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来自施氏假单胞菌质粒的汞和有机汞抗性决定因子的克隆与比较

Cloning and comparison of mercury- and organomercurial-resistance determinants from a Pseudomonas stutzeri plasmid.

作者信息

Reniero D, Galli E, Barbieri P

机构信息

Dipartimento di Genetica e di Biologia dei Microrganismi, Milano, Italy.

出版信息

Gene. 1995 Dec 1;166(1):77-82. doi: 10.1016/0378-1119(95)00546-4.

Abstract

Plasmid pPB confers broad-spectrum mercury resistance (HgR) to a Pseudomonas stutzeri strain. Two pPB regions, separated by 25-30 kb and sharing homology with Tn501 mer (Hg detoxification) genes, were cloned separately and each was shown to carry a cluster of functional and independently regulated mer genes. One of the two gene clusters conferred resistance only to inorganic mercury, and had a structure identical to the classical model of narrow-spectrum mer operons. In the other cluster a novel merB gene, not homologous to the other known merB, but with the same function, was mapped upstream from merA, interposed between an organomercurial-responsive regulatory element and transport genes. Evidence suggests that merB and the other structural mer genes might be transcribed from two distinct promoters. The presence of two inverted repeat-like elements, identical to those of Tn5053, upstream from merR suggests that the pPB broad-spectrum-gene cluster could be part of a transposon-like element.

摘要

质粒pPB赋予施氏假单胞菌菌株广谱汞抗性(HgR)。两个被25 - 30 kb间隔且与Tn501 mer(汞解毒)基因具有同源性的pPB区域被分别克隆,并且每个区域都显示携带一组功能性且独立调控的mer基因。两个基因簇中的一个仅赋予对无机汞的抗性,其结构与窄谱mer操纵子的经典模型相同。在另一个基因簇中,一个与其他已知merB无同源性但功能相同的新型merB基因,被定位在merA上游,介于有机汞响应调控元件和转运基因之间。有证据表明merB和其他结构mer基因可能从两个不同的启动子转录。merR上游存在两个与Tn5053相同的反向重复样元件,这表明pPB广谱基因簇可能是转座子样元件的一部分。

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