Production of 2-butanol and 2-butanone employing aminobutanol phosphate phospholyase
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.
1. A recombinant microbial host cell comprising at least one heterologous DNA molecule encoding a polypeptide that catalyzes a substrate to product conversion of 3-amino-2-butanol phosphate to 2-butanone and at least one heteroloqous DNA molecule encoding a polypeptide that catalyzes a substrate to product conversion of 3-amino-2-butanol to 3-amino-2-butanol phosphate;
wherein said microbial host cell produces 2-butanol by the conversion of 3-amino-2butanol phosphate to 2-butanone; and
wherein the polypeptide that catalyzes a substrate to product conversion of 3-amino-2-butanol phosphate to 2-butanone is aminobutanol phosphate phospho-lyase having the amino acid sequence that has at least 95% identity to the amino acid sequence of SEQ ID NO:126 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.
2. A recombinant microbial host cell comprising at least one heteroloqous DNA molecule encoding a polypeptide that catalyzes a substrate to product conversion of 3-amino-2-butanol phosphate to 2-butanone and at least one heterologous DNA molecule encoding a polypeptide that catalyzes a substrate to product conversion of 3-amino-2-butanol to 3-amino-2-butanol phosphate;
wherein said microbial host cell produces 2-butanone by the conversion of 3-amino-2-butanol phosphate to 2-butanone; and
wherein the polypeptide that catalyzes a substrate to product conversion of 3-amino-2-butanol phosphate to 2-butanone is aminobutanol phosphate phospho-lyase having the amino acid sequence that has at least 95% identity to the amino acid sequence of SEQ ID NO:126 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.
3. A host cell according to claim 1 or 2 wherein the cell is a member of a genus selected from the group consisting of Clostridium, Zymomonas, Escherichia, Salmonella, Rhodococcus, Pseudomonas, Bacillus, Lactobacillus, Enterococcus, Pediococcus, Alcaligenes, Klebsiella, Paenibacillus, Arthrobacter, Corynebacterium, Brevibacterium, Pichia, Candida, Hansenula and Saccharomyces.
4. The recombinant host cell of claim 1 wherein the at least one heterologous DNA molecule encoding a polypeptide that catalyzes a substrate to product conversion of 3-amino-2-butanol to 3-amino-2-butanol phosphate has at least 80% identity to SEQ ID NO: 124 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. The recombinant host cell of claim 2 wherein the at least one heterologous DNA molecule encoding a polypeptide that catalyzes a substrate to product conversion of 3-amino-2-butanol to 3-amino-2-butanol phosphate has at least 80% identity to SEQ ID NO: 124 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.
6. The recombinant host cell of claim 1 further comprising heterologous DNA molecules encoding polypeptides that catalyze the following substrate to product conversions:
(a) pyruvate to alpha-acetolactate;
(b) alpha-acetolactate to acetoin; and
(c) acetoin to 3-amino-2-butanol.
7. The recombinant host cell of claim 2 further comprising heterologous DNA molecules encoding polypeptides that catalyze the following substrate to product conversions:
(a) pyruvate to alpha-acetolactate;
(b) alpha-acetolactate to acetoin; and
(c) acetoin to 3-amino-2-butanol.
8. The recombinant host cell of claim 1 , further comprising at least one heterologous DNA molecule encoding a polypeptide that catalyzes a substrate to product conversion selected from the group consisting of:
(a) pyruvate to alpha-acetolactate;
(b) alpha-acetolactate to acetoin;
(c) acetoin to 3-amino-2-butanol; and
(d) 2-butanone to 2-butanol.
9. The recombinant host cell of claim 2 , further comprising at least one heterologous DNA molecule encoding a polypeptide that catalyzes a substrate to product conversion selected from the group consisting of:
(a) pyruvate to alpha-acetolactate;
(b) alpha-acetolactate to acetoin; and
(c) acetoin to 3-amino-2-butanol.
10. The recombinant host cell of claim 1 wherein the polypeptide that catalyzes a substrate to product conversion of 3-amino-2-butanol phosphate to 2-butanone is aminobutanol phosphate phospho-lyase having the amino acid sequence of SEQ ID NO:126.
11. The recombinant host cell of claim 1 , wherein the at least one heterologous DNA molecule encoding a polypeptide that catalyzes a substrate to product conversion of 3-amino-2-butanol to 3-amino-2-butanol phosphate has at least 95% identity to SEQ ID NO: 124 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.
12. The recombinant host cell of claim 2 wherein the polypeptide that catalyzes a substrate to product conversion of 3-amino-2-butanol phosphate to 2-butanone is aminobutanol phosphate phospho-lyase having the amino acid sequence of SEQ ID NO:126.
13. The recombinant host cell of claim 2 , wherein the at least one heterologous DNA molecule encoding a polypeptide that catalyzes a substrate to product conversion of 3-amino-2-butanol to 3-amino-2-butanol phosphate has at least 95% identity to SEQ ID NO: 124 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.