An Jieun, Kwon Hyeji, Kim Eunjung, Lee Young Mi, Ko Hyeok Jin, Park Hongjae, Choi In-Geol, Kim Sooah, Kim Kyoung Heon, Kim Wankee, Choi Wonja
Division of Life and Pharmaceutical Sciences, Ewha Womans University, Seoul, 120-750, Korea.
Environ Microbiol. 2015 Mar;17(3):656-69. doi: 10.1111/1462-2920.12489. Epub 2014 May 20.
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.
对TATA结合基因SPT15的过表达突变等位基因文库进行筛选,得到了两株对乙酸耐受性增强的酿酒酵母菌株(MRRC 3252和3253)。它们对丙酸和过氧化氢也具有耐受性。转录组谱分析确定了MRRC 3252中58个上调基因和106个下调基因。与应激和蛋白质合成相关的转录因子分别主要富集在上调基因和下调基因中。一些高度下调基因的八个缺失突变体对乙酸具有耐受性。在暴露于乙酸时,MRRC 3252和3253中的细胞内活性氧水平显著降低。代谢组谱分析显示,MRRC 3252中细胞内5种和102种代谢物的浓度分别增加和降低,其特征是尿素大幅增加而氨基酸显著减少。缺失尿素降解基因DUR1/2的dur1/2Δ突变体对乙酸的耐受性增强。在含有低浓度氨基酸的培养基上也观察到对乙酸的耐受性增强。综上所述,本研究确定了两个SPT15等位基因、九个基因缺失以及培养基中低浓度氨基酸可赋予对乙酸的耐受性增强。