Diacylglycerol acyltransferases for alteration of polyunsaturated fatty acids and oil content in oleaginous organisms
View Patent ↗Acyltransferases are provided, suitable for use in the manufacture of microbial oils enriched in omega fatty acids in oleaginous yeast (e.g., Yarrowia lipolytica ). Specifically, genes encoding diacylglycerol acyltransferase (DGAT1) have been isolated from Y. lipolytica and Mortierella alpina . These genes encode enzymes that participate in the terminal step in oil biosynthesis in yeast. Each is expected to play a key role in altering the quantity of polyunsaturated fatty acids produced in oils of oleaginous yeasts.
1. A method of increasing triacylglycerol content in a transformed host cell comprising:
(a) providing a transformed host cell comprising:
(i) at least one gene encoding a diacylglycerol acyltransferase 1 enzyme having the amino acid sequence of SEQ ID NO:14 under the control of suitable regulatory sequences, and,
(ii) a source of fatty acids;
(b) growing the cell of step (a) under conditions whereby the at least one gene encoding a diacylglycerol acyltransferase 1 enzyme is expressed, resulting in the transfer of the fatty acids to triacylglycerol; and
(c) optionally recovering the triacylglycerol of step (b).
2. A method of increasing the ω-3 or ω-6 fatty add content of triacylglycerols in a transformed host cell comprising:
(a) providing a transformed host cell comprising:
(i) genes encoding a functional ω-3/ω-6 fatty acid biosynthetic pathway; and,
(ii) at least one gene encoding a diacylglycerol acyltransferase 1 enzyme having the amino acid sequence of SEQ ID NO:14 under the control of suitable regulatory sequences;
(b) growing the cell of step (a) under conditions whereby the genes of (i) and (ii) are expressed, resulting in the production of at least one ω-3 or ω-6 fatty acid and its transfer to triacylglycerol; and,
(c) optionally recovering the triacylglycerol of step (b).
3. A method of increasing triacylglycerol content in a transformed host cell comprising:
(a) providing a transformed host cell comprising:
(i) at least one isolated gene under the control of suitable regulatory sequences, said gene encoding a diacylglycerol acyltransferase 1 enzyme, wherein the polypeptide encoding said diacylglycerol acyltransferase I enzyme comprises all of the amino acid motifs as set forth in:
1) SEQ ID NO:31:
2) SEQ ID NO:32:
3) SEQ ID NO:33;
4) SEQ ID NO:34;
5) SEQ ID NO;35;
6) SEQ ID NO:36; and
7) SEQ ID NO:37;
wherein said motifs are located at conserved amino acid positions in a sequence alignment when compared to the amino acid sequence as set forth in SEQ ID NO. 14 and wherein the polypeptide has at least 90% identity based on the BLASTP method of alignment when compared to a polypeptide having a sequence as set forth in SEQ ID NO:14, and
(ii) a source of fatty acids;
(b) growing the cell of step (a) under conditions whereby the at least one isolated gene encoding a diacylglycerol acyltransferase 1 enzyme is expressed, resulting in the transfer of the fatty acids to triacylglycerol; and,
(c) optionally recovering the triacylglycerol of step (b).
4. A method of increasing the ω-3 and ω-6 fatty acid content of triacylglycerols in a transformed host cell comprising:
(a) providing a transformed host cell comprising:
(i) genes encoding a functional the ω-3 and ω-6 fatty acid biosynthetic pathway; and,
(ii) at least one isolated gene under the control of suitable regulatory sequences, said gene encoding a diacylglycerol acyltransferase 1 enzyme, wherein the polypeptide encoding
said diacylglycerol acyltransferase 1 enzyme comprises all of the amino acid motifs as set forth in:
1) SEQ ID NO:31:
2) SEQ ID NO:32:
3) SEQ ID NO:33;
4) SEQ ID NO:34;
5) SEQ ID NO:35;
6) SEQ ID NO:36; and
7) SEQ ID NO:37;
wherein said motifs are located at conserved amino acid positions in a sequence alignment when compared to the amino acid sequence as set forth in SEQ ID NO. 14 and wherein the polypeptide has at least 90% identity based on the BLASTP method of alignment when compared to a polypeptide having a sequence as set forth in SEQ ID NO:14, and
(ii) a source of fatty acids;
(b) growing the cell of step (a) under conditions whereby the at least one isolated gene encoding a diacylglycerol acyltransferase 1 enzyme is expressed, resulting in the transfer of the fatty acids to triacylglycerol; and,
(c) optionally recovering the triacylglycerol of step (b).
5. The method according to claim 2 or 4 , wherein the genes encoding a functional ω-3/ω-6 fatty acid biosynthetic pathway are selected from the group consisting of desaturases and elongases.
6. The method according to claim 5 , wherein the desaturase is selected from the group consisting of: Δ9 desaturase, Δ12 desaturase, ≢6 desaturase, Δ5 desaturase, Δ17 desaturase, Δ8 desaturase, Δ15 desaturase and Δ4 desaturase.
7. The method according to claim 1 , wherein the host cell is selected from the group consisting of algae, bacteria, molds, fungi and yeasts.
8. The method according to claim 7 , wherein the host cell is an oleaginous yeast.
9. The method according to claim 8 wherein the oleaginous yeast is a member of a genus selected from the group of consisting of Yarrowia, Candida, Rhodotorula, Rhodospondium, Cryptococcus, Trichosporon and Lipomyces.
10. The method according to claim 9 , wherein the oleaginous yeast is Yarrowia lipolytica.
11. The method according to any one of claim 1 , 2 , 3 or 4 , wherein the fatty acid is selected from the group consisting of: stearate, oleic acid, linoleic acid, γ-linolenic acid, dihomo-γ-linolenic acid, arachidonic acid, α-linolenic acid, stearidonic acid, eicosatetraenoic acid, eicosapentaenoic acid, docosapentaenoic acid, docosahexaenoic acid, eicosadienoic acid and eicosatrienoic acid.
12. The method according to claim 3 or claim 4 , wherein the host cell is selected from the group consisting of algae, bacteria, molds, fungi and yeasts.
13. The method according to claim 12 , wherein the host cell is an oleaginous yeast.