IP Library Granted Patent US 9,951,357
Granted Patent B2
US 9,951,357 · App. 15/274,454 · Granted Apr 24, 2018

Synthesis of long-chain polyunsaturated fatty acids by recombinant cell

Inventors: Surinder Pal Singh (Downer, AU); Stanley Suresh Robert (Oyster Cove, AU); Peter David Nichols (West Hobart, AU); Susan Irene Ellis Blackburn (Battery Point, AU); Xue-Rong Zhou (Harrison, AU); James Robertson Petrie (Goulburn, AU); Allan Graham Green (Cremorne Point, AU)
Assignee: COMMONWEATLH SCIENTIFIC AND INDUSTRIAL RESEARCH ORGANISATION
C12P7/6427A23K10/12A23K10/30A23K20/158C11B1/10C11C3/12C12N9/0071C12N9/0083C12N9/1029C12N15/52C12N15/8247C12P7/64C12P7/6472C12Y114/19004Y02P20/52
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Quick Facts
Patent No.
US 9,951,357
App. No.
15/274,454
Granted
Apr 24, 2018
Kind
B2
Abstract

The present invention relates to methods of synthesizing long-chain polyunsaturated fatty acids, especially eicosapentaenoic acid, docosapentaenoic acid and docosahexaenoic acid, in recombinant cells such as yeast or plant cells. Also provided are recombinant cells or plants which produce long-chain polyunsaturated fatty acids. Furthermore, the present invention relates to a group of new enzymes which possess desatorase or elongase activity that can be used in methods of synthesizing long-chain polyunsaturated fatty acids.

Claims (60)

1. A recombinant plant cell which synthesises eicosapentaenoic acid (EPA), comprising more than one heterologous polynucleotide, wherein said polynucleotides encode:

a) a Δ6 desaturase, a Δ6 elongase and a Δ5 desaturase; or

b) a Δ5/Δ6 bifunctional desaturase and a Δ5/Δ6 bifunctional elongase;

wherein the more than one polynucleotides are operably linked to one or more promoters that are capable of directing expression of said polynucleotides in the cell, wherein the enzymes encoded by said polynucleotides comprise at least one desaturase which is able to act on an acyl-CoA substrate, and wherein the synthesis of EPA requires the sequential action of said enzymes.

2. The cell of claim 1 , wherein the enzymes encoded by the polynucleotides comprise at least one Δ5 elongase which catalyses the conversion of EPA to docosapentaenoic acid (DPA) in the cell.

3. The cell of claim 1 which is a plant cell from an angiosperm, an oilseed plant cell or a cell in a seed.

4. The cell of claim 1 , wherein at least one promoter is a seed specific promoter.

5. The cell of claim 1 , wherein said cell is capable of synthesising DPA.

6. The cell of claim 5 , wherein said cell is capable of synthesising docosahexaenoic acid (DHA).

7. The cell of claim 1 , wherein said cell

i) is capable of producing EPA from a fatty acid which is α-linolenic acid (ALA), linoleic acid (LA), γ-linolenic acid (GLA), stearidonic acid (SDA), eicosatetraenoic acid (ETA), or any combination or mixture of these,

ii) is capable of producing DHA from a fatty acid which is ALA, LA, GLA, arachidonic acid (ARA), SDA, ETA, EPA, DPA, or any combination or mixture of these, and/or

iii) is capable of producing DPA from a fatty acid which is ALA, LA, GLA, ARA, SDA, ETA, EPA, or any combination or mixture of these.

8. A method of producing a recombinant plant cell which synthesises one or more long-chain polyunsaturated fatty acids (LC-PUFA(s)), the method comprising introducing into the cell more than one heterologous polynucleotide, wherein said polynucleotides encode:

a) a Δ6 desaturase, a Δ6 elongase and a Δ5 desaturase; or

b) a Δ5/Δ6 bifunctional′ desaturase and a Δ5/Δ6 bifunctional elongase;

wherein the more than one polynucleotides are operably linked to one or more promoters that are capable of directing expression of said polynucleotides in the cell,

wherein said one or more LC-PUFAs comprise EPA,

wherein the enzymes encoded by said polynucleotides comprise at least one desaturase which is able to act on an acyl-CoA substrate, and

wherein the synthesis of EPA requires the sequential action of said enzymes.

9. A transgenic plant or plant part comprising at least one cell according to claim 1 .

10. The plant or plant part of claim 9 wherein said plant is an angiosperm.

11. The plant of claim 9 which comprises

at least one plant part synthesizing DHA.

12. A transgenic seed comprising a cell according to claim 1 .

13. The seed of claim 12 which further comprises

i) DPA, or

ii) DNA, and DPA.

14. The seed of claim 13 , wherein the seed is derived from an oilseed plant.

15. The seed of claim 14 , wherein the oilseed plant is oilseed rape, maize, sunflower, soybean, sorghum, flax, sugar beet, cotton, peanut, poppy, mustard, castor bean, sesame, or safflower.

16. The seed of claim 12 , wherein the seed has a germination rate which is substantially the same as that of an isogenic non-transgenic seed.

17. The seed of claim 16 which comprises DHA which is synthesized in the seed.

18. The seed of claim 12 which is homozygous for the heterologous polynucleotides.

19. A transgenic plant which comprises the transgenic seed of claim 12 .

20. A method of producing a long-chain polyunsaturated fatty acid (LC-PUFA), the method comprising culturing, under suitable conditions, a recombinant cell according to claim 1 , wherein said LC-PUFA comprises EPA.

21. A method of producing oil comprising LC-PUFA, wherein said LC-PUFA comprises EPA, comprising obtaining the seed according to claim 12 , and extracting oil from said seed.

22. The method according to claim 21 , wherein said oil is further purified.

23. The method according to claim 21 , wherein said oil is further treated by hydrolysis with a strong base to release the free fatty acids.

24. A feedstuff comprising the recombinant cell of claim 1 .

25. The plant of claim 9 which is a Brassica napus plant or Arabidopsis thaliana plant, comprising seed which synthesizes EPA, wherein the total fatty acid of the seed comprises 1.5% EPA.

26. The plant of claim 9 which is a Brassica napus plant or Arabidopsis thaliana plant, comprising seed which synthesizes DPA, wherein the total fatty acid of the seed comprises 0.13% DPA.

27. The plant of claim 9 which is a Brassica napus plant or Arabidopsis thaliana plant, comprising seed which synthesizes at least one ω3 C20 LC-PUFA, wherein the total fatty acid of the seed comprises 4.1% ω3 C20 LC-PUFA.

28. The plant of claim 9 which is a Brassica napus plant or Arabidopsis thaliana plant, comprising seed which synthesizes EPA, wherein the efficiency of conversion of ALA to EPA in the seed is at least 14.6%.

29. The plant of claim 9 which is a Brassica napus plant or Arabidopsis thaliana plant, comprising seed which synthesizes ω3 polyunsaturated fatty acids that are the products of Δ6-desaturation of ALA and/or the products of Δ9 elongation of ALA, wherein the efficiency of conversion of ALA to said products in the seed is at least 22%.

30. The plant of claim 9 which is a Brassica napus plant or Arabidopsis thaliana plant, comprising seed which synthesizes DPA from EPA, and wherein the efficiency of conversion of EPA to DPA in the seed is at least 7%.

31. The plant cell of claim 1 which is a Brassica napus cell or Arabidopsis thaliana cell, wherein the heterologous polynucleotides encode a Δ6 desaturase, a 46 elongase and a Δ5 desaturase.

32. The cell of claim 31 , comprising a heterologous polynucleotide encoding a Δ5 elongase which catalyses the conversion of EPA to DPA in the cell.

33. The cell of claim 32 , wherein said cell is capable of synthesising DHA.

34. The plant cell of claim 1 which is a Brassica napus cell or Arabidopsis thaliana cell, wherein the heterologous polynucleotides encode a Δ5/Δ6 bifunctional desaturase and a Δ5/Δ6 bifunctional elongase.

35. The cell of claim 34 , wherein said cell is capable of synthesising DHA.

36. The method of claim 8 , wherein the plant cell is a Brassica napus cell or Arabidopsis thaliana cell, and wherein the heterologous polynucleotides encode a Δ6 desaturase, a Δ6 elongase and a Δ5 desaturase.

37. The method of claim 8 , wherein the plant cell is a Brassica napus cell or Arabidopsis thaliana cell, and wherein the heterologous polynucleotides encode a Δ5/Δ6 bifunctional desaturase and a Δ5/Δ6 bifunctional elongase.

38. The seed of claim 12 which is a Brassica napus seed or Arabidopsis thaliana seed comprising at least one ω3 C20 long-chain polyunsaturated fatty acid (LC-PUFA) which is synthesized in the seed, wherein the total fatty acid of the seed comprises 2.5% ω3 C20 LC-PUFA, wherein the heterologous polynucleotides encode a Δ6 desaturase, a Δ6 elongase and a Δ5 desaturase, and wherein the polynucleotides are operably linked to one or more promoters that are capable of directing expression of said polynucleotides in Brassica napus seed or Arabidopsis thaliana seed.

39. The seed of claim 12 which is a Brassica napus seed or Arabidopsis thaliana seed comprising ALA and EPA, wherein the efficiency of conversion of ALA to EPA in the seed is at least 14.6%, wherein the heterologous polynucleotides encode a Δ6 desaturase, a Δ6 elongase and a Δ5 desaturase, and wherein the polynucleotides are operably linked to one or more promoters that are capable of directing expression of said polynucleotides in Brassica napus seed or Arabidopsis thaliana seed.

40. The seed of claim 12 which is a Brassica napus seed or Arabidopsis thaliana seed comprising ω3 polyunsaturated fatty acids that are the products of Δ6-desaturation of ALA and/or the products of Δ9 elongation of ALA, which products are synthesized in the seed, wherein the efficiency of conversion of ALA to said products in the seed is at least 22%, wherein the heterologous polynucleotides encode a Δ6 desaturase, a Δ6 elongase and a Δ5 desaturase, and wherein the polynucleotides are operably linked to one or more promoters that are capable of directing expression of said polynucleotides in Brassica napus seed or Arabidopsis thaliana seed.

41. The seed of claim 12 which is a Brassica napus seed or Arabidopsis thaliana seed comprising DPA which is synthesized from EPA in the seed, wherein the efficiency of conversion of EPA to DPA in the seed is at least 7%, wherein the heterologous polynucleotides encode a 46 desaturase, a Δ6 elongase and a Δ5 desaturase, and wherein the polynucleotides are operably linked to one or more promoters that are capable of directing expression of said polynucleotides in Brassica napus seed or Arabidopsis thaliana seed.

42. The seed of claim 12 which is a Brassica napus seed or Arabidopsis thaliana seed comprising at least one ω3 C20 LC-PUFA which is synthesized in the seed, wherein the total fatty acid of the seed comprises 2.5% ω3 C20 LC-PUFA, wherein the heterologous polynucleotides encode a Δ5/Δ6 bifunctional desaturase and a Δ5/Δ6 bifunctional elongase, and wherein the polynucleotides are operably linked to one or more promoters that are capable of directing expression of said polynucleotides in Brassica napus seed or Arabidopsis thaliana seed.

43. The seed of claim 12 which is a Brassica napus seed or Arabidopsis thaliana seed comprising ALA and EPA, wherein the efficiency of conversion of ALA to EPA in the seed is at least 14.6%, wherein the heterologous polynucleotides encode a Δ5/Δ6 bifunctional desaturase and a Δ5/Δ6 bifunctional elongase, and wherein the polynucleotides are operably linked to one or more promoters that are capable of directing expression of said polynucleotides in Brassica napus seed or Arabidopsis thaliana seed.

44. The seed of claim 12 which is a Brassica napus seed or Arabidopsis thaliana seed comprising n3 polyunsaturated fatty acids that are the products of Δ6-desaturation of ALA and/or the products of Δ9 elongation of ALA, which products are synthesized in the seed, wherein the efficiency of conversion of ALA to said products in the seed is at least 22%, wherein the heterologous polynucleotides encode a Δ5/Δ6 bifunctional desaturase and a Δ5/Δ6 bifunctional elongase, and wherein the polynucleotides are operably linked to one or more promoters that are capable of directing expression of said polynucleotides in Brassica napus seed or Arabidopsis thaliana seed.

45. The seed of claim 12 which is a Brassica napus seed or Arabidopsis thaliana seed comprising DPA which is synthesized from EPA in the seed, wherein the efficiency of conversion of EPA to DPA in the seed is at least 7%, wherein the heterologous polynucleotides encode a Δ5/Δ6 bifunctional desaturase and a Δ5/Δ6 bifunctional elongase, and wherein the polynucleotides are operably linked to one or more promoters that are capable of directing expression of said polynucleotides in Brassica napus seed or Arabidopsis thaliana seed.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 9, 2017
From: SINGH, SURINDER PAL; ROBERT, STANLEY SURESH; PETER DAVID NICHOLS; BLACKBURN, SUSAN IRENE ELLIS; ZHOU, XUE-RONG; PETRIE, JAMES ROBERTSON; GREEN, ALLAN GRAHAM
To: COMMONWEALTH SCIENTIFIC AND INDUSTRIAL RESEARCH ORGANISATION
Reel/Frame 041213/0782 →
Priority Claims (1)
AU 2005901673 · Apr 5, 2005 · national
Continuity (11)
Continuation 14323512 · Jul 3, 2014
Continuation 14027727 · Sep 16, 2013
Continuation 13448107 · Apr 16, 2012
Continuation 13311240 · Dec 5, 2011
Continuation 13093252 · Apr 25, 2011
Continuation 12945708 · Nov 12, 2010
Continuation 11587092
Provisional Application 60668705 · Apr 5, 2005
Provisional Application 60613861 · Sep 27, 2004
Provisional Application 60564627 · Apr 22, 2004
Related Publication 20170073712A1 · Mar 16, 2017