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质粒pBR322上tetA(C)基因的遗传分析。

Genetic analysis of the tetA(C) gene on plasmid pBR322.

作者信息

McNicholas P, Chopra I, Rothstein D M

机构信息

Department of Microbial Genetics, Lederle Laboratories, Pearl River, New York 10965.

出版信息

J Bacteriol. 1992 Dec;174(24):7926-33. doi: 10.1128/jb.174.24.7926-7933.1992.

Abstract

The TetA(C) protein, encoded by the tetA(C) gene of plasmid pBR322, is a member of a family of membrane-bound proteins that mediate energy-dependent efflux of tetracycline from the bacterial cell. The tetA(C) gene was mutagenized with hydroxylamine, and missense mutations causing the loss of tetracycline resistance were identified at 30 distinct codons. Mutations that encoded substitutions within putative membrane-spanning alpha-helical regions were scattered throughout the gene. In contrast, mutations outside the alpha-helical regions were clustered in two cytoplasmic loops, between helices 2 and 3 and helices 10 and 11, suggesting that these regions play a critical role in the recognition of tetracycline and/or energy transduction. All of the missense mutations encoded a protein that retained the ability to rescue an Escherichia coli strain defective in potassium uptake, suggesting that the loss of tetracycline resistance was not due to an unstable TetA(C) protein or to the failure of the protein to be inserted in the membrane. We postulate that the mutations encode residues that are critical for the active efflux of tetracycline, except for mutations that result in the introduction of charged residues within hydrophobic regions of the TetA(C) protein.

摘要

由质粒pBR322的tetA(C)基因编码的TetA(C)蛋白,是一类膜结合蛋白家族的成员,该家族介导四环素从细菌细胞中进行能量依赖性外排。用羟胺对tetA(C)基因进行诱变,并在30个不同密码子处鉴定出导致四环素抗性丧失的错义突变。编码假定跨膜α螺旋区域内替换的突变分散在整个基因中。相比之下,α螺旋区域外的突变聚集在两个胞质环中,分别在螺旋2和3之间以及螺旋10和11之间,这表明这些区域在四环素识别和/或能量转导中起关键作用。所有错义突变编码的蛋白都保留了拯救钾摄取缺陷型大肠杆菌菌株的能力,这表明四环素抗性的丧失不是由于TetA(C)蛋白不稳定或该蛋白未能插入膜中。我们推测,除了导致在TetA(C)蛋白疏水区域内引入带电荷残基的突变外,这些突变编码的残基对于四环素的主动外排至关重要。

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Genetic analysis of the tetA(C) gene on plasmid pBR322.质粒pBR322上tetA(C)基因的遗传分析。
J Bacteriol. 1992 Dec;174(24):7926-33. doi: 10.1128/jb.174.24.7926-7933.1992.

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