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首页> 外文期刊>The Biochemical Journal >Weak acid and alkali stress regulate phosphatidylinositol bisphosphate synthesis in Saccharomyces cerevisiae
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Weak acid and alkali stress regulate phosphatidylinositol bisphosphate synthesis in Saccharomyces cerevisiae

机译:弱酸和碱胁迫调节酿酒酵母中磷脂酰肌醇二磷酸酯的合成

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Weak organic acids are used as food preservatives to inhibit the growth of spoilage yeasts, including Saccharomyces cerevisiae. Long-term adaptation to weak acids requires the increased expression of the ATP-binding cassette transporter Pdr12p, which catalyses the active efflux of the weak acids from the cytosol; however, very little is known about the signalling events immediately following application of weak acid stress. We have investigated the effects of weak acids on two stress-responsive signalling molecules, PtdIns(3,5)P-2 and PtdIns(4,5)P-2, which in S. cercvisiae are synthesized by Fab1p and Mss4p respectively. At low extracellular pH, benzoic acid, sorbic acid and acetic acid all cause a transient reduction in PtdIns(3,5)P-2 accumulation and a more persistent rise in PtdIns(4,5)P-2 levels. The increase in PtdIns(4,5)P-2 levels is accompanied by a reorganization of the actin cytoskeleton. However, changes in PtdInSP(2) levels are independent of weak acid-induced Pdr12p expression. In contrast, changing the extracellular medium to alkaline pH provokes a prolonged and substantial rise in PtdIns(3,5)P-2 levels. As PtdIns(3,5)P-2 synthesis is required for correct vacuole acidification, it is possible that levels of this molecule are modulated to maintain intracellular pH homoeostasis in response to weak acid and alkali stresses. In conclusion, we have expanded the repertoire of stress responses that affect PtdInsP(2) levels to include weak acid and alkali stresses.
机译:弱有机酸被用作食品防腐剂,以抑制腐败酵母(包括酿酒酵母)的生长。长期适应弱酸需要增加ATP结合盒转运蛋白Pdr12p的表达,这会催化弱酸从细胞质中主动流出。然而,对施加弱酸胁迫后的信号传递事件知之甚少。我们已经研究了弱酸对两个应激反应信号分子PtdIns(3,5)P-2和PtdIns(4,5)P-2的影响,这两个基因分别在酿酒酵母中由Fab1p和Mss4p合成。在低的细胞外pH值下,苯甲酸,山梨酸和乙酸都会引起PtdIns(3,5)P-2积累的瞬时减少,并导致PtdIns(4,5)P-2的水平持续升高。 PtdIns(4,5)P-2水平的增加伴随着肌动蛋白细胞骨架的重组。但是,PtdInSP(2)水平的变化与弱酸诱导的Pdr12p表达无关。相比之下,将细胞外培养基更改为碱性pH会引起PtdIns(3,5)P-2水平的长期显着上升。由于正确的液泡酸化需要PtdIns(3,5)P-2合成,因此该分子的水平可能会受到调节,以响应弱酸和碱胁迫维持细胞内pH的同质性。总之,我们扩大了影响PtdInsP(2)水平的应激反应的范围,使其包括弱酸和弱碱应激。

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