Engineered microbes and methods for microbial oil production

Patent metadata

Field	Value
Publication number	US-9862977-B2
Application number	US-201414547304-A
Country	US
Kind code	B2
Filing date	Nov 19, 2014
Priority date	Oct 19, 2011
Publication date	Jan 9, 2018
Grant date	Jan 9, 2018

Abstract

Some aspects of this invention provide engineered microbes for oil production. Methods for microbe engineering and for use of engineered microbes are also provided herein. In some embodiments, microbes are provided that are engineered to modulate a combination of rate-controlling steps of lipid synthesis, for example, a combination of a step generating metabolites, acetyl-CoA, ATP or NADPH for lipid synthesis (a push step), and a step sequestering a product or an intermediate of a lipid synthesis pathway that mediates feedback inhibition of lipid synthesis (a pull step). Such push-and-pull engineered microbes exhibit greatly enhanced conversion yields and TAG synthesis and storage properties.

First claim

The invention claimed is:

1. An isolated oleaginous yeast cell, comprising a genetic modification that increases expression of a diacylglycerol acyltransferase (DGA1) gene product and an acetyl-CoA carboxylase (ACC1) gene product, wherein the genetic modification comprises
(a) a first nucleic acid construct comprising an expression cassette comprising a coding nucleic acid encoding the DGA1 gene product,
wherein the coding nucleic acid encoding the DGA1 gene product comprises a nucleic acid sequence that is at least 85% identical to SEQ ID NO: 1,
wherein the first nucleic acid construct comprises an intron-enhanced promoter; and
(b) a second nucleic acid construct comprising an expression cassette comprising a coding nucleic acid encoding the ACC1 gene product,
wherein the coding nucleic acid encoding the ACC1 gene product encodes for a protein comprising the amino acid sequence of SEQ ID NO: 4,
wherein the isolated oleaginous yeast cell converts a carbon source to a fatty acid or a triacylglycerol (TAG) at a conversion rate within the range of about 0.025 g/g to about 0.32 g/g (g TAG produced/g Glucose consumed).

2. The isolated oleaginous yeast cell of claim 1 , further comprising a genetic modification that increases expression of a stearoyl-CoA-desaturase (SCD) gene product or of an ATP-citrate lyase (ACL) gene product or of a SCD gene product and of an ACL gene product.

3. The isolated oleaginous yeast cell of claim 1 , wherein the increased expression of the gene product confers a beneficial phenotype for the conversion of a carbon source to a fatty acid, fatty acid derivative or TAG to the isolated oleaginous yeast cell, and wherein the beneficial phenotype comprises a modified fatty acid profile, a modified TAG profile, an increased fatty acid or triacylglycerol synthesis rate, an increased conversion yield, an increased triacylglycerol accumulation in the isolated oleaginous yeast cell, or an increased triacylglycerol accumulation in a lipid body of the isolated oleaginous yeast cell.

4. The isolated oleaginous yeast cell of claim 3 , wherein the synthesis rate of a fatty acid or a TAG of the cell is at least 2-fold increased as compared to unmodified cells of the same cell type.

5. The isolated oleaginous yeast cell of claim 1 , wherein the isolated oleaginous yeast cell is a Y. lipolytica cell or is derived from Yarrowia lipolytica.

6. A culture, comprising the oleaginous yeast cell of claim 1 .

7. The culture of claim 6 , further comprising a carbon source.

8. The culture of claim 7 , wherein the carbon source comprises a fermentable sugar, an organic acid, and/or acetate.

9. The culture of claim 6 , wherein the culture comprises glycerol.

10. The culture of claim 6 , wherein the culture comprises ammonium sulfate.

11. A method, comprising
contacting a carbon source with the isolated oleaginous yeast cell of claim 1 ; and
incubating the carbon source contacted with the isolated oleaginous yeast cell under conditions suitable for at least partial conversion of the carbon source into a fatty acid or a triacylglycerol by the isolated oleaginous yeast cell.

12. The method of claim 11 , wherein the isolated oleaginous yeast cell further comprises a genetic modification that increases expression of an SCD gene product and/or an ACL gene product.

13. The isolated oleaginous yeast cell of claim 1 , wherein the coding nucleic acid encoding the DGA1 gene product comprises the nucleic acid sequence of SEQ ID NO: 1.

14. The isolated oleaginous yeast cell of claim 1 , wherein the coding nucleic acid encoding the DGA1 gene product encodes for a protein comprising the amino acid sequence of SEQ ID NO: 2.

15. The isolated oleaginous yeast cell of claim 1 , wherein the coding nucleic acid encoding the ACC1 gene product comprises the nucleic acid sequence of SEQ ID NO: 3.

Assignees

• Massachusetts Inst Technology

Inventors

• Stephanopoulos Gregory
• Tai Mitchell
• Chakraborty Sagar

Classifications

• C12N9/0083

  Miscellaneous (1.14.99) · CPC title

• C12N1/16 Primary

  Yeasts; Culture media therefor · CPC title

• C12N9/1029

  transferring groups other than amino-acyl groups (2.3.1) · CPC title

• C12N9/93

  Ligases (6) · CPC title

• C12N15/815

  for yeasts other than Saccharomyces · CPC title