Glucoamylase engineered yeast and fermentation methods

Patent metadata

Field	Value
Publication number	US-11939619-B2
Application number	US-202217657241-A
Country	US
Kind code	B2
Filing date	Mar 30, 2022
Priority date	Feb 28, 2018
Publication date	Mar 26, 2024
Grant date	Mar 26, 2024

Abstract

The invention is directed to an engineered yeast including an exogenous nucleic acid encoding a glucoamylase comprising SEQ ID NO:1 and SEQ ID NO:4, or a variant thereof. The engineered yeast are able to provide glucoamylase into a fermentation media and cause degradation of starch material generating glucose for fermentation to a desired bioproduct, such as ethanol. High titers of bioproduct (e.g., 70 g/kg of ethanol) can be achieved, along with low residual glucose levels. Further the yeast exhibit good growth and bioproduct product at temperatures of 32° C. or greater.

First claim

What is claimed is:

1. An engineered yeast comprising an exogenous nucleic acid encoding a glucoamylase comprising a sequence having 97% or greater sequence identity to SEQ ID NO:4, wherein the yeast is capable of producing ethanol at a rate of 1 g/L*h or greater during a fermentation process.

2. The engineered yeast of claim 1 , wherein the glucoamylase comprises a sequence having 98% or greater sequence identity to SEQ ID NO:4.

3. The engineered yeast of claim, wherein the glucoamylase comprises a sequence having 99% or greater sequence identity to SEQ ID NO:4.

4. The engineered yeast of claim 1 , wherein there are 2-8 copies of the exogenous nucleic acid in the cell.

5. The engineered yeast of claim 1 , wherein the engineered yeast a Saccharomyces cerevisiae yeast.

6. The engineered yeast of claim 1 , wherein the yeast is tolerant to growth in a fermentation medium having a concentration of ethanol of greater than 90 g/L.

7. The engineered yeast of claim 1 , wherein the yeast is tolerant to growth at temperatures in the range of greater than 31° C.-35° C.

8. A fermentation method for producing a bioproduct, comprising:
forming a fermentation medium from a glucose polymer-containing feedstock; and
fermenting the fermentation medium using an engineered yeast comprising an exogenous nucleic acid encoding a glucoamylase comprising a sequence having 97% or greater sequence identity to SEQ ID NO:4, wherein fermenting produces a bioproduct.

9. The fermentation method of claim 8 , wherein the glucose polymer-containing feedstock or the fermentation medium, at the beginning of fermentation, has a dextrose equivalent (“DE”) of about 50 or less.

10. The fermentation method of claim 8 , wherein the glucose polymer-containing feedstock comprises glucose polymer having a degree of polymerization of 4 or greater and present in an amount of 75% weight or greater total fermentable carbohydrates in the feedstock.

11. The fermentation of claim 8 , wherein ethanol is produced to a concentration of 70 g/L or greater in the medium.

12. The fermentation method of claim 8 , comprising adding supplemental glucoamylase to the feedstock, or supplemental glucoamylase to the medium during the fermentation period.

13. An engineered yeast comprising an exogenous nucleic acid encoding a glucoamylase comprising (i) a sequence at least 97% identical to amino acids 26-604 of SEQ ID NO:4 and (ii) a heterologous N-terminal signal sequence.

14. The engineered yeast of claim 13 , wherein the yeast is capable of producing ethanol at a rate of 1 g/L*h or greater during a fermentation process.

15. The engineered yeast of claim 13 , wherein the glucoamylase comprises a sequence at least 98% identical to amino acids 26-604 of SEQ ID NO:4.

16. The engineered yeast of claim 13 , wherein the glucoamylase comprises a sequence at least 99% identical to amino acids 26-604 of SEQ ID NO:4.

17. The engineered yeast of claim 13 , wherein the heterologous N-terminal signal sequence is selected from the group consisting of Sc FAKS, Sc AKS, Sc MFal, Sc IV, Gg LZ, and Hs SA signal sequences.

18. The engineered yeast of claim 13 , wherein the yeast is a Saccharomyces cerevisiae yeast.

Assignees

• Cargill Inc

Inventors

• Miller Chris
• Rush Brian
• Dunn Joshua
• Stanton Brynne

Classifications

• C12P7/10 Primary

  substrate containing cellulosic material · CPC title

• C12N9/2428 Primary

  Glucan 1,4-alpha-glucosidase (3.2.1.3), i.e. glucoamylase · CPC title

• C12N1/185

  Saccharomyces isolates · CPC title

• C12P2203/00

  Fermentation products obtained from optionally pretreated or hydrolyzed cellulosic or lignocellulosic material as the carbon source · CPC title

• C12R2001/865

  Saccharomyces cerevisiae · CPC title