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Transcriptional changes associated with ethanol tolerance in saccharomyces cerevisiae
journal contribution
posted on 2017-12-06, 00:00 authored by P Chambers, Grant StanleyGrant Stanley, A Borneman, S Fraser, Dragana StanleyDragana StanleySaccharomyces spp. are widely used for ethanol production; however, fermentation productivity is negatively affected by the impact of ethanol accumulation on yeast metabolic rate and viability. This study used microarray and statistical two-way ANOVA analysis to compare and evaluate gene expression profiles of two previously generated ethanol-tolerant mutants, CM1 and SM1, with their parent, Saccharomyces cerevisiae W303-1A, in the presence and absence of ethanol stress. Although sharing the same parentage, the mutants were created differently: SM1 by adaptive evolution involving long-term exposure to ethanol stress and CM1 using chemical mutagenesis followed by adaptive evolution-based screening. Compared to the parent, differences in the expression levels of genes associated with a number of gene ontology categories in the mutants suggest that their improved ethanol stress response isa consequence of increased mitochondrial and NADH oxidation activities, stimulating glycolysis and other energy yielding pathways. This leads to increased activity of energy demanding processes associated with the production of proteins and plasma membrane components, which are necessary for acclimation to ethanol stress. It is suggested that a key function of the ethanol stress response is restoration of the NAD+/NADH redox balance, which increasingly ceraldehyde-3-phosphate dehydrogenase activity, and higher glycolytic flux in the ethanol-stressed cell. Both mutants achieved this by a constitutive increase in carbon flux in the glycerol pathway as a means of increasing NADH oxidation.
Funding
Category 1 - Australian Competitive Grants (this includes ARC, NHMRC)
History
Volume
88Start Page
231End Page
239Number of Pages
9eISSN
1432-0614ISSN
0175-7598Location
Berlin, GermanyPublisher
Springer VerlagPublisher DOI
Full Text URL
Language
en-ausPeer Reviewed
- Yes
Open Access
- No
Era Eligible
- Yes