Disruption of PHO13 improves ethanol production via the xylose isomerase pathway
Xylose is the second most abundant sugar in lignocellulosic materials and can be converted to ethanol by recombinant Saccharomyces cerevisiae yeast strains expressing heterologous genes involved in xylose assimilation pathways. Recent research demonstrated that disruption of the alkaline phosphatase...
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Published in | AMB Express Vol. 6; no. 1; pp. 4 - 10 |
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Main Authors | , , |
Format | Journal Article |
Language | English |
Published |
Berlin/Heidelberg
Springer Science and Business Media LLC
14.01.2016
Springer Berlin Heidelberg Springer Nature B.V |
Subjects | |
Online Access | Get full text |
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Summary: | Xylose is the second most abundant sugar in lignocellulosic materials and can be converted to ethanol by recombinant
Saccharomyces cerevisiae
yeast strains expressing heterologous genes involved in xylose assimilation pathways. Recent research demonstrated that disruption of the alkaline phosphatase gene,
PHO13
, enhances ethanol production from xylose by a strain expressing the xylose reductase (XR) and xylitol dehydrogenase (XDH) genes; however, the yield of ethanol is poor. In this study,
PHO13
was disrupted in a recombinant strain harboring multiple copies of the xylose isomerase (XI) gene derived from
Orpinomyces
sp., coupled with overexpression of the endogenous xylulokinase (XK) gene and disruption of
GRE3
, which encodes aldose reductase. The resulting YΔGP/XK/XI strain consumed 2.08 g/L/h of xylose and produced 0.88 g/L/h of volumetric ethanol, for an 86.8 % theoretical ethanol yield, and only YΔGP/XK/XI demonstrated increase in cell concentration. Transcriptome analysis indicated that expression of genes involved in the pentose phosphate pathway (
GND1
,
SOL3
,
TAL1
,
RKI1
, and
TKL1
) and TCA cycle and respiratory chain (
NDE1
,
ACO1
,
ACO2
,
SDH2
,
IDH1
,
IDH2
,
ATP7
,
ATP19
,
SDH4
,
SDH3
,
CMC2
, and
ATP15
) was upregulated in the YΔGP/XK/XI strain. And the expression levels of 125 cell cycle genes were changed by deletion of
PHO13
. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 content type line 23 |
ISSN: | 2191-0855 2191-0855 |
DOI: | 10.1186/s13568-015-0175-7 |