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在大肠杆菌中表达的鳗弧菌锌金属蛋白酶empA的特性及致病性

Characterization and pathogenicity of the zinc metalloprotease empA of Vibrio anguillarum expressed in Escherichia coli.

作者信息

Yang Hui, Chen Jixiang, Yang Guanpin, Zhang Xiao-Hua, Li Yun, Wang Min

机构信息

Department of Marine Biology, College of Marine Life Sciences, Ocean University of China, 5 Yushan Road, Qingdao 266003, PRC.

出版信息

Curr Microbiol. 2007 Mar;54(3):244-8. doi: 10.1007/s00284-006-0495-6.

Abstract

The extracellular zinc metalloprotease (EmpA) is a putative pathogenic factor involved in the invasive process of the fish pathogen Vibrio anguillarum. It is synthesized as a 611-amino-acid preproprotease. The gene encoding EmpA (empA) has already been cloned and sequenced. In this study, empA was inserted into pET24d(+) and expressed in Escherichia coli BL21(DE3). Recombinant EmpA with His-tag was purified in a single step with a His-binding Ni-affinity column to a purity >95%. In addition, proteolytic activity, cytotoxicity, fish pathogenicity, and solubility of the recombinant protein were determined.

摘要

细胞外锌金属蛋白酶(EmpA)是一种推测参与鱼类病原菌鳗弧菌侵袭过程的致病因子。它最初被合成为一种含有611个氨基酸的前体蛋白酶。编码EmpA的基因(empA)已被克隆和测序。在本研究中,将empA插入pET24d(+)载体并在大肠杆菌BL21(DE3)中表达。带有His标签的重组EmpA通过His结合镍亲和柱一步纯化,纯度>95%。此外,还测定了重组蛋白的蛋白水解活性、细胞毒性、鱼类致病性和溶解性。

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