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大肠杆菌中secA基因的核苷酸序列及阻止蛋白质输出的secA(Ts)突变

Nucleotide sequence of the secA gene and secA(Ts) mutations preventing protein export in Escherichia coli.

作者信息

Schmidt M G, Rollo E E, Grodberg J, Oliver D B

机构信息

Department of Microbiology, State University of New York, Stony Brook 11794-8621.

出版信息

J Bacteriol. 1988 Aug;170(8):3404-14. doi: 10.1128/jb.170.8.3404-3414.1988.

Abstract

The DNA sequence of the secA gene, essential for protein export in Escherichia coli, was determined and found to encode a hydrophilic protein of 901 amino acid residues with a predicted molecular weight of 101,902, consistent with its previously determined size and subcellular location. Sequence analysis of 9 secA(Ts) mutations conferring general protein export and secA regulatory defects revealed that these mutations were clustered in three specific regions within the first 170 amino acid residues of the SecA protein and were the result of single amino acid changes predicted to be severely disruptive of protein structure and function. The DNA sequence immediately upstream of secA was shown to encode a previously inferred gene, gene X. Sequence analysis of a conditionally lethal amber mutation, am109, previously inferred to be located proximally in the secA gene, revealed that it was located distally in gene X and was conditionally lethal due to its polar effect on secA expression. This and additional evidence are presented indicating that gene X and secA are cotranscribed.

摘要

确定了大肠杆菌中蛋白质输出所必需的secA基因的DNA序列,发现它编码一种由901个氨基酸残基组成的亲水性蛋白质,预测分子量为101,902,与其先前确定的大小和亚细胞定位一致。对9个导致一般蛋白质输出和secA调节缺陷的secA(Ts)突变进行序列分析,发现这些突变聚集在SecA蛋白前170个氨基酸残基内的三个特定区域,是单个氨基酸变化的结果,预计会严重破坏蛋白质的结构和功能。secA上游紧邻的DNA序列显示编码一个先前推断的基因,即基因X。对先前推断位于secA基因近端的条件致死性琥珀突变am109进行序列分析,发现它位于基因X的远端,由于其对secA表达的极性效应而具有条件致死性。本文提供了这一证据及其他证据,表明基因X和secA是共转录的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d86d/211308/5e730b45d13d/jbacter00186-0101-a.jpg

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