Tolerance to acetic acid is improved by mutations of the TATA-binding protein gene
Summary Screening a library of overexpressing mutant alleles of the TATA‐binding gene SPT15 yielded two Saccharomyces cerevisiae strains (MRRC 3252 and 3253) with enhanced tolerance to acetic acid. They were also tolerant to propionic acid and hydrogen peroxide. Transcriptome profile analysis identi...
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Published in | Environmental microbiology Vol. 17; no. 3; pp. 656 - 669 |
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Main Authors | , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
England
Blackwell Publishing Ltd
01.03.2015
Wiley Subscription Services, Inc |
Subjects | |
Online Access | Get full text |
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Summary: | Summary
Screening a library of overexpressing mutant alleles of the TATA‐binding gene SPT15 yielded two Saccharomyces cerevisiae strains (MRRC 3252 and 3253) with enhanced tolerance to acetic acid. They were also tolerant to propionic acid and hydrogen peroxide. Transcriptome profile analysis identified 58 upregulated genes and 106 downregulated genes in MRRC 3252. Stress‐ and protein synthesis‐related transcription factors were predominantly enriched in the upregulated and downregulated genes respectively. Eight deletion mutants for some of the highly downregulated genes were acetic acid‐tolerant. The level of intracellular reactive oxygen species was considerably lessened in MRRC 3252 and 3253 upon exposure to acetic acid. Metabolome profile analysis revealed that intracellular concentrations of 5 and 102 metabolites were increased and decreased, respectively, in MRRC 3252, featuring a large increase of urea and a significant decrease of amino acids. The dur1/2Δmutant, in which the urea degradation gene DUR1/2 is deleted, displayed enhanced tolerance to acetic acid. Enhanced tolerance to acetic acid was also observed on the medium containing a low concentration of amino acids. Taken together, this study identified two SPT15 alleles, nine gene deletions and low concentration of amino acids in the medium that confer enhanced tolerance to acetic acid. |
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Bibliography: | Ministry of Science, ICT and Technology - No. NRF-2008-2000110 Fig. S1. Effect of mutated SPT15on the regulation of FPS1 and HAA1. Northern analysis was performed with total RNAs prepared from cells treated with none or 0.9% acetic acid for 0 or 10 h. Probes were prepared as in Fig. 4B.Table S1. Oligonucleotides used for PCR.Table S2. Genes regulated by SPT15-AA311.Table S3. TF clustering.Table S4. Metabolites changed in MRRC 3252. ark:/67375/WNG-T35H3BG3-F ArticleID:EMI12489 istex:2A57426639F3800F33890A39FF92B8FF8FD2AD23 ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 1462-2912 1462-2920 |
DOI: | 10.1111/1462-2920.12489 |