Response of Saccharomyces cerevisiae to Ethanol Stress Involves Actions of Protein Asr1p

被引:10
|
作者
Ding Junmei
Huang, Xiaowei
Zhao, Na
Gao, Feng
Lu, Qian
Zhang, Ke-Qin [1 ]
机构
[1] Yunnan Univ, Minist Educ, Lab Conservat & Utilizat Bioresources, Kunming 650091, Yunnan, Peoples R China
关键词
Saccharomyces cerevisiae; ethanol tolerance; gene knockout and tagging; translocation; HETEROLOGOUS MODULES; NUCLEAR-LOCALIZATION; TRANSCRIPTION FACTOR; GENE-EXPRESSION; FINGER PROTEIN; ELEMENT STRE; YEAST; PCR; MSN2P; QUANTIFICATION;
D O I
10.4014/jmb.1007.07021
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
During the fermentation process of Saccharomyces cerevisiae, yeast cells must rapidly respond to a wide variety of external stresses in order to survive the constantly changing environment, including ethanol stress. The accumulation of ethanol can severely inhibit cell growth activity and productivity. Thus, the response to changing ethanol concentrations is one of the most important stress reactions in S. cerevisiae and worthy of thorough investigation. Therefore, this study examined the relationship between ethanol tolerance in S. cerevisiae and a unique protein called alcohol sensitive RING/PHD finger 1 protein (Asr1p). A real-time PCR showed that upon exposure to 8% ethanol, the expression of Asr1 was continuously enhanced, reaching a peak 2 h after stimulation. This result was confirmed by monitoring the fluorescence levels using a strain with a green fluorescent protein tagged to the C-terminal of Asr1p. The fluorescent microscopy also revealed a change in the subcellular localization before and after stimulation. Furthermore, the disruption of the Asr1 gene resulted in hypersensitivity on the medium containing ethanol, when compared with the wild-type strain. Thus, when taken together, the present results suggest that Asr1 is involved in the response to ethanol stress in the yeast S. cerevisiae.
引用
收藏
页码:1630 / 1636
页数:7
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