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由产气荚膜梭菌多拷贝质粒携带的解离酶基因res的分子特征:原核生物位点特异性重组酶的共同进化起源

Molecular characterization of the resolvase gene, res, carried by a multicopy plasmid from Clostridium perfringens: common evolutionary origin for prokaryotic site-specific recombinases.

作者信息

Garnier T, Saurin W, Cole S T

机构信息

Unité des Applications du Génie Génétique, Institut Pasteur, Paris, France.

出版信息

Mol Microbiol. 1987 Nov;1(3):371-6. doi: 10.1111/j.1365-2958.1987.tb01944.x.

Abstract

Clostridium perfringens strain CPN50 harbours a 10.2 kb plasmid known as pIP404 which, in addition to a set of UV-inducible genes involved in bacteriocin production, carries res, a gene probably encoding a site-specific recombinase. The RES protein is highly homologous to the resolvases of transposons from both Gram-negative and Gram-positive bacteria as well as enzymes involved in site-specific DNA inversion. A likely role for the RES protein would be to stabilize pIP404 by reducing the number of plasmid multimers resulting from homologous recombination. A putative resolution site for RES action was found overlapping the res promoter. Phylogenetic analysis of the primary structures of ten site-specific recombinases suggested a common descent and showed the RES protein to be closest to the resolvase encoded by Tn917 from Streptococcus faecalis.

摘要

产气荚膜梭菌菌株CPN50含有一个10.2 kb的质粒,称为pIP404,除了一组参与细菌素产生的紫外线诱导基因外,还携带res,一个可能编码位点特异性重组酶的基因。RES蛋白与革兰氏阴性菌和革兰氏阳性菌转座子的解离酶以及参与位点特异性DNA倒位的酶高度同源。RES蛋白的一个可能作用是通过减少同源重组产生的质粒多聚体数量来稳定pIP404。发现一个RES作用的假定切割位点与res启动子重叠。对十种位点特异性重组酶一级结构的系统发育分析表明它们有共同的起源,并显示RES蛋白与粪肠球菌Tn917编码的解离酶关系最为密切。

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