Identification of Genes Associated with Stress Tolerance of High Ethanol–Producing Saccharomyces cerevisiae Strain, NCIM3186, by Differential Gene Expression Analysis
Lignocellulosic bioethanol production by Saccharomyces cerevisiae is constrained by different stresses. The main aim of this work was to study the complexities and identify the genes associated with the yeast stress response by using NGS-based high throughput RNA-seq analysis. In this study, a bioet...
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Published in | Bioenergy research Vol. 15; no. 3; pp. 1459 - 1471 |
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Main Authors | , , |
Format | Journal Article |
Language | English |
Published |
New York
Springer US
01.09.2022
Springer Springer Nature B.V |
Subjects | |
Online Access | Get full text |
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Summary: | Lignocellulosic bioethanol production by
Saccharomyces cerevisiae
is constrained by different stresses. The main aim of this work was to study the complexities and identify the genes associated with the yeast stress response by using NGS-based high throughput RNA-seq analysis. In this study, a bioethanol-producing
S. cerevisiae
strain, NCIM3186, treated with 4% glucose for 4 h, 8% (v/v) ethanol for 2 h, and 1 g L
−1
furfural for 4 h was employed for Illumina-based RNA-seq analysis. Comparative RNA-seq analysis and differential gene expression profiling using de novo assembled transcripts have unveiled 573 differentially expressed genes (DEGs), wherein thiamine metabolism genes,
SOD2
,
GRE2
,
GLR1
,
HSP12
, and
GLC7
under furfural stress;
TDH1
,
HSP26
, glucose-sensing
SNF1
,
SSA3
,
HXK1
,
SNF1
,
STR3
,
ATG1
, and
HXT7
under ethanol stress; and
MSN2
,
TPS2
,
SNF2
,
MEP3
,
PHO4
, and
STE20
under glucose stress treatments were highly up-regulated (> twofold). Moreover, seven (
TPS1
,
TPS2
,
SIN3
,
PTK2
,
SSQ1
,
ZAP1
,
DOA4
) out of nine stuck fermentome genes which are essential for the timely completion of fermentation process have shown significant expression under stress. The expression of highly up-regulated genes,
TDH1
,
HXT6
,
THI13
, and
HSP12
, and two other unknown genes (UK-1, UK-2) were experimentally validated using qRT-PCR analysis. The expression pattern of DEGs in NCIM3186 signified the key role of oxidative stress response, trehalose accumulation, heat shock proteins, and thiamine metabolism under stress. This study serves as a significant value addition to RNA-seq-based research for the identification of stress associated genes in host yeast strains to be used in bioethanol production. |
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ISSN: | 1939-1234 1939-1242 |
DOI: | 10.1007/s12155-021-10389-8 |