The invention generally relates to polyunsaturated fatty acid (PUFA) polyketide synthase (PKS) systems, to homologues thereof, to isolated nucleic acid molecules and recombinant nucleic acid molecules encoding biologically active domains of such a PUFA PKS system, to genetically modified organisms comprising PUFA PKS systems, to methods of making and using such systems for the production of bioactive molecules of interest, and to novel methods for identifying new bacterial and non-bacterial microorganisms having such a PUFA PKS system.

Inventors:  Metz; James G. (Longmont, CO), Weaver; Craig A. (Boulder, CO), Barclay; William R. (Boulder, CO), Flatt; James H. (Colorado Springs, CO) 
Assignee: Martek Biosciences Corporation (Columbia, MD)
 
Appl. No.:  11/778,575
Filed:  July 16, 2007

--------------------------------------------------------------------------------

Related U.S. Patent Documents

--------------------------------------------------------------------------------
     
 Application Number Filing Date Patent Number Issue Date
 11676971 Feb., 2007  
 10810352 Mar., 2004 7211418 
 10124800 Apr., 2002 7247461 
 09231899 Jan., 1999 6566583 
 60457979 Mar., 2003  
 60323269 Sep., 2001  
 60298796 Jun., 2001  
 60284066 Apr., 2001  
 

--------------------------------------------------------------------------------

Current U.S. Class: 800/281 ; 435/134; 435/183; 435/320.1; 435/419; 536/23.2; 800/295; 800/298
Current International Class:  C12N 15/82 (20060101); C12N 15/52 (20060101); C12P 7/64 (20060101)

--------------------------------------------------------------------------------

References Cited [Referenced By]

--------------------------------------------------------------------------------

U.S. Patent Documents
  
5130242 July 1992 Barclay et al.
5246841 September 1993 Yazawa et al.
5310242 May 1994 Golder
5639790 June 1997 Voelker et al.
5672491 September 1997 Khosia et al.
5683898 November 1997 Yazawa et al.
5798259 August 1998 Yazawa et al.
5908622 June 1999 Barclay
6033883 March 2000 Barr et al.
6140486 October 2000 Facciotti et al.
6503706 January 2003 Abken et al.
6566583 May 2003 Facciotti et al.
7001772 February 2006 Roessler et al.
7125672 October 2006 Picataggio et al.
7211418 May 2007 Metz et al.
7214853 May 2007 Facciotti et al.
7217856 May 2007 Weaver et al.
7256022 August 2007 Metz et al.
7256023 August 2007 Metz et al.
7259295 August 2007 Metz et al.
7271315 September 2007 Metz et al.
2002/0138874 September 2002 Mukerji et al.
2002/0156254 October 2002 Qiu et al.
2002/0194641 December 2002 Metz et al.
2004/0005672 January 2004 Santi et al.
2004/0010817 January 2004 Shockey et al.
2004/0139498 July 2004 Jaworski et al.
2004/0172682 September 2004 Kinney et al.
2005/0014231 January 2005 Mukerji et al.
2005/0089865 April 2005 Napier et al.
2005/0164192 July 2005 Graham et al.
2007/0244192 October 2007 Metz
2007/0245431 October 2007 Metz et al.
2007/0256146 November 2007 Metz et al.
2007/0270494 November 2007 Metz et al.
2008/0022422 January 2008 Weaver et al.
2008/0026434 January 2008 Weaver et al.
2008/0026435 January 2008 Weaver et al.
2008/0026438 January 2008 Metz et al.
2008/0026439 January 2008 Metz et al.
2008/0026440 January 2008 Metz et al.
2008/0032351 February 2008 Metz et al.
2008/0038378 February 2008 Metz et al.
2008/0038379 February 2008 Metz et al.
2008/0038790 February 2008 Metz et al.
2008/0038791 February 2008 Metz et al.
2008/0038792 February 2008 Metz et al.
2008/0038793 February 2008 Metz et al.
2008/0038794 February 2008 Metz et al.
2008/0038795 February 2008 Metz et al.
2008/0038796 February 2008 Metz et al.
2008/0038797 February 2008 Metz et al.
2008/0040822 February 2008 Metz et al.
2008/0044867 February 2008 Metz et al.
2008/0044869 February 2008 Metz et al.
2008/0044870 February 2008 Metz et al.
2008/0044871 February 2008 Metz et al.
2008/0044872 February 2008 Metz et al.
2008/0044873 February 2008 Metz et al.
2008/0050790 February 2008 Metz et al.
2008/0148433 June 2008 Metz et al.
 

Foreign Patent Documents
     
 2520795  Oct., 2004  CA
 0594868  May., 1994  EP
 0823475  Feb., 1998  EP
 9323545  Nov., 1993  WO
 9621735  Jul., 1996  WO
 9846764  Oct., 1998  WO
 9855625  Dec., 1998  WO
 WO 02/083870  Oct., 2002  WO
 WO 2004/087879  Oct., 2004  WO
 WO 2006/008099  Jan., 2006  WO
 WO 2006/034228  Mar., 2006  WO
 0042195  Jul., 2007  WO
 

Other References
Abbadi et al., Eur. J. Lipid Sci. Technol., 103:106-113 (2001). cited by other .
Allen et al., Appl. Envir. Microbiol., 65(4):1710-1720 (1999). cited by other .
Bateman et al., Nucl. Acids Res., 30(1):276-280 (2002). cited by other .
Bentley et al., Annu. Rev. Microbiol., 53:411-46 (1999). cited by other .
Bisang et al., Nature, 401:502-505 (1999). cited by other .
Bork, TIG, 12(10):425-427 (1996). cited by other .
Brenner, TIG, 15(4):132-133 (1999). cited by other .
Broun et al., Science, 282:1315-1317 (1998). cited by other .
Creelman et al., Annu. Rev. Plan Physiol. Plant Mol. Biol., 48:355-81 (1997). cited by other .
DeLong & Yayanos, Appl. Environ. Microbiol., 51(4):730-737 (1986). cited by other .
Doerks, TIG, 14(6):248-250 (1998). cited by other .
Facciotti et al., "Cloning and Characterization of Polyunsaturated Fatty Acids (PUFA) Genes from Marine Bacteria" in Proceedings of the international symposium on progress and prospect of marine biotechnology (China Ocean Pres 1999), pp. 404-405 Abstract. cited by other .
Heath et al., J. Biol. Chem., 271(44):27795-27801 (1996). cited by other .
Hopwood & Sherman, Annu. Rev. Genet., 24:37-66 (1990). cited by other .
Hutchinson, Annu. Rev. Microbiol., 49:201-238 (1995). cited by other .
Jostensen & Landfald, FEMS Microbiology Letters, 151:95-101 (1997). cited by other .
Katz & Donadio, Annu. Rev. Microbiol., 47:875-912 (1993). cited by other .
Kealing et al., Curr. Opin. Chem. Biol., 3:598-606 (1999). cited by other .
Kyle et al., HortScience, 25:1523-26 (1990). cited by other .
Magnuson, Microbil. Rev., 57(3):522-542 (1993) Abstract. cited by other .
Metz et al., Science, 293:290-293 (2001). cited by other .
Nakahara, Yukagaku, 44(10):821-7 (1995). cited by other .
Nasu et al., J. Ferment. Bioeng., 122:467-473 (1997). cited by other .
Nichols et al., Curr. Opin. Biotechnol., 10:240-246 (1999). cited by other .
Nogi et al., Extremophiles, 2:1-7 (1998). cited by other .
Parker-Barnes et al., PNAS, 97(15):8284-8289 (2000). cited by other .
Sanchez et al., Chemistry & Biolosy, 8:725-738 (2001). cited by other .
Shanklin et al., Annu. Rev. Plant Physiol. Plant Mol. Biol., 49:611-41 (1998). cited by other .
Smith et al., Nature Biotechnol., 15:1222-1223 (1997). cited by other .
Somerville Am. J. Clin. Nutr., 58(2 supp):270S-275S (1993). cited by other .
Van de Loo, Proc. Natl. Acad. Sci. USA, 92:6743-6747 (1995). cited by other .
Watanabe et al., J. Biochem., 122:467-473 (1997). cited by other .
Yalpani et al., The Plant Cell, 13:1401-1409 (2001). cited by other .
Yazawa, Lipids, 31(supp):S297-S300 (1996). cited by other .
Metz et al. Production of Polyunsaturated Fatty Acids by Polyketide Synthase in Both Prokaryotes and Eukaryotes. Science Jul. 12, 2001, vol. 293, pp. 290-293. cited by other .
Qiu et al. Identification of a delta4 fatty acid desaturase from Thraustochytrium sp. involved in the biosynthesis. J. Biol. Chem. Aug. 24, 2001, vol. 276, No. 34, pp. 31561-31566. cited by other .
Yokochi et al. Optimization of docosahexaenoic acid production. App. Microbiol. Biotechnol. 1998, vol. 49, pp. 72-76. cited by other .
Nakahara et al. Production of docosahexaenoic and docosapentaenoic acids by Schizochytrium sp. isloated from Yap Islands. 1996 J. Am. Oil Chem. Soc. 1996, vol. 73, No. 11, pp. 1421-1426. cited by other .
Weete et al. Lipids and Ultrasctructure of Thrauchytrium sp. ATCC26185. 1997, Am Oil Chem. Soc. vol. 32, No. 8, pp. 839-845. cited by other .
Singh et al. Microbial Production of Docosahexaenoic Acid (DHA, C22:6) Adv. Appl. Microbial, 1997. vol. 45, pp. 271-312. cited by other .
International Search Report for International (PCT) Patent Application No. PCT/US04/09323, mailed Apr. 4, 2007. cited by other .
Written Opinion for International (PCT) Patent Application No. PCT/US04/09323, mailed Apr. 4, 2007. cited by other .
International Preliminary Report on Patentability for International (PCT) Patent Application No. PCT/US04/09323, mailed May 9, 2007. cited by other .
Examiner's First Report for Australian Patent Application No. 2004225485, mailed Nov. 17, 2006. cited by other .
First Examination Report for Indian Patent Application No. 4359/DELNP/2005, dated Mar. 14, 2007. cited by other .
U.S. Appl. No. 11/674,574, filed Feb. 13, 2007, Facciotti et al. cited by other .
U.S. Appl. No. 11/777,277, filed Jul. 12, 2007, Metz et al. cited by other .
U.S. Appl. No. 11/778,594, filed Jul. 16, 2007, Metz et al. cited by other .
Allen E.A. et al. 2002 "Structure and regulation of the omega-3 polyunsaturated fatty acid synthase genes from the deep-sea bacterium Photobacterium profundum strain SS9" Microbiology vol. 148 pp. 1903-1913. cited by other .
Cane et al., "Harnessing the Biosynthetic Code: Combinations, Permutations, and Mutations." Science 1998, vol. 282, pp. 63-68. cited by other .
Chuck et al., "Molecular recognition of diketide substrates by a beta-ketoacyl-acyl carrier protein synthase domain within a bimodular polyketide synthase", Chem and Bio, Current Bio, (London), GB,, vol. 4, No. 10, 1997, pp. 757-766, XP000884721. cited by other .
Database Geneseq 'Online! Dec. 11, 2000, "S. aggregatum PKS cluster ORF6 homolog DNA." XP002368912, retrieved from EBI accession No. GSN:AAA71567Database accession No. AAA71567--& Database Geneseq 'Online! Dec. 11, 2000, "S. aggregatum PKS cluster ORF6 homolog protein." XP002368914 retrieved from EBI accession No. GSP:AAB10482 Database accession No. AAB10482 & WO 00/42195 A (Calgene, LLC) Jul. 20, 2000. cited by other .
GenBank Accession No. AF4091 00, (Allen et al.) 2002. cited by other .
GenBank Accession No. U09865. Alcaligenes eutrophus pyruvate dehydrogenase (pdhA), dihydrolipoamide acetyltransferase (pdhB), dihydrolipoamide dehydrogenase (pdhL), and ORF3 genes, complete cds (1994). cited by other .
Harlow et al. Antibodies: A Laboratory Manual (1988) Cold Spring Harbor Laboratory Press, p. 76. cited by other .
Jez et al., "Structural control of polyketide formation in plant-specific polyketide synthases", Chem and Bio (London), vol. 7, No. 12, Dec. 2000, pp. 919-930, XP002338564. cited by other .
Kaulmann et al. "Biosynthesis of Polyunsaturated Fatty Acids by Polyketide Synthases", Angew. Chem. Int. Ed. 2002, 41, No. 11, pp. 1866-1869. cited by other .
Kealey et al., "Production of a polyketide natural product in non-polyketide-producing prokaryotic and eukaryotic hosts", Proceedings of the National Academy of Sciences of the United States of America, vol. 95, No. 2, Jan. 20, 1998, pp. 505-509, XP002338563. cited by other .
Khosla et al., "Tolerance and Specificity of Polyketide Synthases", Annu. Rev. Biochem. 1999. 68:219-253. cited by other .
Leadlay PF. "Combinatorial Approaches to Polyketides Biosynthesis" Current Opinion in Chemical Biology (1997) 1: 162-168. cited by other .
Nasu et al., "Efficient Transformation of Marchantia polymorpha That is Haploid and Has Very Small Genome DNA," Journal of Fermentation and Bioengineering vol. 84, No. 6, 519-523 1997. cited by other .
Nicholson et al., "Design and utility of oligonucleotide gene probes for fungal polyketide synthases", Chem & Bio (London) vol. 8, No. 2, Feb. 2001, pp. 157-178, XP002338562. cited by other .
Oliynuk et al. "A hybrid modular polyketide synthase obtained by domain swapping." Chemistry & Biology (1996) 3: 833-839. cited by other .
Orikasa et al. Characterization of the eicosapentaenoic acid biosynthesis gene cluster from Shewanella sp. strain SCRC-2738, Cellular and Molecular Biology (Noisy-le-grand), Jul. 2004, vol. 50, No. 5, pp. 625-630. cited by other .
Satomi et al. Shewanelia marinintesina sp. nov., Shewanella schlegeliana sp. nov. and Shewanelia sairae sp. nov., novel eicosapentaenoic-acid-producing marine bacteria isolated from see-animal intestines. Internat. J. Syst. Evol. Microbiol. 2003, vol. 53, pp. 491-499. cited by other .
Takeyama et al. Expression of eicosapentaenoic acid synthesis gene clustter from Shewanella sp. in transgenic marine cyanobacterium. Synechecoccus sp. Microbiology. 1997, vol. 143, pp. 2725-2731. cited by other .
UniProt Accession No. Q93CG6.sub.--PHOPR, (Allen et al.) 2002. cited by other .
Wallis et al., "Polyunsaturated fatty acid synthesis: what will they think of next?", Tibs Trends in Bio Sciences, Elsevier Publ., Cambridge, EN, vol. 27, No. 9, Sep. 2002, pp. 467-473, XP004378766. cited by other .
Wiesmann et al. "The molecular basis of Celmer's rules: the stereochemistry of the condensation step in chain extension on the erythromycin polyketide synthase." Biochemistry (1997) 36: 13849-13855. cited by other .
Wiesmann et al. "Origin of starter units for erythromycin biosynthesis." Biochemistry (1998) 37: 11012-11017. cited by other .
Wiesmann et al. "Polyketide synthesis in vitro on a modular polyketide synthase." Chemistry & Biology (Sep. 1995) 2: 583-589. cited by other .
International Search Report for International (PCT) Patent Application No. PCT/US02/12254, mailed Nov. 15, 2002. cited by other .
International Preliminary Examination Report for International (PCT) Patent Application No. PCT/US02/12254, mailed Oct. 16, 2006. cited by other .
International Search Report for International (PCT) Patent Application No. PCT/US00/00956, mailed Jul. 6, 2000. cited by other .
Written Opinion for International (PCT) Patent Application No. PCT/US00/00956, mailed Dec. 19, 2000. cited by other .
International Preliminary Examination Report for International (PCT) Patent Application No. PCT/US00/00956, mailed Apr. 19, 2001. cited by other .
International Search Report for International (PCT) Patent Application No. PCT/US05/36998, mailed Mar. 22, 2007. cited by other .
Written Opinion for International (PCT) Patent Application No. PCT/US05/36998, mailed Mar. 22, 2007. cited by other .
International Search Report for International (PCT) Patent Application No. PCT/US08/63835, mailed Nov. 3, 2008. cited by other .
Written Opinion for International (PCT) Patent Application No. PCT/US08/63835, mailed Nov. 3, 2008. cited by other .
International Search Report for International (PCT) Patent Application No. PCT/US06/22893, mailed Feb. 29, 2008. cited by other .
Written Opinion for International (PCT) Patent Application No. PCT/US06/22893, mailed Feb. 29, 2008. cited by other .
International Search Report for International (PCT) Patent Application No. PCT/US07/64105, mailed Nov. 23, 2007. cited by other .
Written Opinion for International (PCT) Patent Application No. PCT/US07/64105, mailed Nov. 23, 2007. cited by other .
International Preliminary Report on Patentability for International (PCT) Patent Application No. PCT/US07/64105, mailed Sep. 25, 2008. cited by other .
International Search Report for International (PCT) Patent Application No. PCT/US07/64104, mailed Dec. 5, 2008. cited by other .
Written Opinion for International (PCT) Patent Application No. PCT/US07/64104, mailed Dec. 5, 2008. cited by other .
International Search Report for International (PCT) Patent Application No. PCT/US2007/064106, mailed Sep. 16, 2008. cited by other .
Written Opinion for International (PCT) Patent Application No. PCT/US2007/064106, mailed Sep. 16, 2008. cited by other .
International Preliminary Report on Patentability for International (PCT) Patent Application No. PCT/US2007/064106, mailed Oct. 30, 2008. cited by other .
Napier, Trends Plant Sci. Feb. 2002; 7(2): 51-4. cited by other .
Fan K W et al: "Eicosapentaenoic and docosahexaenoic acids production by and okara-utilizing potential of thraustochytrids" Journal of Industrial Microbiology and Biotechnology, Basingstoke, GB, vol. 27, No. 4, Oct. 1, 2001 (Oct. 1, 2001), pp. 199-202, XP002393382 ISSN: 1367-5435. cited by other .
Wolff et al, Arachidonic, Eicosapentaenoic and Biosynthetically Related Fatty Acids in Seed Lipids from a primitive Gymnosperm, Agathis robusta. Lipids 34(10), 1994, 1083-1097. cited by other .
Grimsley et al, "Fatty acid composition of mutants of the moss Physcomitrella patens" Phytochemistry 20(7): 1519-1524, 1981. cited by other .
Bedford et al, "A functional chimeric modular polyketide synthase generated via domain replacement." Chemistry & Biology 3: 827 -831, Oct. 1996. cited by other. 

Primary Examiner: Desai; Anand U
Assistant Examiner: Moore; William W
Attorney, Agent or Firm: Sheridan Ross P.C.

--------------------------------------------------------------------------------

Parent Case Text

--------------------------------------------------------------------------------

CROSS-REFERENCE TO RELATED APPLICATIONS

This application is a divisional of U.S. application Ser. No. 11/676,971, filed Feb. 20, 2007, which is a divisional of U.S. application Ser. No. 10/810,352, filed Mar. 26, 2004, now U.S. Pat. No. 7,211,418, which claims the benefit of priority under 35 U.S.C. .sctn. 119(e) from U.S. Provisional Application Ser. No. 60/457,979, filed Mar. 26, 2003, entitled "Modification of a Schizochytrium PKS System to Facilitate Production of Lipids Rich in Polyunsaturated Fatty Acids". U.S. application Ser. No. 10/810,352 is also a continuation-in-part of U.S. patent application Ser. No. 10/124,800, filed Apr. 16, 2002, now U.S. Pat. No. 7,247,461, which claims the benefit of priority under 35 U.S.C. .sctn. 119(e) to: U.S. Provisional Application Ser. No. 60/284,066, filed Apr. 16, 2001; U.S. Provisional Application Ser. No. 60/298,796, filed Jun. 15, 2001; and U.S. Provisional Application Ser. No. 60/323,269, filed Sep. 18, 2001. U.S. patent application Ser. No. 10/124,800, supra, is also a continuation-in-part of U.S. application Ser. No. 09/231,899, filed Jan. 14, 1999, now U.S. Pat. No. 6,566,583. Each of the above-identified patent applications is incorporated herein by reference in its entirety.

This application does not claim the benefit of priority from U.S. application Ser. No. 09/090,793, filed Jun. 4, 1998, now U.S. Pat. No. 6,140,486, although U.S. application Ser. No. 09/090,793 is incorporated herein by reference in its entirety.
--------------------------------------------------------------------------------

Claims

--------------------------------------------------------------------------------

What is claimed is:

1. A genetically modified plant, wherein cells of the plant are transfected with at least one recombinant nucleic acid molecule encoding a polyketide synthase (PKS) system for the production of polyunsaturated fatty acids (PUFAs), wherein the PKS system comprises the following proteins: a) a protein comprising an amino acid sequence that is at least 95% identical to SEQ ID NO:39 and has .beta.-keto acyl-ACP synthase (KS) activity, malonyl-CoA:ACP acyltransferase (MAT) activity, acyl carrier protein (ACP) activity and ketoreductase (KR) activity; b) a protein comprising an amino acid sequence that is at least 95% identical to SEQ ID NO:52 and has .beta.-keto acyl-ACP synthase (KS) activity, chain length factor (CLF) activity, acyl transferase (AT) activity, and enoyl ACP-reductase (ER) activity; and c) a protein comprising an amino acid sequence that is at least 95% identical to SEQ ID NO:62 and has FabA-like .beta.-hydroxy acyl-ACP dehydrase (DH) activity and enoyl ACP-reductase (ER) activity.

2. The genetically modified plant of claim 1, wherein the protein of (a) comprises the amino acid sequence of SEQ ID NO:39.

3. The genetically modified plant of claim 1, wherein the protein of (b) comprises the amino acid sequence of SEQ ID NO:52.

4. The genetically modified plant of claim 1, wherein the protein of (c) comprises the amino acid sequence of SEQ ID NO:62.

5. The genetically modified plant of claim 1, wherein the PKS system comprises: a) a protein comprising the amino acid sequence of SEQ ID NO:39; b) a protein comprising the amino acid sequence of SEQ ID NO:52; and c) a protein comprising the amino acid sequence of SEQ ID NO:62.

6. The genetically modified plant of claim 1, wherein the protein of (a) is encoded by SEQ ID NO:38.

7. The genetically modified plant of claim 1, wherein the protein of (b) is encoded by SEQ ID NO:51.

8. The genetically modified plant of claim 1, wherein the protein of (c) is encoded by SEQ ID NO:61.

9. The genetically modified plant of claim 1, wherein cells of the plant have been further transfected with a phosphopantetheinyl transferase (PPTase).

10. The genetically modified plant of claim 1, wherein the plant produces docosahexaenoic acid (DHA).

11. The genetically modified plant of claim 1, wherein the plant produces docosahexaenoic acid (DHA) and docosapentaenoic acid (DPA).

12. The genetically modified plant of claim 1, wherein the plant produces a polyunsaturated fatty acid (PUFA) profile that differs from the naturally occurring plant without a genetic modification.

13. A recombinant plant cell, wherein the plant cell expresses at least one recombinant nucleic acid molecule encoding a polyketide synthase (PKS) system for the production of polyunsaturated fatty acids (PUFAs), wherein the PKS system comprises the following proteins: a) a protein comprising an amino acid sequence that is at least 95% identical to SEQ ID NO:39 and has .beta.-keto acyl-ACP synthase (KS) activity, malonyl-CoA:ACP acyltransferase (MAT) activity, acyl carrier protein (ACP) activity and ketoreductase (KR) activity; b) a protein comprising an amino acid sequence that is at least 95% identical to SEQ ID NO:52 and has .beta.-keto acyl-ACP synthase (KS) activity, chain length factor (CLF) activity, acyl transferase (AT) activity, and enoyl ACP-reductase (ER) activity; and c) a protein comprising an amino acid sequence that is at least 95% identical to SEQ ID NO:62 and has FabA-like .beta.-hydroxy acyl-ACP dehydrase (DH) activity and enoyl ACP-reductase (ER) activity.

14. The recombinant plant cell of claim 13, wherein the protein of (a) comprises the amino acid sequence of SEQ ID NO:39.

15. The recombinant plant cell of claim 13, wherein the protein of (b) comprises the amino acid sequence of SEQ ID NO:52.

16. The recombinant plant cell of claim 13, wherein the protein of (c) comprises the amino acid sequence of SEQ ID NO:62.

17. The recombinant plant cell of claim 13, wherein the PKS system comprises: a) a protein comprising the amino acid sequence of SEQ ID NO:39; b) a protein comprising the amino acid sequence of SEQ ID NO:52; and c) a protein comprising the amino acid sequence of SEQ ID NO:62.

18. The recombinant plant cell of claim 13, wherein the protein of (a is encoded by SEQ ID NO:38.

19. The recombinant plant cell of claim 13, wherein the protein of (b) is encodec by SEQ ID NO:51.

20. The recombinant plant cell of claim 13, wherein the protein of (c) is encodec by SEQ ID NO:61.

21. A method to produce a genetically modified plant that has a polyunsaturated fatty acid (PUFA) profile that differs from the naturally occurring plant and that produces at least one long chain polyunsaturated fatty acid (PUFA), comprising transfecting plant cells with at least one recombinant nucleic acid molecule encoding a polyketide synthase (PKS) system for the production of polyunsaturated fatty acids (PUFAs) and producing the plant using the plant cells, wherein the PKS system comprises the following proteins: a) a protein comprising an amino acid sequence that is at least 95% identical to SEQ ID NO39 and has 13-keto acyl-ACP synthase (KS) activity, malonyl-CoA:ACP acyltransferase (MAT) activity, acyl carrier protein (ACP) activity and ketoreductase (KR) activity; b) a protein comprising an amino acid sequence that is at least 95% identical to SEQ ID NO:52 and has 13-keto acyl-ACP synthase (KS) activity, chain length factor (CLF) activity, acyl transferase (AT) activity, and enoyl ACP-reductase (ER) activity; and c) a protein comprising an amino acid sequence that is at least 95% identical to SEQ ID NO:62 and has FabA-like .beta.-hydroxy acyl-ACP dehydrase (DH) activity and enoyl ACP-reductase (ER) activity.
--------------------------------------------------------------------------------
 
Description

--------------------------------------------------------------------------------

REFERENCE TO SEQUENCE LISTING

This application contains a Sequence Listing submitted as an electronic text file named "Sequence_Listing.txt", having a size in bytes of 593 kb, and created on 26 Mar. 2004. The information contained in this electronic file is hereby incorporated by reference in its entirety pursuant to 37 CFR .sctn.1.52(e)(5).

FIELD OF THE INVENTION

This invention relates to polyunsaturated fatty acid (PUFA) polyketide synthase (PKS) systems from microorganisms, including eukaryotic organisms, such as Thraustochytrid microorganisms. More particularly, this invention relates to nucleic acids encoding non-bacterial PUFA PKS systems, to non-bacterial PUFA PKS systems, to genetically modified organisms comprising non-bacterial PUFA PKS systems, and to methods of making and using the non-bacterial PUFA PKS systems disclosed herein. This invention also relates to genetically modified microorganisms and methods to efficiently produce lipids (triacylglyerols (TAG), as well as membrane-associated phospholipids (PL)) enriched in various polyunsaturated fatty acids (PUFAs) and particularly, eicosapentaenoic acid (C20:5, .omega.-3; EPA) by manipulation of a PUFA polyketide synthase (PKS) system.

BACKGROUND OF THE INVENTION

Polyketide synthase (PKS) systems are generally known in the art as enzyme complexes derived from fatty acid synthase (FAS) systems, but which are often highly modified to produce specialized products that typically show little resemblance to fatty acids. It has now been shown, however, that polyketide synthase systems exist in marine bacteria and certain microalgae that are capable of synthesizing PUFAs from malonyl-CoA. The PKS pathways for PUFA synthesis in Shewanella and another marine bacteria, Vibrio marinus, are described in detail in U.S. Pat. No. 6,140,486. The PKS pathways for PUFA synthesis in the eukaryotic Thraustochytrid, Schizochytrium is described in detail in U.S. Pat. No. 6,566,583. Finally, the PKS pathways for PUFA synthesis in eukaryotes such as members of Thraustochytriales, including the complete structural description of the PUFA PKS pathway in Schizochytrium and the identification of the PUFA PKS pathway in Thraustochytrium, including details regarding uses of these pathways, are described in detail in U.S. Patent Application Publication No. 20020194641, published Dec. 19, 2002 (corresponding to U.S. patent application Ser. No. 10/124,800, filed Apr. 16, 2002).

Researchers have attempted to exploit polyketide synthase (PKS) systems that have been described in the literature as falling into one of three basic types, typically referred to as: Type II, Type I and modular. The Type II system is characterized by separable proteins, each of which carries out a distinct enzymatic reaction. The enzymes work in concert to produce the end product and each individual enzyme of the system typically participates several times in the production of the end product. This type of system operates in a manner analogous to the fatty acid synthase (FAS) systems found in plants and bacteria. Type I PKS systems are similar to the Type II system in that the enzymes are used in an iterative fashion to produce the end product. The Type I differs from Type II in that enzymatic activities, instead of being associated with separable proteins, occur as domains of largerproteins. This system is analogous to the Type I FAS systems found in animals and fungi.

In contrast to the Type I and II systems, in modular PKS systems, each enzyme domain is used only once in the production of the end product. The domains are found in very large proteins and the product of each reaction is passed on to another domain in the PKS protein. Additionally, in all of the PKS systems described above, if a carbon-carbon double bond is incorporated into the end product, it is always in the trans configuration.

In the Type I and Type II PKS systems described above, the same set of reactions is carried out in each cycle until the end product is obtained. There is no allowance for the introduction of unique reactions during the biosynthetic procedure. The modular PKS systems require huge proteins that do not utilize the economy of iterative reactions (i.e., a distinct domain is required for each reaction). Additionally, as stated above, carbon-carbon double bonds are introduced in the trans configuration in all of the previously described PKS systems.

Polyunsaturated fatty acids (PUFAs) are critical components of membrane lipids in most eukaryotes (Lauritzen et al., Prog. Lipid Res. 40 1 (2001); McConn et al., Plant J. 15, 521 (1998)) and are precursors of certain hormones and signaling molecules (Heller et al., Drugs 55, 487 (1998); Creelman et al., Annu. Rev. Plant Physiol. Plant Mol. Biol. 48, 355 (1997)). Known pathways of PUFA synthesis involve the processing of saturated 16:0 or 18:0 fatty acids (the abbreviationX:Y indicates an acyl group containing X carbon atoms and Y double bonds (usually cis in PUFAs); double-bond positions of PUFAs are indicated relative to the methyl carbon of the fatty acid chain (.omega.3 or .omega.6) with systematic methylene interruption of the double bonds) derived from fatty acid synthase (FAS) by elongation and aerobic desaturation reactions (Sprecher, Curr. Opin. Clin. Nutr. Metab. Care 2, 135 (1999); Parker-Barnes et al., Proc. Natl. Acad. Sci. USA 97, 8284 (2000); Shanklin et al., Annu. Rev. Plant Physiol. Plant Nol. Biol. 49, 611 (1998)). Starting from acetyl-CoA, the synthesis of docosahexaenoic acid (DHA) requires approximately 30 distinct enzyme activities and nearly 70 reactions including the four repetitive steps of the fatty acid synthesis cycle. Polyketide synthases (PKSs) carry out some of the same reactions as FAS (Hopwood et al., Annu. Rev. Genet. 24, 37 (1990); Bentley et al., Annu. Rev. Microbiol. 53, 411 (1999)) and use the same small protein (or domain), acyl carrier protein (ACP), as a covalent attachment site for the growing carbon chain. However, in these enzyme systems, the complete cycle of reduction, dehydration and reduction seen in FAS is often abbreviated so that a highly derivatized carbon chain is produced, typically containing many keto- and hydroxy-groups as well as carbon-carbon double bonds in the trans configuration. The linear products of PKSs are often cyclized to form complex biochemicals that include antibiotics and many other secondary products (Hopwood et al., (1990) supra; Bentley et al., (1999), supra; Keating et al., Curr. Opin. Chem. Biol. 3, 598 (1999)).

Very long chain PUFAs such as docosahexaenoic acid (DHA; 22:6.omega.3) and eicosapentaenoic acid (EPA; 20:5.omega.63) have been reported from several species of marine bacteria, including Shewanella sp (Nichols et al., Curr. Op. Biotechnol. 10, 240 (1999); Yazawa, Lipids 31, S (1996); DeLong et al., Appl. Environ. Microbiol. 51, 730 (1986)). Analysis of a genomic fragment (cloned as plasmid pEPA) from Shewanella sp. strain SCRC2738 led to the identification of five open reading frames (Orfs), totaling 20 Kb, that are necessary and sufficient for EPA production in E. coli (Yazawa, (1996), supra). Several of the predicted protein domains were homologues of FAS enzymes, while other regions showed no homology to proteins of known function. At least 11 regions within the five Orfs were identifiable as putative enzyme domains (See Metz et al., Science 293:290-293 (2001)). When compared with sequences in the gene databases, seven of these were more strongly related to PKS proteins than to FAS proteins. Included in this group were domains putatively encoding malonyl-CoA:ACP acyltransferase (MAT), .beta.-ketoacyl-ACP synthase (KS), .beta.-ketoacyl-ACP reductase (KR), acyltransferase (AT), phosphopantetheine transferase, chain length (or chain initiation) factor (CLF) and a highly unusual cluster of six ACP domains (i.e., the presence of more than two clustered ACP domains had not previously been reported in PKS or FAS sequences). It is likely that the PKS pathway for PUFA synthesis that has been identified in Shewanella is widespread in marine bacteria. Genes with high homology to the Shewanella gene cluster have been identified in Photobacterium profundum (Allen et al., Appli. Environ. Microbiol. 65:1710 (1999)) and in Moritella marina (Vibrio marinus) (see U.S. Pat. No. 6,140,486, ibid., and Tanaka et al., Biotechnol. Lett. 21:939 (1999)).

Polyunsaturated fatty acids (PUFAs) are considered to be useful for nutritional, pharmaceutical, industrial, and other purposes. An expansive supply of PUFAs from natural sources and from chemical synthesis are not sufficient for commercial needs. A major current source for PUFAs is from marine fish; however, fish stocks are declining, and this may not be a sustainable resource. Additionally, contamination, both heavy metal and toxic organic molecules, is a serious issue with oil derived from marine fish. Vegetable oils derived from oil seed crops are relatively inexpensive and do not have the contamination issues associated with fish oils. However, the PUFAs found in commercially developed plant oils are typically limited to linoleic acid (eighteen carbons with 2 double bonds, in the delta 9 and 12 positions--18:2 delta 9,12) and linolenic acid (18:3 delta 9,12,15). In the conventional pathway for PUFA synthesis, medium chain-length saturated fatty acids (products of a fatty acid synthase (FAS) system) are modified by a series of elongation and desaturation reactions. Because a number of separate desaturase and elongase enzymes are required for fatty acid synthesis from linoleic and linolenic acids to produce the more saturated and longer chain PUFAs, engineering plant host cells for the expression of PUFAs such as EPA and docosahexaenoic acid (DHA) may require expression of several separate enzymes to achieve synthesis. Additionally, for production of useable quantities of such PUFAs, additional engineering efforts may be required, for example, engineering the down regulation of enzymes that compete for substrate, engineering of higher enzyme activities such as by mutagenesis or targeting of enzymes to plastid organelles. Therefore it is of interest to obtain genetic material involved in PUFA biosynthesis from species that naturally produce these fatty acids and to express the isolated material alone or in combination in a heterologous system which can be manipulated to allow production of commercial quantities of PUFAs.

The discovery of a PUFA PKS system in marine bacteria such as Shewanella and Vibrio marinus (see U.S. Pat. No. 6,140,486, ibid.) provides a resource for new methods of commercial PUFA production. However, these marine bacteria have limitations which may ultimately restrict their usefulness on a commercial level. First, although U.S. Pat. No. 6,140,486 discloses that these marine bacteria PUFA PKS systems can be used to genetically modify plants, the marine bacteria naturally live and grow in cold marine environments and the enzyme systems of these bacteria do not function well above 22.degree. C.

In contrast, many crop plants, which are attractive targets for genetic manipulation using the PUFA PKS system, have normal growth conditions at temperatures above 22.degree. C. and ranging to higher than 40.degree. C. Therefore, the PUFA PKS systems from these marine bacteria are not predicted to be readily adaptable to plant expression under normal growth conditions. Additionally, the known marine bacteria PUFA PKS systems do not directly produce triacylglyerols (TAG), whereas direct production of TAG would be desirable because TAG are a lipid storage product, and as a result, can be accumulated at very high levels in cells, as opposed to a "structural" lipid product (e.g. phospholipids), which can generally only accumulate at low levels.

With regard to the production of eicosapentaenoic acid (EPA) in particular, researchers have tried to produce EPA with microbes by growing them in both photosynthetic and heterotrophic cultures. They have also used both classical and directed genetic approaches in attempts to increase the productively of the organisms under culture conditions. Other researchers have attempted to produce EPA in oil-seed crop plants by introduction of genes encoding various desaturase and elongase enzymes.

Researchers have attempted to use cultures of red microalgae (Monodus), diatoms (e.g. Phaeodactylum), other microalgae and fungi (e.g. Mortierella cultivated at low temperatures). However, in all cases, productivity was low compared to existing commercial microbial production systems for other long chain PUFAs such as DHA. In many cases, the EPA occurred primarily in the phospholipids (PL) rather than the triacylglycerols (TAG). Since productivity of microalgae under heterotrophic growth conditions can be much higher than under phototrophic conditions, researchers have attempted, and achieved, trophic conversion by introduction of genes encoding specific sugar transporters. However, even with the newly acquired heterotrophic capability, productivity in terms of oil remained relatively low.

Efforts to produce EPA in oil-seed crop plants by modification of the endogenous fatty acid biosynthesis pathway have only yielded plants with very low levels of the PUFA in their oils. As discussed above, several marine bacteria have been shown to produce PUFAs (EPA as well as DHA). However, these bacteria do not produce TAG and the EPA is found primarily in the PL membranes. The levels of EPA produced as well as the growth characteristics of these particular marine bacteria (discussed above) limit their utility for commercial production of EPA.

Therefore, there is a need in the art for other PUFA PKS systems having greater flexibility for commercial use, and for a biological system that efficiently produces quantities of lipids (PL and TAG) enriched in desired PUFAs, such as EPA, in a commercially useful production process.

SUMMARY OF THE INVENTION

One embodiment of the present invention relates to an isolated nucleic acid molecule.

The nucleic acid molecule comprises a nucleic acid sequence selected from: (a) a nucleic acid sequence encoding an amino acid sequence selected from the group consisting of: SEQ ID NO:39, SEQ ID NO:41, SEQ ID NO:43, SEQ ID NO:45, SEQ ID NO:48, SEQ ID NO:50, SEQ ID NO:52, SEQ ID NO:54, SEQ ID NO:56, SEQ ID NO:58, SEQ ID NO:60, SEQ ID NO:62, SEQ ID NO:64, SEQ ID NO:66, SEQ ID NO:68 and biologically active fragments thereof; (b) a nucleic acid sequence encoding an amino acid sequence that is at least about 60% identical, and more preferably at least about 70% identical, and more preferably at least about 80% identical, and more preferably at least about 90% identical, to an amino acid sequence selected from the group consisting of: SEQ ID NO:39, SEQ ID NO:43, SEQ ID NO:50, SEQ ID NO:52, SEQ ID NO:56 and SEQ ID NO:58, wherein the amino acid sequence has a biological activity of at least one domain of a polyunsaturated fatty acid (PUFA) polyketide synthase (PKS) system; (c) a nucleic acid sequence encoding an amino acid sequence that is at least about 65% identical, and more preferably at least about 70% identical, and more preferably at least about 80% identical, and more preferably at least about 90% identical, to SEQ ID NO:54, wherein the amino acid sequence has a biological activity of at least one domain of a polyunsaturated fatty acid (PUFA) polyketide synthase (PKS) system; (d) a nucleic acid sequence encoding an amino acid sequence that is at least about 70% identical, and more preferably at least about 80% identical, and more preferably at least about 90% identical, to an amino acid sequence selected from the group consisting of: SEQ ID NO:45, SEQ ID NO:48, SEQ ID NO:60, SEQ ID NO:62 and SEQ ID NO:64, wherein the amino acid sequence has a biological activity of at least one domain of a polyunsaturated fatty acid (PUFA) polyketide synthase (PKS) system; (e) a nucleic acid sequence encoding an amino acid sequence that is at least about 80% identical, and more preferably at least about 90% identical, to an amino acid sequence selected from the group consisting of: SEQ ID NO:41, SEQ ID NO:66, SEQ ID NO:68, wherein the amino acid sequence has a biological activity of at least one domain of a polyunsaturated fatty acid (PUFA) polyketide synthase (PKS) system; and/or (f) a nucleic acid sequence that is fully complementary to the nucleic acid sequence of (a), (b), (c), (d), or (e). In one aspect, the nucleic acid sequence encodes an amino acid sequence selected from: SEQ ID NO:39, SEQ ID NO:41, SEQ ID NO:43, SEQ ID NO:45, SEQ ID NO:48, SEQ ID NO:50, SEQ ID NO:52, SEQ ID NO:54, SEQ ID NO:56, SEQ ID NO:58, SEQ ID NO:60, SEQ ID NO:62, SEQ ID NO:64, SEQ ID NO:66, SEQ ID NO:68, and biologically active fragments thereof. In one aspect, the nucleic acid sequence is selected from the group consisting of: SEQ ID NO:38, SEQ ID NO:40, SEQ ID NO:42, SEQ ID NO:44, SEQ ID NO:47, SEQ ID NO:49, SEQ ID NO:51, SEQ ID NO:53, SEQ ID NO:55, SEQ ID NO:57, SEQ ID NO:59, SEQ ID NO:61, SEQ ID NO:63, SEQ ID NO:65, and SEQ ID NO:67.

Another embodiment of the present invention relates to a recombinant nucleic acid molecule comprising any of the above-described nucleic acid molecules, operatively linked to at least one transcription control sequence.

Yet another embodiment of the present invention relates to a recombinant cell transfected with any of the above-described recombinant nucleic acid molecules.

Another embodiment of the present invention relates to a genetically modified microorganism, wherein the microorganism expresses a PKS system comprising at least one biologically active domain of a polyunsaturated fatty acid (PUFA) polyketide synthase (PKS) system, wherein the at least one domain of the PUFA PKS system comprises an amino acid sequence selected from: (a) an amino acid sequence selected from the group consisting of: SEQ ID NO:39, SEQ ID NO:41, SEQ ID NO:43, SEQ ID NO:45, SEQ ID NO:48, SEQ ID NO:50, SEQ ID NO:52, SEQ ID NO:54, SEQ ID NO:56, SEQ ID NO:58, SEQ ID NO:60, SEQ ID NO:62, SEQ ID NO:64, SEQ ID NO:66, SEQ ID NO:68 and biologically active fragments thereof; (b) an amino acid sequence that is at least about 60% identical, and more preferably at least about 70% identical, and more preferably at least about 80% identical, and more preferably at least about 90% identical, to an amino acid sequence selected from the group consisting of: SEQ ID NO:39, SEQ ID NO:43, SEQ ID NO:50, SEQ ID NO:52, SEQ ID NO:56 and SEQ ID NO:58, wherein the amino acid sequence has a biological activity of at least one domain of a polyunsaturated fatty acid (PUFA) polyketide synthase (PKS) system; (c) an amino acid sequence that is at least about 65% identical, and more preferably at least about 70% identical, and more preferably at least about 80% identical, and more preferably at least about 90% identical, to SEQ ID NO:54, wherein the amino acid sequence has a biological activity of at least one domain of a polyunsaturated fatty acid (PUFA) polyketide synthase (PKS) system; (d) an amino acid sequence that is at least about 70% identical, and more preferably at least about 80% identical, and more preferably at least about 90% identical, to an amino acid sequence selected from the group consisting of: SEQ ID NO:45, SEQ ID NO:48, SEQ ID NO:60, SEQ ID NO:62 and SEQ ID NO:64, wherein the amino acid sequence has a biological activity of at least one domain of a polyunsaturated fatty acid (PUFA) polyketide synthase (PKS) system; and/or (e) an amino acid sequence that is at least about 80% identical, and more preferably at least about 90% identical, to an amino acid sequence selected from the group consisting of: SEQ ID NO:41, SEQ ID NO:66, SEQ ID NO:68, wherein the amino acid sequence has a biological activity of at least one domain of a polyunsaturated fatty acid (PUFA) polyketide synthase (PKS) system. The microorganism is genetically modified to affect the activity of the PKS system.

In one aspect, the microorganism is genetically modified by transfection with a recombinant nucleic acid molecule encoding the at least one domain of a polyunsaturated fatty acid (PUFA) polyketide synthase (PKS) system. For example, the microorganism can include a Thraustochytrid, such as a Schizochytrium. In one aspect, such a microorganism has been further genetically modified to recombinantly express at least one nucleic acid molecule encoding at least one biologically active domain from a PKS system selected from the group consisting of: a bacterial PUFA PKS system, a Type I PKS system, a Type II PKS system, a modular PKS system, and a non-bacterial PUFA PKS system. The non-bacterial PUFA PKS system can include a Thraustochytrid PUFA PKS system and in one aspect, a Schizochytrium PUFA PKS system.

In another aspect, the microorganism endogenously expresses a PKS system comprising the at least one domain of the PUFA PKS system, and wherein the genetic modification is in a nucleic acid sequence encoding at least one domain of the PUFA PKS system. In another aspect, such a microorganism has been further genetically modified to recombinantly express at least one nucleic acid molecule encoding at least one biologically active domain from a PKS system selected from the group consisting of: a bacterial PUFA PKS system, a Type I PKS system, a Type II PKS system, a modular PKS system, and a non-bacterial PUFA PKS system (e.g., a Thraustochytrid PUFA PKS system, such as a Schizochytrium PUFA PKS system).

In another aspect, the microorganism endogenously expresses a PUFA PKS system comprising the at least one biologically active domain of a PUFA PKS system, and wherein the genetic modification comprises expression of a recombinant nucleic acid molecule selected from the group consisting of a recombinant nucleic acid molecule encoding at least one biologically active domain from a second PKS system and a recombinant nucleic acid molecule encoding a protein that affects the activity of the endogenous PUFA PKS system. The biologically active domain from a second PKS system can include, but is not limited to: (a) a domain of a polyunsaturated fatty acid (PUFA) polyketide synthase (PKS) system from a Thraustochytrid microorganism; (b) a domain of a PUFA PKS system from a microorganism identified by the following method: (i) selecting a microorganism that produces at least one PUFA; and, (ii) identifying a microorganism from (i) that has an ability to produce increased PUFAs under dissolved oxygen conditions of less than about 5% of saturation in the fermentation medium, as compared to production of PUFAs by the microorganism under dissolved oxygen conditions of greater than about 5% of saturation in the fermentation medium; (c) a domain comprising an amino acid sequence selected from the group consisting of: SEQ ID NO:2, SEQ ID NO:4, SEQ ID NO:6, SEQ ID NO:8, SEQ ID NO:10, SEQ ID NO:13, SEQ ID NO:18, SEQ ID NO:20, SEQ ID NO:22, SEQ ID NO:24, SEQ ID NO:26, SEQ ID NO:28, SEQ ID NO:30, SEQ ID NO:32, and biologically active fragments thereof; and (d) a domain comprising an amino acid sequence that is at least about 60% identical, and more preferably at least about 70% identical, and more preferably at least about 80% identical, and more preferably at least about 90% identical, to the amino acid sequence of (c), wherein the amino acid sequence has a biological activity of at least one domain of a polyunsaturated fatty acid (PUFA) polyketide synthase (PKS) system. In one aspect, recombinant nucleic acid molecule encodes a phosphopantetheine transferase. In one aspect, the second PKS system is selected from the group consisting of: a bacterial PUFA PKS system, a type I PKS system, a type II PKS system, a modular PKS system, and a non-bacterial PUFA PKS system (e.g., a eukaryotic PUFA PKS system, such as a Thraustochytrid PUFA PKS system, including, but not limited to a Schizochytrium PUFA PKS system).

Yet another embodiment of the present invention relates to a genetically modified plant, wherein the plant has been genetically modified to recombinantly express a PKS system comprising at least one biologically active domain of a polyunsaturated fatty acid (PUFA) polyketide synthase (PKS) system, wherein the domain comprises an amino acid sequence selected from the group consisting of: (a) an amino acid sequence selected from the group consisting of: SEQ ID NO:39, SEQ ID NO:41, SEQ ID NO:43, SEQ ID NO:45, SEQ ID NO:48, SEQ ID NO:50, SEQ ID NO:52, SEQ ID NO:54, SEQ ID NO:56, SEQ ID NO:58, SEQ ID NO:60, SEQ ID NO:62, SEQ ID NO:64, SEQ ID NO:66, SEQ ID NO:68 and biologically active fragments thereof; (b) an amino acid sequence that is at least about 60% identical, and more preferably at least about 70% identical, and more preferably at least about 80% identical, and more preferably at least about 90% identical, to an amino acid sequence selected from the group consisting of: SEQ ID NO:39, SEQ ID NO:43, SEQ ID NO:50, SEQ ID NO:52, SEQ ID NO:56 and SEQ ID NO:58, wherein the amino acid sequence has a biological activity of at least one domain of a polyunsaturated fatty acid (PUFA) polyketide synthase (PKS) system; (c) an amino acid sequence that is at least about 65% identical, and more preferably at least about 70% identical, and more preferably at least about 80% identical, and more preferably at least about 90% identical, to SEQ ID NO:54, wherein the amino acid sequence has a biological activity of at least one domain of a polyunsaturated fatty acid (PUFA) polyketide synthase (PKS) system; (d) an amino acid sequence that is at least about 70% identical, and more preferably at least about 80% identical, and more preferably at least about 90% identical, to an amino acid sequence selected from the group consisting of: SEQ ID NO:45, SEQ ID NO:48, SEQ ID NO:60, SEQ ID NO:62 and SEQ ID NO:64, wherein the amino acid sequence has a biological activity of at least one domain of a polyunsaturated fatty acid (PUFA) polyketide synthase (PKS) system; and/or (e) an amino acid sequence that is at least about 80% identical, and more preferably at least about 90% identical, to an amino acid sequence selected from the group consisting of: SEQ ID NO:41, SEQ ID NO:66, SEQ ID NO:68, wherein the amino acid sequence has a biological activity of at least one domain of a polyunsaturated fatty acid (PUFA) polyketide synthase (PKS) system. In one aspect, the at least one domain of the PUFA PKS system comprises an amino acid sequence selected from the group consisting of: SEQ ID NO:39, SEQ ID NO:41, SEQ ID NO:43, SEQ ID NO:45, SEQ ID NO:48, SEQ ID NO:50, SEQ ID NO:52, SEQ ID NO:54, SEQ ID NO:56, SEQ ID NO:58, SEQ ID NO:60, SEQ ID NO:62, SEQ ID NO:64, SEQ ID NO:66 and SEQ ID NO:68 and biologically active fragments thereof. In one aspect, the plant has been further genetically modified to recombinantly express at least one nucleic acid molecule encoding at least one biologically active domain from a PKS system selected from the group consisting of: a bacterial PUFA PKS system, a Type I PKS system, a Type II PKS system, a modular PKS system, and a non-bacterial PUFA PKS system (e.g., a Thraustochytrid PUFA PKS system, such as a Schizochytrium PUFA PKS system).

Yet another embodiment of the present invention relates to a method to produce a bioactive molecule that is produced by a polyketide synthase system, comprising culturing under conditions effective to produce the bioactive molecule a genetically modified organism that expresses a PKS system comprising at least one biologically active domain of a polyunsaturated fatty acid (PUFA) polyketide synthase (PKS) system, wherein the at least one domain of the PUFA PKS system comprises an amino acid sequence selected from the group consisting of: (a) an amino acid sequence selected from the group consisting of: SEQ ID NO:39, SEQ ID NO:41, SEQ ID NO:43, SEQ ID NO:45, SEQ ID NO:48, SEQ ID NO:50, SEQ ID NO:52, SEQ ID NO:54, SEQ ID NO:56, SEQ ID NO:58, SEQ ID NO:60, SEQ ID NO:62, SEQ ID NO:64, SEQ ID NO:66, SEQ ID NO:68 and biologically active fragments thereof; (b) an amino acid sequence that is at least about 60% identical, and more preferably at least about 70% identical, and more preferably at least about 80% identical, and more preferably at least about 90% identical, to an amino acid sequence selected from the group consisting of: SEQ ID NO:39, SEQ ID NO:43, SEQ ID NO:50, SEQ ID NO:52, SEQ ID NO:56 and SEQ ID NO:58, wherein the amino acid sequence has a biological activity of at least one domain of a polyunsaturated fatty acid (PUFA) polyketide synthase (PKS) system; (c) an amino acid sequence that is at least about 65% identical, and more preferably at least about 70% identical, and more preferably at least about 80% identical, and more preferably at least about 90% identical, to SEQ ID NO:54, wherein the amino acid sequence has a biological activity of at least one domain of a polyunsaturated fatty acid (PUFA) polyketide synthase (PKS) system; (d) an amino acid sequence that is at least about 70% identical, and more preferably at least about 80% identical, and more preferably at least about 90% identical, to an amino acid sequence selected from the group consisting of: SEQ ID NO:45, SEQ ID NO:48, SEQ ID NO:60, SEQ ID NO:62 and SEQ ID NO:64, wherein the amino acid sequence has a biological activity of at least one domain of a polyunsaturated fatty acid (PUFA) polyketide synthase (PKS) system; and/or (e) an amino acid sequence that is at least about 80% identical, and more preferably at least about 90% identical, to an amino acid sequence selected from the group consisting of: SEQ ID NO:41, SEQ ID NO:66, SEQ ID NO:68, wherein the amino acid sequence has a biological activity of at least one domain of a polyunsaturated fatty acid (PUFA) polyketide synthase (PKS) system.

In one aspect, the organism endogenously expresses a PKS system comprising the at least one domain of the PUFA PKS system, and wherein the genetic modification is in a nucleic acid sequence encoding the at least one domain of the PUFA PKS system. In one aspect, the genetic modification changes at least one product produced by the endogenous PKS system, as compared to an organism wherein the PUFA PKS system has not been genetically modified.

In another aspect, the organism endogenously expresses a PKS system comprising the at least one biologically active domain of the PUFA PKS system, and the genetic s modification comprises transfection of the organism with a recombinant nucleic acid molecule selected from the group consisting of: a recombinant nucleic acid molecule encoding at least one biologically active domain from a second PKS system and a recombinant nucleic acid molecule encoding a protein that affects the activity of the PUFA PKS system. In one aspect, the genetic modification changes at least one product produced by the endogenous PKS system, as compared to an organism that has not been genetically modified to affect PUFA production.

In another aspect, the organism is genetically modified by transfection with a recombinant nucleic acid molecule encoding the at least one domain of the polyunsaturated fatty acid (PUFA) polyketide synthase (PKS) system.

In another aspect, the organism produces a polyunsaturated fatty acid (PUFA) profile that differs from the naturally occurring organism without a genetic modification.

In another aspect, the organism endogenously expresses a non-bacterial PUFA PKS system, and wherein the genetic modification comprises substitution of a domain from a different PKS system for a nucleic acid sequence encoding at least one domain of the non-bacterial PUFA PKS system.

In yet another aspect, the organism endogenously expresses a non-bacterial PUFA PKS system that has been modified by transfecting the organism with a recombinant nucleic acid molecule encoding a protein that regulates the chain length of fatty acids produced by the PUFA PKS system.

In another aspect, the bioactive molecule is selected from: an anti-inflammatory formulation, a chemotherapeutic agent, an active excipient, an osteoporosis drug, an anti-depressant, an anti-convulsant, an anti-Heliobactor pylori drug, a drug for treatment of neurodegenerative disease, a drug for treatment of degenerative liver disease, an antibiotic, and/or a cholesterol lowering formulation. In one aspect, the bioactive molecule is an antibiotic. In another aspect, the bioactive molecule is a polyunsaturated fatty acid (PUFA). In yet another aspect, the bioactive molecule is a molecule including carbon-carbon double bonds in the cis configuration. In one aspect, the bioactive molecule is a molecule including a double bond at every third carbon. In one aspect, the organism is a microorganism. In another aspect, the organism is a plant.

Another embodiment of the present invention relates to a method to produce a plant that has a polyunsaturated fatty acid (PUFA) profile that differs from the naturally occurring plant, comprising genetically modifying cells of the plant to express a PKS system comprising at least one recombinant nucleic acid molecule comprising a nucleic acid sequence encoding at least one biologically active domain of a PUFA PKS system, wherein the at least one domain of the PUFA PKS system comprises an amino acid sequence selected from the group consisting of: (a) an amino acid sequence selected from the group consisting of: SEQ ID NO:39, SEQ ID NO:41, SEQ ID NO:43, SEQ ID NO:45, SEQ ID NO:48, SEQ ID NO:50, SEQ ID NO:52, SEQ ID NO:54, SEQ ID NO:56, SEQ ID NO:58, SEQ ID NO:60, SEQ ID NO:62, SEQ ID NO:64, SEQ ID NO:66, SEQ ID NO:68 and biologically active fragments thereof; (b) an amino acid sequence that is at least about 60% identical, and more preferably at least about 70% identical, and more preferably at least about 80% identical, and more preferably at least about 90% identical, to an amino acid sequence selected from the group consisting of: SEQ ID NO:39, SEQ ID NO:43, SEQ ID NO:50, SEQ ID NO:52, SEQ ID NO:56 and SEQ ID NO:58, wherein the amino acid sequence has a biological activity of at least one domain of a polyunsaturated fatty acid (PUFA) polyketide synthase (PKS) system; (c) an amino acid sequence that is at least about 65% identical, and more preferably at least about 70% identical, and more preferably at least about 80% identical, and more preferably at least about 90% identical, to SEQ ID NO:54, wherein the amino acid sequence has a biological activity of at least one domain of a polyunsaturated fatty acid (PUFA) polyketide synthase (PKS) system; (d) an amino acid sequence that is at least about 70% identical, and more preferably at least about 80% identical, and more preferably at least about 90% identical, to an amino acid sequence selected from the group consisting of: SEQ ID NO:45, SEQ ID NO:48, SEQ ID NO:60, SEQ ID NO:62 and SEQ ID NO:64, wherein the amino acid sequence has a biological activity of at least one domain of a polyunsaturated fatty acid (PUFA) polyketide synthase (PKS) system; and (e) an amino acid sequence that is at least about 80% identical, and more preferably at least about 90% identical, to an amino acid sequence selected from the group consisting of: SEQ ID NO:41, SEQ ID NO:66, SEQ ID NO:68, wherein the amino acid sequence has a biological activity of at least one domain of a polyunsaturated fatty acid (PUFA) polyketide synthase (PKS) system.

Another embodiment of the present invention relates to a method to modify an endproduct containing at least one fatty acid, comprising adding to the endproduct an oil produced by a recombinant host cell that expresses at least one recombinant nucleic acid molecule comprising a nucleic acid sequence encoding at least one biologically active domain of a PUFA PKS system, wherein the at least one domain of a PUFA PKS system comprises an amino acid sequence selected from the group consisting of: (a) an amino acid sequence selected from the group consisting of: SEQ ID NO:39, SEQ ID NO:41, SEQ ID NO:43, SEQ ID NO:45, SEQ ID NO:48, SEQ ID NO:50, SEQ ID NO:52, SEQ ID NO:54, SEQ ID NO:56, SEQ ID NO:58, SEQ ID NO:60, SEQ ID NO:62, SEQ ID NO:64, SEQ ID NO:66, SEQ ID NO:68 and biologically active fragments thereof; (b) an amino acid sequence that is at least about 60% identical, and more preferably at least about 70% identical, and more preferably at least about 80% identical, and more preferably at least about 90% identical, to an amino acid sequence selected from the group consisting of: SEQ ID NO:39, SEQ ID NO:43, SEQ ID NO:50, SEQ ID NO:52, SEQ ID NO:56 and SEQ ID NO:58, wherein the amino acid sequence has a biological activity of at least one domain of a polyunsaturated fatty acid (PUFA) polyketide synthase (PKS) system; (c) an amino acid sequence that is at least about 65% identical, and more preferably at least about 70% identical, and more preferably at least about 80% identical, and more preferably at least about 90% identical, to SEQ ID NO:54, wherein the amino acid sequence has a biological activity of at least one domain of a polyunsaturated fatty acid (PUFA) polyketide synthase (PKS) system; (d) an amino acid sequence that is at least about 70% identical, and more preferably at least about 80% identical, and more preferably at least about 90% identical, to an amino acid sequence selected from the group consisting of: SEQ ID NO:45, SEQ ID NO:48, SEQ ID NO:60, SEQ ID NO:62 and SEQ ID NO:64, wherein the amino acid sequence has a biological activity of at least one domain of a polyunsaturated fatty acid (PUFA) polyketide synthase (PKS) system; and (e) an amino acid sequence that is at least about 80% identical, and more preferably at least about 90% identical, to an amino acid sequence selected from the group consisting of: SEQ ID NO:41, SEQ ID NO:66, SEQ ID NO:68, wherein the amino acid sequence has a biological activity of at least one domain of a polyunsaturated fatty acid (PUFA) polyketide synthase (PKS) system. In one aspect, the endproduct is selected from: a dietary supplement, a food product, a pharmaceutical formulation, a humanized animal milk, and an infant formula. In one aspect, the pharmaceutical formulation is selected from the group consisting of an anti-inflammatory formulation, a chemotherapeutic agent, an active excipient, an osteoporosis drug, an anti-depressant, an anti-convulsant, an anti-Heliobactor pylori drug, a drug for treatment of neurodegenerative disease, a drug for treatment of degenerative liver disease, an antibiotic, and a cholesterol lowering formulation. In one aspect, the endproduct is used to treat a condition selected from the group consisting of: chronic inflammation, acute inflammation, gastrointestinal disorder, cancer, cachexia, cardiac restenosis, neurodegenerative disorder, degenerative disorder of the liver, blood lipid disorder, osteoporosis, osteoarthritis, autoimmune disease, preeclampsia, preterm birth, age related maculopathy, pulmonary disorder, and peroxisomal disorder.

Yet another embodiment of the present invention relates to a method to produce a humanized animal milk, comprising genetically modifying milk-producing cells of a milk-producing animal with at least one recombinant nucleic acid molecule comprising a nucleic acid sequence encoding at least one biologically active domain of a PUFA PKS system, wherein the at least one domain of the PUFA PKS system comprises an amino acid sequence selected from the group consisting of: (a) an amino acid sequence selected from the group consisting of: SEQ ID NO:39, SEQ ID NO:41, SEQ ID NO:43, SEQ ID NO:45, SEQ ID NO:48, SEQ ID NO:50, SEQ ID NO:52, SEQ ID NO:54, SEQ ID NO:56, SEQ ID NO:58, SEQ ID NO:60, SEQ ID NO:62, SEQ ID NO:64, SEQ ID NO:66, SEQ ID NO:68 and biologically active fragments thereof; (b) an amino acid sequence that is at least about 60% identical, and more preferably at least about 70% identical, and more preferably at least about 80% identical, and more preferably at least about 90% identical, to an amino acid sequence selected from the group consisting of: SEQ ID NO:39, SEQ ID NO:43, SEQ ID NO:50, SEQ ID NO:52, SEQ ID NO:56 and SEQ ID NO:58, wherein the amino acid sequence has a biological activity of at least one domain of a polyunsaturated fatty acid (PUFA) polyketide synthase (PKS) system; (c) an amino acid sequence that is at least about 65% identical, and more preferably at least about 70% identical, and more preferably at least about 80% identical, and more preferably at least about 90% identical, to SEQ ID NO:54, wherein the amino acid sequence has a biological activity of at least one domain of a polyunsaturated fatty acid (PUFA) polyketide synthase (PKS) system; (d) an amino acid sequence that is at least about 70% identical, and more preferably at least about 80% identical, and more preferably at least about 90% identical, to an amino acid sequence selected from the group consisting of: SEQ ID NO:45, SEQ ID NO:48, SEQ ID NO:60, SEQ ID NO:62 and SEQ ID NO:64, wherein the amino acid sequence has a biological activity of at least one domain of a polyunsaturated fatty acid (PUFA) polyketide synthase (PKS) system; and (e) an amino acid sequence that is at least about 80% identical, and more preferably at least about 90% identical, to an amino acid sequence selected from the group consisting of: SEQ ID NO:41, SEQ ID NO:66, SEQ ID NO:68, wherein the amino acid sequence has a biological activity of at least one domain of a polyunsaturated fatty acid (PUFA) polyketide synthase (PKS) system.

Another embodiment of the present invention relates to a genetically modified Thraustochytrid microorganism, wherein the microorganism has an endogenous polyunsaturated fatty acid (PUFA) polyketide synthase (PKS) system, and wherein the endogenous PUFA PKS system has been genetically modified to alter the expression profile of a polyunsaturated fatty acid (PUFA) by the Thraustochytrid microorganism as compared to the Thraustochytrid microorganism in the absence of the genetic modification.

In one aspect, the endogenous PUFA PKS system has been modified by mutagenesis of a nucleic acid sequence that encodes at least one domain of the endogenous PUFA PKS system. In one aspect, the modification is produced by targeted mutagenesis. In another aspect, the modification is produced by classical mutagenesis and screening.

In another aspect, the endogenous PUFA PKS system has been modified by deleting at least one nucleic acid sequence that encodes at least one domain of the endogenous PUFA PKS system and inserting therefore a nucleic acid sequence encoding a homologue of the endogenous domain to alter the PUFA production profile of the Thraustochytrid microorganism, wherein the homologue has a biological activity of at least one domain of a PKS system. In one aspect, the homologue of the endogenous domain comprises a modification, as compared to the endogenous domain, selected from the group consisting of at least one deletion, insertion or substitution that results in an alteration of PUFA production profile by the microorganism. In another aspect, the amino acid sequence of the homologue is at least about 60% identical, and more preferably about 70% identical, and more preferably about 80% identical, and more preferably about 90% identical to the amino acid sequence of the endogenous domain. In one aspect, homologue of the endogenous domain is a domain from a PUFA PKS system of another Thraustochytrid microorganism.

In another aspect, the endogenous PUFA PKS system has been modified by deleting at least one nucleic acid sequence that encodes at least one domain of the endogenous PUFA PKS system and inserting therefore a nucleic acid sequence encoding at least one domain of a PKS system from a different microorganism. In one aspect, the nucleic acid sequence encoding at least one domain of a PKS system from a different microorganism is from a bacterial PUFA PKS system. For example, the different microorganism can be a marine bacteria having a PUFA PKS system that naturally produces PUFAs at a temperature of about 25.degree. C. or greater. In one aspect, the marine bacteria is selected from the group consisting of Shewanella olleyana and Shewanella japonica. In one aspect, the domain of a PKS system from a different microorganism is from a PKS system selected from the group consisting of: a Type I PKS system, a Type II PKS system, a modular PKS system, and a PUFA PKS system from a different Thraustochytrid microorganism.

In any of the above aspects, the domain of the endogenous PUFA PKS system can include, but is not limited to, a domain having a biological activity of at least one of the following proteins: malonyl-CoA:ACP acyltransferase (MAT), .beta.-keto acyl-ACP synthase (KS), ketoreductase (KR), acyltransferase (AT), FabA-like .beta.-hydroxy acyl-ACP dehydrase (DH), phosphopantetheine transferase, chain length factor (CLF), acyl carrier protein (ACP), enoyl ACP-reductase (ER), an enzyme that catalyzes the synthesis of trans-2-acyl-ACP, an enzyme that catalyzes the reversible isomerization of trans-2-acyl-ACP to cis-3-acyl-ACP, and an enzyme that catalyzes the elongation of cis-3-acyl-ACP to cis-5-.beta.-keto-acyl-ACP. In any of the above aspects, the domain of the endogenous PUFA PKS system can include an amino acid sequence selected from the group consisting of: (a) an amino acid sequence selected from the group consisting of: SEQ ID NO:2, SEQ ID NO:4, SEQ ID NO:6, SEQ ID NO:8, SEQ ID NO:10, SEQ ID NO:13, SEQ ID NO:18, SEQ ID NO:20, SEQ ID NO:22, SEQ ID NO:24, SEQ ID NO:26, SEQ ID NO:28, SEQ ID NO:30, SEQ ID NO:32, SEQ ID NO:39, SEQ ID NO:41, SEQ ID NO:43, SEQ ID NO:45, SEQ ID NO:48, SEQ ID NO:50, SEQ ID NO:52, SEQ ID NO:54, SEQ ID NO:56, SEQ ID NO:58, SEQ ID NO:60, SEQ ID NO:62, SEQ ID NO:64, SEQ ID NO:66, SEQ ID NO:68 and biologically active fragments thereof; and (b) an amino acid sequence that is at least about 60% identical, and more preferably at least about 70% identical, and more preferably at least about 80% identical, and more preferably at least about 90% identical, to an amino acid sequence of (a), wherein the amino acid sequence has a biological activity of at least one domain of a polyunsaturated fatty acid (PUFA) polyketide synthase (PKS) system.

In one aspect, the PUFA production profile is altered to initiate, increase or decrease production of eicosapentaenoic acid (EPA) by the microorganism. In another aspect, the PUFA production profile is altered to initiate, increase or decrease production of docosahexaenoic acid (DHA) by the microorganism. In another aspect, the PUFA production profile is altered to initiate, increase or decrease production of one or both isomers of docosapentaenoic acid (DPA) by the microorganism. In another aspect, the PUFA production profile is altered to initiate, increase or decrease production of arachidonic acid (ARA) by the microorganism. In another aspect, the Thraustochytrid is from a genus selected from the group consisting of Schizochytrium, Thraustochytrium, and Japonochytrium. In another aspect, the Thraustochytrid is from the genus Schizochytrium.

In another aspect, the Thraustochytrid is from a Schizochytrium species selected from the group consisting of: Schizochytrium aggregatum, Schizochytrium limacinum, and Schizochytrium minutum. In another aspect, the Thraustochytrid is from the genus Thraustochytrium.

Yet another embodiment of the present invention relates to a genetically modified Schizochytrium that produces eicosapentaenoic acid (EPA), wherein the Schizochytrium has an endogenous polyunsaturated fatty acid (PUFA) polyketide synthase (PKS) system comprising a genetic modification in at least one nucleic acid sequence that encodes at least one domain of the endogenous PUFA PKS system that results in the production of EPA by the Schizochytrium. In one aspect, the Schizochytrium comprises a genetic modification in at least one nucleic acid sequence encoding at least one domain having a biological activity of at least one of the following proteins: malonyl-CoA:ACP acyltransferase (MAT), .beta.-keto acyl-ACP synthase (KS), ketoreductase (KR), acyltransferase (AT), FabA-like .beta.-hydroxy acyl-ACP dehydrase (DH), phosphopantetheine transferase, chain length factor (CLF), acyl carrier protein (ACP), enoyl ACP-reductase (ER), an enzyme that catalyzes the synthesis of trans-2-acyl-ACP, an enzyme that catalyzes the reversible isomerization of trans-2-acyl-ACP to cis-3-acyl-ACP, and an enzyme that catalyzes the elongation of cis-3-acyl-ACP to cis-5-.beta.-keto-acyl-ACP. In one aspect, the Schizochytrium comprises a genetic modification in at least one nucleic acid sequence encoding at least one domain from the open reading frame encoding SEQ ID NO:2 of the endogenous PUFA PKS system. In one aspect, the Schizochytrium comprises a genetic modification in at least one nucleic acid sequence encoding at least one domain from the open reading frame encoding SEQ ID NO:4 of the endogenous PUFA PKS system. In one aspect, the Schizochytrium comprises a genetic modification in at least one nucleic acid sequence encoding at least one domain from the open reading frame encoding SEQ ID NO:6 of the endogenous PUFA PKS system. In one aspect, the Schizochytrium comprises a genetic modification in at least one nucleic acid sequence encoding at least one domain having a biological activity of at least one of the following proteins: .beta.-keto acyl-ACP synthase (KS), FabA-like .beta.-hydroxy acyl-ACP dehydrase (DH), chain length factor (CLF), an enzyme that catalyzes the synthesis of trans-2-acyl-ACP, an enzyme that catalyzes the reversible isomerization of trans-2-acyl-ACP to cis-3-acyl-ACP, and an enzyme that catalyzes the elongation of cis-3-acyl-ACP to cis-5-.beta.-keto-acyl-ACP. In one aspect, the Schizochytrium comprises a genetic modification in at least one nucleic acid sequence encoding an amino acid sequence selected from the group consisting of SEQ ID NO:20, SEQ ID NO:22, SEQ ID NO:28 and SEQ ID NO:30 of the endogenous PUFA PKS system. In one aspect, the Schizochytrium has been modified by deleting at least one nucleic acid sequence that encodes at least one domain of the endogenous PUFA PKS system and inserting therefore a nucleic acid sequence encoding at least one domain of a PKS system from a non-Schizochytrium microorganism. In one aspect, the non-Schizochytrium microorganism grows and produces PUFAs at temperature of at least about 15.degree. C., and more preferably at least about 20.degree. C., and more preferably at least about 25.degree. C., and more preferably at least about 30.degree. C., and more preferably between about 20.degree. C. and about 40.degree. C. In one aspect, the nucleic acid sequence encoding at least one domain of a PKS system from a non-Schizochytrium microorganism is from a bacterial PUFA PKS system. In one aspect, the bacterial PUFA PKS system is from a bacterium selected from the group consisting of Shewanella olleyana and Shewanellajaponica. In another aspect, the nucleic acid sequence encoding at least one domain of a PKS system is selected from the group consisting of a Type I PKS system, a Type II PKS system, a modular PKS system, and a non-bacterial PUFA PKS system (e.g., a eukaryotic PUFA PKS system, such as a Thraustochytrid PUFA PKS system).

Another embodiment of the present invention relates to a genetically modified Schizochytrium that produces increased amounts of docosahexaenoic acid (DHA) as compared to a non-genetically modified Schizochytrium, wherein the Schizochytrium has an endogenous polyunsaturated fatty acid (PUFA) polyketide synthase (PKS) system comprising a genetic modification in at least one nucleic sequence that encodes at least one domain of the endogenous PUFA PKS system that results in increased the production of DHA by the Schizochytrium. In one aspect, at least one domain of the endogenous PUFA PKS system has been modified by substitution for at least one domain of a PUFA PKS system from Thraustochytrium. In one aspect, the ratio of DHA to DPA produced by the Schizochytrium is increased as compared to a non-genetically modified Schizochytrium.

Another embodiment of the present invention relates to a method to produce lipids enriched for at least one selected polyunsaturated fatty acid (PUFA), comprising culturing under conditions effective to produce the lipids a genetically modified Thraustochytrid microorganism as described above or a genetically modified Schizochytrium as described above. In one aspect, the selected PUFA is eicosapentaenoic acid (EPA).

Yet another embodiment of the present invention relates to a method to produce eicosapentaenoic acid (EPA)-enriched lipids, comprising culturing under conditions effective to produce the EPA-enriched lipids a genetically modified Thraustochytrid microorganism, wherein the microorganism has an endogenous polyunsaturated fatty acid (PUFA) polyketide synthase (PKS) system, and wherein the endogenous PUFA PKS system has been genetically modified in at least one domain to initiate or increase the production of EPA in the lipids of the microorganism as compared to in the absence of the modification.

BRIEF DESCRIPTION OF THE FIGURES

FIG. 1 is a graphical representation of the domain structure of the Schizochytrium PUFA PKS system.

FIG. 2 shows a comparison of domains of PUFA PKS systems from Schizochytrium and Shewanella.

FIG. 3 shows a comparison of domains of PUFA PKS systems from Schizochytrium and a related PKS system from Nostoc whose product is a long chain fatty acid that does not contain any double bonds.

DETAILED DESCRIPTION OF THE INVENTION

The present invention generally relates to polyunsaturated fatty acid (PUFA) polyketide synthase (PKS) systems, to genetically modified organisms comprising such PUFA PKS systems, to methods of making and using such systems for the production of products of interest, including bioactive molecules and particularly, PUFAs, such as DHA, DPA and EPA. As used herein, a PUFA PKS system generally has the following identifying features: (1) it produces PUFAs as a natural product of the system; and (2) it comprises several multifunctional proteins assembled into a complex that conducts both iterative processing of the fatty acid chain as well non-iterative processing, including trans-cis isomerization and enoyl reduction reactions in selected cycles (See FIG. 1, for example). Reference to a PUFA PKS system refers collectively to all of the genes and their encoded products that work in a complex to produce PUFAs in an organism. Therefore, the PUFA PKS system refers specifically to a PKS system for which the natural products are PUFAs.

More specifically, first, a PUFA PKS system that forms the basis of this invention produces polyunsaturated fatty acids (PUFAs) as products (i.e., an organism that endogenously (naturally) contains such a PKS system makes PUFAs using this system). The PUFAs referred to herein are preferably polyunsaturated fatty acids with a carbon chain length of at least 16 carbons, and more preferably at least 18 carbons, and more preferably at least 20 carbons, and more preferably 22 or more carbons, with at least 3 or more double bonds, and preferably 4 or more, and more preferably 5 or more, and even more preferably 6 or more double bonds, wherein all double bonds are in the cis configuration. It is an object of the present invention to find or create via genetic manipulation or manipulation of the endproduct, PKS systems which produce polyunsaturated fatty acids of desired chain length and with desired numbers of double bonds. Examples of PUFAs include, but are not limited to, DHA (docosahexaenoic acid (C22:6, .omega.-3)), ARA (eicosatetraenoic acid or arachidonic acid (C20:4, n-6)), DPA (docosapentaenoic acid (C22:5, .omega.-6 or .omega.-3)), and EPA (eicosapentaenoic acid (C20:5, .omega.-3)).

Second, the PUFA PKS system described herein incorporates both iterative and non-iterative reactions, which distinguish the system from previously described PKS systems (e.g., type I, type II or modular). More particularly, the PUFA PKS system described herein contains domains that appear to function during each cycle as well as those which appear to function during only some of the cycles. A key aspect of this functionality may be related to the domains showing homology to the bacterial Fab-A enzymes. For example, the Fab-A enzyme of E. coli has been shown to possess two enzymatic activities. It possesses a dehydration activity in which a water molecule (H.sub.2O) is abstracted from a carbon chain containing a hydroxy group, leaving a trans double bond in that carbon chain. In addition, it has an isomerase activity in which the trans double bond is converted to the cis configuration. This isomerization is accomplished in conjunction with a migration of the double bond position to adjacent carbons. In PKS (and FAS) systems, the main carbon chain is extended in 2 carbon increments. One can therefore predict the number of extension reactions required to produce the PUFA products of these PKS systems. For example, to produce DHA (C22:6, all cis) requires 10 extension reactions. Since there are only 6 double bonds in the end product, it means that during some of the reaction cycles, a double bond is retained (as a cis isomer), and in others, the double bond is reduced prior to the next extension.

Before the discovery of a PUFA PKS system in marine bacteria (see U.S. Pat. No. 6,140,486), PKS systems were not known to possess this combination of iterative and selective enzymatic reactions, and they were not thought of as being able to produce carbon-carbon double bonds in the cis configuration. However, the PUFA PKS system described by the present invention has the capacity to introduce cis double bonds and the capacity to vary the reaction sequence in the cycle.

The present inventors propose to use these features of the PUFA PKS system to produce a range of bioactive molecules that could not be produced by the previously described (Type II, Type I and modular) PKS systems. These bioactive molecules include, but are not limited to, polyunsaturated fatty acids (PUFAs), antibiotics or other bioactive compounds, many of which will be discussed below. For example, using the knowledge of the PUFA PKS gene structures described herein, any of a number of methods can be used to alter the PUFA PKS genes, or combine portions of these genes with other synthesis systems, including other PKS systems, such that new products are produced. The inherent ability of this particular type of system to do both iterative and selective reactions will enable this system to yield products that would not be found if similar methods were applied to other types of PKS systems.

Much of the structure of the PKS system for PUFA synthesis in the eukaryotic Thraustochytrid, Schizochytrium has been described in detail in U.S. Pat. No. 6,566,583. Complete sequencing of cDNA and genomic clones in Schizochytrium by the present inventors allowed the identification of the full-length genomic sequence of each of OrfA, OrfB and OrfC and the complete identification of the specific domains in these Schizochytrium Orfs with homology to those in Shewanella (see FIG. 2 and U.S. patent application Ser. No. 10/124,800, supra). In U.S. patent application Ser. No. 10/124,800, the inventors also identified a Thraustochytrium species as meeting the criteria for having a PUFA PKS system and then demonstrated that this organism was likely to contain genes with homology to Schizochytrium PUFA PKS genes by Southern blot analysis. However, the isolation and determination of the structure of such genes and the domain organization of the genes was not described in U.S. patent application Ser. No. 10/124,800. In the present invention, the inventors have now cloned and sequenced the full-length genomic sequence of homologous open reading frames (Orfs) in this Thraustochytrid of the genus Thraustochytrium (specifically, Thraustochytrium sp. 23B (ATCC 20892)), and have identified the domains comprising the PUFA PKS system in this Thraustochytrium. Therefore, the present invention solves the above-mentioned problem of providing additional PUFA PKS systems that have the flexibility for commercial use. The Thraustochytrium PUFA PKS system is described in detail below.

The present invention also solves the above-identified problem for production of commercially valuable lipids enriched in a desired PUFA, such as EPA, by the present inventors' development of genetically modified microorganisms and methods for efficiently producing lipids (triacylglyerols (TAG) as well as membrane-associated phospholipids (PL)) enriched in PUFAs by manipulation of the polyketide synthase-like system that produces PUFAs in eukaryotes, including members of the order Thraustochytriales such as Schizochytrium and Thraustochytrium. Specifically, and by way of example, the present inventors describe herein a strain of Schizochytrium that has previously been optimized for commercial production of oils enriched in PUFA, primarily docosahexaenoic acid (DHA; C22:6 n-3) and docosapentaenoic acid (DPA; C22:5 n-6), and that will now be genetically modified such that EPA (C20:5 n-3) production (or other PUFA production) replaces the DHA production, without sacrificing the oil productivity characteristics of the organism. In addition, the present inventors describe herein the genetic modification of Schizochytrium with PUFA PKS genes from Thraustochytrium to improve the DHA production by the Schizochytrium organism, specifically by altering the ratio of DHA to DPA produced by the microorganism through the modification of the PUFA PKS system. These are only a few examples of the technology encompassed by the invention, as the concepts of the invention can readily be applied to other production organisms and other desired PUFAs as described in detail below.

In one embodiment, a PUFA PKS system according to the present invention comprises at least the following biologically active domains: (a) at least two enoyl-ACP reductase (ER) domains; (b) at least six acyl carrier protein (ACP) domains; (c) at least two .beta.-ketoacyl-ACP synthase (KS) domains; (d) at least one acyltransferase (AT) domain; (e) at least one .beta.-ketoacyl-ACP reductase (KR) domain; (f) at least two FabA-like .beta.-hydroxyacyl-ACP dehydrase (DH) domains; (g) at least one chain length factor (CLF) domain; and (h) at least one malonyl-CoA:ACP acyltransferase (MAT) domain. The functions of these domains are generally individually known in the art and will be described in detail below with regard to the PUFA PKS system of the present invention.

In another embodiment, the PUFA PKS system comprises at least the following biologically active domains: (a) at least one enoyl-ACP reductase (ER) domain; (b) multiple acyl carrier protein (ACP) domains (at least from one to four, and preferably at least five, and more preferably at least six, and even more preferably seven, eight, nine, or more than nine); (c) at least two .beta.-ketoacyl-ACP synthase (KS) domains; (d) at least one acyltransferase (AT) domain; (e) at least one .beta.-ketoacyl-ACP reductase (KR) domain; (f) at least two FabA-like .beta.-hydroxyacyl-ACP dehydrase (DH) domains; (g) at least one chain length factor (CLF) domain; and (h) at least one malonyl-CoA:ACP acyltransferase (MAT) domain. Preferably, such a PUFA PKS system is a non-bacterial PUFA-PKS system.

In one embodiment, a PUFA PKS system of the present invention is a non-bacterial PUFA PKS system. In other words, in one embodiment, the PUFA PKS system of the present invention is isolated from an organism that is not a bacterium, or is a homologue of, or derived from, a PUFA PKS system from an organism that is not a bacterium, such as a eukaryote or an archaebacterium. Eukaryotes are separated from prokaryotes based on the degree of differentiation of the cells, with eukaryotes having more highly differentiated cells and prokaryotes having less differentiated cells. In general, prokaryotes do not possess a nuclear membrane, do not exhibit mitosis during cell division, have only one chromosome, their cytoplasm contains 70S ribosomes, they do not possess any mitochondria, endoplasmic reticulum, chloroplasts, lysosomes or Golgi apparatus, their flagella (if present) consists of a single fibril. In contrast, eukaryotes have a nuclear membrane, they do exhibit mitosis during cell division, they have many chromosomes, their cytoplasm contains 80S ribosomes, they do possess mitochondria, endoplasmic reticulum, chloroplasts (in algae), lysosomes and Golgi apparatus, and their flagella (if present) consists of many fibrils. In general, bacteria are prokaryotes, while algae, fungi, protist, protozoa and higher plants are eukaryotes.

The PUFA PKS systems of the marine bacteria (e.g., Shewanella sp. strain SCRC2738 and Vibrio marinus) are not the basis of the present invention, although the present invention does contemplate the use of domains from these bacterial PUFA PKS systems in conjunction with domains from the non-bacterial PUFA PKS systems of the present invention. In addition, the present invention does contemplate the isolation and use of PUFA PKS gene sets (and proteins and domains encoded thereby) isolated from other bacteria (e.g. Shewanella olleyana and Shewanella japonica) that will be particularly suitable for use as sources of PUFA PKS genes for modifying or combining with the non-bacterial PUFA PKS genes described herein to produce hybrid constructs and genetically modified microorganisms and plants. For example, according to the present invention, genetically modified organisms can be produced which incorporate non-bacterial PUFA PKS functional domains with bacterial PUFA PKS functional domains, as well as PKS functional domains or proteins from other PKS systems (type I, type II, modular) or FAS systems. As discussed in more detail below, PUFA PKS genes from two species of Shewanella, namely Shewanella olleyana or Shewanella japonica, are exemplary bacterial genes that are preferred for use in genetically modified microorganisms, plants, and methods of the invention. PUFA PKS systems (genes and the proteins and domains encoded thereby) from such marine bacteria (e.g., Shewanella olleyana or Shewanella japonica) are encompassed by the present invention as novel PUFA PKS sequences.

According to the present invention, the terms/phrases "Thraustochytrid", "Thraustochytriales microorganism" and "microorganism of the order Thraustochytriales" can be used interchangeably and refer to any members of the order Thraustochytriales, which includes both the family Thraustochytriaceae and the family Labyrinthulaceae. The terms "Labyrinthulid" and "Labyrinthulaceae" are used herein to specifically refer to members of the family Labyrinthulaceae. To specifically reference Thraustochytrids that are members of the family Thraustochytriaceae, the term "Thraustochytriaceae" is used herein. Thus, for the present invention, members of the Labyrinthulids are considered to be included in the Thraustochytrids.

Developments have resulted in frequent revision of the taxonomy of the Thraustochytrids. Taxonomic theorists generally place Thraustochytrids with the algae or algae-like protists. However, because of taxonomic uncertainty, it would be best for the purposes of the present invention to consider the strains described in the present invention as Thraustochytrids to include the following organisms: Order: Thraustochytriales; Family: Thraustochytriaceae (Genera: Thraustochytrium, Schizochytrium, Japonochytrium, Aplanochytrium, or Elina) or Labyrinthulaceae (Genera Labyrinthula, Labyrinthuloides, or Labyrinthomyxa). Also, the following genera are sometimes included in either family Thraustochytriaceae or Labyrinthulaceae: Althornia, Corallochytrium, Diplophyrys, and Pyrrhosorus), and for the purposes of this invention are encompassed by reference to a Thraustochytrid or a member of the order Thraustochytriales. It is recognized that at the time of this invention, revision in the taxonomy of Thraustochytrids places the genus Labyrinthuloides in the family of Labyrinthulaceae and confirms the placement of the two families Thraustochytriaceae and Labyrinthulaceae within the Stramenopile lineage. It is noted that the Labyrinthulaceae are sometimes commonly called labyrinthulids or labyrinthula, or labyrinthuloides and the Thraustochytriaceae are commonly called thraustochytrids, although, as discussed above, for the purposes of clarity of this invention, reference to Thraustochytrids encompasses any member of the order Thraustochytriales and/or includes members of both Thraustochytriaceae and Labyrinthulaceae. Recent taxonomic changes are summarized below.

Strains of certain unicellular microorganisms disclosed herein are members of the order Thraustochytriales. Thraustochytrids are marine eukaryotes with an evolving taxonomic history. Problems with the taxonomic placement of the Thraustochytrids have been reviewed by Moss (1986), Bahnweb and Jackle (1986) and Chamberlain and Moss (1988).

For convenience purposes, the Thraustochytrids were first placed by taxonomists with other colorless zoosporic eukaryotes in the Phycomycetes (algae-like fungi). The name Phycomycetes, however, was eventually dropped from taxonomic status, and the Thraustochytrids were retained in the Oomycetes (the biflagellate zoosporic fungi). It was initially assumed that the Oomycetes were related to the heterokont algae, and eventually a wide range of ultrastructural and biochemical studies, summarized by Barr (Barr, 1981, Biosystems 14:359-370) supported this assumption. The Oomycetes were in fact accepted by Leedale (Leedale, 1974, Taxon 23:261-270) and other phycologists as part of the heterokont algae. However, as a matter of convenience resulting from their heterotrophic nature, the Oomycetes and Thraustochytrids have been largely studied by mycologists (scientists who study fungi) rather than phycologists (scientists who study algae).

From another taxonomic perspective, evolutionary biologists have developed two general schools of thought as to how eukaryotes evolved. One theory proposes an exogenous origin of membrane-bound organelles through a series of endosymbioses (Margulis, 1970, Origin of Eukarvotic Cells. Yale University Press, New Haven); e.g., mitochondria were derived from bacterial endosymbionts, chloroplasts from cyanophytes, and flagella from spirochaetes. The other theory suggests a gradual evolution of the membrane-bound organelles from the non-membrane-bounded systems of the prokaryote ancestor via an autogenous process (Cavalier-Smith, 1975, Nature (Lond.) 256:462-468). Both groups of evolutionary biologists however, have removed the Oomycetes and Thraustochytrids from the fungi and place them either with the chromophyte algae in the kingdom Chromophyta (Cavalier-Smith, 1981, BioSystems 14:461-481) (this kingdom has been more recently expanded to include other protists and members of this kingdom are now called Stramenopiles) or with all algae in the kingdom Protoctista (Margulis and Sagen, 1985, Biosystems 18:141-147).

With the development of electron microscopy, studies on the ultrastructure of the zoospores of two genera of Thraustochytrids, Thraustochytrium and Schizochytrium, (Perkins, 1976, pp.279-312 in "Recent Advances in Aquatic Mycology" (ed. E. B. G. Jones), John Wiley & Sons, New York; Kazama, 1980, Can. J. Bot. 58:2434-2446; Barr, 1981, Biosystems 14:359-370) have provided good evidence that the Thraustochytriaceae are only distantly related to the Oomycetes. Additionally, genetic data representing a correspondence analysis (a form of multivariate statistics) of 5-S ribosomal RNA sequences indicate that Thraustochytriales are clearly a unique group of eukaryotes, completely separate from the fungi, and most closely related to the red and brown algae, and to members of the Oomycetes (Mannella, et al., 1987, Mol. Evol. 24:228-235). Most taxonomists have agreed to remove the Thraustochytrids from the Oomycetes (Bartnicki-Garcia, 1987, pp. 389-403 in "Evolutionary Biology of the Fungi" (eds. Rayner, A. D. M., Brasier, C. M. & Moore, D.), Cambridge University Press, Cambridge).

In summary, employing the taxonomic system of Cavalier-Smith (Cavalier-Smith, 1981, BioSystems 14:461-481, 1983; Cavalier-Smith, 1993, Microbiol Rev. 57:953-994), the Thraustochytrids are classified with the chromophyte algae in the kingdom Chromophyta (Stramenopiles). This taxonomic placement has been more recently reaffirmed by Cavalier-Smith et al. using the 18s rRNA signatures of the Heterokonta to demonstrate that Thraustochytrids are chromists not Fungi (Cavalier-Smith et al., 1994, Phil. Tran. Roy. Soc. London Series BioSciences 346:387-397). This places the Thraustochytrids in a completely different kingdom from the fungi, which are all placed in the kingdom Eufungi.

Currently, there are 71 distinct groups of eukaryotic organisms (Patterson 1999) and within these groups four major lineages have been identified with some confidence: (1) Alveolates, (2) Stramenopiles, (3) a Land Plant-green algae-Rhodophyte_Glaucophyte ("plant") lade and (4) an Opisthokont lade (Fungi and Animals). Formerly these four major lineages would have been labeled Kingdoms but use of the "kingdom" concept is no longer considered useful by some researchers.

As noted by Armstrong, Stramenopile refers to three-parted tubular hairs, and most members of this lineage have flagella bearing such hairs. Motile cells of the Stramenopiles (unicellular organisms, sperm, zoopores) are asymmetrical having two laterally inserted flagella, one long, bearing three-parted tubular hairs that reverse the thrust of the flagellum, and one short and smooth. Formerly, when the group was less broad, the Stramenopiles were called Kingdom Chromista or the heterokont (=different flagella) algae because those groups consisted of the Brown Algae or Phaeophytes, along with the yellow-green Algae, Golden-brown Algae, Eustigmatophytes and Diatoms. Subsequently some heterotrophic, fungal-like organisms, the water molds, and labyrinthulids (slime net amoebas), were found to possess similar motile cells, so a group name referring to photosynthetic pigments or algae became inappropriate. Currently, two of the families within the Stramenopile lineage are the Labyrinthulaceae and the Thraustochytriaceae. Historically, there have been numerous classification strategies for these unique microorganisms and they are often classified under the same order (i.e., Thraustochytriales). Relationships of the members in these groups are still developing. Porter and Leander have developed data based on 18S small subunit ribosomal DNA indicating the thraustochytrid-labyrinthulid lade in monophyletic. However, the lade is supported by two branches; the first contains three species of Thraustochytrium and Ulkenia profunda, and the second includes three species of Labyrinthula, two species of Labyrinthuloides and Schizochytrium aggregatum.

The taxonomic placement of the Thraustochytrids as used in the present invention is therefore summarized below: Kingdom: Chromophyta (Stramenopiles) Phylum: Heterokonta Order: Thraustochytriales (Thraustochytrids) Family: Thraustochytriaceae or Labyrinthulaceae Genera: Thraustochytrium, Schizochytrium, Japonochytrium, Aplanochytrium, Elina, Labyrinthula, Labyrinthuloides, or Labyrinthulomyxa

Some early taxonomists separated a few original members of the genus Thraustochytrium (those with an amoeboid life stage) into a separate genus called Ulkenia. However it is now known that most, if not all, Thraustochytrids (including Thraustochytrium and Schizochytrium), exhibit amoeboid stages and as such, Ulkenia is not considered by some to be a valid genus. As used herein, the genus Thraustochytrium will include Ulkenia.

Despite the uncertainty of taxonomic placement within higher classifications of Phylum and Kingdom, the Thraustochytrids remain a distinctive and characteristic grouping whose members remain classifiable within the order Thraustochytriales.

Schizochytrium is a Thraustochytrid marine microorganism that accumulates large quantities of triacylglycerols rich in DHA and docosapentaenoic acid (DPA; 22:5.omega.-6); e.g., 30% DHA+DPA by dry weight (Barclay et al., J. Appl. Phycol. 6, 123 (1994)). In eukaryotes that synthesize 20- and 22-carbon PUFAs by an elongation/desaturation pathway, the pools of 18-, 20- and 22-carbon intermediates are relatively large so that in vivo labeling experiments using [.sup.14C]-acetate reveal clear precursor-product kinetics for the predicted intermediates (Gellerman et al., Biochim. Biophys. Acta 573:23 (1979)). Furthermore, radiolabeled intermediates provided exogenously to such organisms are converted to the final PUFA products. The present inventors have shown that [1-.sup.14C]-acetate was rapidly taken up by Schizochytrium cells and incorporated into fatty acids, but at the shortest labeling time (1 min), DHA contained 31% of the label recovered in fatty acids, and this percentage remained essentially unchanged during the 10-15 min of [.sup.14C]-acetate incorporation and the subsequent 24 hours of culture growth. Similarly, DPA represented 10% of the label throughout the experiment. There is no evidence for a precursor-product relationship between 16- or 18-carbon fatty acids and the 22-carbon polyunsaturated fatty acids. These results are consistent with rapid synthesis of DHA from [.sup.14C]-acetate involving very small (possibly enzyme-bound) pools of intermediates. A cell-free homogenate derived from Schizochytrium cultures incorporated [1-.sup.14C]-malonyl-CoA into DHA, DPA, and saturated fatty acids. The same biosynthetic activities were retained by a 100,000.times.g supernatant fraction but were not present in the membrane pellet. Thus, DHA and DPA synthesis in Schizochytrium does not involve membrane-bound desaturases or fatty acid elongation enzymes like those described for other eukaryotes (Parker-Barnes et al., 2000, supra; Shanklin et al., 1998, supra). These fractionation data contrast with those obtained from the Shewanella enzymes (See Metz et al., 2001, supra) and may indicate use of a different (soluble) acyl acceptor molecule, such as CoA, by the Schizochytrium enzyme. It is expected that Thraustochytrium will have a similar biochemistry.

In U.S. Pat. No. 6,566,583, a cDNA library from Schizochytrium was constructed and approximately 8500 random clones (ESTs) were sequenced. Sequences that exhibited homology to 8 of the 11 domains of the Shewanella PKS genes shown in FIG. 2 were all identified at frequencies of 0.2-0.5%. In U.S. Pat. No. 6,566,583, several cDNA clones from Schizochytrium showing homology to the Shewanella PKS genes were sequenced, and various clones were assembled into nucleic acid sequences representing two partial open reading frames and one complete open reading frame.

Further sequencing of cDNA and genomic clones by the present inventors allowed the identification of the full-length genomic sequence of each of OrfA, OrfB and OrfC in Schizochytrium and the complete identification of the domains in Schizochytrium with homology to those in Shewanella (see FIG. 2). These genes are described in detail in U.S. patent application Ser. No. 10/124,800, supra and are described in some detail below.

The present inventors have now identified, cloned, and sequenced the full-length genomic sequence of homologous Orfs in a Thraustochytrid of the genus Thraustochytrium (specifically, Thraustochytrium sp. 23B (ATCC 20892)) and have identified the domains comprising the PUFA PKS system in this Thraustochytrium.

Based on the comparison of the domains of the PUFA PKS system of Schizochytrium with the domains of the PUFA PKS system of Shewanella, clearly, the Schizochytrium genome encodes proteins that are highly similar to the proteins in Shewanella that are capable of catalyzing EPA synthesis. The proteins in Schizochytrium constitute a PUFA PKS system that catalyzes DHA and DPA synthesis. Simple modification of the reaction scheme identified for Shewanella will allow for DHA synthesis in Schizochytrium. The homology between the prokaryotic Shewanella and eukaryotic Schizochytrium genes suggests that the PUFA PKS has undergone lateral gene transfer.

A similar comparison can be made for Thraustochytrium. In all cases, comparison of the Thraustochytrium 23B (Th. 23B) PUFA PKS proteins or domains to other known sequences revealed that the closest match was one of the Schizochytrium PUFA PKS proteins (OrfA, B or C, or a domain therefrom) as described in U.S. patent application Ser. No. 10/124,800, supra. The next closest matches in all cases were to one of the PUFA PKS proteins from marine bacteria (Shewanella SCRC-2738, Shewanella oneidensis, Photobacter profundum and Moritella marina) or from a related system found in nitrogen fixing cyanobacteria (e.g., Nostoc punctiforme and Nostoc sp. PCC 7120). The products of the cyanobacterial enzyme systems lack double bonds and the proteins lack domains related to the DH domains implicated in cis double bond formation (i.e., the FabA related DH domains).

According to the present invention, the phrase "open reading frame" is denoted by the abbreviation "Orf". It is noted that the protein encoded by an open reading frame can also be denoted in all upper case letters as "ORF" and a nucleic acid sequence for an open reading frame can also be denoted in all lower case letters as "orf", but for the sake of consistency, the spelling "Orf" is preferentially used herein to describe either the nucleic acid sequence or the protein encoded thereby. It will be obvious from the context of the usage of the term whether a protein or nucleic acid sequence is referenced.

Schizochytrium PUFA PKS

FIG. 1 is a graphical representation of the three open reading frames from the Schizochytrium PUFA PKS system, and includes the domain structure of this PUFA PKS system. As described in detail in U.S. patent application Ser. No. 10/124,800, the domain structure of each open reading frame is as follows:

Open Reading Frame A (OrfA):

The complete nucleotide sequence for OrfA is represented herein as SEQ ID NO:1. OrfA is a 8730 nucleotide sequence (not including the stop codon) which encodes a 2910 amino acid sequence, represented herein as SEQ ID NO:2. Within OrfA are twelve domains: (a) one .beta.-ketoacyl-ACP synthase (KS) domain; (b) one malonyl-CoA:ACP acyltransferase (MAT) domain; (c) nine acyl carrier protein (ACP) domains; and (d) one .beta.-ketoacyl-ACP reductase (KR) domain. The nucleotide sequence for OrfA has been deposited with GenBank as Accession No. AF378327 (amino acid sequence Accession No. AAK728879).

The first domain in Schizochytrium OrfA is a .beta.-ketoacyl-ACP synthase (KS) domain, also referred to herein as OrfA-KS. This domain is contained within the nucleotide sequence spanning from a starting point of between about positions 1 and 40 of SEQ ID NO:1 (OrfA) to an ending point of between about positions 1428 and 1500 of SEQ ID NO:1. The nucleotide sequence containing the sequence encoding the OrfA-KS domain is represented herein as SEQ ID NO:7 (positions 1-1500 of SEQ ID NO:1). The amino acid sequence containing the KS domain spans from a starting point of between about positions 1 and 14 of SEQ ID NO:2 (OrfA) to an ending point of between about positions 476 and 500 of SEQ ID NO:2. The amino acid sequence containing the OrfA-KS domain is represented herein as SEQ ID NO:8 (positions 1-500 of SEQ ID NO:2). It is noted that the OrfA-KS domain contains an active site motif: DXAC* (*acyl binding site C.sub.215).

According to the present invention, a domain or protein having .beta.-ketoacyl-ACP synthase (KS) biological activity (function) is characterized as the enzyme that carries out the initial step of the FAS (and PKS) elongation reaction cycle. The term ".beta.-ketoacyl-ACP synthase" can be used interchangeably with the terms "3-keto acyl-ACP synthase", ".beta.-keto acyl-ACP synthase", and "keto-acyl ACP synthase", and similar derivatives. The acyl group destined for elongation is linked to a cysteine residue at the active site of the enzyme by a thioester bond. In the multi-step reaction, the acyl-enzyme undergoes condensation with malonyl-ACP to form -ketoacyl-ACP, CO.sub.2 and free enzyme. The KS plays a key role in the elongation cycle and in many systems has been shown to possess greater substrate specificity than other enzymes of the reaction cycle. For example, E. coli has three distinct KS enzymes--each with its own particular role in the physiology of the organism (Magnuson et al., Microbiol. Rev. 57, 522 (1993)). The two KS domains of the PUFA-PKS systems could have distinct roles in the PUFA biosynthetic reaction sequence.

As a class of enzymes, KS's have been well characterized. The sequences of many verified KS genes are known, the active site motifs have been identified and the crystal structures of several have been determined. Proteins (or domains of proteins) can be readily identified as belonging to the KS family of enzymes by homology to known KS sequences.

The second domain in OrfA is a malonyl-CoA:ACP acyltransferase (MAT) domain, also referred to herein as OrfA-MAT. This domain is contained within the nucleotide sequence spanning from a starting point of between about positions 1723 and 1798 of SEQ ID NO:1 (OrfA) to an ending point of between about positions 2805 and 3000 of SEQ ID NO:1. The nucleotide sequence containing the sequence encoding the OrfA-MAT domain is represented herein as SEQ ID NO:9 (positions 1723-3000 of SEQ ID NO:1). The amino acid sequence containing the MAT domain spans from a starting point of between about positions 575 and 600 of SEQ ID NO:2 (OrfA) to an ending point of between about positions 935 and 1000 of SEQ ID NO:2. The amino acid sequence containing the OrfA-MAT domain is represented herein as SEQ ID NO:10 (positions 575-1000 of SEQ ID NO:2). It is noted that the OrfA-MAT domain contains an active site motif: GHS*XG (*acyl binding site S.sub.706), represented herein as SEQ ID NO:11.

According to the present invention, a domain or protein having malonyl-CoA:ACP acyltransferase (MAT) biological activity (function) is characterized as one that transfers the malonyl moiety from malonyl-CoA to ACP. The term "malonyl-CoA:ACP acyltransferase" can be used interchangeably with "malonyl acyltransferase" and similar derivatives. In addition to the active site motif (GxSxG), these enzymes possess an extended motif (R and Q amino acids in key positions) that identifies them as MAT enzymes (in contrast to the AT domain of Schizochytrium Orf B). In some PKS systems (but not the PUFA PKS domain) MAT domains will preferentially load methyl- or ethyl-malonate on to the ACP group (from the corresponding CoA ester), thereby introducing branches into the linear carbon chain. MAT domains can be recognized by their homology to known MAT sequences and by their extended motif structure.

Domains 3-11 of OrfA are nine tandem acyl carrier protein (ACP) domains, also referred to herein as OrfA-ACP (the first domain in the sequence is OrfA-ACP1, the second domain is OrfA-ACP2, the third domain is OrfA-ACP3, etc.). The first ACP domain, OrfA-ACP1, is contained within the nucleotide sequence spanning from about position 3343 to about position 3600 of SEQ ID NO:1 (OrfA). The nucleotide sequence containing the sequence encoding the OrfA-ACP1 domain is represented herein as SEQ ID NO:12 (positions 3343-3600 of SEQ ID NO:1). The amino acid sequence containing the first ACP domain spans from about position 1115 to about position 1200 of SEQ ID NO:2. The amino acid sequence containing the OrfA-ACP1 domain is represented herein as SEQ ID NO:13 (positions 1115-1200 of SEQ ID NO:2). It is noted that the OrfA-ACP1 domain contains an active site motif: LGIDS * (*pantetheine binding motif S .sub.1157), represented herein by SEQ ID NO:14.

The nucleotide and amino acid sequences of all nine ACP domains are highly conserved and therefore, the sequence for each domain is not represented herein by an individual sequence identifier. However, based on the information disclosed herein, one of skill in the art can readily determine the sequence containing each of the other eight ACP domains (see discussion below).

All nine ACP domains together span a region of OrfA of from about position 3283 to about position 6288 of SEQ ID NO:1, which corresponds to amino acid positions of from about 1095 to about 2096 of SEQ ID NO:2. The nucleotide sequence for the entire ACP region containing all nine domains is represented herein as SEQ ID NO:16. The region represented by SEQ ID NO:16 includes the linker segments between individual ACP domains. The repeat interval for the nine domains is approximately every 330 nucleotides of SEQ ID NO:16 (the actual number of amino acids measured between adjacent active site serines ranges from 104 to 116 amino acids). Each of the nine ACP domains contains a pantetheine binding motif LGIDS* (represented herein by SEQ ID NO:14), wherein S* is the pantetheine binding site serine (S). The pantetheine binding site serine (S) is located near the center of each ACP domain sequence. At each end of the ACP domain region and between each ACP domain is a region that is highly enriched for proline (P) and alanine (A), which is believed to be a linker region. For example, between ACP domains 1 and 2 is the sequence: APAPVKAAAPAAPVASAPAPA, represented herein as SEQ ID NO:15. The locations of the active site serine residues (i.e., the pantetheine binding site) for each of the nine ACP domains, with respect to the amino acid sequence of SEQ ID NO:2, are as follows: ACP1=S.sub.1157; ACP2=S.sub.1266; ACP3=S.sub.1377; ACP4=S.sub.1488; ACP5=S.sub.1604; ACP6=ACP7=S.sub.1819; ACP8=S.sub.1930; and ACP9=S.sub.2034. Given that the average size of an ACP domain is about 85 amino acids, excluding the linker, and about 110 amino acids including the linker, with the active site serine being approximately in the center of the domain, one of skill in the art can readily determine the positions of each of the nine ACP domains in OrfA.

According to the present invention, a domain or protein having acyl carrier protein (ACP) biological activity (function) is characterized as being small polypeptides (typically, 80 to 100 amino acids long), that function as carriers for growing fatty acyl chains via a thioester linkage to a covalently bound co-factor of the protein. They occur as separate units or as domains within larger proteins. ACPs are converted from inactive apo-forms to functional holo-forms by transfer of the phosphopantetheinyl moeity of CoA to a highly conserved serine residue of the ACP. Acyl groups are attached to ACP by a thioester linkage at the free terminus of the phosphopantetheinyl moiety. ACPs can be identified by labeling with radioactive pantetheine and by sequence homology to known ACPs. The presence of variations of the above mentioned motif (LGIDS*) is also a signature of an ACP.

Domain 12 in OrfA is a .beta.-ketoacyl-ACP reductase (KR) domain, also referred to herein as OrfA-KR. This domain is contained within the nucleotide sequence spanning from a starting point of about position 6598 of SEQ ID NO:1 to an ending point of about position 8730 of SEQ ID NO:1. The nucleotide sequence containing the sequence encoding the OrfA-KR domain is represented herein as SEQ ID NO:17 (positions 6598-8730 of SEQ ID NO:1). The amino acid sequence containing the KR domain spans from a starting point of about position 2200 of SEQ ID NO:2 (OrfA) to an ending point of about position 2910 of SEQ ID NO:2. The amino acid sequence containing the OrfA-KR domain is represented herein as SEQ ID NO:18 (positions 2200-2910 of SEQ ID NO:2). Within the KR domain is a core region with homology to short chain aldehyde-dehydrogenases (KR is a member of this family). This core region spans from about position 7198 to about position 7500 of SEQ ID NO:1, which corresponds to amino acid positions 2400-2500 of SEQ ID NO:2.

According to the present invention, a domain or protein having .beta.-ketoacyl-ACP reductase (KR) activity is characterized as one that catalyzes the pyridine-nucleotide-dependent reduction of 3-ketoacyl forms of ACP. The term ".beta.-ketoacyl-ACP reductase" can be used interchangeably with the terms "ketoreductase", "3-ketoacyl-ACP reductase", "keto-acyl ACP reductase" and similar derivatives of the term. It is the first reductive step in the de novo fatty acid biosynthesis elongation cycle and a reaction often performed in polyketide biosynthesis. Significant sequence similarity is observed with one family of enoyl-ACP reductases (ER), the other reductase of FAS (but not the ER family present in the PUFA PKS system), and the short-chain alcohol dehydrogenase family. Pfam analysis of the PUFA PKS region indicated above reveals the homology to the short-chain alcohol dehydrogenase family in the core region. Blast analysis of the same region reveals matches in the core area to known KR enzymes as well as an extended region of homology to domains from the other characterized PUFA PKS systems.

Open Reading Frame B (OrfB):

The complete nucleotide sequence for OrfB is represented herein as SEQ ID NO:3. OrfB is a 6177 nucleotide sequence (not including the stop codon) which encodes a 2059 amino acid sequence, represented herein as SEQ ID NO:4. Within OrfB are four domains: (a) one .beta.-ketoacyl-ACP synthase (KS) domain; (b) one chain length factor (CLF) domain; (c) one acyltransferase (AT) domain; and, (d) one enoyl-ACP reductase (ER) domain. The nucleotide sequence for OrfB has been deposited with GenBank as Accession No. AF378328 (amino acid sequence Accession No. AAK728880).

The first domain in OrfB is a .beta.-ketoacyl-ACP synthase (KS) domain, also referred to herein as OrfB-KS. This domain is contained within the nucleotide sequence spanning from a starting point of between about positions 1 and 43 of SEQ ID NO:3 (OrfB) to an ending point of between about positions 1332 and 1350 of SEQ ID NO:3. The nucleotide sequence containing the sequence encoding the OrfB-KS domain is represented herein as SEQ ID NO:19 (positions 1-1350 of SEQ ID NO:3). The amino acid sequence containing the KS domain spans from a starting point of between about positions 1 and 15 of SEQ ID NO:4 (OrfB) to an ending point of between about positions 444 and 450 of SEQ ID NO:4. The amino acid sequence containing the OrfB-KS domain is represented herein as SEQ ID NO:20 (positions 1-450 of SEQ ID NO:4). It is noted that the OrfB-KS domain contains an active site motif: DXAC* (*acyl binding site C.sub.196). KS biological activity and methods of identifying proteins or domains having such activity is described above.

The second domain in OrfB is a chain length factor (CLF) domain, also referred to herein as OrfB-CLF. This domain is contained within the nucleotide sequence spanning from a starting point of between about positions 1378 and 1402 of SEQ ID NO:3 (OrfB) to an ending point of between about positions 2682 and 2700 of SEQ ID NO:3. The nucleotide sequence containing the sequence encoding the OrfB-CLF domain is represented herein as SEQ ID NO:21 (positions 1378-2700 of SEQ ID NO:3). The amino acid sequence containing the CLF domain spans from a starting point of between about positions 460 and 468 of SEQ ID NO:4 (OrfB) to an ending point of between about positions 894 and 900 of SEQ ID NO:4. The amino acid sequence containing the OrfB-CLF domain is represented herein as SEQ ID NO:22 (positions 460-900 of SEQ ID NO:4). It is noted that the OrfB-CLF domain contains a KS active site motif without the acyl-binding cysteine.

According to the present invention, a domain or protein is referred to as a chain length factor (CLF) based on the following rationale. The CLF was originally described as characteristic of Type II (dissociated enzymes) PKS systems and was hypothesized to play a role in determining the number of elongation cycles, and hence the chain length, of the end product. CLF amino acid sequences show homology to KS domains (and are thought to form heterodimers with a KS protein), but they lack the active site cysteine. CLF's role in PKS systems is currently controversial. New evidence (C. Bisang et al., Nature 401, 502 (1999)) suggests a role in priming (providing the initial acyl group to be elongated) the PKS systems. In this role the CLF domain is thought to decarboxylate malonate (as malonyl-ACP), thus forming an acetate group that can be transferred to the KS active site. This acetate therefore acts as the `priming` molecule that can undergo the initial elongation (condensation) reaction. Homologues of the Type II CLF have been identified as `loading` domains in some modular PKS systems. A domain with the sequence features of the CLF is found in all currently identified PUFA PKS systems and in each case is found as part of a multidomain protein.

The third domain in OrfB is an AT domain, also referred to herein as OrfB-AT. This domain is contained within the nucleotide sequence spanning from a starting point of between about positions 2701 and 3598 of SEQ ID NO:3 (OrfB) to an ending point of between about positions 3975 and 4200 of SEQ ID NO:3. The nucleotide sequence containing the sequence encoding the OrfB-AT domain is represented herein as SEQ ID NO:23 (positions 2701-4200 of SEQ ID NO:3). The amino acid sequence containing the AT domain spans from a starting point of between about positions 901 and 1200 of SEQ ID NO:4 (OrfB) to an ending point of between about positions 1325 and 1400 of SEQ ID NO:4. The amino acid sequence containing the OrfB-AT domain is represented herein as SEQ ID NO:24 (positions 901-1400 of SEQ ID NO:4). It is noted that the OrfB-AT domain contains an active site motif of GxS*xG (*acyl binding site S.sub.1140) that is characteristic of acyltransferse (AT) proteins.

An "acyltransferase" or "AT" refers to a general class of enzymes that can carry out a number of distinct acyl transfer reactions. The term "acyltransferase" can be used interchangeably with the term "acyl transferase". The Schizochytrium domain shows good homology to a domain present in all of the other PUFA PKS systems currently examined and very weak homology to some acyltransferases whose specific functions have been identified (e.g. to malonyl-CoA:ACP acyltransferase, MAT). In spite of the weak homology to MAT, this AT domain is not believed to function as a MAT because it does not possess an extended motif structure characteristic of such enzymes (see MAT domain description, above). For the purposes of this disclosure, the functions of the AT domain in a PUFA PKS system include, but are not limited to: transfer of the fatty acyl group from the OrfA ACP domain(s) to water (i.e. a thioesterase--releasing the fatty acyl group as a free fatty acid), transfer of a fatty acyl group to an acceptor such as CoA, transfer of the acyl group among the various ACP domains, or transfer of the fatty acyl group to a lipophilic acceptor molecule (e.g. to lysophosphadic acid).

The fourth domain in OrfB is an ER domain, also referred to herein as OrfB-ER. This domain is contained within the nucleotide sequence spanning from a starting point of about position 4648 of SEQ ID NO:3 (OrfB) to an ending point of about position 6177 of SEQ ID NO:3. The nucleotide sequence containing the sequence encoding the OrfB-ER domain is represented herein as SEQ ID NO:25 (positions 4648-6177 of SEQ ID NO:3). The amino acid sequence containing the ER domain spans from a starting point of about position 1550 of SEQ ID NO:4 (OrfB) to an ending point of about position 2059 of SEQ ID NO:4. The amino acid sequence containing the OrfB-ER domain is represented herein as SEQ ID NO:26 (positions 1550-2059 of SEQ ID NO:4).

According to the present invention, this domain has enoyl-ACP reductase (ER) biological activity. According to the present invention, the term "enoyl-ACP reductase" can be used interchangeably with "enoyl reductase", "enoyl ACP-reductase" and "enoyl acyl-ACP reductase". The ER enzyme reduces the trans-double bond (introduced by the DH activity) in the fatty acyl-ACP, resulting in fully saturating those carbons. The ER domain in the PUFA-PKS shows homology to a newly characterized family of ER enzymes (Heath et al., Nature 406, 145 (2000)). Heath and Rock identified this new class of ER enzymes by cloning a gene of interest from Streptococcus pneumoniae, purifying a protein expressed from that gene, and showing that it had ER activity in an in vitro assay. The sequence of the Schizochytrium ER domain of OrfB shows homology to the S. pneumoniae ER protein. All of the PUFA PKS systems currently examined contain at least one domain with very high sequence homology to the Schizochytrium ER domain. The Schizochytrium PUFA PKS system contains two ER domains (one on OrfB and one on OrfC).

Open Reading Frame C (OrfC):

The complete nucleotide sequence for OrfC is represented herein as SEQ ID NO:5. OrfC is a 4509 nucleotide sequence (not including the stop codon) which encodes a 1503 amino acid sequence, represented herein as SEQ ID NO:6. Within OrfC are three domains: (a) two FabA-like .beta.-hydroxyacyl-ACP dehydrase (DH) domains; and (b) one enoyl-ACP reductase (ER) domain. The nucleotide sequence for OrfC has been deposited with GenBank as Accession No. AF378329 (amino acid sequence Accession No. AAK728881).

The first domain in OrfC is a DH domain, also referred to herein as OrfC-DH1. This is one of two DH domains in OrfC, and therefore is designated DH1. This domain is contained within the nucleotide sequence spanning from a starting point of between about positions 1 and 778 of SEQ ID NO:5 (OrfC) to an ending point of between about positions 1233 and 1350 of SEQ ID NO:5. The nucleotide sequence containing the sequence encoding the OrfC-DH1 domain is represented herein as SEQ ID NO:27 (positions 1-1350 of SEQ ID NO:5). The amino acid sequence containing the DH1 domain spans from a starting point of between about positions 1 and 260 of SEQ ID NO:6 (OrfC) to an ending point of between about positions 411 and 450 of SEQ ID NO:6. The amino acid sequence containing the OrfC-DH1 domain is represented herein as SEQ ID NO:28 (positions 1-450 of SEQ ID NO:6).

According to the present invention, this domain has FabA-like .beta.-hydroxyacyl-ACP dehydrase (DH) biological activity. The term "FabA-like .beta.-hydroxyacyl-ACP dehydrase" can be used interchangeably with the terms "FabA-like .beta.-hydroxy acyl-ACP dehydrase", ".beta.-hydroxyacyl-ACP dehydrase", "dehydrase" and similar derivatives. The characteristics of both the DH domains (see below for DH 2) in the PUFA PKS systems have been described in the preceding sections. This class of enzyme removes HOH from a .beta.-ketoacyl-ACP and leaves a trans double bond in the carbon chain. The DH domains of the PUFA PKS systems show homology to bacterial DH enzymes associated with their FAS systems (rather than to the DH domains of other PKS systems). A subset of bacterial DH's, the FabA-like DH's, possesses cis-trans isomerase activity (Heath et al., J. Biol. Chem., 271, 27795 (1996)). It is the homologies to the FabA-like DH's that indicate that one or both of the DH domains is responsible for insertion of the cis double bonds in the PUFA PKS products.

The second domain in OrfC is a DH domain, also referred to herein as OrfC-DH2. This is the second of two DH domains in OrfC, and therefore is designated DH2. This domain is contained within the nucleotide sequence spanning from a starting point of between about positions 1351 and 2437 of SEQ ID NO:5 (OrfC) to an ending point of between about positions 2607 and 2850 of SEQ ID NO:5. The nucleotide sequence containing the sequence encoding the OrfC-DH2 domain is represented herein as SEQ ID NO:29 (positions 1351-2850 of SEQ ID NO:5). The amino acid sequence containing the DH2 domain spans from a starting point of between about positions 451 and 813 of SEQ ID NO:6 (OrfC) to an ending point of between about positions 869 and 950 of SEQ ID NO:6. The amino acid sequence containing the OrfC-DH2 domain is represented herein as SEQ ID NO:30 (positions 451-950 of SEQ ID NO:6). DH biological activity has been described above.

The third domain in OrfC is an ER domain, also referred to herein as OrfC-ER. This domain is contained within the nucleotide sequence spanning from a starting point of about position 2998 of SEQ ID NO:5 (OrfC) to an ending point of about position 4509 of SEQ ID NO:5. The nucleotide sequence containing the sequence encoding the OrfC-ER domain is represented herein as SEQ ID NO:31 (positions 2998-4509 of SEQ ID NO:5). The amino acid sequence containing the ER domain spans from a starting point of about position 1000 of SEQ ID NO:6 (OrfC) to an ending point of about position 1502 of SEQ ID NO:6. The amino acid sequence containing the OrfC-ER domain is representedherein as SEQ ID NO:32 (positions 1000-1502 of SEQ ID NO:6). ER biological activity has been described above.

Thraustochytrium 23B PUFA PKS

Th. 23B Open Reading Frame A (OrfA):

The complete nucleotide sequence for Th. 23B OrfA is represented herein as SEQ ID NO:38. SEQ ID NO:38 encodes the following domains in Th. 23B OrfA: (a) one .beta.-ketoacyl-ACP synthase (KS) domain; (b) one malonyl-CoA:ACP acyltransferase (MAT) domain; (c) eight acyl carrier protein (ACP) domains; and (d) one .beta.-ketoacyl-ACP reductase (KR) domain. This domain organization is the same as is present in Schizochytrium Orf A (SEQ ID NO:1) with the exception that the Th. 23B Orf A has 8 adjacent ACP domains, while Schizochytrium Orf A has 9 adjacent ACP domains. Th. 23B OrfA is a 8433 nucleotide sequence (not including the stop codon) which encodes a 2811 amino acid sequence, represented herein as SEQ ID NO:39. The Th. 23B OrfA amino acid sequence (SEQ ID NO:39) was compared with known sequences in a standard BLAST search (BLAST parameters: Blastp, low complexity filter Off, program--BLOSUM62,Gap cost--Existence: 11, Extension 1; (BLAST described in Altschul, S. F., Madden, T. L., Schaaffer, A. A., Zhang, J., Zhang, Z., Miller, W. & Lipman, D. J. (1997) "Gapped BLAST and PSI-BLAST: a new generation of protein database search programs." Nucleic Acids Res. 25:3389-3402, incorporated herein by reference in its entirety))). At the amino acid level, the sequences with the greatest degree of homology to Th. 23B OrfA was Schizochytrium Orf A (gb AAK72879.1) (SEQ ID NO:2). The alignment extends over the entire query but is broken into 2 pieces (due to the difference in numbers of ACP repeats). SEQ ID NO:39 first aligns at positions 6 through 1985 (including 8 ACP domains) with SEQ ID NO:2 and shows a sequence identity to SEQ ID NO:2 of 54% over 2017 amino acids. SEQ ID NO:39 also aligns at positions 980 through 2811 with SEQ ID NO:2 and shows a sequence identity to SEQ ID NO:2 of 43% over 1861 amino acids. In this second alignment, the match is evident for the Th. 23B 8X ACPs in the regions of the conserved pantetheine attachment site motif, but is very poor over the 1st Schizochytrium ACP domain (i.e., there is not a 9th ACP domain in the Th. 23B query sequence, but the Blastp output under theses conditions attempts to align them anyway). SEQ ID NO:39 shows the next closest identity with sequences from Shewanella oneidensis (Accession No. NP.sub.--717214) and Photobacter profundum (Accession No. AAL01060).

The first domain in Th. 23B OrfA is a KS domain, also referred to herein as Th. 23B OrfA-KS. KS domain function has been described in detail above. This domain is contained within the nucleotide sequence spanning from about position 1 to about position 1500 of SEQ ID NO:38, represented herein as SEQ ID NO:40. The amino acid sequence containing the Th. 23B KS domain is a region of SEQ ID NO:39 spanning from about position 1 to about position 500 of SEQ ID NO:39, represented herein as SEQ ID NO:41. This region of SEQ ID NO:39 has a Pfam match to FabB (.beta.-ketoacyl-ACP synthase) spanning from position 1 to about position 450 of SEQ ID NO:39 (also positions 1 to about 450 of SEQ ID NO:41). It is noted that the Th. 23B OrfA-KS domain contains an active site motif: DXAC* (*acyl binding site C.sub.207). Also, a characteristic motif at the end of the Th. 23B KS region, GFGG, is present in positions 453-456 of SEQ ID NO:39 (also positions 453-456 of SEQ ID NO:41). The amino acid sequence spanning positions 1-500 of SEQ ID NO:39 is about 79% identical to Schizochytrium OrfA (SEQ ID NO:2) over 496 amino acids. The amino acid sequence spanning positions 1-450 of SEQ ID NO:39 is about 81% identical to Schizochytrium OrfA (SEQ ID NO:2) over 446 amino acids.

The second domain in Th. 23B OrfA is a MAT domain, also referred to herein as Th. 23B OrfA-MAT. MAT domain function has been described in detail above. This domain is contained within the nucleotide sequence spanning from between about position 1503 and about position 3000 of SEQ ID NO:38, represented herein as SEQ ID NO:42. The amino acid sequence containing the Th. 23B MAT domain is a region of SEQ ID NO:39 spanning from about position 501 to about position 1000, represented herein by SEQ ID NO:43. This region of SEQ ID NO:39 has a Pfam match to FabD (malonyl-CoA:ACP acyltransferase) spanning from about position 580 to about position 900 of SEQ ID NO:39 (positions 80-400 of SEQ ID NO:43). It is noted that the Th. 23B OrfA-MAT domain contains an active site motif: GHS*XG (*acyl binding site S.sub.697), represented by positions 695-699 of SEQ ID NO:39. The amino acid sequence spanning positions 501-1000 of SEQ ID NO:39 is about 46% identical to Schizochytrium OrfA (SEQ ID NO:2) over 481 amino acids. The amino acid sequence spanning positions 580-900 of SEQ ID NO:39 is about 50% identical to Schizochytrium OrfA (SEQ ID NO:2) over 333 amino acids.

Domains 3-10 of Th. 23B OrfA are eight tandem ACP domains, also referred to herein as Th. 23B OrfA-ACP (the first domain in the sequence is OrfA-ACP1, the second domain is OrfA-ACP2, the third domain is OrfA-ACP3, etc.). The function of ACP domains has been described in detail above. The first Th. 23B ACP domain, Th. 23B OrfA-ACP1, is contained within the nucleotide sequence spanning from about position 3205 to about position 3555 of SEQ ID NO:38 (OrfA), represented herein as SEQ ID NO:44. The amino acid sequence containing the first Th. 23B ACP domain is a region of SEQ ID NO:39 spanning from about position 1069 to about position 1185 of SEQ ID NO:39, represented herein by SEQ ID NO:45. The amino acid sequence spanning positions 1069-1185 of SEQ ID NO:39 is about 65% identical to Schizochytrium OrfA (SEQ ID NO:2) over 85 amino acids. Th. 23B OrfA-ACP1 has a similar identity to any one of the nine ACP domains in Schizochytrium OrfA.

The eight ACP domains in Th. 23B OrfA are adjacent to one another and can be identified by the presence of the phosphopantetheine binding site motif, LGXDS* (represented by SEQ ID NO:46), wherein the S* is the phosphopantetheine attachment site. The amino acid position of each of the eight S* sites, with reference to SEQ ID NO:39, are 1128 (ACP1), 1244 (ACP2), 1360 (ACP3), 1476 (ACP4), 1592 (ACP5), 1708 (ACP6), 1824 (ACP7) and 1940 (ACP8). The nucleotide and amino acid sequences of all eight Th. 23B ACP domains are highly conserved and therefore, the sequence for each domain is not represented herein by an individual sequence identifier. However, based on the information disclosed herein, one of skill in the art can readily determine the sequence containing each of the other seven ACP domains in SEQ ID NO:38 and SEQ ID NO:39.

All eight Th. 23B ACP domains together span a region of Th. 23B OrfA of from about position 3205 to about postion 5994 of SEQ ID NO:38, which corresponds to amino acidpositions of from about 1069 to about 1998 of SEQ ID NO:39. The nucleotide sequence for the entire ACP region containing all eight domains is represented herein as SEQ ID NO:47. SEQ ID NO:47 encodes an amino acid sequence represented herein by SEQ ID NO:48. SEQ ID NO:48 includes the linker segments between individual ACP domains. The repeat interval for the eight domains is approximately every 116 amino acids of SEQ ID NO:48, and each domain can be considered to consist of about 116 amino acids centered on the active site motif (described above). It is noted that the linker regions between the nine adjacent ACP domains in OrfA in Schizochytrium are highly enriched in proline and alanine residues, while the linker regions between the eight adjacent ACP domains in OrfA of Thraustochytrium are highly enriched in serine residues (and not proline or alanine residues).

The last domain in Th. 23B OrfA is a KR domain, also referred to herein as Th. 23B OrfA-KR. KR domain function has been discussed in detail above. This domain is contained within the nucleotide sequence spanning from between about position 6001 to about position 8433 of SEQ ID NO:38, represented herein by SEQ ID NO:49. The amino acid sequence containing the Th. 23B KR domain is a region of SEQ ID NO:39 spanning from about position 2001 to about position 2811 of SEQ ID NO:39, represented herein by SEQ ID NO:50. This region of SEQ ID NO:39 has a Pfam match to FabG (.beta.-ketoacyl-ACP reductase) spanning from about position 2300 to about 2550 of SEQ ID NO:39 (positions 300-550 of SEQ ID NO:50). The amino acid sequence spanning positions 2001-2811 of SEQ ID NO:39 is about 40% identical to Schizochytrium OrfA (SEQ ID NO:2) over 831 amino acids. The amino acid sequence spanning positions 2300-2550 of SEQ ID NO:39 is about 51% identical to Schizochytrium OrfA (SEQ ID NO:2) over 235 amino acids.

Th. 23B Open Reading Frame B (OrfB):

The complete nucleotide sequence for Th. 23B OrfB is represented herein as SEQ ID NO:51. SEQ ID NO:51 encodes the following domains in Th. 23B OrfB: (a) one .beta.-ketoacyl-ACP synthase (KS) domain; (b) one chain length factor (CLF) domain; (c) one acyltransferase (AT) domain; and, (d) one enoyl-ACP reductase (ER) domain. This domain organization is the same as in Schizochytrium Orf B (SEQ ID NO:3) with the exception that the linker region between the AT and ER domains of the Schizochytrium protein is longer than that of Th. 23B by about 50-60 amino acids. Also, this linker region in Schizochytrium has a specific area that is highly enriched in serine residues (it contains 15 adjacent serine residues, in addition to other serines in the region), whereas the corresponding linker region in Th. 23B OrfB is not enriched in serine residues. This difference in the AT/ER linker region most likely accounts for a break in the alignment between Schizochytrium OrfB and Th. 23B OrfB at the start of this region.

Th. 23B OrfB is a 5805 nucleotide sequence (not including the stop codon) which encodes a 1935 amino acid sequence, represented herein as SEQ ID NO:52. The Th. 23B OrfB amino acid sequence (SEQ ID NO:52) was compared with known sequences in a standard BLAST search (BLAST parameters: Blastp, low complexity filter Off, program--BLOSUM62,Gap cost--Existence: 11, Extension 1; (BLAST described in Altschul, S. F., Madden, T. L., Schaaffer, A. A., Zhang, J., Zhang, Z., Miller, W. & Lipman, D. J. (1997) "Gapped BLAST and PSI-BLAST: a new generation of protein database search programs." Nucleic Acids Res. 25:3389-3402, incorporated herein by reference in its entirety))). At the amino acid level, the sequences with the greatest degree of homology to Th. 23B OrfB were Schizochytrium Orf B (gb AAK72880.1) (SEQ ID NO:4), over most of OrfB; and Schizochytrium OrfC (gb AAK728881.1) (SEQ ID NO:6), over the last domain (the alignment is broken into 2 pieces, as mentioned above). SEQ ID NO:52 first aligns at positions 10 through about 1479 (including the KS, CLF and AT domains) with SEQ ID NO:4 and shows a sequence identity to SEQ ID NO:4 of 52% over 1483 amino acids. SEQ ID NO:52 also aligns at positions 1491 through 1935 (including the ER domain) with SEQ ID NO:6 and shows a sequence identity to SEQ ID NO:4 of 64% over 448 amino acids.

The first domain in the Th. 23B OrfB is a KS domain, also referred to herein as Th. 23B OrfB-KS. KS domain function has been described in detail above. This domain is contained within the nucleotide sequence spanning from between about position 1 and about postion 1500 of SEQ ID NO:51 (Th. 23B OrfB), represented herein as SEQ ID NO:53. The amino acid sequence containing the Th. 23B KS domain is a region of SEQ ID NO: 52 spanning from about position 1 to about position 500 of SEQ ID NO:52, represented herein as SEQ ID NO:54. This region of SEQ ID NO:52 has a Pfam match to FabB (.beta.-ketoacyl-ACP synthase) spanning from about position 1 to about position 450 (positions 1-450 of SEQ ID NO:54). It is noted that the Th. 23B OrfB-KS domain contains an active site motif: DXAC*, where C* is the site of acyl group attachment and wherein the C* is at position 201 of SEQ ID NO:52. Also, a characteristic motif at the end of the KS region, GFGG is present in amino acid positions 434-437 of SEQ ID NO:52. The amino acid sequence spanning positions 1-500 of SEQ ID NO:52 is about 64% identical to Schizochytrium OrfB (SEQ ID NO:4) over 500 amino acids. The amino acid sequence spanning positions 1-450 of SEQ ID NO:52 is about 67% identical to Schizochytrium OrfB (SEQ ID NO:4) over 442 amino acids.

The second domain in Th. 23B OrfB is a CLF domain, also referred to herein as Th. 23B OrfB-CLF. CLF domain function has been described in detail above. This domain is contained within the nucleotide sequence spanning from between about position 1501 and about position 3000 of SEQ ID NO:51 (OrfB), represented herein as SEQ ID NO:55. The amino acid sequence containing the CLF domain is a region of SEQ ID NO: 52 spanning from about position 501 to aboutposition 1000 of SEQ ID NO:52, represented herein as SEQ ID NO:56. This region of SEQ ID NO:52 has a Pfam match to FabB (.beta.-ketoacyl-ACP synthase) spanning from about position 550 to about position 910 (positions 50-410 of SEQ ID NO:56). Although CLF has homology to KS proteins, it lacks an active site cysteine to 25 which the acyl group is attached in KS proteins. The amino acid sequence spanning positions 501-1000 of SEQ ID NO:52 is about 49% identical to Schizochytrium OrfB (SEQ ID NO:4) over 517 amino acids. The amino acid sequence spanning positions 550-910 of SEQ ID NO:52 is about 54% identical to Schizochytrium OrfB (SEQ ID NO:4) over 360 amino acids.

The third domain in Th. 23B OrfB is an AT domain, also referred to herein as Th. 23B OrfB-AT. AT domain function has been described in detail above. This domain is contained within the nucleotide sequence spanning from between about position 3001 and about position 4500 of SEQ ID NO:51 (Th. 23B OrfB), represented herein as SEQ ID NO:58. The amino acid sequence containing the Th. 23B AT domain is a region of SEQ ID NO: 52 spanning from about position 1001 to about position 1500 of SEQ ID NO:52, represented herein as SEQ ID NO:58. This region of SEQ ID NO:52 has a Pfam match to FabD (malonyl-CoA:ACP acyltransferase) spanning from about position 1100 to about position 1375 (positions 100-375 of SEQ ID NO:58). Although this AT domain of the PUFA synthases has homology to MAT proteins, it lacks the extended motif of the MAT (key arginine and glutamine residues) and it is not thought to be involved in malonyl-CoA transfers. The GXS*XG motif of acyltransferases is present, with the S* being the site of acyl attachment and located at position 1123 with respect to SEQ ID NO:52. The amino acid sequence spanning positions 1001-1500 of SEQ ID NO:52 is about 44% identical to Schizochytrium OrfB (SEQ ID NO:4) over 459 amino acids. The amino acid sequence spanning positions 1100-1375 of SEQ ID NO:52 is about 45% identical to Schizochytrium OrfB (SEQ ID NO:4) over 283 amino acids.

The fourth domain in Th. 23B OrfB is an ER domain, also referred to herein as Th. 23B OrfB-ER. ER domain function has been described in detail above. This domain is contained within the nucleotide sequence spanning from between about position 4501 and about position 5805 of SEQ ID NO:51 (OrfB), represented herein as SEQ ID NO:59. The amino acid sequence containing the Th. 23B ER domain is a region of SEQ ID NO: 52 spanning from about position 1501 to about position 1935 of SEQ ID NO:52, represented herein as SEQ ID NO:60. This region of SEQ ID NO:52 has a Pfam match to a family of dioxygenases related to 2-nitropropane dioxygenases spanning from about position 1501 to about position 1810 (positions 1-310 of SEQ ID NO:60). That this domain functions as an ER can be further predicted due to homology to a newly characterized ER enzyme from Streptococcus pneumoniae. The amino acid sequence spanning positions 1501-1935 of SEQ ID NO:52 is about 66% identical to Schizochytrium OrfB (SEQ ID NO:4) over 433 amino acids. The amino acid sequence spanning positions 1501-1810 of SEQ ID NO:52 is about 70% identical to Schizochytrium OrfB (SEQ ID NO:4) over 305 amino acids.

Th. 23B Open Reading Frame C (OrfC):

The complete nucleotide sequence for Th. 23B OrfC is represented herein as SEQ ID NO:61. SEQ ID NO:61 encodes the following domains in Th. 23B OrfC: (a) two FabA-like .beta.-hydroxyacyl-ACP dehydrase (DH) domains, both with homology to the FabA protein (an enzyme that catalyzes the synthesis of trans-2-decenoyl-ACP and the reversible isomerization of this product to cis-3-decenoyl-ACP); and (b) one enoyl-ACP reductase (ER) domain with high homology to the ER domain of Schizochytrium OrfB. This domain organization is the same as in Schizochytrium Orf C (SEQ ID NO:5).

Th. 23B OrfC is a 4410 nucleotide sequence (not including the stop codon) which encodes a 1470 amino acid sequence, represented herein as SEQ ID NO:62. The Th. 23B OrfC amino acid sequence (SEQ ID NO:62) was compared with known sequences in a standard BLAST search (BLAST parameters: Blastp, low complexity filter Off, program--BLOSUM62,Gap cost--Existence: 11, Extension 1; (BLAST described in Altschul, S. F., Madden, T. L., Schaaffer, A. A., Zhang, J., Zhang, Z., Miller, W. & Lipman, D. J. (1997) "Gapped BLAST and PSI-BLAST: a new generation of protein database search programs." Nucleic Acids Res. 25:3389-3402, incorporated herein by reference in its entirety))). At the amino acid level, the sequences with the greatest degree of homology to Th. 23B OrfC was Schizochytrium OrfC (gb AAK728881.1) (SEQ ID NO:6). SEQ ID NO:52 is 66% identical to Schizochytrium OrfC (SEQ ID NO:6).

The first domain in Th. 23B OrfC is a DH domain, also referred to herein as Th. 23B OrfC-DH1. DH domain function has been described in detail above. This domain is contained within the nucleotide sequence spanning from between about position 1 to about position 1500 of SEQ ID NO:61 (OrfC), represented herein as SEQ ID NO:63. The amino acid sequence containing the Th. 23B DH1 domain is a region of SEQ ID NO:62 spanning from about position 1 to about position 500 of SEQ ID NO:62, represented herein as SEQ ID NO:64. This region of SEQ ID NO:62 has a Pfam match to FabA, as mentioned above, spanning from about position 275 to about position 400 (positions 275-400 of SEQ ID NO:64). The amino acid sequence spanning positions 1-500 of SEQ ID NO:62 is about 66% identical to Schizochytrium OrfC (SEQ ID NO:6) over 526 amino acids. The amino acid sequence spanning positions 275-400 of SEQ ID NO:62 is about 81% identical to Schizochytrium OrfC (SEQ ID NO:6) over 126 amino acids.

The second domain in Th. 23B OrfC is also a DH domain, also referred to herein as Th. 23B OrfC-DH2. This is the second of two DH domains in OrfC, and therefore is designated DH2. This domain is contained within the nucleotide sequence spanning from between about position 1501 to about 3000 of SEQ ID NO:61 (OrfC), represented herein as SEQ ID NO:65. The amino acid sequence containing the Th. 23B DH2 domain is a region of SEQ ID NO: 62 spanning from about position 501 to about position 1000 of SEQ ID NO:62, represented herein as SEQ ID NO:66. This region of SEQ ID NO:62 has a Pfam match to FabA, as mentioned above, spanning from about position 800 to about position 925 (positions 300-425 of SEQ ID NO:66). The amino acid sequence spanning positions 501-1000 of SEQ ID NO:62 is about 56% identical to Schizochytrium OrfC (SEQ ID NO:6) over 518 amino acids. The amino acid sequence spanning positions 800-925 of SEQ ID NO:62 is about 58% identical to Schizochytrium OrfC (SEQ ID NO:6) over 124 amino acids.

The third domain in Th. 23B OrfC is an ER domain, also referred to herein as Th. 23B OrfC-ER. ER domain function has been described in detail above. This domain is contained within the nucleotide sequence spanning from between about position 3001 to about position 4410 of SEQ ID NO:61 (OrfC), represented herein as SEQ ID NO:67. The amino acid sequence containing the Th. 23B ER domain is a region of SEQ ID NO:62 spanning from about position 1001 to about position 1470 of SEQ ID NO:62, represented herein as SEQ ID NO:68. This region of SEQ ID NO:62 has a Pfam match to the dioxygenases related to 2-nitropropane dioxygenases, as mentioned above, spanning from about position 1025 to about position 1320 (positions 25-320 of SEQ ID NO:68). This domain function as an ER can also be predicted due to homology to a newly characterized ER enzyme from Streptococcus pneumoniae. The amino acid sequence spanning positions 1001-1470 of SEQ ID NO:62 is about 75% identical to Schizochytrium OrfB (SEQ ID NO:4) over 474 amino acids. The amino acid sequence spanning positions 1025-1320 of SEQ ID NO:62 is about 81% identical to Schizochytrium OrfB (SEQ ID NO:4) over 296 amino acids.

One embodiment of the present invention relates to an isolated protein or domain from a non-bacterial PUFA PKS system, a homologue thereof, and/or a fragment thereof. Also included in the invention are isolated nucleic acid molecules encoding any of the proteins, domains or peptides described herein (discussed in detail below). According to the present invention, an isolated protein or peptide, such as a protein or peptide from a PUFA PKS system, is a protein or a fragment thereof (including a polypeptide or peptide) that has been removed from its natural milieu (i.e., that has been subject to human manipulation) and can include purified proteins, partially purified proteins, recombinantly produced proteins, and synthetically produced proteins, for example. As such, "isolated" does not reflect the extent to which the protein has been purified. Preferably, an isolated protein of the present invention is produced recombinantly. An isolated peptide can be produced synthetically (e.g., chemically, such as by peptide synthesis) or recombinantly. In addition, and by way of example, a "Thraustochytrium PUFA PKS protein" refers to a PUFA PKS protein (generally including a homologue of a naturally occurring PUFA PKS protein) from a Thraustochytrium microorganism, or to a PUFA PKS protein that has been otherwise produced from the knowledge of the structure (e.g., sequence), and perhaps the function, of a naturally occurring PUFA PKS protein from Thraustochytrium. In other words, general reference to a Thraustochytrium PUFA PKS protein includes any PUFA PKS protein that has substantially similar structure and function of a naturally occurring PUFA PKS protein from Thraustochytrium or that is a biologically active (i.e., has biological activity) homologue of a naturally occurring PUFA PKS protein from Thraustochytrium as described in detail herein. As such, a Thraustochytrium PUFA PKS protein can include purified, partially purified, recombinant, mutated/modified and synthetic proteins. The same description applies to reference to other proteins or peptides described herein, such as the PUFA PKS proteins and domains from Schizochytrium or from other microorganisms.

According to the present invention, the terms "modification" and "mutation" can be used interchangeably, particularly with regard to the modifications/mutations to the primary amino acid sequences of a protein or peptide (or nucleic acid sequences) described herein. The term "modification" can also be used to describe post-translational modifications to a protein or peptide including, but not limited to, methylation, famesylation, carboxymethylation, geranyl geranylation, glycosylation, phosphorylation, acetylation, myristoylation, prenylation, palmitation, and/or amidation. Modifications can also include, for example, complexing a protein or peptide with another compound. Such modifications can be considered to be mutations, for example, if the modification is different than the post-translational modification that occurs in the natural, wild-type protein or peptide.

As used herein, the term "homologue" is used to refer to a protein or peptide which differs from a naturally occurring protein or peptide (i.e., the "prototype" or "wild-type" protein) by one or more minor modifications or mutations to the naturally occurring protein or peptide, but which maintains the overall basic protein and side chain structure of the naturally occurring form (i.e., such that the homologue is identifiable as being related to the wild-type protein). Such changes include, but are not limited to: changes in one or a few amino acid side chains; changes one or a few amino acids, including deletions (e.g., a truncated version of the protein or peptide) insertions and/or substitutions; changes in stereochemistry of one or a few atoms; and/or minor derivatizations, including but not limited to: methylation, farnesylation, geranyl geranylation, glycosylation, carboxymethylation, phosphorylation, acetylation, myristoylation, prenylation, palmitation, and/or amidation. A homologue can have either enhanced, decreased, or substantially similar properties as compared to the naturally occurring protein or peptide. Preferred homologues of a PUFA PKS protein or domain are described in detail below. It is noted that homologues can include synthetically produced homologues, naturally occurring allelic variants of a given protein or domain, or homologous sequences from organisms other than the organism from which the reference sequence was derived.

Conservative substitutions typically include substitutions within the following groups: glycine and alanine; valine, isoleucine and leucine; aspartic acid, glutamic acid, asparagine, and glutamine; serine and threonine; lysine and arginine; and phenylalanine and tyrosine. Substitutions may also be made on the basis of conserved hydrophobicity or hydrophilicity (Kyte and Doolittle, J. Mol. Biol. (1982) 157: 105-132), or on the basis of the ability to assume similar polypeptide secondary structure (Chou and Fasman, Adv. Enzymol. (1978) 47: 45-148, 1978).

Homologues can be the result of natural allelic variation or natural mutation. A naturally occurring allelic variant of a nucleic acid encoding a protein is a gene that occurs at essentially the same locus (or loci) in the genome as the gene which encodes such protein, but which, due to natural variations caused by, for example, mutation or recombination, has a similar but not identical sequence. Allelic variants typically encode proteins having similar activity to that of the protein encoded by the gene to which they are being compared. One class of allelic variants can encode the same protein but have different nucleic acid sequences due to the degeneracy of the genetic code. Allelic variants can also comprise alterations in the 5' or 3' untranslated regions of the gene (e.g., in regulatory control regions). Allelic variants are well known to those skilled in the art.

Homologues can be produced using techniques known in the art for the production of proteins including, but not limited to, direct modifications to the isolated, naturally occurring protein, direct protein synthesis, or modifications to the nucleic acid sequence encoding the protein using, for example, classic or recombinant DNA techniques to effect random or targeted mutagenesis.

Modifications or mutations in protein homologues, as compared to the wild-type protein, either increase, decrease, or do not substantially change, the basic biological activity of the homologue as compared to the naturally occurring (wild-type) protein. In general, the biological activity or biological action of a protein refers to any function(s) exhibited or performed by the protein that is ascribed to the naturally occurring form of the protein as measured or observed in vivo (i.e., in the natural physiological environment of the protein) or in vitro (i.e., under laboratory conditions). Biological activities of PUFA PKS systems and the individual proteins/domains that make up a PUFA PKS system have been described in detail elsewhere herein. Modifications of a protein, such as in a homologue or mimetic (discussed below), may result in proteins having the same biological activity as the naturally occurring protein, or in proteins having decreased or increased biological activity as compared to the naturally occurring protein. Modifications which result in a decrease in protein expression or a decrease in the activity of the protein, can be referred to as inactivation (complete or partial), down-regulation, or decreased action (or activity) of a protein. Similarly, modifications which result in an increase in protein expression or an increase in the activity of the protein, can be referred to as amplification, overproduction, activation, enhancement, up-regulation or increased action (or activity) of a protein. It is noted that general reference to a homologue having the biological activity of the wild-type protein does not necessarily mean that the homologue has identical biological activity as the wild-type protein, particularly with regard to the level of biological activity. Rather, a homologue can perform the same biological activity as the wild-type protein, but at a reduced or increased level of activity as compared to the wild-type protein. A functional domain of a PUFA PKS system is a domain (i.e., a domain can be a portion of a protein) that is capable of performing a biological function (i.e., has biological activity).

Methods of detecting and measuring PUFA PKS protein or domain biological activity include, but are not limited to, measurement of transcription of a PUFA PKS protein or domain, measurement of translation of a PUFA PKS protein or domain, measurement of posttranslational modification of a PUFA PKS protein or domain, measurement of enzymatic activity of a PUFA PKS protein or domain, and/or measurement production of one or more products of a PUFA PKS system (e.g., PUFA production). It is noted that an isolated protein of the present invention (including a homologue) is not necessarily required to have the biological activity of the wild-type protein. For example, a PUFA PKS protein or domain can be a truncated, mutated or inactive protein, for example. Such proteins are useful in screening assays, for example, or for other purposes such as antibody production. In a preferred embodiment, the isolated proteins of the present invention have biological activity that is similar to that of the wild-type protein (although not necessarily equivalent, as discussed above).

Methods to measure protein expression levels generally include, but are not limited to: Western blot, immunoblot, enzyme-linked immunosorbant assay (ELISA), radioimmunoassay (RIA), immunoprecipitation, surface plasmon resonance, chemiluminescence, fluorescent polarization, phosphorescence, immunohistochemical analysis, matrix-assisted laser desorption/ionization time-of-flight (MALDI-TOF) mass spectrometry, microcytometry, microarray, microscopy, fluorescence activated cell sorting (FACS), and flow cytometry, as well as assays based on a property of the protein including but not limited to enzymatic activity or interaction with other protein partners. Binding assays are also well known in the art. For example, a BIAcore machine can be used to determine the binding constant of a complex between two proteins. The dissociation constant for the complex can be determined by monitoring changes in the refractive index with respect to time as buffer is passed over the chip (O'Shannessy et al. Anal. Biochem. 212:457-468 (1993); Schuster et al., Nature 365:343-347 (1993)). Other suitable assays for measuring the binding of one protein to another include, for example, immunoassays such as enzyme linked immunoabsorbent assays (ELISA) and radioimmunoassays (RIA); or determination of binding by monitoring the change in the spectroscopic or optical properties of the proteins through fluorescence, UV absorption, circular dichrosim, or nuclear magnetic resonance (NMR).

In one embodiment, the present invention relates to an isolated protein comprising an amino acid sequence selected from the group consisting of: (a) an amino acid sequence selected from the group consisting of: SEQ ID NO:39, SEQ ID NO:52, SEQ ID NO:62, and biologically active fragments thereof; (b) an amino acid sequence selected from the group consisting of: SEQ ID NO:41, SEQ ID NO:43, SEQ ID NO:45, SEQ ID NO:48, SEQ ID NO:50, SEQ ID NO:54, SEQ ID NO:56, SEQ ID NO:58, SEQ ID NO:60, SEQ ID NO:64, SEQ ID NO:66, SEQ ID NO:68 and biologically active fragments thereof; (c) an amino acid sequence that is at least about 60% identical to at least 500 consecutive amino acids of the amino acid sequence of (a), wherein the amino acid sequence has a biological activity of at least one domain of a polyunsaturated fatty acid (PUFA) polyketide synthase (PKS) system; and/or (d) an amino acid sequence that is at least about 60% identical to the amino acid sequence of (b), wherein the amino acid sequence has a biological activity of at least one domain of a polyunsaturated fatty acid (PUFA) polyketide synthase (PKS) system. In a further embodiment, an amino acid sequence including the active site domains or other functional motifs described above for several of the PUFA PKS domains are encompassed by the invention. In one embodiment, the amino acid sequence described above does not include any of the following amino acid sequences: SEQ ID NO:2, SEQ ID NO:4, SEQ ID NO:6, SEQ ID NO:8, SEQ ID NO: 10, SEQ ID NO:13, SEQ ID NO:18, SEQ ID NO:20, SEQ ID NO:22, SEQ ID NO:24, SEQ ID NO:26, SEQ ID NO:28, SEQ ID NO:30, SEQ ID NO:32.

In one aspect of the invention, a PUFA PKS protein or domain encompassed by the present invention, including a homologue of a particular PUFA PKS protein or domain described herein, comprises an amino acid sequence that is at least about 60% identical to at least 500 consecutive amino acids of an amino acid sequence chosen from: SEQ ID NO:39, SEQ ID NO:52, or SEQ ID NO:62, wherein the amino acid sequence has a biological activity of at least one domain of a PUFA PKS system. In a further aspect, the amino acid sequence of the protein is at least about 60% identical to at least about 600 consecutive amino acids, and more preferably to at least about 700 consecutive amino acids, and more preferably to at least about 800 consecutive amino acids, and more preferably to at least about 900 consecutive amino acids, and more preferably to at least about 1000 consecutive amino acids, and more preferably to at least about 1100 consecutive amino acids, and more preferably to at least about 1200 consecutive amino acids, and more preferably to at least about 1300 consecutive amino acids, and more preferably to at least about 1400 consecutive amino acids of any of SEQ ID NO:39, SEQ ID NO:52, or SEQ ID NO:62, or to the full length of SEQ ID NO:62. In a further aspect, the amino acid sequence of the protein is at least about 60% identical to at least about 1500 consecutive amino acids, and more preferably to at least about 1600 consecutive amino acids, and more preferably to at least about 1700 consecutive amino acids, and more preferably to at least about 1800 consecutive amino acids, and more preferably to at least about 1900 consecutive amino acids, of any of SEQ ID NO:39 or SEQ ID NO:52, or to the full length of SEQ ID NO:52. In a further aspect, the amino acid sequence of the protein is at least about 60% identical to at least about 2000 consecutive amino acids, and more preferably to at least about 2100 consecutive amino acids, and more preferably to at least about 2200 consecutive amino acids, and more preferably to at least about 2300 consecutive amino acids, and more preferably to at least about 2400 consecutive amino acids, and more preferably to at least about 2500 consecutive amino acids, and more preferably to at least about 2600 consecutive amino acids, and more preferably to at least about 2700 consecutive amino acids, and more preferably to at least about 2800 consecutive amino acids, and even more preferably, to the full length of SEQ ID NO:39. In one embodiment, the amino acid sequence described above does not include any of the following amino acid sequences: SEQ ID NO:2, SEQ ID NO:4, SEQ ID NO:6, SEQ ID NO:8, SEQ ID NO: 10, SEQ ID NO: 13, SEQ ID NO: 18, SEQ ID NO:20, SEQ ID NO:22, SEQ ID NO:24, SEQ ID NO:26, SEQ ID NO:28, SEQ ID NO:30, SEQ ID NO:32.

In another aspect, a PUFA PKS protein or domain encompassed by the present invention, including homologues as described above, comprises an amino acid sequence that is at least about 65% identical, and more preferably at least about 70% identical, and more preferably at least about 75% identical, and more preferably at least about 80% identical, and more preferably at least about 85% identical, and more preferably at least about 90% identical, and more preferably at least about 95% identical, and more preferably at least about 96% identical, and more preferably at least about 97% identical, and more preferably at least about 98% identical, and more preferably at least about 99% identical to an amino acid sequence chosen from: SEQ ID NO:39, SEQ ID NO:52, or SEQ ID NO:62, over any of the consecutive amino acid lengths described in the paragraph above, wherein the amino acid sequence has a biological activity of at least one domain of a PUFA PKS system. In one embodiment, the amino acid sequence described above does not include any of the following amino acid sequences: SEQ ID NO:2, SEQ ID NO:4, SEQ ID NO:6, SEQ ID NO:8, SEQ ID NO:10, SEQ ID NO:13, SEQ ID NO:18, SEQ ID NO:20, SEQ ID NO:22, SEQ ID NO:24, SEQ ID NO:26, SEQ ID NO:28, SEQ ID NO:30, SEQ ID NO:32.

In one aspect of the invention, a PUFA PKS protein or domain encompassed by the present invention, including a homologue as described above, comprises an amino acid sequence that is at least about 60% identical to an amino acid sequence chosen from: SEQ ID NO:39, SEQ ID NO:41, SEQ ID NO:43, SEQ ID NO:45, SEQ ID NO:48, SEQ ID NO:50, SEQ ID NO:52, SEQ ID NO:54, SEQ ID NO:56, SEQ ID NO:58, SEQ ID NO:60, SEQ ID NO:62, SEQ ID NO:64, SEQ ID NO:66, SEQ ID NO:68, wherein the amino acid sequence has a biological activity of at least one domain of a PUFA PKS system. In a further aspect, the amino acid sequence of the protein is at least about 65% identical, and more preferably at least about 70% identical, and more preferably at least about 75% identical, and more preferably at least about 80% identical, and more preferably at least about 85% identical, and more preferably at least about 90% identical, and more preferably at least about 95% identical, and more preferably at least about 96% identical, and more preferably at least about 97% identical, and more preferably at least about 98% identical, and more preferably at least about 99% identical to an amino acid sequence chosen from: SEQ ID NO:39, SEQ ID NO:41, SEQ ID NO:43, SEQ ID NO:45, SEQ ID NO:48, SEQ ID NO:50, SEQ ID NO:52, SEQ ID NO:54, SEQ ID NO:56, SEQ ID NO:58, SEQ ID NO:60, SEQ ID NO:62, SEQ ID NO:64, SEQ ID NO:66, SEQ ID NO:68, wherein the amino acid sequence has a biological activity of at least one domain of a PUFA PKS system. In one embodiment, the amino acid sequence described above does not include any of the following amino acid sequences: SEQ ID NO:2, SEQ ID NO:4, SEQ ID NO:6, SEQ ID NO:8, SEQ ID NO:10, SEQ ID NO:13, SEQ ID NO:18, SEQ ID NO:20, SEQ ID NO:22, SEQ ID NO:24, SEQ ID NO:26, SEQ ID NO:28, SEQ ID NO:30, SEQ ID NO:32.

In another aspect, a PUFA PKS protein or domain encompassed by the present invention, including ahomologue as described above, comprises an amino acid sequence that is at least about 50% identical to an amino acid sequence chosen from: SEQ ID NO:39, SEQ ID NO:43, SEQ ID NO:50, SEQ ID NO:52, and SEQ ID NO:58, wherein the amino acid sequence has a biological activity of at least one domain of a PUFA PKS system. In another aspect, the amino acid sequence of the protein is at least about 55% identical, and more preferably at least about 60% identical, to an amino acid sequence chosen from: SEQ ID NO:39, SEQ ID NO:43, SEQ ID NO:50, SEQ ID NO:52, SEQ ID NO:56 and SEQ ID NO:58, wherein the amino acid sequence has a biological activity of at least one domain of a PUFA PKS system. In a further aspect, the amino acid sequence of the protein is at least about 65% identical to an amino acid sequence chosen from SEQ ID NO:39, SEQ ID NO:43, SEQ ID NO:50, SEQ ID NO:52, SEQ ID NO:54, SEQ ID NO:56 and SEQ ID NO:58, wherein the amino acid sequence has a biological activity of at least one domain of a PUFA PKS system. In another aspect, the amino acid sequence of the protein is at least about 70% identical, and more preferably at least about 75% identical, to an amino acid sequence chosen from: SEQ ID NO:39, SEQ ID NO:43, SEQ ID NO:45, SEQ ID NO:48, SEQ ID NO:50, SEQ ID NO:52, SEQ ID NO:54, SEQ ID NO:56, SEQ ID NO:58, SEQ ID NO:60, SEQ ID NO:62, and SEQ ID NO:64, wherein the amino acid sequence has a biological activity of at least one domain of a PUFA PKS system. In another aspect, the amino acid sequence of the protein is at least about 80% identical, and more preferably at least about 85% identical, and more preferably at least about 90% identical, and more preferably at least about 95% identical, and more preferably at least about 96% identical, and more preferably at least about 97% identical, and more preferably at least about 98% identical, and more preferably at least about 99% identical, to an amino acid sequence chosen from: SEQ ID NO:39, SEQ ID NO:41, SEQ ID NO:43, SEQ ID NO:45, SEQ ID NO:48, SEQ ID NO:50, SEQ ID NO:52, SEQ ID NO:54, SEQ ID NO:56, SEQ ID NO:58, SEQ ID NO:60, SEQ ID NO:62, SEQ ID NO:64, SEQ ID NO:66, SEQ ID NO:68, wherein the amino acid sequence has a biological activity of at least one domain of a PUFA PKS system. In one embodiment, the amino acid sequence described above does not include any of the following amino acid sequences: SEQ ID NO:2, SEQ ID NO:4, SEQ ID NO:6, SEQ ID NO:8, SEQ ID NO:10, SEQ ID NO:13, SEQ ID NO:18, SEQ ID NO:20, SEQ ID NO:22, SEQ ID NO:24, SEQ ID NO:26, SEQ ID NO:28, SEQ ID NO:30, SEQ ID NO:32.

In a preferred embodiment an isolated protein or domain of the present invention comprises, consists essentially of, or consists of, an amino acid sequence chosen from: SEQ ID NO:39, SEQ ID NO:41, SEQ ID NO:43, SEQ ID NO:45, SEQ ID NO:48, SEQ ID NO:50, SEQ ID NO:52, SEQ ID NO:54, SEQ ID NO:56, SEQ ID NO:58, SEQ ID NO:60, SEQ ID NO:62, SEQ ID NO:64, SEQ ID NO:66, SEQ ID NO:68, or any biologically active fragments thereof, including any fragments that have a biological activity of at least one domain of a PUFA PKS system.

In one aspect of the present invention, the following Schizochytrium proteins and domains are useful in one or more embodiments of the present invention, all of which have been previously described in detail in U.S. patent application Ser. No. 10/124,800, supra. In one aspect of the invention, a PUFA PKS protein or domain useful in the present invention comprises an amino acid sequence that is at least about 60% identical to at least 500 consecutive amino acids of an amino acid sequence chosen from: SEQ ID NO:2, SEQ ID NO:4, and SEQ ID NO:6; wherein the amino acid sequence has a biological activity of at least one domain of a PUFA PKS system. In a further aspect, the amino acid sequence of the protein is at least about 60% identical to at least about 600 consecutive amino acids, and more preferably to at least about 700 consecutive amino acids, and more preferably to at least about 800 consecutive amino acids, and more preferably to at least about 900 consecutive amino acids, and more preferably to at least about 1000 consecutive amino acids, and more preferably to at least about 1100 consecutive amino acids, and more preferably to at least about 1200 consecutive amino acids, and more preferably to at least about 1300 consecutive amino acids, and more preferably to at least about 1400 consecutive amino acids, and more preferably to at least about 1500 consecutive amino acids of any of SEQ ID NO:2, SEQ ID NO:4 and SEQ ID NO:6, or to the full length of SEQ ID NO:6. In a further aspect, the amino acid sequence of the protein is at least about 60% identical to at least about 1600 consecutive amino acids, and more preferably to at least about 1700 consecutive amino acids, and more preferably to at least about 1800 consecutive amino acids, and more preferably to at least about 1900 consecutive amino acids, and more preferably to at least about 2000 consecutive amino acids of any of SEQ ID NO:2 or SEQ ID NO:4, or to the full length of SEQ ID NO:4. In a further aspect, the amino acid sequence of the protein is at least about 60% identical to at least about 2100 consecutive amino acids, and more preferably to at least about 2200 consecutive amino acids, and more preferably to at least about 2300 consecutive amino acids, and more preferably to at least about 2400 consecutive amino acids, and more preferably to at least about 2500 consecutive amino acids, and more preferably to at least about 2600 consecutive amino acids, and more preferably to at least about 2700 consecutive amino acids, and more preferably to at least about 2800 consecutive amino acids, and even more preferably, to the full length of SEQ ID NO:2.

In another aspect, a PUFA PKS protein or domain useful in one or more embodiments of the present invention comprises an amino acid sequence that is at least about 65% identical, and more preferably at least about 70% identical, and more preferably at least about 75% identical, and more preferably at least about 80% identical, and more preferably at least about 85% identical, and more preferably at least about 90% identical, and more preferably at least about 95% identical, and more preferably at least about 96% identical, and more preferably at least about 97% identical, and more preferably at least about 98% identical, and more preferably at least about 99% identical to an amino acid sequence chosen from: SEQ ID NO:2, SEQ ID NO:4, or SEQ ID NO:6, over any of the consecutive amino acid lengths described in the paragraph above, wherein the amino acid sequence has a biological activity of at least one domain of a PUFA PKS system.

In another aspect of the invention, a PUFA PKS protein or domain useful in one or more embodiments of the present invention comprises an amino acid sequence that is at least about 60% identical to an amino acid sequence chosen from: SEQ ID NO:8, SEQ ID NO: 10, SEQ ID NO:13, SEQ ID NO:18, SEQ ID NO:20, SEQ ID NO:22, SEQ ID NO:24, SEQ ID NO:26, SEQ ID NO:28, SEQ ID NO:30, or SEQ ID NO:32, wherein the amino acid sequence has a biological activity of at least one domain of a PUFA PKS system. In a further aspect, the amino acid sequence of the protein is at least about 65% identical, and more preferably at least about 70% identical, and more preferably at least about 75% identical, and more preferably at least about 80% identical, and more preferably at least about 85% identical, and more preferably at least about 90% identical, and more preferably at least about 95% identical, and more preferably at least about 96% identical, and more preferably at least about 97% identical, and more preferably at least about 98% identical, and more preferably at least about 99% identical to an amino acid sequence chosen from: SEQ ID NO:8, SEQ ID NO:10, SEQ ID NO:13, SEQ ID NO:18, SEQ ID NO:20, SEQ ID NO:22, SEQ ID NO:24, SEQ ID NO:26, SEQ ID NO:28, SEQ ID NO:30, SEQ ID NO:32, wherein the amino acid sequence has a biological activity of at least one domain of a PUFA PKS system.

In yet another aspect of the invention, a PUFA PKS protein or domain useful in one or more embodiments of the present invention comprises, consists essentially of, or consists of, an amino acid sequence chosen from: SEQ ID NO:2, SEQ ID NO:4, SEQ ID NO:6, SEQ ID NO:8, SEQ ID NO: 10, SEQ ID NO: 13, SEQ ID NO: 18, SEQ ID NO:20, SEQ ID NO:22, SEQ ID NO:24, SEQ ID NO:26, SEQ ID NO:28, SEQ ID NO:30, SEQ ID NO:32 or any biologically active fragments thereof, including any fragments that have a biological activity of at least one domain of a PUFA PKS system.

According to the present invention, the term "contiguous" or "consecutive", with regard to nucleic acid or amino acid sequences described herein, means to be connected in an unbroken sequence. For example, for a first sequence to comprise 30 contiguous (or consecutive) amino acids of a second sequence, means that the first sequence includes an unbroken sequence of 30 amino acid residues that is 100% identical to an unbroken sequence of 30 amino acid residues in the second sequence. Similarly, for a first sequence to have "100% identity" with a second sequence means that the first sequence exactly matches the second sequence with no gaps between nucleotides or amino acids.

As used herein, unless otherwise specified, reference to a percent (%) identity refers to an evaluation of homology which is performed using: (1) a BLAST 2.0 Basic BLAST homology search using blastp for amino acid searches, blastn for nucleic acid searches, and blastX for nucleic acid searches and searches of translated amino acids in all 6 open reading frames, all with standard default parameters, wherein the query sequence is filtered for low complexity regions by default (described in Altschul, S. F., Madden, T. L., Schaaffer, A. A., Zhang, J., Zhang, Z., Miller, W. & Lipman, D. J. (1997) "Gapped BLAST and PSI-BLAST: a new generation of protein database search programs." Nucleic Acids Res. 25:3389-3402, incorporated herein by reference in its entirety); (2) a BLAST 2 alignment (using the parameters described below); (3) and/or PSI-BLAST with the standard default parameters (Position-Specific Iterated BLAST). It is noted that due to some differences in the standard parameters between BLAST 2.0 Basic BLAST and BLAST 2, two specific sequences might be recognized as having significant homology using the BLAST 2 program, whereas a search performed in BLAST 2.0 Basic BLAST using one of the sequences as the query sequence may not identify the second sequence in the top matches. In addition, PSI-BLAST provides an automated, easy-to-use version of a "profile" search, which is a sensitive way to look for sequence homologues. The program first performs a gapped BLAST database search. The PSI-BLAST program uses the information from any significant alignments returned to construct a position-specific score matrix, which replaces the query sequence for the next round of database searching. Therefore, it is to be understood that percent identity can be determined by using any one of these programs.

Two specific sequences can be aligned to one another using BLAST 2 sequence as described in Tatusova and Madden, (1999), "Blast 2 sequences--a new tool for comparing protein and nucleotide sequences", FEMS Microbiol Lett. 174, 247, incorporated herein by reference in its entirety. BLAST 2 sequence alignment is performed in blastp or blastn using the BLAST 2.0 algorithm to perform a Gapped BLAST search (BLAST 2.0) between the two sequences allowing for the introduction of gaps (deletions and insertions) in the resulting alignment. For purposes of clarity herein, a BLAST 2 sequence alignment is performed using the standard default parameters as follows.

For blastn, using 0 BLOSUM62 matrix:

Reward for match=1

Penalty for mismatch=-2

Open gap (5) and extension gap (2) penalties

gap x_dropoff (50) expect (10) word size (11) filter (on)

For blastp, using 0 BLOSUM62 matrix:

Open gap (11) and extension gap (1) penalties

gap x_dropoff (50) expect (10) word size (3) filter (on).

According to the present invention, an amino acid sequence that has a biological activity of at least one domain of a PUFA PKS system is an amino acid sequence that has the biological activity of at least one domain of the PUFA PKS system described in detail herein, as previously exemplified by the Schizochytrium PUFA PKS system or as additionally exemplified herein by the Thraustochytrium PUFA PKS system. The biological activities of the various domains within the Schizochytrium or Thraustochytrium PUFA PKS systems have been described in detail above. Therefore, an isolated protein useful in the present invention can include the translation product of any PUFA PKS open reading frame, any PUFA PKS domain, biologically active fragment thereof, or any homologue of a naturally occurring PUFA PKS open reading frame product or domain which has biological activity.

In another embodiment of the invention, an amino acid sequence having the biological activity of at least one domain of a PUFA PKS system of the present invention includes an amino acid sequence that is sufficiently similar to a naturally occurring PUFA PKS protein or polypeptide that a nucleic acid sequence encoding the amino acid sequence is capable of hybridizing under moderate, high, or very high stringency conditions (described below) to (i.e., with) a nucleic acid molecule encoding the naturally occurring PUFA PKS protein or polypeptide (i.e., to the complement of the nucleic acid strand encoding the naturally occurring PUFA PKS protein or polypeptide). Preferably, an amino acid sequence having the biological activity of at least one domain of a PUFA PKS system of the present invention is encoded by a nucleic acid sequence that hybridizes under moderate, high or very high stringency conditions to the complement of a nucleic acid sequence that encodes any of the above-described amino acid sequences for a PUFA PKS protein or domain. Methods to deduce a complementary sequence are known to those skilled in the art. It should be noted that since amino acid sequencing and nucleic acid sequencing technologies are not entirely error-free, the sequences presented herein, at best, represent apparent sequences of PUFA PKS domains and proteins of the present invention.

As used herein, hybridization conditions refer to standard hybridization conditions under which nucleic acid molecules are used to identify similar nucleic acid molecules. Such standard conditions are disclosed, for example, in Sambrook et al., Molecular Cloning: A Laboratory Manual, Cold Spring Harbor Labs Press, 1989. Sambrook et al., ibid., is incorporated by reference herein in its entirety (see specifically, pages 9.31-9.62). In addition, formulae to calculate the appropriate hybridization and wash conditions to achieve hybridization permitting varying degrees of mismatch of nucleotides are disclosed, for example, in Meinkoth et al., 1984, Anal. Biochem. 138, 267-284; Meinkoth et al., ibid., is incorporated by reference herein in its entirety.

More particularly, moderate stringency hybridization and washing conditions, as referred to herein, refer to conditions which permit isolation of nucleic acid molecules having at least about 70% nucleic acid sequence identity with the nucleic acid molecule being used to probe in the hybridization reaction (i.e., conditions permitting about 30% or less mismatch of nucleotides). High stringency hybridization and washing conditions, as referred to herein, refer to conditions which permit isolation of nucleic acid molecules having at least about 80% nucleic acid sequence identity with the nucleic acid molecule being used to probe in the hybridization reaction (i.e., conditions permitting about 20% or less mismatch of nucleotides). Very high stringency hybridization and washing conditions, as referred to herein, refer to conditions which permit isolation of nucleic acid molecules having at least about 90% nucleic acid sequence identity with the nucleic acid molecule being used to probe in the hybridization reaction (i.e., conditions permitting about 10% or less mismatch of nucleotides). As discussed above, one of skill in the art can use the formulae in Meinkoth et al., ibid. to calculate the appropriate hybridization and wash conditions to achieve these particular levels of nucleotide mismatch. Such conditions will vary, depending on whether DNA:RNA or DNA:DNA hybrids are being formed. Calculated melting temperatures for DNA:DNA hybrids are 10.degree. C. less than for DNA:RNA hybrids. In particular embodiments, stringent hybridization conditions for DNA:DNA hybrids include hybridization at an ionic strength of 6.times.SSC (0.9 M Na.sup.+) at a temperature of between about 20.degree. C. and about 35.degree. C. (lower stringency), more preferably, between about 28.degree. C. and about 40.degree. C. (more stringent), and even more preferably, between about 35.degree. C. and about 45.degree. C. (even more stringent), with appropriate wash conditions. In particular embodiments, stringent hybridization conditions for DNA:RNA hybrids include hybridization at an ionic strength of 6.times.SSC (0.9 M Na.sup.+) at a temperature of between about 30.degree. C. and about 45.degree. C., more preferably, between about 38.degree. C. and about 50.degree. C., and even more preferably, between about 45.degree. C. and about 55.degree. C., with similarly stringent wash conditions. These values are based on calculations of a melting temperature for molecules larger than about 100 nucleotides, 0% formamide and a G+C content of about 40%. Alternatively, T.sub.m can be calculated empirically as set forth in Sambrook et al., supra, pages 9.31 to 9.62. In general, the wash conditions should be as stringent as possible, and should be appropriate for the chosen hybridization conditions. For example, hybridization conditions can include a combination of salt and temperature conditions that are approximately 20-25.degree. C. below the calculated T.sub.m of a particular hybrid, and wash conditions typically include a combination of salt and temperature conditions that are approximately 12-20.degree. C. below the calculated T.sub.m of the particular hybrid. One example of hybridization conditions suitable for use with DNA:DNA hybrids includes a 2-24 hour s hybridization in 6.times.SSC (50% formamide) at about 42.degree. C., followed by washing steps that include one or more washes at room temperature in about 2.times.SSC, followed by additional washes at higher temperatures and lower ionic strength (e.g., at least one wash as about 37.degree. C. in about 0.1.times.-0.5.times.SSC, followed by at least one wash at about 68.degree. C. in about 0.1.times.-0.5.times.SSC).

The present invention also includes a fusion protein that includes any PUFA PKS protein or domain or any homologue or fragment thereof attached to one or more fusion segments. Suitable fusion segments for use with the present invention include, but are not limited to, segments that can: enhance a protein's stability; provide other desirable biological activity; and/or assist with the purification of the protein (e.g., by affinity chromatography). A suitable fusion segment can be a domain of any size that has the desired function (e.g., imparts increased stability, solubility, biological activity; and/or simplifies purification of a protein). Fusion segments can be joined to amino and/or carboxyl termini of the protein and can be susceptible to cleavage in order to enable straight-forward recovery of the desired protein. Fusion proteins are preferably produced by culturing a recombinant cell transfected with a fusion nucleic acid molecule that encodes a protein including the fusion segment attached to either the carboxyl and/or amino terminal end of the protein of the invention as discussed above.

In one embodiment of the present invention, any of the above-described PUFA PKS amino acid sequences, as well as homologues of such sequences, can be produced with from at least one, and up to about 20, additional heterologous amino acids flanking each of the C- and/or N-terminal end of the given amino acid sequence. The resulting protein or polypeptide can be referred to as "consisting essentially of" a given amino acid sequence. According to the present invention, the heterologous amino acids are a sequence of amino acids that are not naturally found (i.e., not found in nature, in vivo) flanking the given amino acid sequence or which would not be encoded by the nucleotides that flank the naturally occurring nucleic acid sequence encoding the given amino acid sequence as it occurs in the gene, if such nucleotides in the naturally occurring sequence were translated using standard codon usage for the organism from which the given amino acid sequence is derived. Similarly, the phrase "consisting essentially of", when used with reference to a nucleic acid sequence herein, refers to a nucleic acid sequence encoding a given amino acid sequence that can be flanked by from at least one, and up to as many as about 60, additional heterologous nucleotides at each of the 5' and/or the 3' end of the nucleic acid sequence encoding the given amino acid sequence. The heterologous nucleotides are not naturally found (i.e., not found in nature, in vivo) flanking the nucleic acid sequence encoding the given amino acid sequence as it occurs in the natural gene.

The minimum size of a protein or domain and/or a homologue or fragment thereof of the present invention is, in one aspect, a size sufficient to have the requisite biological activity, or sufficient to serve as an antigen for the generation of an antibody or as a target in an in vitro assay. In one embodiment, a protein of the present invention is at least about 8 amino acids in length (e.g., suitable for an antibody epitope or as a detectable peptide in an assay), or at least about 25 amino acids in length, or at least about 50 amino acids in length, or at least about 100 amino acids in length, or at least about 150 amino acids in length, or at least about 200 amino acids in length, or at least about 250 amino acids in length, or at least about 300 amino acids in length, or at least about 350 amino acids in length, or at least about 400 amino acids in length, or at least about 450 amino acids in length, or at least about 500 amino acids in length, or at least about 750 amino acids in length, and so on, in any length between 8 amino acids and up to the full length of a protein or domain of the invention or longer, in whole integers (e.g., 8, 9, 10, . . . 25, 26, . . . 500, 501 . . . 1234, 1235, . . . ). There is no limit, other than a practical limit, on the maximum size of such a protein in that the protein can include a portion of a PUFA PKS protein, domain, or biologically active or useful fragment thereof, or a full-length PUFA PKS protein or domain, plus additional sequence (e.g., a fusion protein sequence), if desired.

Further embodiments of the present invention include isolated nucleic acid molecules comprising, consisting essentially of, or consisting of nucleic acid sequences that encode any of the above-identified proteins or domains, including a homologue or fragment thereof, as well as nucleic acid sequences that are fully complementary thereto. In accordance with the present invention, an isolated nucleic acid molecule is a nucleic acid molecule that has been removed from its natural milieu (i.e., that has been subject to human manipulation), its natural milieu being the genome or chromosome in which the nucleic acid molecule is found in nature. As such, "isolated" does not necessarily reflect the extent to which the nucleic acid molecule has been purified, but indicates that the molecule does not include an entire genome or an entire chromosome in which the nucleic acid molecule is found in nature. An isolated nucleic acid molecule can include a gene. An isolated nucleic acid molecule that includes a gene is not a fragment of a chromosome that includes such gene, but rather includes the coding region and regulatory regions associated with the gene, but no additional genes naturally found on the same chromosome. An isolated nucleic acid molecule can also include a specified nucleic acid sequence flanked by (i.e., at the 5' and/or the 3' end of the sequence) additional nucleic acids that do not normally flank the specified nucleic acid sequence in nature (i.e., heterologous sequences). Isolated nucleic acid molecule can include DNA, RNA (e.g., mRNA), or derivatives of either DNA or RNA (e.g., cDNA). Although the phrase "nucleic acid molecule" primarily refers to the physical nucleic acid molecule and the phrase "nucleic acid sequence" primarily refers to the sequence of nucleotides on the nucleic acid molecule, the two phrases can be used interchangeably, especially with respect to a nucleic acid molecule, or a nucleic acid sequence, being capable of encoding a protein or domain of a protein.

Preferably, an isolated nucleic acid molecule of the present invention is produced using recombinant DNA technology (e.g., polymerase chain reaction (PCR) amplification, cloning) or chemical synthesis. Isolated nucleic acid molecules include natural nucleic acid molecules and homologues thereof, including, but not limited to, natural allelic variants and modified nucleic acid molecules in which nucleotides have been inserted, deleted, substituted, and/or inverted in such a manner that such modifications provide the desired effect on PUFA PKS system biological activity as described herein. Protein homologues (e.g., proteins encoded by nucleic acid homologues) have been discussed in detail above.

A nucleic acid molecule homologue can be produced using a number of methods known to those skilled in the art (see, for example, Sambrook et al., Molecular Cloning: A Laboratory Manual, Cold Spring Harbor Labs Press, 1989). For example, nucleic acid molecules can be modified using a variety of techniques including, but not limited to, classic mutagenesis techniques and recombinant DNA techniques, such as site-directed mutagenesis, chemical treatment of a nucleic acid molecule to induce mutations, restriction enzyme cleavage of a nucleic acid fragment, ligation of nucleic acid fragments, PCR amplification and/or mutagenesis of selected regions of a nucleic acid sequence, synthesis of oligonucleotide mixtures and ligation of mixture groups to "build" a mixture of nucleic acid molecules and combinations thereof. Nucleic acid molecule homologues can be selected from a mixture of modified nucleic acids by screening for the function of the protein encoded by the nucleic acid and/or by hybridization with a wild-type gene.

The minimum size of a nucleic acid molecule of the present invention is a size sufficient to form a probe or oligonucleotide primer that is capable of forming a stable hybrid (e.g., under moderate, high or very high stringency conditions) with the complementary sequence of a nucleic acid molecule useful in the present invention, or of a size sufficient to encode an amino acid sequence having a biological activity of at least one domain of a PUFA PKS system according to the present invention. As such, the size of the nucleic acid molecule encoding such a protein can be dependent on nucleic acid composition and percent homology or identity between the nucleic acid molecule and complementary sequence as well as upon hybridization conditions per se (e.g., temperature, salt concentration, and formamide concentration). The minimal size of a nucleic acid molecule that is used as an oligonucleotide primer or as a probe is typically at least about 12 to about 15 nucleotides in length if the nucleic acid molecules are GC-rich and at least about 15 to about 18 bases in length if they are AT-rich. There is no limit, other than a practical limit, on the maximal size of a nucleic acid molecule of the present invention, in that the nucleic acid molecule can include a sequence sufficient to encode a biologically active fragment of a domain of a PUFA PKS system, an entire domain of a PUFA PKS system, several domains within an open reading frame (Orf) of a PUFA PKS system, an entire Orf of a PUFA PKS system, or more than one Orf of a PUFA PKS system.

In one embodiment of the present invention, an isolated nucleic acid molecule comprises, consists essentially of, or consists of a nucleic acid sequence encoding any of the above-described amino acid sequences, including any of the amino acid sequences, or homologues thereof, from a Schizochytrium or Thraustochytrium described herein. In one aspect, the nucleic acid sequence is selected from the group of: SEQ ID NO:1, SEQ ID NO:3, SEQ ID NO:5, SEQ ID NO:7, SEQ ID NO:9, SEQ ID NO:12, SEQ ID NO:17, SEQ ID NO:19, SEQ ID NO:21, SEQ ID NO:23, SEQ ID NO:25, SEQ ID NO:27, SEQ ID NO:29, SEQ ID NO:31, SEQ ID NO:38, SEQ ID NO:40, SEQ ID NO:42, SEQ ID NO:44, SEQ ID NO:47, SEQ ID NO:49, SEQ ID NO:51, SEQ ID NO:53, SEQ ID NO:55, SEQ ID NO:57, SEQ ID NO:59, SEQ ID NO:61, SEQ ID NO:63, SEQ ID NO:65, or SEQ ID NO:67, orhomologues (including sequences that are at least about 50%, 55%, 60%, 65%, 70%, 75%, 80%, 85%, 90%, 95%, 96%, 97%, 98%, or 99% identical to such sequences), or fragments thereof, or any complementary sequences thereof.

Another embodiment of the present invention includes a recombinant nucleic acid molecule comprising a recombinant vector and a nucleic acid sequence encoding protein or peptide having a biological activity of at least one domain (or homologue or fragment thereof) of a PUFA PKS system as described herein. Such nucleic acid sequences are described in detail above. According to the present invention, a recombinant vector is an engineered (i.e., artificially produced) nucleic acid molecule that is used as a tool for manipulating a nucleic acid sequence of choice and for introducing such a nucleic acid sequence into a host cell. The recombinant vector is therefore suitable for use in cloning, sequencing, and/or otherwise manipulating the nucleic acid sequence of choice, such as by expressing and/or delivering the nucleic acid sequence of choice into a host cell to form a recombinant cell. Such a vector typically contains heterologous nucleic acid sequences, that is nucleic acid sequences that are not naturally found adjacent to nucleic acid sequence to be cloned or delivered, although the vector can also contain regulatory nucleic acid sequences (e.g., promoters, untranslated regions) which are naturally found adjacent to nucleic acid molecules of the present invention or which are useful for expression of the nucleic acid molecules of the present invention (discussed in detail below). The vector can be either RNA or DNA, either prokaryotic or eukaryotic, and typically is a plasmid. The vector can be maintained as an extrachromosomal element (e.g., a plasmid) or it can be integrated into the chromosome of a recombinant organism (e.g., a microbe or a plant). The entire vector can remain in place within a host cell, or under certain conditions, the plasmid DNA can be deleted, leaving behind the nucleic acid molecule of the present invention. The integrated nucleic acid molecule can be under chromosomal promoter control, under native or plasmid promoter control, or under a combination of several promoter controls. Single or multiple copies of the nucleic acid molecule can be integrated into the chromosome. A recombinant vector of the present invention can contain at least one selectable marker.

In one embodiment, a recombinant vector used in a recombinant nucleic acid molecule of the present invention is an expression vector. As used herein, the phrase "expression vector" is used to refer to a vector that is suitable for production of an encoded product (e.g., a protein of interest). In this embodiment, a nucleic acid sequence encoding the product to be produced (e.g., a PUFA PKS domain) is inserted into the recombinant vector to produce a recombinant nucleic acid molecule. The nucleic acid sequence encoding the protein to be produced is inserted into the vector in a manner that operatively links the nucleic acid sequence to regulatory sequences in the vector which enable the transcription and translation of the nucleic acid sequence within the recombinant host cell.

In another embodiment, a recombinant vector used in a recombinant nucleic acid molecule of the present invention is a targeting vector. As used herein, the phrase "targeting vector" is used to refer to a vector that is used to deliver a particular nucleic acid molecule into a recombinant host cell, wherein the nucleic acid molecule is used to delete or inactivate an endogenous gene within the host cell or microorganism (i.e., used for targeted gene disruption or knock-out technology). Such a vector may also be known in the art as a "knock-out" vector. In one aspect of this embodiment, a portion of the vector, but more typically, the nucleic acid molecule inserted into the vector (i.e., the insert), has a nucleic acid sequence that is homologous to a nucleic acid sequence of a target gene in the host cell (i.e., a gene which is targeted to be deleted or inactivated). The nucleic acid sequence of the vector insert is designed to bind to the target gene such that the target gene and the insert undergo homologous recombination, whereby the endogenous target gene is deleted, inactivated or attenuated (i.e., by at least a portion of the endogenous target gene being mutated or deleted). The use of this type of recombinant vector to replace an endogenous Schizochytrium gene with a recombinant gene is described in the Examples section, and the general technique for genetic transformation of Thraustochytrids is described in detail in U.S. patent application Ser. No. 10/124,807, published as U.S. Patent Application Publication No. 20030166207, published Sep. 4, 2003.

Typically, a recombinant nucleic acid molecule includes at least one nucleic acid molecule of the present invention operatively linked to one or more expression control sequences. As used herein, the phrase "recombinant molecule" or "recombinant nucleic acid molecule" primarily refers to a nucleic acid molecule or nucleic acid sequence operatively linked to a expression control sequence, but can be used interchangeably with the phrase "nucleic acid molecule", when such nucleic acid molecule is a recombinant molecule as discussed herein. According to the present invention, the phrase "operatively linked" refers to linking a nucleic acid molecule to an expression control sequence (e.g., a transcription control sequence and/or a translation control sequence) in a manner such that the molecule is able to be expressed when transfected (i.e., transformed, transduced, transfected, conjugated or conduced) into a host cell. Transcription control sequences are sequences which control the initiation, elongation, or termination of transcription. Particularly important transcription control sequences are those which control transcription initiation, such as promoter, enhancer, operator and repressor sequences. Suitable transcription control sequences include any transcription control sequence that can function in a host cell or organism into which the recombinant nucleic acid molecule is to be introduced.

Recombinant nucleic acid molecules of the present invention can also contain additional regulatory sequences, such as translation regulatory sequences, origins of replication, and other regulatory sequences that are compatible with the recombinant cell. In one embodiment, a recombinant molecule of the present invention, including those which are integrated into the host cell chromosome, also contains secretory signals (i.e., signal segment nucleic acid sequences) to enable an expressed protein to be secreted from the cell that produces the protein. Suitable signal segments include a signal segment that is naturally associated with the protein to be expressed or any heterologous signal segment capable of directing the secretion of the protein according to the present invention. In another embodiment, a recombinant molecule of the present invention comprises a leader sequence to enable an expressed protein to be delivered to and inserted into the membrane of a host cell. Suitable leader sequences include a leader sequence that is naturally associated with the protein, or any heterologous leader sequence capable of directing the delivery and insertion of the protein to the membrane of a cell.

The present inventors have found that the Schizochytrium PUFA PKS Orfs A and B are closely linked in the genome and region between the Orfs has been sequenced. The Orfs are oriented in opposite directions and 4244 base pairs separate the start (ATG) codons (i.e. they are arranged as follows: 3'OrfA5'-4244 bp -5'OrfB3'). Examination of the 4244 bp intergenic region did not reveal any obvious Orfs (no significant matches were found on a BlastX search). Both Orfs A and B are highly expressed in Schizochytrium, at least during the time of oil production, implying that active promoter elements are embedded in this intergenic region. These genetic elements are believed to have utility as a bi-directional promoter sequence for transgenic applications. For example, in a preferred embodiment, one could clone this region, place any genes of interest at each end and introduce the construct into Schizochytrium (or some other host in which the promoters can be shown to function). It is predicted that the regulatory elements, under the appropriate conditions, would provide for coordinated, high level expression of the two introduced genes. The complete nucleotide sequence for the regulatory region containing Schizochytrium PUFA PKS regulatory elements (e.g., a promoter) is represented herein as SEQ ID NO:36.

In a similar manner, OrfC is highly expressed in Schizochytrium during the time of oil production and regulatory elements are expected to reside in the region upstream of its start codon. A region of genomic DNA upstream of OrfC has been cloned and sequenced and is represented herein as (SEQ ID NO:37). This sequence contains the 3886 nt immediately upstream of the OrfC start codon. Examination of this region did not reveal any obvious Orfs (i.e., no significant matches were found on a BlastX search). It is believed that regulatory elements contained in this region, under the appropriate conditions, will provide for high-level expression of a gene placed behind them. Additionally, under the appropriate conditions, the level of expression may be coordinated with genes under control of the A-B intergenic region (SEQ ID NO:36).

Therefore, in one embodiment, a recombinant nucleic acid molecule useful in the present invention, as disclosed herein, can include a PUFA PKS regulatory region contained within SEQ ID NO:36 and/or SEQ ID NO:37. Such a regulatory region can include any portion (fragment) of SEQ ID NO:36 and/or SEQ ID NO:37 that has at least basal PUFA PKS transcriptional activity.

One or more recombinant molecules of the present invention can be used to produce an encoded product (e.g., a PUFA PKS domain, protein, or system) of the present invention. In one embodiment, an encoded product is produced by expressing a nucleic acid molecule as described herein under conditions effective to produce the protein. A preferred method to produce an encoded protein is by transfecting a host cell with one or more recombinant molecules to form a recombinant cell. Suitable host cells to transfect include, but are not limited to, any bacterial, fungal (e.g., yeast), insect, plant or animal cell that can be transfected. In one embodiment of the invention, a preferred host cell is a Thraustochytrid host cell (described in detail below) or a plant host cell. Host cells can be either untransfected cells or cells that are already transfected with at least one other recombinant nucleic acid molecule.

According to the present invention, the term "transfection" is used to refer to any method by which an exogenous nucleic acid molecule (i.e., a recombinant nucleic acid molecule) can be inserted into a cell. The term "transformation" can be used interchangeably with the term "transfection" when such term is used to refer to the introduction of nucleic acid molecules into microbial cells, such as algae, bacteria and yeast, or into plants. In microbial systems, the term "transformation" is used to describe an inherited change due to the acquisition of exogenous nucleic acids by the microorganism or plant and is essentially synonymous with the term "transfection." However, in animal cells, transformation has acquired a second meaning which can refer to changes in the growth properties of cells in culture after they become cancerous, for example. Therefore, to avoid confusion, the term "transfection" is preferably used with regard to the introduction of exogenous nucleic acids into animal cells, and the term "transfection" will be used herein to generally encompass transfection of animal cells, and transformation of microbial cells or plant cells, to the extent that the terms pertain to the introduction of exogenous nucleic acids into a cell. Therefore, transfection techniques include, but are not limited to, transformation, particle bombardment, diffusion, active transport, bath sonication, electroporation, microinjection, lipofection, adsorption, infection and protoplast fusion.

It will be appreciated by one skilled in the art that use of recombinant DNA technologies can improve control of expression of transfected nucleic acid molecules by manipulating, for example, the number of copies of the nucleic acid molecules within the host cell, the efficiency with which those nucleic acid molecules are transcribed, the efficiency with which the resultant transcripts are translated, and the efficiency of post-translational modifications. Additionally, the promoter sequence might be genetically engineered to improve the level of expression as compared to the native promoter.

Recombinant techniques useful for controlling the expression of nucleic acid molecules include, but are not limited to, integration of the nucleic acid molecules into one or more host cell chromosomes, addition of vector stability sequences to plasmids, substitutions or modifications of transcription control signals (e.g., promoters, operators, enhancers), substitutions or modifications of translational control signals (e.g., ribosome binding sites, Shine-Dalgamo sequences), modification of nucleic acid molecules to correspond to the codon usage of the host cell, and deletion of sequences that destabilize transcripts.

General discussion above with regard to recombinant nucleic acid molecules and transfection of host cells is intended to be applied to any recombinant nucleic acid molecule discussed herein, including those encoding any amino acid sequence having a biological activity of at least one domain from a PUFA PKS, those encoding amino acid sequences from other PKS systems, and those encoding other proteins or domains.

Polyunsaturated fatty acids (PUFAs) are essential membrane components in higher eukaryotes and the precursors of many lipid-derived signaling molecules. The PUFA PKS system of the present invention uses pathways for PUFA synthesis that do not require desaturation and elongation of saturated fatty acids. The pathways catalyzed by PUFA PKSs that are distinct from previously recognized PKSs in both structure and mechanism. Generation of cis double bonds is suggested to involve position-specific isomerases; these enzymes are believed to be useful in the production of new families of antibiotics.

To produce significantly high yields of one or more desired polyunsaturated fatty acids or other bioactive molecules, an organism, preferably a microorganism or a plant, and most preferably a Thraustochytrid microorganism, can be genetically modified to alter the activity and particularly, the end product, of the PUFA PKS system in the microorganism or plant.

Therefore, one embodiment of the present invention relates to a genetically modified microorganism, wherein the microorganism expresses a PKS system comprising at least one biologically active domain of a polyunsaturated fatty acid (PUFA) polyketide synthase (PKS) system. The domain of the PUFA PKS system can include any of the domains, including homologues thereof, for PUFA PKS systems as described above (e.g., for Schizochytrium and Thraustochytrium), and can also include any domain of a PUFA PKS system from any other non-bacterial microorganism, including any eukaryotic microorganism, including any Thraustochytrid microorganism or any domain of a PUFA PKS system from a microorganism identified by a screening method as described in U.S. patent application Ser. No. 10/124,800, supra. The genetic modification affects the activity of the PKS system in the organism. The screening process described in U.S. patent application Ser. No. 10/124,800 includes the steps of: (a) selecting a microorganism that produces at least one PUFA; and, (b) identifying a microorganism from (a) that has an ability to produce increased PUFAs under dissolved oxygen conditions of less than about 5% of saturation in the fermentation medium, as compared to production of PUFAs by the microorganism under dissolved oxygen conditions of greater than about 5% of saturation, and preferably about 10%, and more preferably about 15%, and more preferably about 20% of saturation in the fermentation medium.

In one aspect, such an organism can endogenously contain and express a PUFA PKS system, and the genetic modification can be a genetic modification of one or more of the functional domains of the endogenous PUFA PKS system, whereby the modification has some effect on the activity of the PUFA PKS system. In another aspect, such an organism can endogenously contain and express a PUFA PKS system, and the genetic modification can be an introduction of at least one exogenous nucleic acid sequence (e.g., a recombinant nucleic acid molecule), wherein the exogenous nucleic acid sequence encodes at least one biologically active domain or protein from a second PKS system and/or a protein that affects the activity of the PUFA PKS system (e.g., a phosphopantetheinyl transferases (PPTase), discussed below). In yet another aspect, the organism does not necessarily endogenously (naturally) contain a PUFA PKS system, but is genetically modified to introduce at least one recombinant nucleic acid molecule encoding an amino acid sequence having the biological activity of at least one domain of a PUFA PKS system. In this aspect, PUFA PKS activity is affected by introducing or increasing PUFA PKS activity in the organism. Various embodiments associated with each of these aspects will be discussed in greater detail below.

It is to be understood that a genetic modification of a PUFA PKS system or an organism comprising a PUFA PKS system can involve the modification of at least one domain of a PUFA PKS system (including a portion of a domain), more than one or several domains of a PUFA PKS system (including adjacent domains, non-contiguous domains, or domains on different proteins in the PUFA PKS system), entire proteins of the PUFA PKS system, and the entire PUFA PKS system (e.g., all of the proteins encoded by the PUFA PKS genes). As such, modifications can include a small modification to a single domain of an endogenous PUFA PKS system; to substitution, deletion or addition to one or more domains or proteins of a given PUFA PKS system; up to replacement of the entire PUFA PKS system in an organism with the PUFA PKS system from a different organism. One of skill in the art will understand that any genetic modification to a PUFA PKS system is encompassed by the invention.

As used herein, a genetically modified microorganism can include a genetically modified bacterium, protist, microalgae, fungus, or other microbe, and particularly, any of the genera of the order Thraustochytriales (e.g., a Thraustochytrid) described herein (e.g., Schizochytrium, Thraustochytrium, Japonochytrium, Labyrinthula, Labyrinthuloides, etc.). Such a genetically modified microorganism has a genome which is modified (i.e., mutated or changed) from its normal (i.e., wild-type or naturally occurring) form such that the desired result is achieved (i.e., increased or modified PUFA PKS activity and/or production of a desired product using the PKS system). Genetic modification of a microorganism can be accomplished using classical strain development and/or molecular genetic techniques. Such techniques known in the art and are generally disclosed for microorganisms, for example, in Sambrook et al., 1989, Molecular Cloning: A Laboratory Manual, Cold Spring Harbor Labs Press. The reference Sambrook et al., ibid., is incorporated by reference herein in its entirety. A genetically modified microorganism can include a microorganism in which nucleic acid molecules have been inserted, deleted or modified (i.e., mutated; e.g., by insertion, deletion, substitution, and/or inversion of nucleotides), in such a manner that such modifications provide the desired effect within the microorganism.

Preferred microorganism host cells to modify according to the present invention include, but are not limited to, any bacteria, protist, microalga, fungus, or protozoa. In one aspect, preferred microorganisms to genetically modify include, but are not limited to, any microorganism of the order Thraustochytriales, including any microorganism in the families Thraustochytriaceae and Labyrinthulaceae. Particularly preferred host cells for use in the present invention could include microorganisms from a genus including, but not limited to: Thraustochytrium, Japonochytrium, Aplanochytrium, Elina and Schizochytrium within the Thraustochytriaceae and Labyrinthula, Labyrinthuloides, and Labyrinthomyxa within the Labyrinthulaceae. Preferred species within these genera include, but are not limited to: any species within Labyrinthula, including Labrinthula sp., Labyrinthula algeriensis, Labyrinthula cienkowskii, Labyrinthula chattonii, Labyrinthula coenocystis, Labyrinthula macrocystis, Labyrinthula macrocystis atlantica, Labyrinthula macrocystis macrocystis, Labyrinthula magnifica, Labyrinthula minuta, Labyrinthula roscoffensis, Labyrinthula valkanovii, Labyrinthula vitellina, Labyrinthula vitellina pacifica, Labyrinthula vitellina vitellina, Labyrinthula zopfii; any Labyrinthuloides species, including Labyrinthuloides sp., Labyrinthuloides minuta, Labyrinthuloides schizochytrops; any Labyrinthomyxa species, including Labyrinthomyxa sp., Labyrinthomyxa pohlia, Labyrinthomyxa sauvageaui, any Aplanochytrium species, including Aplanochytrium sp. and Aplanochytrium kerguelensis; any Elina species, including Elina sp., Elina marisalba, Elina sinorifica; any Japanochytrium species, including Japanochytrium sp., Japanochytrium marinum; any Schizochytrium species, including Schizochytrium sp., Schizochytrium aggregatum, Schizochytrium limacinum, Schizochytrium minutum, Schizochytrium octosporum; and any Thraustochytrium species, including Thraustochytrium sp., Thraustochytrium aggregatum, Thraustochytrium arudimentale, Thraustochytrium aureum, Thraustochytrium benthicola, Thraustochytrium globosum, Thraustochytrium kinnei, Thraustochytrium motivum, Thraustochytrium pachydermum, Thraustochytrium proliferum, Thraustochytrium roseum, Thraustochytrium striatum, Ulkenia sp., Ulkenia minuta, Ulkenia profunda, Ulkenia radiate, Ulkenia sarkariana, and Ulkenia visurgensis. Particularly preferred species within these genera include, but are not limited to: any Schizochytrium species, including Schizochytrium aggregatum, Schizochytrium limacinum, Schizochytrium minutum; any Thraustochytrium species (including former Ulkenia species such as U. visurgensis, U. amoeboida, U. sarkariana, U. profunda, U. radiata, U. minuta and Ulkenia sp. BP-5601), and including Thraustochytrium striatum, Thraustochytrium aureum, Thraustochytrium roseum; and any Japonochytrium species. Particularly preferred strains of Thraustochytriales include, but are not limited to: Schizochytrium sp. (S31)(ATCC 20888); Schizochytrium sp. (S8)(ATCC 20889); Schizochytrium sp. (LC-RM)(ATCC 18915); Schizochytrium sp. (SR21); Schizochytrium aggregatum (Goldsteinet Belsky)(ATCC 28209); Schizochytrium limacinum (Honda et Yokochi)(IFO 32693); Thraustochytrium sp. (23B)(ATCC 20891); Thraustochytrium striatum (Schneider)(ATCC 24473); Thraustochytrium aureum (Goldstein)(ATCC 34304); Thraustochytrium roseum (Goldstein)(ATCC 28210); and Japonochytrium sp. (L1)(ATCC 28207). Other examples of suitable host microorganisms for genetic modification include, but are not limited to, yeast including Saccharomyces cerevisiae, Saccharomyces carlsbergensis, or other yeast such as Candida, Kluyveromyces, or other fungi, for example, filamentous fungi such as Aspergillus, Neurospora, Penicillium, etc. Bacterial cells also may be used as hosts. These include, but are not limited to, Escherichia coli, which can be useful in fermentation processes. Alternatively, and only by way of example, a host such as a Lactobacillus species or Bacillus species can be used as a host.

Another embodiment of the present invention relates to a genetically modified plant, wherein the plant has been genetically modified to recombinantly express a PKS system comprising at least one biologically active domain of a polyunsaturated fatty acid (PUFA) polyketide synthase (PKS) system. The domain of the PUFA PKS system can include any of the domains, including homologues thereof, for PUFA PKS systems as described above (e.g., for Schizochytrium and/or Thraustochytrium), and can also include any domain of a PUFA PKS system from any non-bacterial microorganism (including any eukaryotic microorganism and any other Thraustochytrid microorganism) or any domain of a PUFA PKS system from a microorganism identified by a screening method as described in U.S. patent application Ser. No. 10/124,800, supra. The plant can also be further modified with at least one domain or biologically active fragment thereof of another PKS system, including, but not limited to, bacterial PUFA PKS or PKS systems, Type I PKS systems, Type II PKS systems, modular PKS systems, and/or any non-bacterial PUFA PKS system (e.g., eukaryotic, Thraustochytrid, Thraustochytriaceae or Labyrinthulaceae, Schizochytrium, etc.).

As used herein, a genetically modified plant can include any genetically modified plant including higher plants and particularly, any consumable plants or plants useful for producing a desired bioactive molecule of the present invention. Such a genetically modified plant has a genome which is modified (i.e., mutated or changed) from its normal (i.e., wild-type or naturally occurring) form such that the desired result is achieved (i.e., increased or modified PUFA PKS activity and/or production of a desired product using the PKS system). Genetic modification of a plant can be accomplished using classical strain development and/or molecular genetic techniques. Methods for producing a transgenic plant, wherein a recombinant nucleic acid molecule encoding a desired amino acid sequence is incorporated into the genome of the plant, are known in the art. A preferred plant to genetically modify according to the present invention is preferably a plant suitable for consumption by animals, including humans.

Preferred plants to genetically modify according to the present invention (i.e., plant host cells) include, but are not limited to any higher plants, and particularly consumable plants, including crop plants and especially plants used for their oils. Such plants can include, for example: canola, soybeans, rapeseed, linseed, corn, safflowers, sunflowers and tobacco. Other preferred plants include those plants that are known to produce compounds used as pharmaceutical agents, flavoring agents, neutraceutical agents, functional food ingredients or cosmetically active agents or plants that are genetically engineered to produce these compounds/agents.

According to the present invention, a genetically modified microorganism or plant includes a microorganism or plant that has been modified using recombinant technology or by classical mutagenesis and screening techniques. As used herein, genetic modifications which result in a decrease in gene expression, in the function of the gene, or in the function of the gene product (i.e., the protein encoded by the gene) can be referred to as inactivation (complete or partial), deletion, interruption, blockage or down-regulation of a gene. For example, a genetic modification in a gene which results in a decrease in the function of the protein encoded by such gene, can be the result of a complete deletion of the gene (i.e., the gene does not exist, and therefore the protein does not exist), a mutation in the gene which results in incomplete or no translation of the protein (e.g., the protein is not expressed), or a mutation in the gene which decreases or abolishes the natural function of the protein (e.g., a protein is expressed which has decreased or no enzymatic activity or action). Genetic modifications that result in an increase in gene expression or function can be referred to as amplification, overproduction, overexpression, activation, enhancement, addition, or up-regulation of a gene.

The genetic modification of a microorganism or plant according to the present invention preferably affects the activity of the PKS system expressed by the microorganism or plant, whether the PKS system is endogenous and genetically modified, endogenous with the introduction of recombinant nucleic acid molecules into the organism (with the option of modifying the endogenous system or not), or provided completely by recombinant technology. To alter the PUFA production profile of a PUFA PKS system or organism expressing such system includes causing any detectable or measurable change in the production of any one or more PUFAs by the host microorganism or plant as compared to in the absence of the genetic modification (i.e., as compared to the unmodified, wild-type microorganism or plant or the microorganism or plant that is unmodified at least with respect to PUFA synthesis--i.e., the organism might have other modifications not related to PUFA synthesis). To affect the activity of a PKS system includes any genetic modification that causes any detectable or measurable change or modification in the PKS system expressed by the organism as compared to in the absence of the genetic modification. A detectable change or modification in the PKS system can include, but is not limited to: a change or modification (introduction of, increase or decrease) of the expression and/or biological activity of any one or more of the domains in a modified PUFA PKS system as compared to the endogenous PUFA PKS system in the absence of genetic modification, the introduction of PKS system activity into an organism such that the organism now has measurable/detectable PKS system activity (i.e., the organism did not contain a PKS system prior to the genetic modification), the introduction into the organism of a functional domain from a different PKS system than a PKS system endogenously expressed by the organism such that the PKS system activity is modified (e.g., a bacterial PUFA PKS domain or a type I PKS domain is introduced into an organism that endogenously expresses a non-bacterial PUFAPKS system), a change in the amount of a bioactive molecule (e.g., a PUFA) produced by the PKS system (e.g., the system produces more (increased amount) or less (decreased amount) of a given product as compared to in the absence of the genetic modification), a change in the type of a bioactive molecule (e.g., a change in the type of PUFA) produced by the PKS system (e.g., the system produces an additional or different PUFA, a new or different product, or a variant of a PUFA or other product that is naturally produced by the system), and/or a change in the ratio of multiple bioactive molecules produced by the PKS system (e.g., the system produces a different ratio of one PUFA to another PUFA, produces a completely different lipid profile as compared to in the absence of the genetic modification, or places various PUFAs in different positions in a triacylglycerol as compared to the natural configuration). Such a genetic modification includes any type of genetic modification and specifically includes modifications made by recombinant technology and by classical mutagenesis.

It should be noted that reference to increasing the activity of a functional domain or protein in a PUFA PKS system refers to any genetic modification in the organism containing the domain or protein (or into which the domain or protein is to be introduced) which results in increased functionality of the domain or protein system and can include higher activity of the domain or protein (e.g., specific activity or in vivo enzymatic activity), reduced inhibition or degradation of the domain or protein system, and overexpression of the domain or protein. For example, gene copy number can be increased, expression levels can be increased by use of a promoter that gives higher levels of expression than that of the native promoter, or a gene can be altered by genetic engineering or classical mutagenesis to increase the activity of the domain or protein encoded by the gene.

Similarly, reference to decreasing the activity of a functional domain or protein in a PUFA PKS system refers to any genetic modification in the organism containing such domain or protein (or into which the domain or protein is to be introduced) which results in decreased functionality of the domain or protein and includes decreased activity of the domain or protein, increased inhibition or degradation of the domain or protein and a reduction or elimination of expression of the domain or protein. For example, the action of domain or protein of the present invention can be decreased by blocking or reducing the production of the domain or protein, "knocking out" the gene or portion thereof encoding the domain or protein, reducing domain or protein activity, or inhibiting the activity of the domain or protein. Blocking or reducing the production of a domain or protein can include placing the gene encoding the domain or protein under the control of a promoter that requires the presence of an inducing compound in the growth medium. By establishing conditions such that the inducer becomes depleted from the medium, the expression of the gene encoding the domain or protein (and therefore, of protein synthesis) could be turned off. The present inventors demonstrate the ability to delete (knock out) targeted genes in a Thraustochytrid microorganism in the Examples section. Blocking or reducing the activity of domain or protein could also include using an excision technology approach similar to that described in U.S. Pat. No. 4,743,546, incorporated herein by reference. To use this approach, the gene encoding the protein of interest is cloned between specific genetic sequences that allow specific, controlled excision of the gene from the genome. Excision could be prompted by, for example, a shift in the cultivation temperature of the culture, as in U.S. Pat. No. 4,743,546, or by some other physical or nutritional signal.

In one embodiment of the present invention, a genetic modification includes a modification of a nucleic acid sequence encoding an amino acid sequence that has a biological activity of at least one domain of a non-bacterial PUFA PKS system as described herein (e.g., a domain, more than one domain, a protein, or the entire PUFA PKS system, of an endogenous PUFA PKS system of a Thraustochytrid host). Such a modification can be made to an amino acid sequence within an endogenously (naturally) expressed non-bacterial PUFA PKS system, whereby a microorganism that naturally contains such a system is genetically modified by, for example, classical mutagenesis and selection techniques and/or molecular genetic techniques, include genetic engineering techniques. Genetic engineering techniques can include, for example, using a targeting recombinant vector to delete a portion of an endogenous gene (demonstrated in the Examples), or to replace a portion of an endogenous gene with a heterologous sequence (demonstrated in the Examples). Examples of heterologous sequences that could be introduced into a host genome include sequences encoding at least one functional domain from another PKS system, such as a different non-bacterial PUFA PKS system (e.g., from a eukaryote, including another Thraustochytrid), a bacterial PUFA PKS system, a type I PKS system, a type II PKS system, or a modular PKS system. A heterologous sequence can also include an entire PUFA PKS system (e.g., all genes associated with the PUFA PKS system) that is used to replace the entire endogenous PUFA PKS system (e.g., all genes of the endogenous PUFA PKS system) in a host. A heterologous sequence can also include a sequence encoding a modified functional domain (a homologue) of a natural domain from a PUFA PKS system of a host Thraustochytrid (e.g., a nucleic acid sequence encoding a modified domain from OrfB of a Schizochytrium, wherein the modified domain will, when used to replace the naturally occurring domain expressed in the Schizochytrium, alter the PUFA production profile by the Schizochytrium). Other heterologous sequences to introduce into the genome of a host includes a sequence encoding a protein or functional domain that is not a domain of a PKS system, but which will affect the activity of the endogenous PKS system. For example, one could introduce into the host genome a nucleic acid molecule encoding a phosphopantetheinyl transferase (discussed below). Specific modifications that could be made to an endogenous PUFA PKS system are discussed in detail herein.

In another aspect of this embodiment of the invention, the genetic modification can include: (1) the introduction of a recombinant nucleic acid molecule encoding an amino acid sequence having a biological activity of at least one domain of a PUFA PKS system; and/or (2) the introduction of a recombinant nucleic acid molecule encoding a protein or functional domain that affects the activity of a PUFA PKS system, into a host. The host can include: (1) a host cell that does not express any PKS system, wherein all functional domains of a PKS system are introduced into the host cell, and wherein at least one functional domain is from a non-bacterial PUFA PKS system; (2) a host cell that expresses a PKS system (endogenous or recombinant) having at least one functional domain of a non-bacterial PUFA PKS system, wherein the introduced recombinant nucleic acid molecule can encode at least one additional non-bacterial PUFA PKS domain function or another protein or domain that affects the activity of the host PKS system; and (3) a host cell that expresses a PKS system (endogenous or recombinant) which does not necessarily include a domain function from a non-bacterial PUFA PKS, and wherein the introduced recombinant nucleic acid molecule includes a nucleic acid sequence encoding at least one functional domain of a non-bacterial PUFA PKS system. In other words, the present invention intends to encompass any genetically modified organism (e.g., microorganism or plant), wherein the organism comprises at least one non-bacterial PUFA PKS domain function (either endogenously or introduced by recombinant modification), and wherein the genetic modification has a measurable effect on the non-bacterial PUFA PKS domain function or on the PKS system when the organism comprises a functional PKS system.

The present invention encompasses many possible non-bacterial and bacterial microorganisms as either possible host cells for the PUFA PKS systems described herein and/or as sources for additional genetic material encoding PUFA PKS system proteins and domains for use in the genetic modifications and methods described herein. For example, microbial organisms with a PUFA PKS system similar to that found in Schizochytrium, such as the Thraustochytrium microorganism discovered by the present inventors and described in Example 1, can be readily identified/isolated/screened by methods to identify other non-bacterial microorganisms that have a polyunsaturated fatty acid (PUFA) polyketide synthase (PKS) system that are described in detail in U.S. Patent Application Publication No. 20020194641, supra (corresponding to U.S. patent application Ser. No. 10/124,800).

Locations for collection of the preferred types of microbes for screening for a PUFA PKS system according to the present invention include any of the following: low oxygen environments (or locations near these types of low oxygen environments including in the guts of animals including invertebrates that consume microbes or microbe-containing foods (including types of filter feeding organisms), low or non-oxygen containing aquatic habitats (including freshwater, saline and marine), and especially at-or near-low oxygen environments (regions) in the oceans. The microbial strains would preferably not be obligate anaerobes but be adapted to live in both aerobic and low or anoxic environments. Soil environments containing both aerobic and low oxygen or anoxic environments would also excellent environments to find these organisms in and especially in these types of soil in aquatic habitats or temporary aquatic habitats.

A particularly preferred non-bacterial microbial strain to screen for use as a host and/or a source of PUFA PKS genes according to the present invention would be a strain (selected from the group consisting of algae, fungi (including yeast), protozoa or protists) that, during a portion of its life cycle, is capable of consuming whole bacterial cells (bacterivory) by mechanisms such as phagocytosis, phagotrophic or endocytic capability and/or has a stage of its life cycle in which it exists as an amoeboid stage or naked protoplast. This method of nutrition would greatly increase the potential for transfer of a bacterial PKS system into a eukaryotic cell if a mistake occurred and the bacterial cell (or its DNA) did not get digested and instead are functionally incorporated into the eukaryotic cell.

Included in the present invention as sources of PUFA PKS genes (and proteins and domains encoded thereby) are any Thraustochytrids other than those specifically described herein that contain a PUFA PKS system. Such Thraustochytrids include, but are not limited to, but are not limited to, any microorganism of the order Thraustochytriales, including any microorganism in the families Thraustochytriaceae and Labyrinthulaceae, which further comprise a genus including, but not limited to: Thraustochytrium, Japonochytrium, Aplanochytrium, Elina and Schizochytrium within the Thraustochytriaceae and Labyrinthula, Labyrinthuloides, and Labyrinthomyxa within the Labyrinthulaceae. Preferred species within these genera include, but are not limited to: any species within Labyrinthula, including Labrinthula sp., Labyrinthula algeriensis, Labyrinthula cienkowskii, Labyrinthula chattonii, Labyrinthula coenocystis, Labyrinthula macrocystis, Labyrinthula macrocystis atlantica, Labyrinthula macrocystis macrocystis, Labyrinthula magnifica, Labyrinthula minuta, Labyrinthula roscoffensis, Labyrinthula valkanovii, Labyrinthula vitellina, Labyrinthula vitellina pacifica, Labyrinthula vitellina vitellina, Labyrinthula zopfii; any Labyrinthuloides species, including Labyrinthuloides sp., Labyrinthuloides minuta, Labyrinthuloides schizochytrops; any Labyrinthomyxa species, including Labyrinthomyxa sp., Labyrinthomyxa pohlia, Labyrinthomyxa sauvageaui, any Aplanochytrium species, including Aplanochytrium sp. and Aplanochytrium kerguelensis; any Elina species, including Elina sp., Elina marisalba, Elina sinorifica; any Japanochytrium species, including Japanochytrium sp., Japanochytrium marinum; any Schizochytrium species, including Schizochytrium sp., Schizochytrium aggregatum, Schizochytrium limacinum, Schizochytrium minutum, Schizochytrium octosporum; and any Thraustochytrium species, including Thraustochytrium sp., Thraustochytrium aggregatum, Thraustochytrium arudimentale, Thraustochytrium aureum, Thraustochytrium benthicola, Thraustochytrium globosum, Thraustochytrium kinnei, Thraustochytrium motivum, Thraustochytrium pachydeum, Thraustochytrium proliferum, Thraustochytrium roseum, Thraustochytrium striatum, Ulkenia sp., Ulkenia minuta, Ulkenia profunda, Ulkenia radiate, Ulkenia sarkariana, and Ulkenia visurgensis.

It is noted that, without being bound by theory, the present inventors consider Labyrinthula and other Labyrinthulaceae as sources of PUFA PKS genes because the Labyrinthulaceae are closely related to the Thraustochytriaceae which are known to possess PUFA PKS genes, the Labyrinthulaceae are known to bebactivorous/phagocytotic, and some members of the Labyrinthulaceae have fatty acid/PUFA profiles consistent with having a PUFA PKS system.

Strains of microbes (other than the members of the Thraustochytrids) capable of bacterivory (especially by phagocytosis or endocytosis) can be found in the following microbial classes (including but not limited to example genera):

In the algae and algae-like microbes (including Stramenopiles): of the class Euglenophyceae (for example genera Euglena, and Peranema), the class Chrysophyceae (for example the genus Ochromonas), the class Dinobryaceae (for example the genera Dinobryon, Platychysis, and Chrysochromulina), the Dinophyceae (including the genera Crypthecodinium, Gymnodinium, Peridinium, Ceratium, Gyrodinium, and Oxyrrhis), the class Cryptophyceae (for example the genera Cryptomonas, and Rhodomonas), the class Xanthophyceae (for example the genus Olisthodiscus) (and including forms of algae in which an amoeboid stage occurs as in the flagellates Rhizochloridaceae, and zoospores/gametes of Aphanochaete pascheri, Bumilleria stigeoclonium and Vaucheria geminata), the class Eustigmatophyceae, and the class Prymnesiopyceae (including the genera Prymnesium and Diacronema).

In the Stramenopiles including the: Proteromonads, Opalines, Developayella, Diplophorys, Labyrinthulids, Thraustochytrids, Bicosecids, Oomycetes, Hypochytridiomycetes, Commation, Reticulosphaera, Pelagomonas, Pelapococcus, Ollicola, Aureococcus, Parmales, Raphidiophytes, Synurids, Rhizochromulinaales, Pedinellales, Dictyochales, Chrysomeridales, Sarcinochrysidales, Hydrurales, Hibberdiales, and Chromulinales.

In the Fungi: Class Myxomycetes (form myxamoebae)--slime molds, class Acrasieae including the orders Acrasiceae (for example the genus Sappinia), class Guttulinaceae (for example the genera Guttulinopsis, and Guttulina), class Dictysteliaceae (for example the genera Acrasis, Dictyostelium, Polysphondylium, and Coenonia), and class Phycomyceae including the orders Chytridiales, Ancylistales, Blastocladiales, Monoblepharidales, Saprolegniales, Peronosporales, Mucorales, and Entomophthorales.

In the Protozoa: Protozoa strains with life stages capable of bacterivory (including by phageocytosis) can be selected from the types classified as ciliates, flagellates or amoebae. Protozoan ciliates include the groups: Chonotrichs, Colpodids, Cyrtophores, Haptorids, Karyorelicts, Oligohymenophora, Polyhymenophora (spirotrichs), Prostomes and Suctoria. Protozoan flagellates include the Biosoecids, Bodonids, Cercomonads, Chrysophytes (for example the genera Anthophysa, Chrysamoemba, Chrysosphaerella, Dendromonas, Dinobryon, Mallomonas, Ochromonas, Paraphysomonas, Poterioochromonas, Spumella, Syncrypta, Synura, and Uroglena), Collar flagellates, Cryptophytes (for example the genera Chilomonas, Cryptomonas, Cyanomonas, and Goniomonas), Dinoflagellates, Diplomonads, Euglenoids, Heterolobosea, Pedinellids, Pelobionts, Phalansteriids, Pseudodendromonads, Spongomonads and Volvocales (and other flagellates including the unassigned flagellate genera of Artodiscus, Clautriavia, Helkesimastix, Kathablepharis and Multicilia). Amoeboid protozoans include the groups: Actinophryids, Centrohelids, Desmothoricids, Diplophryids, Eumamoebae, Heterolobosea, Leptomyxids, Nucleariid filose amoebae, Pelebionts, Testate amoebae and Vampyrellids (and including the unassigned amoebid genera Gymnophrys, Biomyxa, Microcometes, Reticulomyxa, Belonocystis, Elaeorhanis, Allelogromia, Gromia or Lieberkuhnia). The protozoan orders include the following: Percolomonadeae, Heterolobosea, Lyromonadea, Pseudociliata, Trichomonadea, Hypermastigea, Heteromiteae, Telonemea, Cyathobodonea, Ebridea, Pyytomyxea, Opalinea, Kinetomonadea, Hemimastigea, ,Protostelea, Myxagastrea, Dictyostelea, Choanomonadea, Apicomonadea, Eogregarinea, Neogregarinea, Coelotrolphea, Eucoccidea, Haemosporea, Piroplasmea, Spirotrichea, Prostomatea, Litostomatea, Phyllopharyngea, Nassophorea, Oligohymenophorea, Colpodea, Karyorelicta, Nucleohelea, Centrohelea, Acantharea, Sticholonchea, Polycystinea, Phaeodarea, Lobosea, Filosea, Athalamea, Monothalamea, Polythalamea, Xenophyophorea, Schizocladea, Holosea, Entamoebea, Myxosporea, Actinomyxea, Halosporea, Paramyxea, Rhombozoa and Orthonectea.

A preferred embodiment of the present invention includes strains of the microorganisms listed above that have been collected from one of the preferred habitats listed above.

In some embodiments of this method of the present invention, PUFA PKS systems from bacteria, including genes and portions thereof (encoding entire PUFA PKS systems, proteins thereof and/or domains thereof) can be used to genetically modify other PUFA PKS systems (e.g., any non-bacterial PUFA PKS system) and/or microorganisms containing the same (or vice versa) in the embodiments of the invention. In one aspect, novel PUFA PKS systems can be identified in bacteria that are expected to be particularly useful for creating genetically modified microorganisms (e.g., genetically modified Thraustochytrids) and/or novel hybrid constructs encoding PUFA PKS systems for use in the methods and genetically modified microorganisms and plants of the present invention. In one aspect, bacteria that may be particularly useful in the embodiments of the present invention have PUFA PKS systems, wherein the PUFA PKS system is capable of producing PUFAs at temperatures exceeding about 20.degree. C., preferably exceeding about 25.degree. C. and even more preferably exceeding about 30.degree. C. As described previously herein, the marine bacteria, Shewanella and Vibrio marinus, described in U.S. Pat. No. 6,140,486, do not produce PUFAs at higher temperatures, which limits the usefulness of PUFA PKS systems derived from these bacteria, particularly in plant applications under field conditions. Therefore, in one embodiment, the screening method of the present invention can be used to identify bacteria that have a PUFA PKS system, wherein the bacteria are capable of growth and PUFA production at higher temperatures (e.g., above about 15.degree. C., 20.degree. C., 25.degree. C., or 30.degree. C. or even higher). However, even if the bacteria sources do not grow well and/or produce PUFAs at the higher temperatures, the present invention encompasses the identification, isolation and use of the PUFA PKS systems (genes and proteins/domains encoded thereby), wherein the PUFA PKS systems from the bacteria have enzymatic/biological activity at temperatures above about 15.degree. C., 20.degree. C., 25.degree. C., or 30.degree. C. or even higher. In one aspect of this embodiment, inhibitors of eukaryotic growth such as nystatin (antifungal) or cycloheximide (inhibitor of eukaryotic protein synthesis) can be added to agar plates used to culture/select initial strains from water samples/soil samples collected from the types of habitats/niches such as marine or estuarian habits, or any other habitat where such bacteria can be found. This process would help select for enrichment of bacterial strains without (or minimal) contamination of eukaryotic strains. This selection process, in combination with culturing the plates at elevated temperatures (e.g. 30.degree. C.), and then selecting strains that produce at least one PUFA would initially identify candidate bacterial strains with a PUFA PKS system that is operative at elevated temperatures (as opposed to those bacterial strains in the prior art which only exhibit PUFA production at temperatures less than about 20.degree. C. and more preferably below about 5.degree. C.).

However, even in bacteria that do not grow well (or at all) at higher temperatures, or that do not produce at least one PUFA at higher temperatures, such strains can be identified and selected as comprising a PUFA PKS system by the identification of the ability of the bacterium to produce PUFAs under any conditions and/or by screening the genome of the bacterium for genes that are homologous to other known PUFA PKS genes from bacteria or non-bacterial organisms (e.g., see Example 7). To evaluate PUFA PKS function at higher temperatures for genes from any bacterial source, one can produce cell-free extracts and test for PUFA production at various temperatures, followed by selection of microorganisms that contain PUFA PKS genes that have enzymatic/biological activity at higher temperature ranges (e.g., 15.degree. C., 20.degree. C., 25.degree. C., or 30.degree. C. or even higher).

Suitable bacteria to use as hosts for genetic modification include any bacterial strain as discussed above. Particularly suitable bacteria to use as a source of PUFA PKS genes (and proteins and domains encoded thereby) for the production of genetically modified sequences and organisms according to the present invention include any bacterium that comprises a PUFA PKS system. Such bacteria are typically isolated from marine or estuarian habitats and can be readily identified by their ability to product PUFAs and/or by the presence of one or more genes having homology to known PUFA PKS genes in the organism. Such bacteria can include, but are not limited to, bacteria of the genera Shewanella and Vibrio. Preferred bacteria for use in the present invention include those with PUFA PKS systems that are biologically active at higher temperatures (e.g., above about 15.degree. C., 20.degree. C., 25.degree. C., or 30.degree. C. or even higher). The present inventors have identified two exemplary bacteria (e.g. Shewanella olleyana and Shewanellajaponica; see Examples 7 and 8) that will be particularly suitable for use as sources of PUFA PKS genes, and others can be readily identified or are known to comprise PUFA PKS genes and may be useful in an embodiment of the present invention (e.g., Shewanella gelidimarina).

Furthermore, it is recognized that not all bacterial or non-bacterial microorganisms can be readily cultured from natural habitats. However, genetic characteristics of such un-culturable microorganisms can be evaluated by isolating genes from DNA prepared en mass from mixed or crude environmental samples. Particularly suitable to the present invention, PUFA PKS genes derived from un-culturable microorganisms can be isolated from environmental DNA samples by degenerate PCR using primers designed to generally match regions of high similarity in known PUFA PKS genes (e.g., see Example 7). Alternatively, whole DNA fragments can be cloned directly from purified environmental DNA by any of several methods known to the art. Sequence of the DNA fragments thus obtained can reveal homologs to known genes such as PUFA PKS genes. Homologs of OrfB and OrfC (referring to the domain structure of Schizochytrium and Thraustochytrium, for example) may be particularly useful in defining the PUFA PKS end product. Whole coding regions of PUFA PKS genes can then be expressed in host organisms (such as Escherichia coli or yeast) in combination with each other or with known PUFA PKS gene or gene fragment combinations to evaluate their effect on PUFA production. As described above, activity in cell-free extracts can be used to determine function at desired temperatures. Isolated PUFA PKS genes can also be transformed directly into appropriate Schizochytrium or other suitable strains to measure function. PUFA PKS system-encoding constructs identified or produced in such a manner, including hybrid constructs, can also be used to transform other organisms, such as plants.

Therefore, using the non-bacterial PUFA PKS systems of the present invention, which, for example, makes use of genes from Thraustochytrid PUFA PKS systems, as well as PUFA PKS systems and PKS systems from bacteria, gene mixing can be used to extend the range of PUFA products to include EPA, DHA, ARA, GLA, SDA and others (described in detail below), as well as to produce a wide variety of bioactive molecules, including antibiotics, other pharmaceutical compounds, and other desirable products. The method to obtain these bioactive molecules includes not only the mixing of genes from various organisms but also various methods of genetically modifying the non-bacterial PUFA PKS genes disclosed herein. Knowledge of the genetic basis and domain structure of the non-bacterial PUFA PKS system of the present invention provides a basis for designing novel genetically modified organisms which produce a variety of bioactive molecules. Although mixing and modification of any PKS domains and related genes are contemplated by the present inventors, by way of example, various possible manipulations of the PUFA-PKS system are discussed below with regard to genetic modification and bioactive molecule production.

Accordingly, encompassed by the present invention are methods to genetically modify microbial or plant cells by: genetically modifying at least one nucleic acid sequence in the organism that encodes an amino acid sequence having the biological activity of at least one functional domain of a non-bacterial PUFA PKS system according to the present invention, and/or expressing at least one recombinant nucleic acid molecule comprising a nucleic acid sequence encoding such amino acid sequence. Various embodiments of such sequences, methods to genetically modify an organism, and specific modifications have been described in detail above. Typically, the method is used to produce a particular genetically modified organism that produces a particular bioactive molecule or molecules.

One embodiment of the present invention relates to a genetically modified Thraustochytrid microorganism, wherein the microorganism has an endogenous polyunsaturated fatty acid (PUFA) polyketide synthase (PKS) system, and wherein the endogenous PUFA PKS system has been genetically modified to alter the expression profile of a polyunsaturated fatty acid (PUFA) by the microorganism as compared to the Thraustochytrid microorganism in the absence of the modification. Thraustochytrid microorganisms useful as host organisms in the present invention endogenously contain and express a PUFA PKS system. The genetic modification can be a genetic modification of one or more of the functional domains of the endogenous PUFA PKS system, whereby the modification alters the PUFA production profile of the endogenous PUFA PKS system. In addition, or as an alternative, the genetic modification can be an introduction of at least one exogenous nucleic acid sequence (e.g., a recombinant nucleic acid molecule) to the microorganism, wherein the exogenous nucleic acid sequence encodes at least one biologically active domain or protein from a second PKS system and/or a protein that affects the activity of the PUFA PKS system (e.g., a phosphopantetheinyl transferases (PPTase)). The second PKS system can be any PKS system, including other PUFA PKS systems and including homologues of genes from the Thraustochytrid PUFA PKS system to be genetically modified.

This embodiment of the invention is particularly useful for the production of commercially valuable lipids enriched in a desired PUFA, such as EPA, via the present inventors' development of genetically modified microorganisms and methods for efficiently producing lipids (triacylglyerols (TAG) as well as membrane-associated phospholipids (PL)) enriched in PUFAs.

This particular embodiment of the present invention is derived in part from the following knowledge: (1) utilization of the inherent TAG production capabilities of selected microorganisms, and particularly, of Thraustochytrids, such as the commercially developed Schizochytrium strain described herein; (2) the present inventors' detailed understanding of PUFA PKS biosynthetic pathways (i.e., PUFA PKS systems) in eukaryotes and in particular, in members of the order Thraustochytriales; and, (3) utilization of a homologous genetic recombination system in Schizochytrium. Based on the inventors' knowledge of the systems involved, the same general approach may be exploited to produce PUFAs other than EPA.

In one embodiment of the invention, the endogenous Thraustochytrid PUFA PKS genes, such as the Schizochytrium genes encoding PUFA PKS enzymes that normally produce DHA and DPA, are modified by random or targeted mutagenesis, replaced with genes from other organisms that encode homologous PKS proteins (e.g., from bacteria or other sources), or replaced with genetically modified Schizochytrium, Thraustochytrium or other Thraustochytrid PUFA PKS genes. The product of the enzymes encoded by these introduced and/or modified genes can be EPA, for example, or it could be some other related molecule, including other PUFAs. One feature of this method is the utilization of endogenous components of Thraustochytrid PUFA synthesis and accumulation machinery that is essential for efficient production and incorporation of the PUFA into PL and TAG. In particular, this embodiment of the invention is directed to the modification of the type of PUFA produced by the organism, while retaining the high oil productivity of the parent strain.

Although some of the following discussion uses the organism Schizochytrium as an exemplary host organism, any Thraustochytrid can be modified according to the present invention, including members of the genera Thraustochytrium, Labyrinthuloides, and Japonochytrium. For example, the genes encoding the PUFA PKS system for a species of Thraustochytrium have been identified (see Example 6), and this organism can also serve as a host organism for genetic modification using the methods described herein, although it is more likely that the Thraustochytrium PKS genes will be used to modify the endogenous PUFA PKS genes of another Thraustochytrid, such as Schizochytrium. Furthermore, using methods for screening organisms as set forth in U.S. application Ser. No. 10/124,800, supra, one can identify other organisms useful in the present method and all such organisms are encompassed herein.

This embodiment of the present invention can be illustrated as follows. By way of example, based on the present inventors' current understanding of PUFA synthesis and accumulation in Schizochytrium, the overall biochemical process can be divided into three parts.

First, the PUFAs that accumulate in Schizochytrium oil (DHA and DPA) are the product of a PUFA PKS system as discussed above. The PUFA PKS system in Schizochytrium converts malonyl-CoA into the end product PUFA without release of significant amounts of intermediate compounds. In Schizochytrium, three genes have been identified (Orfs A, B and C; also represented by SEQ ID NO:1, SEQ ID NO:3 and SEQ ID NO:5, respectively) that encode all of the enzymatic domains known to be required for actual synthesis of PUFAs. Similar sets of genes (encoding proteins containing homologous sets of enzymatic domains) have been cloned and characterized from several other non-eukaryotic organisms that produce PUFAs, namely, several strains of marine bacteria. In addition, the present inventors have identified and now sequenced PUFA PKS genes in at least one other marine protist (Thraustochytrium strain 23B) (described in detail below).

The PUFA products of marine bacteria include EPA (e.g., produced by Shewanella SRC2738 and Photobacter profundum) as well as DHA (Vibrio marinus, now known as Moritella marina) (described in U.S. Pat. No. 6,140,486, supra; and in U.S. Pat. No. 6,566,583, supra). It is an embodiment of the invention that any PUFA PKS gene set could be envisioned to substitute for the Schizochytrium genes described in the example herein, as long as the physiological growth requirements of the production organism (e.g., Schizochytrium) in fermentation conditions were satisfied. In particular, the PUFA-producing bacterial strains described above grow only at relatively low temperatures (typically less than 20.degree. C.) which further indicates that their PUFA PKS gene products will not function at standard growth temperatures for Schizochytrium (25-30.degree. C.). However, the inventors have recently identified at least two other marine bacteria that grow and produce EPA at standard growth temperatures for Schizochytrium and other Thraustochytrids (see Example 7). These alternate marine bacteria have been shown to possess PUFA-PKS-like genes that will serve as material for modification of Schizochytrium and other Thraustochytrids by methods described herein. It will be apparent to those skilled in the art from this disclosure that other currently unstudied or unidentified PUFA-producing bacteria could also contain PUFA PKS genes useful for modification of Thraustochytrids.

Second, in addition to the genes that encode the enzymes directly involved in PUFA synthesis, an "accessory" enzyme is required. The gene encodes a phosphopantetheine transferase (PPTase) that activates the acyl-carrier protein (ACP) domains present in the PUFA PKS complex. Activation of the ACP domains by addition of this co-factor is required for the PUFA PKS enzyme complex to function. All of the ACP domains of the PUFA PKS systems identified so far show a high degree of amino acid sequence conservation and, without being bound by theory, the present inventors believe that the PPTase of Schizochytrium and other Thraustochytrids will recognize and activate ACP domains from other PUFA PKS systems. As proof of principle that heterologous PPTases and PUFA PKS genes can function together to produce a PUFA product, the present inventors demonstrate herein the use of two different heterologous PPTases with the PUFA PKS genes from Schizochytrium to produce a PUFA in a bacterial host cell.

Third, in Schizochytrium, the products of the PUFA PKS system are efficiently channeled into both the phospholipids (PL) and triacylglycerols (TAG). The present inventors' data suggest that the PUFA is transferred from the ACP domains of the PKS complex to coenzyme A (CoA). As in other eukaryotic organisms, this acyl-CoA would then serve as the substrate for the various acyl-transferases that form the PL and TAG molecules. In contrast, the data indicate that in bacteria, transfer to CoA does not occur; rather, there is a direct transfer from the ACP domains of the PKS complex to the acyl-transferases that form PL. The enzymatic system in Schizochytrium that transfers PUFA from ACP to CoA clearly can recognize both DHA and DPA and therefore, the present inventors believe that it is predictable that any PUFA product of the PUFA PKS system (as attached to the PUFA PKS ACP domains) will serve as a substrate.

Therefore, in one embodiment of the present invention, the present inventors propose to alter the genes encoding the components of the PUFA PKS enzyme complex (part 1) while utilizing the endogenous PPTase from Schizochytrium or another Thraustochytrid host (part 2) and PUFA-ACP to PUFA-CoA transferase activity and TAG/PL synthesis systems (or other endogenous PUFA ACP to TAG/PL mechanism) (part 3). These methods of the present invention are supported by experimental data, some of which are presented in the Examples section in detail.

First, the present inventors have found that the PUFA PKS system can be transferred between organisms, and that some parts are interchangeable. More particularly, it has been previously shown that the PUFA PKS pathways of the marine bacteria, Shewanella SCR2738 (Yazawa, 1996, Lipids 31:S297-300) and Vibrio marinus (along with the PPTase from Shewanella) (U.S. Pat. No. 6,140,486), can be successfully transferred to a heterologous host (i.e., to E. coli). Additionally, the degree of structural homology between the subunits of the PUFA PKS enzymes from these two organisms (Shewanella SCRC2738 and Vibrio marinus) is such that it has been possible to mix and match genes from the two systems (U.S. Pat. No. 6,140,486, supra). The PUFA end product of the mixed sets of genes varied depending on the origins of the specific gene homologues. At least one open reading frame (Shewanella's Orf 7 and its Vibrio marinus homologue; see FIG. 13 of U.S. Pat. No. 6,140,486; note that the nomenclature for this Orf has changed; it is labeled as Orf8 in the patent, but was submitted to Genbank as Orf 7, and is now referred to by its GenBank designation) could be associated with determination of whether DHA or EPA would be the product of the composite system. The functional domains of all of the PUFA PKS enzymes identified so far show sequence homology to one another. Similarly, these data indicated that PUFA PKS systems, including those from the marine bacteria, can be transferred to, and will function in, Schizochytrium and other Thraustochytrids.

The present inventors have now expressed the PUFA PKS genes (Orfs A, B and C) from Schizochytrium in an E. coli host and have demonstrated that the cells made DHA and DPA in about the same ratio as the endogenous production of these PUFAs in Schizochytrium (see Example 2). Therefore, it has been demonstrated that the recombinant Schizochytrium PUFA PKS genes encode a functional PUFA synthesis system. Additionally, all or portions of the Thraustochytrium 23B OrfA and OrfC genes have been shown to function in Schizochytrium (see Example 6).

Second, the present inventors have previously found that PPTases can activate heterologous PUFA PKS ACP domains. Production of DHA in E. coli transformed with the PUFA PKS genes from Vibrio marinus occurred only when an appropriate PPTase gene (in this case, from Shewanella SCRC2738) was also present (see U.S. Pat. No. 6,140,486, supra). This demonstrated that the Shewanella PPTase was able to activate the Vibrio PUFA PKS ACP domains. Additionally, the present inventors have now demonstrated the activation (pantetheinylation) of ACP domains from Schizochytrium Orf A using a PPTase (sfp) from Bacillus subtilus (see Example 2). The present inventors have also demonstrated activation (pantetheinylation) of ACP domains from Schizochytrium Orf A by a PPTase called Het I from Nostoc (see Example 2). The HetI enzyme was additionally used as the PPTase in the experiments discussed above for the production of DHA and DPA in E. coli using the recombinant Schizochytrium PUFA PKS genes (Example 2).

Third, data indicate that DHA-CoA and DPA-CoA may be metabolic intermediates in the Schizochytrium TAG and PL synthesis pathway. Published biochemical data suggest that in bacteria, the newly synthesized PUFAs are transferred directly from the PUFA PKS ACP domains to the phospholipid synthesis enzymes. In contrast, the present inventors' data indicate that in Schizochytrium, a eukaryotic organism, there may be an intermediate between the PUFA on the PUFA PKS ACP domains and the target TAG and PL molecules. The typical carrier of fatty acids in the eukaryotic cytoplasm is CoA. The inventors examined extracts of Schizochytrium cells and found significant levels of compounds that co-migrated during HPLC fractionation with authentic standards of DHA-CoA, DPA-CoA, 16:0-CoA and 18:1-CoA. The identity of the putative DHA-CoA and DPA-CoA peaks were confirmed using mass spectroscopy. In contrast, the inventors were not able to detect DHA-CoA in extracts of Vibrio marinus, again suggesting that a different mechanism exists in bacteria for transfer of the PUFA to its final target (e.g., direct transfer to PL). The data indicate a mechanism likely exists in Schizochytrium for transfer of the newly synthesized PUFA to CoA (probably via a direct transfer from the ACP to CoA). Both TAG and PL synthesis enzymes could then access this PUFA-CoA. The observation that both DHA and DPA CoA are produced suggests that the enzymatic transfer machinery may recognize a range of PUFAs.

Fourth, the present inventors have now created knockouts of Orf A, Orf B, and Orf C in Schizochytrium (see Example 3). The knockout strategy relies on the homologous recombination that has been demonstrated to occur in Schizochytrium (see U.S. patent application Ser. No. 10/124,807, supra). Several strategies can be employed in the design of knockout constructs. The specific strategy used to inactivate these three genes utilized insertion of a Zeocin.TM. resistance gene coupled to a tubulin promoter (derived from pMON50000, see U.S. patent application Ser. No. 10/124,807) into a cloned portion of the Orf. The new construct containing the interrupted coding region was then used for the transformation of wild type Schizochytrium cells via particle bombardment (see U.S. patent application Ser. No. 10/124,807). Bombarded cells were spread on plates containing both Zeocin.TM. and a supply of PUFA (see below). Colonies that grew on these plates were then streaked onto Zeocin.TM. plates that were not supplemented with PUFAs. Those colonies that required PUFA supplementation for growth were candidates for having had the PUFA PKS Orf inactivated via homologous recombination. In all three cases, this presumption was confirmed by rescuing the knockout by transforming the cells with a full-length genomic DNA clones of the respective Schizochytrium Orfs. Furthermore, in some cases, it was found that the Zeocin.TM. resistance gene had been removed (see Example 5), indicating that the introduced functional gene had integrated into the original site by double homologous recombination (i.e. deleting the resistance marker). One key to the success of this strategy was supplementation of the growth medium with PUFAs. In the present case, an effective means of supplementation was found to be sequestration of the PUFA by mixing with partially methylated beta-cyclodextrin prior to adding to the growth medium (see Example 5). Together, these experiments demonstrate the principle that one of skill in the art, given the guidance provided herein, can inactivate one or more of the PUFA PKS genes in a PUFA PKS-containing microorganism such as Schizochytrium, and create a PUFA auxotroph which can then be used for further genetic modification (e.g., by introducing other PKS genes) according to the present invention (e.g., to alter the fatty acid profile of the recombinant organism).

One important element of the genetic modification of the organisms of the present invention is the ability to directly transform a Thraustochytrid genome. In U.S. application Ser. No. 10/124,807, supra, transformation of Schizochytrium via single crossover homologous recombination and targeted gene replacement via double crossover homologous recombination were demonstrated. As discussed above, the present inventors have now used this technique for homologous recombination to inactivate Orf A, Orf B and OrfC of the PUFA-PKA system in Schizochytrium. The resulting mutants are dependent on supplementation of the media with PUFA. Several markers of transformation, promoter elements for high level expression of introduced genes and methods for delivery of exogenous genetic material have been developed and are available. Therefore, the tools are in place for knocking out endogenous PUFA PKS genes in Thraustochytrids and other eukaryotes having similar PUFA PKS systems and replacing them with genes from other organisms (or with modified Schizochytrium genes) as proposed above.

In one approach for production of EPA-rich TAG, the PUFA PKS system of Schizochytrium can be altered by the addition of heterologous genes encoding a PUFA PKS system whose product is EPA. It is anticipated that the endogenous PPTase will activate the ACP domains of that heterologous PUFA PKS system. Additionally, it is anticipated that the EPA will be converted to EPA-CoA and will readily be incorporated into Schizochytrium TAG and PL membranes. In one modification of this approach, techniques can be used to modify the relevant domains of the endogenous Schizochytrium system (either by introduction of specific regions of heterologous genes or by mutagenesis of the Schizochytrium genes themselves) such that its end product is EPA rather than DHA and DPA. This is an exemplary approach, as this technology can be applied to the production of other PUFA end products and to any eukaryotic microorganism that comprises a PUFA PKS system and that has the ability to efficiently channel the products of the PUFA PKS system into both the phospholipids (PL) and triacylglycerols (TAG). In particular, the invention is applicable to any Thraustochytrid microorganism or any other eukaryote that has an endogenous PUFA PKS system, which is described in detail below by way of example. In addition, the invention is applicable to any suitable host organism, into which the modified genetic material for production of various PUFA profiles as described herein can be transformed. For example, in the Examples, the PUFA PKS system from Schizochytrium is transformed into an E. coli. Such a transformed organism could then be further modified to alter the PUFA production profile using the methods described herein.

The present invention can make use of genes and nucleic acid sequences which encode proteins or domains from PKS systems other than the PUFA PKS system described herein and in U.S. patent application Ser. No. 10/124,800, and include genes and nucleic acid sequences from bacterial and non-bacterial PKS systems, including PKS systems of Type II, Type I and modular, described above. Organisms which express each of these types of PKS systems are known in the art and can serve as sources for nucleic acids useful in the genetic modification process of the present invention.

In a preferred embodiment, genes and nucleic acid sequences which encode proteins or domains from PKS systems other than the PUFA PKS system or from other PUFA PKS systems are isolated or derived from organisms which have preferred growth characteristics for production of PUFAs. In particular, it is desirable to be able to culture the genetically modified Thraustochytrid microorganism at temperatures greater than about 15.degree. C., greater than 20.degree. C., greater than 25.degree. C., greater than 30.degree. C., greater than 35.degree. C., greater than 40.degree. C., or in one embodiment, at any temperature between about 20.degree. C. and 40.degree. C. Therefore, PKS proteins or domains having functional enzymatic activity at these temperatures are preferred. For example, the present inventors describe herein the use of PKS genes from Shewanella olleyana or Shewanella japonica, which are marine bacteria that naturally produce EPA and grow at temperatures up to 30.degree. C. and 35.degree. C., respectively (see Example 7). PKS proteins or domains from these organisms are examples of proteins and domains that can be mixed with Thraustochytrid PUFA PKS proteins and domains as described herein to produce a genetically modified organism that has a specifically designed or modified PUFA production profile.

In another preferred embodiment, the genes and nucleic acid sequences that encode proteins or domains from a PUFA PKS system that produces one fatty acid profile are used to modify another PUFA PKS system and thereby alter the fatty acid profile of the host. For example, Thraustochytrium 23B (ATCC 20892) is significantly different from Schizochytrium sp. (ATCC 20888) in its fatty acid profile. Thraustochytrium 23B can have DHA:DPA(n-6) ratios as high as 40:1 compared to only 2-3:1 in Schizochytrium (ATCC 20888). Thraustochytrium 23B can also have higher levels of C20:5(n-3). However, Schizochytrium (ATCC 20888) is an excellent oil producer as compared to Thraustochytrium 23B. Schizochytrium accumulates large quantities of triacylglycerols rich in DHA and docosapentaenoic acid (DPA; 22:5.omega.6); e.g., 30% DHA+DPA by dry weight. Therefore, the present inventors describe herein the modification of the Schizochytrium endogenous PUFA PKS system with Thraustochytrium 23B PUFA PKS genes to create a genetically modified Schizochytrium with a DHA:DPA profile more similar to Thraustochytrium 23B (i.e., a "super-DHA-producer" Schizochytrium, wherein the production capabilities of the Schizochytrium combine with the DHA:DPA ratio of Thraustochytrium).

Therefore, the present invention makes use of genes from Thraustochytrid PUFA PKS systems, and further utilizes gene mixing to extend and/or alter the range of PUFA products to include EPA, DHA, DPA, ARA, GLA, SDA and others. The method to obtain these altered PUFA production profiles includes not only the mixing of genes from various organisms into the Thrasustochytrid PUFA PKS genes, but also various methods of genetically modifying the endogenous Thraustochytrid PUFA PKS genes disclosed herein. Knowledge of the genetic basis and domain structure of the Thraustochytrid PUFA PKS system of the present invention (e.g., described in detail for Schizochytrium above) provides a basis for designing novel genetically modified organisms which produce a variety of PUFA profiles. Novel PUFA PKS constructs prepared in microorganisms such as a Thraustochytrid can be isolated and used to transform plants to impart similar PUFA production properties onto the plants.

Any one or more of the endogenous Thraustochytrid PUFA PKS domains can be altered or replaced according to the present invention, provided that the modification produces the desired result (i.e., alteration of the PUFA production profile of the microorganism). Particularly preferred domains to alter or replace include, but are not limited to, any of the domains corresponding to the domains in Schizochytrium OrfB or OrfC (.beta.-keto acyl-ACP synthase (KS), acyltransferase (AT), FabA-like .beta.-hydroxy acyl-ACP dehydrase (DH), chain length factor (CLF), enoyl ACP-reductase (ER), an enzyme that catalyzes the synthesis of trans-2-acyl-ACP, an enzyme that catalyzes the reversible isomerization of trans-2-acyl-ACP to cis-3-acyl-ACP, and an enzyme that catalyzes the elongation of cis-3-acyl-ACP to cis-5-.beta.-keto-acyl-ACP). In one embodiment, preferred domains to alter or replace include, but are not limited to, .beta.-keto acyl-ACP synthase (KS), FabA-like .beta.-hydroxy acyl-ACP dehydrase (DH), and chain length factor (CLF).

In one aspect of the invention, Thraustochytrid PUFA-PKS PUFA production is altered by modifying the CLF (chain length factor) domain. This domain is characteristic of Type II (dissociated enzymes) PKS systems. Its amino acid sequence shows homology to KS (keto synthase pairs) domains, but it lacks the active site cysteine. CLF may function to determine the number of elongation cycles, and hence the chain length, of the end product. In this embodiment of the invention, using the current state of knowledge of FAS and PKS synthesis, a rational strategy for production of ARA by directed modification of the non-bacterial PUFA-PKS system is provided. There is controversy in the literature concerning the function of the CLF in PKS systems (Bisang et al., Nature 401, 502 (1999); Yi et al., J. Am. Chem. Soc. 125, 12708 (2003)) and it is realized that other domains may be involved in determination of the chain length of the end product. However, it is significant that Schizochytrium produces both DHA (C22:6, .omega.-3) and DPA (C22:5, .omega.-6). In the PUFA-PKS system the cis double bonds are introduced during synthesis of the growing carbon chain. Since placement of the .omega.-3 and .omega.-6 double bonds occurs early in the synthesis of the molecules, one would not expect that they would affect subsequent end-product chain length determination. Thus, without being bound by theory, the present inventors believe that introduction of a factor (e.g. CLF) that directs synthesis of C20 units (instead of C22 units) into the Schizochytrium PUFA-PKS system will result in the production of EPA (C20:5, .omega.-3) and ARA (C20:4, .omega.-6). For example, in heterologous systems, one could exploit the CLF by directly substituting a CLF from an EPA producing system (such as one from Photobacterium, or preferably from a microorganism with the preferred growth requirements as described below) into the Schizochytrium gene set. The fatty acids of the resulting transformants can then be analyzed for alterations in profiles to identify the transformants producing EPA and/or ARA.

By way of example, in this aspect of the invention, one could construct a clone with the CLF of OrfB replaced with a CLF from a C20 PUFA-PKS system. A marker gene could be inserted downstream of the coding region. More specifically, one can use the homologous recombination system for transformation of Thraustochytrids as described herein and in detail in U.S. patent application Ser. No. 10/124,807, supra. One can then transform the wild type Thraustochytrid cells (e.g., Schizochytrium cells), select for the marker phenotype, and then screen for those that had incorporated the new CLF. Again, one would analyze these transformants for any effects on fatty acid profiles to identify transformants producing EPA and/or ARA. If some factor other than those associated with the CLF is found to influence the chain length of the end product, a similar strategy could be employed to alter those factors.

In another aspect of the invention, modification or substitution of the .beta.-hydroxy acyl-ACP dehydrase/keto synthase pairs is contemplated. During cis-vaccenic acid (C18:1, .DELTA.11) synthesis in E. coli, creation of the cis double bond is believed to depend on a specific DH enzyme, .beta.-hydroxy acyl-ACP dehydrase, the product of the fabA gene. This enzyme removes HOH from a .beta.-keto acyl-ACP and leaves a trans double bond in the carbon chain. A subset of DH's, FabA-like, possess cis-trans isomerase activity (Heath et al., 1996, supra). A novel aspect of bacterial and non-bacterial PUFA-PKS systems is the presence of two FabA-like DH domains. Without being bound by theory, the present inventors believe that one or both of these DH domains will possess cis-trans isomerase activity (manipulation of the DH domains is discussed in greater detail below).

Another aspect of the unsaturated fatty acid synthesis in E. coli is the requirement for a particular KS enzyme, .beta.-ketoacyl-ACP synthase, the product of the fabB gene. This is the enzyme that carries out condensation of a fatty acid, linked to a cysteine residue at the active site (by a thio-ester bond), with a malonyl-ACP. In the multi-step reaction, C0.sub.2 is released and the linear chain is extended by two carbons. It is believed that only this KS can extend a carbon chain that contains a double bond. This extension occurs only when the double bond is in the cis configuration; if it is in the trans configuration, the double bond is reduced by enoyl-ACP reductase (ER) prior to elongation (Heath et al., 1996, supra). All of the PUFA-PKS systems characterized so far have two KS domains, one of which shows greater homology to the FabB-like KS of E. coli than the other. Again, without being bound by theory, the present inventors believe that in PUFA-PKS systems, the specificities and interactions of the DH (FabA-like) and KS (FabB-like) enzymatic domains determine the number and placement of cis double bonds in the end products. Because the number of 2-carbon elongation reactions is greater than the number of double bonds present in the PUFA-PKS end products, it can be determined that in some extension cycles complete reduction occurs. Thus the DH and KS domains can be used as targets for alteration of the DHA/DPA ratio or ratios of other long chain fatty acids. These can be modified and/or evaluated by introduction of homologous domains from other systems or by mutagenesis of these gene fragments.

In another embodiment, the ER (enoyl-ACP reductase--an enzyme which reduces the trans-double bond in the fatty acyl-ACP resulting in fully saturated carbons) domains can be modified or substituted to change the type of product made by the PKS system. For example, the present inventors know that Schizochytrium PUFA-PKS system differs from the previously described bacterial systems in that it has two (rather than one) ER domains. Without being bound by theory, the present inventors believe these ER domains can strongly influence the resulting PKS production product. The resulting PKS product could be changed by separately knocking out the individual domains or by modifying their nucleotide sequence or by substitution of ER domains from other organisms.

In another aspect of the invention, substitution of one of the DH (FabA-like) domains of the PUFA-PKS system for a DH domain that does not posses isomerization activity is contemplated, potentially creating a molecule with a mix of cis- and trans-double bonds. The current products of the Schizochytrium PUFA PKS system are DHA and DPA (C22:5 .omega.6). If one manipulated the system to produce C20 fatty acids, one would expect the products to be EPA and ARA (C20:4 .omega.6). This could provide a new source for ARA. One could also substitute domains from related PUFA-PKS systems that produced a different DHA to DPA ratio--for example by using genes from Thraustochytrium 23B (the PUFA PKS system of which is identified in U.S. patent application Ser. No. 10/124,800, supra).

Additionally, in one embodiment, one of the ER domains is altered in the Thraustochytrid PUFA PKS system (e.g. by removing or inactivating) to alter the end product profile. Similar strategies could be attempted in a directed manner for each of the distinct domains of the PUFA-PKS proteins using more or less sophisticated approaches. Of course one would not be limited to the manipulation of single domains. Finally, one could extend the approach by mixing domains from the PUFA-PKS system and other PKS or FAS systems (e.g., type I, type II, modular) to create an entire range of new PUFA end products.

It is recognized that many genetic alterations, either random or directed, which one may introduce into a native (endogenous, natural) PKS system, will result in an inactivation of enzymatic functions. Therefore, in order to test for the effects of genetic manipulation of a Thraustochytrid PUFA PKS system in a controlled environment, one could first use a recombinant system in another host, such as E. coli, to manipulate various aspects of the system and evaluate the results. For example, the FabB-strain of E. coli is incapable of synthesizing unsaturated fatty acids and requires supplementation of the medium with fatty acids that can substitute for its normal unsaturated fatty acids in order to grow (see Metz et al., 2001, supra). However, this requirement (for supplementation of the medium) can be removed when the strain is transformed with a functional PUFA-PKS system (i.e. one that produces a PUFA product in the E. coli host--see (Metz et al., 2001, supra, FIG. 2A). The transformed FabB- strain now requires a functional PUFA-PKS system (to produce the unsaturated fatty acids) for growth without supplementation. The key element in this example is that production of a wide range of unsaturated fatty acid will suffice (even unsaturated fatty acid substitutes such as branched chain fatty acids). Therefore, in another preferred embodiment of the invention, one could create a large number of mutations in one or more of the PUFA PKS genes disclosed herein, and then transform the appropriately modified FabB-strain (e.g. create mutations in an expression construct containing an ER domain and transform a FabB-strain having the other essential domains on a separate plasmid--or integrated into the chromosome) and select only for those transformants that grow without supplementation of the medium (i.e., that still possessed an ability to produce a molecule that could complement the FabB-defect).

One test system for genetic modification of a PUFA PKS is exemplified in the Examples section. Briefly, a host microorganism such as E. coli is transformed with genes encoding a PUFA PKS system including all or a portion of a Thraustochytrid PUFA PKS system (e.g., Orfs A, B and C of Schizochytrium) and a gene encoding a phosphopantetheinyl transferases (PPTase), which is required for the attachment of a phosphopantetheine cofactor to produce the active, holo-ACP in the PKS system. The genes encoding the PKS system can be genetically engineered to introduce one or more modifications to the Thraustochytrid PUFA PKS genes and/or to introduce nucleic acids encoding domains from other PKS systems into the Thraustochytrid genes (including genes from non-Thraustochytrid microorganisms and genes from different Thraustochytrid microorganisms). The PUFA PKS system can be expressed in the E. coli and the PUFA production profile measured. In this manner, potential genetic modifications can be evaluated prior to manipulation of the Thraustochytrid PUFA production organism.

The present invention includes the manipulation of endogenous nucleic acid molecules and/or the use of isolated nucleic acid molecules comprising a nucleic acid sequence from a Thraustochytrid PUFA PKS system or a homologue thereof. In one aspect, the present invention relates to the modification and/or use of a nucleic acid molecule comprising a nucleic acid sequence encoding a domain from a PUFA PKS system having a biological activity of at least one of the following proteins: malonyl-CoA:ACP acyltransferase (MAT), .beta.-keto acyl-ACP synthase (KS), ketoreductase (KR), acyltransferase (AT), FabA-like .beta.-hydroxy acyl-ACP dehydrase (DH), phosphopantetheine transferase, chain length factor (CLF), acyl carrier protein (ACP), enoyl ACP-reductase (ER), an enzyme that catalyzes the synthesis of trans-2-acyl-ACP, an enzyme that catalyzes the reversible isomerization of trans-2-acyl-ACP to cis-3-acyl-ACP, and/or an enzyme that catalyzes the elongation of cis-3-acyl-ACP to cis-5-.beta.-keto-acyl-ACP. Preferred domains to modify in order to alter the PUFA production profile of a host Thraustochytrid have been discussed previously herein.

The genetic modification of a Thraustochytrid microorganism according to the present invention preferably affects the type, amounts, and/or activity of the PUFAs produced by the microorganism, whether the endogenous PUFA PKS system is genetically modified and/or whether recombinant nucleic acid molecules are introduced into the organism. According to the present invention, to affect an activity of a PUFA PKS system, such as to affect the PUFA production profile, includes any genetic modification in the PUFA PKS system or genes that interact with the PUFA PKS system that causes any detectable or measurable change or modification in any biological activity the PUFA PKS system expressed by the organism as compared to in the absence of the genetic modification. According to the present invention, the phrases "PUFA profile", "PUFA expression profile" and "PUFA production profile" can be used interchangeably and describe the overall profile of PUFAs expressed/produced by a microorganism. The PUFA expression profile can include the types of PUFAs expressed by the microorganism, as well as the absolute and relative amounts of the PUFAs produced. Therefore, a PUFA profile can be described in terms of the ratios of PUFAs to one another as produced by the microorganism, in terms of the types of PUFAs produced by the microorganism, and/or in terms of the types and absolute or relative amounts of PUFAs produced by the microorganism.

As discussed above, while the host microorganism can include any eukaryotic microorganism with an endogenous PUFA PKS system and the ability to efficiently channel the products of the PUFA PKS system into both the phospholipids (PL) and triacylglycerols (TAG), the preferred host microorganism is any member of the order Thraustochytriales, including the families Thraustochytriaceae and Labyrinthulaceae. Particularly preferred host cells for use in the present invention could include microorganisms from a genus including, but not limited to: Thraustochytrium, Japonochytrium, Aplanochytrium, Elina, and Schizochytrium within the Thraustochytriaceae, and Labyrinthula, Labyrinthuloides, and Labyrinthomyxa within the Labyrinthulaceae. Preferred species within these genera include, but are not limited to: any species within Labyrinthula, including Labrinthula sp., Labyrinthula algeriensis, Labyrinthula cienkowskii, Labyrinthula chattonii, Labyrinthula coenocystis, Labyrinthula macrocystis, Labyrinthula macrocystis atlantica, Labyrinthula macrocystis macrocystis, Labyrinthula magnifica, Labyrinthula minuta, Labyrinthula roscoffensis, Labyrinthula valkanovii, Labyrinthula vitellina, Labyrinthula vitellina pacifica, Labyrinthula vitellina vitellina, Labyrinthula zopfii; any Labyrinthuloides species, including Labyrinthuloides sp., Labyrinthuloides minuta, Labyrinthuloides schizochytrops; any Labyrinthomyxa species, including Labyrinthomyxa sp., Labyrinthomyxa pohlia, Labyrinthomyxa sauvageaui, any Aplanochytrium species, including Aplanochytrium sp. and Aplanochytrium kerguelensis; any Elina species, including Elina sp., Elina marisalba, Elina sinorifica; any Japanochytrium species, including Japanochytrium sp., Japanochytrium marinum; any Schizochytrium species, including Schizochytrium sp., Schizochytrium aggregatum, Schizochytrium limacinum, Schizochytrium minutum, Schizochytrium octosporum; and any Thraustochytrium species, including Thraustochytrium sp., Thraustochytrium aggregatum, Thraustochytrium arudimentale, Thraustochytrium aureum, Thraustochytrium benthicola, Thraustochytrium globosum, Thraustochytrium kinnei, Thraustochytrium motivum, Thraustochytrium pachydermum, Thraustochytrium proliferum, Thraustochytrium roseum, Thraustochytrium striatum, Ulkenia sp., Ulkenia minuta, Ulkenia profunda, Ulkenia radiate, Ulkenia sarkariana, and Ulkenia visurgensis. Particularly preferred species within these genera include, but are not limited to: any Schizochytrium species, including Schizochytrium aggregatum, Schizochytrium limacinum, Schizochytrium minutum; any Thraustochytrium species (including former Ulkenia species such as U. visurgensis, U. amoeboida, U. sarkariana, U. profunda, U. radiata, U. minuta and Ulkenia sp. BP-5601), and including Thraustochytrium striatum, Thraustochytrium aureum, Thraustochytrium roseum; and any Japonochytrium species. Particularly preferred strains of Thraustochytriales include, but are not limited to: Schizochytrium sp. (S31)(ATCC 20888); Schizochytrium sp. (S8)(ATCC 20889); Schizochytrium sp. (LC-RM)(ATCC 18915); Schizochytrium sp. (SR21); Schizochytrium aggregatum (Goldstein et Belsky)(ATCC 28209); Schizochytrium limacinum (Honda et Yokochi)(IFO 32693); Thraustochytrium sp. (23B)(ATCC 20891); Thraustochytrium striatum (Schneider)(ATCC 24473); Thraustochytrium aureum (Goldstein)(ATCC 34304); Thraustochytrium roseum (Goldstein)(ATCC 28210); and Japonochytrium sp. (L1)(ATCC 28207).

In one embodiment of the present invention, it is contemplated that a mutagenesis program could be combined with a selective screening process to obtain a Thraustochytrid microorganism with the PUFA production profile of interest. The mutagenesis methods could include, but are not limited to: chemical mutagenesis, gene shuffling, switching regions of the genes encoding specific enzymatic domains, or mutagenesis restricted to specific regions of those genes, as well as other methods.

For example, high throughput mutagenesis methods could be used to influence or optimize production of the desired PUFA profile. Once an effective model system has been developed, one could modify these genes in a high throughput manner. Utilization of these technologies can be envisioned on two levels. First, if a sufficiently selective screen for production of a product of interest (e.g., EPA) can be devised, it could be used to attempt to alter the system to produce this product (e.g., in lieu of, or in concert with, other strategies such as those discussed above). Additionally, if the strategies outlined above resulted in a set of genes that did produce the PUFA profile of interest, the high throughput technologies could then be used to optimize the system. For example, if the introduced domain only functioned at relatively low temperatures, selection methods could be devised to permit removing that limitation.

In one embodiment of the present invention, a genetically modified Thraustochytrid microorganism has an enhanced ability to synthesize desired PUFAs and/or has a newly introduced ability to synthesize a different profile of PUFAs. According to the present invention, "an enhanced ability to synthesize" a product refers to any enhancement, or up-regulation, in a pathway related to the synthesis of the product such that the microorganism produces an increased amount of the product (including any production of a product where there was none before) as compared to the wild-type microorganism, cultured or grown, under the same conditions. Methods to produce such genetically modified organisms have been described in detail above.

As described above, in one embodiment of the present invention, a genetically modified microorganism or plant includes a microorganism or plant which has an enhanced ability to synthesize desired bioactive molecules (products) or which has a newly introduced ability to synthesize specific products (e.g., to synthesize a specific antibiotic). According to the present invention, "an enhanced ability to synthesize" a product refers to any enhancement, or up-regulation, in a pathway related to the synthesis of the product such that the microorganism or plant produces an increased amount of the product (including any production of a product where there was none before) as compared to the wild-type microorganism or plant, cultured or grown, under the same conditions. Methods to produce such genetically modified organisms have been described in detail above.

One embodiment of the present invention is a method to produce desired bioactive molecules (also referred to as products or compounds) by growing or culturing a genetically modified microorganism or plant of the present invention (described in detail above). Such a method includes the step of culturing in a fermentation medium or growing in a suitable environment, such as soil, a microorganism or plant, respectively, that has a genetic modification as described previously herein and in accordance with the present invention. Preferred host cells for genetic modification related to the PUFA PKS system of the invention are described above.

One embodiment of the present invention is a method to produce desired PUFAs by culturing a genetically modified Thraustochytrid microorganism of the present invention (described in detail above). Such a method includes the step of culturing in a fermentation medium and under conditions effective to produce the PUFA(s) a Thraustochytrid microorganism that has a genetic modification as described previously herein and in accordance with the present invention. An appropriate, or effective, medium refers to any medium in which a genetically modified microorganism of the present invention, including Thraustochytrids and other microorganisms, when cultured, is capable of producing the desired PUFA product(s). Such a medium is typically an aqueous medium comprising assimilable carbon, nitrogen and phosphate sources. Such a medium can also include appropriate salts, minerals, metals and other nutrients. Any microorganisms of the present invention can be cultured in conventional fermentation bioreactors. The microorganisms can be cultured by any fermentation process which includes, but is not limited to, batch, fed-batch, cell recycle, and continuous fermentation. Preferred growth conditions for Thraustochytrid microorganisms according to the present invention are well known in the art and are described in detail, for example, in U.S. Pat. Nos. 5,130,242, 5,340,742, and 5,698,244, each of which is incorporated herein by reference in its entirety.

In one embodiment, the genetically modified microorganism is cultured at a temperature of greater than about 15.degree. C., and in another embodiment, greater than about 20.degree. C., and in another embodiment, greater than about 25.degree. C., and in another embodiment, greater than about 30.degree. C., and in another embodiment, greater than about 35.degree. C., and in another embodiment, greater than about 40.degree. C., and in one embodiment, at any temperature between about 20.degree. C. and 40.degree. C.

The desired PUFA(s) and/or other bioactive molecules produced by the genetically modified microorganism can be recovered from the fermentation medium using conventional separation and purification techniques. For example, the fermentation medium can be filtered or centrifuged to remove microorganisms, cell debris and other particulate matter, and the product can be recovered from the cell-free supernatant by conventional methods, such as, for example, ion exchange, chromatography, extraction, solvent extraction, phase separation, membrane separation, electrodialysis, reverse osmosis, distillation, chemical derivatization and crystallization. Alternatively, microorganisms producing the PUFA(s), or extracts and various fractions thereof, can be used without removal of the microorganism components from the product.

Preferably, a genetically modified Thraustochytrid microorganism of the invention produces one or more polyunsaturated fatty acids including, but not limited to, EPA (C20:5, .omega.-3), DHA (C22:6, .omega.-3), DPA (C22:5, .omega.-6), ARA (C20:4, .omega.-6), GLA (C18:3, n-6), and SDA (C18:4, n-3)). In one preferred embodiment, a Schizochytrium that, in wild-type form, produces high levels of DHA and DPA, is genetically modified according to the invention to produce high levels of EPA. As discussed above, one advantage of using genetically modified Thraustochytrid microorganisms to produce PUFAs is that the PUFAs are directly incorporated into both the phospholipids (PL) and triacylglycerides (TAG).

Preferably, PUFAs are produced in an amount that is greater than about 5% of the dry weight of the microorganism, and in one aspect, in an amount that is greater than 6%, and in another aspect, in an amount that is greater than 7%, and in another aspect, in an amount that is greater than 8%, and in another aspect, in an amount that is greater than 9%, and in another aspect, in an amount that is greater than 10%, and so on in whole integer percentages, up to greater than 90% dry weight of the microorganism (e.g., 15%, 20%, 30%, 40%, 50%, and any percentage in between).

In the method for production of desired bioactive compounds of the present invention, a genetically modified plant is cultured in a fermentation medium or grown in a suitable medium such as soil. An appropriate, or effective, fermentation medium has been discussed in detail above. A suitable growth medium for higher plants includes any growth medium for plants, including, but not limited to, soil, sand, any other particulate media that support root growth (e.g. vermiculite, perlite, etc.) or hydroponic culture, as well as suitable light, water and nutritional supplements which optimize the growth of the higher plant. The genetically modified plants of the present invention are engineered to produce significant quantities of the desired product through the activity of the PKS system that is genetically modified according to the present invention. The compounds can be recovered through purification processes which extract the compounds from the plant. In a preferred embodiment, the compound is recovered by harvesting the plant. In this embodiment, the plant can be consumed in its natural state or further processed into consumable products.

Many genetic modifications useful for producing bioactive molecules will be apparent to those of skill in the art, given the present disclosure, and various other modifications have been discussed previously herein. The present invention contemplates any genetic modification related to a PUFA PKS system as described herein which results in the production of a desired bioactive molecule.

Bioactive molecules, according to the present invention, include any molecules (compounds, products, etc.) that have a biological activity, and that can be produced by a PKS system that comprises at least one amino acid sequence having a biological activity of at least one functional domain of a non-bacterial PUFA PKS system as described herein. Such bioactive molecules can include, but are not limited to: a polyunsaturated fatty acid (PUFA), an anti-inflammatory formulation, a chemotherapeutic agent, an active excipient, an osteoporosis drug, an anti-depressant, an anti-convulsant, an anti-Heliobactor pylori drug, a drug for treatment of neurodegenerative disease, a drug for treatment of degenerative liver disease, an antibiotic, and a cholesterol lowering formulation. One advantage of the non-bacterial PUFA PKS system of the present invention is the ability of such a system to introduce carbon-carbon double bonds in the cis configuration, and molecules including a double bond at every third carbon. This ability can be utilized to produce a variety of compounds.

Preferably, bioactive compounds of interest are produced by the genetically modified microorganism in an amount that is greater than about 0.05%, and preferably greater than about 0.1%, and more preferably greater than about 0.25%, and more preferably greater than about 0.5%, and more preferably greater than about 0.75%, and more preferably greater than about 1%, and more preferably greater than about 2.5%, and more preferably greater than about 5%, and more preferably greater than about 10%, and more preferably greater than about 15%, and even more preferably greater than about 20% of the dry weight of the microorganism. For lipid compounds, preferably, such compounds are produced in an amount that is greater than about 5% of the dry weight of the microorganism. For other bioactive compounds, such as antibiotics or compounds that are synthesized in smaller amounts, those strains possessing such compounds at of the dry weight of the microorganism are identified as predictably containing a novel PKS system of the type described above. In some embodiments, particular bioactive molecules (compounds) are secreted by the microorganism, rather than accumulating. Therefore, such bioactive molecules are generally recovered from the culture medium and the concentration of molecule produced will vary depending on the microorganism and the size of the culture.

One embodiment of the present invention relates to a method to modify an endproduct containing at least one fatty acid, comprising adding to the endproduct an oil produced by a recombinant host cell that expresses at least one recombinant nucleic acid molecule comprising a nucleic acid sequence encoding at least one biologically active domain of a PUFA PKS system. The PUFA PKS system includes any suitable bacterial or non-bacterial PUFA PKS system described herein, including the PUFA PKS systems from Thraustochytrium and Schizochytrium, or any PUFA PKS system from bacteria that normally (i.e., under normal or natural conditions) are capable of growing and producing PUFAs at temperatures above 22.degree. C., such as Shewanella olleyana or Shewanella japonica.

Preferably, the endproduct is selected from the group consisting of a food, a dietary supplement, a pharmaceutical formulation, a humanized animal milk, and an infant formula. Suitable pharmaceutical formulations include, but are not limited to, an anti-inflammatory formulation, a chemotherapeutic agent, an active excipient, an osteoporosis drug, an anti-depressant, an anti-convulsant, an anti-Heliobactor pylori drug, a drug for treatment of neurodegenerative disease, a drug for treatment of degenerative liver disease, an antibiotic, and a cholesterol lowering formulation. In one embodiment, the endproduct is used to treat a condition selected from the group consisting of: chronic inflammation, acute inflammation, gastrointestinal disorder, cancer, cachexia, cardiac restenosis, neurodegenerative disorder, degenerative disorder of the liver, blood lipid disorder, osteoporosis, osteoarthritis, autoimmune disease, preeclampsia, preterm birth, age related maculopathy, pulmonary disorder, and peroxisomal disorder.

Suitable food products include, but are not limited to, fine bakery wares, bread and rolls, breakfast cereals, processed and unprocessed cheese, condiments (ketchup, mayonnaise, etc.), dairy products (milk, yogurt), puddings and gelatin desserts, carbonated drinks, teas, powdered beverage mixes, processed fish products, fruit-based drinks, chewing gum, hard confectionery, frozen dairy products, processed meat products, nut and nut-based spreads, pasta, processed poultry products, gravies and sauces, potato chips and other chips or crisps, chocolate and other confectionery, soups and soup mixes, soya based products (milks, drinks, creams, whiteners), vegetable oil-based spreads, and vegetable-based drinks.

Yet another embodiment of the present invention relates to a method to produce a humanized animal milk. This method includes the steps of genetically modifying milk-producing cells of a milk-producing animal with at least one recombinant nucleic acid molecule comprising a nucleic acid sequence encoding at least one biologically active domain of a PUFA PKS system as described herein.

Methods to genetically modify a host cell and to produce a genetically modified non-human, milk-producing animal, are known in the art. Examples of host animals to modify include cattle, sheep, pigs, goats, yaks, etc., which are amenable to genetic manipulation and cloning for rapid expansion of a transgene expressing population. For animals, PKS-like transgenes can be adapted for expression in target organelles, tissues and body fluids through modification of the gene regulatory regions. Of particular interest is the production of PUFAs in the breast milk of the host animal.

The following examples are provided for the purpose of illustration and are not intended to limit the scope of the present invention.

EXAMPLES

Example 1

The following example, from U.S. patent application Ser. No.10/124,800, describes the use of the screening process of the present invention to identify other non-bacterial organisms comprising a PUFA PKS system according to the present invention.

Thraustochytrium sp. 23B (ATCC 20892) was cultured as described in detail herein.

A frozen vial of Thraustochytrium sp. 23B (ATCC 20892) was used to inoculate a 250 mL shake flask containing 50 mL of RCA medium. The culture was shaken on a shaker table (200 rpm) for 72 hr at 25.degree. C. RCA medium contains the following:

TABLE-US-00001 RCA Medium Deionized water 1000 mL Reef Crystals .RTM. sea salts 40 g/L Glucose 20 g/L Monosodium glutamate (MSG) 20 g/L Yeast extract 1 g/L PII metals* 5 mL/L Vitamin mix* 1 mL/L pH 7.0 *PII metal mix and vitamin mix are same as those outlined in U.S. Pat. No. 5,130,742, incorporated herein by reference in its entirety.

25 mL of the 72 hr old culture was then used to inoculate another 250 mL shake flask containing 50 mL of low nitrogen RCA medium (10 g/L MSG instead of 20 g/L) and the other 25 mL of culture was used to inoculate a 250 mL shake flask containing 175 mL of low-nitrogen RCA medium. The two flasks were then placed on a shaker table (200 rpm) for 72 hr at 25.degree. C. The cells were then harvested via centrifugation and dried by lyophilization. The dried cells were analyzed for fat content and fatty acid profile and content using standard gas chromatograph procedures.

The screening results for Thraustochytrium 23B under low oxygen conditions relative to high oxygen conditions were as follows:

TABLE-US-00002 Did DHA as % FAME increase? Yes (38 -> 44%) C14:0 + C16:0 + C16:1 greater than about Yes (44%) 40% TFA? No C18:3(n - 3) or C18:3(n - 6)? Yes (0%) Did fat content increase? Yes (2-fold increase) Did DHA (or other HUFA content increase)? Yes (2.3-fold increase)

The results, especially the significant increase in DHA content (as % FAME) under low oxygen conditions, conditions, strongly indicates the presence of a PUFA producing PKS system in this strain of Thraustochytrium.

In order to provide additional data confirming the presence of a PUFA PKS system, a Southern blot of Thraustochytrium 23B was conducted using PKS probes from Schizochytrium strain 20888, a strain which has already been determined to contain a PUFA producing PKS system (i.e., SEQ ID Nos: 1-32 described above). Fragments of Thraustochytrium 23B genomic DNA which are homologous to hybridization probes from PKS PUFA synthesis genes were detected using the Southern blot technique. Thraustochytrium 23B genomic DNA was digested with either ClaI or KpnI restriction endonucleases, separated by agarose gel electrophoresis (0.7% agarose, in standard tris-acetate-EDTA buffer), and blotted to a Schleicher & Schuell Nytran Supercharge membrane by capillary transfer. Two digoxigenin labeled hybridization probes were used--one specific for the enoyl-ACP reductase (ER) region of Schizochytrium PKS Orf B (nucleotides 5012-5511 of Orf B; SEQ ID NO:3), and the other specific for a conserved region at the beginning of Schizochytrium PKS Orf C (nucleotides 76-549 of OrfC; SEQ ID NO:5).

The OrfB-ER probe detected an approximately 13 kb ClaI fragment and an approximately 3.6 kb KpnI fragment in the Thraustochytrium 23B genomic DNA. The OrfC probe detected an approximately 7.5 kb ClaI fragment and an approximately 4.6 kb KpnI fragment in the Thraustochytrium 23B genomic DNA.

Finally, a recombinant genomic library, consisting of DNA fragments from Thraustochytrium 23B genomic DNA inserted into vector lambda FIX II (Stratagene), was screened using digoxigenin labeled probes corresponding to the following segments of Schizochytrium 20888 PUFA-PKS genes: nucleotides 7385-7879 of Orf A (SEQ ID NO:1), nucleotides 5012-5511 of Orf B (SEQ ID NO:3), and nucleotides 76-549 of Orf C (SEQ ID NO:5). Each of these probes detected positive plaques from the Thraustochytrium 23B library, indicating extensive homology between the Schizochytrium PUFA-PKS genes and the genes of Thraustochytrium 23B.

These results demonstrate that Thraustochytrium 23B genomic DNA contains sequences that are homologous to PKS genes from Schizochytrium 20888.

Example 2

The following example demonstrates that Schizochytrium Orfs A, B and C encode a functional DHA/DPA synthesis enzyme via functional expression in E. coli.

General Preparation of E. coli Transformants

The three genes encoding the Schizochytrium PUFA PKS system that produces DHA and DPA in Schizochytrium (Orfs A, B & C; SEQ ID NO:1, SEQ ID NO:3 and SEQ ID NO:5, respectively) were cloned into a single E. coli expression vector (derived from pET21c (Novagen)). The genes are transcribed as a single message (by the T7 RNA-polymerase), and a ribosome-binding site cloned in front of each of the genes initiates translation. Modification of the Orf B coding sequence was needed to obtain production of a full-length Orf B protein in E. coli (see below). An accessory gene, encoding a PPTase (see below) was cloned into a second plasmid (derived from pACYC184, New England Biolabs).

OrfB

The Orf B gene is predicted to encode a protein with a mass of .about.224 kDa. Initial attempts at expression of the gene in E. coli resulted in accumulation of a protein with an apparent molecular mass of .about.165 kDa (as judged by comparison to proteins of known mass during SDS-PAGE). Examination of the Orf B nucleotide sequence revealed a region containing 15 sequential serine codons--all of them being the TCT codon. The genetic code contains 6 different serine codons, and three of these are used frequently in E. coli. The present inventors used four overlapping oligonucleotides in combination with a polymerase chain reaction protocol to resynthesize a small portion of the Orf B gene (a .about.195 base pair, BspHI to SacII restriction enzyme fragment) that contained the serine codon repeat region. In the synthetic Orf B fragment, a random mixture of the 3 serine codons commonly used by E. coli was used, and some other potentially problematic codons were changed as well (i.e., other codons rarely used by E. coli). The B spHI to S acII fragment present in the original Orf B was replaced by the resynthesized fragment (to yield Orf B*) and the modified gene was cloned into the relevant expression vectors. The modified OrfB* still encodes the amino acid sequence of SEQ ID NO:4. Expression of the modified Orf B* clone in E. coli resulted in the appearance of a .about.224 kDa protein, indicating that the full-length product of OrfB was produced. The sequence of the resynthesized Orf B* BspHI to SacI fragment is shown in SEQ ID NO:80. Referring to SEQ ID NO:80, the nucleotide sequence of the resynthesized BspHI to SacII region of Orf B is shown. The BspHI restriction site and the SacII restriction site are identified. The BspHI site starts at nucleotide 4415 of the Orf B CDS (SEQ ID NO:3) (note: there are a total of three BspHI sites in the Orf B CDS, while the SacII site is unique). The sequence of the unmodified Orf B CDS is given in GenBank Accession number AF378328 and in SEQ ID NO:3.

PPTase

The ACP domains of the Orf A protein (SEQ ID NO:2 in Schizochytrium) must be activated by addition of phosphopantetheine group in order to function. The enzymes that catalyze this general type of reaction are called phosphopantetheine transferases (PPTases). E. coli contains two endogenous PPTases, but it was anticipated that they would not recognize the Orf A ACP domains from Schizochytrium. This was confirmed by expressing Orfs A, B* (see above) and C in E. coli without an additional PPTase. In this transformant, no DHA production was detected. The inventors tested two heterologous PPTases in the E. coli PUFA PKS expression system: (1) sfp (derived from Bacillus subtilis) and (2) Het I (from the cyanobacterium Nostoc strain 7120).

The sfp PPTase has been well characterized and is widely used due to its ability to recognize a broad range of substrates. Based on published sequence information (Nakana, et al., 1992, Molecular and General Genetics 232: 313-321), an expression vector for sfp was built by cloning the coding region, along with defined up- and downstream flanking DNA sequences, into a pACYC-184 cloning vector. The oligonucleotides:

TABLE-US-00003 CGGGGTACCCGGGAGCCGCCTTGGCTTTGT; (forward; SEQ ID NO: 73) and AAACTGCAGCCCGGGTCCAGCTGGCAGGCACCCTG, (reverse; SEQ ID NO: 74)

were used to amplify the region of interest from genomic B. subtilus DNA. Convenient restriction enzyme sites were included in the oligonucleotides to facilitate cloning in an intermediate, high copy number vector and finally into the EcoRV site of pACYC184 to create the plasmid: pBR301. Examination of extracts of E. coli transformed with this plasmid revealed the presence of a novel protein with the mobility expected for sfp. Co-expression of the sfp construct in cells expressing the Orf A, B*, C proteins, under certain conditions, resulted in DHA production. This experiment demonstrated that sfp was able to activate the Schizochytrium Orf A ACP domains. In addition, the regulatory elements associated with the sfp gene were used to create an expression cassette into which other genes could be inserted. Specifically, the sfp coding region (along with three nucleotides immediately upstream of the ATG) in pBR301 was replaced with a 53 base pair section of DNA designed so that it contains several unique (for this construct) restriction enzyme sites. The initial restriction enzyme site in this region is NdeI (CATATG; SEQ ID NO:79). The ATG sequence embedded in this site is utilized as the initiation methionine codon for introduced genes. The additional restriction sites (BglLL, NotI, Smal, PmeII, HindIII, SpeI and XhoI) were included to facilitate the cloning process. The functionality of this expression vector cassette was tested by using PCR to generate a version of sfp with a NdeI site at the 5' end and an XhoI site ate the 3' end. This fragment was cloned into the expression cassette and transferred into E. coli along with the Orf A, B* and C expression vector. Under appropriate conditions, these cells accumulated DHA, demonstrating that a functional sfp had been produced.

To the present inventors' knowledge, Het I has not been tested previously in a heterologous situation. Het I is present in a cluster of genes in Nostoc known to be responsible for the synthesis of long chain hydroxy-fatty acids that are a component of a glyco-lipid layer present in heterocysts of that organism. The present inventors, without being bound by theory, believe that Het I activates the ACP domains of a protein, Hgl E, present in that cluster. The two ACP domains of Hgl E have a high degree of sequence homology to the ACP domains found in Schizochytrium Orf A. The endogenous start codon of Het I has not been identified (there is no methionine present in the putative protein). There are several potential alternative start codons (e.g., TTG and ATT) near the 5' end of the open reading frame. The sequence of the region of Nostoc DNA encoding the HetI gene is shown in SEQ ID NO:81. SEQ ID NO:82 represents the amino acid sequence encoded by SEQ ID NO:81. Referring to SEQ ID NO:81, limit to the upstream coding region indicated by the inframe nonsense triplet (TAA) at positions 1-3 of SEQ ID NO: 81 and ends with the stop codon (TGA) at positions 715-717 of SEQ ID NO:81. No methionine codons (ATG) are present in the sequence. Potential alternative initiation codons are: 3 TTG codons (positions 4-6,7-9 and 49-51 of SEQ ID NO:81), ATT (positions 76-78 of SEQ ID NO:81) and GTG (positions 235-237 of SEQ ID NO:81). A Het I expression construct was made by using PCR to replace the furthest 5' potential alternative start codon (TTG) with a methionine codon (ATG, as part of the above described NdeI restriction enzyme recognition site), and introducing an XhoI site at the 3' end of the coding sequence. The modified HetI coding sequence was then inserted into the NdeI and XhoI sites of the pACYC 184 vector construct containing the sfp regulatory elements. Expression of this Het I construct in E. coli resulted in the appearance of a new protein of the size expected from the sequence data. Co-expression of Het I with Schizochytrium Orfs A, B*, C in E. coli under several conditions resulted in the accumulation of DHA and DPA in those cells. In all of the experiments in which sfp and Het I were compared, more DHA and DPA accumulated in the cells containing the Het I construct than in cells containing the sfp construct.

Production of DHA and DPA in E. coli Transformants

The two plasmids encoding: (1) the Schizochytrium PUFA PKS genes (Orfs A, B* and C) and (2) the PPTase (from sfp or from Het I) were transformed into E. coli strain BL21 which contains an inducible T7 RNA polymerase gene. Synthesis of the Schizochytrium proteins was induced by addition of IPTG to the medium, while PPTase expression was controlled by a separate regulatory element (see above). Cells were grown under various defined conditions and using either of the two heterologous PPTase genes. The cells were harvested and the fatty acids were converted to methyl-esters (FAME) and analyzed using gas-liquid chromatography.

Under several conditions, DHA and DPA were detected in E. coli cells expressing the Schizochytrium PUFA PKS genes, plus either of the two heterologous PPTases. No DHA or DPA was detected in FAMEs prepared from control cells (i.e., cells transformed with a plasmid lacking one of the Orfs). The ratio of DHA to DPA observed in E. coli approximates that of the endogenous DHA and DPA production observed in Schizochytrium. The highest level of PUFA (DHA plus DPA), representing .about.17% of the total FAME, was found in cells grown at 32.degree. C. in 765 medium (recipe available from the American Type Culture Collection) supplemented with 10% (by weight) glycerol. Note that PUFA accumulation was also observed when cells were grown in Luria Broth supplemented with 5 or 10% glycerol, and when grown at 20.degree. C. Selection for the presence of the respective plasmids was maintained by inclusion of the appropriate antibiotics during the growth and IPTG (to a final concentration of 0.5 mM) was used to induce expression of Orfs A, B* and C.

FIG. 4 shows an example chromatogram from gas-liquid chromatographic analysis of FAMEs derived from control cells and from cells expressing the Schizochytrium PUFA PKS genes plus a PPTase (in this case Het I). Identity of the labeled FAMEs has been confirmed using mass spectroscopy.

Example 3

The following example shows demonstrates that genes encoding the Schizochytrium PUFA PKS enzyme complex can be selectively inactivated (knocked out), and that it is a lethal phenotype unless the medium is supplemented with polyunsaturated fatty acids.

Homologous recombination has been demonstrated in Schizochytrium (see copending U.S. patent application Ser. No. 10/124,807, incorporated herein by reference in its entirety). A plasmid designed to inactivate Schizochytrium Orf A (SEQ ID NO:1) was made by inserting a Zeocin.TM. resistance marker into the Sma I site of a clone containing the Orf A coding sequence. The Zeocin.TM. resistance marker was obtained from the plasmid pMON50000--expression of the Zeocin.TM. resistance gene is driven by a Schizochytrium derived tubulin promoter element (see U.S. patent application Ser. No. 10/124,807, ibid.). The knock-out construct thus consists of: 5' Schizochytrium Orf A coding sequence, the tub-Zeocin.TM. resistance element and 3' Schizochytrium Orf A coding sequence, all cloned into pBluescript II SK (+) vector (Stratagene).

The plasmid was introduced into Schizochytrium cells by particle bombardment and transformants were selected on plates containing Zeocin.TM. and supplemented with polyunsaturated fatty acids (PUFA) (see Example 4). Colonies that grew on the Zeocin.TM. plus PUFA plates were tested for ability to grow on plates without the PUFA supplementation and several were found that required the PUFA. These PUFA auxotrophs are putative Orf A knockouts. Northern blot analysis of RNA extracted from several of these mutants confirmed that a full-length Orf A message was not produced in these mutants.

These experiments demonstrate that a Schizochytrium gene (e.g., Orf A) can be inactivated via homologous recombination, that inactivation of Orf A results in a lethal phenotype, and that those mutants can be rescued by supplementation of the media with PUFA.

Similar sets of experiments directed to the inactivation of Schizochytrium Orf B (SEQ ID NO:3) and Orf C (SEQ ID NO:5) have yielded similar results. That is, Orf B and Orf C can be individually inactivated by homologous recombination and those cells require PUFA supplementation for growth.

Example 4

The following example shows that PUFA auxotrophs can be maintained on medium supplemented with EPA, demonstrating that EPA can substitute for DHA in Schizochytrium.

As indicated in Example 3, Schizochytrium cells in which the PUFA PKS complex has been inactivated required supplementation with PUFA to survive. Aside from demonstrating that Schizochytrium is dependent on the products of this system for growth, this experimental system permits the testing of various fatty acids for their ability to rescue the mutants. It was discovered that the mutant cells (in which any of the three genes have been inactivated) grew as well on media supplemented with EPA as they did on media supplemented with DHA. This result indicates that, if the endogenous PUFA PKS complex which produces DHA were replaced with one whose product was EPA, the cells would be viable. Additionally, these mutant cells could be rescued by supplementation with either ARA or GLA, demonstrating the feasibility of producing genetically modified Schizochytrium that produce these products. It is noted that a preferred method for supplementation with PUFAs involves combining the free fatty acids with partially methylated beta-cyclodextrin prior to addition of the PUFAs to the medium.

Example 5

The following example shows that inactivated PUFA genes can be replaced at the same site with active forms of the genes in order to restore PUFA synthesis.

Double homologous recombination at the acetolactate synthase gene site has been demonstrated in Schizochytrium (see U.S. patent application Ser. No. 10/124,807, supra). The present inventors tested this concept for replacement of the Schizochytrium PUFA PKS genes by transformation of a Schizochytrium Orf A knockout strain (described in Example 2) with a full-length Schizochytrium Orf A genomic clone. The transformants were selected by their ability to grow on media without supplemental PUFAs. These PUFA prototrophs were then tested for resistance to Zeocin.TM. and several were found that were sensitive to the antibiotic. These results indicate that the introduced Schizochytrium Orf A has replaced the Zeocin.TM. resistance gene in the knockout strain via double homologous recombination. This experiment demonstrates the proof of concept for gene replacement within the PUFA PKS genes. Similar experiments for Schizochytrium Orf B and Orf C knock-outs have given identical results.

Example 6

This example shows that all or some portions of the Thraustochytrium 23B PUFA PKS genes can function in Schizochytrium.

As described in U.S. patent application Ser. No. 10/124,800 (supra), the DHA-producing protist Thraustochytrium 23B (Th. 23B) has been shown to contain orfA, orfb, and orfC homologs. Complete genomic clones of the three Th. 23B genes were used to transform the Schizochytrium strain containing the cognate orf "knock-out". Direct selection for complemented transformants was carried out in the absence of PUFA supplementation. By this method, it was shown that the Th. 23B orfA and orfC genes could complement the Schizochytrium orfA and orfC knock-out strains, respectively, to PUFA prototrophy. Complemented transformants were found that either retained or lost Zeocin.TM. resistance (the marker inserted into the Schizochytrium genes thereby defining the knock-outs). The Zeocin.TM.-resistant complemented transformants are likely to have arisen by a single cross-over integration of the entire Thraustochytrium gene into the Schizochytrium genome outside of the respective orf region. This result suggests that the entire Thraustochytrium gene is functioning in Schizochytrium. The Zeocin.TM.-sensitive complemented transformants are likely to have arisen by double cross-over events in which portions (or conceivably all) of the Thraustochytrium genes functionally replaced the cognate regions of the Schizochytrium genes that had contained the disruptive Zeocin.TM. resistance marker. This result suggests that a fraction of the Thraustochytrium gene is functioning in Schizochytrium.

Example 7

The following example shows that certain EPA-producing bacteria contain PUFA PKS-like genes that appear to be suitable for modification of Schizochytrium.

Two EPA-producing marine bacterial strains of the genus Shewanella have been shown to grow at temperatures typical of Schizochytrium fermentations and to possess PUFA PKS-like genes. Shewanella olleyana (Australian Collection of Antarctic Microorganisms (ACAM) strain number 644; Skerratt et al., Int. J. Syst. Evol. Microbiol 52, 2101 (2002)) produces EPA and grows up to 30.degree. C. Shewanella japonica (American Type Culture Collection (ATCC) strain number BAA-316; Ivanova et al., Int. J. Syst. Evol. Microbiol. 51, 1027 (2001)) produces EPA and grows up to 35.degree. C.

To identify and isolate the PUFA-PKS genes from these bacterial strains, degenerate PCR primer pairs for the KS-MAT region of bacterial orf5/pfaA genes and the DH-DH region of bacterial orf7/pfaC genes were designed based on published gene sequences for Shewanella SCRC-2738, Shewanella oneidensis MR-1; Shewanella sp. GA-22; Photobacter profundum, and Moritella marina (see discussion above). Specifically, the primers and PCR conditions were designed as follows:

Primers for the KS/AT region; based on the following published sequences: Shewanella sp. SCRC-2738; Shewanella oneidensis MR-1; Photobacter profundum; Moritella marina:

TABLE-US-00004 prRZ23 GGYATGMTGRTTGGTGAAGG (forward; SEQ ID NO: 69) prRZ24 TRTTSASRTAYTGYGAACCTTG (reverse; SEQ ID NO: 70)

Primers for the DH region; based on the following published sequences: Shewanella sp. GA-22; Shewanella sp. SCRC-2738; Photobacter profundum; Moritella marina:

TABLE-US-00005 prRZ28 ATGKCNGAAGGTTGTGGCCA (forward; SEQ ID NO: 71) prRZ29 CCWGARATRAAGCCRTTDGGTTG (reverse; SEQ ID NO: 72)

The PCR conditions (with bacterial chromosomal DNA as templates) were as follows:

Reaction Mixture:

0.2 .mu.M dNTPs

0.1 .mu.M each primer

8% DMSO

250 ng chromosomal DNA

2.5U Herculase.RTM. DNA polymerase (Stratagene)

1X Herculase.RTM. buffer

50 .mu.L total volume

PCR Protocol: (1) 98.degree. C. for 3 min.; (2) 98.degree. C. for 40 sec.; (3) 56.degree. C. for 30 sec.; (4) 72.degree. C. for 90 sec.; (5) Repeat steps 2-4 for 29 cycles; (6) 72.degree. C. for 10 min.; (7) Hold at 6.degree. C.

For both primer pairs, PCR gave distinct products with expected sizes using chromosomal DNA templates from either Shewanella olleyana or Shewanellajaponica. The four respective PCR products were cloned into pCR-BLUNT II-TOPO (Invitrogen) and insert sequences were determined using the M13 forward and reverse primers. In all cases, the DNA sequences thus obtained were highly homologous to known bacterial PUFA PKS gene regions.

The DNA sequences obtained from the bacterial PCR products were compared with known sequences and with PUFA PKS genes from Schizochytrium ATCC 20888 in a standard Blastx search (BLAST parameters: Low Complexity filter: On; Matrix: BLOSUM62; Word Size: 3; Gap Costs: Existance11, Extension 1 (BLAST described in Altschul, S. F., Madden, T. L., Schaaffer, A. A., Zhang, J., Zhang, Z., Miller, W. & Lipman, D. J. (1997) "Gapped BLAST and PSI-BLAST: a new generation of protein database search programs." Nucleic Acids Res. 25:3389-3402, incorporated herein by reference in its entirety)).

At the amino acid level, the sequences with the greatest degree of homology to the Shewanella olleyana ACAM644 ketoacyl synthase/acyl transferase (KS-AT) deduced amino acid sequence encoded by SEQ ID NO:76 were: Photobacter profundum pfaA (identity=70%; positives=81%); Shewanella oneidensis MR-1 "multi-domain .beta.-ketoacyl synthase" (identity=66%; positives=77%); and Moritella marina ORF8 (identity=56%; positives=71%). The Schizochytrium sp. ATCC20888 orfA was 41% identical and 56% positive to the deduced amino acid sequence encoded by SEQ ID NO:76.

At the amino acid level, the sequences with the greatest degree of homology to the Shewanella japonica ATCC BAA-316 ketoacyl synthase/acyl transferase (KS-AT) deduced amino acid sequence encoded by SEQ ID NO:78 were: Shewanella oneidensis MR-1 "multi-domain .beta.-ketoacyl synthase" (identity=67%; positives=79%); Shewanella sp. SCRC-2738 orf5 (identity=69%; positives=77%); and Moritella marina ORF8 (identity=56%; positives=70%). The Schizochytrium sp. ATCC20888 orfA was 41% identical and 55% positive to the deduced amino acid sequence encoded by SEQ ID NO:78.

At the amino acid level, the sequences with the greatest degree of homology to the Shewanella olleyana ACAM644 dehydrogenase (DH) deduced amino acid sequence encoded by SEQ ID NO:75 were: Shewanella sp. SCRC-2738 orf7 (identity=77%; positives=86%); Photobacter profundum pfaC (identity=72%; positives 81%); and Shewanella oneidensis MR-1 "multi-domain .beta.-ketoacyl synthase" (identity 75%; positives=83%). The Schizochytrium sp. ATCC20888 orfC was 26% identical and 42% positive to the deduced amino acid sequence encoded by SEQ ID NO:75.

At the amino acid level, the sequences with the greatest degree of homology to the Shewanella japonica ATCC BAA-316 dehydrogenase (DH) deduced amino acid sequence encodedby SEQ ID NO:77 were: Shewanella sp. SCRC-2738 orf7 (identity=77%; positives=86%); Photobacter profundum pfaC (identity=73%; positives=83%) and Shewanella oneidensis MR-1 "multi-domain .beta.-ketoacyl synthase" (identity=74%; positives=81%). The Schizochytrium sp. ATCC20888 orfC was 27% identical and 42% positive to the deduced amino acid sequence encoded by SEQ ID NO:77.

It is expected that the PUFA PKS gene sets from these two Shewanella strains will provide beneficial sources of whole genes or individual domains for the modification of Schizochytrium PUFA production. PUFA PKS genes and the proteins and domains encoded thereby from either of Shewanella olleyana or Shewanella japonica are explicitly encompassed by the present invention.

Example 8

This example demonstrates how the bacterial PUFA PKS gene fragments described in Example 7 can be used to modify PUFA production in Schizochytrium.

All presently-known examples of PUFA PKS genes from bacteria exist as four closely linked genes that contain the same domains as in the three-gene Schizochytrium set. It is anticipated that the PUFA PKS genes from Shewanella olleyana and Shewanella japonica will likewise be found in this tightly clustered arrangement. The homologous regions identified in Example 7 are used to isolate the PUFA PKS gene clusters from clone banks of Sh. olleyana and Sh. japonica DNAs. Clone banks can be constructed in bacteriophage lambda vectors, cosmid vectors, bacterial artificial chromosome ("BAC") vectors, or by other methods known in the art. Desired clones containing bacterial PUFA PKS genes can be identified by colony or plaque hybridization (as described in Example 1) using probes generated by PCR of the partial gene sequences of Example 7 employing primers designed from these sequences. The complete DNA sequence of the new bacterial PUFA PKS gene sets are then used to design vectors for transformation of Schizochytrium strains defective in the endogenous PUFA PKS genes (e.g., see Examples 3, 5, and 6). Whole bacterial genes (coding sequences) may be used to replace whole Schizochytrium genes (coding sequences), thus utilizing the Schizochytrium gene expression regions, and the fourth bacterial gene may be targeted to a different location within the genome. Alternatively, individual bacterial PUFA PKS functional domains may be "swapped" or exchanged with the analogous Schizochytrium domains by similar techniques of homologous recombination. It is understood that the sequence of the bacterial PUFA PKS genes or domains may have to be modified to accommodate details of Schizochytrium codon usage, but this is within the ability of those of skill in the art.

Each publication cited or discussed herein is incorporated herein by reference in its entirety.

While various embodiments of the present invention have been described in detail, it is apparent that modifications and adaptations of those embodiments will occur to those skilled in the art. It is to be expressly understood, however, that such modifications and adaptations are within the scope of the present invention, as set forth in the following claims.

>

82 DNA Schizochytrium sp. CDS (3g gcg gcc cgt ctg cag gag caa aag gga ggc gag atg gat acc cgc 48 Met Ala Ala Arg Leu Gln Glu Gln Lys Gly Gly Glu Met Asp Thr Arg gcc atc atc ggc atg tcg gcc atc ctc ccc tgc ggc acg acc gtg 96 Ile Ala Ile Ile Gly Met Ser Ala Ile Leu Pro Cys Gly Thr Thr Val 2 cgc gag tcg tgg gag acc atc cgc gcc ggc atc gac tgc ctg tcg gat Glu Ser Trp Glu Thr Ile Arg Ala Gly Ile Asp Cys Leu Ser Asp 35 4c ccc gag gac cgc gtc gac gtg acg gcg tac ttt gac ccc gtc aag Pro Glu Asp Arg Val Asp Val Thr Ala Tyr Phe Asp Pro Val Lys 5 acc acc aag gac aag atc tac tgc aag cgc ggt ggc ttc att ccc gag 24hr Lys Asp Lys Ile Tyr Cys Lys Arg Gly Gly Phe Ile Pro Glu 65 7 tac gac ttt gac gcc cgc gag ttc gga ctc aac atg ttc cag atg gag 288 Tyr Asp Phe Asp Ala Arg Glu Phe Gly Leu Asn Met Phe Gln Met Glu 85 9c tcg gac gca aac cag acc atc tcg ctt ctc aag gtc aag gag gcc 336 Asp Ser Asp Ala Asn Gln Thr Ile Ser Leu Leu Lys Val Lys Glu Ala cag gac gcc ggc atc gac gcc ctc ggc aag gaa aag aag aac atc 384 Leu Gln Asp Ala Gly Ile Asp Ala Leu Gly Lys Glu Lys Lys Asn Ile tgc gtg ctc ggc att ggc ggc ggc caa aag tcc agc cac gag ttc 432 Gly Cys Val Leu Gly Ile Gly Gly Gly Gln Lys Ser Ser His Glu Phe tcg cgc ctt aat tat gtt gtc gtg gag aag gtc ctc cgc aag atg 48er Arg Leu Asn Tyr Val Val Val Glu Lys Val Leu Arg Lys Met ggc atg ccc gag gag gac gtc aag gtc gcc gtc gaa aag tac aag gcc 528 Gly Met Pro Glu Glu Asp Val Lys Val Ala Val Glu Lys Tyr Lys Ala ttc ccc gag tgg cgc ctc gac tcc ttc cct ggc ttc ctc ggc aac 576 Asn Phe Pro Glu Trp Arg Leu Asp Ser Phe Pro Gly Phe Leu Gly Asn acc gcc ggt cgc tgc acc aac acc ttc aac ctc gac ggc atg aac 624 Val Thr Ala Gly Arg Cys Thr Asn Thr Phe Asn Leu Asp Gly Met Asn 2gtt gtc gac gcc gca tgc gcc tcg tcc ctc atc gcc gtc aag gtc 672 Cys Val Val Asp Ala Ala Cys Ala Ser Ser Leu Ile Ala Val Lys Val 222tc gac gag ctg ctc tac ggt gac tgc gac atg atg gtc acc ggt 72le Asp Glu Leu Leu Tyr Gly Asp Cys Asp Met Met Val Thr Gly 225 234cc tgc acg gat aac tcc atc ggc atg tac atg gcc ttc tcc aag 768 Ala Thr Cys Thr Asp Asn Ser Ile Gly Met Tyr Met Ala Phe Ser Lys 245 25cc ccc gtg ttc tcc acg gac ccc agc gtg cgc gcc tac gac gaa aag 8Pro Val Phe Ser Thr Asp Pro Ser Val Arg Ala Tyr Asp Glu Lys 267ag ggc atg ctc atc ggc gag ggc tcc gcc atg ctc gtc ctc aag 864 Thr Lys Gly Met Leu Ile Gly Glu Gly Ser Ala Met Leu Val Leu Lys 275 28gc tac gcc gac gcc gtc cgc gac ggc gat gag atc cac gct gtt att 9Tyr Ala Asp Ala Val Arg Asp Gly Asp Glu Ile His Ala Val Ile 29ggc tgc gcc tcc tcc agt gat ggc aag gcc gcc ggc atc tac acg 96ly Cys Ala Ser Ser Ser Asp Gly Lys Ala Ala Gly Ile Tyr Thr 33ccc acc att tcg ggc cag gag gag gcc ctc cgc cgc gcc tac aac cgc o Thr Ile Ser Gly Gln Glu Glu Ala Leu Arg Arg Ala Tyr Asn Arg 325 33cc tgt gtc gac ccg gcc acc gtc act ctc gtc gag ggt cac ggc acc a Cys Val Asp Pro Ala Thr Val Thr Leu Val Glu Gly His Gly Thr 345ct ccc gtt ggc gac cgc atc gag ctc acc gcc ttg cgc aac ctc y Thr Pro Val Gly Asp Arg Ile Glu Leu Thr Ala Leu Arg Asn Leu 355 36tt gac aag gcc tac ggc gag ggc aac acc gaa aag gtc gct gtg ggc e Asp Lys Ala Tyr Gly Glu Gly Asn Thr Glu Lys Val Ala Val Gly 378tc aag tcc agc atc ggc cat ctc aag gcc gtc gcc ggt ctc gcc r Ile Lys Ser Ser Ile Gly His Leu Lys Ala Val Ala Gly Leu Ala 385 39atg atc aag gtc atc atg gcg ctc aag cac aag act ctc ccg ggc y Met Ile Lys Val Ile Met Ala Leu Lys His Lys Thr Leu Pro Gly 44atc aac gtc gac aac cca ccc aac ctc tac gac aac acg ccc atc r Ile Asn Val Asp Asn Pro Pro Asn Leu Tyr Asp Asn Thr Pro Ile 423ag tcc tcg ctc tac att aac acc atg aac cgc ccc tgg ttc ccg n Glu Ser Ser Leu Tyr Ile Asn Thr Met Asn Arg Pro Trp Phe Pro 435 44cc cct ggt gtg ccc cgc cgc gcc ggc att tcg agc ttt ggc ttt ggt o Pro Gly Val Pro Arg Arg Ala Gly Ile Ser Ser Phe Gly Phe Gly 456cc aac tac cac gcc gtc ctc gag gag gcc gag ccc gag cac acg y Ala Asn Tyr His Ala Val Leu Glu Glu Ala Glu Pro Glu His Thr 465 478cg tac cgc ctc aac aag cgc ccg cag ccc gtg ctc atg atg gcc r Ala Tyr Arg Leu Asn Lys Arg Pro Gln Pro Val Leu Met Met Ala 485 49cc acg ccc gcg gcc ctc cag tcg ctc tgc gag gcc cag ctc aag gag a Thr Pro Ala Ala Leu Gln Ser Leu Cys Glu Ala Gln Leu Lys Glu 55gag gcc gcc atc aag gag aac gag acc gtc aag aac acc gcc tac e Glu Ala Ala Ile Lys Glu Asn Glu Thr Val Lys Asn Thr Ala Tyr 5525 atc aag tgc gtc aag ttc ggc gag cag ttc aaa ttc cct ggc tcc atc e Lys Cys Val Lys Phe Gly Glu Gln Phe Lys Phe Pro Gly Ser Ile 534cc aca aac gcg cgc ctc ggc ttc ctc gtc aag gat gct gag gat o Ala Thr Asn Ala Arg Leu Gly Phe Leu Val Lys Asp Ala Glu Asp 545 556gc tcc acc ctc cgt gcc atc tgc gcc caa ttc gcc aag gat gtc a Cys Ser Thr Leu Arg Ala Ile Cys Ala Gln Phe Ala Lys Asp Val 565 57cc aag gag gcc tgg cgc ctc ccc cgc gag ggc gtc agc ttc cgc gcc r Lys Glu Ala Trp Arg Leu Pro Arg Glu Gly Val Ser Phe Arg Ala 589gc atc gcc acc aac ggc gct gtc gcc gcg ctc ttc tcc ggc cag s Gly Ile Ala Thr Asn Gly Ala Val Ala Ala Leu Phe Ser Gly Gln 595 6ggc gcg cag tac acg cac atg ttt agc gag gtg gcc atg aac tgg ccc y Ala Gln Tyr Thr His Met Phe Ser Glu Val Ala Met Asn Trp Pro 662tc cgc cag agc att gcc gcc atg gac gcc gcc cag tcc aag gtc n Phe Arg Gln Ser Ile Ala Ala Met Asp Ala Ala Gln Ser Lys Val 625 634ga agc gac aag gac ttt gag cgc gtc tcc cag gtc ctc tac ccg a Gly Ser Asp Lys Asp Phe Glu Arg Val Ser Gln Val Leu Tyr Pro 645 65gc aag ccg tac gag cgt gag ccc gag cag aac ccc aag aag atc tcc 2 Lys Pro Tyr Glu Arg Glu Pro Glu Gln Asn Pro Lys Lys Ile Ser 667cc gcc tac tcg cag ccc tcg acc ctg gcc tgc gct ctc ggt gcc 2 Thr Ala Tyr Ser Gln Pro Ser Thr Leu Ala Cys Ala Leu Gly Ala 675 68tt gag atc ttc aag gag gcc ggc ttc acc ccg gac ttt gcc gcc ggc 2 Glu Ile Phe Lys Glu Ala Gly Phe Thr Pro Asp Phe Ala Ala Gly 69tcg ctc ggt gag ttc gcc gcc ctc tac gcc gcg ggc tgc gtc gac 2 Ser Leu Gly Glu Phe Ala Ala Leu Tyr Ala Ala Gly Cys Val Asp 77cgc gac gag ctc ttt gag ctt gtc tgc cgc cgc gcc cgc atc atg ggc 22Asp Glu Leu Phe Glu Leu Val Cys Arg Arg Ala Arg Ile Met Gly 725 73gc aag gac gca ccg gcc acc ccc aag gga tgc atg gcc gcc gtc att 2256 Gly Lys Asp Ala Pro Ala Thr Pro Lys Gly Cys Met Ala Ala Val Ile 745cc aac gcc gag aac atc aag gtc cag gcc gcc aac gtc tgg ctc 23Pro Asn Ala Glu Asn Ile Lys Val Gln Ala Ala Asn Val Trp Leu 755 76gc aac tcc aac tcg cct tcg cag acc gtc atc acc ggc tcc gtc gaa 2352 Gly Asn Ser Asn Ser Pro Ser Gln Thr Val Ile Thr Gly Ser Val Glu 778tc cag gcc gag agc gcc cgc ctc cag aag gag ggc ttc cgc gtc 24Ile Gln Ala Glu Ser Ala Arg Leu Gln Lys Glu Gly Phe Arg Val 785 79cct ctt gcc tgc gag agc gcc ttc cac tcg ccc cag atg gag aac 2448 Val Pro Leu Ala Cys Glu Ser Ala Phe His Ser Pro Gln Met Glu Asn 88tcg tcg gcc ttc aag gac gtc atc tcc aag gtc tcc ttc cgc acc 2496 Ala Ser Ser Ala Phe Lys Asp Val Ile Ser Lys Val Ser Phe Arg Thr 823ag gcc gag acc aag ctc ttc agc aac gtc tct ggc gag acc tac 2544 Pro Lys Ala Glu Thr Lys Leu Phe Ser Asn Val Ser Gly Glu Thr Tyr 835 84cc acg gac gcc cgc gag atg ctt acg cag cac atg acc agc agc gtc 2592 Pro Thr Asp Ala Arg Glu Met Leu Thr Gln His Met Thr Ser Ser Val 856tc ctc acc cag gtc cgc aac atg cac cag gcc ggt gcg cgc atc 264he Leu Thr Gln Val Arg Asn Met His Gln Ala Gly Ala Arg Ile 865 878tc gag ttc gga ccc aag cag gtg ctc tcc aag ctt gtc tcc gag 2688 Phe Val Glu Phe Gly Pro Lys Gln Val Leu Ser Lys Leu Val Ser Glu 885 89cc ctc aag gat gac ccc tcg gtt gtc acc gtc tct gtc aac ccg gcc 2736 Thr Leu Lys Asp Asp Pro Ser Val Val Thr Val Ser Val Asn Pro Ala 99ggc acg gat tcg gac atc cag ctc cgc gac gcg gcc gtc cag ctc 2784 Ser Gly Thr Asp Ser Asp Ile Gln Leu Arg Asp Ala Ala Val Gln Leu 9925 gtt gtc gct ggc gtc aac ctt cag ggc ttt gac aag tgg gac gcc ccc 2832 Val Val Ala Gly Val Asn Leu Gln Gly Phe Asp Lys Trp Asp Ala Pro 934cc acc cgc atg cag gcc atc aag aag aag cgc act acc ctc cgc 288la Thr Arg Met Gln Ala Ile Lys Lys Lys Arg Thr Thr Leu Arg 945 956cg gcc gcc acc tac gtc tcg gac aag acc aag aag gtc cgc gac 2928 Leu Ser Ala Ala Thr Tyr Val Ser Asp Lys Thr Lys Lys Val Arg Asp 965 97cc gcc atg aac gat ggc cgc tgc gtc acc tac ctc aag ggc gcc gca 2976 Ala Ala Met Asn Asp Gly Arg Cys Val Thr Tyr Leu Lys Gly Ala Ala 989tc atc aag gcc ccg gag ccc gtt gtc gac gag gcc gcc aag cgc 3 Leu Ile Lys Ala Pro Glu Pro Val Val Asp Glu Ala Ala Lys Arg 995 gcc gag cgt ctc cag aag gag ctt cag gat gcc cag cgc cag 3 Ala Glu Arg Leu Gln Lys Glu Leu Gln Asp Ala Gln Arg Gln ctc gac gac gcc aag cgc gcc gcc gcc gag gcc aac tcc aag ctc 3 Asp Asp Ala Lys Arg Ala Ala Ala Glu Ala Asn Ser Lys Leu 3gcc gct gcc aag gag gag gcc aag acc gcc gct gct tcg gcc aag 3 Ala Ala Lys Glu Glu Ala Lys Thr Ala Ala Ala Ser Ala Lys 45 c gca gtt gac act gct gtt gtc gaa aag cat cgt gcc atc ctc 32Ala Val Asp Thr Ala Val Val Glu Lys His Arg Ala Ile Leu 6aag tcc atg ctc gcg gag ctc gat ggc tac gga tcg gtc gac gct 3249 Lys Ser Met Leu Ala Glu Leu Asp Gly Tyr Gly Ser Val Asp Ala 75 t tcc ctc cag cag cag cag cag cag cag acg gcc ccc gcc ccg 3294 Ser Ser Leu Gln Gln Gln Gln Gln Gln Gln Thr Ala Pro Ala Pro 9gtc aag gct gct gcg cct gcc gcc ccc gtt gcc tcg gcc cct gcc 3339 Val Lys Ala Ala Ala Pro Ala Ala Pro Val Ala Ser Ala Pro Ala ccg gct gtc tcg aac gag ctt ctt gag aag gcc gag act gtc gtc 3384 Pro Ala Val Ser Asn Glu Leu Leu Glu Lys Ala Glu Thr Val Val 2atg gag gtc ctc gcc gcc aag acc ggc tac gag acc gac atg atc 3429 Met Glu Val Leu Ala Ala Lys Thr Gly Tyr Glu Thr Asp Met Ile 35 g gct gac atg gag ctc gag acc gag ctc ggc att gac tcc atc 3474 Glu Ala Asp Met Glu Leu Glu Thr Glu Leu Gly Ile Asp Ser Ile 5aag cgt gtc gag atc ctc tcc gag gtc cag gcc atg ctc aat gtc 35Arg Val Glu Ile Leu Ser Glu Val Gln Ala Met Leu Asn Val 65 g gcc aag gat gtc gat gcc ctc agc cgc act cgc act gtt ggt 3564 Glu Ala Lys Asp Val Asp Ala Leu Ser Arg Thr Arg Thr Val Gly 8gag gtt gtc aac gcc atg aag gcc gag atc gct ggc agc tct gcc 36Val Val Asn Ala Met Lys Ala Glu Ile Ala Gly Ser Ser Ala 95 g gcg cct gct gcc gct gct ccg gct ccg gcc aag gct gcc cct 3654 Pro Ala Pro Ala Ala Ala Ala Pro Ala Pro Ala Lys Ala Ala Pro gcc gcc gct gcg cct gct gtc tcg aac gag ctt ctc gag aag gcc 3699 Ala Ala Ala Ala Pro Ala Val Ser Asn Glu Leu Leu Glu Lys Ala 25 g acc gtc gtc atg gag gtc ctc gcc gcc aag act ggc tac gag 3744 Glu Thr Val Val Met Glu Val Leu Ala Ala Lys Thr Gly Tyr Glu 4act gac atg atc gag tcc gac atg gag ctc gag act gag ctc ggc 3789 Thr Asp Met Ile Glu Ser Asp Met Glu Leu Glu Thr Glu Leu Gly 55 t gac tcc atc aag cgt gtc gag atc ctc tcc gag gtt cag gcc 3834 Ile Asp Ser Ile Lys Arg Val Glu Ile Leu Ser Glu Val Gln Ala 7atg ctc aac gtc gag gcc aag gac gtc gac gct ctc agc cgc act 3879 Met Leu Asn Val Glu Ala Lys Asp Val Asp Ala Leu Ser Arg Thr 85 c act gtg ggt gag gtc gtc aac gcc atg aag gct gag atc gct 3924 Arg Thr Val Gly Glu Val Val Asn Ala Met Lys Ala Glu Ile Ala ggt ggc tct gcc ccg gcg cct gcc gcc gct gcc cca ggt ccg gct 3969 Gly Gly Ser Ala Pro Ala Pro Ala Ala Ala Ala Pro Gly Pro Ala gct gcc gcc cct gcg cct gcc gcc gcc gcc cct gct gtc tcg aac 4 Ala Ala Pro Ala Pro Ala Ala Ala Ala Pro Ala Val Ser Asn 3gag ctt ctt gag aag gcc gag acc gtc gtc atg gag gtc ctc gcc 4 Leu Leu Glu Lys Ala Glu Thr Val Val Met Glu Val Leu Ala 45 c aag act ggc tac gag act gac atg atc gag tcc gac atg gag 4 Lys Thr Gly Tyr Glu Thr Asp Met Ile Glu Ser Asp Met Glu 6ctc gag acc gag ctc ggc att gac tcc atc aag cgt gtc gag att 4 Glu Thr Glu Leu Gly Ile Asp Ser Ile Lys Arg Val Glu Ile 75 c tcc gag gtc cag gcc atg ctc aac gtc gag gcc aag gac gtc 4 Ser Glu Val Gln Ala Met Leu Asn Val Glu Ala Lys Asp Val 9gac gct ctc agc cgc acc cgc act gtt ggc gag gtc gtc gat gcc 4239 Asp Ala Leu Ser Arg Thr Arg Thr Val Gly Glu Val Val Asp Ala atg aag gcc gag atc gct ggt ggc tct gcc ccg gcg cct gcc gcc 4284 Met Lys Ala Glu Ile Ala Gly Gly Ser Ala Pro Ala Pro Ala Ala 2gct gct cct gct ccg gct gct gcc gcc cct gcg cct gcc gcc cct 4329 Ala Ala Pro Ala Pro Ala Ala Ala Ala Pro Ala Pro Ala Ala Pro 35 g cct gct gtc tcg agc gag ctt ctc gag aag gcc gag act gtc 4374 Ala Pro Ala Val Ser Ser Glu Leu Leu Glu Lys Ala Glu Thr Val 5gtc atg gag gtc ctc gcc gcc aag act ggc tac gag act gac atg 44Met Glu Val Leu Ala Ala Lys Thr Gly Tyr Glu Thr Asp Met 65 c gag tcc gac atg gag ctc gag acc gag ctc ggc att gac tcc 4464 Ile Glu Ser Asp Met Glu Leu Glu Thr Glu Leu Gly Ile Asp Ser 8atc aag cgt gtc gag att ctc tcc gag gtc cag gcc atg ctc aac 45Lys Arg Val Glu Ile Leu Ser Glu Val Gln

Ala Met Leu Asn 95 c gag gcc aag gac gtc gac gct ctc agc cgc acc cgc act gtt 4554 Val Glu Ala Lys Asp Val Asp Ala Leu Ser Arg Thr Arg Thr Val ggc gag gtc gtc gat gcc atg aag gcc gag atc gct ggt ggc tct 4599 Gly Glu Val Val Asp Ala Met Lys Ala Glu Ile Ala Gly Gly Ser 25 c ccg gcg cct gcc gcc gct gct cct gct ccg gct gct gcc gcc 4644 Ala Pro Ala Pro Ala Ala Ala Ala Pro Ala Pro Ala Ala Ala Ala 4cct gcg cct gcc gcc cct gcg cct gcc gcc cct gcg cct gct gtc 4689 Pro Ala Pro Ala Ala Pro Ala Pro Ala Ala Pro Ala Pro Ala Val 55 g agc gag ctt ctc gag aag gcc gag act gtc gtc atg gag gtc 4734 Ser Ser Glu Leu Leu Glu Lys Ala Glu Thr Val Val Met Glu Val 7ctc gcc gcc aag act ggc tac gag act gac atg att gag tcc gac 4779 Leu Ala Ala Lys Thr Gly Tyr Glu Thr Asp Met Ile Glu Ser Asp 85 g gag ctc gag acc gag ctc ggc att gac tcc atc aag cgt gtc 4824 Met Glu Leu Glu Thr Glu Leu Gly Ile Asp Ser Ile Lys Arg Val gag att ctc tcc gag gtt cag gcc atg ctc aac gtc gag gcc aag 4869 Glu Ile Leu Ser Glu Val Gln Ala Met Leu Asn Val Glu Ala Lys gac gtc gac gct ctc agc cgc act cgc act gtt ggt gag gtc gtc 49Val Asp Ala Leu Ser Arg Thr Arg Thr Val Gly Glu Val Val 3gat gcc atg aag gct gag atc gct ggc agc tcc gcc tcg gcg cct 4959 Asp Ala Met Lys Ala Glu Ile Ala Gly Ser Ser Ala Ser Ala Pro 45 c gcc gct gct cct gct ccg gct gct gcc gct cct gcg ccc gct 5 Ala Ala Ala Pro Ala Pro Ala Ala Ala Ala Pro Ala Pro Ala 6gcc gcc gcc cct gct gtc tcg aac gag ctt ctc gag aaa gcc gag 5 Ala Ala Pro Ala Val Ser Asn Glu Leu Leu Glu Lys Ala Glu 75 t gtc gtc atg gag gtc ctc gcc gcc aag act ggc tac gag act 5 Val Val Met Glu Val Leu Ala Ala Lys Thr Gly Tyr Glu Thr 9gac atg atc gag tcc gac atg gag ctc gag act gag ctc ggc att 5 Met Ile Glu Ser Asp Met Glu Leu Glu Thr Glu Leu Gly Ile gac tcc atc aag cgt gtc gag atc ctc tcc gag gtt cag gcc atg 5 Ser Ile Lys Arg Val Glu Ile Leu Ser Glu Val Gln Ala Met 2ctc aac gtc gag gcc aag gac gtc gat gcc ctc agc cgc acc cgc 5229 Leu Asn Val Glu Ala Lys Asp Val Asp Ala Leu Ser Arg Thr Arg 35 t gtt ggc gag gtt gtc gat gcc atg aag gcc gag atc gct ggt 5274 Thr Val Gly Glu Val Val Asp Ala Met Lys Ala Glu Ile Ala Gly 5ggc tct gcc ccg gcg cct gcc gcc gct gcc cct gct ccg gct gcc 53Ser Ala Pro Ala Pro Ala Ala Ala Ala Pro Ala Pro Ala Ala 65 c gcc cct gct gtc tcg aac gag ctt ctc gag aag gcc gag act 5364 Ala Ala Pro Ala Val Ser Asn Glu Leu Leu Glu Lys Ala Glu Thr 8gtc gtc atg gag gtc ctc gcc gcc aag act ggc tac gag acc gac 54Val Met Glu Val Leu Ala Ala Lys Thr Gly Tyr Glu Thr Asp 95 g atc gag tcc gac atg gag ctc gag acc gag ctc ggc att gac 5454 Met Ile Glu Ser Asp Met Glu Leu Glu Thr Glu Leu Gly Ile Asp tcc atc aag cgt gtc gag att ctc tcc gag gtt cag gcc atg ctc 5499 Ser Ile Lys Arg Val Glu Ile Leu Ser Glu Val Gln Ala Met Leu 25 c gtc gag gcc aag gac gtc gat gct ctc agc cgc act cgc act 5544 Asn Val Glu Ala Lys Asp Val Asp Ala Leu Ser Arg Thr Arg Thr 4gtt ggc gag gtc gtc gat gcc atg aag gct gag atc gcc ggc agc 5589 Val Gly Glu Val Val Asp Ala Met Lys Ala Glu Ile Ala Gly Ser 55 c gcc ccg gcg cct gcc gcc gct gct cct gct ccg gct gct gcc 5634 Ser Ala Pro Ala Pro Ala Ala Ala Ala Pro Ala Pro Ala Ala Ala 7gct cct gcg ccc gct gcc gct gcc cct gct gtc tcg agc gag ctt 5679 Ala Pro Ala Pro Ala Ala Ala Ala Pro Ala Val Ser Ser Glu Leu 85 c gag aag gcc gag acc gtc gtc atg gag gtc ctc gcc gcc aag 5724 Leu Glu Lys Ala Glu Thr Val Val Met Glu Val Leu Ala Ala Lys act ggc tac gag act gac atg att gag tcc gac atg gag ctc gag 5769 Thr Gly Tyr Glu Thr Asp Met Ile Glu Ser Asp Met Glu Leu Glu act gag ctc ggc att gac tcc atc aag cgt gtc gag atc ctc tcc 58Glu Leu Gly Ile Asp Ser Ile Lys Arg Val Glu Ile Leu Ser 3gag gtt cag gcc atg ctc aac gtc gag gcc aag gac gtc gat gcc 5859 Glu Val Gln Ala Met Leu Asn Val Glu Ala Lys Asp Val Asp Ala 45 c agc cgc acc cgc act gtt ggc gag gtt gtc gat gcc atg aag 59Ser Arg Thr Arg Thr Val Gly Glu Val Val Asp Ala Met Lys 6gcc gag atc gct ggt ggc tct gcc ccg gcg cct gcc gcc gct gcc 5949 Ala Glu Ile Ala Gly Gly Ser Ala Pro Ala Pro Ala Ala Ala Ala 75 t gct ccg gct gcc gcc gcc cct gct gtc tcg aac gag ctt ctt 5994 Pro Ala Pro Ala Ala Ala Ala Pro Ala Val Ser Asn Glu Leu Leu 9gag aag gcc gag acc gtc gtc atg gag gtc ctc gcc gcc aag act 6 Lys Ala Glu Thr Val Val Met Glu Val Leu Ala Ala Lys Thr 25 2 tac gag acc gac atg atc gag tcc gac atg gag ctc gag acc 6 Tyr Glu Thr Asp Met Ile Glu Ser Asp Met Glu Leu Glu Thr 2gag ctc ggc att gac tcc atc aag cgt gtc gag att ctc tcc gag 6 Leu Gly Ile Asp Ser Ile Lys Arg Val Glu Ile Leu Ser Glu 25 2 cag gcc atg ctc aac gtc gag gcc aag gac gtc gac gct ctc 6 Gln Ala Met Leu Asn Val Glu Ala Lys Asp Val Asp Ala Leu 2agc cgc act cgc act gtt ggc gag gtc gtc gat gcc atg aag gct 62Arg Thr Arg Thr Val Gly Glu Val Val Asp Ala Met Lys Ala 25 2 atc gct ggt ggc tct gcc ccg gcg cct gcc gcc gct gct cct 6264 Glu Ile Ala Gly Gly Ser Ala Pro Ala Pro Ala Ala Ala Ala Pro 2gcc tcg gct ggc gcc gcg cct gcg gtc aag att gac tcg gtc cac 63Ser Ala Gly Ala Ala Pro Ala Val Lys Ile Asp Ser Val His 25 2 gct gac tgt gat gat ctt tcc ctg atg cac gcc aag gtg gtt 6354 Gly Ala Asp Cys Asp Asp Leu Ser Leu Met His Ala Lys Val Val 2gac atc cgc cgc ccg gac gag ctc atc ctg gag cgc ccc gag aac 6399 Asp Ile Arg Arg Pro Asp Glu Leu Ile Leu Glu Arg Pro Glu Asn 25 2 ccc gtt ctc gtt gtc gat gac ggc agc gag ctc acc ctc gcc 6444 Arg Pro Val Leu Val Val Asp Asp Gly Ser Glu Leu Thr Leu Ala 2ctg gtc cgc gtc ctc ggc gcc tgc gcc gtt gtc ctg acc ttt gag 6489 Leu Val Arg Val Leu Gly Ala Cys Ala Val Val Leu Thr Phe Glu 25 2 ctc cag ctc gct cag cgc gct ggt gcc gct gcc atc cgc cac 6534 Gly Leu Gln Leu Ala Gln Arg Ala Gly Ala Ala Ala Ile Arg His 2gtg ctc gcc aag gat ctt tcc gcg gag agc gcc gag aag gcc atc 6579 Val Leu Ala Lys Asp Leu Ser Ala Glu Ser Ala Glu Lys Ala Ile 25 2 gag gcc gag cag cgc ttt ggc gct ctc ggc ggc ttc atc tcg 6624 Lys Glu Ala Glu Gln Arg Phe Gly Ala Leu Gly Gly Phe Ile Ser 2cag cag gcg gag cgc ttc gag ccc gcc gaa atc ctc ggc ttc acg 6669 Gln Gln Ala Glu Arg Phe Glu Pro Ala Glu Ile Leu Gly Phe Thr 22 222tg tgc gcc aag ttc gcc aag gct tcc ctc tgc acg gct gtg 67Met Cys Ala Lys Phe Ala Lys Ala Ser Leu Cys Thr Ala Val 2225 223gct ggc ggc cgc ccg gcc ttt atc ggt gtg gcg cgc ctt gac ggc 6759 Ala Gly Gly Arg Pro Ala Phe Ile Gly Val Ala Arg Leu Asp Gly 224225tc gga ttc act tcg cag ggc act tct gac gcg ctc aag cgt 68Leu Gly Phe Thr Ser Gln Gly Thr Ser Asp Ala Leu Lys Arg 2255 226gcc cag cgt ggt gcc atc ttt ggc ctc tgc aag acc atc ggc ctc 6849 Ala Gln Arg Gly Ala Ile Phe Gly Leu Cys Lys Thr Ile Gly Leu 227228gg tcc gag tct gac gtc ttt tcc cgc ggc gtg gac att gct 6894 Glu Trp Ser Glu Ser Asp Val Phe Ser Arg Gly Val Asp Ile Ala 2285 229cag ggc atg cac ccc gag gat gcc gcc gtg gcg att gtg cgc gag 6939 Gln Gly Met His Pro Glu Asp Ala Ala Val Ala Ile Val Arg Glu 23 23gcg tgc gct gac att cgc att cgc gag gtc ggc att ggc gca 6984 Met Ala Cys Ala Asp Ile Arg Ile Arg Glu Val Gly Ile Gly Ala 23 2325 aac cag cag cgc tgc acg atc cgt gcc gcc aag ctc gag acc ggc 7 Gln Gln Arg Cys Thr Ile Arg Ala Ala Lys Leu Glu Thr Gly 233234cg cag cgc cag atc gcc aag gac gac gtg ctg ctc gtt tct 7 Pro Gln Arg Gln Ile Ala Lys Asp Asp Val Leu Leu Val Ser 2345 235ggc ggc gct cgc ggc atc acg cct ctt tgc atc cgg gag atc acg 7 Gly Ala Arg Gly Ile Thr Pro Leu Cys Ile Arg Glu Ile Thr 236237ag atc gcg ggc ggc aag tac att ctg ctt ggc cgc agc aag 7 Gln Ile Ala Gly Gly Lys Tyr Ile Leu Leu Gly Arg Ser Lys 2375 238gtc tct gcg agc gaa ccg gca tgg tgc gct ggc atc act gac gag 72Ser Ala Ser Glu Pro Ala Trp Cys Ala Gly Ile Thr Asp Glu 23924gct gtg caa aag gct gct acc cag gag ctc aag cgc gcc ttt 7254 Lys Ala Val Gln Lys Ala Ala Thr Gln Glu Leu Lys Arg Ala Phe 24 24gct ggc gag ggc ccc aag ccc acg ccc cgc gct gtc act aag 7299 Ser Ala Gly Glu Gly Pro Lys Pro Thr Pro Arg Ala Val Thr Lys 242243tg ggc tct gtt ctt ggc gct cgc gag gtg cgc agc tct att 7344 Leu Val Gly Ser Val Leu Gly Ala Arg Glu Val Arg Ser Ser Ile 2435 244gct gcg att gaa gcg ctc ggc ggc aag gcc atc tac tcg tcg tgc 7389 Ala Ala Ile Glu Ala Leu Gly Gly Lys Ala Ile Tyr Ser Ser Cys 245246tg aac tct gcc gcc gac gtg gcc aag gcc gtg cgc gat gcc 7434 Asp Val Asn Ser Ala Ala Asp Val Ala Lys Ala Val Arg Asp Ala 2465 247gag tcc cag ctc ggt gcc cgc gtc tcg ggc atc gtt cat gcc tcg 7479 Glu Ser Gln Leu Gly Ala Arg Val Ser Gly Ile Val His Ala Ser 248249tg ctc cgc gac cgt ctc atc gag aag aag ctc ccc gac gag 7524 Gly Val Leu Arg Asp Arg Leu Ile Glu Lys Lys Leu Pro Asp Glu 2495 25 ttc gac gcc gtc ttt ggc acc aag gtc acc ggt ctc gag aac ctc 7569 Phe Asp Ala Val Phe Gly Thr Lys Val Thr Gly Leu Glu Asn Leu 25 252cc gcc gtc gac cgc gcc aac ctc aag cac atg gtc ctc ttc 76Ala Ala Val Asp Arg Ala Asn Leu Lys His Met Val Leu Phe 2525 253agc tcg ctc gcc ggc ttc cac ggc aac gtc ggc cag tct gac tac 7659 Ser Ser Leu Ala Gly Phe His Gly Asn Val Gly Gln Ser Asp Tyr 254255tg gcc aac gag gcc ctt aac aag atg ggc ctc gag ctc gcc 77Met Ala Asn Glu Ala Leu Asn Lys Met Gly Leu Glu Leu Ala 2555 256aag gac gtc tcg gtc aag tcg atc tgc ttc ggt ccc tgg gac ggt 7749 Lys Asp Val Ser Val Lys Ser Ile Cys Phe Gly Pro Trp Asp Gly 257258tg gtg acg ccg cag ctc aag aag cag ttc cag gag atg ggc 7794 Gly Met Val Thr Pro Gln Leu Lys Lys Gln Phe Gln Glu Met Gly 2585 259gtg cag atc atc ccc cgc gag ggc ggc gct gat acc gtg gcg cgc 7839 Val Gln Ile Ile Pro Arg Glu Gly Gly Ala Asp Thr Val Ala Arg 26 26gtg ctc ggc tcc tcg ccg gct gag atc ctt gtc ggc aac tgg 7884 Ile Val Leu Gly Ser Ser Pro Ala Glu Ile Leu Val Gly Asn Trp 26 2625 cgc acc ccg tcc aag aag gtc ggc tcg gac acc atc acc ctg cac 7929 Arg Thr Pro Ser Lys Lys Val Gly Ser Asp Thr Ile Thr Leu His 263264ag att tcc gcc aag tcc aac ccc ttc ctc gag gac cac gtc 7974 Arg Lys Ile Ser Ala Lys Ser Asn Pro Phe Leu Glu Asp His Val 2645 265atc cag ggc cgc cgc gtg ctg ccc atg acg ctg gcc att ggc tcg 8 Gln Gly Arg Arg Val Leu Pro Met Thr Leu Ala Ile Gly Ser 266267cg gag acc tgc ctc ggc ctc ttc ccc ggc tac tcg ctc tgg 8 Ala Glu Thr Cys Leu Gly Leu Phe Pro Gly Tyr Ser Leu Trp 2675 268gcc att gac gac gcc cag ctc ttc aag ggt gtc act gtc gac ggc 8 Ile Asp Asp Ala Gln Leu Phe Lys Gly Val Thr Val Asp Gly 26927gtc aac tgc gag gtg acc ctc acc ccg tcg acg gcg ccc tcg 8 Val Asn Cys Glu Val Thr Leu Thr Pro Ser Thr Ala Pro Ser 27 27cgc gtc aac gtc cag gcc acg ctc aag acc ttt tcc agc ggc 8 Arg Val Asn Val Gln Ala Thr Leu Lys Thr Phe Ser Ser Gly 272273tg gtc ccg gcc tac cgc gcc gtc atc gtg ctc tcc aac cag 8244 Lys Leu Val Pro Ala Tyr Arg Ala Val Ile Val Leu Ser Asn Gln 2735 274ggc gcg ccc ccg gcc aac gcc acc atg cag ccg ccc tcg ctc gat 8289 Gly Ala Pro Pro Ala Asn Ala Thr Met Gln Pro Pro Ser Leu Asp 275276at ccg gcg ctc cag ggc tcc gtc tac gac ggc aag acc ctc 8334 Ala Asp Pro Ala Leu Gln Gly Ser Val Tyr Asp Gly Lys Thr Leu 2765 277ttc cac ggc ccg gcc ttc cgc ggc atc gat gac gtg ctc tcg tgc 8379 Phe His Gly Pro Ala Phe Arg Gly Ile Asp Asp Val Leu Ser Cys 278279ag agc cag ctt gtg gcc aag tgc agc gct gtc ccc ggc tcc 8424 Thr Lys Ser Gln Leu Val Ala Lys Cys Ser Ala Val Pro Gly Ser 2795 28 gac gcc gct cgc ggc gag ttt gcc acg gac act gac gcc cat gac 8469 Asp Ala Ala Arg Gly Glu Phe Ala Thr Asp Thr Asp Ala His Asp 28 282tc gtg aac gac ctg gcc ttt cag gcc atg ctc gtc tgg gtg 85Phe Val Asn Asp Leu Ala Phe Gln Ala Met Leu Val Trp Val 2825 283cgc cgc acg ctc ggc cag gct gcg ctc ccc aac tcg atc cag cgc 8559 Arg Arg Thr Leu Gly Gln Ala Ala Leu Pro Asn Ser Ile Gln Arg 284285tc cag cac cgc ccg gtc ccg cag gac aag ccc ttc tac att 86Val Gln His Arg Pro Val Pro Gln Asp Lys Pro Phe Tyr Ile 2855 286acc ctc cgc tcc aac cag tcg ggc ggt cac tcc cag cac aag cac 8649 Thr Leu Arg Ser Asn Gln Ser Gly Gly His Ser Gln His Lys His 287288tt cag ttc cac aac gag cag ggc gat ctc ttc att gat gtc 8694 Ala Leu Gln Phe His Asn Glu Gln Gly Asp Leu Phe Ile Asp Val 2885 289cag gct tcg gtc atc gcc acg gac agc ctt gcc ttc 873la Ser Val Ile Ala Thr Asp Ser Leu Ala Phe 29 29Schizochytrium sp. 2 Met Ala Ala Arg Leu Gln Glu Gln Lys Gly Gly Glu Met Asp Thr Arg Ala Ile Ile Gly Met Ser Ala Ile Leu Pro Cys Gly Thr Thr Val 2 Arg Glu Ser Trp Glu Thr Ile Arg Ala Gly Ile Asp Cys Leu Ser Asp 35 4u Pro Glu Asp Arg Val Asp Val Thr Ala Tyr Phe Asp Pro Val Lys 5 Thr Thr Lys Asp Lys Ile Tyr Cys Lys Arg Gly Gly Phe Ile Pro Glu 65 7R>
8sp Phe Asp Ala Arg Glu Phe Gly Leu Asn Met Phe Gln Met Glu 85 9p Ser Asp Ala Asn Gln Thr Ile Ser Leu Leu Lys Val Lys Glu Ala Gln Asp Ala Gly Ile Asp Ala Leu Gly Lys Glu Lys Lys Asn Ile Cys Val Leu Gly Ile Gly Gly Gly Gln Lys Ser Ser His Glu Phe Ser Arg Leu Asn Tyr Val Val Val Glu Lys Val Leu Arg Lys Met Gly Met Pro Glu Glu Asp Val Lys Val Ala Val Glu Lys Tyr Lys Ala Phe Pro Glu Trp Arg Leu Asp Ser Phe Pro Gly Phe Leu Gly Asn Thr Ala Gly Arg Cys Thr Asn Thr Phe Asn Leu Asp Gly Met Asn 2Val Val Asp Ala Ala Cys Ala Ser Ser Leu Ile Ala Val Lys Val 222le Asp Glu Leu Leu Tyr Gly Asp Cys Asp Met Met Val Thr Gly 225 234hr Cys Thr Asp Asn Ser Ile Gly Met Tyr Met Ala Phe Ser Lys 245 25hr Pro Val Phe Ser Thr Asp Pro Ser Val Arg Ala Tyr Asp Glu Lys 267ys Gly Met Leu Ile Gly Glu Gly Ser Ala Met Leu Val Leu Lys 275 28rg Tyr Ala Asp Ala Val Arg Asp Gly Asp Glu Ile His Ala Val Ile 29Gly Cys Ala Ser Ser Ser Asp Gly Lys Ala Ala Gly Ile Tyr Thr 33Pro Thr Ile Ser Gly Gln Glu Glu Ala Leu Arg Arg Ala Tyr Asn Arg 325 33la Cys Val Asp Pro Ala Thr Val Thr Leu Val Glu Gly His Gly Thr 345hr Pro Val Gly Asp Arg Ile Glu Leu Thr Ala Leu Arg Asn Leu 355 36he Asp Lys Ala Tyr Gly Glu Gly Asn Thr Glu Lys Val Ala Val Gly 378le Lys Ser Ser Ile Gly His Leu Lys Ala Val Ala Gly Leu Ala 385 39Met Ile Lys Val Ile Met Ala Leu Lys His Lys Thr Leu Pro Gly 44Ile Asn Val Asp Asn Pro Pro Asn Leu Tyr Asp Asn Thr Pro Ile 423lu Ser Ser Leu Tyr Ile Asn Thr Met Asn Arg Pro Trp Phe Pro 435 44ro Pro Gly Val Pro Arg Arg Ala Gly Ile Ser Ser Phe Gly Phe Gly 456la Asn Tyr His Ala Val Leu Glu Glu Ala Glu Pro Glu His Thr 465 478la Tyr Arg Leu Asn Lys Arg Pro Gln Pro Val Leu Met Met Ala 485 49la Thr Pro Ala Ala Leu Gln Ser Leu Cys Glu Ala Gln Leu Lys Glu 55Glu Ala Ala Ile Lys Glu Asn Glu Thr Val Lys Asn Thr Ala Tyr 5525 Ile Lys Cys Val Lys Phe Gly Glu Gln Phe Lys Phe Pro Gly Ser Ile 534la Thr Asn Ala Arg Leu Gly Phe Leu Val Lys Asp Ala Glu Asp 545 556ys Ser Thr Leu Arg Ala Ile Cys Ala Gln Phe Ala Lys Asp Val 565 57hr Lys Glu Ala Trp Arg Leu Pro Arg Glu Gly Val Ser Phe Arg Ala 589ly Ile Ala Thr Asn Gly Ala Val Ala Ala Leu Phe Ser Gly Gln 595 6Gly Ala Gln Tyr Thr His Met Phe Ser Glu Val Ala Met Asn Trp Pro 662he Arg Gln Ser Ile Ala Ala Met Asp Ala Ala Gln Ser Lys Val 625 634ly Ser Asp Lys Asp Phe Glu Arg Val Ser Gln Val Leu Tyr Pro 645 65rg Lys Pro Tyr Glu Arg Glu Pro Glu Gln Asn Pro Lys Lys Ile Ser 667hr Ala Tyr Ser Gln Pro Ser Thr Leu Ala Cys Ala Leu Gly Ala 675 68he Glu Ile Phe Lys Glu Ala Gly Phe Thr Pro Asp Phe Ala Ala Gly 69Ser Leu Gly Glu Phe Ala Ala Leu Tyr Ala Ala Gly Cys Val Asp 77Arg Asp Glu Leu Phe Glu Leu Val Cys Arg Arg Ala Arg Ile Met Gly 725 73ly Lys Asp Ala Pro Ala Thr Pro Lys Gly Cys Met Ala Ala Val Ile 745ro Asn Ala Glu Asn Ile Lys Val Gln Ala Ala Asn Val Trp Leu 755 76ly Asn Ser Asn Ser Pro Ser Gln Thr Val Ile Thr Gly Ser Val Glu 778le Gln Ala Glu Ser Ala Arg Leu Gln Lys Glu Gly Phe Arg Val 785 79Pro Leu Ala Cys Glu Ser Ala Phe His Ser Pro Gln Met Glu Asn 88Ser Ser Ala Phe Lys Asp Val Ile Ser Lys Val Ser Phe Arg Thr 823ys Ala Glu Thr Lys Leu Phe Ser Asn Val Ser Gly Glu Thr Tyr 835 84ro Thr Asp Ala Arg Glu Met Leu Thr Gln His Met Thr Ser Ser Val 856he Leu Thr Gln Val Arg Asn Met His Gln Ala Gly Ala Arg Ile 865 878al Glu Phe Gly Pro Lys Gln Val Leu Ser Lys Leu Val Ser Glu 885 89hr Leu Lys Asp Asp Pro Ser Val Val Thr Val Ser Val Asn Pro Ala 99Gly Thr Asp Ser Asp Ile Gln Leu Arg Asp Ala Ala Val Gln Leu 9925 Val Val Ala Gly Val Asn Leu Gln Gly Phe Asp Lys Trp Asp Ala Pro 934la Thr Arg Met Gln Ala Ile Lys Lys Lys Arg Thr Thr Leu Arg 945 956er Ala Ala Thr Tyr Val Ser Asp Lys Thr Lys Lys Val Arg Asp 965 97la Ala Met Asn Asp Gly Arg Cys Val Thr Tyr Leu Lys Gly Ala Ala 989eu Ile Lys Ala Pro Glu Pro Val Val Asp Glu Ala Ala Lys Arg 995 Ala Glu Arg Leu Gln Lys Glu Leu Gln Asp Ala Gln Arg Gln Leu Asp Asp Ala Lys Arg Ala Ala Ala Glu Ala Asn Ser Lys Leu 3Ala Ala Ala Lys Glu Glu Ala Lys Thr Ala Ala Ala Ser Ala Lys 45 o Ala Val Asp Thr Ala Val Val Glu Lys His Arg Ala Ile Leu 6Lys Ser Met Leu Ala Glu Leu Asp Gly Tyr Gly Ser Val Asp Ala 75 r Ser Leu Gln Gln Gln Gln Gln Gln Gln Thr Ala Pro Ala Pro 9Val Lys Ala Ala Ala Pro Ala Ala Pro Val Ala Ser Ala Pro Ala Pro Ala Val Ser Asn Glu Leu Leu Glu Lys Ala Glu Thr Val Val 2Met Glu Val Leu Ala Ala Lys Thr Gly Tyr Glu Thr Asp Met Ile 35 u Ala Asp Met Glu Leu Glu Thr Glu Leu Gly Ile Asp Ser Ile 5Lys Arg Val Glu Ile Leu Ser Glu Val Gln Ala Met Leu Asn Val 65 u Ala Lys Asp Val Asp Ala Leu Ser Arg Thr Arg Thr Val Gly 8Glu Val Val Asn Ala Met Lys Ala Glu Ile Ala Gly Ser Ser Ala 95 o Ala Pro Ala Ala Ala Ala Pro Ala Pro Ala Lys Ala Ala Pro Ala Ala Ala Ala Pro Ala Val Ser Asn Glu Leu Leu Glu Lys Ala 25 u Thr Val Val Met Glu Val Leu Ala Ala Lys Thr Gly Tyr Glu 4Thr Asp Met Ile Glu Ser Asp Met Glu Leu Glu Thr Glu Leu Gly 55 e Asp Ser Ile Lys Arg Val Glu Ile Leu Ser Glu Val Gln Ala 7Met Leu Asn Val Glu Ala Lys Asp Val Asp Ala Leu Ser Arg Thr 85 g Thr Val Gly Glu Val Val Asn Ala Met Lys Ala Glu Ile Ala Gly Gly Ser Ala Pro Ala Pro Ala Ala Ala Ala Pro Gly Pro Ala Ala Ala Ala Pro Ala Pro Ala Ala Ala Ala Pro Ala Val Ser Asn 3Glu Leu Leu Glu Lys Ala Glu Thr Val Val Met Glu Val Leu Ala 45 a Lys Thr Gly Tyr Glu Thr Asp Met Ile Glu Ser Asp Met Glu 6Leu Glu Thr Glu Leu Gly Ile Asp Ser Ile Lys Arg Val Glu Ile 75 u Ser Glu Val Gln Ala Met Leu Asn Val Glu Ala Lys Asp Val 9Asp Ala Leu Ser Arg Thr Arg Thr Val Gly Glu Val Val Asp Ala Met Lys Ala Glu Ile Ala Gly Gly Ser Ala Pro Ala Pro Ala Ala 2Ala Ala Pro Ala Pro Ala Ala Ala Ala Pro Ala Pro Ala Ala Pro 35 a Pro Ala Val Ser Ser Glu Leu Leu Glu Lys Ala Glu Thr Val 5Val Met Glu Val Leu Ala Ala Lys Thr Gly Tyr Glu Thr Asp Met 65 e Glu Ser Asp Met Glu Leu Glu Thr Glu Leu Gly Ile Asp Ser 8Ile Lys Arg Val Glu Ile Leu Ser Glu Val Gln Ala Met Leu Asn 95 l Glu Ala Lys Asp Val Asp Ala Leu Ser Arg Thr Arg Thr Val Gly Glu Val Val Asp Ala Met Lys Ala Glu Ile Ala Gly Gly Ser 25 a Pro Ala Pro Ala Ala Ala Ala Pro Ala Pro Ala Ala Ala Ala 4Pro Ala Pro Ala Ala Pro Ala Pro Ala Ala Pro Ala Pro Ala Val 55 r Ser Glu Leu Leu Glu Lys Ala Glu Thr Val Val Met Glu Val 7Leu Ala Ala Lys Thr Gly Tyr Glu Thr Asp Met Ile Glu Ser Asp 85 t Glu Leu Glu Thr Glu Leu Gly Ile Asp Ser Ile Lys Arg Val Glu Ile Leu Ser Glu Val Gln Ala Met Leu Asn Val Glu Ala Lys Asp Val Asp Ala Leu Ser Arg Thr Arg Thr Val Gly Glu Val Val 3Asp Ala Met Lys Ala Glu Ile Ala Gly Ser Ser Ala Ser Ala Pro 45 a Ala Ala Ala Pro Ala Pro Ala Ala Ala Ala Pro Ala Pro Ala 6Ala Ala Ala Pro Ala Val Ser Asn Glu Leu Leu Glu Lys Ala Glu 75 r Val Val Met Glu Val Leu Ala Ala Lys Thr Gly Tyr Glu Thr 9Asp Met Ile Glu Ser Asp Met Glu Leu Glu Thr Glu Leu Gly Ile Asp Ser Ile Lys Arg Val Glu Ile Leu Ser Glu Val Gln Ala Met 2Leu Asn Val Glu Ala Lys Asp Val Asp Ala Leu Ser Arg Thr Arg 35 r Val Gly Glu Val Val Asp Ala Met Lys Ala Glu Ile Ala Gly 5Gly Ser Ala Pro Ala Pro Ala Ala Ala Ala Pro Ala Pro Ala Ala 65 a Ala Pro Ala Val Ser Asn Glu Leu Leu Glu Lys Ala Glu Thr 8Val Val Met Glu Val Leu Ala Ala Lys Thr Gly Tyr Glu Thr Asp 95 t Ile Glu Ser Asp Met Glu Leu Glu Thr Glu Leu Gly Ile Asp Ser Ile Lys Arg Val Glu Ile Leu Ser Glu Val Gln Ala Met Leu 25 n Val Glu Ala Lys Asp Val Asp Ala Leu Ser Arg Thr Arg Thr 4Val Gly Glu Val Val Asp Ala Met Lys Ala Glu Ile Ala Gly Ser 55 r Ala Pro Ala Pro Ala Ala Ala Ala Pro Ala Pro Ala Ala Ala 7Ala Pro Ala Pro Ala Ala Ala Ala Pro Ala Val Ser Ser Glu Leu 85 u Glu Lys Ala Glu Thr Val Val Met Glu Val Leu Ala Ala Lys Thr Gly Tyr Glu Thr Asp Met Ile Glu Ser Asp Met Glu Leu Glu Thr Glu Leu Gly Ile Asp Ser Ile Lys Arg Val Glu Ile Leu Ser 3Glu Val Gln Ala Met Leu Asn Val Glu Ala Lys Asp Val Asp Ala 45 u Ser Arg Thr Arg Thr Val Gly Glu Val Val Asp Ala Met Lys 6Ala Glu Ile Ala Gly Gly Ser Ala Pro Ala Pro Ala Ala Ala Ala 75 o Ala Pro Ala Ala Ala Ala Pro Ala Val Ser Asn Glu Leu Leu 9Glu Lys Ala Glu Thr Val Val Met Glu Val Leu Ala Ala Lys Thr 25 2 Tyr Glu Thr Asp Met Ile Glu Ser Asp Met Glu Leu Glu Thr 2Glu Leu Gly Ile Asp Ser Ile Lys Arg Val Glu Ile Leu Ser Glu 25 2 Gln Ala Met Leu Asn Val Glu Ala Lys Asp Val Asp Ala Leu 2Ser Arg Thr Arg Thr Val Gly Glu Val Val Asp Ala Met Lys Ala 25 2 Ile Ala Gly Gly Ser Ala Pro Ala Pro Ala Ala Ala Ala Pro 2Ala Ser Ala Gly Ala Ala Pro Ala Val Lys Ile Asp Ser Val His 25 2 Ala Asp Cys Asp Asp Leu Ser Leu Met His Ala Lys Val Val 2Asp Ile Arg Arg Pro Asp Glu Leu Ile Leu Glu Arg Pro Glu Asn 25 2 Pro Val Leu Val Val Asp Asp Gly Ser Glu Leu Thr Leu Ala 2Leu Val Arg Val Leu Gly Ala Cys Ala Val Val Leu Thr Phe Glu 25 2 Leu Gln Leu Ala Gln Arg Ala Gly Ala Ala Ala Ile Arg His 2Val Leu Ala Lys Asp Leu Ser Ala Glu Ser Ala Glu Lys Ala Ile 25 2 Glu Ala Glu Gln Arg Phe Gly Ala Leu Gly Gly Phe Ile Ser 2Gln Gln Ala Glu Arg Phe Glu Pro Ala Glu Ile Leu Gly Phe Thr 22 222et Cys Ala Lys Phe Ala Lys Ala Ser Leu Cys Thr Ala Val 2225 223Ala Gly Gly Arg Pro Ala Phe Ile Gly Val Ala Arg Leu Asp Gly 224225eu Gly Phe Thr Ser Gln Gly Thr Ser Asp Ala Leu Lys Arg 2255 226Ala Gln Arg Gly Ala Ile Phe Gly Leu Cys Lys Thr Ile Gly Leu 227228rp Ser Glu Ser Asp Val Phe Ser Arg Gly Val Asp Ile Ala 2285 229Gln Gly Met His Pro Glu Asp Ala Ala Val Ala Ile Val Arg Glu 23 23Ala Cys Ala Asp Ile Arg Ile Arg Glu Val Gly Ile Gly Ala 23 2325 Asn Gln Gln Arg Cys Thr Ile Arg Ala Ala Lys Leu Glu Thr Gly 233234ro Gln Arg Gln Ile Ala Lys Asp Asp Val Leu Leu Val Ser 2345 235Gly Gly Ala Arg Gly Ile Thr Pro Leu Cys Ile Arg Glu Ile Thr 236237ln Ile Ala Gly Gly Lys Tyr Ile Leu Leu Gly Arg Ser Lys 2375 238Val Ser Ala Ser Glu Pro Ala Trp Cys Ala Gly Ile Thr Asp Glu 23924Ala Val Gln Lys Ala Ala Thr Gln Glu Leu Lys Arg Ala Phe 24 24Ala Gly Glu Gly Pro Lys Pro Thr Pro Arg Ala Val Thr Lys 242243al Gly Ser Val Leu Gly Ala Arg Glu Val Arg Ser Ser Ile 2435 244Ala Ala Ile Glu Ala Leu Gly Gly Lys Ala Ile Tyr Ser Ser Cys 245246al Asn Ser Ala Ala Asp Val Ala Lys Ala Val Arg Asp Ala 2465 247Glu Ser Gln Leu Gly Ala Arg Val Ser Gly Ile Val His Ala Ser 248249al Leu Arg Asp Arg

Leu Ile Glu Lys Lys Leu Pro Asp Glu 2495 25 Phe Asp Ala Val Phe Gly Thr Lys Val Thr Gly Leu Glu Asn Leu 25 252la Ala Val Asp Arg Ala Asn Leu Lys His Met Val Leu Phe 2525 253Ser Ser Leu Ala Gly Phe His Gly Asn Val Gly Gln Ser Asp Tyr 254255et Ala Asn Glu Ala Leu Asn Lys Met Gly Leu Glu Leu Ala 2555 256Lys Asp Val Ser Val Lys Ser Ile Cys Phe Gly Pro Trp Asp Gly 257258et Val Thr Pro Gln Leu Lys Lys Gln Phe Gln Glu Met Gly 2585 259Val Gln Ile Ile Pro Arg Glu Gly Gly Ala Asp Thr Val Ala Arg 26 26Val Leu Gly Ser Ser Pro Ala Glu Ile Leu Val Gly Asn Trp 26 2625 Arg Thr Pro Ser Lys Lys Val Gly Ser Asp Thr Ile Thr Leu His 263264ys Ile Ser Ala Lys Ser Asn Pro Phe Leu Glu Asp His Val 2645 265Ile Gln Gly Arg Arg Val Leu Pro Met Thr Leu Ala Ile Gly Ser 266267la Glu Thr Cys Leu Gly Leu Phe Pro Gly Tyr Ser Leu Trp 2675 268Ala Ile Asp Asp Ala Gln Leu Phe Lys Gly Val Thr Val Asp Gly 26927Val Asn Cys Glu Val Thr Leu Thr Pro Ser Thr Ala Pro Ser 27 27Arg Val Asn Val Gln Ala Thr Leu Lys Thr Phe Ser Ser Gly 272273eu Val Pro Ala Tyr Arg Ala Val Ile Val Leu Ser Asn Gln 2735 274Gly Ala Pro Pro Ala Asn Ala Thr Met Gln Pro Pro Ser Leu Asp 275276sp Pro Ala Leu Gln Gly Ser Val Tyr Asp Gly Lys Thr Leu 2765 277Phe His Gly Pro Ala Phe Arg Gly Ile Asp Asp Val Leu Ser Cys 278279ys Ser Gln Leu Val Ala Lys Cys Ser Ala Val Pro Gly Ser 2795 28 Asp Ala Ala Arg Gly Glu Phe Ala Thr Asp Thr Asp Ala His Asp 28 282he Val Asn Asp Leu Ala Phe Gln Ala Met Leu Val Trp Val 2825 283Arg Arg Thr Leu Gly Gln Ala Ala Leu Pro Asn Ser Ile Gln Arg 284285al Gln His Arg Pro Val Pro Gln Asp Lys Pro Phe Tyr Ile 2855 286Thr Leu Arg Ser Asn Gln Ser Gly Gly His Ser Gln His Lys His 287288eu Gln Phe His Asn Glu Gln Gly Asp Leu Phe Ile Asp Val 2885 289Gln Ala Ser Val Ile Ala Thr Asp Ser Leu Ala Phe 29 2977 DNA Schizochytrium sp. CDS (77) 3 atg gcc gct cgg aat gtg agc gcc gcg cat gag atg cac gat gaa aag 48 Met Ala Ala Arg Asn Val Ser Ala Ala His Glu Met His Asp Glu Lys atc gcc gtc gtc ggc atg gcc gtc cag tac gcc gga tgc aaa acc 96 Arg Ile Ala Val Val Gly Met Ala Val Gln Tyr Ala Gly Cys Lys Thr 2 aag gac gag ttc tgg gag gtg ctc atg aac ggc aag gtc gag tcc aag Asp Glu Phe Trp Glu Val Leu Met Asn Gly Lys Val Glu Ser Lys 35 4g atc agc gac aaa cga ctc ggc tcc aac tac cgc gcc gag cac tac Ile Ser Asp Lys Arg Leu Gly Ser Asn Tyr Arg Ala Glu His Tyr 5 aaa gca gag cgc agc aag tat gcc gac acc ttt tgc aac gaa acg tac 24la Glu Arg Ser Lys Tyr Ala Asp Thr Phe Cys Asn Glu Thr Tyr 65 7 ggc acc ctt gac gag aac gag atc gac aac gag cac gaa ctc ctc ctc 288 Gly Thr Leu Asp Glu Asn Glu Ile Asp Asn Glu His Glu Leu Leu Leu 85 9c ctc gcc aag cag gca ctc gca gag aca tcc gtc aaa gac tcg aca 336 Asn Leu Ala Lys Gln Ala Leu Ala Glu Thr Ser Val Lys Asp Ser Thr tgc ggc atc gtc agc ggc tgc ctc tcg ttc ccc atg gac aac ctc 384 Arg Cys Gly Ile Val Ser Gly Cys Leu Ser Phe Pro Met Asp Asn Leu ggt gaa ctc ctc aac gtg tac caa aac cat gtc gag aaa aag ctc 432 Gln Gly Glu Leu Leu Asn Val Tyr Gln Asn His Val Glu Lys Lys Leu gcc cgc gtc ttc aag gac gcc tcc cat tgg tcc gaa cgc gag cag 48la Arg Val Phe Lys Asp Ala Ser His Trp Ser Glu Arg Glu Gln tcc aac aaa ccc gag gcc ggt gac cgc cgc atc ttc atg gac ccg gcc 528 Ser Asn Lys Pro Glu Ala Gly Asp Arg Arg Ile Phe Met Asp Pro Ala ttc gtc gcc gaa gaa ctc aac ctc ggc gcc ctt cac tac tcc gtc 576 Ser Phe Val Ala Glu Glu Leu Asn Leu Gly Ala Leu His Tyr Ser Val gca gca tgc gcc acg gcg ctc tac gtg ctc cgc ctc gcg cag gat 624 Asp Ala Ala Cys Ala Thr Ala Leu Tyr Val Leu Arg Leu Ala Gln Asp 2ctc gtc tcc ggc gcc gcc gac gtc atg ctc tgc ggt gcc acc tgc 672 His Leu Val Ser Gly Ala Ala Asp Val Met Leu Cys Gly Ala Thr Cys 222cg gag ccc ttt ttc atc ctt tcg ggc ttt tcc acc ttc cag gcc 72ro Glu Pro Phe Phe Ile Leu Ser Gly Phe Ser Thr Phe Gln Ala 225 234cc gtc ggc acg ggc cag aac gtg tcc atg ccg ctg cac aag gac 768 Met Pro Val Gly Thr Gly Gln Asn Val Ser Met Pro Leu His Lys Asp 245 25gc cag ggc ctc acc ccg ggt gag ggc ggc tcc atc atg gtc ctc aag 8Gln Gly Leu Thr Pro Gly Glu Gly Gly Ser Ile Met Val Leu Lys 267tc gat gat gcc atc cgc gac ggc gac cac att tac ggc acc ctt 864 Arg Leu Asp Asp Ala Ile Arg Asp Gly Asp His Ile Tyr Gly Thr Leu 275 28tc ggc gcc aat gtc agc aac tcc ggc aca ggt ctg ccc ctc aag ccc 9Gly Ala Asn Val Ser Asn Ser Gly Thr Gly Leu Pro Leu Lys Pro 29ctc ccc agc gag aaa aag tgc ctc atg gac acc tac acg cgc att 96eu Pro Ser Glu Lys Lys Cys Leu Met Asp Thr Tyr Thr Arg Ile 33aac gtg cac ccg cac aag att cag tac gtc gag tgc cac gcc acc ggc n Val His Pro His Lys Ile Gln Tyr Val Glu Cys His Ala Thr Gly 325 33cg ccc cag ggt gat cgt gtg gaa atc gac gcc gtc aag gcc tgc ttt r Pro Gln Gly Asp Arg Val Glu Ile Asp Ala Val Lys Ala Cys Phe 345gc aag gtc ccc cgt ttc ggt acc aca aag ggc aac ttt gga cac u Gly Lys Val Pro Arg Phe Gly Thr Thr Lys Gly Asn Phe Gly His 355 36cc cts gyc gca gcc ggc ttt gcc ggt atg tgc aag gtc ctc ctc tcc r Xaa Xaa Ala Ala Gly Phe Ala Gly Met Cys Lys Val Leu Leu Ser 378ag cat ggc atc atc ccg ccc acc ccg ggt atc gat gac gag acc t Lys His Gly Ile Ile Pro Pro Thr Pro Gly Ile Asp Asp Glu Thr 385 39atg gac cct ctc gtc gtc tcc ggt gag gcc atc cca tgg cca gag s Met Asp Pro Leu Val Val Ser Gly Glu Ala Ile Pro Trp Pro Glu 44aac ggc gag ccc aag cgc gcc ggt ctc tcg gcc ttt ggc ttt ggt r Asn Gly Glu Pro Lys Arg Ala Gly Leu Ser Ala Phe Gly Phe Gly 423cc aac gcc cat gcc gtc ttt gag gag cat gac ccc tcc aac gcc y Thr Asn Ala His Ala Val Phe Glu Glu His Asp Pro Ser Asn Ala 435 44cc tgc acg ggc cac gac tcc att tct gcg ctc tcg gcc cgc tgc ggc a Cys Thr Gly His Asp Ser Ile Ser Ala Leu Ser Ala Arg Cys Gly 456aa agc aac atg cgc atc gcc atc act ggt atg gac gcc acc ttt y Glu Ser Asn Met Arg Ile Ala Ile Thr Gly Met Asp Ala Thr Phe 465 478ct ctc aag gga ctc gac gcc ttc gag cgc gcc att tac acc ggc y Ala Leu Lys Gly Leu Asp Ala Phe Glu Arg Ala Ile Tyr Thr Gly 485 49ct cac ggt gcc atc cca ctc cca gaa aag cgc tgg cgc ttt ctc ggc a His Gly Ala Ile Pro Leu Pro Glu Lys Arg Trp Arg Phe Leu Gly 55gac aag gac ttt ctt gac ctc tgc ggc gtc aag gcc acc ccg cac s Asp Lys Asp Phe Leu Asp Leu Cys Gly Val Lys Ala Thr Pro His 5525 ggc tgc tac att gaa gat gtt gag gtc gac ttc cag cgc ctc cgc acg y Cys Tyr Ile Glu Asp Val Glu Val Asp Phe Gln Arg Leu Arg Thr 534tg acc cct gaa gac atg ctc ctc cct cag cag ctt ctg gcc gtc o Met Thr Pro Glu Asp Met Leu Leu Pro Gln Gln Leu Leu Ala Val 545 556cc att gac cgc gcc atc ctc gac tcg gga atg aaa aag ggt ggc r Thr Ile Asp Arg Ala Ile Leu Asp Ser Gly Met Lys Lys Gly Gly 565 57at gtc gcc gtc ttt gtc ggc ctc ggc acc gac ctc gag ctc tac cgt n Val Ala Val Phe Val Gly Leu Gly Thr Asp Leu Glu Leu Tyr Arg 589gt gct cgc gtc gct ctc aag gag cgc gtc cgc cct gaa gcc tcc s Arg Ala Arg Val Ala Leu Lys Glu Arg Val Arg Pro Glu Ala Ser 595 6aag aag ctc aat gac atg atg cag tac att aac gac tgc ggc aca tcc s Lys Leu Asn Asp Met Met Gln Tyr Ile Asn Asp Cys Gly Thr Ser 662cg tac acc tcg tac att ggc aac ctc gtc gcc acg cgc gtc tcg r Ser Tyr Thr Ser Tyr Ile Gly Asn Leu Val Ala Thr Arg Val Ser 625 634ag tgg ggc ttc acg ggc ccc tcc ttt acg atc acc gag ggc aac r Gln Trp Gly Phe Thr Gly Pro Ser Phe Thr Ile Thr Glu Gly Asn 645 65ac tcc gtc tac cgc tgc gcc gag ctc ggc aag tac ctc ctc gag acc 2 Ser Val Tyr Arg Cys Ala Glu Leu Gly Lys Tyr Leu Leu Glu Thr 667ag gtc gat ggc gtc gtc gtt gcg ggt gtc gat ctc tgc ggc agt 2 Glu Val Asp Gly Val Val Val Ala Gly Val Asp Leu Cys Gly Ser 675 68cc gaa aac ctt tac gtc aag tct cgc cgc ttc aag gtg tcc acc tcc 2 Glu Asn Leu Tyr Val Lys Ser Arg Arg Phe Lys Val Ser Thr Ser 69acc ccg cgc gcc agc ttt gac gcc gcc gcc gat ggc tac ttt gtc 2 Thr Pro Arg Ala Ser Phe Asp Ala Ala Ala Asp Gly Tyr Phe Val 77ggc gag ggc tgc ggt gcc ttt gtg ctc aag cgt gag act agc tgc acc 22Glu Gly Cys Gly Ala Phe Val Leu Lys Arg Glu Thr Ser Cys Thr 725 73ag gac gac cgt atc tac gct tgc atg gat gcc atc gtc cct ggc aac 2256 Lys Asp Asp Arg Ile Tyr Ala Cys Met Asp Ala Ile Val Pro Gly Asn 745ct agc gcc tgc ttg cgc gag gcc ctc gac cag gcg cgc gtc aag 23Pro Ser Ala Cys Leu Arg Glu Ala Leu Asp Gln Ala Arg Val Lys 755 76cg ggc gat atc gag atg ctc gag ctc agc gcc gac tcc gcc cgc cac 2352 Pro Gly Asp Ile Glu Met Leu Glu Leu Ser Ala Asp Ser Ala Arg His 778ag gac ccg tcc gtc ctg ccc aag gag ctc act gcc gag gag gaa 24Lys Asp Pro Ser Val Leu Pro Lys Glu Leu Thr Ala Glu Glu Glu 785 79ggc ggc ctt cag acg atc ctt cgt gac gat gac aag ctc ccg cgc 2448 Ile Gly Gly Leu Gln Thr Ile Leu Arg Asp Asp Asp Lys Leu Pro Arg 88gtc gca acg ggc agt gtc aag gcc acc gtc ggt gac acc ggt tat 2496 Asn Val Ala Thr Gly Ser Val Lys Ala Thr Val Gly Asp Thr Gly Tyr 823ct ggt gct gcc agc ctc atc aag gct gcg ctt tgc atc tac aac 2544 Ala Ser Gly Ala Ala Ser Leu Ile Lys Ala Ala Leu Cys Ile Tyr Asn 835 84gc tac ctg ccc agc aac ggc gac gac tgg gat gaa ccc gcc cct gag 2592 Arg Tyr Leu Pro Ser Asn Gly Asp Asp Trp Asp Glu Pro Ala Pro Glu 856cc tgg gac agc acc ctc ttt gcg tgc cag acc tcg cgc gct tgg 264ro Trp Asp Ser Thr Leu Phe Ala Cys Gln Thr Ser Arg Ala Trp 865 878ag aac cct ggc gag cgt cgc tat gcg gcc gtc tcg ggc gtc tcc 2688 Leu Lys Asn Pro Gly Glu Arg Arg Tyr Ala Ala Val Ser Gly Val Ser 885 89ag acg cgc tcg tgc tat tcc gtg ctc ctc tcc gaa gcc gag ggc cac 2736 Glu Thr Arg Ser Cys Tyr Ser Val Leu Leu Ser Glu Ala Glu Gly His 99gag cgc gag aac cgc atc tcg ctc gac gag gag gcg ccc aag ctc 2784 Tyr Glu Arg Glu Asn Arg Ile Ser Leu Asp Glu Glu Ala Pro Lys Leu 9925 att gtg ctt cgc gcc gac tcc cac gag gag atc ctt ggt cgc ctc gac 2832 Ile Val Leu Arg Ala Asp Ser His Glu Glu Ile Leu Gly Arg Leu Asp 934tc cgc gag cgc ttc ttg cag ccc acg ggc gcc gcc ccg cgc gag 288le Arg Glu Arg Phe Leu Gln Pro Thr Gly Ala Ala Pro Arg Glu 945 956ag ctc aag gcg cag gcc cgc cgc atc ttc ctc gag ctc ctc ggc 2928 Ser Glu Leu Lys Ala Gln Ala Arg Arg Ile Phe Leu Glu Leu Leu Gly 965 97ag acc ctt gcc cag gat gcc gct tct tca ggc tcg caa aag ccc ctc 2976 Glu Thr Leu Ala Gln Asp Ala Ala Ser Ser Gly Ser Gln Lys Pro Leu 989tc agc ctc gtc tcc acg ccc tcc aag ctc cag cgc gag gtc gag 3 Leu Ser Leu Val Ser Thr Pro Ser Lys Leu Gln Arg Glu Val Glu 995 gcg gcc aag ggt atc ccg cgc tgc ctc aag atg cgc cgc gat 3 Ala Ala Lys Gly Ile Pro Arg Cys Leu Lys Met Arg Arg Asp tgg agc tcc cct gct ggc agc cgc tac gcg cct gag ccg ctc gcc 3 Ser Ser Pro Ala Gly Ser Arg Tyr Ala Pro Glu Pro Leu Ala 3agc gac cgc gtc gcc ttc atg tac ggc gaa ggt cgc agc cct tac 3 Asp Arg Val Ala Phe Met Tyr Gly Glu Gly Arg Ser Pro Tyr 45 c ggc atc acc caa gac att cac cgc att tgg ccc gaa ctc cac 32Gly Ile Thr Gln Asp Ile His Arg Ile Trp Pro Glu Leu His 6gag gtc atc aac gaa aag acg aac cgt ctc tgg gcc gaa ggc gac 3249 Glu Val Ile Asn Glu Lys Thr Asn Arg Leu Trp Ala Glu Gly Asp 75 c tgg gtc atg ccg cgc gcc agc ttc aag tcg gag ctc gag agc 3294 Arg Trp Val Met Pro Arg Ala Ser Phe Lys Ser Glu Leu Glu Ser 9cag cag caa gag ttt gat cgc aac atg att gaa atg ttc cgt ctt 3339 Gln Gln Gln Glu Phe Asp Arg Asn Met Ile Glu Met Phe Arg Leu gga atc ctc acc tca att gcc ttc acc aat ctg gcg cgc gac gtt 3384 Gly Ile Leu Thr Ser Ile Ala Phe Thr Asn Leu Ala Arg Asp Val 2ctc aac atc acg ccc aag gcc gcc ttt ggc ctc agt ctt ggc gag 3429 Leu Asn Ile Thr Pro Lys Ala Ala Phe Gly Leu Ser Leu Gly Glu 35 t tcc atg att ttt gcc ttt tcc aag aag aac ggt ctc atc tcc 3474 Ile Ser Met Ile Phe Ala Phe Ser Lys Lys Asn Gly Leu Ile Ser 5gac cag ctc acc aag gat ctt cgc gag tcc gac gtg tgg aac aag 35Gln Leu Thr Lys Asp Leu Arg Glu Ser Asp Val Trp Asn Lys 65 t ctg gcc gtt gaa ttt aat gcg ctg cgc gag gcc tgg ggc att 3564 Ala Leu Ala Val Glu Phe Asn Ala Leu Arg Glu Ala Trp Gly Ile 8cca cag agt gtc ccc aag gac gag ttc tgg caa ggc tac att gtg 36Gln Ser Val Pro Lys Asp Glu Phe Trp Gln Gly Tyr Ile Val 95 c ggc acc aag cag gat atc gag gcg gcc atc gcc ccg gac agc 3654 Arg Gly Thr Lys Gln Asp Ile Glu Ala Ala Ile Ala Pro Asp Ser aag tac gtg cgc ctc acc atc atc aat gat gcc aac acc gcc ctc 3699 Lys Tyr Val Arg Leu Thr Ile Ile Asn Asp Ala Asn Thr Ala Leu 25 t agc ggc aag ccc gac gcc tgc aag gct gcg atc gcg cgt ctc 3744 Ile Ser Gly Lys Pro Asp Ala Cys Lys Ala Ala Ile Ala Arg

Leu 4ggt ggc aac att cct gcg ctt ccc gtg acc cag ggc atg tgc ggc 3789 Gly Gly Asn Ile Pro Ala Leu Pro Val Thr Gln Gly Met Cys Gly 55 c tgc ccc gag gtg gga cct tat acc aag gat atc gcc aag atc 3834 His Cys Pro Glu Val Gly Pro Tyr Thr Lys Asp Ile Ala Lys Ile 7cat gcc aac ctt gag ttc ccc gtt gtc gac ggc ctt gac ctc tgg 3879 His Ala Asn Leu Glu Phe Pro Val Val Asp Gly Leu Asp Leu Trp 85 c aca atc aac cag aag cgc ctc gtg cca cgc gcc acg ggc gcc 3924 Thr Thr Ile Asn Gln Lys Arg Leu Val Pro Arg Ala Thr Gly Ala aag gac gaa tgg gcc cct tct tcc ttt ggc gag tac gcc ggc cag 3969 Lys Asp Glu Trp Ala Pro Ser Ser Phe Gly Glu Tyr Ala Gly Gln ctc tac gag aag cag gct aac ttc ccc caa atc gtc gag acc att 4 Tyr Glu Lys Gln Ala Asn Phe Pro Gln Ile Val Glu Thr Ile 3tac aag caa aac tac gac gtc ttt gtc gag gtt ggg ccc aac aac 4 Lys Gln Asn Tyr Asp Val Phe Val Glu Val Gly Pro Asn Asn 45 c cgt agc acc gca gtg cgc acc acg ctt ggt ccc cag cgc aac 4 Arg Ser Thr Ala Val Arg Thr Thr Leu Gly Pro Gln Arg Asn 6cac ctt gct ggc gcc atc gac aag cag aac gag gat gct tgg acg 4 Leu Ala Gly Ala Ile Asp Lys Gln Asn Glu Asp Ala Trp Thr 75 c atc gtc aag ctt gtg gct tcg ctc aag gcc cac ctt gtt cct 4 Ile Val Lys Leu Val Ala Ser Leu Lys Ala His Leu Val Pro 9ggc gtc acg atc tcg ccg ctg tac cac tcc aag ctt gtg gcg gag 4239 Gly Val Thr Ile Ser Pro Leu Tyr His Ser Lys Leu Val Ala Glu gct cag gct tgc tac gct gcg ctc tgc aag ggt gaa aag ccc aag 4284 Ala Gln Ala Cys Tyr Ala Ala Leu Cys Lys Gly Glu Lys Pro Lys 2aag aac aag ttt gtg cgc aag att cag ctc aac ggt cgc ttc aac 4329 Lys Asn Lys Phe Val Arg Lys Ile Gln Leu Asn Gly Arg Phe Asn 35 c aag gcg gac ccc atc tcc tcg gcc gat ctt gcc agc ttt ccg 4374 Ser Lys Ala Asp Pro Ile Ser Ser Ala Asp Leu Ala Ser Phe Pro 5cct gcg gac cct gcc att gaa gcc gcc atc tcg agc cgc atc atg 44Ala Asp Pro Ala Ile Glu Ala Ala Ile Ser Ser Arg Ile Met 65 g cct gtc gct ccc aag ttc tac gcg cgt ctc aac att gac gag 4464 Lys Pro Val Ala Pro Lys Phe Tyr Ala Arg Leu Asn Ile Asp Glu 8cag gac gag acc cga gat ccg atc ctc aac aag gac aac gcg ccg 45Asp Glu Thr Arg Asp Pro Ile Leu Asn Lys Asp Asn Ala Pro 95 t tct tct tct tct tct tct tct tct tct tct tct tct tct tct 4554 Ser Ser Ser Ser Ser Ser Ser Ser Ser Ser Ser Ser Ser Ser Ser ccg tcg cct gct cct tcg gcc ccc gtg caa aag aag gct gct ccc 4599 Pro Ser Pro Ala Pro Ser Ala Pro Val Gln Lys Lys Ala Ala Pro 25 c gcg gag acc aag gct gtt gct tcg gct gac gca ctt cgc agt 4644 Ala Ala Glu Thr Lys Ala Val Ala Ser Ala Asp Ala Leu Arg Ser 4gcc ctg ctc gat ctc gac agt atg ctt gcg ctg agc tct gcc agt 4689 Ala Leu Leu Asp Leu Asp Ser Met Leu Ala Leu Ser Ser Ala Ser 55 c tcc ggc aac ctt gtt gag act gcg cct agc gac gcc tcg gtc 4734 Ala Ser Gly Asn Leu Val Glu Thr Ala Pro Ser Asp Ala Ser Val 7att gtg ccg ccc tgc aac att gcg gat ctc ggc agc cgc gcc ttc 4779 Ile Val Pro Pro Cys Asn Ile Ala Asp Leu Gly Ser Arg Ala Phe 85 g aaa acg tac ggt gtt tcg gcg cct ctg tac acg ggc gcc atg 4824 Met Lys Thr Tyr Gly Val Ser Ala Pro Leu Tyr Thr Gly Ala Met gcc aag ggc att gcc tct gcg gac ctc gtc att gcc gcc ggc cgc 4869 Ala Lys Gly Ile Ala Ser Ala Asp Leu Val Ile Ala Ala Gly Arg cag ggc atc ctt gcg tcc ttt ggc gcc ggc gga ctt ccc atg cag 49Gly Ile Leu Ala Ser Phe Gly Ala Gly Gly Leu Pro Met Gln 3gtt gtg cgt gag tcc atc gaa aag att cag gcc gcc ctg ccc aat 4959 Val Val Arg Glu Ser Ile Glu Lys Ile Gln Ala Ala Leu Pro Asn 45 c ccg tac gct gtc aac ctt atc cat tct ccc ttt gac agc aac 5 Pro Tyr Ala Val Asn Leu Ile His Ser Pro Phe Asp Ser Asn 6ctc gaa aag ggc aat gtc gat ctc ttc ctc gag aag ggt gtc acc 5 Glu Lys Gly Asn Val Asp Leu Phe Leu Glu Lys Gly Val Thr 75 t gtc gag gcc tcg gcc ttt atg acg ctc acc ccg cag gtc gtg 5 Val Glu Ala Ser Ala Phe Met Thr Leu Thr Pro Gln Val Val 9cgg tac cgc gcg gct ggc ctc acg cgc aac gcc gac ggc tcg gtc 5 Tyr Arg Ala Ala Gly Leu Thr Arg Asn Ala Asp Gly Ser Val aac atc cgc aac cgt atc att ggc aag gtc tcg cgc acc gag ctc 5 Ile Arg Asn Arg Ile Ile Gly Lys Val Ser Arg Thr Glu Leu 2gcc gag atg ttc atg cgt cct gcg ccc gag cac ctt ctt cag aag 5229 Ala Glu Met Phe Met Arg Pro Ala Pro Glu His Leu Leu Gln Lys 35 c att gct tcc ggc gag atc aac cag gag cag gcc gag ctc gcc 5274 Leu Ile Ala Ser Gly Glu Ile Asn Gln Glu Gln Ala Glu Leu Ala 5cgc cgt gtt ccc gtc gct gac gac atc gcg gtc gaa gct gac tcg 53Arg Val Pro Val Ala Asp Asp Ile Ala Val Glu Ala Asp Ser 65 t ggc cac acc gac aac cgc ccc atc cac gtc att ctg ccc ctc 5364 Gly Gly His Thr Asp Asn Arg Pro Ile His Val Ile Leu Pro Leu 8atc atc aac ctt cgc gac cgc ctt cac cgc gag tgc ggc tac ccg 54Ile Asn Leu Arg Asp Arg Leu His Arg Glu Cys Gly Tyr Pro 95 c aac ctt cgc gtc cgt gtg ggc gcc ggc ggt ggc att ggg tgc 5454 Ala Asn Leu Arg Val Arg Val Gly Ala Gly Gly Gly Ile Gly Cys ccc cag gcg gcg ctg gcc acc ttc aac atg ggt gcc tcc ttt att 5499 Pro Gln Ala Ala Leu Ala Thr Phe Asn Met Gly Ala Ser Phe Ile 25 c acc ggc acc gtg aac cag gtc gcc aag cag tcg ggc acg tgc 5544 Val Thr Gly Thr Val Asn Gln Val Ala Lys Gln Ser Gly Thr Cys 4gac aat gtg cgc aag cag ctc gcg aag gcc act tac tcg gac gta 5589 Asp Asn Val Arg Lys Gln Leu Ala Lys Ala Thr Tyr Ser Asp Val 55 c atg gcc ccg gct gcc gac atg ttc gag gaa ggc gtc aag ctt 5634 Cys Met Ala Pro Ala Ala Asp Met Phe Glu Glu Gly Val Lys Leu 7cag gtc ctc aag aag gga acc atg ttt ccc tcg cgc gcc aac aag 5679 Gln Val Leu Lys Lys Gly Thr Met Phe Pro Ser Arg Ala Asn Lys 85 c tac gag ctc ttt tgc aag tac gac tcg ttc gag tcc atg ccc 5724 Leu Tyr Glu Leu Phe Cys Lys Tyr Asp Ser Phe Glu Ser Met Pro ccc gca gag ctt gcg cgc gtc gag aag cgc atc ttc agc cgc gcg 5769 Pro Ala Glu Leu Ala Arg Val Glu Lys Arg Ile Phe Ser Arg Ala ctc gaa gag gtc tgg gac gag acc aaa aac ttt tac att aac cgt 58Glu Glu Val Trp Asp Glu Thr Lys Asn Phe Tyr Ile Asn Arg 3ctt cac aac ccg gag aag atc cag cgc gcc gag cgc gac ccc aag 5859 Leu His Asn Pro Glu Lys Ile Gln Arg Ala Glu Arg Asp Pro Lys 45 c aag atg tcg ctg tgc ttt cgc tgg tac ctg agc ctg gcg agc 59Lys Met Ser Leu Cys Phe Arg Trp Tyr Leu Ser Leu Ala Ser 6cgc tgg gcc aac act gga gct tcc gat cgc gtc atg gac tac cag 5949 Arg Trp Ala Asn Thr Gly Ala Ser Asp Arg Val Met Asp Tyr Gln 75 c tgg tgc ggt cct gcc att ggt tcc ttc aac gat ttc atc aag 5994 Val Trp Cys Gly Pro Ala Ile Gly Ser Phe Asn Asp Phe Ile Lys 9gga act tac ctt gat ccg gcc gtc gca aac gag tac ccg tgc gtc 6 Thr Tyr Leu Asp Pro Ala Val Ala Asn Glu Tyr Pro Cys Val 25 2 cag att aac aag cag atc ctt cgt gga gcg tgc ttc ttg cgc 6 Gln Ile Asn Lys Gln Ile Leu Arg Gly Ala Cys Phe Leu Arg 2cgt ctc gaa att ctg cgc aac gca cgc ctt tcc gat ggc gct gcc 6 Leu Glu Ile Leu Arg Asn Ala Arg Leu Ser Asp Gly Ala Ala 25 2 ctt gtg gcc agc atc gat gac aca tac gtc ccg gcc gag aag 6 Leu Val Ala Ser Ile Asp Asp Thr Tyr Val Pro Ala Glu Lys 2ctg 6 4 2 Schizochytrium sp. misc_feature (37'Xaa' at location 37s for Leu. 4 Met Ala Ala Arg Asn Val Ser Ala Ala His Glu Met His Asp Glu Lys Ile Ala Val Val Gly Met Ala Val Gln Tyr Ala Gly Cys Lys Thr 2 Lys Asp Glu Phe Trp Glu Val Leu Met Asn Gly Lys Val Glu Ser Lys 35 4l Ile Ser Asp Lys Arg Leu Gly Ser Asn Tyr Arg Ala Glu His Tyr 5 Lys Ala Glu Arg Ser Lys Tyr Ala Asp Thr Phe Cys Asn Glu Thr Tyr 65 7 Gly Thr Leu Asp Glu Asn Glu Ile Asp Asn Glu His Glu Leu Leu Leu 85 9n Leu Ala Lys Gln Ala Leu Ala Glu Thr Ser Val Lys Asp Ser Thr Cys Gly Ile Val Ser Gly Cys Leu Ser Phe Pro Met Asp Asn Leu Gly Glu Leu Leu Asn Val Tyr Gln Asn His Val Glu Lys Lys Leu Ala Arg Val Phe Lys Asp Ala Ser His Trp Ser Glu Arg Glu Gln Ser Asn Lys Pro Glu Ala Gly Asp Arg Arg Ile Phe Met Asp Pro Ala Phe Val Ala Glu Glu Leu Asn Leu Gly Ala Leu His Tyr Ser Val Ala Ala Cys Ala Thr Ala Leu Tyr Val Leu Arg Leu Ala Gln Asp 2Leu Val Ser Gly Ala Ala Asp Val Met Leu Cys Gly Ala Thr Cys 222ro Glu Pro Phe Phe Ile Leu Ser Gly Phe Ser Thr Phe Gln Ala 225 234ro Val Gly Thr Gly Gln Asn Val Ser Met Pro Leu His Lys Asp 245 25er Gln Gly Leu Thr Pro Gly Glu Gly Gly Ser Ile Met Val Leu Lys 267eu Asp Asp Ala Ile Arg Asp Gly Asp His Ile Tyr Gly Thr Leu 275 28eu Gly Ala Asn Val Ser Asn Ser Gly Thr Gly Leu Pro Leu Lys Pro 29Leu Pro Ser Glu Lys Lys Cys Leu Met Asp Thr Tyr Thr Arg Ile 33Asn Val His Pro His Lys Ile Gln Tyr Val Glu Cys His Ala Thr Gly 325 33hr Pro Gln Gly Asp Arg Val Glu Ile Asp Ala Val Lys Ala Cys Phe 345ly Lys Val Pro Arg Phe Gly Thr Thr Lys Gly Asn Phe Gly His 355 36hr Xaa Xaa Ala Ala Gly Phe Ala Gly Met Cys Lys Val Leu Leu Ser 378ys His Gly Ile Ile Pro Pro Thr Pro Gly Ile Asp Asp Glu Thr 385 39Met Asp Pro Leu Val Val Ser Gly Glu Ala Ile Pro Trp Pro Glu 44Asn Gly Glu Pro Lys Arg Ala Gly Leu Ser Ala Phe Gly Phe Gly 423hr Asn Ala His Ala Val Phe Glu Glu His Asp Pro Ser Asn Ala 435 44la Cys Thr Gly His Asp Ser Ile Ser Ala Leu Ser Ala Arg Cys Gly 456lu Ser Asn Met Arg Ile Ala Ile Thr Gly Met Asp Ala Thr Phe 465 478la Leu Lys Gly Leu Asp Ala Phe Glu Arg Ala Ile Tyr Thr Gly 485 49la His Gly Ala Ile Pro Leu Pro Glu Lys Arg Trp Arg Phe Leu Gly 55Asp Lys Asp Phe Leu Asp Leu Cys Gly Val Lys Ala Thr Pro His 5525 Gly Cys Tyr Ile Glu Asp Val Glu Val Asp Phe Gln Arg Leu Arg Thr 534et Thr Pro Glu Asp Met Leu Leu Pro Gln Gln Leu Leu Ala Val 545 556hr Ile Asp Arg Ala Ile Leu Asp Ser Gly Met Lys Lys Gly Gly 565 57sn Val Ala Val Phe Val Gly Leu Gly Thr Asp Leu Glu Leu Tyr Arg 589rg Ala Arg Val Ala Leu Lys Glu Arg Val Arg Pro Glu Ala Ser 595 6Lys Lys Leu Asn Asp Met Met Gln Tyr Ile Asn Asp Cys Gly Thr Ser 662er Tyr Thr Ser Tyr Ile Gly Asn Leu Val Ala Thr Arg Val Ser 625 634ln Trp Gly Phe Thr Gly Pro Ser Phe Thr Ile Thr Glu Gly Asn 645 65sn Ser Val Tyr Arg Cys Ala Glu Leu Gly Lys Tyr Leu Leu Glu Thr 667lu Val Asp Gly Val Val Val Ala Gly Val Asp Leu Cys Gly Ser 675 68la Glu Asn Leu Tyr Val Lys Ser Arg Arg Phe Lys Val Ser Thr Ser 69Thr Pro Arg Ala Ser Phe Asp Ala Ala Ala Asp Gly Tyr Phe Val 77Gly Glu Gly Cys Gly Ala Phe Val Leu Lys Arg Glu Thr Ser Cys Thr 725 73ys Asp Asp Arg Ile Tyr Ala Cys Met Asp Ala Ile Val Pro Gly Asn 745ro Ser Ala Cys Leu Arg Glu Ala Leu Asp Gln Ala Arg Val Lys 755 76ro Gly Asp Ile Glu Met Leu Glu Leu Ser Ala Asp Ser Ala Arg His 778ys Asp Pro Ser Val Leu Pro Lys Glu Leu Thr Ala Glu Glu Glu 785 79Gly Gly Leu Gln Thr Ile Leu Arg Asp Asp Asp Lys Leu Pro Arg 88Val Ala Thr Gly Ser Val Lys Ala Thr Val Gly Asp Thr Gly Tyr 823er Gly Ala Ala Ser Leu Ile Lys Ala Ala Leu Cys Ile Tyr Asn 835 84rg Tyr Leu Pro Ser Asn Gly Asp Asp Trp Asp Glu Pro Ala Pro Glu 856ro Trp Asp Ser Thr Leu Phe Ala Cys Gln Thr Ser Arg Ala Trp 865 878ys Asn Pro Gly Glu Arg Arg Tyr Ala Ala Val Ser Gly Val Ser 885 89lu Thr Arg Ser Cys Tyr Ser Val Leu Leu Ser Glu Ala Glu Gly His 99Glu Arg Glu Asn Arg Ile Ser Leu Asp Glu Glu Ala Pro Lys Leu 9925 Ile Val Leu Arg Ala Asp Ser His Glu Glu Ile Leu Gly Arg Leu Asp 934le Arg Glu Arg Phe Leu Gln Pro Thr Gly Ala Ala Pro Arg Glu 945 956lu Leu Lys Ala Gln Ala Arg Arg Ile Phe Leu Glu Leu Leu Gly 965 97lu Thr Leu Ala Gln Asp Ala Ala Ser Ser Gly Ser Gln Lys Pro Leu 989eu Ser Leu Val Ser Thr Pro Ser Lys Leu Gln Arg Glu Val Glu 995 Ala Ala Lys Gly Ile Pro Arg Cys Leu Lys Met Arg Arg Asp Trp Ser Ser Pro Ala Gly Ser Arg Tyr Ala Pro Glu Pro Leu Ala 3Ser Asp Arg Val Ala Phe Met Tyr Gly Glu Gly Arg Ser Pro Tyr 45 r Gly Ile Thr Gln Asp Ile His Arg Ile Trp

Pro Glu Leu His 6Glu Val Ile Asn Glu Lys Thr Asn Arg Leu Trp Ala Glu Gly Asp 75 g Trp Val Met Pro Arg Ala Ser Phe Lys Ser Glu Leu Glu Ser 9Gln Gln Gln Glu Phe Asp Arg Asn Met Ile Glu Met Phe Arg Leu Gly Ile Leu Thr Ser Ile Ala Phe Thr Asn Leu Ala Arg Asp Val 2Leu Asn Ile Thr Pro Lys Ala Ala Phe Gly Leu Ser Leu Gly Glu 35 e Ser Met Ile Phe Ala Phe Ser Lys Lys Asn Gly Leu Ile Ser 5Asp Gln Leu Thr Lys Asp Leu Arg Glu Ser Asp Val Trp Asn Lys 65 a Leu Ala Val Glu Phe Asn Ala Leu Arg Glu Ala Trp Gly Ile 8Pro Gln Ser Val Pro Lys Asp Glu Phe Trp Gln Gly Tyr Ile Val 95 g Gly Thr Lys Gln Asp Ile Glu Ala Ala Ile Ala Pro Asp Ser Lys Tyr Val Arg Leu Thr Ile Ile Asn Asp Ala Asn Thr Ala Leu 25 e Ser Gly Lys Pro Asp Ala Cys Lys Ala Ala Ile Ala Arg Leu 4Gly Gly Asn Ile Pro Ala Leu Pro Val Thr Gln Gly Met Cys Gly 55 s Cys Pro Glu Val Gly Pro Tyr Thr Lys Asp Ile Ala Lys Ile 7His Ala Asn Leu Glu Phe Pro Val Val Asp Gly Leu Asp Leu Trp 85 r Thr Ile Asn Gln Lys Arg Leu Val Pro Arg Ala Thr Gly Ala Lys Asp Glu Trp Ala Pro Ser Ser Phe Gly Glu Tyr Ala Gly Gln Leu Tyr Glu Lys Gln Ala Asn Phe Pro Gln Ile Val Glu Thr Ile 3Tyr Lys Gln Asn Tyr Asp Val Phe Val Glu Val Gly Pro Asn Asn 45 s Arg Ser Thr Ala Val Arg Thr Thr Leu Gly Pro Gln Arg Asn 6His Leu Ala Gly Ala Ile Asp Lys Gln Asn Glu Asp Ala Trp Thr 75 r Ile Val Lys Leu Val Ala Ser Leu Lys Ala His Leu Val Pro 9Gly Val Thr Ile Ser Pro Leu Tyr His Ser Lys Leu Val Ala Glu Ala Gln Ala Cys Tyr Ala Ala Leu Cys Lys Gly Glu Lys Pro Lys 2Lys Asn Lys Phe Val Arg Lys Ile Gln Leu Asn Gly Arg Phe Asn 35 r Lys Ala Asp Pro Ile Ser Ser Ala Asp Leu Ala Ser Phe Pro 5Pro Ala Asp Pro Ala Ile Glu Ala Ala Ile Ser Ser Arg Ile Met 65 s Pro Val Ala Pro Lys Phe Tyr Ala Arg Leu Asn Ile Asp Glu 8Gln Asp Glu Thr Arg Asp Pro Ile Leu Asn Lys Asp Asn Ala Pro 95 r Ser Ser Ser Ser Ser Ser Ser Ser Ser Ser Ser Ser Ser Ser Pro Ser Pro Ala Pro Ser Ala Pro Val Gln Lys Lys Ala Ala Pro 25 a Ala Glu Thr Lys Ala Val Ala Ser Ala Asp Ala Leu Arg Ser 4Ala Leu Leu Asp Leu Asp Ser Met Leu Ala Leu Ser Ser Ala Ser 55 a Ser Gly Asn Leu Val Glu Thr Ala Pro Ser Asp Ala Ser Val 7Ile Val Pro Pro Cys Asn Ile Ala Asp Leu Gly Ser Arg Ala Phe 85 t Lys Thr Tyr Gly Val Ser Ala Pro Leu Tyr Thr Gly Ala Met Ala Lys Gly Ile Ala Ser Ala Asp Leu Val Ile Ala Ala Gly Arg Gln Gly Ile Leu Ala Ser Phe Gly Ala Gly Gly Leu Pro Met Gln 3Val Val Arg Glu Ser Ile Glu Lys Ile Gln Ala Ala Leu Pro Asn 45 y Pro Tyr Ala Val Asn Leu Ile His Ser Pro Phe Asp Ser Asn 6Leu Glu Lys Gly Asn Val Asp Leu Phe Leu Glu Lys Gly Val Thr 75 e Val Glu Ala Ser Ala Phe Met Thr Leu Thr Pro Gln Val Val 9Arg Tyr Arg Ala Ala Gly Leu Thr Arg Asn Ala Asp Gly Ser Val Asn Ile Arg Asn Arg Ile Ile Gly Lys Val Ser Arg Thr Glu Leu 2Ala Glu Met Phe Met Arg Pro Ala Pro Glu His Leu Leu Gln Lys 35 u Ile Ala Ser Gly Glu Ile Asn Gln Glu Gln Ala Glu Leu Ala 5Arg Arg Val Pro Val Ala Asp Asp Ile Ala Val Glu Ala Asp Ser 65 y Gly His Thr Asp Asn Arg Pro Ile His Val Ile Leu Pro Leu 8Ile Ile Asn Leu Arg Asp Arg Leu His Arg Glu Cys Gly Tyr Pro 95 a Asn Leu Arg Val Arg Val Gly Ala Gly Gly Gly Ile Gly Cys Pro Gln Ala Ala Leu Ala Thr Phe Asn Met Gly Ala Ser Phe Ile 25 l Thr Gly Thr Val Asn Gln Val Ala Lys Gln Ser Gly Thr Cys 4Asp Asn Val Arg Lys Gln Leu Ala Lys Ala Thr Tyr Ser Asp Val 55 s Met Ala Pro Ala Ala Asp Met Phe Glu Glu Gly Val Lys Leu 7Gln Val Leu Lys Lys Gly Thr Met Phe Pro Ser Arg Ala Asn Lys 85 u Tyr Glu Leu Phe Cys Lys Tyr Asp Ser Phe Glu Ser Met Pro Pro Ala Glu Leu Ala Arg Val Glu Lys Arg Ile Phe Ser Arg Ala Leu Glu Glu Val Trp Asp Glu Thr Lys Asn Phe Tyr Ile Asn Arg 3Leu His Asn Pro Glu Lys Ile Gln Arg Ala Glu Arg Asp Pro Lys 45 u Lys Met Ser Leu Cys Phe Arg Trp Tyr Leu Ser Leu Ala Ser 6Arg Trp Ala Asn Thr Gly Ala Ser Asp Arg Val Met Asp Tyr Gln 75 l Trp Cys Gly Pro Ala Ile Gly Ser Phe Asn Asp Phe Ile Lys 9Gly Thr Tyr Leu Asp Pro Ala Val Ala Asn Glu Tyr Pro Cys Val 25 2 Gln Ile Asn Lys Gln Ile Leu Arg Gly Ala Cys Phe Leu Arg 2Arg Leu Glu Ile Leu Arg Asn Ala Arg Leu Ser Asp Gly Ala Ala 25 2 Leu Val Ala Ser Ile Asp Asp Thr Tyr Val Pro Ala Glu Lys 2Leu 5 45Schizochytrium sp. CDS (tg gcg ctc cgt gtc aag acg aac aag aag cca tgc tgg gag atg acc 48 Met Ala Leu Arg Val Lys Thr Asn Lys Lys Pro Cys Trp Glu Met Thr gag gag ctg acc agc ggc aag acc gag gtg ttc aac tat gag gaa 96 Lys Glu Glu Leu Thr Ser Gly Lys Thr Glu Val Phe Asn Tyr Glu Glu 2 ctc ctc gag ttc gca gag ggc gac atc gcc aag gtc ttc gga ccc gag Leu Glu Phe Ala Glu Gly Asp Ile Ala Lys Val Phe Gly Pro Glu 35 4c gcc gtc atc gac aag tac ccg cgc cgc gtg cgc ctg ccc gcc cgc Ala Val Ile Asp Lys Tyr Pro Arg Arg Val Arg Leu Pro Ala Arg 5 gag tac ctg ctc gtg acc cgc gtc acc ctc atg gac gcc gag gtc aac 24yr Leu Leu Val Thr Arg Val Thr Leu Met Asp Ala Glu Val Asn 65 7 aac tac cgc gtc ggc gcc cgc atg gtc acc gag tac gat ctc ccc gtc 288 Asn Tyr Arg Val Gly Ala Arg Met Val Thr Glu Tyr Asp Leu Pro Val 85 9c gga gag ctc tcc gag ggc gga gac tgc ccc tgg gcc gtc ctg gtc 336 Asn Gly Glu Leu Ser Glu Gly Gly Asp Cys Pro Trp Ala Val Leu Val agt ggc cag tgc gat ctc atg ctc atc tcc tac atg ggc att gac 384 Glu Ser Gly Gln Cys Asp Leu Met Leu Ile Ser Tyr Met Gly Ile Asp cag aac cag ggc gac cgc gtc tac cgc ctg ctc aac acc acg ctc 432 Phe Gln Asn Gln Gly Asp Arg Val Tyr Arg Leu Leu Asn Thr Thr Leu ttt tac ggc gtg gcc cac gag ggc gag acc ctc gag tac gac att 48he Tyr Gly Val Ala His Glu Gly Glu Thr Leu Glu Tyr Asp Ile cgc gtc acc ggc ttc gcc aag cgt ctc gac ggc ggc atc tcc atg ttc 528 Arg Val Thr Gly Phe Ala Lys Arg Leu Asp Gly Gly Ile Ser Met Phe ttc gag tac gac tgc tac gtc aac ggc cgc ctc ctc atc gag atg 576 Phe Phe Glu Tyr Asp Cys Tyr Val Asn Gly Arg Leu Leu Ile Glu Met gat ggc tgc gcc ggc ttc ttc acc aac gag gag ctc gac gcc ggc 624 Arg Asp Gly Cys Ala Gly Phe Phe Thr Asn Glu Glu Leu Asp Ala Gly 2ggc gtc gtc ttc acc cgc ggc gac ctc gcc gcc cgc gcc aag atc 672 Lys Gly Val Val Phe Thr Arg Gly Asp Leu Ala Ala Arg Ala Lys Ile 222ag cag gac gtc tcc ccc tac gcc gtc gcc ccc tgc ctc cac aag 72ys Gln Asp Val Ser Pro Tyr Ala Val Ala Pro Cys Leu His Lys 225 234ag ctc aac gaa aag gag atg cag acc ctc gtc gac aag gac tgg 768 Thr Lys Leu Asn Glu Lys Glu Met Gln Thr Leu Val Asp Lys Asp Trp 245 25ca tcc gtc ttt ggc tcc aag aac ggc atg ccg gaa atc aac tac aaa 8Ser Val Phe Gly Ser Lys Asn Gly Met Pro Glu Ile Asn Tyr Lys 267gc gcg cgt aag atg ctc atg att gac cgc gtc acc agc att gac 864 Leu Cys Ala Arg Lys Met Leu Met Ile Asp Arg Val Thr Ser Ile Asp 275 28ac aag ggc ggt gtc tac ggc ctc ggt cag ctc gtc ggt gaa aag atc 9Lys Gly Gly Val Tyr Gly Leu Gly Gln Leu Val Gly Glu Lys Ile 29gag cgc gac cac tgg tac ttt ccc tgc cac ttt gtc aag gat cag 96lu Arg Asp His Trp Tyr Phe Pro Cys His Phe Val Lys Asp Gln 33gtc atg gcc gga tcc ctc gtc tcc gac ggc tgc agc cag atg ctc aag l Met Ala Gly Ser Leu Val Ser Asp Gly Cys Ser Gln Met Leu Lys 325 33tg tac atg atc tgg ctc ggc ctc cac ctc acc acc gga ccc ttt gac t Tyr Met Ile Trp Leu Gly Leu His Leu Thr Thr Gly Pro Phe Asp 345gc ccg gtc aac ggc cac ccc aac aag gtc cgc tgc cgc ggc caa e Arg Pro Val Asn Gly His Pro Asn Lys Val Arg Cys Arg Gly Gln 355 36tc tcc ccg cac aag ggc aag ctc gtc tac gtc atg gag atc aag gag e Ser Pro His Lys Gly Lys Leu Val Tyr Val Met Glu Ile Lys Glu 378gc ttc gac gag gac aac gac ccg tac gcc att gcc gac gtc aac t Gly Phe Asp Glu Asp Asn Asp Pro Tyr Ala Ile Ala Asp Val Asn 385 39att gat gtc gac ttc gaa aag ggc cag gac ttt agc ctc gac cgc e Ile Asp Val Asp Phe Glu Lys Gly Gln Asp Phe Ser Leu Asp Arg 44agc gac tac ggc aag ggc gac ctc aac aag aag atc gtc gtc gac e Ser Asp Tyr Gly Lys Gly Asp Leu Asn Lys Lys Ile Val Val Asp 423ag ggc atc gct ctc aag atg cag aag cgc tcc acc aac aag aac e Lys Gly Ile Ala Leu Lys Met Gln Lys Arg Ser Thr Asn Lys Asn 435 44cc tcc aag gtt cag ccc gtc ttt gcc aac ggc gcc gcc act gtc ggc o Ser Lys Val Gln Pro Val Phe Ala Asn Gly Ala Ala Thr Val Gly 456ag gcc tcc aag gct tcc tcc ggc gcc agc gcc agc gcc agc gcc o Glu Ala Ser Lys Ala Ser Ser Gly Ala Ser Ala Ser Ala Ser Ala 465 478cg gcc aag cct gcc ttc agc gcc gat gtt ctt gcg ccc aag ccc a Pro Ala Lys Pro Ala Phe Ser Ala Asp Val Leu Ala Pro Lys Pro 485 49tt gcc ctt ccc gag cac atc ctc aag ggc gac gcc ctc gcc ccc aag l Ala Leu Pro Glu His Ile Leu Lys Gly Asp Ala Leu Ala Pro Lys 55atg tcc tgg cac ccc atg gcc cgc atc ccg ggc aac ccg acg ccc u Met Ser Trp His Pro Met Ala Arg Ile Pro Gly Asn Pro Thr Pro 5525 tct ttt gcg ccc tcg gcc tac aag ccg cgc aac atc gcc ttt acg ccc r Phe Ala Pro Ser Ala Tyr Lys Pro Arg Asn Ile Ala Phe Thr Pro 534cc ggc aac ccc aac gat aac gac cac acc ccg ggc aag atg ccg e Pro Gly Asn Pro Asn Asp Asn Asp His Thr Pro Gly Lys Met Pro 545 556cc tgg ttc aac atg gcc gag ttc atg gcc ggc aag gtc agc atg u Thr Trp Phe Asn Met Ala Glu Phe Met Ala Gly Lys Val Ser Met 565 57gc ctc ggc ccc gag ttc gcc aag ttc gac gac tcg aac acc agc cgc s Leu Gly Pro Glu Phe Ala Lys Phe Asp Asp Ser Asn Thr Ser Arg 589cc gct tgg gac ctc gct ctc gtc acc cgc gcc gtg tct gtg tct r Pro Ala Trp Asp Leu Ala Leu Val Thr Arg Ala Val Ser Val Ser 595 6gac ctc aag cac gtc aac tac cgc aac atc gac ctc gac ccc tcc aag p Leu Lys His Val Asn Tyr Arg Asn Ile Asp Leu Asp Pro Ser Lys 662cc atg gtc ggc gag ttc gac tgc ccc gcg gac gcc tgg ttc tac y Thr Met Val Gly Glu Phe Asp Cys Pro Ala Asp Ala Trp Phe Tyr 625 634gc gcc tgc aac gat gcc cac atg ccg tac tcg atc ctc atg gag s Gly Ala Cys Asn Asp Ala His Met Pro Tyr Ser Ile Leu Met Glu 645 65tc gcc ctc cag acc tcg ggt gtg ctc acc tcg gtg ctc aag gcg ccc 2 Ala Leu Gln Thr Ser Gly Val Leu Thr Ser Val Leu Lys Ala Pro 667cc atg gag aag gac gac atc ctc ttc cgc aac ctc gac gcc aac 2 Thr Met Glu Lys Asp Asp Ile Leu Phe Arg Asn Leu Asp Ala Asn 675 68cc gag ttc gtg cgc gcc gac ctc gac tac cgc ggc aag act atc cgc 2 Glu Phe Val Arg Ala Asp Leu Asp Tyr Arg Gly Lys Thr Ile Arg 69gtc acc aag tgc act ggc tac agc atg ctc ggc gag atg ggc gtc 2 Val Thr Lys Cys Thr Gly Tyr Ser Met Leu Gly Glu Met Gly Val 77cac cgc ttc acc ttt gag ctc tac gtc gat gat gtg ctc ttt tac aag 22Arg Phe Thr Phe Glu Leu Tyr Val Asp Asp Val Leu Phe Tyr Lys 725 73gc tcg acc tcg ttc ggc tgg ttc gtg ccc gag gtc ttt gcc gcc cag 2256 Gly Ser Thr Ser Phe Gly Trp Phe Val Pro Glu Val Phe Ala Ala Gln 745gc ctc gac aac ggc cgc aag tcg gag ccc tgg ttc att gag aac 23Gly Leu Asp Asn Gly Arg Lys Ser Glu Pro Trp Phe Ile Glu Asn 755 76ag gtt ccg gcc tcg cag gtc tcc tcc ttt gac gtg cgc ccc aac ggc 2352 Lys Val Pro Ala Ser Gln Val Ser Ser Phe Asp Val Arg Pro Asn Gly 778gc cgc acc gcc atc ttc gcc aac gcc ccc agc ggc gcc cag ctc 24Gly Arg Thr Ala Ile Phe Ala Asn Ala Pro Ser Gly Ala Gln Leu 785 79cgc cgc acg gac cag ggc cag tac ctc gac gcc gtc gac att gtc 2448 Asn Arg Arg Thr Asp Gln Gly Gln Tyr Leu Asp Ala Val Asp Ile Val 88ggc agc ggc aag aag agc ctc ggc tac gcc cac ggt tcc aag acg 2496 Ser Gly Ser Gly Lys Lys Ser Leu Gly Tyr Ala His Gly Ser Lys Thr 823ac ccg aac gac tgg ttc ttc tcg tgc cac ttt tgg ttt gac tcg 2544 Val Asn Pro Asn Asp Trp Phe Phe Ser Cys His Phe Trp Phe Asp Ser 835 84tc atg ccc gga agt ctc ggt gtc gag tcc atg ttc cag ctc gtc gag 2592 Val Met Pro Gly Ser Leu Gly Val Glu Ser Met Phe Gln Leu Val Glu 856tc gcc gcc cac gag gat ctc gct ggc aaa gca cgg cat tgc caa 264le Ala Ala His Glu Asp Leu Ala Gly Lys Ala Arg His Cys Gln 865 878ac ctt tgt gca cgc ccc

cgg gca aga tca agc tgg aag tac cgc 2688 Pro His Leu Cys Ala Arg Pro Arg Ala Arg Ser Ser Trp Lys Tyr Arg 885 89gc cag ctc acg ccc aag agc aag aag atg gac tcg gag gtc cac atc 2736 Gly Gln Leu Thr Pro Lys Ser Lys Lys Met Asp Ser Glu Val His Ile 99tcc gtg gac gcc cac gac ggc gtt gtc gac ctc gtc gcc gac ggc 2784 Val Ser Val Asp Ala His Asp Gly Val Val Asp Leu Val Ala Asp Gly 9925 ttc ctc tgg gcc gac agc ctc cgc gtc tac tcg gtg agc aac att cgc 2832 Phe Leu Trp Ala Asp Ser Leu Arg Val Tyr Ser Val Ser Asn Ile Arg 934gc atc gcc tcc ggt gag gcc cct gcc gcc gcc tcc tcc gcc gcc 288rg Ile Ala Ser Gly Glu Ala Pro Ala Ala Ala Ser Ser Ala Ala 945 956tg ggc tcc tcg gct tcg tcc gtc gag cgc acg cgc tcg agc ccc 2928 Ser Val Gly Ser Ser Ala Ser Ser Val Glu Arg Thr Arg Ser Ser Pro 965 97ct gtc gcc tcc ggc ccg gcc cag acc atc gac ctc aag cag ctc aag 2976 Ala Val Ala Ser Gly Pro Ala Gln Thr Ile Asp Leu Lys Gln Leu Lys 989ag ctc ctc gag ctc gat gcc ccg ctc tac ctc tcg cag gac ccg 3 Glu Leu Leu Glu Leu Asp Ala Pro Leu Tyr Leu Ser Gln Asp Pro 995 agc ggc cag ctc aag aag cac acc gac gtg gcc tcc ggc cag 3 Ser Gly Gln Leu Lys Lys His Thr Asp Val Ala Ser Gly Gln gcc acc atc gtg cag ccc tgc acg ctc ggc gac ctc ggt gac cgc 3 Thr Ile Val Gln Pro Cys Thr Leu Gly Asp Leu Gly Asp Arg 3tcc ttc atg gag acc tac ggc gtc gtc gcc ccg ctg tac acg ggc 3 Phe Met Glu Thr Tyr Gly Val Val Ala Pro Leu Tyr Thr Gly 45 c atg gcc aag ggc att gcc tcg gcg gac ctc gtc atc gcc gcc 32Met Ala Lys Gly Ile Ala Ser Ala Asp Leu Val Ile Ala Ala 6ggc aag cgc aag atc ctc ggc tcc ttt ggc gcc ggc ggc ctc ccc 3249 Gly Lys Arg Lys Ile Leu Gly Ser Phe Gly Ala Gly Gly Leu Pro 75 g cac cac gtg cgc gcc gcc ctc gag aag atc cag gcc gcc ctg 3294 Met His His Val Arg Ala Ala Leu Glu Lys Ile Gln Ala Ala Leu 9cct cag ggc ccc tac gcc gtc aac ctc atc cac tcg cct ttt gac 3339 Pro Gln Gly Pro Tyr Ala Val Asn Leu Ile His Ser Pro Phe Asp agc aac ctc gag aag ggc aac gtc gat ctc ttc ctc gag aag ggc 3384 Ser Asn Leu Glu Lys Gly Asn Val Asp Leu Phe Leu Glu Lys Gly 2gtc act gtg gtg gag gcc tcg gca ttc atg acc ctc acc ccg cag 3429 Val Thr Val Val Glu Ala Ser Ala Phe Met Thr Leu Thr Pro Gln 35 c gtg cgc tac cgc gcc gcc ggc ctc tcg cgc aac gcc gac ggt 3474 Val Val Arg Tyr Arg Ala Ala Gly Leu Ser Arg Asn Ala Asp Gly 5tcg gtc aac atc cgc aac cgc atc atc ggc aag gtc tcg cgc acc 35Val Asn Ile Arg Asn Arg Ile Ile Gly Lys Val Ser Arg Thr 65 g ctc gcc gag atg ttc atc cgc ccg gcc ccg gag cac ctc ctc 3564 Glu Leu Ala Glu Met Phe Ile Arg Pro Ala Pro Glu His Leu Leu 8gag aag ctc atc gcc tcg ggc gag atc acc cag gag cag gcc gag 36Lys Leu Ile Ala Ser Gly Glu Ile Thr Gln Glu Gln Ala Glu 95 c gcg cgc cgc gtt ccc gtc gcc gac gat atc gct gtc gag gct 3654 Leu Ala Arg Arg Val Pro Val Ala Asp Asp Ile Ala Val Glu Ala gac tcg ggc ggc cac acc gac aac cgc ccc atc cac gtc atc ctc 3699 Asp Ser Gly Gly His Thr Asp Asn Arg Pro Ile His Val Ile Leu 25 g ctc atc atc aac ctc cgc aac cgc ctg cac cgc gag tgc ggc 3744 Pro Leu Ile Ile Asn Leu Arg Asn Arg Leu His Arg Glu Cys Gly 4tac ccc gcg cac ctc cgc gtc cgc gtt ggc gcc ggc ggt ggc gtc 3789 Tyr Pro Ala His Leu Arg Val Arg Val Gly Ala Gly Gly Gly Val 55 c tgc ccg cag gcc gcc gcc gcc gcg ctc acc atg ggc gcc gcc 3834 Gly Cys Pro Gln Ala Ala Ala Ala Ala Leu Thr Met Gly Ala Ala 7ttc atc gtc acc ggc act gtc aac cag gtc gcc aag cag tcc ggc 3879 Phe Ile Val Thr Gly Thr Val Asn Gln Val Ala Lys Gln Ser Gly 85 c tgc gac aac gtg cgc aag cag ctc tcg cag gcc acc tac tcg 3924 Thr Cys Asp Asn Val Arg Lys Gln Leu Ser Gln Ala Thr Tyr Ser gat atc tgc atg gcc ccg gcc gcc gac atg ttc gag gag ggc gtc 3969 Asp Ile Cys Met Ala Pro Ala Ala Asp Met Phe Glu Glu Gly Val aag ctc cag gtc ctc aag aag gga acc atg ttc ccc tcg cgc gcc 4 Leu Gln Val Leu Lys Lys Gly Thr Met Phe Pro Ser Arg Ala 3aac aag ctc tac gag ctc ttt tgc aag tac gac tcc ttc gac tcc 4 Lys Leu Tyr Glu Leu Phe Cys Lys Tyr Asp Ser Phe Asp Ser 45 g cct cct gcc gag ctc gag cgc atc gag aag cgt atc ttc aag 4 Pro Pro Ala Glu Leu Glu Arg Ile Glu Lys Arg Ile Phe Lys 6cgc gca ctc cag gag gtc tgg gag gag acc aag gac ttt tac att 4 Ala Leu Gln Glu Val Trp Glu Glu Thr Lys Asp Phe Tyr Ile 75 c ggt ctc aag aac ccg gag aag atc cag cgc gcc gag cac gac 4 Gly Leu Lys Asn Pro Glu Lys Ile Gln Arg Ala Glu His Asp 9ccc aag ctc aag atg tcg ctc tgc ttc cgc tgg tac ctt ggt ctt 4239 Pro Lys Leu Lys Met Ser Leu Cys Phe Arg Trp Tyr Leu Gly Leu gcc agc cgc tgg gcc aac atg ggc gcc ccg gac cgc gtc atg gac 4284 Ala Ser Arg Trp Ala Asn Met Gly Ala Pro Asp Arg Val Met Asp 2tac cag gtc tgg tgt ggc ccg gcc att ggc gcc ttc aac gac ttc 4329 Tyr Gln Val Trp Cys Gly Pro Ala Ile Gly Ala Phe Asn Asp Phe 35 c aag ggc acc tac ctc gac ccc gct gtc tcc aac gag tac ccc 4374 Ile Lys Gly Thr Tyr Leu Asp Pro Ala Val Ser Asn Glu Tyr Pro 5tgt gtc gtc cag atc aac ctg caa atc ctc cgt ggt gcc tgc tac 44Val Val Gln Ile Asn Leu Gln Ile Leu Arg Gly Ala Cys Tyr 65 g cgc cgt ctc aac gcc ctg cgc aac gac ccg cgc att gac ctc 4464 Leu Arg Arg Leu Asn Ala Leu Arg Asn Asp Pro Arg Ile Asp Leu 8gag acc gag gat gct gcc ttt gtc tac gag ccc acc aac gcg ctc 45Thr Glu Asp Ala Ala Phe Val Tyr Glu Pro Thr Asn Ala Leu 95 T Schizochytrium sp. 6 Met Ala Leu Arg Val Lys Thr Asn Lys Lys Pro Cys Trp Glu Met Thr Glu Glu Leu Thr Ser Gly Lys Thr Glu Val Phe Asn Tyr Glu Glu 2 Leu Leu Glu Phe Ala Glu Gly Asp Ile Ala Lys Val Phe Gly Pro Glu 35 4e Ala Val Ile Asp Lys Tyr Pro Arg Arg Val Arg Leu Pro Ala Arg 5 Glu Tyr Leu Leu Val Thr Arg Val Thr Leu Met Asp Ala Glu Val Asn 65 7 Asn Tyr Arg Val Gly Ala Arg Met Val Thr Glu Tyr Asp Leu Pro Val 85 9n Gly Glu Leu Ser Glu Gly Gly Asp Cys Pro Trp Ala Val Leu Val Ser Gly Gln Cys Asp Leu Met Leu Ile Ser Tyr Met Gly Ile Asp Gln Asn Gln Gly Asp Arg Val Tyr Arg Leu Leu Asn Thr Thr Leu Phe Tyr Gly Val Ala His Glu Gly Glu Thr Leu Glu Tyr Asp Ile Arg Val Thr Gly Phe Ala Lys Arg Leu Asp Gly Gly Ile Ser Met Phe Phe Glu Tyr Asp Cys Tyr Val Asn Gly Arg Leu Leu Ile Glu Met Asp Gly Cys Ala Gly Phe Phe Thr Asn Glu Glu Leu Asp Ala Gly 2Gly Val Val Phe Thr Arg Gly Asp Leu Ala Ala Arg Ala Lys Ile 222ys Gln Asp Val Ser Pro Tyr Ala Val Ala Pro Cys Leu His Lys 225 234ys Leu Asn Glu Lys Glu Met Gln Thr Leu Val Asp Lys Asp Trp 245 25la Ser Val Phe Gly Ser Lys Asn Gly Met Pro Glu Ile Asn Tyr Lys 267ys Ala Arg Lys Met Leu Met Ile Asp Arg Val Thr Ser Ile Asp 275 28is Lys Gly Gly Val Tyr Gly Leu Gly Gln Leu Val Gly Glu Lys Ile 29Glu Arg Asp His Trp Tyr Phe Pro Cys His Phe Val Lys Asp Gln 33Val Met Ala Gly Ser Leu Val Ser Asp Gly Cys Ser Gln Met Leu Lys 325 33et Tyr Met Ile Trp Leu Gly Leu His Leu Thr Thr Gly Pro Phe Asp 345rg Pro Val Asn Gly His Pro Asn Lys Val Arg Cys Arg Gly Gln 355 36le Ser Pro His Lys Gly Lys Leu Val Tyr Val Met Glu Ile Lys Glu 378ly Phe Asp Glu Asp Asn Asp Pro Tyr Ala Ile Ala Asp Val Asn 385 39Ile Asp Val Asp Phe Glu Lys Gly Gln Asp Phe Ser Leu Asp Arg 44Ser Asp Tyr Gly Lys Gly Asp Leu Asn Lys Lys Ile Val Val Asp 423ys Gly Ile Ala Leu Lys Met Gln Lys Arg Ser Thr Asn Lys Asn 435 44ro Ser Lys Val Gln Pro Val Phe Ala Asn Gly Ala Ala Thr Val Gly 456lu Ala Ser Lys Ala Ser Ser Gly Ala Ser Ala Ser Ala Ser Ala 465 478ro Ala Lys Pro Ala Phe Ser Ala Asp Val Leu Ala Pro Lys Pro 485 49al Ala Leu Pro Glu His Ile Leu Lys Gly Asp Ala Leu Ala Pro Lys 55Met Ser Trp His Pro Met Ala Arg Ile Pro Gly Asn Pro Thr Pro 5525 Ser Phe Ala Pro Ser Ala Tyr Lys Pro Arg Asn Ile Ala Phe Thr Pro 534ro Gly Asn Pro Asn Asp Asn Asp His Thr Pro Gly Lys Met Pro 545 556hr Trp Phe Asn Met Ala Glu Phe Met Ala Gly Lys Val Ser Met 565 57ys Leu Gly Pro Glu Phe Ala Lys Phe Asp Asp Ser Asn Thr Ser Arg 589ro Ala Trp Asp Leu Ala Leu Val Thr Arg Ala Val Ser Val Ser 595 6Asp Leu Lys His Val Asn Tyr Arg Asn Ile Asp Leu Asp Pro Ser Lys 662hr Met Val Gly Glu Phe Asp Cys Pro Ala Asp Ala Trp Phe Tyr 625 634ly Ala Cys Asn Asp Ala His Met Pro Tyr Ser Ile Leu Met Glu 645 65le Ala Leu Gln Thr Ser Gly Val Leu Thr Ser Val Leu Lys Ala Pro 667hr Met Glu Lys Asp Asp Ile Leu Phe Arg Asn Leu Asp Ala Asn 675 68la Glu Phe Val Arg Ala Asp Leu Asp Tyr Arg Gly Lys Thr Ile Arg 69Val Thr Lys Cys Thr Gly Tyr Ser Met Leu Gly Glu Met Gly Val 77His Arg Phe Thr Phe Glu Leu Tyr Val Asp Asp Val Leu Phe Tyr Lys 725 73ly Ser Thr Ser Phe Gly Trp Phe Val Pro Glu Val Phe Ala Ala Gln 745ly Leu Asp Asn Gly Arg Lys Ser Glu Pro Trp Phe Ile Glu Asn 755 76ys Val Pro Ala Ser Gln Val Ser Ser Phe Asp Val Arg Pro Asn Gly 778ly Arg Thr Ala Ile Phe Ala Asn Ala Pro Ser Gly Ala Gln Leu 785 79Arg Arg Thr Asp Gln Gly Gln Tyr Leu Asp Ala Val Asp Ile Val 88Gly Ser Gly Lys Lys Ser Leu Gly Tyr Ala His Gly Ser Lys Thr 823sn Pro Asn Asp Trp Phe Phe Ser Cys His Phe Trp Phe Asp Ser 835 84al Met Pro Gly Ser Leu Gly Val Glu Ser Met Phe Gln Leu Val Glu 856le Ala Ala His Glu Asp Leu Ala Gly Lys Ala Arg His Cys Gln 865 878is Leu Cys Ala Arg Pro Arg Ala Arg Ser Ser Trp Lys Tyr Arg 885 89ly Gln Leu Thr Pro Lys Ser Lys Lys Met Asp Ser Glu Val His Ile 99Ser Val Asp Ala His Asp Gly Val Val Asp Leu Val Ala Asp Gly 9925 Phe Leu Trp Ala Asp Ser Leu Arg Val Tyr Ser Val Ser Asn Ile Arg 934rg Ile Ala Ser Gly Glu Ala Pro Ala Ala Ala Ser Ser Ala Ala 945 956al Gly Ser Ser Ala Ser Ser Val Glu Arg Thr Arg Ser Ser Pro 965 97la Val Ala Ser Gly Pro Ala Gln Thr Ile Asp Leu Lys Gln Leu Lys 989lu Leu Leu Glu Leu Asp Ala Pro Leu Tyr Leu Ser Gln Asp Pro 995 Ser Gly Gln Leu Lys Lys His Thr Asp Val Ala Ser Gly Gln Ala Thr Ile Val Gln Pro Cys Thr Leu Gly Asp Leu Gly Asp Arg 3Ser Phe Met Glu Thr Tyr Gly Val Val Ala Pro Leu Tyr Thr Gly 45 a Met Ala Lys Gly Ile Ala Ser Ala Asp Leu Val Ile Ala Ala 6Gly Lys Arg Lys Ile Leu Gly Ser Phe Gly Ala Gly Gly Leu Pro 75 t His His Val Arg Ala Ala Leu Glu Lys Ile Gln Ala Ala Leu 9Pro Gln Gly Pro Tyr Ala Val Asn Leu Ile His Ser Pro Phe Asp Ser Asn Leu Glu Lys Gly Asn Val Asp Leu Phe Leu Glu Lys Gly 2Val Thr Val Val Glu Ala Ser Ala Phe Met Thr Leu Thr Pro Gln 35 l Val Arg Tyr Arg Ala Ala Gly Leu Ser Arg Asn Ala Asp Gly 5Ser Val Asn Ile Arg Asn Arg Ile Ile Gly Lys Val Ser Arg Thr 65 u Leu Ala Glu Met Phe Ile Arg Pro Ala Pro Glu His Leu Leu 8Glu Lys Leu Ile Ala Ser Gly Glu Ile Thr Gln Glu Gln Ala Glu 95 u Ala Arg Arg Val Pro Val Ala Asp Asp Ile Ala Val Glu Ala Asp Ser Gly Gly His Thr Asp Asn Arg Pro Ile His Val Ile Leu 25 o Leu Ile Ile Asn Leu Arg Asn Arg Leu His Arg Glu Cys Gly 4Tyr Pro Ala His Leu Arg Val Arg Val Gly Ala Gly Gly Gly Val 55 y Cys Pro Gln Ala Ala Ala Ala Ala Leu Thr Met Gly Ala Ala 7Phe Ile Val Thr Gly Thr Val Asn Gln Val Ala Lys Gln Ser Gly 85 r Cys Asp Asn Val Arg Lys Gln Leu Ser Gln Ala Thr Tyr Ser Asp Ile Cys Met Ala Pro Ala Ala Asp Met Phe Glu Glu Gly Val Lys Leu Gln Val Leu Lys Lys Gly Thr Met Phe Pro Ser Arg Ala 3Asn Lys Leu Tyr Glu Leu Phe Cys Lys Tyr Asp Ser Phe Asp Ser 45 t Pro Pro Ala Glu Leu Glu Arg Ile Glu Lys Arg Ile Phe Lys 6Arg Ala Leu Gln Glu Val Trp Glu Glu Thr Lys Asp Phe Tyr Ile 75 n Gly Leu Lys Asn Pro Glu Lys Ile Gln Arg Ala Glu His Asp 9Pro Lys Leu Lys Met Ser Leu Cys Phe Arg Trp Tyr Leu Gly

Leu Ala Ser Arg Trp Ala Asn Met Gly Ala Pro Asp Arg Val Met Asp 2Tyr Gln Val Trp Cys Gly Pro Ala Ile Gly Ala Phe Asn Asp Phe 35 e Lys Gly Thr Tyr Leu Asp Pro Ala Val Ser Asn Glu Tyr Pro 5Cys Val Val Gln Ile Asn Leu Gln Ile Leu Arg Gly Ala Cys Tyr 65 u Arg Arg Leu Asn Ala Leu Arg Asn Asp Pro Arg Ile Asp Leu 8Glu Thr Glu Asp Ala Ala Phe Val Tyr Glu Pro Thr Asn Ala Leu 95 6Schizochytrium sp. CDS (g gcg gcc cgt ctg cag gag caa aag gga ggc gag atg gat acc cgc 48 Met Ala Ala Arg Leu Gln Glu Gln Lys Gly Gly Glu Met Asp Thr Arg gcc atc atc ggc atg tcg gcc atc ctc ccc tgc ggc acg acc gtg 96 Ile Ala Ile Ile Gly Met Ser Ala Ile Leu Pro Cys Gly Thr Thr Val 2 cgc gag tcg tgg gag acc atc cgc gcc ggc atc gac tgc ctg tcg gat Glu Ser Trp Glu Thr Ile Arg Ala Gly Ile Asp Cys Leu Ser Asp 35 4c ccc gag gac cgc gtc gac gtg acg gcg tac ttt gac ccc gtc aag Pro Glu Asp Arg Val Asp Val Thr Ala Tyr Phe Asp Pro Val Lys 5 acc acc aag gac aag atc tac tgc aag cgc ggt ggc ttc att ccc gag 24hr Lys Asp Lys Ile Tyr Cys Lys Arg Gly Gly Phe Ile Pro Glu 65 7 tac gac ttt gac gcc cgc gag ttc gga ctc aac atg ttc cag atg gag 288 Tyr Asp Phe Asp Ala Arg Glu Phe Gly Leu Asn Met Phe Gln Met Glu 85 9c tcg gac gca aac cag acc atc tcg ctt ctc aag gtc aag gag gcc 336 Asp Ser Asp Ala Asn Gln Thr Ile Ser Leu Leu Lys Val Lys Glu Ala cag gac gcc ggc atc gac gcc ctc ggc aag gaa aag aag aac atc 384 Leu Gln Asp Ala Gly Ile Asp Ala Leu Gly Lys Glu Lys Lys Asn Ile tgc gtg ctc ggc att ggc ggc ggc caa aag tcc agc cac gag ttc 432 Gly Cys Val Leu Gly Ile Gly Gly Gly Gln Lys Ser Ser His Glu Phe tcg cgc ctt aat tat gtt gtc gtg gag aag gtc ctc cgc aag atg 48er Arg Leu Asn Tyr Val Val Val Glu Lys Val Leu Arg Lys Met ggc atg ccc gag gag gac gtc aag gtc gcc gtc gaa aag tac aag gcc 528 Gly Met Pro Glu Glu Asp Val Lys Val Ala Val Glu Lys Tyr Lys Ala ttc ccc gag tgg cgc ctc gac tcc ttc cct ggc ttc ctc ggc aac 576 Asn Phe Pro Glu Trp Arg Leu Asp Ser Phe Pro Gly Phe Leu Gly Asn acc gcc ggt cgc tgc acc aac 6Thr Ala Gly Arg Cys Thr Asn 8 2Schizochytrium sp. 8 Met Ala Ala Arg Leu Gln Glu Gln Lys Gly Gly Glu Met Asp Thr Arg Ala Ile Ile Gly Met Ser Ala Ile Leu Pro Cys Gly Thr Thr Val 2 Arg Glu Ser Trp Glu Thr Ile Arg Ala Gly Ile Asp Cys Leu Ser Asp 35 4u Pro Glu Asp Arg Val Asp Val Thr Ala Tyr Phe Asp Pro Val Lys 5 Thr Thr Lys Asp Lys Ile Tyr Cys Lys Arg Gly Gly Phe Ile Pro Glu 65 7 Tyr Asp Phe Asp Ala Arg Glu Phe Gly Leu Asn Met Phe Gln Met Glu 85 9p Ser Asp Ala Asn Gln Thr Ile Ser Leu Leu Lys Val Lys Glu Ala Gln Asp Ala Gly Ile Asp Ala Leu Gly Lys Glu Lys Lys Asn Ile Cys Val Leu Gly Ile Gly Gly Gly Gln Lys Ser Ser His Glu Phe Ser Arg Leu Asn Tyr Val Val Val Glu Lys Val Leu Arg Lys Met Gly Met Pro Glu Glu Asp Val Lys Val Ala Val Glu Lys Tyr Lys Ala Phe Pro Glu Trp Arg Leu Asp Ser Phe Pro Gly Phe Leu Gly Asn Thr Ala Gly Arg Cys Thr Asn 9 A Schizochytrium sp. CDS (78) 9 gat gtc acc aag gag gcc tgg cgc ctc ccc cgc gag ggc gtc agc ttc 48 Asp Val Thr Lys Glu Ala Trp Arg Leu Pro Arg Glu Gly Val Ser Phe gcc aag ggc atc gcc acc aac ggc gct gtc gcc gcg ctc ttc tcc 96 Arg Ala Lys Gly Ile Ala Thr Asn Gly Ala Val Ala Ala Leu Phe Ser 2 ggc cag ggc gcg cag tac acg cac atg ttt agc gag gtg gcc atg aac Gln Gly Ala Gln Tyr Thr His Met Phe Ser Glu Val Ala Met Asn 35 4g ccc cag ttc cgc cag agc att gcc gcc atg gac gcc gcc cag tcc Pro Gln Phe Arg Gln Ser Ile Ala Ala Met Asp Ala Ala Gln Ser 5 aag gtc gct gga agc gac aag gac ttt gag cgc gtc tcc cag gtc ctc 24al Ala Gly Ser Asp Lys Asp Phe Glu Arg Val Ser Gln Val Leu 65 7 tac ccg cgc aag ccg tac gag cgt gag ccc gag cag aac ccc aag aag 288 Tyr Pro Arg Lys Pro Tyr Glu Arg Glu Pro Glu Gln Asn Pro Lys Lys 85 9c tcc ctc acc gcc tac tcg cag ccc tcg acc ctg gcc tgc gct ctc 336 Ile Ser Leu Thr Ala Tyr Ser Gln Pro Ser Thr Leu Ala Cys Ala Leu gcc ttt gag atc ttc aag gag gcc ggc ttc acc ccg gac ttt gcc 384 Gly Ala Phe Glu Ile Phe Lys Glu Ala Gly Phe Thr Pro Asp Phe Ala ggc cat tcg ctc ggt gag ttc gcc gcc ctc tac gcc gcg ggc tgc 432 Ala Gly His Ser Leu Gly Glu Phe Ala Ala Leu Tyr Ala Ala Gly Cys gac cgc gac gag ctc ttt gag ctt gtc tgc cgc cgc gcc cgc atc 48sp Arg Asp Glu Leu Phe Glu Leu Val Cys Arg Arg Ala Arg Ile atg ggc ggc aag gac gca ccg gcc acc ccc aag gga tgc atg gcc gcc 528 Met Gly Gly Lys Asp Ala Pro Ala Thr Pro Lys Gly Cys Met Ala Ala att ggc ccc aac gcc gag aac atc aag gtc cag gcc gcc aac gtc 576 Val Ile Gly Pro Asn Ala Glu Asn Ile Lys Val Gln Ala Ala Asn Val ctc ggc aac tcc aac tcg cct tcg cag acc gtc atc acc ggc tcc 624 Trp Leu Gly Asn Ser Asn Ser Pro Ser Gln Thr Val Ile Thr Gly Ser 2gaa ggt atc cag gcc gag agc gcc cgc ctc cag aag gag ggc ttc 672 Val Glu Gly Ile Gln Ala Glu Ser Ala Arg Leu Gln Lys Glu Gly Phe 222tc gtg cct ctt gcc tgc gag agc gcc ttc cac tcg ccc cag atg 72al Val Pro Leu Ala Cys Glu Ser Ala Phe His Ser Pro Gln Met 225 234ac gcc tcg tcg gcc ttc aag gac gtc atc tcc aag gtc tcc ttc 768 Glu Asn Ala Ser Ser Ala Phe Lys Asp Val Ile Ser Lys Val Ser Phe 245 25gc acc ccc aag gcc gag acc aag ctc ttc agc aac gtc tct ggc gag 8Thr Pro Lys Ala Glu Thr Lys Leu Phe Ser Asn Val Ser Gly Glu 267ac ccc acg gac gcc cgc gag atg ctt acg cag cac atg acc agc 864 Thr Tyr Pro Thr Asp Ala Arg Glu Met Leu Thr Gln His Met Thr Ser 275 28gc gtc aag ttc ctc acc cag gtc cgc aac atg cac cag gcc ggt gcg 9Val Lys Phe Leu Thr Gln Val Arg Asn Met His Gln Ala Gly Ala 29atc ttt gtc gag ttc gga ccc aag cag gtg ctc tcc aag ctt gtc 96le Phe Val Glu Phe Gly Pro Lys Gln Val Leu Ser Lys Leu Val 33tcc gag acc ctc aag gat gac ccc tcg gtt gtc acc gtc tct gtc aac r Glu Thr Leu Lys Asp Asp Pro Ser Val Val Thr Val Ser Val Asn 325 33cg gcc tcg ggc acg gat tcg gac atc cag ctc cgc gac gcg gcc gtc o Ala Ser Gly Thr Asp Ser Asp Ile Gln Leu Arg Asp Ala Ala Val 345tc gtt gtc gct ggc gtc aac ctt cag ggc ttt gac aag tgg gac n Leu Val Val Ala Gly Val Asn Leu Gln Gly Phe Asp Lys Trp Asp 355 36cc ccc gat gcc acc cgc atg cag gcc atc aag aag aag cgc act acc a Pro Asp Ala Thr Arg Met Gln Ala Ile Lys Lys Lys Arg Thr Thr 378gc ctt tcg gcc gcc acc tac gtc tcg gac aag acc aag aag gtc u Arg Leu Ser Ala Ala Thr Tyr Val Ser Asp Lys Thr Lys Lys Val 385 39gac gcc gcc atg aac gat ggc cgc tgc gtc acc tac ctc aag ggc g Asp Ala Ala Met Asn Asp Gly Arg Cys Val Thr Tyr Leu Lys Gly 44gca ccg ctc atc aag gcc ccg gag ccc a Ala Pro Leu Ile Lys Ala Pro Glu Pro 42RT Schizochytrium sp. Val Thr Lys Glu Ala Trp Arg Leu Pro Arg Glu Gly Val Ser Phe Ala Lys Gly Ile Ala Thr Asn Gly Ala Val Ala Ala Leu Phe Ser 2 Gly Gln Gly Ala Gln Tyr Thr His Met Phe Ser Glu Val Ala Met Asn 35 4p Pro Gln Phe Arg Gln Ser Ile Ala Ala Met Asp Ala Ala Gln Ser 5 Lys Val Ala Gly Ser Asp Lys Asp Phe Glu Arg Val Ser Gln Val Leu 65 7 Tyr Pro Arg Lys Pro Tyr Glu Arg Glu Pro Glu Gln Asn Pro Lys Lys 85 9e Ser Leu Thr Ala Tyr Ser Gln Pro Ser Thr Leu Ala Cys Ala Leu Ala Phe Glu Ile Phe Lys Glu Ala Gly Phe Thr Pro Asp Phe Ala Gly His Ser Leu Gly Glu Phe Ala Ala Leu Tyr Ala Ala Gly Cys Asp Arg Asp Glu Leu Phe Glu Leu Val Cys Arg Arg Ala Arg Ile Met Gly Gly Lys Asp Ala Pro Ala Thr Pro Lys Gly Cys Met Ala Ala Ile Gly Pro Asn Ala Glu Asn Ile Lys Val Gln Ala Ala Asn Val Leu Gly Asn Ser Asn Ser Pro Ser Gln Thr Val Ile Thr Gly Ser 2Glu Gly Ile Gln Ala Glu Ser Ala Arg Leu Gln Lys Glu Gly Phe 222al Val Pro Leu Ala Cys Glu Ser Ala Phe His Ser Pro Gln Met 225 234sn Ala Ser Ser Ala Phe Lys Asp Val Ile Ser Lys Val Ser Phe 245 25rg Thr Pro Lys Ala Glu Thr Lys Leu Phe Ser Asn Val Ser Gly Glu 267yr Pro Thr Asp Ala Arg Glu Met Leu Thr Gln His Met Thr Ser 275 28er Val Lys Phe Leu Thr Gln Val Arg Asn Met His Gln Ala Gly Ala 29Ile Phe Val Glu Phe Gly Pro Lys Gln Val Leu Ser Lys Leu Val 33Ser Glu Thr Leu Lys Asp Asp Pro Ser Val Val Thr Val Ser Val Asn 325 33ro Ala Ser Gly Thr Asp Ser Asp Ile Gln Leu Arg Asp Ala Ala Val 345eu Val Val Ala Gly Val Asn Leu Gln Gly Phe Asp Lys Trp Asp 355 36la Pro Asp Ala Thr Arg Met Gln Ala Ile Lys Lys Lys Arg Thr Thr 378rg Leu Ser Ala Ala Thr Tyr Val Ser Asp Lys Thr Lys Lys Val 385 39Asp Ala Ala Met Asn Asp Gly Arg Cys Val Thr Tyr Leu Lys Gly 44Ala Pro Leu Ile Lys Ala Pro Glu Pro 42 Schizochytrium sp. MISC_FEATURE ( Xaa = any amino acid His Ser Xaa Gly 258 DNA Schizochytrium sp. CDS (8) gtc tcg aac gag ctt ctt gag aag gcc gag act gtc gtc atg gag 48 Ala Val Ser Asn Glu Leu Leu Glu Lys Ala Glu Thr Val Val Met Glu ctc gcc gcc aag acc ggc tac gag acc gac atg atc gag gct gac 96 Val Leu Ala Ala Lys Thr Gly Tyr Glu Thr Asp Met Ile Glu Ala Asp 2 atg gag ctc gag acc gag ctc ggc att gac tcc atc aag cgt gtc gag Glu Leu Glu Thr Glu Leu Gly Ile Asp Ser Ile Lys Arg Val Glu 35 4c ctc tcc gag gtc cag gcc atg ctc aat gtc gag gcc aag gat gtc Leu Ser Glu Val Gln Ala Met Leu Asn Val Glu Ala Lys Asp Val 5 gat gcc ctc agc cgc act cgc act gtt ggt gag gtt gtc aac gcc atg 24la Leu Ser Arg Thr Arg Thr Val Gly Glu Val Val Asn Ala Met 65 7 aag gcc gag atc gct ggc 258 Lys Ala Glu Ile Ala Gly 85 RT Schizochytrium sp. Val Ser Asn Glu Leu Leu Glu Lys Ala Glu Thr Val Val Met Glu Leu Ala Ala Lys Thr Gly Tyr Glu Thr Asp Met Ile Glu Ala Asp 2 Met Glu Leu Glu Thr Glu Leu Gly Ile Asp Ser Ile Lys Arg Val Glu 35 4e Leu Ser Glu Val Gln Ala Met Leu Asn Val Glu Ala Lys Asp Val 5 Asp Ala Leu Ser Arg Thr Arg Thr Val Gly Glu Val Val Asn Ala Met 65 7 Lys Ala Glu Ile Ala Gly 85 T Schizochytrium sp. Gly Ile Asp Ser 2chizochytrium sp. Pro Ala Pro Val Lys Ala Ala Ala Pro Ala Ala Pro Val Ala Ser Pro Ala Pro Ala 2Schizochytrium sp. ccgccc cggtcaaggc tgctgcgcct gccgcccccg ttgcctcggc ccctgccccg 6ctcga acgagcttct tgagaaggcc gagactgtcg tcatggaggt cctcgccgcc accggct acgagaccga catgatcgag gctgacatgg agctcgagac cgagctcggc gactcca tcaagcgtgt cgagatcctc tccgaggtcc aggccatgct caatgtcgag 24ggatg tcgatgccct cagccgcact cgcactgttg gtgaggttgt caacgccatg 3ccgaga tcgctggcag ctctgccccg gcgcctgctg ccgctgctcc ggctccggcc 36tgccc ctgccgccgc tgcgcctgct gtctcgaacg agcttctcga gaaggccgag 42cgtca tggaggtcct cgccgccaag actggctacg agactgacat gatcgagtcc 48ggagc tcgagactga gctcggcatt gactccatca agcgtgtcga gatcctctcc 54tcagg ccatgctcaa cgtcgaggcc aaggacgtcg acgctctcag ccgcactcgc 6tgggtg aggtcgtcaa cgccatgaag gctgagatcg ctggtggctc tgccccggcg 66cgccg ctgccccagg tccggctgct gccgcccctg cgcctgccgc cgccgcccct 72ctcga acgagcttct tgagaaggcc gagaccgtcg tcatggaggt cctcgccgcc 78tggct acgagactga catgatcgag tccgacatgg agctcgagac cgagctcggc 84ctcca tcaagcgtgt cgagattctc tccgaggtcc aggccatgct caacgtcgag 9aggacg tcgacgctct cagccgcacc cgcactgttg gcgaggtcgt cgatgccatg 96cgaga tcgctggtgg ctctgccccg gcgcctgccg ccgctgctcc tgctccggct tgccgccc ctgcgcctgc cgcccctgcg cctgctgtct cgagcgagct tctcgagaag cgagactg tcgtcatgga ggtcctcgcc gccaagactg gctacgagac tgacatgatc gtccgaca tggagctcga gaccgagctc ggcattgact ccatcaagcg tgtcgagatt ctccgagg tccaggccat gctcaacgtc gaggccaagg acgtcgacgc tctcagccgc ccgcactg ttggcgaggt cgtcgatgcc atgaaggccg agatcgctgg tggctctgcc ggcgcctg ccgccgctgc tcctgctccg gctgctgccg cccctgcgcc tgccgcccct gcctgccg cccctgcgcc tgctgtctcg agcgagcttc tcgagaaggc cgagactgtc catggagg tcctcgccgc caagactggc tacgagactg acatgattga gtccgacatg gctcgaga ccgagctcgg cattgactcc atcaagcgtg tcgagattct ctccgaggtt ggccatgc tcaacgtcga ggccaaggac gtcgacgctc tcagccgcac tcgcactgtt tgaggtcg tcgatgccat gaaggctgag atcgctggca gctccgcctc ggcgcctgcc cgctgctc ctgctccggc tgctgccgct cctgcgcccg ctgccgccgc ccctgctgtc gaacgagc ttctcgagaa agccgagact gtcgtcatgg aggtcctcgc cgccaagact ctacgaga ctgacatgat cgagtccgac atggagctcg agactgagct cggcattgac catcaagc gtgtcgagat cctctccgag gttcaggcca tgctcaacgt cgaggccaag cgtcgatg ccctcagccg cacccgcact gttggcgagg ttgtcgatgc catgaaggcc gatcgctg gtggctctgc cccggcgcct gccgccgctg cccctgctcc ggctgccgcc 2cctgctg tctcgaacga gcttctcgag aaggccgaga ctgtcgtcat ggaggtcctc 2gccaaga ctggctacga gaccgacatg atcgagtccg acatggagct cgagaccgag 2ggcattg actccatcaa gcgtgtcgag attctctccg aggttcaggc catgctcaac 222ggcca aggacgtcga tgctctcagc cgcactcgca ctgttggcga ggtcgtcgat 228gaagg ctgagatcgc cggcagctcc gccccggcgc ctgccgccgc tgctcctgct 234tgctg ccgctcctgc gcccgctgcc gctgcccctg ctgtctcgag cgagcttctc 24aggccg

agaccgtcgt catggaggtc ctcgccgcca agactggcta cgagactgac 246tgagt ccgacatgga gctcgagact gagctcggca ttgactccat caagcgtgtc 252cctct ccgaggttca ggccatgctc aacgtcgagg ccaaggacgt cgatgccctc 258caccc gcactgttgg cgaggttgtc gatgccatga aggccgagat cgctggtggc 264cccgg cgcctgccgc cgctgcccct gctccggctg ccgccgcccc tgctgtctcg 27agcttc ttgagaaggc cgagaccgtc gtcatggagg tcctcgccgc caagactggc 276gaccg acatgatcga gtccgacatg gagctcgaga ccgagctcgg cattgactcc 282gcgtg tcgagattct ctccgaggtt caggccatgc tcaacgtcga ggccaaggac 288cgctc tcagccgcac tcgcactgtt ggcgaggtcg tcgatgccat gaaggctgag 294tggtg gctctgcccc ggcgcctgcc gccgctgctc ctgcctcggc tggcgccgcg 3gcg 32 Schizochytrium sp. CDS (33) ggc gct ctc ggc ggc ttc atc tcg cag cag gcg gag cgc ttc gag 48 Phe Gly Ala Leu Gly Gly Phe Ile Ser Gln Gln Ala Glu Arg Phe Glu gcc gaa atc ctc ggc ttc acg ctc atg tgc gcc aag ttc gcc aag 96 Pro Ala Glu Ile Leu Gly Phe Thr Leu Met Cys Ala Lys Phe Ala Lys 2 gct tcc ctc tgc acg gct gtg gct ggc ggc cgc ccg gcc ttt atc ggt Ser Leu Cys Thr Ala Val Ala Gly Gly Arg Pro Ala Phe Ile Gly 35 4g gcg cgc ctt gac ggc cgc ctc gga ttc act tcg cag ggc act tct Ala Arg Leu Asp Gly Arg Leu Gly Phe Thr Ser Gln Gly Thr Ser 5 gac gcg ctc aag cgt gcc cag cgt ggt gcc atc ttt ggc ctc tgc aag 24la Leu Lys Arg Ala Gln Arg Gly Ala Ile Phe Gly Leu Cys Lys 65 7 acc atc ggc ctc gag tgg tcc gag tct gac gtc ttt tcc cgc ggc gtg 288 Thr Ile Gly Leu Glu Trp Ser Glu Ser Asp Val Phe Ser Arg Gly Val 85 9c att gct cag ggc atg cac ccc gag gat gcc gcc gtg gcg att gtg 336 Asp Ile Ala Gln Gly Met His Pro Glu Asp Ala Ala Val Ala Ile Val gag atg gcg tgc gct gac att cgc att cgc gag gtc ggc att ggc 384 Arg Glu Met Ala Cys Ala Asp Ile Arg Ile Arg Glu Val Gly Ile Gly aac cag cag cgc tgc acg atc cgt gcc gcc aag ctc gag acc ggc 432 Ala Asn Gln Gln Arg Cys Thr Ile Arg Ala Ala Lys Leu Glu Thr Gly ccg cag cgc cag atc gcc aag gac gac gtg ctg ctc gtt tct ggc 48ro Gln Arg Gln Ile Ala Lys Asp Asp Val Leu Leu Val Ser Gly ggc gct cgc ggc atc acg cct ctt tgc atc cgg gag atc acg cgc cag 528 Gly Ala Arg Gly Ile Thr Pro Leu Cys Ile Arg Glu Ile Thr Arg Gln gcg ggc ggc aag tac att ctg ctt ggc cgc agc aag gtc tct gcg 576 Ile Ala Gly Gly Lys Tyr Ile Leu Leu Gly Arg Ser Lys Val Ser Ala gaa ccg gca tgg tgc gct ggc atc act gac gag aag gct gtg caa 624 Ser Glu Pro Ala Trp Cys Ala Gly Ile Thr Asp Glu Lys Ala Val Gln 2gct gct acc cag gag ctc aag cgc gcc ttt agc gct ggc gag ggc 672 Lys Ala Ala Thr Gln Glu Leu Lys Arg Ala Phe Ser Ala Gly Glu Gly 222ag ccc acg ccc cgc gct gtc act aag ctt gtg ggc tct gtt ctt 72ys Pro Thr Pro Arg Ala Val Thr Lys Leu Val Gly Ser Val Leu 225 234ct cgc gag gtg cgc agc tct att gct gcg att gaa gcg ctc ggc 768 Gly Ala Arg Glu Val Arg Ser Ser Ile Ala Ala Ile Glu Ala Leu Gly 245 25gc aag gcc atc tac tcg tcg tgc gac gtg aac tct gcc gcc gac gtg 8Lys Ala Ile Tyr Ser Ser Cys Asp Val Asn Ser Ala Ala Asp Val 267ag gcc gtg cgc gat gcc gag tcc cag ctc ggt gcc cgc gtc tcg 864 Ala Lys Ala Val Arg Asp Ala Glu Ser Gln Leu Gly Ala Arg Val Ser 275 28gc atc gtt cat gcc tcg ggc gtg ctc cgc gac cgt ctc atc gag aag 9Ile Val His Ala Ser Gly Val Leu Arg Asp Arg Leu Ile Glu Lys 29ctc ccc gac gag ttc gac gcc gtc ttt ggc acc aag gtc acc ggt 96eu Pro Asp Glu Phe Asp Ala Val Phe Gly Thr Lys Val Thr Gly 33ctc gag aac ctc ctc gcc gcc gtc gac cgc gcc aac ctc aag cac atg u Glu Asn Leu Leu Ala Ala Val Asp Arg Ala Asn Leu Lys His Met 325 33tc ctc ttc agc tcg ctc gcc ggc ttc cac ggc aac gtc ggc cag tct l Leu Phe Ser Ser Leu Ala Gly Phe His Gly Asn Val Gly Gln Ser 345ac gcc atg gcc aac gag gcc ctt aac aag atg ggc ctc gag ctc p Tyr Ala Met Ala Asn Glu Ala Leu Asn Lys Met Gly Leu Glu Leu 355 36cc aag gac gtc tcg gtc aag tcg atc tgc ttc ggt ccc tgg gac ggt a Lys Asp Val Ser Val Lys Ser Ile Cys Phe Gly Pro Trp Asp Gly 378tg gtg acg ccg cag ctc aag aag cag ttc cag gag atg ggc gtg y Met Val Thr Pro Gln Leu Lys Lys Gln Phe Gln Glu Met Gly Val 385 39atc atc ccc cgc gag ggc ggc gct gat acc gtg gcg cgc atc gtg n Ile Ile Pro Arg Glu Gly Gly Ala Asp Thr Val Ala Arg Ile Val 44ggc tcc tcg ccg gct gag atc ctt gtc ggc aac tgg cgc acc ccg u Gly Ser Ser Pro Ala Glu Ile Leu Val Gly Asn Trp Arg Thr Pro 423ag aag gtc ggc tcg gac acc atc acc ctg cac cgc aag att tcc r Lys Lys Val Gly Ser Asp Thr Ile Thr Leu His Arg Lys Ile Ser 435 44cc aag tcc aac ccc ttc ctc gag gac cac gtc atc cag ggc cgc cgc a Lys Ser Asn Pro Phe Leu Glu Asp His Val Ile Gln Gly Arg Arg 456tg ccc atg acg ctg gcc att ggc tcg ctc gcg gag acc tgc ctc l Leu Pro Met Thr Leu Ala Ile Gly Ser Leu Ala Glu Thr Cys Leu 465 478tc ttc ccc ggc tac tcg ctc tgg gcc att gac gac gcc cag ctc y Leu Phe Pro Gly Tyr Ser Leu Trp Ala Ile Asp Asp Ala Gln Leu 485 49tc aag ggt gtc act gtc gac ggc gac gtc aac tgc gag gtg acc ctc e Lys Gly Val Thr Val Asp Gly Asp Val Asn Cys Glu Val Thr Leu 55ccg tcg acg gcg ccc tcg ggc cgc gtc aac gtc cag gcc acg ctc r Pro Ser Thr Ala Pro Ser Gly Arg Val Asn Val Gln Ala Thr Leu 5525 aag acc ttt tcc agc ggc aag ctg gtc ccg gcc tac cgc gcc gtc atc s Thr Phe Ser Ser Gly Lys Leu Val Pro Ala Tyr Arg Ala Val Ile 534tc tcc aac cag ggc gcg ccc ccg gcc aac gcc acc atg cag ccg l Leu Ser Asn Gln Gly Ala Pro Pro Ala Asn Ala Thr Met Gln Pro 545 556cg ctc gat gcc gat ccg gcg ctc cag ggc tcc gtc tac gac ggc o Ser Leu Asp Ala Asp Pro Ala Leu Gln Gly Ser Val Tyr Asp Gly 565 57ag acc ctc ttc cac ggc ccg gcc ttc cgc ggc atc gat gac gtg ctc s Thr Leu Phe His Gly Pro Ala Phe Arg Gly Ile Asp Asp Val Leu 589gc acc aag agc cag ctt gtg gcc aag tgc agc gct gtc ccc ggc r Cys Thr Lys Ser Gln Leu Val Ala Lys Cys Ser Ala Val Pro Gly 595 6tcc gac gcc gct cgc ggc gag ttt gcc acg gac act gac gcc cat gac r Asp Ala Ala Arg Gly Glu Phe Ala Thr Asp Thr Asp Ala His Asp 662tc gtg aac gac ctg gcc ttt cag gcc atg ctc gtc tgg gtg cgc o Phe Val Asn Asp Leu Ala Phe Gln Ala Met Leu Val Trp Val Arg 625 634cg ctc ggc cag gct gcg ctc ccc aac tcg atc cag cgc atc gtc g Thr Leu Gly Gln Ala Ala Leu Pro Asn Ser Ile Gln Arg Ile Val 645 65ag cac cgc ccg gtc ccg cag gac aag ccc ttc tac att acc ctc cgc 2 His Arg Pro Val Pro Gln Asp Lys Pro Phe Tyr Ile Thr Leu Arg 667ac cag tcg ggc ggt cac tcc cag cac aag cac gcc ctt cag ttc 2 Asn Gln Ser Gly Gly His Ser Gln His Lys His Ala Leu Gln Phe 675 68ac aac gag cag ggc gat ctc ttc att gat gtc cag gct tcg gtc atc 2 Asn Glu Gln Gly Asp Leu Phe Ile Asp Val Gln Ala Ser Val Ile 69acg gac agc ctt gcc ttc 2 Thr Asp Ser Leu Ala Phe 7PRT Schizochytrium sp. Gly Ala Leu Gly Gly Phe Ile Ser Gln Gln Ala Glu Arg Phe Glu Ala Glu Ile Leu Gly Phe Thr Leu Met Cys Ala Lys Phe Ala Lys 2 Ala Ser Leu Cys Thr Ala Val Ala Gly Gly Arg Pro Ala Phe Ile Gly 35 4l Ala Arg Leu Asp Gly Arg Leu Gly Phe Thr Ser Gln Gly Thr Ser 5 Asp Ala Leu Lys Arg Ala Gln Arg Gly Ala Ile Phe Gly Leu Cys Lys 65 7 Thr Ile Gly Leu Glu Trp Ser Glu Ser Asp Val Phe Ser Arg Gly Val 85 9p Ile Ala Gln Gly Met His Pro Glu Asp Ala Ala Val Ala Ile Val Glu Met Ala Cys Ala Asp Ile Arg Ile Arg Glu Val Gly Ile Gly Asn Gln Gln Arg Cys Thr Ile Arg Ala Ala Lys Leu Glu Thr Gly Pro Gln Arg Gln Ile Ala Lys Asp Asp Val Leu Leu Val Ser Gly Gly Ala Arg Gly Ile Thr Pro Leu Cys Ile Arg Glu Ile Thr Arg Gln Ala Gly Gly Lys Tyr Ile Leu Leu Gly Arg Ser Lys Val Ser Ala Glu Pro Ala Trp Cys Ala Gly Ile Thr Asp Glu Lys Ala Val Gln 2Ala Ala Thr Gln Glu Leu Lys Arg Ala Phe Ser Ala Gly Glu Gly 222ys Pro Thr Pro Arg Ala Val Thr Lys Leu Val Gly Ser Val Leu 225 234la Arg Glu Val Arg Ser Ser Ile Ala Ala Ile Glu Ala Leu Gly 245 25ly Lys Ala Ile Tyr Ser Ser Cys Asp Val Asn Ser Ala Ala Asp Val 267ys Ala Val Arg Asp Ala Glu Ser Gln Leu Gly Ala Arg Val Ser 275 28ly Ile Val His Ala Ser Gly Val Leu Arg Asp Arg Leu Ile Glu Lys 29Leu Pro Asp Glu Phe Asp Ala Val Phe Gly Thr Lys Val Thr Gly 33Leu Glu Asn Leu Leu Ala Ala Val Asp Arg Ala Asn Leu Lys His Met 325 33al Leu Phe Ser Ser Leu Ala Gly Phe His Gly Asn Val Gly Gln Ser 345yr Ala Met Ala Asn Glu Ala Leu Asn Lys Met Gly Leu Glu Leu 355 36la Lys Asp Val Ser Val Lys Ser Ile Cys Phe Gly Pro Trp Asp Gly 378et Val Thr Pro Gln Leu Lys Lys Gln Phe Gln Glu Met Gly Val 385 39Ile Ile Pro Arg Glu Gly Gly Ala Asp Thr Val Ala Arg Ile Val 44Gly Ser Ser Pro Ala Glu Ile Leu Val Gly Asn Trp Arg Thr Pro 423ys Lys Val Gly Ser Asp Thr Ile Thr Leu His Arg Lys Ile Ser 435 44la Lys Ser Asn Pro Phe Leu Glu Asp His Val Ile Gln Gly Arg Arg 456eu Pro Met Thr Leu Ala Ile Gly Ser Leu Ala Glu Thr Cys Leu 465 478eu Phe Pro Gly Tyr Ser Leu Trp Ala Ile Asp Asp Ala Gln Leu 485 49he Lys Gly Val Thr Val Asp Gly Asp Val Asn Cys Glu Val Thr Leu 55Pro Ser Thr Ala Pro Ser Gly Arg Val Asn Val Gln Ala Thr Leu 5525 Lys Thr Phe Ser Ser Gly Lys Leu Val Pro Ala Tyr Arg Ala Val Ile 534eu Ser Asn Gln Gly Ala Pro Pro Ala Asn Ala Thr Met Gln Pro 545 556er Leu Asp Ala Asp Pro Ala Leu Gln Gly Ser Val Tyr Asp Gly 565 57ys Thr Leu Phe His Gly Pro Ala Phe Arg Gly Ile Asp Asp Val Leu 589ys Thr Lys Ser Gln Leu Val Ala Lys Cys Ser Ala Val Pro Gly 595 6Ser Asp Ala Ala Arg Gly Glu Phe Ala Thr Asp Thr Asp Ala His Asp 662he Val Asn Asp Leu Ala Phe Gln Ala Met Leu Val Trp Val Arg 625 634hr Leu Gly Gln Ala Ala Leu Pro Asn Ser Ile Gln Arg Ile Val 645 65ln His Arg Pro Val Pro Gln Asp Lys Pro Phe Tyr Ile Thr Leu Arg 667sn Gln Ser Gly Gly His Ser Gln His Lys His Ala Leu Gln Phe 675 68is Asn Glu Gln Gly Asp Leu Phe Ile Asp Val Gln Ala Ser Val Ile 69Thr Asp Ser Leu Ala Phe 7 DNA Schizochytrium sp. CDS (5tg gcc gct cgg aat gtg agc gcc gcg cat gag atg cac gat gaa aag 48 Met Ala Ala Arg Asn Val Ser Ala Ala His Glu Met His Asp Glu Lys atc gcc gtc gtc ggc atg gcc gtc cag tac gcc gga tgc aaa acc 96 Arg Ile Ala Val Val Gly Met Ala Val Gln Tyr Ala Gly Cys Lys Thr 2 aag gac gag ttc tgg gag gtg ctc atg aac ggc aag gtc gag tcc aag Asp Glu Phe Trp Glu Val Leu Met Asn Gly Lys Val Glu Ser Lys 35 4g atc agc gac aaa cga ctc ggc tcc aac tac cgc gcc gag cac tac Ile Ser Asp Lys Arg Leu Gly Ser Asn Tyr Arg Ala Glu His Tyr 5 aaa gca gag cgc agc aag tat gcc gac acc ttt tgc aac gaa acg tac 24la Glu Arg Ser Lys Tyr Ala Asp Thr Phe Cys Asn Glu Thr Tyr 65 7 ggc acc ctt gac gag aac gag atc gac aac gag cac gaa ctc ctc ctc 288 Gly Thr Leu Asp Glu Asn Glu Ile Asp Asn Glu His Glu Leu Leu Leu 85 9c ctc gcc aag cag gca ctc gca gag aca tcc gtc aaa gac tcg aca 336 Asn Leu Ala Lys Gln Ala Leu Ala Glu Thr Ser Val Lys Asp Ser Thr tgc ggc atc gtc agc ggc tgc ctc tcg ttc ccc atg gac aac ctc 384 Arg Cys Gly Ile Val Ser Gly Cys Leu Ser Phe Pro Met Asp Asn Leu ggt gaa ctc ctc aac gtg tac caa aac cat gtc gag aaa aag ctc 432 Gln Gly Glu Leu Leu Asn Val Tyr Gln Asn His Val Glu Lys Lys Leu gcc cgc gtc ttc aag gac gcc tcc cat tgg tcc gaa cgc gag cag 48la Arg Val Phe Lys Asp Ala Ser His Trp Ser Glu Arg Glu Gln tcc aac aaa ccc gag gcc ggt gac cgc cgc atc ttc atg gac ccg gcc 528 Ser Asn Lys Pro Glu Ala Gly Asp Arg Arg Ile Phe Met Asp Pro Ala ttc gtc gcc gaa gaa ctc aac ctc ggc gcc ctt cac tac tcc gtc 576 Ser Phe Val Ala Glu Glu Leu Asn Leu Gly Ala Leu His Tyr Ser Val gca gca tgc gcc acg gcg ctc tac gtg ctc cgc ctc gcg cag gat 624 Asp Ala Ala Cys Ala Thr Ala Leu Tyr Val Leu Arg Leu Ala Gln Asp 2ctc gtc tcc ggc gcc gcc gac gtc atg ctc tgc ggt gcc acc tgc 672 His Leu Val Ser Gly Ala Ala Asp Val Met Leu Cys Gly Ala Thr Cys 222cg gag ccc ttt ttc atc ctt tcg ggc ttt tcc acc ttc cag gcc 72ro Glu Pro Phe Phe Ile Leu Ser Gly Phe Ser Thr Phe Gln Ala 225 234cc gtc ggc acg ggc cag aac gtg tcc atg ccg ctg cac aag gac 768 Met Pro Val Gly Thr Gly Gln Asn Val Ser Met Pro Leu His Lys Asp 245 25gc cag ggc ctc acc ccg ggt gag ggc ggc tcc atc atg gtc ctc aag 8Gln Gly Leu Thr Pro Gly Glu Gly Gly Ser Ile Met Val Leu Lys 267tc gat gat gcc atc cgc gac ggc gac cac att tac ggc acc ctt 864 Arg Leu Asp Asp Ala Ile Arg Asp Gly Asp His Ile Tyr Gly Thr Leu 275 28tc ggc gcc

aat gtc agc aac tcc ggc aca ggt ctg ccc ctc aag ccc 9Gly Ala Asn Val Ser Asn Ser Gly Thr Gly Leu Pro Leu Lys Pro 29ctc ccc agc gag aaa aag tgc ctc atg gac acc tac acg cgc att 96eu Pro Ser Glu Lys Lys Cys Leu Met Asp Thr Tyr Thr Arg Ile 33aac gtg cac ccg cac aag att cag tac gtc gag tgc cac gcc acc ggc n Val His Pro His Lys Ile Gln Tyr Val Glu Cys His Ala Thr Gly 325 33cg ccc cag ggt gat cgt gtg gaa atc gac gcc gtc aag gcc tgc ttt r Pro Gln Gly Asp Arg Val Glu Ile Asp Ala Val Lys Ala Cys Phe 345gc aag gtc ccc cgt ttc ggt acc aca aag ggc aac ttt gga cac u Gly Lys Val Pro Arg Phe Gly Thr Thr Lys Gly Asn Phe Gly His 355 36cc cts gyc gca gcc ggc ttt gcc ggt atg tgc aag gtc ctc ctc tcc r Xaa Xaa Ala Ala Gly Phe Ala Gly Met Cys Lys Val Leu Leu Ser 378ag cat ggc atc atc ccg ccc acc ccg ggt atc gat gac gag acc t Lys His Gly Ile Ile Pro Pro Thr Pro Gly Ile Asp Asp Glu Thr 385 39atg gac cct ctc gtc gtc tcc ggt gag gcc atc cca tgg cca gag s Met Asp Pro Leu Val Val Ser Gly Glu Ala Ile Pro Trp Pro Glu 44aac ggc gag ccc aag cgc gcc ggt ctc tcg gcc ttt ggc ttt ggt r Asn Gly Glu Pro Lys Arg Ala Gly Leu Ser Ala Phe Gly Phe Gly 423cc aac gcc cat gcc gtc ttt gag gag cat gac ccc tcc aac gcc y Thr Asn Ala His Ala Val Phe Glu Glu His Asp Pro Ser Asn Ala 435 44cc tgc a Cys 45chizochytrium sp. misc_feature (37'Xaa' at location 37s for Leu. 2la Ala Arg Asn Val Ser Ala Ala His Glu Met His Asp Glu Lys Ile Ala Val Val Gly Met Ala Val Gln Tyr Ala Gly Cys Lys Thr 2 Lys Asp Glu Phe Trp Glu Val Leu Met Asn Gly Lys Val Glu Ser Lys 35 4l Ile Ser Asp Lys Arg Leu Gly Ser Asn Tyr Arg Ala Glu His Tyr 5 Lys Ala Glu Arg Ser Lys Tyr Ala Asp Thr Phe Cys Asn Glu Thr Tyr 65 7 Gly Thr Leu Asp Glu Asn Glu Ile Asp Asn Glu His Glu Leu Leu Leu 85 9n Leu Ala Lys Gln Ala Leu Ala Glu Thr Ser Val Lys Asp Ser Thr Cys Gly Ile Val Ser Gly Cys Leu Ser Phe Pro Met Asp Asn Leu Gly Glu Leu Leu Asn Val Tyr Gln Asn His Val Glu Lys Lys Leu Ala Arg Val Phe Lys Asp Ala Ser His Trp Ser Glu Arg Glu Gln Ser Asn Lys Pro Glu Ala Gly Asp Arg Arg Ile Phe Met Asp Pro Ala Phe Val Ala Glu Glu Leu Asn Leu Gly Ala Leu His Tyr Ser Val Ala Ala Cys Ala Thr Ala Leu Tyr Val Leu Arg Leu Ala Gln Asp 2Leu Val Ser Gly Ala Ala Asp Val Met Leu Cys Gly Ala Thr Cys 222ro Glu Pro Phe Phe Ile Leu Ser Gly Phe Ser Thr Phe Gln Ala 225 234ro Val Gly Thr Gly Gln Asn Val Ser Met Pro Leu His Lys Asp 245 25er Gln Gly Leu Thr Pro Gly Glu Gly Gly Ser Ile Met Val Leu Lys 267eu Asp Asp Ala Ile Arg Asp Gly Asp His Ile Tyr Gly Thr Leu 275 28eu Gly Ala Asn Val Ser Asn Ser Gly Thr Gly Leu Pro Leu Lys Pro 29Leu Pro Ser Glu Lys Lys Cys Leu Met Asp Thr Tyr Thr Arg Ile 33Asn Val His Pro His Lys Ile Gln Tyr Val Glu Cys His Ala Thr Gly 325 33hr Pro Gln Gly Asp Arg Val Glu Ile Asp Ala Val Lys Ala Cys Phe 345ly Lys Val Pro Arg Phe Gly Thr Thr Lys Gly Asn Phe Gly His 355 36hr Xaa Xaa Ala Ala Gly Phe Ala Gly Met Cys Lys Val Leu Leu Ser 378ys His Gly Ile Ile Pro Pro Thr Pro Gly Ile Asp Asp Glu Thr 385 39Met Asp Pro Leu Val Val Ser Gly Glu Ala Ile Pro Trp Pro Glu 44Asn Gly Glu Pro Lys Arg Ala Gly Leu Ser Ala Phe Gly Phe Gly 423hr Asn Ala His Ala Val Phe Glu Glu His Asp Pro Ser Asn Ala 435 44la Cys 4523 DNA Schizochytrium sp. CDS (23) 2cc cgc tgc ggc ggt gaa agc aac atg cgc atc gcc atc act ggt 48 Ser Ala Arg Cys Gly Gly Glu Ser Asn Met Arg Ile Ala Ile Thr Gly gac gcc acc ttt ggc gct ctc aag gga ctc gac gcc ttc gag cgc 96 Met Asp Ala Thr Phe Gly Ala Leu Lys Gly Leu Asp Ala Phe Glu Arg 2 gcc att tac acc ggc gct cac ggt gcc atc cca ctc cca gaa aag cgc Ile Tyr Thr Gly Ala His Gly Ala Ile Pro Leu Pro Glu Lys Arg 35 4g cgc ttt ctc ggc aag gac aag gac ttt ctt gac ctc tgc ggc gtc Arg Phe Leu Gly Lys Asp Lys Asp Phe Leu Asp Leu Cys Gly Val 5 aag gcc acc ccg cac ggc tgc tac att gaa gat gtt gag gtc gac ttc 24la Thr Pro His Gly Cys Tyr Ile Glu Asp Val Glu Val Asp Phe 65 7 cag cgc ctc cgc acg ccc atg acc cct gaa gac atg ctc ctc cct cag 288 Gln Arg Leu Arg Thr Pro Met Thr Pro Glu Asp Met Leu Leu Pro Gln 85 9g ctt ctg gcc gtc acc acc att gac cgc gcc atc ctc gac tcg gga 336 Gln Leu Leu Ala Val Thr Thr Ile Asp Arg Ala Ile Leu Asp Ser Gly aaa aag ggt ggc aat gtc gcc gtc ttt gtc ggc ctc ggc acc gac 384 Met Lys Lys Gly Gly Asn Val Ala Val Phe Val Gly Leu Gly Thr Asp gag ctc tac cgt cac cgt gct cgc gtc gct ctc aag gag cgc gtc 432 Leu Glu Leu Tyr Arg His Arg Ala Arg Val Ala Leu Lys Glu Arg Val cct gaa gcc tcc aag aag ctc aat gac atg atg cag tac att aac 48ro Glu Ala Ser Lys Lys Leu Asn Asp Met Met Gln Tyr Ile Asn gac tgc ggc aca tcc aca tcg tac acc tcg tac att ggc aac ctc gtc 528 Asp Cys Gly Thr Ser Thr Ser Tyr Thr Ser Tyr Ile Gly Asn Leu Val acg cgc gtc tcg tcg cag tgg ggc ttc acg ggc ccc tcc ttt acg 576 Ala Thr Arg Val Ser Ser Gln Trp Gly Phe Thr Gly Pro Ser Phe Thr acc gag ggc aac aac tcc gtc tac cgc tgc gcc gag ctc ggc aag 624 Ile Thr Glu Gly Asn Asn Ser Val Tyr Arg Cys Ala Glu Leu Gly Lys 2ctc ctc gag acc ggc gag gtc gat ggc gtc gtc gtt gcg ggt gtc 672 Tyr Leu Leu Glu Thr Gly Glu Val Asp Gly Val Val Val Ala Gly Val 222tc tgc ggc agt gcc gaa aac ctt tac gtc aag tct cgc cgc ttc 72eu Cys Gly Ser Ala Glu Asn Leu Tyr Val Lys Ser Arg Arg Phe 225 234tg tcc acc tcc gat acc ccg cgc gcc agc ttt gac gcc gcc gcc 768 Lys Val Ser Thr Ser Asp Thr Pro Arg Ala Ser Phe Asp Ala Ala Ala 245 25at ggc tac ttt gtc ggc gag ggc tgc ggt gcc ttt gtg ctc aag cgt 8Gly Tyr Phe Val Gly Glu Gly Cys Gly Ala Phe Val Leu Lys Arg 267ct agc tgc acc aag gac gac cgt atc tac gct tgc atg gat gcc 864 Glu Thr Ser Cys Thr Lys Asp Asp Arg Ile Tyr Ala Cys Met Asp Ala 275 28tc gtc cct ggc aac gtc cct agc gcc tgc ttg cgc gag gcc ctc gac 9Val Pro Gly Asn Val Pro Ser Ala Cys Leu Arg Glu Ala Leu Asp 29gcg cgc gtc aag ccg ggc gat atc gag atg ctc gag ctc agc gcc 96la Arg Val Lys Pro Gly Asp Ile Glu Met Leu Glu Leu Ser Ala 33gac tcc gcc cgc cac ctc aag gac ccg tcc gtc ctg ccc aag gag ctc p Ser Ala Arg His Leu Lys Asp Pro Ser Val Leu Pro Lys Glu Leu 325 33ct gcc gag gag gaa atc ggc ggc ctt cag acg atc ctt cgt gac gat r Ala Glu Glu Glu Ile Gly Gly Leu Gln Thr Ile Leu Arg Asp Asp 345ag ctc ccg cgc aac gtc gca acg ggc agt gtc aag gcc acc gtc p Lys Leu Pro Arg Asn Val Ala Thr Gly Ser Val Lys Ala Thr Val 355 36gt gac acc ggt tat gcc tct ggt gct gcc agc ctc atc aag gct gcg y Asp Thr Gly Tyr Ala Ser Gly Ala Ala Ser Leu Ile Lys Ala Ala 378gc atc tac aac cgc tac ctg ccc agc aac ggc gac gac tgg gat u Cys Ile Tyr Asn Arg Tyr Leu Pro Ser Asn Gly Asp Asp Trp Asp 385 39ccc gcc cct gag gcg ccc tgg gac agc acc ctc ttt gcg tgc cag u Pro Ala Pro Glu Ala Pro Trp Asp Ser Thr Leu Phe Ala Cys Gln 44tcg cgc gct tgg ctc aag aac cct ggc gag cgt cgc tat gcg gcc r Ser Arg Ala Trp Leu Lys Asn Pro Gly Glu Arg Arg Tyr Ala Ala 423cg ggc gtc tcc gag acg cgc tcg l Ser Gly Val Ser Glu Thr Arg Ser 435 44chizochytrium sp. 22 Ser Ala Arg Cys Gly Gly Glu Ser Asn Met Arg Ile Ala Ile Thr Gly Asp Ala Thr Phe Gly Ala Leu Lys Gly Leu Asp Ala Phe Glu Arg 2 Ala Ile Tyr Thr Gly Ala His Gly Ala Ile Pro Leu Pro Glu Lys Arg 35 4p Arg Phe Leu Gly Lys Asp Lys Asp Phe Leu Asp Leu Cys Gly Val 5 Lys Ala Thr Pro His Gly Cys Tyr Ile Glu Asp Val Glu Val Asp Phe 65 7 Gln Arg Leu Arg Thr Pro Met Thr Pro Glu Asp Met Leu Leu Pro Gln 85 9n Leu Leu Ala Val Thr Thr Ile Asp Arg Ala Ile Leu Asp Ser Gly Lys Lys Gly Gly Asn Val Ala Val Phe Val Gly Leu Gly Thr Asp Glu Leu Tyr Arg His Arg Ala Arg Val Ala Leu Lys Glu Arg Val Pro Glu Ala Ser Lys Lys Leu Asn Asp Met Met Gln Tyr Ile Asn Asp Cys Gly Thr Ser Thr Ser Tyr Thr Ser Tyr Ile Gly Asn Leu Val Thr Arg Val Ser Ser Gln Trp Gly Phe Thr Gly Pro Ser Phe Thr Thr Glu Gly Asn Asn Ser Val Tyr Arg Cys Ala Glu Leu Gly Lys 2Leu Leu Glu Thr Gly Glu Val Asp Gly Val Val Val Ala Gly Val 222eu Cys Gly Ser Ala Glu Asn Leu Tyr Val Lys Ser Arg Arg Phe 225 234al Ser Thr Ser Asp Thr Pro Arg Ala Ser Phe Asp Ala Ala Ala 245 25sp Gly Tyr Phe Val Gly Glu Gly Cys Gly Ala Phe Val Leu Lys Arg 267hr Ser Cys Thr Lys Asp Asp Arg Ile Tyr Ala Cys Met Asp Ala 275 28le Val Pro Gly Asn Val Pro Ser Ala Cys Leu Arg Glu Ala Leu Asp 29Ala Arg Val Lys Pro Gly Asp Ile Glu Met Leu Glu Leu Ser Ala 33Asp Ser Ala Arg His Leu Lys Asp Pro Ser Val Leu Pro Lys Glu Leu 325 33hr Ala Glu Glu Glu Ile Gly Gly Leu Gln Thr Ile Leu Arg Asp Asp 345ys Leu Pro Arg Asn Val Ala Thr Gly Ser Val Lys Ala Thr Val 355 36ly Asp Thr Gly Tyr Ala Ser Gly Ala Ala Ser Leu Ile Lys Ala Ala 378ys Ile Tyr Asn Arg Tyr Leu Pro Ser Asn Gly Asp Asp Trp Asp 385 39Pro Ala Pro Glu Ala Pro Trp Asp Ser Thr Leu Phe Ala Cys Gln 44Ser Arg Ala Trp Leu Lys Asn Pro Gly Glu Arg Arg Tyr Ala Ala 423er Gly Val Ser Glu Thr Arg Ser 435 44Schizochytrium sp. CDS (tgc tat tcc gtg ctc ctc tcc gaa gcc gag ggc cac tac gag cgc gag 48 Cys Tyr Ser Val Leu Leu Ser Glu Ala Glu Gly His Tyr Glu Arg Glu cgc atc tcg ctc gac gag gag gcg ccc aag ctc att gtg ctt cgc 96 Asn Arg Ile Ser Leu Asp Glu Glu Ala Pro Lys Leu Ile Val Leu Arg 2 gcc gac tcc cac gag gag atc ctt ggt cgc ctc gac aag atc cgc gag Asp Ser His Glu Glu Ile Leu Gly Arg Leu Asp Lys Ile Arg Glu 35 4c ttc ttg cag ccc acg ggc gcc gcc ccg cgc gag tcc gag ctc aag Phe Leu Gln Pro Thr Gly Ala Ala Pro Arg Glu Ser Glu Leu Lys 5 gcg cag gcc cgc cgc atc ttc ctc gag ctc ctc ggc gag acc ctt gcc 24ln Ala Arg Arg Ile Phe Leu Glu Leu Leu Gly Glu Thr Leu Ala 65 7 cag gat gcc gct tct tca ggc tcg caa aag ccc ctc gct ctc agc ctc 288 Gln Asp Ala Ala Ser Ser Gly Ser Gln Lys Pro Leu Ala Leu Ser Leu 85 9c tcc acg ccc tcc aag ctc cag cgc gag gtc gag ctc gcg gcc aag 336 Val Ser Thr Pro Ser Lys Leu Gln Arg Glu Val Glu Leu Ala Ala Lys atc ccg cgc tgc ctc aag atg cgc cgc gat tgg agc tcc cct gct 384 Gly Ile Pro Arg Cys Leu Lys Met Arg Arg Asp Trp Ser Ser Pro Ala agc cgc tac gcg cct gag ccg ctc gcc agc gac cgc gtc gcc ttc 432 Gly Ser Arg Tyr Ala Pro Glu Pro Leu Ala Ser Asp Arg Val Ala Phe tac ggc gaa ggt cgc agc cct tac tac ggc atc acc caa gac att 48yr Gly Glu Gly Arg Ser Pro Tyr Tyr Gly Ile Thr Gln Asp Ile cac cgc att tgg ccc gaa ctc cac gag gtc atc aac gaa aag acg aac 528 His Arg Ile Trp Pro Glu Leu His Glu Val Ile Asn Glu Lys Thr Asn ctc tgg gcc gaa ggc gac cgc tgg gtc atg ccg cgc gcc agc ttc 576 Arg Leu Trp Ala Glu Gly Asp Arg Trp Val Met Pro Arg Ala Ser Phe tcg gag ctc gag agc cag cag caa gag ttt gat cgc aac atg att 624 Lys Ser Glu Leu Glu Ser Gln Gln Gln Glu Phe Asp Arg Asn Met Ile 2atg ttc cgt ctt gga atc ctc acc tca att gcc ttc acc aat ctg 672 Glu Met Phe Arg Leu Gly Ile Leu Thr Ser Ile Ala Phe Thr Asn Leu 222gc gac gtt ctc aac atc acg ccc aag gcc gcc ttt ggc ctc agt 72rg Asp Val Leu Asn Ile Thr Pro Lys Ala Ala Phe Gly Leu Ser 225 234gc gag att tcc atg att ttt gcc ttt tcc aag aag aac ggt ctc 768 Leu Gly Glu Ile Ser Met Ile Phe Ala Phe Ser Lys Lys Asn Gly Leu 245 25tc tcc gac cag ctc acc aag gat ctt cgc gag tcc gac gtg tgg aac 8Ser Asp Gln Leu Thr Lys Asp Leu Arg Glu Ser Asp Val Trp Asn 267ct ctg gcc gtt gaa ttt aat gcg ctg cgc gag gcc tgg ggc att 864 Lys Ala Leu Ala Val Glu Phe Asn Ala Leu Arg Glu Ala Trp Gly Ile 275 28ca cag agt gtc ccc aag gac gag ttc tgg caa ggc tac att gtg cgc 9Gln Ser Val Pro Lys Asp Glu Phe Trp Gln Gly Tyr Ile Val Arg 29acc aag cag gat atc gag gcg gcc atc gcc ccg gac agc aag tac 96hr Lys Gln Asp Ile Glu Ala Ala Ile Ala Pro Asp Ser Lys Tyr 33gtg cgc ctc acc atc atc aat gat gcc aac acc gcc ctc att agc ggc l Arg Leu Thr Ile Ile Asn Asp Ala Asn Thr Ala Leu Ile Ser Gly 325 33ag ccc gac gcc

tgc aag gct gcg atc gcg cgt ctc ggt ggc aac att s Pro Asp Ala Cys Lys Ala Ala Ile Ala Arg Leu Gly Gly Asn Ile 345cg ctt ccc gtg acc cag ggc atg tgc ggc cac tgc ccc gag gtg o Ala Leu Pro Val Thr Gln Gly Met Cys Gly His Cys Pro Glu Val 355 36ga cct tat acc aag gat atc gcc aag atc cat gcc aac ctt gag ttc y Pro Tyr Thr Lys Asp Ile Ala Lys Ile His Ala Asn Leu Glu Phe 378tt gtc gac ggc ctt gac ctc tgg acc aca atc aac cag aag cgc o Val Val Asp Gly Leu Asp Leu Trp Thr Thr Ile Asn Gln Lys Arg 385 39gtg cca cgc gcc acg ggc gcc aag gac gaa tgg gcc cct tct tcc u Val Pro Arg Ala Thr Gly Ala Lys Asp Glu Trp Ala Pro Ser Ser 44ggc gag tac gcc ggc cag ctc tac gag aag cag gct aac ttc ccc e Gly Glu Tyr Ala Gly Gln Leu Tyr Glu Lys Gln Ala Asn Phe Pro 423tc gtc gag acc att tac aag caa aac tac gac gtc ttt gtc gag n Ile Val Glu Thr Ile Tyr Lys Gln Asn Tyr Asp Val Phe Val Glu 435 44tt ggg ccc aac aac cac cgt agc acc gca gtg cgc acc acg ctt ggt l Gly Pro Asn Asn His Arg Ser Thr Ala Val Arg Thr Thr Leu Gly 456ag cgc aac cac ctt gct ggc gcc atc gac aag cag aac gag gat o Gln Arg Asn His Leu Ala Gly Ala Ile Asp Lys Gln Asn Glu Asp 465 478gg acg acc atc gtc aag ctt gtg gct tcg ctc aag gcc cac ctt a Trp Thr Thr Ile Val Lys Leu Val Ala Ser Leu Lys Ala His Leu 485 49tt cct ggc gtc l Pro Gly Val 5Schizochytrium sp. 24 Cys Tyr Ser Val Leu Leu Ser Glu Ala Glu Gly His Tyr Glu Arg Glu Arg Ile Ser Leu Asp Glu Glu Ala Pro Lys Leu Ile Val Leu Arg 2 Ala Asp Ser His Glu Glu Ile Leu Gly Arg Leu Asp Lys Ile Arg Glu 35 4g Phe Leu Gln Pro Thr Gly Ala Ala Pro Arg Glu Ser Glu Leu Lys 5 Ala Gln Ala Arg Arg Ile Phe Leu Glu Leu Leu Gly Glu Thr Leu Ala 65 7 Gln Asp Ala Ala Ser Ser Gly Ser Gln Lys Pro Leu Ala Leu Ser Leu 85 9l Ser Thr Pro Ser Lys Leu Gln Arg Glu Val Glu Leu Ala Ala Lys Ile Pro Arg Cys Leu Lys Met Arg Arg Asp Trp Ser Ser Pro Ala Ser Arg Tyr Ala Pro Glu Pro Leu Ala Ser Asp Arg Val Ala Phe Tyr Gly Glu Gly Arg Ser Pro Tyr Tyr Gly Ile Thr Gln Asp Ile His Arg Ile Trp Pro Glu Leu His Glu Val Ile Asn Glu Lys Thr Asn Leu Trp Ala Glu Gly Asp Arg Trp Val Met Pro Arg Ala Ser Phe Ser Glu Leu Glu Ser Gln Gln Gln Glu Phe Asp Arg Asn Met Ile 2Met Phe Arg Leu Gly Ile Leu Thr Ser Ile Ala Phe Thr Asn Leu 222rg Asp Val Leu Asn Ile Thr Pro Lys Ala Ala Phe Gly Leu Ser 225 234ly Glu Ile Ser Met Ile Phe Ala Phe Ser Lys Lys Asn Gly Leu 245 25le Ser Asp Gln Leu Thr Lys Asp Leu Arg Glu Ser Asp Val Trp Asn 267la Leu Ala Val Glu Phe Asn Ala Leu Arg Glu Ala Trp Gly Ile 275 28ro Gln Ser Val Pro Lys Asp Glu Phe Trp Gln Gly Tyr Ile Val Arg 29Thr Lys Gln Asp Ile Glu Ala Ala Ile Ala Pro Asp Ser Lys Tyr 33Val Arg Leu Thr Ile Ile Asn Asp Ala Asn Thr Ala Leu Ile Ser Gly 325 33ys Pro Asp Ala Cys Lys Ala Ala Ile Ala Arg Leu Gly Gly Asn Ile 345la Leu Pro Val Thr Gln Gly Met Cys Gly His Cys Pro Glu Val 355 36ly Pro Tyr Thr Lys Asp Ile Ala Lys Ile His Ala Asn Leu Glu Phe 378al Val Asp Gly Leu Asp Leu Trp Thr Thr Ile Asn Gln Lys Arg 385 39Val Pro Arg Ala Thr Gly Ala Lys Asp Glu Trp Ala Pro Ser Ser 44Gly Glu Tyr Ala Gly Gln Leu Tyr Glu Lys Gln Ala Asn Phe Pro 423le Val Glu Thr Ile Tyr Lys Gln Asn Tyr Asp Val Phe Val Glu 435 44al Gly Pro Asn Asn His Arg Ser Thr Ala Val Arg Thr Thr Leu Gly 456ln Arg Asn His Leu Ala Gly Ala Ile Asp Lys Gln Asn Glu Asp 465 478rp Thr Thr Ile Val Lys Leu Val Ala Ser Leu Lys Ala His Leu 485 49al Pro Gly Val 553chizochytrium sp. CDS (3tg ctc gat ctc gac agt atg ctt gcg ctg agc tct gcc agt gcc tcc 48 Leu Leu Asp Leu Asp Ser Met Leu Ala Leu Ser Ser Ala Ser Ala Ser aac ctt gtt gag act gcg cct agc gac gcc tcg gtc att gtg ccg 96 Gly Asn Leu Val Glu Thr Ala Pro Ser Asp Ala Ser Val Ile Val Pro 2 ccc tgc aac att gcg gat ctc ggc agc cgc gcc ttc atg aaa acg tac Cys Asn Ile Ala Asp Leu Gly Ser Arg Ala Phe Met Lys Thr Tyr 35 4t gtt tcg gcg cct ctg tac acg ggc gcc atg gcc aag ggc att gcc Val Ser Ala Pro Leu Tyr Thr Gly Ala Met Ala Lys Gly Ile Ala 5 tct gcg gac ctc gtc att gcc gcc ggc cgc cag ggc atc ctt gcg tcc 24la Asp Leu Val Ile Ala Ala Gly Arg Gln Gly Ile Leu Ala Ser 65 7 ttt ggc gcc ggc gga ctt ccc atg cag gtt gtg cgt gag tcc atc gaa 288 Phe Gly Ala Gly Gly Leu Pro Met Gln Val Val Arg Glu Ser Ile Glu 85 9g att cag gcc gcc ctg ccc aat ggc ccg tac gct gtc aac ctt atc 336 Lys Ile Gln Ala Ala Leu Pro Asn Gly Pro Tyr Ala Val Asn Leu Ile tct ccc ttt gac agc aac ctc gaa aag ggc aat gtc gat ctc ttc 384 His Ser Pro Phe Asp Ser Asn Leu Glu Lys Gly Asn Val Asp Leu Phe gag aag ggt gtc acc ttt gtc gag gcc tcg gcc ttt atg acg ctc 432 Leu Glu Lys Gly Val Thr Phe Val Glu Ala Ser Ala Phe Met Thr Leu ccg cag gtc gtg cgg tac cgc gcg gct ggc ctc acg cgc aac gcc 48ro Gln Val Val Arg Tyr Arg Ala Ala Gly Leu Thr Arg Asn Ala gac ggc tcg gtc aac atc cgc aac cgt atc att ggc aag gtc tcg cgc 528 Asp Gly Ser Val Asn Ile Arg Asn Arg Ile Ile Gly Lys Val Ser Arg gag ctc gcc gag atg ttc atg cgt cct gcg ccc gag cac ctt ctt 576 Thr Glu Leu Ala Glu Met Phe Met Arg Pro Ala Pro Glu His Leu Leu aag ctc att gct tcc ggc gag atc aac cag gag cag gcc gag ctc 624 Gln Lys Leu Ile Ala Ser Gly Glu Ile Asn Gln Glu Gln Ala Glu Leu 2cgc cgt gtt ccc gtc gct gac gac atc gcg gtc gaa gct gac tcg 672 Ala Arg Arg Val Pro Val Ala Asp Asp Ile Ala Val Glu Ala Asp Ser 222gc cac acc gac aac cgc ccc atc cac gtc att ctg ccc ctc atc 72ly His Thr Asp Asn Arg Pro Ile His Val Ile Leu Pro Leu Ile 225 234ac ctt cgc gac cgc ctt cac cgc gag tgc ggc tac ccg gcc aac 768 Ile Asn Leu Arg Asp Arg Leu His Arg Glu Cys Gly Tyr Pro Ala Asn 245 25tt cgc gtc cgt gtg ggc gcc ggc ggt ggc att ggg tgc ccc cag gcg 8Arg Val Arg Val Gly Ala Gly Gly Gly Ile Gly Cys Pro Gln Ala 267tg gcc acc ttc aac atg ggt gcc tcc ttt att gtc acc ggc acc 864 Ala Leu Ala Thr Phe Asn Met Gly Ala Ser Phe Ile Val Thr Gly Thr 275 28tg aac cag gtc gcc aag cag tcg ggc acg tgc gac aat gtg cgc aag 9Asn Gln Val Ala Lys Gln Ser Gly Thr Cys Asp Asn Val Arg Lys 29ctc gcg aag gcc act tac tcg gac gta tgc atg gcc ccg gct gcc 96eu Ala Lys Ala Thr Tyr Ser Asp Val Cys Met Ala Pro Ala Ala 33gac atg ttc gag gaa ggc gtc aag ctt cag gtc ctc aag aag gga acc p Met Phe Glu Glu Gly Val Lys Leu Gln Val Leu Lys Lys Gly Thr 325 33tg ttt ccc tcg cgc gcc aac aag ctc tac gag ctc ttt tgc aag tac t Phe Pro Ser Arg Ala Asn Lys Leu Tyr Glu Leu Phe Cys Lys Tyr 345cg ttc gag tcc atg ccc ccc gca gag ctt gcg cgc gtc gag aag p Ser Phe Glu Ser Met Pro Pro Ala Glu Leu Ala Arg Val Glu Lys 355 36gc atc ttc agc cgc gcg ctc gaa gag gtc tgg gac gag acc aaa aac g Ile Phe Ser Arg Ala Leu Glu Glu Val Trp Asp Glu Thr Lys Asn 378ac att aac cgt ctt cac aac ccg gag aag atc cag cgc gcc gag e Tyr Ile Asn Arg Leu His Asn Pro Glu Lys Ile Gln Arg Ala Glu 385 39gac ccc aag ctc aag atg tcg ctg tgc ttt cgc tgg tac ctg agc g Asp Pro Lys Leu Lys Met Ser Leu Cys Phe Arg Trp Tyr Leu Ser 44gcg agc cgc tgg gcc aac act gga gct tcc gat cgc gtc atg gac u Ala Ser Arg Trp Ala Asn Thr Gly Ala Ser Asp Arg Val Met Asp 423ag gtc tgg tgc ggt cct gcc att ggt tcc ttc aac gat ttc atc r Gln Val Trp Cys Gly Pro Ala Ile Gly Ser Phe Asn Asp Phe Ile 435 44ag gga act tac ctt gat ccg gcc gtc gca aac gag tac ccg tgc gtc s Gly Thr Tyr Leu Asp Pro Ala Val Ala Asn Glu Tyr Pro Cys Val 456ag att aac aag cag atc ctt cgt gga gcg tgc ttc ttg cgc cgt l Gln Ile Asn Lys Gln Ile Leu Arg Gly Ala Cys Phe Leu Arg Arg 465 478aa att ctg cgc aac gca cgc ctt tcc gat ggc gct gcc gct ctt u Glu Ile Leu Arg Asn Ala Arg Leu Ser Asp Gly Ala Ala Ala Leu 485 49tg gcc agc atc gat gac aca tac gtc ccg gcc gag aag ctg l Ala Ser Ile Asp Asp Thr Tyr Val Pro Ala Glu Lys Leu 55Schizochytrium sp. 26 Leu Leu Asp Leu Asp Ser Met Leu Ala Leu Ser Ser Ala Ser Ala Ser Asn Leu Val Glu Thr Ala Pro Ser Asp Ala Ser Val Ile Val Pro 2 Pro Cys Asn Ile Ala Asp Leu Gly Ser Arg Ala Phe Met Lys Thr Tyr 35 4y Val Ser Ala Pro Leu Tyr Thr Gly Ala Met Ala Lys Gly Ile Ala 5 Ser Ala Asp Leu Val Ile Ala Ala Gly Arg Gln Gly Ile Leu Ala Ser 65 7 Phe Gly Ala Gly Gly Leu Pro Met Gln Val Val Arg Glu Ser Ile Glu 85 9s Ile Gln Ala Ala Leu Pro Asn Gly Pro Tyr Ala Val Asn Leu Ile Ser Pro Phe Asp Ser Asn Leu Glu Lys Gly Asn Val Asp Leu Phe Glu Lys Gly Val Thr Phe Val Glu Ala Ser Ala Phe Met Thr Leu Pro Gln Val Val Arg Tyr Arg Ala Ala Gly Leu Thr Arg Asn Ala Asp Gly Ser Val Asn Ile Arg Asn Arg Ile Ile Gly Lys Val Ser Arg Glu Leu Ala Glu Met Phe Met Arg Pro Ala Pro Glu His Leu Leu Lys Leu Ile Ala Ser Gly Glu Ile Asn Gln Glu Gln Ala Glu Leu 2Arg Arg Val Pro Val Ala Asp Asp Ile Ala Val Glu Ala Asp Ser 222ly His Thr Asp Asn Arg Pro Ile His Val Ile Leu Pro Leu Ile 225 234sn Leu Arg Asp Arg Leu His Arg Glu Cys Gly Tyr Pro Ala Asn 245 25eu Arg Val Arg Val Gly Ala Gly Gly Gly Ile Gly Cys Pro Gln Ala 267eu Ala Thr Phe Asn Met Gly Ala Ser Phe Ile Val Thr Gly Thr 275 28al Asn Gln Val Ala Lys Gln Ser Gly Thr Cys Asp Asn Val Arg Lys 29Leu Ala Lys Ala Thr Tyr Ser Asp Val Cys Met Ala Pro Ala Ala 33Asp Met Phe Glu Glu Gly Val Lys Leu Gln Val Leu Lys Lys Gly Thr 325 33et Phe Pro Ser Arg Ala Asn Lys Leu Tyr Glu Leu Phe Cys Lys Tyr 345er Phe Glu Ser Met Pro Pro Ala Glu Leu Ala Arg Val Glu Lys 355 36rg Ile Phe Ser Arg Ala Leu Glu Glu Val Trp Asp Glu Thr Lys Asn 378yr Ile Asn Arg Leu His Asn Pro Glu Lys Ile Gln Arg Ala Glu 385 39Asp Pro Lys Leu Lys Met Ser Leu Cys Phe Arg Trp Tyr Leu Ser 44Ala Ser Arg Trp Ala Asn Thr Gly Ala Ser Asp Arg Val Met Asp 423ln Val Trp Cys Gly Pro Ala Ile Gly Ser Phe Asn Asp Phe Ile 435 44ys Gly Thr Tyr Leu Asp Pro Ala Val Ala Asn Glu Tyr Pro Cys Val 456ln Ile Asn Lys Gln Ile Leu Arg Gly Ala Cys Phe Leu Arg Arg 465 478lu Ile Leu Arg Asn Ala Arg Leu Ser Asp Gly Ala Ala Ala Leu 485 49al Ala Ser Ile Asp Asp Thr Tyr Val Pro Ala Glu Lys Leu 555Schizochytrium sp. CDS (atg gcg ctc cgt gtc aag acg aac aag aag cca tgc tgg gag atg acc 48 Met Ala Leu Arg Val Lys Thr Asn Lys Lys Pro Cys Trp Glu Met Thr gag gag ctg acc agc ggc aag acc gag gtg ttc aac tat gag gaa 96 Lys Glu Glu Leu Thr Ser Gly Lys Thr Glu Val Phe Asn Tyr Glu Glu 2 ctc ctc gag ttc gca gag ggc gac atc gcc aag gtc ttc gga ccc gag Leu Glu Phe Ala Glu Gly Asp Ile Ala Lys Val Phe Gly Pro Glu 35 4c gcc gtc atc gac aag tac ccg cgc cgc gtg cgc ctg ccc gcc cgc Ala Val Ile Asp Lys Tyr Pro Arg Arg Val Arg Leu Pro Ala Arg 5 gag tac ctg ctc gtg acc cgc gtc acc ctc atg gac gcc gag gtc aac 24yr Leu Leu Val Thr Arg Val Thr Leu Met Asp Ala Glu Val Asn 65 7 aac tac cgc gtc ggc gcc cgc atg gtc acc gag tac gat ctc ccc gtc 288 Asn Tyr Arg Val Gly Ala Arg Met Val Thr Glu Tyr Asp Leu Pro Val 85 9c gga gag ctc tcc gag ggc gga gac tgc ccc tgg gcc gtc ctg gtc 336 Asn Gly Glu Leu Ser Glu Gly Gly Asp Cys Pro Trp Ala Val Leu Val agt ggc cag tgc gat ctc atg ctc atc tcc tac atg ggc att gac 384 Glu Ser Gly Gln Cys Asp Leu Met Leu Ile Ser Tyr Met Gly Ile Asp cag aac cag ggc gac cgc gtc tac cgc ctg ctc aac acc acg ctc 432 Phe Gln Asn Gln Gly Asp Arg Val Tyr Arg Leu Leu Asn Thr Thr Leu ttt tac ggc gtg gcc cac gag ggc gag acc ctc gag tac gac att 48he Tyr Gly Val Ala His Glu Gly Glu Thr Leu Glu Tyr Asp Ile cgc gtc acc ggc ttc gcc aag cgt ctc gac ggc ggc atc tcc atg ttc 528 Arg Val Thr Gly Phe Ala Lys Arg Leu Asp Gly Gly Ile Ser Met Phe ttc gag tac gac tgc tac gtc aac ggc cgc ctc ctc atc gag atg 576 Phe Phe Glu Tyr Asp Cys Tyr Val Asn Gly Arg Leu Leu Ile Glu Met gat ggc tgc gcc ggc ttc ttc acc aac gag gag ctc gac gcc ggc 624 Arg Asp Gly Cys Ala Gly Phe Phe Thr Asn Glu

Glu Leu Asp Ala Gly 2ggc gtc gtc ttc acc cgc ggc gac ctc gcc gcc cgc gcc aag atc 672 Lys Gly Val Val Phe Thr Arg Gly Asp Leu Ala Ala Arg Ala Lys Ile 222ag cag gac gtc tcc ccc tac gcc gtc gcc ccc tgc ctc cac aag 72ys Gln Asp Val Ser Pro Tyr Ala Val Ala Pro Cys Leu His Lys 225 234ag ctc aac gaa aag gag atg cag acc ctc gtc gac aag gac tgg 768 Thr Lys Leu Asn Glu Lys Glu Met Gln Thr Leu Val Asp Lys Asp Trp 245 25ca tcc gtc ttt ggc tcc aag aac ggc atg ccg gaa atc aac tac aaa 8Ser Val Phe Gly Ser Lys Asn Gly Met Pro Glu Ile Asn Tyr Lys 267gc gcg cgt aag atg ctc atg att gac cgc gtc acc agc att gac 864 Leu Cys Ala Arg Lys Met Leu Met Ile Asp Arg Val Thr Ser Ile Asp 275 28ac aag ggc ggt gtc tac ggc ctc ggt cag ctc gtc ggt gaa aag atc 9Lys Gly Gly Val Tyr Gly Leu Gly Gln Leu Val Gly Glu Lys Ile 29gag cgc gac cac tgg tac ttt ccc tgc cac ttt gtc aag gat cag 96lu Arg Asp His Trp Tyr Phe Pro Cys His Phe Val Lys Asp Gln 33gtc atg gcc gga tcc ctc gtc tcc gac ggc tgc agc cag atg ctc aag l Met Ala Gly Ser Leu Val Ser Asp Gly Cys Ser Gln Met Leu Lys 325 33tg tac atg atc tgg ctc ggc ctc cac ctc acc acc gga ccc ttt gac t Tyr Met Ile Trp Leu Gly Leu His Leu Thr Thr Gly Pro Phe Asp 345gc ccg gtc aac ggc cac ccc aac aag gtc cgc tgc cgc ggc caa e Arg Pro Val Asn Gly His Pro Asn Lys Val Arg Cys Arg Gly Gln 355 36tc tcc ccg cac aag ggc aag ctc gtc tac gtc atg gag atc aag gag e Ser Pro His Lys Gly Lys Leu Val Tyr Val Met Glu Ile Lys Glu 378gc ttc gac gag gac aac gac ccg tac gcc att gcc gac gtc aac t Gly Phe Asp Glu Asp Asn Asp Pro Tyr Ala Ile Ala Asp Val Asn 385 39att gat gtc gac ttc gaa aag ggc cag gac ttt agc ctc gac cgc e Ile Asp Val Asp Phe Glu Lys Gly Gln Asp Phe Ser Leu Asp Arg 44agc gac tac ggc aag ggc gac ctc aac aag aag atc gtc gtc gac e Ser Asp Tyr Gly Lys Gly Asp Leu Asn Lys Lys Ile Val Val Asp 423ag ggc atc gct ctc aag atg cag aag cgc tcc acc aac aag aac e Lys Gly Ile Ala Leu Lys Met Gln Lys Arg Ser Thr Asn Lys Asn 435 44cc tcc aag gtt cag ccc gtc ttt gcc aac ggc gcc gcc act gtc ggc o Ser Lys Val Gln Pro Val Phe Ala Asn Gly Ala Ala Thr Val Gly 456ag gcc tcc aag gct tcc tcc ggc gcc agc gcc agc gcc agc gcc o Glu Ala Ser Lys Ala Ser Ser Gly Ala Ser Ala Ser Ala Ser Ala 465 478cg gcc aag cct gcc ttc agc gcc gat gtt ctt gcg ccc aag ccc a Pro Ala Lys Pro Ala Phe Ser Ala Asp Val Leu Ala Pro Lys Pro 485 49tt gcc ctt ccc gag cac atc ctc aag ggc gac gcc ctc gcc ccc aag l Ala Leu Pro Glu His Ile Leu Lys Gly Asp Ala Leu Ala Pro Lys 55atg tcc tgg cac ccc atg gcc cgc atc ccg ggc aac ccg acg ccc u Met Ser Trp His Pro Met Ala Arg Ile Pro Gly Asn Pro Thr Pro 5525 tct ttt gcg ccc tcg gcc tac aag ccg cgc aac atc gcc ttt acg ccc r Phe Ala Pro Ser Ala Tyr Lys Pro Arg Asn Ile Ala Phe Thr Pro 534cc ggc aac ccc aac gat aac gac cac acc ccg ggc aag atg ccg e Pro Gly Asn Pro Asn Asp Asn Asp His Thr Pro Gly Lys Met Pro 545 556cc tgg ttc aac atg gcc gag ttc atg gcc ggc aag gtc agc atg u Thr Trp Phe Asn Met Ala Glu Phe Met Ala Gly Lys Val Ser Met 565 57gc ctc ggc ccc gag ttc gcc aag ttc gac gac tcg aac acc agc cgc s Leu Gly Pro Glu Phe Ala Lys Phe Asp Asp Ser Asn Thr Ser Arg 589cc gct tgg gac ctc gct ctc gtc acc cgc gcc gtg tct gtg tct r Pro Ala Trp Asp Leu Ala Leu Val Thr Arg Ala Val Ser Val Ser 595 6gac ctc aag cac gtc aac tac cgc aac atc gac ctc gac ccc tcc aag p Leu Lys His Val Asn Tyr Arg Asn Ile Asp Leu Asp Pro Ser Lys 662cc atg gtc ggc gag ttc gac tgc ccc gcg gac gcc tgg ttc tac y Thr Met Val Gly Glu Phe Asp Cys Pro Ala Asp Ala Trp Phe Tyr 625 634gc gcc tgc aac gat gcc cac atg ccg tac tcg atc ctc atg gag s Gly Ala Cys Asn Asp Ala His Met Pro Tyr Ser Ile Leu Met Glu 645 65tc gcc ctc cag acc tcg ggt gtg ctc acc tcg gtg ctc aag gcg ccc 2 Ala Leu Gln Thr Ser Gly Val Leu Thr Ser Val Leu Lys Ala Pro 667cc atg gag aag gac gac atc ctc ttc cgc aac ctc gac gcc aac 2 Thr Met Glu Lys Asp Asp Ile Leu Phe Arg Asn Leu Asp Ala Asn 675 68cc gag ttc gtg cgc gcc gac ctc gac tac cgc ggc aag act atc cgc 2 Glu Phe Val Arg Ala Asp Leu Asp Tyr Arg Gly Lys Thr Ile Arg 69gtc acc aag tgc act ggc tac agc atg ctc ggc gag atg ggc gtc 2 Val Thr Lys Cys Thr Gly Tyr Ser Met Leu Gly Glu Met Gly Val 77cac cgc ttc acc ttt gag ctc tac gtc gat gat gtg ctc ttt tac aag 22Arg Phe Thr Phe Glu Leu Tyr Val Asp Asp Val Leu Phe Tyr Lys 725 73gc tcg acc tcg ttc ggc tgg ttc gtg ccc gag gtc ttt gcc gcc cag 2256 Gly Ser Thr Ser Phe Gly Trp Phe Val Pro Glu Val Phe Ala Ala Gln 745gc ctc gac aac ggc cgc aag tcg gag ccc tgg ttc att gag aac 23Gly Leu Asp Asn Gly Arg Lys Ser Glu Pro Trp Phe Ile Glu Asn 755 76ag gtt ccg gcc tcg cag gtc tcc tcc ttt gac gtg cgc ccc aac ggc 2352 Lys Val Pro Ala Ser Gln Val Ser Ser Phe Asp Val Arg Pro Asn Gly 778gc cgc acc gcc atc ttc gcc aac gcc ccc agc ggc gcc cag ctc 24Gly Arg Thr Ala Ile Phe Ala Asn Ala Pro Ser Gly Ala Gln Leu 785 79cgc cgc acg gac cag ggc cag tac ctc gac gcc gtc gac att gtc 2448 Asn Arg Arg Thr Asp Gln Gly Gln Tyr Leu Asp Ala Val Asp Ile Val 88ggc agc ggc aag aag agc ctc ggc tac gcc cac ggt tcc aag acg 2496 Ser Gly Ser Gly Lys Lys Ser Leu Gly Tyr Ala His Gly Ser Lys Thr 823ac ccg aac gac tgg ttc ttc tcg tgc cac ttt tgg ttt gac tcg 2544 Val Asn Pro Asn Asp Trp Phe Phe Ser Cys His Phe Trp Phe Asp Ser 835 84tc atg ccc gga agt ctc ggt gtc gag tcc atg ttc cag ctc gtc gag 2592 Val Met Pro Gly Ser Leu Gly Val Glu Ser Met Phe Gln Leu Val Glu 856tc gcc gcc cac gag gat ctc gct ggc aaa gca cgg cat tgc caa 264le Ala Ala His Glu Asp Leu Ala Gly Lys Ala Arg His Cys Gln 865 878ac ctt tgt gca cgc ccc cgg gca aga tca agc tgg aag tac cgc 2688 Pro His Leu Cys Ala Arg Pro Arg Ala Arg Ser Ser Trp Lys Tyr Arg 885 89gc cag ctc acg ccc aag agc aag aag atg gac tcg gag gtc cac atc 2736 Gly Gln Leu Thr Pro Lys Ser Lys Lys Met Asp Ser Glu Val His Ile 99tcc gtg gac gcc cac gac ggc gtt gtc gac ctc gtc gcc gac ggc 2784 Val Ser Val Asp Ala His Asp Gly Val Val Asp Leu Val Ala Asp Gly 9925 ttc ctc tgg gcc gac agc ctc cgc gtc tac tcg gtg agc aac att cgc 2832 Phe Leu Trp Ala Asp Ser Leu Arg Val Tyr Ser Val Ser Asn Ile Arg 934gc atc gcc tcc ggt gag gcc cct gcc gcc gcc tcc tcc gcc gcc 288rg Ile Ala Ser Gly Glu Ala Pro Ala Ala Ala Ser Ser Ala Ala 945 956tg ggc tcc tcg gct tcg tcc gtc gag cgc acg cgc tcg agc ccc 2928 Ser Val Gly Ser Ser Ala Ser Ser Val Glu Arg Thr Arg Ser Ser Pro 965 97ct gtc gcc tcc ggc ccg gcc cag acc atc gac ctc aag cag ctc aag 2976 Ala Val Ala Ser Gly Pro Ala Gln Thr Ile Asp Leu Lys Gln Leu Lys 989ag ctc ctc gag ctc gat gcc ccg ctc tac ctc tcg cag gac ccg 3 Glu Leu Leu Glu Leu Asp Ala Pro Leu Tyr Leu Ser Gln Asp Pro 995 agc ggc cag ctc aag aag cac acc gac gtg gcc tcc ggc cag 3 Ser Gly Gln Leu Lys Lys His Thr Asp Val Ala Ser Gly Gln gcc acc atc gtg cag ccc tgc acg ctc ggc gac ctc ggt gac cgc 3 Thr Ile Val Gln Pro Cys Thr Leu Gly Asp Leu Gly Asp Arg 3tcc ttc atg gag acc tac ggc gtc gtc gcc ccg ctg tac acg ggc 3 Phe Met Glu Thr Tyr Gly Val Val Ala Pro Leu Tyr Thr Gly 45 c atg gcc aag ggc att gcc tcg gcg gac ctc gtc atc gcc gcc 32Met Ala Lys Gly Ile Ala Ser Ala Asp Leu Val Ile Ala Ala 6ggc aag cgc aag atc ctc ggc tcc ttt ggc gcc ggc ggc ctc ccc 3249 Gly Lys Arg Lys Ile Leu Gly Ser Phe Gly Ala Gly Gly Leu Pro 75 g cac cac gtg cgc gcc gcc ctc gag aag atc cag gcc gcc ctg 3294 Met His His Val Arg Ala Ala Leu Glu Lys Ile Gln Ala Ala Leu 9cct cag ggc ccc tac gcc gtc aac ctc atc cac tcg cct ttt gac 3339 Pro Gln Gly Pro Tyr Ala Val Asn Leu Ile His Ser Pro Phe Asp agc aac ctc gag aag ggc aac gtc gat ctc ttc ctc gag aag ggc 3384 Ser Asn Leu Glu Lys Gly Asn Val Asp Leu Phe Leu Glu Lys Gly 2gtc act gtg gtg gag gcc tcg gca ttc atg acc ctc acc ccg cag 3429 Val Thr Val Val Glu Ala Ser Ala Phe Met Thr Leu Thr Pro Gln 35 c gtg cgc tac cgc gcc gcc ggc ctc tcg cgc aac gcc gac ggt 3474 Val Val Arg Tyr Arg Ala Ala Gly Leu Ser Arg Asn Ala Asp Gly 5tcg gtc aac atc cgc aac cgc atc atc ggc aag gtc tcg cgc acc 35Val Asn Ile Arg Asn Arg Ile Ile Gly Lys Val Ser Arg Thr 65 g ctc gcc gag atg ttc atc cgc ccg gcc ccg gag cac ctc ctc 3564 Glu Leu Ala Glu Met Phe Ile Arg Pro Ala Pro Glu His Leu Leu 8gag aag ctc atc gcc tcg ggc gag atc acc cag gag cag gcc gag 36Lys Leu Ile Ala Ser Gly Glu Ile Thr Gln Glu Gln Ala Glu 95 c gcg cgc cgc gtt ccc gtc gcc gac gat atc gct gtc gag gct 3654 Leu Ala Arg Arg Val Pro Val Ala Asp Asp Ile Ala Val Glu Ala gac tcg ggc ggc cac acc gac aac cgc ccc atc cac gtc atc ctc 3699 Asp Ser Gly Gly His Thr Asp Asn Arg Pro Ile His Val Ile Leu 25 g ctc atc atc aac ctc cgc aac cgc ctg cac cgc gag tgc ggc 3744 Pro Leu Ile Ile Asn Leu Arg Asn Arg Leu His Arg Glu Cys Gly 4tac ccc gcg cac ctc cgc gtc cgc gtt ggc gcc ggc ggt ggc gtc 3789 Tyr Pro Ala His Leu Arg Val Arg Val Gly Ala Gly Gly Gly Val 55 c tgc ccg cag gcc gcc gcc gcc gcg ctc acc atg ggc gcc gcc 3834 Gly Cys Pro Gln Ala Ala Ala Ala Ala Leu Thr Met Gly Ala Ala 7ttc atc gtc acc ggc act gtc aac cag gtc gcc aag cag tcc ggc 3879 Phe Ile Val Thr Gly Thr Val Asn Gln Val Ala Lys Gln Ser Gly 85 c tgc gac aac gtg cgc aag cag ctc tcg cag gcc acc tac tcg 3924 Thr Cys Asp Asn Val Arg Lys Gln Leu Ser Gln Ala Thr Tyr Ser gat atc tgc atg gcc ccg gcc gcc gac atg ttc gag gag ggc gtc 3969 Asp Ile Cys Met Ala Pro Ala Ala Asp Met Phe Glu Glu Gly Val aag ctc cag gtc ctc aag aag gga acc atg ttc ccc tcg cgc gcc 4 Leu Gln Val Leu Lys Lys Gly Thr Met Phe Pro Ser Arg Ala 3aac aag ctc tac gag ctc ttt tgc aag tac gac tcc ttc gac tcc 4 Lys Leu Tyr Glu Leu Phe Cys Lys Tyr Asp Ser Phe Asp Ser 45 g cct cct gcc gag ctc gag cgc atc gag aag cgt atc ttc aag 4 Pro Pro Ala Glu Leu Glu Arg Ile Glu Lys Arg Ile Phe Lys 6cgc gca ctc cag gag gtc tgg gag gag acc aag gac ttt tac att 4 Ala Leu Gln Glu Val Trp Glu Glu Thr Lys Asp Phe Tyr Ile 75 c ggt ctc aag aac ccg gag aag atc cag cgc gcc gag cac gac 4 Gly Leu Lys Asn Pro Glu Lys Ile Gln Arg Ala Glu His Asp 9ccc aag ctc aag atg tcg ctc tgc ttc cgc tgg tac ctt ggt ctt 4239 Pro Lys Leu Lys Met Ser Leu Cys Phe Arg Trp Tyr Leu Gly Leu gcc agc cgc tgg gcc aac atg ggc gcc ccg gac cgc gtc atg gac 4284 Ala Ser Arg Trp Ala Asn Met Gly Ala Pro Asp Arg Val Met Asp 2tac cag gtc tgg tgt ggc ccg gcc att ggc gcc ttc aac gac ttc 4329 Tyr Gln Val Trp Cys Gly Pro Ala Ile Gly Ala Phe Asn Asp Phe 35 c aag ggc acc tac ctc gac ccc gct gtc tcc aac gag tac ccc 4374 Ile Lys Gly Thr Tyr Leu Asp Pro Ala Val Ser Asn Glu Tyr Pro 5tgt gtc gtc cag atc aac ctg caa atc ctc cgt ggt gcc tgc tac 44Val Val Gln Ile Asn Leu Gln Ile Leu Arg Gly Ala Cys Tyr 65 g cgc cgt ctc aac gcc ctg cgc aac gac ccg cgc att gac ctc 4464 Leu Arg Arg Leu Asn Ala Leu Arg Asn Asp Pro Arg Ile Asp Leu 8gag acc gag gat gct gcc ttt gtc tac gag ccc acc aac gcg ctc 45Thr Glu Asp Ala Ala Phe Val Tyr Glu Pro Thr Asn Ala Leu 95 a 455Schizochytrium sp. 28 Met Ala Leu Arg Val Lys Thr Asn Lys Lys Pro Cys Trp Glu Met Thr Glu Glu Leu Thr Ser Gly Lys Thr Glu Val Phe Asn Tyr Glu Glu 2 Leu Leu Glu Phe Ala Glu Gly Asp Ile Ala Lys Val Phe Gly Pro Glu 35 4e Ala Val Ile Asp Lys Tyr Pro Arg Arg Val Arg Leu Pro Ala Arg 5 Glu Tyr Leu Leu Val Thr Arg Val Thr Leu Met Asp Ala Glu Val Asn 65 7 Asn Tyr Arg Val Gly Ala Arg Met Val Thr Glu Tyr Asp Leu Pro Val 85 9n Gly Glu Leu Ser Glu Gly Gly Asp Cys Pro Trp Ala Val Leu Val Ser Gly Gln Cys Asp Leu Met Leu Ile Ser Tyr Met Gly Ile Asp Gln Asn Gln Gly Asp Arg Val Tyr Arg Leu Leu Asn Thr Thr Leu Phe Tyr Gly Val Ala His Glu Gly Glu Thr Leu Glu Tyr Asp Ile Arg Val Thr Gly Phe Ala Lys Arg Leu Asp Gly Gly Ile Ser Met Phe Phe Glu Tyr Asp Cys Tyr Val Asn Gly Arg Leu Leu Ile Glu Met Asp Gly Cys Ala Gly Phe Phe Thr Asn Glu Glu Leu Asp Ala Gly 2Gly Val Val Phe Thr Arg Gly Asp Leu Ala Ala Arg Ala Lys Ile 222ys Gln Asp Val Ser Pro Tyr Ala Val Ala Pro Cys Leu His Lys 225 234ys Leu Asn Glu Lys Glu Met Gln Thr Leu Val Asp Lys Asp Trp 245 25la Ser Val Phe Gly Ser Lys Asn Gly Met Pro Glu Ile Asn Tyr Lys 267ys Ala Arg Lys Met Leu Met Ile Asp Arg Val Thr Ser Ile Asp 275 28is Lys Gly Gly Val Tyr Gly Leu Gly Gln Leu Val Gly Glu Lys Ile 29Glu Arg Asp His Trp Tyr Phe Pro

Cys His Phe Val Lys Asp Gln 33Val Met Ala Gly Ser Leu Val Ser Asp Gly Cys Ser Gln Met Leu Lys 325 33et Tyr Met Ile Trp Leu Gly Leu His Leu Thr Thr Gly Pro Phe Asp 345rg Pro Val Asn Gly His Pro Asn Lys Val Arg Cys Arg Gly Gln 355 36le Ser Pro His Lys Gly Lys Leu Val Tyr Val Met Glu Ile Lys Glu 378ly Phe Asp Glu Asp Asn Asp Pro Tyr Ala Ile Ala Asp Val Asn 385 39Ile Asp Val Asp Phe Glu Lys Gly Gln Asp Phe Ser Leu Asp Arg 44Ser Asp Tyr Gly Lys Gly Asp Leu Asn Lys Lys Ile Val Val Asp 423ys Gly Ile Ala Leu Lys Met Gln Lys Arg Ser Thr Asn Lys Asn 435 44ro Ser Lys Val Gln Pro Val Phe Ala Asn Gly Ala Ala Thr Val Gly 456lu Ala Ser Lys Ala Ser Ser Gly Ala Ser Ala Ser Ala Ser Ala 465 478ro Ala Lys Pro Ala Phe Ser Ala Asp Val Leu Ala Pro Lys Pro 485 49al Ala Leu Pro Glu His Ile Leu Lys Gly Asp Ala Leu Ala Pro Lys 55Met Ser Trp His Pro Met Ala Arg Ile Pro Gly Asn Pro Thr Pro 5525 Ser Phe Ala Pro Ser Ala Tyr Lys Pro Arg Asn Ile Ala Phe Thr Pro 534ro Gly Asn Pro Asn Asp Asn Asp His Thr Pro Gly Lys Met Pro 545 556hr Trp Phe Asn Met Ala Glu Phe Met Ala Gly Lys Val Ser Met 565 57ys Leu Gly Pro Glu Phe Ala Lys Phe Asp Asp Ser Asn Thr Ser Arg 589ro Ala Trp Asp Leu Ala Leu Val Thr Arg Ala Val Ser Val Ser 595 6Asp Leu Lys His Val Asn Tyr Arg Asn Ile Asp Leu Asp Pro Ser Lys 662hr Met Val Gly Glu Phe Asp Cys Pro Ala Asp Ala Trp Phe Tyr 625 634ly Ala Cys Asn Asp Ala His Met Pro Tyr Ser Ile Leu Met Glu 645 65le Ala Leu Gln Thr Ser Gly Val Leu Thr Ser Val Leu Lys Ala Pro 667hr Met Glu Lys Asp Asp Ile Leu Phe Arg Asn Leu Asp Ala Asn 675 68la Glu Phe Val Arg Ala Asp Leu Asp Tyr Arg Gly Lys Thr Ile Arg 69Val Thr Lys Cys Thr Gly Tyr Ser Met Leu Gly Glu Met Gly Val 77His Arg Phe Thr Phe Glu Leu Tyr Val Asp Asp Val Leu Phe Tyr Lys 725 73ly Ser Thr Ser Phe Gly Trp Phe Val Pro Glu Val Phe Ala Ala Gln 745ly Leu Asp Asn Gly Arg Lys Ser Glu Pro Trp Phe Ile Glu Asn 755 76ys Val Pro Ala Ser Gln Val Ser Ser Phe Asp Val Arg Pro Asn Gly 778ly Arg Thr Ala Ile Phe Ala Asn Ala Pro Ser Gly Ala Gln Leu 785 79Arg Arg Thr Asp Gln Gly Gln Tyr Leu Asp Ala Val Asp Ile Val 88Gly Ser Gly Lys Lys Ser Leu Gly Tyr Ala His Gly Ser Lys Thr 823sn Pro Asn Asp Trp Phe Phe Ser Cys His Phe Trp Phe Asp Ser 835 84al Met Pro Gly Ser Leu Gly Val Glu Ser Met Phe Gln Leu Val Glu 856le Ala Ala His Glu Asp Leu Ala Gly Lys Ala Arg His Cys Gln 865 878is Leu Cys Ala Arg Pro Arg Ala Arg Ser Ser Trp Lys Tyr Arg 885 89ly Gln Leu Thr Pro Lys Ser Lys Lys Met Asp Ser Glu Val His Ile 99Ser Val Asp Ala His Asp Gly Val Val Asp Leu Val Ala Asp Gly 9925 Phe Leu Trp Ala Asp Ser Leu Arg Val Tyr Ser Val Ser Asn Ile Arg 934rg Ile Ala Ser Gly Glu Ala Pro Ala Ala Ala Ser Ser Ala Ala 945 956al Gly Ser Ser Ala Ser Ser Val Glu Arg Thr Arg Ser Ser Pro 965 97la Val Ala Ser Gly Pro Ala Gln Thr Ile Asp Leu Lys Gln Leu Lys 989lu Leu Leu Glu Leu Asp Ala Pro Leu Tyr Leu Ser Gln Asp Pro 995 Ser Gly Gln Leu Lys Lys His Thr Asp Val Ala Ser Gly Gln Ala Thr Ile Val Gln Pro Cys Thr Leu Gly Asp Leu Gly Asp Arg 3Ser Phe Met Glu Thr Tyr Gly Val Val Ala Pro Leu Tyr Thr Gly 45 a Met Ala Lys Gly Ile Ala Ser Ala Asp Leu Val Ile Ala Ala 6Gly Lys Arg Lys Ile Leu Gly Ser Phe Gly Ala Gly Gly Leu Pro 75 t His His Val Arg Ala Ala Leu Glu Lys Ile Gln Ala Ala Leu 9Pro Gln Gly Pro Tyr Ala Val Asn Leu Ile His Ser Pro Phe Asp Ser Asn Leu Glu Lys Gly Asn Val Asp Leu Phe Leu Glu Lys Gly 2Val Thr Val Val Glu Ala Ser Ala Phe Met Thr Leu Thr Pro Gln 35 l Val Arg Tyr Arg Ala Ala Gly Leu Ser Arg Asn Ala Asp Gly 5Ser Val Asn Ile Arg Asn Arg Ile Ile Gly Lys Val Ser Arg Thr 65 u Leu Ala Glu Met Phe Ile Arg Pro Ala Pro Glu His Leu Leu 8Glu Lys Leu Ile Ala Ser Gly Glu Ile Thr Gln Glu Gln Ala Glu 95 u Ala Arg Arg Val Pro Val Ala Asp Asp Ile Ala Val Glu Ala Asp Ser Gly Gly His Thr Asp Asn Arg Pro Ile His Val Ile Leu 25 o Leu Ile Ile Asn Leu Arg Asn Arg Leu His Arg Glu Cys Gly 4Tyr Pro Ala His Leu Arg Val Arg Val Gly Ala Gly Gly Gly Val 55 y Cys Pro Gln Ala Ala Ala Ala Ala Leu Thr Met Gly Ala Ala 7Phe Ile Val Thr Gly Thr Val Asn Gln Val Ala Lys Gln Ser Gly 85 r Cys Asp Asn Val Arg Lys Gln Leu Ser Gln Ala Thr Tyr Ser Asp Ile Cys Met Ala Pro Ala Ala Asp Met Phe Glu Glu Gly Val Lys Leu Gln Val Leu Lys Lys Gly Thr Met Phe Pro Ser Arg Ala 3Asn Lys Leu Tyr Glu Leu Phe Cys Lys Tyr Asp Ser Phe Asp Ser 45 t Pro Pro Ala Glu Leu Glu Arg Ile Glu Lys Arg Ile Phe Lys 6Arg Ala Leu Gln Glu Val Trp Glu Glu Thr Lys Asp Phe Tyr Ile 75 n Gly Leu Lys Asn Pro Glu Lys Ile Gln Arg Ala Glu His Asp 9Pro Lys Leu Lys Met Ser Leu Cys Phe Arg Trp Tyr Leu Gly Leu Ala Ser Arg Trp Ala Asn Met Gly Ala Pro Asp Arg Val Met Asp 2Tyr Gln Val Trp Cys Gly Pro Ala Ile Gly Ala Phe Asn Asp Phe 35 e Lys Gly Thr Tyr Leu Asp Pro Ala Val Ser Asn Glu Tyr Pro 5Cys Val Val Gln Ile Asn Leu Gln Ile Leu Arg Gly Ala Cys Tyr 65 u Arg Arg Leu Asn Ala Leu Arg Asn Asp Pro Arg Ile Asp Leu 8Glu Thr Glu Asp Ala Ala Phe Val Tyr Glu Pro Thr Asn Ala Leu 95 A Schizochytrium sp. CDS (aag gtt cag ccc gtc ttt gcc aac ggc gcc gcc act gtc ggc ccc gag 48 Lys Val Gln Pro Val Phe Ala Asn Gly Ala Ala Thr Val Gly Pro Glu tcc aag gct tcc tcc ggc gcc agc gcc agc gcc agc gcc gcc ccg 96 Ala Ser Lys Ala Ser Ser Gly Ala Ser Ala Ser Ala Ser Ala Ala Pro 2 gcc aag cct gcc ttc agc gcc gat gtt ctt gcg ccc aag ccc gtt gcc Lys Pro Ala Phe Ser Ala Asp Val Leu Ala Pro Lys Pro Val Ala 35 4t ccc gag cac atc ctc aag ggc gac gcc ctc gcc ccc aag gag atg Pro Glu His Ile Leu Lys Gly Asp Ala Leu Ala Pro Lys Glu Met 5 tcc tgg cac ccc atg gcc cgc atc ccg ggc aac ccg acg ccc tct ttt 24rp His Pro Met Ala Arg Ile Pro Gly Asn Pro Thr Pro Ser Phe 65 7 gcg ccc tcg gcc tac aag ccg cgc aac atc gcc ttt acg ccc ttc ccc 288 Ala Pro Ser Ala Tyr Lys Pro Arg Asn Ile Ala Phe Thr Pro Phe Pro 85 9c aac ccc aac gat aac gac cac acc ccg ggc aag atg ccg ctc acc 336 Gly Asn Pro Asn Asp Asn Asp His Thr Pro Gly Lys Met Pro Leu Thr ttc aac atg gcc gag ttc atg gcc ggc aag gtc agc atg tgc ctc 384 Trp Phe Asn Met Ala Glu Phe Met Ala Gly Lys Val Ser Met Cys Leu ccc gag ttc gcc aag ttc gac gac tcg aac acc agc cgc agc ccc 432 Gly Pro Glu Phe Ala Lys Phe Asp Asp Ser Asn Thr Ser Arg Ser Pro tgg gac ctc gct ctc gtc acc cgc gcc gtg tct gtg tct gac ctc 48rp Asp Leu Ala Leu Val Thr Arg Ala Val Ser Val Ser Asp Leu aag cac gtc aac tac cgc aac atc gac ctc gac ccc tcc aag ggt acc 528 Lys His Val Asn Tyr Arg Asn Ile Asp Leu Asp Pro Ser Lys Gly Thr gtc ggc gag ttc gac tgc ccc gcg gac gcc tgg ttc tac aag ggc 576 Met Val Gly Glu Phe Asp Cys Pro Ala Asp Ala Trp Phe Tyr Lys Gly tgc aac gat gcc cac atg ccg tac tcg atc ctc atg gag atc gcc 624 Ala Cys Asn Asp Ala His Met Pro Tyr Ser Ile Leu Met Glu Ile Ala 2cag acc tcg ggt gtg ctc acc tcg gtg ctc aag gcg ccc ctg acc 672 Leu Gln Thr Ser Gly Val Leu Thr Ser Val Leu Lys Ala Pro Leu Thr 222ag aag gac gac atc ctc ttc cgc aac ctc gac gcc aac gcc gag 72lu Lys Asp Asp Ile Leu Phe Arg Asn Leu Asp Ala Asn Ala Glu 225 234tg cgc gcc gac ctc gac tac cgc ggc aag act atc cgc aac gtc 768 Phe Val Arg Ala Asp Leu Asp Tyr Arg Gly Lys Thr Ile Arg Asn Val 245 25cc aag tgc act ggc tac agc atg ctc ggc gag atg ggc gtc cac cgc 8Lys Cys Thr Gly Tyr Ser Met Leu Gly Glu Met Gly Val His Arg 267cc ttt gag ctc tac gtc gat gat gtg ctc ttt tac aag ggc tcg 864 Phe Thr Phe Glu Leu Tyr Val Asp Asp Val Leu Phe Tyr Lys Gly Ser 275 28cc tcg ttc ggc tgg ttc gtg ccc gag gtc ttt gcc gcc cag gcc ggc 9Ser Phe Gly Trp Phe Val Pro Glu Val Phe Ala Ala Gln Ala Gly 29gac aac ggc cgc aag tcg gag ccc tgg ttc att gag aac aag gtt 96sp Asn Gly Arg Lys Ser Glu Pro Trp Phe Ile Glu Asn Lys Val 33ccg gcc tcg cag gtc tcc tcc ttt gac gtg cgc ccc aac ggc agc ggc o Ala Ser Gln Val Ser Ser Phe Asp Val Arg Pro Asn Gly Ser Gly 325 33gc acc gcc atc ttc gcc aac gcc ccc agc ggc gcc cag ctc aac cgc g Thr Ala Ile Phe Ala Asn Ala Pro Ser Gly Ala Gln Leu Asn Arg 345cg gac cag ggc cag tac ctc gac gcc gtc gac att gtc tcc ggc g Thr Asp Gln Gly Gln Tyr Leu Asp Ala Val Asp Ile Val Ser Gly 355 36gc ggc aag aag agc ctc ggc tac gcc cac ggt tcc aag acg gtc aac r Gly Lys Lys Ser Leu Gly Tyr Ala His Gly Ser Lys Thr Val Asn 378ac gac tgg ttc ttc tcg tgc cac ttt tgg ttt gac tcg gtc atg o Asn Asp Trp Phe Phe Ser Cys His Phe Trp Phe Asp Ser Val Met 385 39gga agt ctc ggt gtc gag tcc atg ttc cag ctc gtc gag gcc atc o Gly Ser Leu Gly Val Glu Ser Met Phe Gln Leu Val Glu Ala Ile 44gcc cac gag gat ctc gct ggc aaa gca cgg cat tgc caa ccc cac a Ala His Glu Asp Leu Ala Gly Lys Ala Arg His Cys Gln Pro His 423gt gca cgc ccc cgg gca aga tca agc tgg aag tac cgc ggc cag u Cys Ala Arg Pro Arg Ala Arg Ser Ser Trp Lys Tyr Arg Gly Gln 435 44tc acg ccc aag agc aag aag atg gac tcg gag gtc cac atc gtg tcc u Thr Pro Lys Ser Lys Lys Met Asp Ser Glu Val His Ile Val Ser 456ac gcc cac gac ggc gtt gtc gac ctc gtc gcc gac ggc ttc ctc l Asp Ala His Asp Gly Val Val Asp Leu Val Ala Asp Gly Phe Leu 465 478cc gac agc ctc cgc gtc tac tcg gtg agc aac att cgc gtg cgc p Ala Asp Ser Leu Arg Val Tyr Ser Val Ser Asn Ile Arg Val Arg 485 49tc gcc tcc ggt e Ala Ser Gly 5Schizochytrium sp. 3al Gln Pro Val Phe Ala Asn Gly Ala Ala Thr Val Gly Pro Glu Ser Lys Ala Ser Ser Gly Ala Ser Ala Ser Ala Ser Ala Ala Pro 2 Ala Lys Pro Ala Phe Ser Ala Asp Val Leu Ala Pro Lys Pro Val Ala 35 4u Pro Glu His Ile Leu Lys Gly Asp Ala Leu Ala Pro Lys Glu Met 5 Ser Trp His Pro Met Ala Arg Ile Pro Gly Asn Pro Thr Pro Ser Phe 65 7 Ala Pro Ser Ala Tyr Lys Pro Arg Asn Ile Ala Phe Thr Pro Phe Pro 85 9y Asn Pro Asn Asp Asn Asp His Thr Pro Gly Lys Met Pro Leu Thr Phe Asn Met Ala Glu Phe Met Ala Gly Lys Val Ser Met Cys Leu Pro Glu Phe Ala Lys Phe Asp Asp Ser Asn Thr Ser Arg Ser Pro Trp Asp Leu Ala Leu Val Thr Arg Ala Val Ser Val Ser Asp Leu Lys His Val Asn Tyr Arg Asn Ile Asp Leu Asp Pro Ser Lys Gly Thr Val Gly Glu Phe Asp Cys Pro Ala Asp Ala Trp Phe Tyr Lys Gly Cys Asn Asp Ala His Met Pro Tyr Ser Ile Leu Met Glu Ile Ala 2Gln Thr Ser Gly Val Leu Thr Ser Val Leu Lys Ala Pro Leu Thr 222lu Lys Asp Asp Ile Leu Phe Arg Asn Leu Asp Ala Asn Ala Glu 225 234al Arg Ala Asp Leu Asp Tyr Arg Gly Lys Thr Ile Arg Asn Val 245 25hr Lys Cys Thr Gly Tyr Ser Met Leu Gly Glu Met Gly Val His Arg 267hr Phe Glu Leu Tyr Val Asp Asp Val Leu Phe Tyr Lys Gly Ser 275 28hr Ser Phe Gly Trp Phe Val Pro Glu Val Phe Ala Ala Gln Ala Gly 29Asp Asn Gly Arg Lys Ser Glu Pro Trp Phe Ile Glu Asn Lys Val 33Pro Ala Ser Gln Val Ser Ser Phe Asp Val Arg Pro Asn Gly Ser Gly 325 33rg Thr Ala Ile Phe Ala Asn Ala Pro Ser Gly Ala Gln Leu Asn Arg 345hr Asp Gln Gly Gln Tyr Leu Asp Ala Val Asp Ile Val Ser Gly 355 36er Gly Lys Lys Ser Leu Gly Tyr Ala His Gly Ser Lys Thr Val Asn 378sn Asp Trp Phe Phe Ser Cys His Phe Trp Phe Asp Ser Val Met 385 39Gly Ser Leu Gly Val Glu Ser Met Phe Gln Leu Val Glu Ala Ile 44Ala His Glu Asp Leu Ala

Gly Lys Ala Arg His Cys Gln Pro His 423ys Ala Arg Pro Arg Ala Arg Ser Ser Trp Lys Tyr Arg Gly Gln 435 44eu Thr Pro Lys Ser Lys Lys Met Asp Ser Glu Val His Ile Val Ser 456sp Ala His Asp Gly Val Val Asp Leu Val Ala Asp Gly Phe Leu 465 478la Asp Ser Leu Arg Val Tyr Ser Val Ser Asn Ile Arg Val Arg 485 49le Ala Ser Gly 55Schizochytrium sp. CDS (gcc ccg ctc tac ctc tcg cag gac ccg acc agc ggc cag ctc aag aag 48 Ala Pro Leu Tyr Leu Ser Gln Asp Pro Thr Ser Gly Gln Leu Lys Lys acc gac gtg gcc tcc ggc cag gcc acc atc gtg cag ccc tgc acg 96 His Thr Asp Val Ala Ser Gly Gln Ala Thr Ile Val Gln Pro Cys Thr 2 ctc ggc gac ctc ggt gac cgc tcc ttc atg gag acc tac ggc gtc gtc Gly Asp Leu Gly Asp Arg Ser Phe Met Glu Thr Tyr Gly Val Val 35 4c ccg ctg tac acg ggc gcc atg gcc aag ggc att gcc tcg gcg gac Pro Leu Tyr Thr Gly Ala Met Ala Lys Gly Ile Ala Ser Ala Asp 5 ctc gtc atc gcc gcc ggc aag cgc aag atc ctc ggc tcc ttt ggc gcc 24al Ile Ala Ala Gly Lys Arg Lys Ile Leu Gly Ser Phe Gly Ala 65 7 ggc ggc ctc ccc atg cac cac gtg cgc gcc gcc ctc gag aag atc cag 288 Gly Gly Leu Pro Met His His Val Arg Ala Ala Leu Glu Lys Ile Gln 85 9c gcc ctg cct cag ggc ccc tac gcc gtc aac ctc atc cac tcg cct 336 Ala Ala Leu Pro Gln Gly Pro Tyr Ala Val Asn Leu Ile His Ser Pro gac agc aac ctc gag aag ggc aac gtc gat ctc ttc ctc gag aag 384 Phe Asp Ser Asn Leu Glu Lys Gly Asn Val Asp Leu Phe Leu Glu Lys gtc act gtg gtg gag gcc tcg gca ttc atg acc ctc acc ccg cag 432 Gly Val Thr Val Val Glu Ala Ser Ala Phe Met Thr Leu Thr Pro Gln gtg cgc tac cgc gcc gcc ggc ctc tcg cgc aac gcc gac ggt tcg 48al Arg Tyr Arg Ala Ala Gly Leu Ser Arg Asn Ala Asp Gly Ser gtc aac atc cgc aac cgc atc atc ggc aag gtc tcg cgc acc gag ctc 528 Val Asn Ile Arg Asn Arg Ile Ile Gly Lys Val Ser Arg Thr Glu Leu gag atg ttc atc cgc ccg gcc ccg gag cac ctc ctc gag aag ctc 576 Ala Glu Met Phe Ile Arg Pro Ala Pro Glu His Leu Leu Glu Lys Leu gcc tcg ggc gag atc acc cag gag cag gcc gag ctc gcg cgc cgc 624 Ile Ala Ser Gly Glu Ile Thr Gln Glu Gln Ala Glu Leu Ala Arg Arg 2ccc gtc gcc gac gat atc gct gtc gag gct gac tcg ggc ggc cac 672 Val Pro Val Ala Asp Asp Ile Ala Val Glu Ala Asp Ser Gly Gly His 222ac aac cgc ccc atc cac gtc atc ctc ccg ctc atc atc aac ctc 72sp Asn Arg Pro Ile His Val Ile Leu Pro Leu Ile Ile Asn Leu 225 234ac cgc ctg cac cgc gag tgc ggc tac ccc gcg cac ctc cgc gtc 768 Arg Asn Arg Leu His Arg Glu Cys Gly Tyr Pro Ala His Leu Arg Val 245 25gc gtt ggc gcc ggc ggt ggc gtc ggc tgc ccg cag gcc gcc gcc gcc 8Val Gly Ala Gly Gly Gly Val Gly Cys Pro Gln Ala Ala Ala Ala 267tc acc atg ggc gcc gcc ttc atc gtc acc ggc act gtc aac cag 864 Ala Leu Thr Met Gly Ala Ala Phe Ile Val Thr Gly Thr Val Asn Gln 275 28tc gcc aag cag tcc ggc acc tgc gac aac gtg cgc aag cag ctc tcg 9Ala Lys Gln Ser Gly Thr Cys Asp Asn Val Arg Lys Gln Leu Ser 29gcc acc tac tcg gat atc tgc atg gcc ccg gcc gcc gac atg ttc 96la Thr Tyr Ser Asp Ile Cys Met Ala Pro Ala Ala Asp Met Phe 33gag gag ggc gtc aag ctc cag gtc ctc aag aag gga acc atg ttc ccc u Glu Gly Val Lys Leu Gln Val Leu Lys Lys Gly Thr Met Phe Pro 325 33cg cgc gcc aac aag ctc tac gag ctc ttt tgc aag tac gac tcc ttc r Arg Ala Asn Lys Leu Tyr Glu Leu Phe Cys Lys Tyr Asp Ser Phe 345cc atg cct cct gcc gag ctc gag cgc atc gag aag cgt atc ttc p Ser Met Pro Pro Ala Glu Leu Glu Arg Ile Glu Lys Arg Ile Phe 355 36ag cgc gca ctc cag gag gtc tgg gag gag acc aag gac ttt tac att s Arg Ala Leu Gln Glu Val Trp Glu Glu Thr Lys Asp Phe Tyr Ile 378gt ctc aag aac ccg gag aag atc cag cgc gcc gag cac gac ccc n Gly Leu Lys Asn Pro Glu Lys Ile Gln Arg Ala Glu His Asp Pro 385 39ctc aag atg tcg ctc tgc ttc cgc tgg tac ctt ggt ctt gcc agc s Leu Lys Met Ser Leu Cys Phe Arg Trp Tyr Leu Gly Leu Ala Ser 44tgg gcc aac atg ggc gcc ccg gac cgc gtc atg gac tac cag gtc g Trp Ala Asn Met Gly Ala Pro Asp Arg Val Met Asp Tyr Gln Val 423gt ggc ccg gcc att ggc gcc ttc aac gac ttc atc aag ggc acc p Cys Gly Pro Ala Ile Gly Ala Phe Asn Asp Phe Ile Lys Gly Thr 435 44ac ctc gac ccc gct gtc tcc aac gag tac ccc tgt gtc gtc cag atc r Leu Asp Pro Ala Val Ser Asn Glu Tyr Pro Cys Val Val Gln Ile 456tg caa atc ctc cgt ggt gcc tgc tac ctg cgc cgt ctc aac gcc n Leu Gln Ile Leu Arg Gly Ala Cys Tyr Leu Arg Arg Leu Asn Ala 465 478gc aac gac ccg cgc att gac ctc gag acc gag gat gct gcc ttt u Arg Asn Asp Pro Arg Ile Asp Leu Glu Thr Glu Asp Ala Ala Phe 485 49tc tac gag ccc acc aac gcg ctc l Tyr Glu Pro Thr Asn Ala Leu 5Schizochytrium sp. 32 Ala Pro Leu Tyr Leu Ser Gln Asp Pro Thr Ser Gly Gln Leu Lys Lys Thr Asp Val Ala Ser Gly Gln Ala Thr Ile Val Gln Pro Cys Thr 2 Leu Gly Asp Leu Gly Asp Arg Ser Phe Met Glu Thr Tyr Gly Val Val 35 4a Pro Leu Tyr Thr Gly Ala Met Ala Lys Gly Ile Ala Ser Ala Asp 5 Leu Val Ile Ala Ala Gly Lys Arg Lys Ile Leu Gly Ser Phe Gly Ala 65 7 Gly Gly Leu Pro Met His His Val Arg Ala Ala Leu Glu Lys Ile Gln 85 9a Ala Leu Pro Gln Gly Pro Tyr Ala Val Asn Leu Ile His Ser Pro Asp Ser Asn Leu Glu Lys Gly Asn Val Asp Leu Phe Leu Glu Lys Val Thr Val Val Glu Ala Ser Ala Phe Met Thr Leu Thr Pro Gln Val Arg Tyr Arg Ala Ala Gly Leu Ser Arg Asn Ala Asp Gly Ser Val Asn Ile Arg Asn Arg Ile Ile Gly Lys Val Ser Arg Thr Glu Leu Glu Met Phe Ile Arg Pro Ala Pro Glu His Leu Leu Glu Lys Leu Ala Ser Gly Glu Ile Thr Gln Glu Gln Ala Glu Leu Ala Arg Arg 2Pro Val Ala Asp Asp Ile Ala Val Glu Ala Asp Ser Gly Gly His 222sp Asn Arg Pro Ile His Val Ile Leu Pro Leu Ile Ile Asn Leu 225 234sn Arg Leu His Arg Glu Cys Gly Tyr Pro Ala His Leu Arg Val 245 25rg Val Gly Ala Gly Gly Gly Val Gly Cys Pro Gln Ala Ala Ala Ala 267eu Thr Met Gly Ala Ala Phe Ile Val Thr Gly Thr Val Asn Gln 275 28al Ala Lys Gln Ser Gly Thr Cys Asp Asn Val Arg Lys Gln Leu Ser 29Ala Thr Tyr Ser Asp Ile Cys Met Ala Pro Ala Ala Asp Met Phe 33Glu Glu Gly Val Lys Leu Gln Val Leu Lys Lys Gly Thr Met Phe Pro 325 33er Arg Ala Asn Lys Leu Tyr Glu Leu Phe Cys Lys Tyr Asp Ser Phe 345er Met Pro Pro Ala Glu Leu Glu Arg Ile Glu Lys Arg Ile Phe 355 36ys Arg Ala Leu Gln Glu Val Trp Glu Glu Thr Lys Asp Phe Tyr Ile 378ly Leu Lys Asn Pro Glu Lys Ile Gln Arg Ala Glu His As