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Possible roles of vacuolar H+-ATPase and mitochondria! function in tolerance to air-drying stress revealed by genome-wide screening of sacchoromyces cerevisiae deletion strains.

机译:液泡H + -ATP酶和线粒体的可能作用!全基因组酿酒酵母缺失菌株的筛选揭示了对风干胁迫的耐受性。

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摘要

Yeasts used in bread making are exposed to air-drying stress during dried yeast production processes. To clarify the genes required for air-drying tolerance, we performed genome-wide screening using the complete deletion strain collection of diploid Saccharomyces cerevisiae. The screening identified 278 gene deletions responsible for air-drying sensitivity. These genes were classified based on their cellular function and on the localization of their gene products. The results showed that the genes required for air-drying tolerance were frequently involved in mitochondrial functions and in connection with vacuolar H+-ATPase, which plays a role in vacuolar acidification. To determine the role of vacuolar acidification in air-drying stress tolerance, we monitored intracellular pH. The results showed that intracellular acidification was induced during air-drying and that this acidification was amplified in a deletion mutant of the VMA2 gene encoding a component of vacuolar H+-ATPase, suggesting that vacuolar H+-ATPase helps maintain intracellular pH homeostasis, which is affected by air-drying stress. To determine the effects of air-drying stress on mitochondria, we analysed the mitochondrial membrane potential under air-drying stress conditions using MitoTracker. The results showed that mitochondria were extremely sensitive to air-drying stress, suggesting that a mitochondrial function is required for tolerance to air-drying stress. We also analysed the correlation between oxidative-stress sensitivity and air-drying-stress sensitivity. The results suggested that oxidative stress is a critical determinant of sensitivity to air-drying stress, although ROS-scavenging systems are not necessary for air-drying stress tolerance.
机译:面包制作中使用的酵母在干酵母生产过程中会承受空气干燥的压力。为了阐明风干耐受性所需的基因,我们使用二倍体酿酒酵母的完整缺失菌株收集进行了全基因组筛选。筛选确定了278个基因缺失,这些基因缺失导致了风干敏感性。这些基因根据其细胞功能和基因产物的定位进行分类。结果表明,风干耐受性所需的基因经常参与线粒体功能,并与液泡中的H + -ATPase有关,后者在液泡酸化中起作用。为了确定液泡酸化在风干胁迫耐受性中的作用,我们监测了细胞内pH。结果表明,在风干过程中诱导了细胞内酸化,并且该酸化在编码液泡H + -ATPase成分的VMA2基因的缺失突变体中得到了放大,表明液泡H + -ATPase有助于维持细胞内的pH稳态,这受到影响。通过风干应力。为了确定风干应力对线粒体的影响,我们使用MitoTracker分析了风干应力条件下的线粒体膜电位。结果表明,线粒体对风干应力极为敏感,这表明线粒体功能是耐风干应力所必需的。我们还分析了氧化应激敏感性和风干应激敏感性之间的相关性。结果表明,氧化应激是对风干应力敏感性的关键决定因素,尽管对于风干应力耐受性而言,ROS清除系统并不是必需的。

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