Methods for regulating nitrogen metabolism during the production of ethanol from corn by metabolically engineered yeast strains

Patent metadata

Field	Value
Publication number	US-11946089-B2
Application number	US-202217592915-A
Country	US
Kind code	B2
Filing date	Feb 4, 2022
Priority date	Mar 15, 2013
Publication date	Apr 2, 2024
Grant date	Apr 2, 2024

Abstract

The present invention provides for a mechanism to reduce glycerol production and increase nitrogen utilization and ethanol production of recombinant microorganisms. One aspect of this invention relates to strains of S. cerevisiae with reduced glycerol productivity that get a kinetic benefit from higher nitrogen concentration without sacrificing ethanol yield. A second aspect of the invention relates to metabolic modifications resulting in altered transport and/or intracellular metabolism of nitrogen sources present in corn mash.

First claim

The invention claimed is:

1. A recombinant yeast comprising:
a) at least one engineered genetic modification that leads to the up-regulation of one or more native and/or heterologous saccharolytic enzyme; and,
b) at least one engineered genetic modification that leads to the up-regulation or down-regulation of an enzyme in a nitrogen-assimilation pathway;
wherein the down-regulated enzyme in the nitrogen-assimilation pathway is glutamate dehydrogenase (Gdh) (EC 1.4.14); or
wherein the up-regulated enzyme in the nitrogen-assimilation pathway is at least one of the following enzyme glutamate dehydrogenase (Gdh) (EC 1.4.1.2), glutamate synthase (Glt) (EC 1.4.1.14), and glutamine synthase (Gln) (EC 6.3.1.2); an ammonium transporter; a urea-amido lyase (EC 6.3.4.6); or a urea transporter.

2. The recombinant yeast of claim 1 , wherein the saccharolytic enzyme is selected from the group consisting of amylases, cellulases, hemicellulases, cellulolytic accessory enzymes, amylolytic accessory enzymes, inulinases, levanases, and pentose sugar utilizing enzymes.

3. The recombinant yeast of claim 2 , wherein the saccharolytic enzymes comprise an amylase.

4. The recombinant yeast of claim 3 , wherein the amylase is selected from the group consisting of H. grisea, T aurantiacus, T emersonii, T reesei, C. lacteus, C. formasamus, N. takasagoensis, C. acinaciformis, M darwinensis, N. walkeri, S. fibuligera, C. luckowense, R. speratus, Thermobfida fusca, Clostridum thermocellum, Clostridium cellulolyticum, Clostridum josui, Bacillus pumilis, Cellulomonas fimi, Saccharophagus degradans, Piromyces equii, Neocallimastix particarum and Arabidopsis thaliana amylase.

5. The recombinant yeast of claim 3 , wherein the amylase comprises a glucoamylase.

6. The recombinant yeast of claim 5 , wherein the glucoamylase is encoded by a polypeptide sequence at least 80%, 90%, 95%, or 100% identical to a polypeptide sequence encoded by SEQ ID NO: 163.

7. The recombinant yeast of claim 1 , wherein the down-regulated enzyme in the nitrogen assimilation pathway comprises a Gdh1 and/or a Gdh3.

8. The recombinant yeast of claim 7 , wherein the down-regulated enzyme in the nitrogen-assimilation pathway is encoded by a polypeptide sequence at least 80%, 90%, 95%, or 100% identical to a polypeptide sequence selected from the group consisting of: SEQ ID NOs: 25 and 31 ( S. cerevisiae Gdh1 and Gdh3).

9. The recombinant yeast of claim 1 , wherein the up-regulated enzyme in the nitrogen-assimilation pathway comprises a Gdh2, a Glt1, a Gln1, a MEP protein, a Dur1/2, a Dur3, and/or a Gln3.

10. The recombinant yeast of claim 9 , wherein the up-regulated enzyme in the nitrogen-assimilation pathway is encoded by an amino acid sequence at least 80%, 90%, 95% or 100% identical to a polypeptide sequence selected from the group consisting of: SEQ ID NOs: 27 and 29 (Gdh2);
at least 80%, 90%, 95% or 100% identical to a polypeptide sequence encoded by SEQ ID NO: 33 (Glt1);
at least 80%, 90%, 95%, 100% identical to a polypeptide sequence encoded by SEQ ID NO: 35 (Gln1);
at least 80%, 90%, 95% or 100% identical to a polypeptide sequence encoded by SEQ ID NO: 19 (Mep1);
at least 80%, 90%, 95% or 100% identical to a polypeptide sequence encoded by SEQ ID NO: 21 (Mep2);
at least 80%, 90%, 95% or 100% identical to a polypeptide sequence encoded by SEQ ID NO: 23 (Mep3);
at least 80%, 90%, 95% or 100% identical to a polypeptide sequence encoded by SEQ ID NO: 37 (Dur1/2);
at least 80%, 90%, 95% or 100% identical to a polypeptide sequence encoded by: SEQ ID NO: 39 (Dur3); and/or
at least 80%, 90%, 95% or 100% identical to a polypeptide sequence encoded by SEQ ID NO: 156 (Gln3).

11. The recombinant yeast of claim 1 , wherein the up-regulated enzyme in the nitrogen-assimilation pathway is an ammonium transporter and/or a urea transporter.

12. The recombinant yeast of claim 1 , wherein the microorganism further comprises at least one engineered genetic modification that leads to the down-regulation of an enzyme in a glycerol-production pathway; wherein the down-regulated enzyme in the glycerol-production pathway is selected from the group consisting of glycerol-3-phosphate dehydrogenase 1 polynucleotide (GPD1) (EC 1.1.1.8), glycerol-3-phosphate dehydrogenase 1 polypeptide (Gpd1) (EC 1.1.1.8), glycerol-3-phosphate dehydrogenase 2 polynucleotide (GPD2) (EC 1.1.1.8), glycerol-3-phosphate dehydrogenase 2 polypeptide (Gpd2) (EC 1.1.1.8), glycerol-3-phosphate phosphatase 1 polynucleotide (GPP1) (EC 3.1.3.21), a glycerol-3-phosphate phosphatase polypeptide 1 (Gpp1) (EC 3.1.3.21), a glycerol-3-phosphate phosphatase 2 polynucleotide (GPP2) (EC 3.1.3.21), and glycerol-3-phosphate phosphatase polypeptide 2 (Gpp2) (EC 3.1.3.21).

13. The recombinant yeast of claim 12 , wherein the enzyme in the glycerol production pathway is encoded by a polypeptide sequence at least 80%, 90%, 95% or 100% identical to the polypeptide sequence encoded by: SEQ ID NO: 5 (Gpd1); a polypeptide sequence at least 80%, 90%, 95% or 100% identical to the polypeptide sequence encoded by: SEQ ID NO: 7 (Gpd2); a polypeptide sequence at least 80%, 90%, 95% or 100% identical to the polypeptide sequence encoded by: SEQ ID NO: 159 (Gpp1); or a polypeptide sequence at least 80%, 90%, 95% or 100% identical to the polypeptide sequence encoded by: SEQ ID NO: 161 (Gpp2).

14. The recombinant yeast of claim 1 , wherein the microorganism further comprises an up-regulation or down-regulation of a regulatory element.

15. The recombinant yeast of claim 14 , wherein the regulatory element is selected from the group consisting of Ure2 and Aua1.

16. The recombinant yeast of claim 15 , wherein the regulatory element is encoded by polypeptide sequence at least 80%, 90%, 95% or 100% identical to a polypeptide sequence encoded by a polynucleotide, sequence of SEQ ID NO: 55 (Ure2) or a polypeptide sequence at least 80%, 90%, 95% or 100% identical to a polypeptide sequence encoded by a polynucleotide sequence of SEQ ID NO: 57 (Aua1).

17. The recombinant yeast of claim 1 , wherein the microorganism further comprises at least one additional up-regulated enzyme, wherein the at least one additional up-regulated enzyme is a permease or a protease with EC number: 3.4.23.41.

18. The recombinant yeast of claim 17 , wherein the up-regulated enzyme is encoded by a polypeptide sequence at least 80%, 90%, 95% or 100% identical to a polypeptide sequence encoded by SEQ ID NO: 53 (Gap); or a polypeptide sequence at least 80%, 90%, 95% or 100% identical to a polypeptide sequence selected from a group consisting of SEQ NOs: 41, 43, 45, 47, 49, and 51 (protease).

19. The recombinant yeast of claim 1 , wherein the up-regulated enzymes are under the control of a heterologous promoter, wherein the heterologous promoter is selected from a group consisting of: a promoter of the TEF2 gene (SEQ ID NO: 58), a promoter of the HXT7 gene (SEQ ID NO: 59), a promoter of the ADH1 gene (SEQ ID NO: 60), and a promoter of a TP1 gene (SEQ ID NO: 61).

20. The recombinant yeast of claim 1 , wherein the yeast is from the genus Saccharomyces.

21. A co-culture comprising at least two host cells wherein
a) one of the host cells comprises a recombinant yeast from claim 1 ; and,
b) another host cell that is genetically distinct from (a).

Assignees

• Lallemand Hungary Liquidity Man Llc

Inventors

• Argyros Aaron
• Barrett Trisha

Classifications

• C12P7/06 Primary

  Ethanol, i.e. non-beverage · CPC title

• C12N9/0004 Primary

  Oxidoreductases (1.) · CPC title

• C12N9/0006

  acting on CH-OH groups as donors (1.1) · CPC title

• C12N9/0008

  acting on the aldehyde or oxo group of donors (1.2) · CPC title

• C12N9/0016

  with NAD or NADP as acceptor (1.4.1) · CPC title