Cloning of a copper resistance gene cluster from the cyanobacterium Synechocystis sp PCC 6803 by recombineering recovery

被引:6
|
作者
Gittins, John R. [1 ]
机构
[1] Univ Southampton, Ocean & Earth Sci, Natl Oceanog Ctr, Southampton SO14 3ZH, Hants, England
关键词
Cloning; Copper resistance gene cluster; Heterologous expression; Homologous recombination; Mutant complementation; Recombineering recovery; ESCHERICHIA-COLI; HOMOLOGOUS RECOMBINATION; IN-VIVO; SYSTEM; EXPRESSION; TRANSFORMATION; CONSTRUCTION; PLASMIDS; GENOME; INTEGRATION;
D O I
10.1016/j.febslet.2015.05.014
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
A copper resistance gene cluster (6 genes, similar to 8.2 kb) was isolated from the cyanobacterium Synechocystis sp. PCC 6803 by recombineering recovery (RR). Following integration of a narrow-host-range plasmid vector adjacent to the target region in the Synechocystis genome (pSYSX), DNA was isolated from transformed cells and the plasmid plus flanking sequence circularized by recombineering to precisely clone the gene cluster. Complementation of a copper-sensitive Escherichia coli mutant demonstrated the functionality of the pcopM gene encoding a copper-binding protein. RR provides a novel alternative method for cloning large DNA fragments from species that can be transformed by homologous recombination. (C) 2015 Federation of European Biochemical Societies. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:1872 / 1878
页数:7
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