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在酿酒酵母KNU5377发酵过程中诱导产生的CPR1基因敲除菌株对各种类型的胁迫敏感。

A knockout strain of CPR1 induced during fermentation of Saccharomyces cerevisiae KNU5377 is susceptible to various types of stress.

作者信息

Kim Il-Sup, Yun Hae-Sun, Park In-Su, Sohn Ho-Yong, Iwahashi Hitoshi, Jin Ing-Nyol

机构信息

Department of Microbiology, School of Life Sciences and Biotechnology, Kyungpook National University, Daegu 702-701, Korea.

出版信息

J Biosci Bioeng. 2006 Oct;102(4):288-96. doi: 10.1263/jbb.102.288.

Abstract

To investigate the tolerance factor of Saccharomyces cerevisiae KNU5377 against various types of environmental stress during fermentation, we identified the protein that is upregulated at high temperatures. The highly upregulated protein was high-score-matched as a cytoplasmic peptidyl-prolyl cis-trans isomerase, cyclophilin (Cpr1p), by matrix-assisted laser desorption ionization time-of-flight mass spectrometry (MALDI-TOF). We constructed a CPR1-deleted KNU5377 strain (KNU5377Y cpr1Delta) to determine the roles of the protein under fermentative or stress condition. The growth of the S. cerevisiae KNU5377Y cpr1Delta strain was completely inhibited under the following conditions: heat (40 degrees C), hydrogen peroxide (20-30 mM), menadione (0.3 mM), ethanol (16%), sulfuric acid (5 mm), and lactic acid (0.4-0.8%). However, the wild-type and cpr1Delta mutant of S. cerevisiae BY4741 as a positive control did not show differences in sensitivity to stress. It is interesting to note that the wild-type KNU5377Y and KNU5377Y cpr1Delta mutant showed high sensitivity against various stresses, particularly, acid stress such as in the presence of sulfuric and lactic acid. Although the alcohol fermentation rate of the KNU5377Y cpr1Delta mutant markedly decreased with an increase in temperature up to 40 degrees C, we observed no decrease in that of the wild-type strain under the same conditions. These results suggest that CPR1 contributes to the stress tolerance of KNU5377 against various types of environmental stress caused during fermentation, thus leading to the physiological role of maintaining an alcohol fermentation yield, even at high temperatures such as 40 degrees C.

摘要

为了研究酿酒酵母KNU5377在发酵过程中对各种环境胁迫的耐受因子,我们鉴定了在高温下上调的蛋白质。通过基质辅助激光解吸电离飞行时间质谱(MALDI-TOF),高度上调的蛋白质与细胞质肽基脯氨酰顺反异构酶亲环蛋白(Cpr1p)进行了高分匹配。我们构建了一个缺失CPR1的KNU5377菌株(KNU5377Y cpr1Δ),以确定该蛋白质在发酵或胁迫条件下的作用。酿酒酵母KNU5377Y cpr1Δ菌株在以下条件下生长完全受到抑制:高温(40℃)、过氧化氢(20-30 mM))、甲萘醌(0.3 mM)、乙醇(16%)、硫酸(5 mM)和乳酸(0.4-0.8%)。然而,作为阳性对照的酿酒酵母BY4741的野生型和cpr1Δ突变体对胁迫的敏感性没有差异。有趣的是,野生型KNU5377Y和KNU5377Y cpr1Δ突变体对各种胁迫表现出高敏感性,特别是在硫酸和乳酸存在下的酸胁迫。尽管KNU5377Y cpr1Δ突变体的酒精发酵速率随着温度升高至40℃而显著降低,但在相同条件下我们未观察到野生型菌株的发酵速率下降。这些结果表明,CPR1有助于KNU5377对发酵过程中引起的各种环境胁迫的耐受性,从而在维持酒精发酵产量方面发挥生理作用,即使在40℃等高温下也是如此。

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