Methods for the improvement of product yield and production in a microorganism through glycerol recycling
View Patent ↗The present invention provides for novel metabolic pathways to reduce or modulate glycerol production and increase product formation. More specifically, the invention provides for a recombinant microorganism comprising one or more native and/or heterologous proteins that function to import glycerol and one or more native and/or heterologous enzymes that function in one or more engineered metabolic pathways to convert a carbohydrate source, such as lignocellulose, to a product, such as ethanol, wherein the one or more native and/or heterologous proteins or enzymes is activated, upregulated, or downregulated. The invention also provides for a recombinant microorganism comprising one or more native or heterologous proteins that function to regulate glycerol synthesis and one or more native and/or heterologous enzymes that function in one or more engineered metabolic pathways to convert a carbohydrate source to ethanol, wherein said one or more native and/or heterologous proteins or enzymes is activated, upregulated or downregulated. Also provided are methods for increasing cellular glycerol uptake and increasing recombinant production of fuels and other chemicals using the recombinant microorganisms of the invention.
1. A recombinant yeast comprising:
(a) a heterologous Sugar Transporter-Like protein (STL1); and
(b) a heterologous enzyme comprising an acetaldehyde dehydrogenase and/or a bifunctional acetaldehyde/alcohol dehydrogenase; and
wherein the recombinant yeast produces increased ethanol relative to a control recombinant yeast without said heterologous STL1 protein.
2. The recombinant yeast of claim 1 , wherein the recombinant yeast further comprises one or more native and/or heterologous proteins that function to export glycerol from the yeast, wherein said one or more native and/or heterologous enzymes that function to export glycerol is activated, upregulated, or downregulated.
3. The recombinant yeast of claim 1 , wherein the recombinant yeast further comprises a deletion or downregulation of one or more native enzymes that function to produce glycerol and/or regulate glycerol synthesis.
4. The recombinant yeast of claim 1 , wherein said one or more engineered metabolic pathways comprises conversion of pyruvate to acetyl-CoA and formate.
5. The recombinant yeast of claim 1 , wherein said one or more engineered metabolic pathways is the pentose phosphate pathway (PPP).
6. The recombinant yeast of claim 1 , wherein said one or more engineered metabolic pathways comprises the conversion of acetate to acetyl-CoA.
7. The recombinant yeast of claim 1 , wherein said one or more engineered metabolic pathways comprises one or more native and/or heterologous enzymes that encodes a saccharolytic enzyme.
8. The recombinant yeast of claim 1 , wherein said yeast further comprises one or more native and/or heterologous enzymes that function in one or more engineered metabolic pathways to convert xylose to xylulose-5-phosphate and/or arabinose to xylulose-5-phosphate, wherein said one or more native and/or heterologous enzymes is activated, upregulated or downregulated.
9. The recombinant yeast of claim 1 , wherein said one or more engineered metabolic pathways comprises the conversion of trehalose to acetyl-CoA.
10. The recombinant yeast of claim 9 , wherein said one or more native and/or heterologous enzymes functions to convert trehalose to glucose.
11. A method for decreasing cellular-produced glycerol comprising contacting biomass with a recombinant yeast according to claim 1 .
12. A process for converting biomass to ethanol comprising contacting biomass with a recombinant yeast according to claim 1 .
13. A process for converting biomass to isopropanol comprising contacting biomass with a recombinant yeast according to claim 1 .
14. The recombinant yeast of claim 1 , wherein said yeast comprises intracellular glycerol.
15. The recombinant yeast of claim 1 , further comprising a functional GPD1 gene and/or a functional GPD2 gene.
16. The recombinant yeast of claim 1 , wherein said heterologous STL1 comprises an STL1 protein from a yeast selected from the group consisting of: S. cerevisiae, P. sorbitophila , and Saccharomyces paradoxus.
17. The recombinant yeast of claim 1 , wherein said heterologous STL1 protein comprises an amino acid sequence selected from the group consisting of: SEQ ID NO: 140, SEQ ID NO: 142, SEQ ID NO: 10, and SEQ ID NO: 225.
18. The recombinant yeast of claim 1 , said yeast being S. cerevisiae.
19. The recombinant yeast of claim 1 , wherein said yeast is able to grow anaerobically independent of the presence of externally supplied glycerol.
20. The recombinant yeast of claim 1 , wherein said yeast produces less glycerol than said recombinant yeast without said heterologous STL1.
21. The recombinant yeast of claim 1 , said yeast being from the genera Saccharomyces.
22. The recombinant yeast of claim 14 , wherein the STL1 increases intracellular glycerol concentration by about 0.05 fold to about 5 fold more intracellular glycerol than is present in a recombinant yeast without the heterologous STL1.
23. The recombinant yeast of claim 14 , wherein the STL reduces glycerol formation by 12% to 23% of the glycerol produced by a recombinant yeast without the heterologous STL1.
24. The recombinant yeast of claim 14 , wherein the STL1 increases intracellular glycerol concentration by at least 0.05-fold more intracellular glycerol than is present in a recombinant yeast without the heterologous STL1.
25. The recombinant yeast of claim 14 , wherein the STL1 reduces glycerol formation by more than 5% of the glycerol produced by a recombinant yeast without the heterologous STL1.