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肺炎克雷伯菌tonB基因的克隆与测序以及大肠杆菌-肺炎克雷伯菌TonB杂合蛋白的特性分析。

Cloning and sequencing of the Klebsiella pneumoniae tonB gene and characterization of Escherichia coli-K. pneumoniae TonB hybrid proteins.

作者信息

Bruske A K, Anton M, Heller K J

机构信息

Fakultät für Biologie, Universität Konstanz, Germany.

出版信息

Gene. 1993 Sep 6;131(1):9-16. doi: 10.1016/0378-1119(93)90663-n.

Abstract

The tonB gene of Klebsiella pneumoniae was cloned on a 1.4-kb EcoRV fragment and expressed in Escherichia coli. Determination of the nucleotide (nt) sequence of the cloned fragment identified tonB as an open reading frame (ORF) of 729 nt. The TonB protein consists of 243 amino acids (aa) and is highly homologous to Enterobacter aerogenes TonB. The genetic context of K. pneumoniae and En. aerogenes tonB is the same, but is different from that of E. coli, Salmonella typhimurium and Serratia marcescens. K. pneumoniae tonB complemented an E. coli tonB mutant as efficiently as E. coli tonB when cloned on the same type of plasmid. Replacement of the highly hydrophobic C terminus of E. coli TonB by the weakly hydrophobic C terminus of K. pneumoniae TonB yielded a hybrid protein of the same activity as E. coli wild-type TonB. The result shows that the strong hydrophobicity of the C-terminal end is not necessary for the function of E. coli TonB.

摘要

肺炎克雷伯菌的tonB基因克隆于一个1.4kb的EcoRV片段上,并在大肠杆菌中表达。对克隆片段的核苷酸(nt)序列测定确定tonB为一个729nt的开放阅读框(ORF)。TonB蛋白由243个氨基酸(aa)组成,与产气肠杆菌的TonB高度同源。肺炎克雷伯菌和产气肠杆菌tonB的遗传背景相同,但与大肠杆菌、鼠伤寒沙门氏菌和粘质沙雷氏菌不同。当克隆于同一类型质粒上时,肺炎克雷伯菌tonB对大肠杆菌tonB突变体的互补效率与大肠杆菌tonB相同。用肺炎克雷伯菌TonB的弱疏水性C末端取代大肠杆菌TonB的高疏水性C末端,产生了一种与大肠杆菌野生型TonB具有相同活性的杂合蛋白。结果表明,C末端的强疏水性对于大肠杆菌TonB的功能并非必需。

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