IP Library Granted Patent US 10,544,411
Granted Patent B2
US 10,544,411 · App. 16/313,613 · Granted Jan 28, 2020

Methods for generating a glucose permease library and uses thereof

Inventors: Shawn Manchester (Oakland, CA); Jeffrey Mellin (Oakland, CA)
Assignee: Zymergen Inc.
C12N15/1037C12N9/1205C12P1/04C12Y207/01001C12Y207/01069
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Quick Facts
Patent No.
US 10,544,411
App. No.
16/313,613
Granted
Jan 28, 2020
Kind
B2
Abstract

The present disclosure describes methods for generating microbial strains expressing a heterologous bacterial glucose permease gene that produce biomolecules of interest. In aspects, the disclosure provides novel bacterial strains, which express a heterologous bacterial glucose permease gene whose expression is controlled by a native Corynebacterium glutamicum promoter or a mutant promoter derived therefrom. Also provided herein are methods for producing a library of bacterial glucose permease genes using a promoter ladder comprising a plurality of promoters derived from Corynebacterium glutamicum.

Claims (24)

1. A host cell comprising a heterologous glucose permease gene functionally linked to a first promoter polynucleotide, wherein the first promoter polynucleotide comprises a nucleotide sequence selected from SEQ ID NO: 1, SEQ ID NO: 2, SEQ ID NO: 3, SEQ ID NO: 4, SEQ ID NO: 5, SEQ ID NO: 6, SEQ ID NO: 7, and SEQ ID NO: 8.

2. The host cell of claim 1 , wherein the glucose permease gene is a gene that encodes a polypeptide with an amino acid sequence selected from SEQ ID NO: 13, SEQ ID NO: 10, SEQ ID NO: 11, SEQ ID NO: 12, SEQ ID NO: 9and SEQ ID NO: 14.

3. The host cell of claim 1 , wherein the glucose permease gene is a gene with a nucleotide sequence selected from SEQ ID NO: 23, SEQ ID NO: 20, SEQ ID NO: 21, SEQ ID NO: 22, SEQ ID NO: 19 and SEQ ID NO: 24.

4. The host cell of claim 1 , further comprising a hexokinase gene functionally linked to a second promoter polynucleotide, wherein the second promoter polynucleotide comprises a nucleotide sequence selected from SEQ ID NO: 2, SEQ ID NO: 1, SEQ ID NO: 3, SEQ ID NO: 4, SEQ ID NO: 5, SEQ ID NO: 6, SEQ ID NO: 7, and SEQ ID NO: 8.

5. The host cell of claim 4 , wherein the hexokinase gene is a gene that encodes a polypeptide sequence selected from SEQ ID NO: 15 and SEQ ID NO: 16.

6. The host cell of claim 4 , wherein the hexokinase gene is a gene with a nucleotide sequence selected from SEQ ID NO: 25 and SEQ ID NO: 26.

7. A method for generating a microorganism capable of increased production of a biomolecule from glucose, the method comprising:

a) genetically modifying a host microorganism, wherein the modifying comprises introducing a glucose permease gene from a library of glucose permease genes into the genome of the host microorganism, wherein each glucose permease gene from the library of glucose permease genes is functionally linked to a promoter comprising a nucleotide sequence selected from SEQ ID NO: 1, SEQ ID NO: 2, SEQ ID NO: 3, SEQ ID NO: 4, SEQ ID NO: 5, SEQ ID NO: 6, SEQ ID NO: 7, and SEQ ID NO: 8 and wherein the modification generates a strain of the host microorganism expressing the glucose permease gene;

b) repeating step a) for a plurality of rounds until a plurality of strains of the host microorganism are generated, wherein each strain of the plurality of strains of the host microorganism expresses a separate glucose permease gene from the library of glucose permease genes;

c) contacting each strain of the plurality of strains of the host microorganism with a carbon source comprising glucose under fermentative conditions; and

d) selecting each strain of the host microorganism that produces an increased amount of a biomolecule from glucose as compared to the amount of the biomolecule produce from glucose from a control microorganism, wherein the control microorganism does not express a glucose permease gene from the library of glucose permease genes.

8. The method of claim 7 , wherein the library of glucose permease genes comprises genes that encode polypeptide sequences of SEQ ID NO: 13, SEQ ID NO: 10, SEQ ID NO: 11, SEQ ID NO: 12, SEQ ID NO: 9, SEQ ID NO: 14 or a combination thereof.

9. The method of claim 7 , wherein the library of glucose permease genes comprises genes with a nucleotide sequence of SEQ ID NO: 23, SEQ ID NO: 20, SEQ ID NO: 21, SEQ ID NO: 22, SEQ ID NO: 19, SEQ ID NO: 24 or a combination thereof.

10. The method of claim 7 , further comprising introducing a hexokinase gene from a library of hexokinase genes, wherein each hexokinase gene from the library of hexokinase genes is functionally linked to a promoter polynucleotide, wherein the promoter polynucleotide comprises a sequence selected from SEQ ID NO: 2, SEQ ID NO: 1, SEQ ID NO: 3, SEQ ID NO: 4, SEQ ID NO: 5, SEQ ID NO: 6, SEQ ID NO: 7, and SEQ ID NO: 8.

11. The method of claim 10 , wherein the library of hexokinase genes comprises genes that encode polypeptide sequences of SEQ ID NO: 15 and/or SEQ ID NO: 16.

12. The method of claim 10 , wherein the library of hexokinase genes comprises genes with nucleotide sequences of SEQ ID NO: 25 and/or SEQ ID NO: 26.

13. A library of glucose permease genes, wherein each glucose permease gene in the library of glucose permease genes is functionally linked to a promoter comprising a nucleotide sequence selected from SEQ ID NO: 1, SEQ ID NO: 2, SEQ ID NO: 3, SEQ ID NO: 4, SEQ ID NO: 5, SEQ ID NO: 6, SEQ ID NO: 7, and SEQ ID NO: 8.

14. The library of claim 13 , wherein the library of glucose permease genes comprises genes that encode polypeptide sequences of SEQ ID NO: 13, SEQ ID NO: 10, SEQ ID NO: 11, SEQ ID NO: 12, SEQ ID NO: 9, SEQ ID NO: 14 or a combination thereof.

15. The library of claim 13 , wherein the library of glucose permease genes comprises genes with nucleotide sequences of SEQ ID NO: 23, SEQ ID NO: 20, SEQ ID NO: 21, SEQ ID NO: 22, SEQ ID NO: 19, SEQ ID NO: 24 or a combination thereof.

16. The library of claim 13 , wherein each glucose permease gene in the library of glucose permease genes is a first portion of a chimeric construct, wherein the chimeric construct comprises a second portion, wherein the second portion is a hexokinase gene.

17. The library of claim 16 , wherein the hexokinase gene is functionally linked to a promoter polynucleotide, wherein the promoter polynucleotide comprises a sequence selected from SEQ ID NO: 2, SEQ ID NO: 1, SEQ ID NO: 3, SEQ ID NO: 4, SEQ ID NO: 5, SEQ ID NO: 6, SEQ ID NO: 7, and SEQ ID NO: 8.

18. The library of claim 17 , wherein the library of hexokinase genes comprises genes that encode polypeptide sequences of SEQ ID NO: 15 and or SEQ ID NO: 16.

19. The library of claim 17 , wherein the library of hexokinase genes comprises genes with nucleotide sequences of SEQ ID NO: 25 and/or SEQ ID NO: 26.

20. A method of producing a biomolecule comprising introducing a glucose permease gene from the library of claim 13 , into a host cell and culturing the host cell under conditions suitable for producing the biomolecule.

Assignments (3)
RELEASE OF SECURITY INTEREST Recorded Jul 1, 2022
From: PERCEPTIVE CREDIT HOLDINGS II, LP, AS ADMINISTRATIVE AGENT
To: ZYMERGEN INC.
Reel/Frame 060421/0533 →
PATENT SECURITY AGREEMENT Recorded Dec 26, 2019
From: ZYMERGEN INC.
To: PERCEPTIVE CREDIT HOLDINGS II, LP, AS ADMINISTRATIVE AGENT
Reel/Frame 051425/0485 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 30, 2019
From: MANCHESTER, SHAWN; MELLIN, JEFFREY
To: ZYMERGEN INC.
Reel/Frame 049898/0180 →
Continuity (2)
Provisional Application 62356924 · Jun 30, 2016
Related Publication 20190194647A1 · Jun 27, 2019