US2006270008A1PendingUtilityA1
Modified yeast consuming L-arabinose
Est. expiryMay 8, 2022(expired)· nominal 20-yr term from priority
C12N 15/52C12P 7/06Y02E50/10
54
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Claims
Abstract
The present invention relates to a method for producing a L-arabinose utilizing yeast strain for the production of ethanol, whereby a yeast strain is modified by introducing and expressing araA gene (L-arabinose isomerase), araB gene (L-ribulokinase D 121 -N) and araD gene (L-ribulose-5-P 4-epimerase) and carrying additional mutations in its genome or overexpressing a TALl (transaldolase) gene, enabling it to consume L-arabinose, to use it as the only carbon source, and to produce ethanol, as well as a method for producing ethanol using such a modified strain.
Claims
exact text as granted — not AI-modified1 . A method for producing an L-arabinose utilizing Saccharomyces cerevisiae yeast strain for the production of ethanol, wherein a yeast strain is modified by introducing and expressing an araA gene (L-arabinose isomerase), an araB gene (L-ribulokinase) and an araD gene (L-ribulose-5-P 4-epimerase), and carrying additional mutations in its genome or overexpressing a TALl (transaldolase) gene, enabling it to consume L-arabinose, and to produce ethanol thereby from a medium comprising L-arabinose, whereby the yeast strain is further modified by expressing a mutant form of the E. coli L-ribulokinase enzyme with reduced activity.
2 . The method according to claim 1 , wherein the araA gene is a B. subtilis araA gene.
3 . The method according to claim 1 , wherein the araA gene is a M. smegmatis araA gene.
4 . The method according to claim 1 , wherein the araB gene is a E. coli araB gene.
5 . The method according to claim 1 , wherein the araD gene is an E. coli araD gene.
6 . The method according to claim 1 , wherein the TALl gene is an S. cerevisiae TALl gene.
7 . (canceled)
8 . The method according to claim 1 , wherein the Saccharomyces cerevisiae strain is a CEN.PK strain, preferably a CEN.PK2-1C.
9 . The method according to claim 1 , wherein the Saccharomyces cerevisiae strain is a Saccharomyces cerevisiae W303-strain.
10 . (canceled)
11 . The method according to claim 1 , wherein the yeast strain is further modified by overexpressing the yeast GAL2 gene.
12 . The method according to claim 1 , wherein the araB gene is placed behind a weak promoter.
13 . The method according to claim 1 , wherein the modifications are made behind the strong HXT7 promoter fragment on multicopy vectors in S. cerevisiae CEN.PK-strains.
14 . The method according to claim 1 , wherein the modifications are made behind the strong HXT7 promoter fragment on multicopy vectors in Saccharomyces cerevisiae W303-strains.
15 . The method according to claim 1 , wherein the amount of L-arabinose of the growth medium is 2 to 200 g/L.
16 . The method according to claim 1 , wherein the strain is Saccharomyces cerevisiae strain JBY25-4M with DSM accession number 15560.
17 . The method according to claim 1 , wherein the strain is Saccharomyces cerevisiae strain JBY24-3T with a DSM accession number 15559.
18 . A method for producing ethanol by fermenting yeast, wherein a modified yeast according to claim 1 ferments a growth medium containing L-arabinose.
19 . The method according to claim 18 , wherein the amount of L-arabinose of the growth medium is 2 to 200 g/L.Cited by (0)
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