Higgins Vincent J, Beckhouse Anthony G, Oliver Anthony D, Rogers Peter J, Dawes Ian W
Clive and Vera Ramaciotti Centre for Gene Function Analysis. School of Biotechnology and Biomolecular Sciences, University of New South Wales, Sydney, New South Wales 2052, Australia.
Appl Environ Microbiol. 2003 Aug;69(8):4777-87. doi: 10.1128/AEM.69.8.4777-4787.2003.
Genome-wide expression analysis of an industrial strain of Saccharomyces cerevisiae during the initial stages of an industrial lager fermentation identified a strong response from genes involved in the biosynthesis of ergosterol and oxidative stress protection. The induction of the ERG genes was confirmed by Northern analysis and was found to be complemented by a rapid accumulation of ergosterol over the initial 6-h fermentation period. From a test of the metabolic activity of deletion mutants in the ergosterol biosynthesis pathway, it was found that ergosterol is an important factor in restoring the fermentative capacity of the cell after storage. Additionally, similar ERG10 and TRR1 gene expression patterns over the initial 24-h fermentation period highlighted a possible interaction between ergosterol biosynthesis and the oxidative stress response. Further analysis showed that erg mutants producing altered sterols were highly sensitive to oxidative stress-generating compounds. Here we show that genome-wide expression analysis can be used in the commercial environment and was successful in identifying environmental conditions that are important in industrial yeast fermentation.
对工业拉格啤酒发酵初期的酿酒酵母工业菌株进行全基因组表达分析,结果表明,参与麦角固醇生物合成和氧化应激保护的基因有强烈反应。通过Northern分析证实了ERG基因的诱导,并发现麦角固醇在发酵初期的6小时内迅速积累,起到了补充作用。通过对麦角固醇生物合成途径中缺失突变体的代谢活性测试发现,麦角固醇是恢复细胞储存后发酵能力的重要因素。此外,在发酵初期的24小时内,ERG10和TRR1基因呈现出相似的表达模式,这突出了麦角固醇生物合成与氧化应激反应之间可能存在的相互作用。进一步分析表明,产生改变的固醇的erg突变体对产生氧化应激的化合物高度敏感。我们在此表明,全基因组表达分析可用于商业环境,并成功识别出在工业酵母发酵中重要的环境条件。