Yeast organism producing isobutanol at a high yield
View Patent ↗There is disclosed a method of producing isobutanol. In an embodiment, the method includes providing a microorganism transformed with an isobutanol producing pathway containing at least one exogenous gene. The microorganism is selected to produce isobutanol from a carbon source at a yield of at least 10 percent theoretical. The method includes cultivating the microorganism in a culture medium containing a feedstock providing the carbon source, until isobutanol is produced. The method includes recovering the isobutanol. In one embodiment, the microorganism is a yeast with a Crabtree-negative phenotype. In another embodiment, the microorganism is a yeast microorganism with a Crabtree-positive phenotype. There is disclosed a microorganism for producing isobutanol. In an embodiment, the microorganism includes an isobutanol producing pathway containing at least one exogenous gene, and is selected to produce a recoverable quantity of isobutanol from a carbon source at a yield of at least 10 percent theoretical.
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 said 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 dihydroxy acid dehydratase to catalyze the conversion of 2,3-dihydroxyisovalerate to α-ketoisovalerate;
(d) an α-ketoisovalerate decarboxylase from Lactococcus 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 disrupt, mutate, or delete one or more endogenous pyruvate decarboxylase (PDC) genes, wherein said recombinant yeast microorganism has reduced endogenous PDC activity as compared to the corresponding yeast microorganism that has not been engineered to have reduce endogenous PDC activity, and wherein said recombinant yeast microorganism produces:
(A) isobutanol at a yield which is at least 10% of the theoretical yield of isobutanol from glucose; and/or
(B) ethanol at a yield which is 1.8% or less of the theoretical yield of ethanol from glucose.
2. The recombinant yeast microorganism of claim 1 , wherein the recombinant yeast microorganism is further engineered or selected to grow on glucose independently of C2-compounds at a growth rate substantially equivalent to the growth rate of the corresponding yeast microorganism that has not been engineered to have reduced endogenous PDC activity.
3. The recombinant yeast microorganism of claim 1 , wherein the recombinant yeast microorganism is a yeast of the Saccharomyces clade.
4. The recombinant yeast microorganism of claim 1 , wherein the recombinant yeast microorganism is a non-fermenting yeast microorganism.
5. The recombinant yeast microorganism of claim 1 , wherein said one or more endogenous PDC genes is selected from the group consisting of PDC1, PDC2, PDC5, and PDC6.
6. The recombinant yeast microorganism of claim 1 , wherein said α-ketoisovalerate decarboxylase is encoded by a gene that has been codon optimized for expression in yeast.
7. A method of producing isobutanol, comprising:
(a) providing the recombinant yeast microorganism according to claim 1 ;
(b) cultivating the recombinant yeast microorganism in a culture medium containing a feedstock providing the carbon source, until the isobutanol is produced; and
(c) recovering the isobutanol.