IP Library Granted Patent US 9,267,157
Granted Patent B2
US 9,267,157 · App. 13/227,016 · Granted Feb 23, 2016

Butanol strain improvement with integration of a polynucleotide encoding a polypeptide that catalyzes pyruvate to acetolactate conversion

View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 9,267,157
App. No.
13/227,016
Granted
Feb 23, 2016
Kind
B2
Abstract

The invention relates to recombinant host cells having at least one integrated polynucleotide encoding a polypeptide that catalyzes a step in a pyruvate-utilizing biosynthetic pathway, e.g., pyruvate to acetolactate conversion. The invention also relates to methods of increasing the biosynthetic production of isobutanol, 2,3-butanediol, 2-butanol or 2-butanone using such host cells.

Claims (11)

1. A method comprising:

(a) providing a recombinant host cell comprising an isobutanol biosynthetic pathway wherein said pathway comprises the substrate to product conversion pyruvate to acetolactate catalyzed by a polypeptide encoded by a heterologous polynucleotide integrated into the chromosome at the PDC1-TRX1 intergenic region and wherein said pathway comprises the substrate to product conversion acetolactate to 2,3-dihydroxyisovalerate catalyzed by a polypeptide that has at least about 90% identity to SEQ ID NO: 224 or 225 and said polypeptide is encoded by a polynucleotide on a plasmid and wherein the titer of isobutanol production is increased as compared to a recombinant host cell wherein the polynucleotide encoding a polypeptide that catalyzes the conversion of pyruvate to acetolactate is not integrated into the chromosome;

(b) contacting the host cell with a fermentable carbon substrate to form a fermentation broth under conditions whereby the isobutanol biosynthetic pathway product is produced; and

(c) contacting the fermentation broth with an extractant to produce a two-phase fermentation mixture, wherein the extractant comprises fatty acids; and

(d) recovering the isobutanol.

2. The method of claim 1 , wherein the fatty acids are derived from corn oil or soybean oil.

3. The method of claim 1 , wherein the extractant further comprises a water immiscible organic extractant selected from the group consisting of: C 12 to C 22 fatty alcohols, esters of C 12 to C 22 fatty acids, C 12 to C 22 fatty aldehydes, and C 12 to C 22 fatty amides.

4. The method of claim 1 , and wherein the method further comprises contacting the fermentation broth with an organic acid and an enzyme capable of esterifying the isobutanol with the organic acid.

5. The method of claim 1 , and wherein the method further comprises vaporizing at least a portion of the fermentation broth to form a vapor stream comprising water and alcohol.

6. The method of claim 1 , wherein the rate of isobutanol production is increased by at least 10% as compared to a recombinant host cell wherein the polynucleotide encoding a polypeptide that catalyzes the conversion of pyruvate to acetolactate is not integrated into the chromosome.

7. The method of claim 1 , wherein the titer of isobutanol production is increased by at least 10% as compared to a recombinant host cell wherein the polynucleotide encoding a polypeptide that catalyzes the conversion of pyruvate to acetolactate is not integrated into the chromosome.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 30, 2021
From: BUTAMAX ADVANCED BIOFUELS LLC
To: GEVO, INC.
Reel/Frame 057677/0477 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 20, 2012
From: ANTHONY, LARRY CAMERON; MAGGIO-HALL, LORI ANN
To: BUTAMAX(TM) ADVANCED BIOFUELS LLC
Reel/Frame 029328/0883 →