IP Library Granted Patent US 9,156,760
Granted Patent B2
US 9,156,760 · App. 14/211,342 · Granted Oct 13, 2015

Method for production of butanol using extractive fermentation

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Quick Facts
Patent No.
US 9,156,760
App. No.
14/211,342
Granted
Oct 13, 2015
Kind
B2
Abstract

Provided herein are methods for recovering butanol from a fermentation medium. The methods comprise providing a fermentation medium comprising butanol, water, and a recombinant microorganism comprising a butanol biosynthetic pathway, wherein the recombinant microorganism produces butanol; contacting the fermentation medium with a water immiscible organic extractant composition comprising a dry solvent to form a butanol-containing organic phase and an aqueous phase; and recovering the butanol from the butanol-containing organic phase.

Claims (20)

1. A method for recovering butanol from a fermentation medium, the method comprising:

a) providing a fermentation medium comprising butanol, water, and a recombinant microorganism comprising a butanol biosynthetic pathway, wherein the recombinant microorganism produces butanol;

b) contacting the fermentation medium with a water immiscible organic extractant composition comprising a dry solvent to form a butanol-containing organic phase and an aqueous phase, wherein the dry solvent is a saturated hydrocarbon that is a branched C 7 to C 22 alkane or a mixture thereof; and

c) recovering the butanol from the butanol-containing organic phase.

2. The method of claim 1 , wherein the C 7 to C 22 alkane is a derivative of isobutanol, wherein the derivative of isobutanol is triisobutylene, diisobutylene, tetraisobutylene, isooctane, isohexadecane, or isododecane.

3. The method of claim 2 , wherein the derivative of isobutanol is isododecane.

4. The method of claim 1 , wherein the contacting of the organic extractant composition with the fermentation medium occurs in a fermentor.

5. The method of claim 1 , further comprising transferring a portion of the fermentation medium from a fermentor to a vessel, wherein the contacting of the organic extractant composition with the fermentation medium occurs in the vessel.

6. The method of claim 1 , wherein the organic extractant composition further comprises a second solvent, wherein the second solvent is a C 4 to C 22 fatty alcohol, a C 4 to C 28 fatty acid, an ester of a C 4 to C 28 fatty acid, a C 4 to C 22 fatty aldehyde, a C 7 to C 22 ether, or mixtures thereof.

7. The method of claim 1 , wherein the organic extractant composition further comprises a second solvent, wherein the second solvent is oleyl alcohol, behenyl alcohol, cetyl alcohol, lauryl alcohol, myristyl alcohol, stearyl alcohol, oleaic acid, lauric acid, myristic acid, stearic acid, octanoic acid, decanoic acid, undecanoic acid, methyl myristate, methyl oleate, 1-nonanol, 1-decanol, 2-undecanol, 1-nonanal, 1-undenol, undecanal, isododecanol, lauric aldehyde, 2-methylundecanal, oleamide, linoleamide, palmitamide, streaylamide, 2-ethyl-1-hexanol, 2-hexyl-1-decanol, 2-octyl-1-dodecanol, or mixtures thereof.

8. The method of claim 6 or 7 , wherein the second solvent increases a butanol partition coefficient of the organic extractant composition.

9. The method of claim 1 , wherein the recovered butanol has an effective titer from about 30 grams per liter to about 50 grams per liter of the fermentation medium.

10. The method of claim 1 , wherein the recovered butanol has an effective titer of at least 37 grams per liter of the fermentation medium.

11. The method of claim 1 , wherein the butanol is isobutanol.

12. A composition comprising butanol in a water immiscible organic extractant composition, wherein the organic extractant composition comprises a solvent, wherein the solvent is a dry solvent, wherein the dry solvent is a saturated hydrocarbon that is a branched C 7 to C 22 alkane or a mixture thereof.

13. The composition of claim 12 , wherein the C 7 to C 22 alkane is a derivative of isobutanol, wherein the derivative of isobutanol is triisobutylene, diisobutylene, tetraisobutylene, isooctane, isohexadecane, or isododecane.

14. The composition of claim 13 , wherein the derivative of isobutanol is isododecane.

15. The composition of claim 12 , further comprising a second solvent, wherein the second solvent is a C 4 to C 22 fatty alcohol, a C 4 to C 28 fatty acid, an ester of a C 4 to C 28 fatty acid, a C 4 to C 22 fatty aldehyde, a C 7 to C 22 ether, or mixtures thereof.

16. The composition of claim 12 , further comprising a second solvent, wherein the second solvent is oleyl alcohol, behenyl alcohol, cetyl alcohol, lauryl alcohol, myristyl alcohol, stearyl alcohol, oleaic acid, lauric acid, myristic acid, stearic acid, octanoic acid, decanoic acid, undecanoic acid, methyl myristate, methyl oleate, 1-nonanol, 1-decanol, 2-undecanol, 1-nonanal, 1-undenol, undecanal, isododecanol, lauric aldehyde, 2-methylundecanal, oleamide, linoleamide, palmitamide, streaylamide, 2-ethyl-1-hexanol, 2-hexyl-1-decanol, 2-octyl-1-dodecanol, or mixtures thereof.

17. The composition of claim 12 , wherein the butanol is isobutanol.

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 Mar 19, 2014
From: ZAHER, JOSEPH J.
To: BUTAMAX ADVANCED BIOFUELS LLC
Reel/Frame 032473/0144 →