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Transcriptional Response of Saccharomyces cerevisiae to Different Nitrogen Concentrations during Alcoholic Fermentation

机译:酒精发酵过程中酿酒酵母对不同氮浓度的转录响应

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Gene expression profiles of a wine strain of Saccharomyces cerevisiae PYCC4072 were monitored during alcoholic fermentations with three different nitrogen supplies: (i) control fermentation (with enough nitrogen to complete sugar fermentation), (ii) nitrogen-limiting fermentation, and (iii) the addition of nitrogen to the nitrogen-limiting fermentation (refed fermentation). Approximately 70% of the yeast transcriptome was altered in at least one of the fermentation stages studied, revealing the continuous adjustment of yeast cells to stressful conditions. Nitrogen concentration had a decisive effect on gene expression during fermentation. The largest changes in transcription profiles were observed when the early time points of the N-limiting and control fermentations were compared. Despite the high levels of glucose present in the media, the early responses of yeast cells to low nitrogen were characterized by the induction of genes involved in oxidative glucose metabolism, including a significant number of mitochondrial associated genes resembling the yeast cell response to glucose starvation. As the N-limiting fermentation progressed, a general downregulation of genes associated with catabolism was observed. Surprisingly, genes encoding ribosomal proteins and involved in ribosome biogenesis showed a slight increase during N starvation; besides, genes that comprise the RiBi regulon behaved distinctively under the different experimental conditions. Here, for the first time, the global response of nitrogen-depleted cells to nitrogen addition under enological conditions is described. An important gene expression reprogramming occurred after nitrogen addition; this reprogramming affected genes involved in glycolysis, thiamine metabolism, and energy pathways, which enabled the yeast strain to overcome the previous nitrogen starvation stress and restart alcoholic fermentation.
机译:在酒精发酵过程中使用三种不同的氮源监测酿酒酵母PYCC4072的葡萄酒菌株的基因表达谱:(i)对照发酵(有足够的氮来完成糖发酵),(ii)限氮发酵和(iii)将氮添加到限氮发酵中(参考发酵)。在所研究的至少一个发酵阶段中,约有70%的酵母转录组发生了变化,表明酵母细胞不断适应压力条件。发酵过程中氮浓度对基因表达具有决定性影响。当比较N-限制发酵和对照发酵的早期时间点时,观察到转录概况的最大变化。尽管培养基中存在高水平的葡萄糖,但是酵母细胞对低氮的早期反应的特征是诱导涉及氧化葡萄糖代谢的基因,包括与酵母细胞对葡萄糖饥饿的反应相似的大量线粒体相关基因。随着N限制发酵的进行,人们观察到与分解代谢相关的基因普遍下调。出乎意料的是,编码核糖体蛋白并参与核糖体生物发生的基因在N饥饿期间显示略有增加。此外,组成RiBi调控区的基因在不同的实验条件下表现出明显的不同。在此,首次描述了在生态条件下,贫氮细胞对氮添加的总体响应。添加氮后发生了重要的基因表达重编程;这种重编程影响了参与糖酵解,硫胺素代谢和能量途径的基因,使酵母菌株能够克服先前的氮饥饿压力并重新开始酒精发酵。

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