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伤寒沙门氏菌中编码3-脱氢奎尼酸酶的aroD基因的分子克隆与特性分析

Molecular cloning and characterization of the aroD gene encoding 3-dehydroquinase from Salmonella typhi.

作者信息

Servos S, Chatfield S, Hone D, Levine M, Dimitriadis G, Pickard D, Dougan G, Fairweather N, Charles I

机构信息

Department of Molecular Biology, Wellcome Biotech, Beckenham, Kent, UK.

出版信息

J Gen Microbiol. 1991 Jan;137(1):147-52. doi: 10.1099/00221287-137-1-147.

Abstract

The aroD gene from Salmonella typhi, encoding 5-dehydroquinate hydrolyase (3-dehydroquinase), has been cloned into Escherichia coli and the DNA sequence determined. The aroD gene was isolated from a cosmid gene bank by complementation of an S. typhimurium aroD mutant. Analysis of the DNA sequence revealed the presence of an open reading frame capable of encoding a protein of 252 amino acids with a calculated Mr of 27706. Comparison of the deduced S. typhi 3-dehydroquinase protein sequence with that elucidated for E. coli revealed 69% homology. Alignment of the S. typhi sequence and equivalent Aspergillus nidulans and Saccharomyces cerevisiae sequences showed that homology was lower, at 24%, but still significant. Use of a minicell expression system demonstrated that a polyclonal antibody raised against E. coli 3-dehydroquinase cross-related with its S. typhi counterpart.

摘要

来自伤寒沙门氏菌的aroD基因编码5-脱氢奎尼酸水解酶(3-脱氢奎尼酸酶),已被克隆到大肠杆菌中并测定了DNA序列。aroD基因是通过对鼠伤寒沙门氏菌aroD突变体进行互补从黏粒基因文库中分离出来的。对DNA序列的分析表明存在一个开放阅读框,能够编码一种由252个氨基酸组成的蛋白质,计算出的分子量为27706。将推导的伤寒沙门氏菌3-脱氢奎尼酸酶蛋白序列与大肠杆菌的序列进行比较,发现同源性为69%。伤寒沙门氏菌序列与构巢曲霉和酿酒酵母的等效序列比对显示同源性较低,为24%,但仍然显著。使用小细胞表达系统表明,针对大肠杆菌3-脱氢奎尼酸酶产生的多克隆抗体与其伤寒沙门氏菌对应物存在交叉反应。

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