초록 ▼

This invention is directed to methods for recovery of C3-C6 alcohols from dilute aqueous solutions, such as fermentation broths. Such methods provide improved volumetric productivity for the fermentation and allows recovery of the alcohol. Such methods also allow for reduced energy use in the produc

This invention is directed to methods for recovery of C3-C6 alcohols from dilute aqueous solutions, such as fermentation broths. Such methods provide improved volumetric productivity for the fermentation and allows recovery of the alcohol. Such methods also allow for reduced energy use in the production and drying of spent fermentation broth due to increased effective concentration of the alcohol product by the simultaneous fermentation and recovery process which increases the quantity of alcohol produced and recovered per quantity of fermentation broth dried. Thus, the invention allows for production and recovery of C3-C6 alcohols at low capital and reduced operating costs.

대표청구항 ▼

1. A method for recovering isobutanol from a fermentation medium, comprising: (a) culturing a genetically engineered microorganism in a fermentation medium comprising water and a feedstock comprising isobutanol, said genetically engineered microorganism, and a fermentable carbon source;(b) extractin

1. A method for recovering isobutanol from a fermentation medium, comprising: (a) culturing a genetically engineered microorganism in a fermentation medium comprising water and a feedstock comprising isobutanol, said genetically engineered microorganism, and a fermentable carbon source;(b) extracting the isobutanol in a portion of the fermentation medium with a water immiscible, isobutanol-selective liquid extractant, thereby forming an isobutanol-rich liquid phase and a water-rich liquid phase;(c) separating the isobutanol-rich liquid phase and a water-rich liquid phase;(d) recovering the isobutanol from the isobutanol-rich liquid phase; wherein: said genetically engineered microorganism is engineered to express or over-express a metabolic pathway that converts pyruvate to isobutanol; andsaid metabolic pathway comprises an acetohydroxy acid synthase (ALS) enzyme; andsaid genetically engineered microorganism includes a deletion of pyruvate decarboxylase. 2. The method of claim 1, wherein the isobutanol-selective liquid extractant is a hydrophobic hydrocarbon solvent. 3. The method of claim 2, wherein the hydrophobic hydrocarbon solvent is a biofuel. 4. The method of claim 1, wherein the ratio of isobutanol to water in the isobutanol-rich phase is greater than about 2. 5. The method of claim 1, wherein the ratio of isobutanol to water in the isobutanol-rich phase is greater than about 8. 6. The method of claim 1, wherein the ratio of isobutanol to water in the isobutanol rich phase is greater than the ratio of isobutanol to water in the fermentation medium by at least 5 fold. 7. The method of claim 1, wherein the ratio of isobutanol to water in the isobutanol rich phase is greater than the ratio of isobutanol to water in the fermentation medium by at least 25-fold. 8. The method of claim 1, further comprising cooling the isobutanol-rich phase, thereby increasing the ratio of isobutanol to water in the isobutanol-rich phase. 9. The method of claim 1, wherein the fermentation medium further comprises ethanol. 10. The method of claim 1, further comprising: (e) conducting the water-rich liquid phase to the fermentation medium. 11. The method of claim 1, wherein the metabolic pathway comprises ketolacid reductoisomerase (KARI) and isobutyraldehyde dehydrogenase (IDH) enzymes. 12. The method of claim 11, wherein the KARI and IDH enzymes utilize a NADPH cofactor. 13. The method of claim 11, wherein the KARI and IDH enzymes utilize a NADH cofactor. 14. The method of claim 11, wherein either KARI or IDH utilizes a NADH cofactor.