Compositions and methods for succinate production

Patent metadata

Field	Value
Publication number	US-11390873-B2
Application number	US-201615386506-A
Country	US
Kind code	B2
Filing date	Dec 21, 2016
Priority date	Jan 25, 2011
Publication date	Jul 19, 2022
Grant date	Jul 19, 2022

Abstract

The present application provides genetically modified yeast cell comprising an active succinate fermentation pathway, as well as methods of using these cells to produce succinate.

First claim

What is claimed is:

1. A method of producing succinate comprising culturing genetically modified yeast cells in the presence of at least one carbon source and isolating succinate from the culture, wherein the genetically modified yeast cells are from the Pichia fermentans/Issatchenkia orientalis clade and have an active succinate fermentation pathway from phosphoenolpyruvate or pyruvate to succinate, wherein the active succinate fermentation pathway comprises the reactions:
(a) pyruvate to oxaloacetate;
(b) oxaloacetate to malate;
(c) malate to fumarate; and
(d) fumarate to succinate,

wherein the cells comprise an exogenous succinate exporter gene that catalyzes export of succinate from inside the cell to the extracellular environment.

2. The method of claim 1 , wherein the cell comprises a further exogenous nucleic acid encoding an enzyme that catalyzes any one of reactions (a) to (d).

3. The method of claim 2 , wherein the cell comprises an exogenous nucleic acid encoding pyruvate carboxylase, malate dehydrogenase, fumarase, or fumarate reductase.

4. The method of claim 3 , wherein the cell comprises an exogenous nucleic acid encoding a pyruvate carboxylase comprising an amino acid sequence with at least 90% sequence identity to the amino acid sequence of SEQ ID NO: 8, 10, or 12.

5. The method of claim 3 , wherein the cell comprises an exogenous nucleic acid encoding a malate dehydrogenase comprising an amino acid sequence with at least 90% sequence identity to the amino acid sequence of SEQ ID NO: 14, 16, 18, 168, 20, 22, or 24.

6. The method of claim 3 , wherein the cell comprises an exogenous nucleic acid encoding a malate dehydrogenase comprising an amino acid sequence with at least 90% sequence identity to the amino acid sequence of SEQ ID NO: 170.

7. The method of claim 3 , wherein the cell comprises an exogenous nucleic acid encoding a fumarase comprising an amino acid sequence with at least 90% sequence identity to the amino acid sequence of SEQ ID NO: 2.

8. The method of claim 3 , wherein the cell comprises an exogenous nucleic acid encoding a fumarate reductase comprising an amino acid sequence with at least 90% sequence identity to the amino acid sequence of SEQ ID NO: 26, 28, 30, or 32.

9. The method of claim 3 , wherein the cell comprises an exogenous nucleic acid encoding a fumarate reductase comprising an amino acid sequence with at least 90% sequence identity to the amino acid sequence of SEQ ID NO: 174, 176, 178, or 180.

10. The method of claim 1 , wherein the cell comprises an exogenous succinate exporter gene encoding a polypeptide comprising an amino acid sequence with at least 90% sequence identity to the amino acid sequence of SEQ ID NO: 182 or 184.

11. The method of claim 1 , wherein the active succinate fermentation pathway comprises the reaction phosphoenolpyruvate to oxaloacetate in addition to reaction (a).

12. The method of claim 11 , wherein the cell comprises an exogenous nucleic acid encoding phosphoenolpyruvate carboxylase.

13. The method of claim 12 , wherein the cell comprises an exogenous nucleic acid encoding a phosphoenolpyruvate carboxylase comprising an amino acid sequence with at least 90% sequence identity to the amino acid sequence of SEQ ID NO: 4 or 6.

14. The method of claim 1 , wherein the cell comprises a deletion or disruption of an endogenous malic enzyme gene.

15. The method of claim 1 , wherein the cell comprises a deletion or disruption of an endogenous pyruvate decarboxylase gene.

16. The method of claim 1 , wherein the cell comprises an exogenous nucleic acid encoding glucose 6-phosphate dehydrogenase.

17. The method of claim 16 , wherein the cell comprises an exogenous nucleic acid encoding a glucose 6-phosphate dehydrogenase comprising an amino acid sequence with at least 90% sequence identity to the amino acid sequence of SEQ ID NO: 34.

18. The method of claim 1 , which produces succinate at a concentration of at least 20 g/L.

19. A method of producing succinate comprising culturing genetically modified yeast cells in the presence of at least one carbon source and isolating succinate from the culture, wherein the genetically modified yeast cells are from the species Issatchenkia orientalis, Pichia kudriavzevii, Candida kruzei , or Candida lambica and have an active succinate fermentation pathway from phosphoenolpyruvate or pyruvate to succinate, wherein the active succinate fermentation pathway comprises the reactions:
(a) pyruvate to oxaloacetate;
(b) oxaloacetate to malate;
(c) malate to fumarate; and
(d) fumarate to succinate,

wherein the cells comprise an exogenous succinate exporter, gene that catalyzes export of succinate from inside the cell to the extracellular environment.

20. The method of claim 19 , which produces succinate at a concentration of at least 20 g/L.

Assignees

• Cargill Inc

Inventors

• Finley Kenneth R
• Huryta Jeanette M
• Mastel Beth M
• Mcmullin Thomas W
• Poynter Gregory M
• Rush Brian J
• Fosmer Arlene M
• Mcintosh Jr Vernon L
• Brady Keith M
• Watts Kevin T

Classifications

• C12Y604/01001

  Pyruvate carboxylase (6.4.1.1) · CPC title

• C12N9/93

  Ligases (6) · CPC title

• C12Y101/01037

  Malate dehydrogenase (1.1.1.37) · CPC title

• C12N15/52

  Genes encoding for enzymes or proenzymes · CPC title

• C12N9/001

  acting on the CH-CH group of donors (1.3) · CPC title