Enzymes and methods for producing ω-3 fatty acids
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 desaturase or elongase activity that can be used in methods of synthesizing long-chain polyunsaturated fatty acids. In particular, the present invention provides ω3 destaurases, Δ5 elongases and Δ6 desaturases with novel activities. Also provided are methods and DNA constructs for transiently and/or stably transforming cells, particularly plant cells, with multiple genes.
1. A process for producing canola oil, comprising a step of extracting oil from canola seed comprising exogenous polynucleotides encoding a microalgal Δ6 desaturase, a Δ6 elongase, a microalgal Δ5 desaturase, a microalgal Δ5 elongase, and a microalgal Δ4 desaturase, wherein each exogenous polynucleotide is operably linked to a promoter that directs expression of said polynucleotide in the cell, and
a total fatty acid content comprising α-linolenic acid (ALA), stearidonic acid (SDA), eicosatetraenoic acid (ETA), eicosapentaenoic acid (EPA), docosapentaenoic acid (DPA) and docosahexaenoic acid (DHA), wherein the EPA, DPA and DHA are each present at a level in the total fatty acid content, each level being expressed as a percentage of the total fatty acid content, such that the sum of the percentages for DPA and DHA divided by the sum of the percentages for EPA, DPA and DHA, expressed as a percentage, is at least 60%,
wherein the microalgal Δ6 desaturase has greater activity on ALA-CoA as a fatty acid substrate than on ALA esterified at the sn-2 position of phosphatidylcholine (PC) as fatty acid substrate,
thereby producing the canola oil.
2. The process of claim 1 , wherein the microalgal Δ4 desaturase has, or the microalgal Δ5 desaturase has, or both the microalgal Δ4 and the microalgal Δ5 desaturases have greater activity on an acyl-CoA substrate than on a corresponding acyl group esterified at the sn-2 position of PC.
3. The process of claim 1 , wherein the microalgal Δ6 desaturase has greater Δ6 desaturase activity on ALA than linoleic acid (LA) as fatty acid substrate.
4. The process of claim 1 , wherein the microalgal Δ6 desaturase is an Ostreococcus tauri or Micromonas pusilla Δ6 desaturase.
5. The process of claim 1 , wherein the microalgal Δ6 desaturase has the amino acid sequence set forth as SEQ ID NO:30.
6. The process of claim 1 , wherein the microalgal Δ5 elongase has an amino acid sequence which is at least 99% identical to the amino acid sequence set forth as SEQ ID NO: 130.
7. The process of claim 1 , wherein the Δ6 elongase has an amino acid sequence identical to the amino acid sequence encoded by the nucleotide sequence set forth as SEQ ID NO: 133, and the Δ5 desaturase has an amino acid sequence identical to the amino acid sequence encoded by the nucleotide sequence set forth as SEQ ID NO: 31.
8. The process of claim 1 , wherein the Δ4 desaturase is a Pavlova spp. Δ4 desaturase.
9. The process of claim 1 , wherein the Δ4 desaturase has an amino acid sequence identical to the amino acid sequence encoded by the nucleotide sequence set forth as SEQ ID NO: 132.
10. The process of claim 1 , wherein ALA, SDA, ETA, EPA, DPA and DHA are each present at a level in the total fatty acid content, each level being expressed as a percentage of the total fatty acid content, such that the sum of the percentages for DPA and DHA divided by the sum of the percentages for ALA, SDA, ETA, EPA, DPA and DHA, expressed as a percentage, is at least 15.4%.
11. The process of claim 10 , wherein arachidonic acid (ARA), EPA, DPA and DHA together comprise 15% of the total fatty acids.
12. The process of claim 10 , wherein 4% of the total fatty acid content is DPA.
13. The process of claim 8 , wherein DHA is present at a level in the total fatty acid content such that the percentage for DHA divided by the sum of the percentages for EPA, DPA and DHA, expressed as a percentage, is at least 45%.
14. The process of claim 1 , which comprises a step of purifying the extracted canola oil.
15. A process for producing canola oil, comprising a step of extracting oil from canola seed comprising exogenous polynucleotides encoding a microalgal Δ6 desaturase which has the amino acid sequence set forth as SEQ ID NO:30, a Δ6 elongase which has an amino acid sequence identical to the amino acid sequence encoded by the nucleotide sequence set forth as SEQ ID NO: 133, a Δ5 desaturase which has the amino acid sequence encoded by the nucleotide sequence set forth as SEQ ID NO: 131, a microalgal Δ5 elongase which has an amino acid sequence which is at least 99% identical to the amino acid sequence set forth as SEQ ID NO: 130, and a Δ4 desaturase which has an amino acid sequence identical to the amino acid sequence encoded by the nucleotide sequence set forth as SEQ ID NO: 132, wherein each exogenous polynucleotide is operably linked to a promoter that directs expression of said polynucleotide in the cell, and
a total fatty acid content comprising α-linolenic acid (ALA), stearidonic acid (SDA), eicosatetraenoic acid (ETA), eicosapentaenoic acid (EPA), docosapentaenoic acid (DPA) and docosahexaenoic acid (DHA), wherein the EPA, DPA and DHA are each present at a level in the total fatty acid content, each level being expressed as a percentage of the total fatty acid content, such that the sum of the percentages for DPA and DHA divided by the sum of the percentages for EPA, DPA and DHA, expressed as a percentage, is at least 60%, thereby producing the canola oil.