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霍乱弧菌血凝素/蛋白酶(HA/蛋白酶)基因的克隆、核苷酸序列测定及HA/蛋白酶阴性菌株的构建

Cloning and nucleotide sequence of the Vibrio cholerae hemagglutinin/protease (HA/protease) gene and construction of an HA/protease-negative strain.

作者信息

Häse C C, Finkelstein R A

机构信息

Department of Molecular Microbiology and Immunology, School of Medicine, University of Missouri, Columbia 65212.

出版信息

J Bacteriol. 1991 Jun;173(11):3311-7. doi: 10.1128/jb.173.11.3311-3317.1991.

Abstract

The structural gene hap for the extracellular hemagglutinin/protease (HA/protease) of Vibrio cholerae was cloned and sequenced. The cloned DNA fragment contained a 1,827-bp open reading frame potentially encoding a 609-amino-acid polypeptide. The deduced protein contains a putative signal sequence followed by a large propeptide. The extracellular HA/protease consists of 414 amino acids with a computed molecular weight of 46,700. In the absence of protease inhibitors, this is processed to the 32-kDa form which is usually isolated. The deduced amino acid sequence of the mature HA/protease showed 61.5% identity with the Pseudomonas aeruginosa elastase. The cloned hap gene was inactivated and introduced into the chromosome of V. cholerae by recombination to construct the HA/protease-negative strain HAP-1. The cloned fragment containing the hap gene was then shown to complement the mutant strain.

摘要

霍乱弧菌细胞外血凝素/蛋白酶(HA/蛋白酶)的结构基因hap被克隆并测序。克隆的DNA片段包含一个1827碱基对的开放阅读框,可能编码一个609个氨基酸的多肽。推导的蛋白质含有一个假定的信号序列,后面跟着一个大的前肽。细胞外HA/蛋白酶由414个氨基酸组成,计算分子量为46700。在没有蛋白酶抑制剂的情况下,它被加工成通常分离得到的32 kDa形式。成熟HA/蛋白酶的推导氨基酸序列与铜绿假单胞菌弹性蛋白酶有61.5%的同一性。克隆的hap基因被灭活,并通过重组导入霍乱弧菌染色体,构建HA/蛋白酶阴性菌株HAP-1。然后显示含有hap基因的克隆片段可互补突变菌株。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1261/207942/3019e7f59b7d/jbacter00101-0053-a.jpg

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