Yeast organism producing isobutanol at a high yield
View Patent ↗The present invention provides recombinant mircoorganisms comprising an isobutanol producing metabolic pathway and methods of using said recombinant microorganisms to produce isobutanol. In various aspects of the invention, the recombinant microorganisms may comprise a modification resulting in the reduction of pyruvate decarboxylase and/or glycerol-3-phosphate dehydrogenase activity. In various embodiments described herein, the recombinant microorganisms may be microorganisms of the Saccharomyces clade, Crabtree-negative yeast microorganisms, Crabtree-positive yeast microorganisms, post-WGD (whole genome duplication) yeast microorganisms, pre-WGD (whole genome duplication) yeast microorganisms, and non-fermenting yeast microorganisms.
1. A recombinant yeast microorganism for producing isobutanol, the recombinant yeast microorganism comprising an isobutanol producing metabolic pathway, wherein said isobutanol producing metabolic pathway comprises the following substrate to product conversions:
(i) pyruvate to acetolactate;
(ii) acetolactate to 2,3-dihydroxyisovalerate;
(iii) 2,3-dihydroxyisovalerate to α-ketoisovalerate;
(iv) α-ketoisovalerate to isobutyraldehyde; and
(v) isobutyraldehyde to isobutanol;
wherein the recombinant yeast microorganism expresses
(a) an acetolactate synthase to catalyze the conversion of pyruvate to acetolactate;
(b) a ketol-acid reductoisomerase to catalyze the conversion of acetolactate to 2,3-dihydroxyisovalerate;
(c) a dihydroxyacid dehydratase to catalyze the conversion of 2,3-dihydroxyisovalerate to α-ketoi sovalerate;
(d) an α-ketoisovalerate decarboxylase from Laciococcus lactis to catalyze the conversion of α-ketoisovalerate to isobutyraldehyde; and
(e) an alcohol dehydrogenase to catalyze the conversion of isobutyraldehyde to isobutanol;
wherein the recombinant yeast microorganism has been engineered to:
(A) disrupt, mutate, or delete one or more endogenous pyruvate decarboxylase (PDC) genes; and
(B) disrupt, mutate, or delete one or more endogenous glycerol-3-phosphate dehydrogenase (GPD) genes;
wherein said recombinant yeast microorganism has reduced endogenous PDC and reduced endogenous GPD activity as compared to the corresponding yeast microorganism that has not been engineered to have reduced endogenous PDC activity and reduced endogenous GPD activity; and wherein the recombinant yeast microorganism produces isobutanol at a yield which is at least 10% of the theoretical yield of isobutanol from glucose.
2. The recombinant yeast microorganism of claim 1 , wherein all endogenous PDC genes and all endogenous GPD genes are disrupted, mutated, or deleted.
3. The recombinant yeast microorganism of claim 1 , wherein said acetolactate synthase is a cytosolically-localized acetolactate synthase.
4. The recombinant yeast microorganism of claim 3 , wherein said cytosolically-localized acetolactate synthase is encoded by the Lactococcus lactis alsS gene.
5. The recombinant yeast microorganism of claim 3 , wherein said cytosolically-localized acetolactate synthase is encoded by the Bacillus subtilis alsS gene.
6. The recombinant yeast microorganism of claim 1 , wherein said recombinant yeast microorganism has been engineered to disrupt or delete an endogenous pyruvate dehydrogenase (PDH) gene.
7. The recombinant yeast microorganism of claim 1 , wherein said recombinant yeast microorganism has an increased capacity to produce acetolactate as compared to the corresponding yeast microorganism that has not been engineered to have reduced endogenous PDC activity and reduced endogenous GPD activity.
8. The recombinant yeast microorganism of claim 1 , wherein said recombinant yeast microorganism is a yeast of a genus selected from the group consisting of Saccharomyces, Kluyveromyces, Candida, Pichia, Issatchenkia, Debaryomyces, Hansenula, Yarrowia , and Schizosaccharomyces.
9. A method of producing isobutanol, comprising:
(a) providing a recombinant yeast microorganism according to claim 1 ;
(b) cultivating the microorganism in a culture medium containing a feedstock providing the carbon source, until the isobutanol is produced; and
(c) recovering the isobutanol.