Ethanol production in non-recombinant hosts
Non-recombinant bacteria that produce ethanol as the primary fermentation product, associated nucleic acids and polypeptides, methods for producing ethanol using the bacteria, and kits are disclosed.
1. A method for producing ethanol from an oligosaccharide source comprising contacting the oligosaccharide with an isolated non-recombinant bacterium comprising an lpd gene having a mutation, wherein the mutation is one that corresponds to the substitution of the His residue at amino acid position 322 relative to an E. coli LPD sequence and the mutation renders the non-recombinant bacterium capable of producing ethanol as the primary fermentation product under anaerobic conditions, thereby producing ethanol from an oligosaccharide source.
2. The method of claim 1 , wherein the ethanol produced comprises greater than 50% of total non-gaseous fermentation products under anaerobic conditions.
3. The method of claim 1 , wherein the bacterium, in the absence of the mutation, is non-ethanologenic.
4. The method of claim 3 , wherein ethanol is the minor fermentation product and comprises less than 40% of total non gaseous fermentation products.
5. The method of claim 1 , wherein the mutation provides a homoethanol fermentation pathway.
6. The method of claim 1 , wherein one or more alternative pathways for fermentation in the bacterium are inactivated.
7. The method of claim 6 , wherein the alternative pathways for fermentation include lactate production by lactate dehydrogenase (ldhA), acetate, ethanol, formate, H 2 and CO 2 starting with pyruvate formate-lyase (pfl) and succinate.
8. The method of claim 7 , wherein the alternative pathways for fermentation are inactivated by mutation.
9. The method of claim 8 , wherein the mutation is in the ldhA gene.
10. The method of claim 8 , wherein the mutation is in the pfl gene.
11. The method of claim 9 , wherein the mutation is in the ldhA or pflB genes.
12. The method of claim 10 , wherein the mutation is in the ldhA or pflB genes.
13. The method of claim 1 , wherein the oligosaccharide is selected from the group consisting of lignocellulose, hemicellulose, cellulose, pectin and any combination thereof.
14. The method of claim 1 , wherein mutation in the lpd gene causes NADH insensitivity.
15. A method for producing ethanol from an oligosaccharide source comprising contacting the oligosaccharide with an isolated non-recombinant bacterium comprising an E. coli lpd gene having a mutation selected from the group consisting of H322Y and E354K, wherein the mutation renders the non-recombinant bacterium capable of producing ethanol as the primary fermentation product under anaerobic conditions, thereby producing ethanol from an oligosaccharide source.
16. The method of claim 15 , wherein the ethanol produced comprises greater than 50% of total non-gaseous fermentation products under anaerobic conditions.
17. The method of claim 15 , wherein the bacterium, in the absence of the mutation, is non-ethanologenic.
18. The method of claim 17 , wherein ethanol is the minor fermentation product and comprises less than 40% of total non gaseous fermentation products.
19. The method of claim 15 , wherein the mutation provides a homoethanol fermentation pathway.
20. The method of claim 15 , wherein one or more alternative pathways for fermentation in the bacterium are inactivated.
21. The method of claim 20 , wherein the alternative pathways for fermentation include lactate production by lactate dehydrogenase (ldhA), acetate, ethanol, formate, H 2 and CO 2 starting with pyruvate formate-lyase (pfl) and succinate.
22. The method of claim 21 , wherein the alternative pathways for fermentation are inactivated by mutation.
23. The method of claim 22 , wherein the mutation is in the ldhA gene.
24. The method of claim 22 , wherein the mutation is in the pfl gene.
25. The method of claim 23 , wherein the mutation is in the ldhA or pflB genes.
26. The method of claim 24 , wherein the mutation is in the ldhA or pflB genes.
27. The method of claim 15 , wherein the oligosaccharide is selected from the group consisting of lignocellulose, hemicellulose, cellulose, pectin and any combination thereof.
28. The method of claim 15 , wherein mutation in the lpd gene causes NADH insensitivity.