Griffin H G, Foster T J, Silver S, Misra T K
Proc Natl Acad Sci U S A. 1987 May;84(10):3112-6. doi: 10.1073/pnas.84.10.3112.
The broad-spectrum mercurial-resistance plasmid pDU1358 was analyzed by cloning the resistance determinants and preparing a physical and genetic map of a 45-kilobase (kb) region of the plasmid that contains two separate mercurial-resistance operons that mapped about 20 kb apart. One encoded narrow-spectrum mercurial resistance to Hg2+ and a few organomercurials; the other specified broad-spectrum resistance to phenylmercury and additional organomercurials. Each determinant governed mercurial transport functions. Southern DNA X DNA hybridization experiments using gene-specific probes from the plasmid R100 mer operon indicated close homology with the R100 determinant. The 2153 base pairs of the promoter-distal part of the broad-spectrum Hg2+-resistance operon of pDU1358 were sequenced. This region included the 3'-terminal part of the merA gene, merD, unidentified reading frame URF1, and a part of URF2 homologous to previously sequenced determinants of plasmid R100. Between the merA and merD genes, an open reading frame encoding a 212 amino acid polypeptide was identified as the merB gene that determines the enzyme organomercurial lyase that cleaves the C--Hg bond of phenylmercury.
通过克隆抗性决定簇并绘制该质粒45千碱基(kb)区域的物理和遗传图谱,对广谱汞抗性质粒pDU1358进行了分析。该区域包含两个独立的汞抗性操纵子,它们在图谱上相距约20 kb。一个编码对Hg2+和少数有机汞的窄谱汞抗性;另一个则赋予对苯基汞和其他有机汞的广谱抗性。每个决定簇都控制汞转运功能。使用来自质粒R100 mer操纵子的基因特异性探针进行的Southern DNA X DNA杂交实验表明,它与R100决定簇具有密切的同源性。对pDU1358广谱Hg2+抗性操纵子启动子远端部分的2153个碱基对进行了测序。该区域包括merA基因的3'末端部分、merD、未鉴定的阅读框URF1以及与质粒R100先前测序的决定簇同源的URF2的一部分。在merA和merD基因之间,一个编码212个氨基酸多肽的开放阅读框被鉴定为merB基因,它决定了可裂解苯基汞C-Hg键的有机汞裂解酶。