Regulation of the RAS/cAMP/PKA signaling pathway in yeasts for obtaining a fermentation product during fermentation
The present disclosure relates to the modulation in the RAS/cAMP/PKA signaling pathway for maintaining the propagation efficiency and increasing fermentation efficiency of yeast cells. The present disclosure provides yeast cells having or engineered to exhibit a modulation in signaling in a RAS/cAMP/PKA pathway, depending on conditions. For example the yeast cells can be selected or genetically modified to express a mutated Ras1 protein, a mutated Ras2 protein, a mutated Ira1 protein and/or a mutated Ira2 protein, optionally in combination with specific promoters. Also provided herewith are methods for propagating the yeast cells as well as using the yeast cells to generate a fermented product (such as ethanol).
1. A method of fermenting a fermentation medium to obtain ethanol, said method comprising:
contacting a recombinant yeast host cell with the fermentation medium under conditions to allow generation of ethanol; and
obtaining ethanol from the fermentation medium;
wherein:
the recombinant yeast host cell expresses a first heterologous nucleic acid molecule comprising a promoter operatively linked to a second nucleic acid molecule coding for a mutated Ras2 protein (a) having increased activity when compared to the wild-type Ras2 protein and (b) comprising an amino acid sequence having at least 90% identity to SEQ ID NO: 1, wherein the amino acid residue at position 66 is substituted with a histidine, an isoleucine, an arginine, a leucine, an asparagine, a lysine, an aspartic acid, a methionine, a cysteine, a phenylalanine, a glutamic acid, a threonine, a glutamine, a tryptophan, a glycine, a valine, a proline, a serine, or a tyrosine residue;
the promoter is capable of increasing expression of the second nucleic acid molecule during fermentation when compared to the expression of the second nucleic acid molecule during propagation;
the fermentation medium comprises xylose and/or arabinose; and
the recombinant yeast host cell is capable of utilizing (i) xylose by expressing a third heterologous nucleic acid molecule coding for (a) a xylose reductase and a xylitol dehydrogenase or (b) a xylose isomerase, and/or (ii) arabinose by expressing a fourth heterologous nucleic acid molecule coding for an arabinose isomerase, a ribulokinase and a ribulose 5-phosphate epimerase.
2. The method of claim 1 , wherein the mutated Ras2 protein has the amino acid sequence of SEQ ID NO: 2 or the second nucleic acid molecule comprises the sequence of SEQ ID NO: 3.
3. The method of claim 1 , wherein the promoter:
(i) is capable of increasing the expression of the second nucleic acid molecule when the recombinant yeast host cell is in at least partial anaerobic conditions when compared to a level of the expression of the second nucleic acid molecule that is obtained when the recombinant yeast host cell is placed in aerobic conditions, or
(ii) is a glucose-repressible promoter.
4. The method of claim 1 , wherein the recombinant yeast host cell comprises at least one copy of a RAS2 gene coding for a wild-type Ras2 protein.
5. The method of claim 1 , wherein the recombinant yeast host cell is a Saccharomyces cerevisiae cell.
6. The method of claim 1 , wherein the recombinant yeast host cell comprises the third heterologous nucleic acid molecule encoding the heterologous xylose isomerase.
7. The method of claim 1 , wherein the third heterologous nucleic acid molecule further encodes a xylulokinase, a xylose reductase, a xylose dehydrogenase, a xylonate dehydratase, a xylose transketolase and/or a xylose transaldolase.
8. The method of claim 1 , wherein the fourth heterologous nucleic acid molecule further encodes an arabinose transporter.
9. The method of claim 1 , wherein the xylose isomerase is from Catonella morbi.
10. The method of claim 1 , wherein the arabinose isomerase ribulokinase is from Bacteroides thetaiotaomicron.
11. The method of claim 1 , wherein the ribulokinase is from Bacteroides thetaiotaomicron.
12. The method of claim 1 , wherein the ribulose 5 -phosphate epimerase is from Bacteroides thetaiotaomicron.
13. The method of claim 1 , wherein the second nucleic acid molecule is a heterologous nucleic acid molecule.
14. The method of claim 1 , wherein the promoter is not a RAS2 promoter from a RAS2 gene.
15. The method of claim 1 , wherein the wild-type Ras2 protein has the amino acid sequence of SEQ ID NO: 1.
16. The method of claim 1 , wherein the amino acid residue at position 66 of the mutated Ras2 protein is substituted with a threonine residue.