IP Library Granted Patent US 10,358,664
Granted Patent B2
US 10,358,664 · App. 15/553,241 · Granted Jul 23, 2019

Mutant host cells for the production of 3-hydroxypropionic acid

Inventors: Janice Frias (New Brighton, MN); Guillaume Barbier (Davis, CA)
Assignee: Novozymes A/S
C12P7/42C12N9/0006C12Y101/01081
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Quick Facts
Patent No.
US 10,358,664
App. No.
15/553,241
Granted
Jul 23, 2019
Kind
B2
Abstract

Provided herein are recombinant host cells having an active 3-Hydroxypropionic Acid (3-HP) pathway wherein the host cells comprise a disruption to an endogenous gene that encodes for a pyruvate reductase. Also described are methods of making the host cells, and methods using the cells to produce 3-HP and derivatives of 3-HP (e.g., acrylic acid).

Claims (38)

1. A recombinant yeast cell, wherein the recombinant yeast cell belongs to the genus Issatchenkia , wherein the recombinant yeast cell comprises (1) an active 3-hydroxypropionic acid (3-HP) pathway capable of producing 3-HP and (2) a disruption to an endogenous gene that encodes a pyruvate reductase, and wherein the amino acid sequence of the pyruvate reductase has at least 95% sequence identity to the amino acid sequence of SEQ ID NO: 205.

2. The recombinant cell of claim 1 , wherein the amino acid sequence of the pyruvate reductase differs by no more than ten amino acids from the amino acid sequence of SEQ ID NO: 205.

3. The recombinant cell of claim 1 , wherein the pyruvate reductase comprises or consists of the amino acid sequence of SEQ ID NO: 205.

4. The recombinant cell of claim 1 , wherein the cell produces less D-lactate compared to a corresponding yeast cell that lacks disruption of the endogenous gene encoding the pyruvate reductase, when cultivated under identical conditions.

5. The recombinant cell of claim 1 , wherein the cell produces less pyruvate reductase compared to a corresponding yeast cell that lacks disruption of the endogenous gene encoding the pyruvate reductase, when cultivated under identical conditions.

6. The recombinant cell of claim 1 , wherein the endogenous gene encoding the pyruvate reductase is inactivated.

7. The recombinant cell of claim 1 , wherein the cell comprises one or more heterologous polynucleotides selected from:

a heterologous polynucleotide encoding a pyruvate dehydrogenase (PDH);

a heterologous polynucleotide encoding an acetyl-CoA carboxylase (ACC);

a heterologous polynucleotide encoding a malonyl-CoA reductase; and

a heterologous polynucleotide encoding a 3-HP dehydrogenase (3-HPDH).

8. The recombinant cell of claim 1 , wherein the cell comprises one or more heterologous polynucleotides selected from:

a heterologous polynucleotide encoding a PEP carboxylase (PPC);

a heterologous polynucleotide encoding a pyruvate carboxylase (PYC);

a heterologous polynucleotide encoding an aspartate aminotransferase (AAT);

a heterologous polynucleotide encoding an aspartate 1-decarboxylase (ADC);

a heterologous polynucleotide encoding a β-alanine aminotransferase (BAAT) or aminobutyrate aminotransferase (gabT); and

a heterologous polynucleotide encoding a 3-HP dehydrogenase (3-HPDH).

9. The recombinant cell of claim 1 , wherein the cell is an Issatchenkia orientalis.

10. The recombinant cell of claim 1 , wherein the yeast cell is unable to ferment pentose sugars.

11. A method of producing 3-hydroxypropionic acid (3-HP), comprising:

(a) cultivating the recombinant yeast cell of claim 1 in a fermentable medium under suitable conditions to produce 3-HP; and

(b) recovering the 3-HP.

12. A method of producing acrylic acid or a salt thereof, comprising:

(a) cultivating the recombinant cell of claim 1 in a fermentable medium under suitable conditions to produce 3-hydroxypropionic acid (3-HP);

(b) recovering the 3-HP;

(c) dehydrating the 3-HP under suitable conditions to produce acrylic acid or a salt thereof; and

(d) recovering the acrylic acid or salt thereof.

13. The method of claim 11 , wherein the fermentable medium comprises less than 1% pentose sugars.

14. A method for obtaining the recombinant yeast cell of claim 1 , comprising:

(a) cultivating a parent yeast strain, wherein the parent strain belongs to the genus Issatchenkia;

(b)(i) transforming the parent strain with one or more 3-hydroxypropionic acid (3-HP) pathway gene(s) to provide an active 3-HP pathway in the parent strain of (a);

(b)(ii) disrupting an endogenous gene encoding a pyruvate reductase in the parent strain of (a), wherein the amino acid sequence of the pyruvate reductase has at least 95% sequence identity to the amino acid sequence of SEQ ID NO: 205; and

(c) isolating the recombinant yeast cell resulting from (b)(i) and (b)(ii).

15. The recombinant cell of claim 1 , wherein the amino acid sequence of the pyruvate reductase has at least 97% sequence identity to the amino acid sequence of SEQ ID NO: 205.

16. The method of claim 11 , wherein the amino acid sequence of the pyruvate reductase has at least 97% sequence identity to the amino acid sequence of SEQ ID NO: 205.

17. The method of claim 11 , wherein the amino acid sequence of the pyruvate reductase comprises or consists of the amino acid sequence of SEQ ID NO: 205.

18. The method of claim 11 , wherein the recombinant cell is an Issatchenkia orientalis cell.

Continuity (2)
Provisional Application 62126377 · Feb 27, 2015
Related Publication 20180237809A1 · Aug 23, 2018
Cited By (1)
US 12,378,580