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酿酒酵母soo1-1突变导致细胞壁结合烯醇化酶向培养基中的分泌增强。

Enhanced secretion of cell wall bound enolase into culture medium by the soo1-1 mutation of Saccharomyces cerevisiae.

作者信息

Kim Ki-Hyun, Park Hee-Moon

机构信息

Department of Microbiology, School of Biosciences and Biotechnology, Chungnam National University, Daejeon 305-764, Korea.

出版信息

J Microbiol. 2004 Sep;42(3):248-52.

Abstract

In order to identify the protein(s) secreted into culture medium by the soo1-1/ret1-1 mutation of Saccharomyces cerevisiae, proteins from the culture medium of cells grown at permissive (28 degrees C) and non-permissive temperatures (37 degrees C), were analyzed. Comparison of protein bands separated by SDS-PAGE identified a prominent band of 47-kDa band from a mutant grown at 37 degrees C. N-terminal amino acid sequencing of this 47-kDa protein showed high identity with enolases 1 and 2. Western blot analysis revealed that most of the cell wall-bound enolase was released into the culture medium of the mutant grown at 37 degrees C, some of which were separated as those with lower molecular weights. Our results, presented here, indicate the impairment of cell wall enolase biogenesis and assembly by the soo1-1/ret1-1 mutation of S. cerevisiae.

摘要

为了鉴定酿酒酵母soo1-1/ret1-1突变体分泌到培养基中的蛋白质,对在允许温度(28℃)和非允许温度(37℃)下生长的细胞的培养基中的蛋白质进行了分析。通过SDS-PAGE分离的蛋白条带比较,鉴定出在37℃下生长的突变体中有一条突出的47-kDa条带。对该47-kDa蛋白的N端氨基酸测序显示与烯醇化酶1和2具有高度同源性。蛋白质印迹分析表明,大多数细胞壁结合的烯醇化酶被释放到在37℃下生长的突变体的培养基中,其中一些以较低分子量的形式分离出来。我们在此展示的结果表明,酿酒酵母的soo1-1/ret1-1突变会损害细胞壁烯醇化酶的生物合成和组装。

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