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首页> 外文期刊>Applied Microbiology >Coordination of the Cell Wall Integrity and High-Osmolarity Glycerol Pathways in Response to Ethanol Stress in Saccharomyces cerevisiae
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Coordination of the Cell Wall Integrity and High-Osmolarity Glycerol Pathways in Response to Ethanol Stress in Saccharomyces cerevisiae

机译:酿酒酵母中细胞壁完整性和高渗甘油途径对乙醇胁迫的响应

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摘要

During fermentation, a high ethanol concentration is a major stress that influences the vitality and viability of yeast cells, which in turn leads to a termination of the fermentation process. In this study, we show that the BCK1 and SLT2 genes encoding mitogen-activated protein kinase kinase kinase (MAPKKK) and mitogen-activated protein kinase (MAPK) of the cell wall integrity (CWI) pathway, respectively, are essential for ethanol tolerance, suggesting that the CWI pathway is involved in the response to ethanol-induced cell wall stress. Upon ethanol exposure, the CWI pathway induces the expression of specific cell wall-remodeling genes, including FKS2, CRH1, and PIR3 (encoding β-1,3-glucan synthase, chitin transglycosylase, and O-glycosylated cell wall protein, respectively), which eventually leads to the remodeling of the cell wall structure. Our results revealed that in response to ethanol stress, the high-osmolarity glycerol (HOG) pathway plays a collaborative role with the CWI pathway in inducing cell wall remodeling via the upregulation of specific cell wall biosynthesis genes such as the CRH1 gene. Furthermore, the substantial expression of CWI-responsive genes is also triggered by external hyperosmolarity, suggesting that the adaptive changes in the cell wall are crucial for protecting yeast cells against not only cell wall stress but also osmotic stress. On the other hand, the cell wall stress-inducing agent calcofluor white has no effect on promoting the expression of GPD1, a major target gene of the HOG pathway. Collectively, these findings suggest that during ethanol stress, the CWI and HOG pathways collaboratively regulate the transcription of specific cell wall biosynthesis genes, thereby leading to adaptive changes in the cell wall.IMPORTANCE The budding yeast Saccharomyces cerevisiae has been widely used in industrial fermentations, including the production of alcoholic beverages and bioethanol. During fermentation, an increased ethanol concentration is the main stress that affects yeast metabolism and inhibits ethanol production. This work presents evidence that in response to ethanol stress, both CWI and HOG pathways cooperate to control the expression of cell wall-remodeling genes in order to build the adaptive strength of the cell wall. These findings will contribute to a better understanding of the molecular mechanisms underlying adaptive responses and tolerance of yeast to ethanol stress, which is essential for successful engineering of yeast strains for improved ethanol tolerance.
机译:在发酵过程中,高乙醇浓度是影响酵母细胞活力和生存力的主要压力,继而导致发酵过程终止。在这项研究中,我们发现BCK1和SLT2基因分别编码细胞壁完整性(CWI)途径的促分裂原激活蛋白激酶激酶(MAPKKK)和促分裂原激活蛋白激酶(MAPK),对于乙醇耐受性至关重要,提示CWI通路参与了乙醇诱导的细胞壁应激反应。暴露于乙醇后,CWI途径诱导特定细胞壁重塑基因的表达,包括FKS2,CRH1和PIR3(分别编码β-1,3-葡聚糖合酶,几丁质转糖基酶和O-糖基化细胞壁蛋白),最终导致细胞壁结构的重塑。我们的研究结果表明,响应于乙醇胁迫,高渗透压甘油(HOG)途径与CWI途径在通过上调特定细胞壁生物合成基因(例如CRH1基因)来诱导细胞壁重塑中起着协同作用。此外,外部高渗也触发了CWI反应基因的大量表达,这表明细胞壁的适应性变化对于保护酵母细胞不仅抗细胞壁压力而且抗渗透压力至关重要。另一方面,细胞壁应激诱导剂钙荧光白对促进HOG途径的主要靶基因GPD1的表达没有影响。总的来说,这些发现表明,在乙醇胁迫期间,CWI和HOG途径协同调节特定细胞壁生物合成基因的转录,从而导致细胞壁的适应性变化。重要的是,出芽的酿酒酵母已广泛用于工业发酵,包括酒精饮料和生物乙醇的生产。在发酵过程中,乙醇浓度升高是影响酵母代谢并抑制乙醇产生的主要压力。这项工作提供了证据,表明响应乙醇压力,CWI和HOG途径都可以共同控制细胞壁重塑基因的表达,从而增强细胞壁的适应性强度。这些发现将有助于更好地理解酵母对乙醇胁迫的适应性反应和耐受性的分子机制,这对于成功改造酵母菌株以改善乙醇耐受性至关重要。

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