IP Library Granted Patent US 9,517,985
Granted Patent B2
US 9,517,985 · App. 14/772,705 · Granted Dec 13, 2016

Method for producing butanol using extractive fermentation

Inventors: Thomas Basham (San Diego, CA); Leslie William Bolton (Hampshire, GB); Ian David Dobson (London, GB); Sarah Richardson Hanson (San Marcus, CA); Aidan Hurley (East Riding of Yorkshire, GB); Karen Kustedjo (La Jolla, CA); Andrew Richard Lucy (Brough East Yorkshire, GB); Liang Song (San Diego, CA)
Assignee: Butamax Advanced Biofuels LLC
C07C29/76C07C29/86C07C31/12C12P7/16Y02E50/10
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Quick Facts
Patent No.
US 9,517,985
App. No.
14/772,705
Granted
Dec 13, 2016
Kind
B2
Abstract

The invention relates to a method for producing butanol through microbial fermentation, in which the butanol product is removed by extraction into a water immiscible organic extractant during the fermentation. The invention also relates to a method for producing butanol through microbial fermentation, in which the butanol product is removed during the fermentation by extraction into a water-immiscible extractant composition. The invention further relates to compositions comprising a solution of butanol in a water immiscible organic extractant composition.

Claims (29)

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 solvent selected from the group consisting of C 12 to C 22 fatty alcohols, C 12 to C 22 ethers, esters of C 12 to C 22 fatty acids, C 10 to C 22 alkanes, and mixtures thereof, to form a butanol-containing organic phase and an aqueous phase,

wherein the solvent is biocompatible with the microorganism such that at least about 90% of the microorganisms are viable after exposure to the organic extractant composition, and

wherein the solvent has a boiling point less than about 300° C, with the proviso that the organic extractant is not oleyl alcohol, 1-dodecanol, behenyl alcohol, cetyl alcohol, myristyl alcohol, or stearyl alcohol; and

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

2. The method of claim 1 , wherein the solvent is trimethylnonanol, methyl laurate, di-n-octyl ether, dodecane, n-undecane, ethyl decanoate, ethyl laurate, or mixtures thereof.

3. 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 solvent is trimethylnonanol, methyl laurate, di-n-octyl ether, dodecane, n-undecane, ethyl decanoate, ethyl laurate, or mixtures thereof, to form a butanol-containing organic phase and an aqueous phase; and

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

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 the 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 butanol is isobutanol.

7. The method of claim 1 , wherein the organic extractant composition further comprises an additional solvent, wherein the additional solvent is n-hexanol, methyl isobutyl carbinol, 2-ethyl-1-hexanol, 2,6-dimethylheptan-4-ol, or mixtures thereof.

8. The method of claim 7 , wherein the additional solvent is 2,6-dimethylheptan-4-ol.

9. The method of claim 1 , wherein the organic extractant composition further comprises an additional solvent with a butanol partition coefficient greater than about 4.

10. The method according to claim 9 , wherein the organic extractant composition further comprises an additional solvent, wherein the additional solvent is n-hexanol, methyl isobutyl carbinol, 2-ethyl-1-hexanol, 2,6-dimethylheptan-4-ol, or mixtures thereof.

11. The method of claim 10 , wherein the additional solvent is 2,6-dimethylheptan-4-ol.

12. The method of claim 1 , wherein the contacting comprises contacting the fermentation medium via a co-current or counter-current stream of the organic extractant composition.

13. The method of claim 1 , wherein the recovered butanol has an effective titer from about 22 g per liter to about 40 g per liter of the fermentation medium.

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

15. A composition comprising a solution of butanol in a water immiscible organic extractant composition, wherein the organic extractant composition comprises a solvent selected from the group consisting of C 12 to C 22 fatty alcohols, C 12 to C 22 ethers, esters of C 12 to C 22 fatty acids, C 10 to C 22 alkanes, and mixtures thereof,

wherein the solvent is biocompatible with a recombinant microorganism comprising a butanol biosynthetic pathway, wherein at least 90% of the recombinant microorganisms are viable after exposure to the organic extractant composition, and wherein the solvent has a boiling point less than about 300° C.,

with the proviso that the solvent is not oleyl alcohol, 1-dodecanol, behenyl alcohol, cetyl alcohol, myristyl alcohol, or stearyl alcohol.

16. The composition of claim 15 , wherein the solvent is trimethylnonanol, methyl laurate, di-n-octyl ether, dodecane, n-undecane, ethyl decanoate, ethyl laurate, or mixtures thereof.

17. The composition of claim 15 , wherein the organic extractant composition further comprises an additional solvent, wherein the additional solvent is n-hexanol, methyl isobutyl carbinol, 2-ethyl-1-hexanol, 2,6-dimethylheptan -4-ol, or mixtures thereof.

18. The composition of claim 17 , wherein the additional solvent is 2,6-dimethylheptan-4-ol.

19. The composition of claim 15 , wherein the butanol is isobutanol.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 30, 2021
From: BUTAMAX ADVANCED BIOFUELS LLC
To: GEVO, INC.
Reel/Frame 057677/0477 →
Continuity (2)
Provisional Application 61788213 · Mar 15, 2013
Related Publication 20160016870A1 · Jan 21, 2016