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IncJ质粒pMERPH的汞抗性操纵子与其他革兰氏阴性菌的mer操纵子在结构和调控方面存在差异。

The mercury resistance operon of the IncJ plasmid pMERPH exhibits structural and regulatory divergence from other Gram-negative mer operons.

作者信息

Osborn A M, Bruce K D, Ritchie D A, Strike P

机构信息

Department of Genetics and Microbiology, Donnan Laboratories, University of Liverpool, PO Box 147, Liverpool L69 3BX, UK.

出版信息

Microbiology (Reading). 1996 Feb;142 ( Pt 2):337-345. doi: 10.1099/13500872-142-2-337.

Abstract

The bacterial mercury resistance determinant carried on the IncJ plasmid pMERPH has been characterized further by DNA sequence analysis. From the sequence of a 4097 bp Bg/II fragment which confers mercury resistance, it is predicted that the determinant consists of the genes merT, merP, merC and merA. The level of DNA sequence similarity between these genes and those of the mer determinant of Tn21 was between 56 center dot 4 and 62 center dot 4%. A neighbour-joining phylogenetic tree of merA gene sequences was constructed which suggested that pMERPH bears the most divergent Gram-negative mer determinant characterized to date. Although the determinant from pMERPH has been shown to be inducible, no regulatory genes have been found within the Bg/II fragment and it is suggested that a regulatory gene may be located elsewhere on the plasmid. The cloned determinant has been shown to express mercury resistance constitutively. Analysis of the pMERPH mer operator/promoter (O/P) region in vivo has shown constitutive expression from the mer PTCPA promoter, which could be partially repressed by the presence of a trans-acting MerR protein from a Tn21-like mer determinant. This incomplete repression of mer PTCPA promoter activity may be due to the presence of an extra base between the -35 and -10 sequences of the promoter and/or to variation in the MerR binding sites in the O/P region. Expression from the partially repressed mer PTCPA promoter could be restored by the addition of inducing levels of Hg2+ ions. Using the polymerase chain reaction with primers designed to amplify regions in the merP and merA genes, 1 center dot 37 kb pMERPH-like sequences have been amplified from the IncJ plasmid R391, the environmental isolate SE2 and from DNA isolated directly from non-cultivated bacteria in River Mersey sediment. This suggests that pMERPH-like sequences, although rare, are nevertheless persistent in natural environments.

摘要

通过DNA序列分析对IncJ质粒pMERPH上携带的细菌汞抗性决定簇进行了进一步表征。从一个赋予汞抗性的4097 bp Bg/II片段的序列预测,该决定簇由merT、merP、merC和merA基因组成。这些基因与Tn21的mer决定簇基因之间的DNA序列相似性水平在56.4%至62.4%之间。构建了merA基因序列的邻接法系统发育树,结果表明pMERPH携带了迄今为止所表征的最具分歧性的革兰氏阴性mer决定簇。尽管已证明来自pMERPH的决定簇是可诱导的,但在Bg/II片段内未发现调控基因,提示调控基因可能位于质粒的其他位置。已证明克隆的决定簇组成性表达汞抗性。对pMERPH mer操纵子/启动子(O/P)区域的体内分析表明,mer PTCPA启动子组成性表达,其可被来自Tn21样mer决定簇的反式作用MerR蛋白部分抑制。mer PTCPA启动子活性的这种不完全抑制可能是由于启动子的-35和-10序列之间存在额外碱基和/或O/P区域中MerR结合位点的变异。通过添加诱导水平的Hg2+离子可恢复部分抑制的mer PTCPA启动子的表达。使用设计用于扩增merP和merA基因区域的引物进行聚合酶链反应,已从IncJ质粒R391、环境分离株SE2以及直接从默西河沉积物中未培养细菌分离的DNA中扩增出1.37 kb的pMERPH样序列。这表明pMERPH样序列虽然罕见,但在自然环境中仍然存在。

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