具有突变H3残基的酿酒酵母乙酸胁迫反应的研究。

IF 4.1 3区 生物学 Q2 CELL BIOLOGY
Microbial Cell Pub Date : 2023-08-18 eCollection Date: 2023-10-02 DOI:10.15698/mic2023.10.806
Nitu Saha, Swati Swagatika, Raghuvir Singh Tomar
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引用次数: 1

摘要

乙酸水平的提高降低了用于基于工业发酵的应用的酵母菌株的活性。因此,揭示酵母对乙酸耐受性和敏感性调节的遗传因素对于优化各种工业工艺至关重要。在这篇通讯中,我们试图破译先前报道的乙酸敏感组蛋白突变体的乙酸应激反应。使用现场测试分析和生长曲线的再验证显示,这些突变体中的五个,即H3K18Q、H3S28A、H3K42Q、H3Q68A和H3F104A,对测试的乙酸浓度最敏感。这些突变体表现出增强的乙酸应激反应,如AIF1的表达水平增加、活性氧(ROS)的产生、染色质断裂和聚集的肌动蛋白细胞骨架所证明的。此外,突变体在乙酸处理后表现出活性细胞壁损伤反应,如Slt2磷酸化和细胞壁完整性基因表达增加所示。有趣的是,突变体对细胞壁应激因子的敏感性增加。最后,组蛋白H3 N-末端尾部截短突变体的筛选表明,尾部截短对乙酸胁迫表现出普遍的敏感性。这些N-末端尾部截短突变体中的一些,即H3[del1-24]、H3[del1-2-8]、H3[del 9-24]和H3[del 25-36]也对细胞壁应激因子如刚果红和咖啡因敏感,这表明它们增强的乙酸敏感性可能是由于乙酸诱导的细胞壁应激。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Investigation of the acetic acid stress response in <i>Saccharomyces cerevisiae</i> with mutated H3 residues.

Investigation of the acetic acid stress response in <i>Saccharomyces cerevisiae</i> with mutated H3 residues.

Investigation of the acetic acid stress response in <i>Saccharomyces cerevisiae</i> with mutated H3 residues.

Investigation of the acetic acid stress response in Saccharomyces cerevisiae with mutated H3 residues.

Enhanced levels of acetic acid reduce the activity of yeast strains employed for industrial fermentation-based applications. Therefore, unraveling the genetic factors underlying the regulation of the tolerance and sensitivity of yeast towards acetic acid is imperative for optimising various industrial processes. In this communication, we have attempted to decipher the acetic acid stress response of the previously reported acetic acid-sensitive histone mutants. Revalidation using spot-test assays and growth curves revealed that five of these mutants, viz., H3K18Q, H3S28A, H3K42Q, H3Q68A, and H3F104A, are most sensitive towards the tested acetic acid concentrations. These mutants demonstrated enhanced acetic acid stress response as evidenced by the increased expression levels of AIF1, reactive oxygen species (ROS) generation, chromatin fragmentation, and aggregated actin cytoskeleton. Additionally, the mutants exhibited active cell wall damage response upon acetic acid treatment, as demonstrated by increased Slt2-phosphorylation and expression of cell wall integrity genes. Interestingly, the mutants demonstrated increased sensitivity to cell wall stress-causing agents. Finally, screening of histone H3 N-terminal tail truncation mutants revealed that the tail truncations exhibit general sensitivity to acetic acid stress. Some of these N-terminal tail truncation mutants viz., H3 [del 1-24], H3 [del 1-28], H3 [del 9-24], and H3 [del 25-36] are also sensitive to cell wall stress agents such as Congo red and caffeine suggesting that their enhanced acetic acid sensitivity may be due to cell wall stress induced by acetic acid.

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来源期刊
Microbial Cell
Microbial Cell Multiple-
CiteScore
6.40
自引率
0.00%
发文量
32
审稿时长
12 weeks
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