METABOLICALLY ENGINEERED YEASTS FOR THE PRODUCTION OF ETHANOL AND OTHER PRODUCTS FROM XYLOSE AND CELLOBIOSE
The present invention provides yeast cells that produce high concentrations of ethanol, culture media and bioreactors comprising the yeast cells, and methods for making and using the yeast cells in efficiently producing ethanol.
1 . An isolated Pichia stipitis cell, recombinantly expressing:
a. a xylose transporter;
b. one or more of a xylose reductase, a xylitol dehydrogenase, and/or a xylulokinase.
2 . The P. stipitis cell of claim 1 , further recombinantly expressing a transketolase and/or a transaldolase.
3 . The P. stipitis cell of claim 1 or 2 , wherein the cell further recombinantly expresses a cellobiose transporter.
4 . The P. stipitis cell of claim 3 , wherein the cell further recombinantly expresses a betaglucosidase and/or an endo-1,4-beta-glucanase.
5 . The P. stipitis cell of claim 1 or 2 , wherein the cell further recombinantly expresses an alcohol dehydrogenase.
6 . The P. stipitis cell of claim 1 , wherein the xylose transporter is selected from the group consisting of Sut1, Sut2, Sut3, Sut4, Xut1 and Xut3.
7 . The P. stipitis cell of claim 1 , wherein the transporter is substantially identical to any one of SEQ ID NOs: 46-51.
8 . The P. stipitis cell of claim 1 , wherein the yeast recombinantly expresses a xylose reductase, a xylitol dehydrogenase, and a xylulokinase.
9 . The P. stipitis cell of claim 1 , wherein the xylose reductase is substantially identical to SEQ ID NO:52; the xylitol dehydrogenase is substantially identical to SEQ ID NO:53; and the xylulokinase is substantially identical to SEQ ID NO:54.
10 . The P. stipitis cell of claim 2 , wherein the transketolase is substantially identical to GenBank EAZ62979 (Tkl2; DHAS; SEQ ID NO: 92) or GenBank ABN64656 (Tkt1; SEQ ID NO: 93).
11 . The P. stipitis cell of claim 2 , wherein the transaldolase is substantially identical to GenBank ABN68690 (PsTal1p; SEQ ID NO: 94).
12 . An isolated yeast cell comprising a first and second expression cassette, wherein the first and second expression cassette each encodes the same xylose transporter, wherein
the first expression cassette comprises a promoter operably linked to a polynucleotide encoding the xylose transporter; and
the second expression cassette comprises a promoter operably linked to a polynucleotide encoding the xylose transporter.
13 . The isolated yeast cell of claim 12 , wherein the xylose transporter is SUT4.
14 . A method of converting xylose to ethanol, the method comprising, contacting a mixture comprising xylose with the yeast of claim 1 under conditions in which the yeast converts the xylose to ethanol.
15 . The method of claim 14 , wherein the mixture further comprises a C6 sugar and the yeast converts the C6 sugar to ethanol.
16 . The method of claim 14 , wherein the mixture comprises at least 0.115% acetic acid.
17 . An isolated yeast cell, recombinantly expressing:
a. a cellobiose transporter; and
b. a betaglucosidase.
18 . The isolated yeast of claim 17 , wherein the cellobiose transporter is substantially identical to any of SEQ ID NOs: 38, 39, 40, 41, 42, 43, or 44.
19 . The isolated yeast of claim 17 , wherein the betaglucosidase is substantially identical to any of SEQ ID NOs: 26, 27, 28, 29, 30, 31, or 32.
20 . The isolated yeast of claim 17 , further recombinantly expressing:
c. an endo-1,4-beta-glucanase.
21 . The isolated yeast of claim 20 , wherein the endo-1,4-beta-glucanase is substantially identical to any of SEQ ID NOs: 33, 34, or 35.
22 . A method of converting cellobiose to ethanol, the method comprising, contacting a mixture comprising cellobiose with the yeast of claim 17 under conditions in which the yeast converts the cellobiose to ethanol.