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Acetic Acid Causes Endoplasmic Reticulum Stress and Induces the Unfolded Protein Response in Saccharomyces cerevisiae

机译:乙酸引起内质网应激并诱导酿酒酵母中未折叠的蛋白质反应

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摘要

Since acetic acid inhibits the growth and fermentation ability of Saccharomyces cerevisiae, it is one of the practical hindrances to the efficient production of bioethanol from a lignocellulosic biomass. Although extensive information is available on yeast response to acetic acid stress, the involvement of endoplasmic reticulum (ER) and unfolded protein response (UPR) has not been addressed. We herein demonstrated that acetic acid causes ER stress and induces the UPR. The accumulation of misfolded proteins in the ER and activation of Ire1p and Hac1p, an ER-stress sensor and ER stress-responsive transcription factor, respectively, were induced by a treatment with acetic acid stress (>0.2% v/v). Other monocarboxylic acids such as propionic acid and sorbic acid, but not lactic acid, also induced the UPR. Additionally, ire1Δ and hac1Δ cells were more sensitive to acetic acid than wild-type cells, indicating that activation of the Ire1p-Hac1p pathway is required for maximum tolerance to acetic acid. Furthermore, the combination of mild acetic acid stress (0.1% acetic acid) and mild ethanol stress (5% ethanol) induced the UPR, whereas neither mild ethanol stress nor mild acetic acid stress individually activated Ire1p, suggesting that ER stress is easily induced in yeast cells during the fermentation process of lignocellulosic hydrolysates. It was possible to avoid the induction of ER stress caused by acetic acid and the combined stress by adjusting extracellular pH.
机译:由于乙酸抑制了酿酒酵母的生长和发酵能力,因此这是从木质纤维素生物质有效生产生物乙醇的实际障碍之一。尽管可以获得大量有关酵母对乙酸应激反应的信息,但是内质网(ER)和未折叠蛋白反应(UPR)的参与尚未得到解决。我们在本文中证明了乙酸引起ER应力并诱导UPR。乙酸应激(> 0.2%v / v)处理分别诱导了ER中错误折叠的蛋白的积累以及ER应激传感器Ire1p和Hac1p的激活以及ER应激响应转录因子的激活。其他一元羧酸(如丙酸和山梨酸,但不包括乳酸)也可引起UPR。另外,ire1Δ和hac1Δ细胞比野生型细胞对乙酸更敏感,这表明激活Ire1p-Hac1p途径对于乙酸具有最大的耐受性。此外,轻度乙酸胁迫(0.1%乙酸)和轻度乙醇胁迫(5%乙醇)的组合诱导了UPR,而轻度乙醇胁迫和轻度乙酸胁迫均未单独激活Ire1p,表明ER应激很容易诱导木质纤维素水解产物发酵过程中的酵母细胞。通过调节细胞外pH可以避免由乙酸引起的内质网应激的诱导和综合应激。

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