Fermentive production of four carbon alcohols
View Patent ↗Methods for the fermentive production of four carbon alcohols are provided. Specifically, butanol, preferably 2-butanol is produced by the fermentive growth of a recombinant bacteria expressing a 2-butanol biosynthetic pathway. The recombinant microorganisms and methods of the invention can also be adapted to produce 2-butanone, an intermediate in the 2-butanol biosynthetic pathways disclosed herein. Specifically disclosed herein are the use of coenzyme B 12 -independent butanediol dehydratases that catalyzes the substrate to product conversion of 2,3-butanediol to 2-butanone in the process of producing 2-butanol and 2-butanone.
1. A recombinant microbial host cell comprising at least one heterologous DNA molecule encoding a polypeptide that catalyzes the substrate to product conversions:
i) pyruvate to alpha-acetolactate;
ii) alpha-acetolactate to acetoin;
iii) acetoin to 2,3-butanediol; and
iv) 2,3-butanediol to 2-butanone;
wherein the at least one DNA molecule that catalyzes the substrate to product conversion of 2,3-butanediol to 2-butanone encodes a coenzyme B12-independent butanediol dehydratase, and further wherein the B12-independent butanediol dehydratase has an amino acid sequence having at least 75% identity to the amino acid sequence of SEQ ID NO:276 based on the Clustal W method of alignment using the default parameters of GAP PENALTY=10, GAP LENGTH PENALTY=0.1, and Gonnet 250 series of protein weight matrix;
and wherein the microbial host cell produces 2 butanol.
2. The recombinant microbial host cell according to claim 1 wherein the B12-independent butanediol dehydratase has the amino acid sequence of SEQ ID NO:276.
3. A recombinant microbial host cell according to claim 1 further comprising a DNA molecule encoding a B12-independent butanediol dehydratase reactivase.
4. A recombinant microbial host cell according to claim 3 wherein the reactivase has an amino acid sequence having at least 75% identity to the amino acid sequence of SEQ ID NO:278 based on the Clustal W method of alignment using the default parameters of GAP PENALTY=10, GAP LENGTH PENALTY=0.1, and Gonnet 250 series of protein weight matrix.
5. A recombinant microbial host cell according to claim 4 wherein the reactivase has the amino acid sequence of SEQ ID NO:278.
6. A method for the production of 2-butanone comprising:
a) providing the recombinant microbial host cell of claim 1 and a source of 2,3-butanediol; and
b) growing the microbial host cell of (a) under conditions whereby the 2,3-butanediol is converted to 2-butanone; and
c) optionally recovering the 2-butanone.
7. A method for the production of 2-butanol comprising:
a) providing the recombinant microbial host cell of claim 1 and a source of 2,3-butanediol; wherein the at least one DNA molecule is heterologous to said microbial host cell; and
b) growing the microbial host cell of (a) under conditions whereby the isolated nucleic acid molecule is expressed and the 2,3-butanediol is converted to 2-butanone, and the 2-butanone is converted to 2-butanol; and
c) optionally recovering the 2-butanol.
8. A recombinant microbial host cell according to claim 3 wherein the reactivase has an amino acid sequence having at least 75% identity to the amino acid sequence of SEQ ID NO:282 based on the Clustal W method of alignment using the default parameters of GAP PENALTY=10, GAP LENGTH PENALTY=0.1, and Gonnet 250 series of protein weight matrix.
9. A recombinant microbial host cell according to claim 8 wherein the reactivase has the amino acid sequence of SEQ ID NO:282.
10. The recombinant microbial host cell of claim 1 further comprising at least one heterologous DNA molecule encoding a polypeptide that catalyzes the substrate to product conversion of 2-butanone to 2-butanol is heterologous to the microbial host cell.