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首页> 外文期刊>Journal of bacteriology >Regulation of the cnr Cobalt and Nickel Resistance Determinant of Ralstonia eutropha (Alcaligenes eutrophus) CH34
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Regulation of the cnr Cobalt and Nickel Resistance Determinant of Ralstonia eutropha (Alcaligenes eutrophus) CH34

机译:富营养小球藻(Alcaligenes eutrophus)CH34的cnr钴和镍抗性决定簇的调节

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The linked resistance to nickel and cobalt of Ralstonia eutropha-like strain CH34 (Alcaligenes eutrophusCH34) is encoded by the cnr operon, which is localized on the megaplasmid pMOL28. The regulatory genes cnrYXH have been cloned, overexpressed, and purified in Escherichia coli. CnrY fractionated as a 10.7-kDa protein in in vitro translation assays. CnrX, a periplasmic protein of 16.5 kDa, was overproduced and purified as a histidine-tagged fusion protein inE. coli. His-CnrX was found to posses a secondary structure content rich in alpha-helical and beta-sheet structures. CnrH, a sigma factor of the extracytoplasmic function family, was purified as an N-terminally histidine-tagged fusion. In gel shift mobility assays, His-CnrH, in the presence of E. coli core RNA polymerase enzyme, could retard at least two different promoter DNA targets,cnrYp and cnrHp, localized within thecnrYXH locus. These promoters and their transcription start sites were confirmed by primer extension. Purified His-CnrX did not inhibit the DNA-binding activity of His-CnrH and is therefore unlikely to be an anti-sigma factor, as previously hypothesized (EMBL M91650description entry). To study the transcriptional response of the regulatory locus to metals and to probe promoter regions, transcriptional fusions were constructed between fragments ofcnrYXH and the luxCDABE, luciferase reporter genes. Nickel and cobalt specifically induced thecnrYXH-luxCDABE fusion at optimal concentrations of 0.3 mM Ni2+ and 2.0 mM Co2+ in a noncomplexing medium for metals. The two promoter regions PY (upstreamcnrY) and PH (upstream cnrH) were probed and characterized using this vector and were found to control the nickel-inducible regulatory response of the cnr operon. The cnrHp promoter was responsible for full transcription of the cnrCBA structural resistance genes, while thecnrYp promoter was necessary to obtain metal-inducible transcription from the cnrHp promoter. The zinc resistance phenotype (ZinB) of a spontaneous cnr mutant strain, AE963, was investigated and could be attributed to an insertion of IS1087, a member of the IS2 family of insertion elements, within the cnrY gene.
机译: Ralstonia eutropha 样菌株CH34( Alcaligenes eutrophus CH34)对镍和钴的连锁抗性由 cnr 操纵子编码,该操纵子位于本地在大质粒pMOL28上。已在大肠杆菌中克隆,过表达并纯化了调控基因 cnrYXH 。在体外翻译测定中,CnrY被分离为10.7-kDa蛋白。 CnrX,16.5 kDa的周质蛋白,在E中被过量生产并纯化为组氨酸标记的融合蛋白。大肠杆菌。发现His-CnrX具有富含α-螺旋和β-折叠结构的二级结构。 CnrH,胞外功能家族的一个西格玛因子,被纯化为N端组氨酸标记的融合体。在存在E的凝胶迁移迁移率测定中,His-CnrH。 核心RNA聚合酶可以延迟至少两个不同的启动子DNA靶标 cnrYp cnrHp ,它们位于 cnrYXH 位点。通过引物延伸证实了这些启动子及其转录起始位点。纯化的His-CnrX不会抑制His-CnrH的DNA结合活性,因此不可能像先前所假设的那样是抗σ因子(EMBL M91650描述条目)。为研究调节基因座对金属和探针启动子区域的转录应答,在 cnrYXH 和萤光素酶报告基因 luxCDABE 的片段之间构建了转录融合体。在非复杂介质中,镍和钴在0.3 mM Ni 2 + 和2.0 mM Co 2 + 的最佳浓度下能特异性诱导 cnrYXH-luxCDABE 融合。用于金属。探测并鉴定了两个启动子区域P Y (上游 cnrY )和P H (上游 cnrH )该载体被发现可以控制 cnr 操纵子的镍诱导的调控反应。 cnrHp 启动子负责 cnrCBA 结构抗性基因的完全转录,而 cnrYp 启动子对于从中获得金属诱导的转录是必需的。 cnrHp 启动子。研究了自发性 cnr 突变株AE963的锌抗性表型(ZinB),其归因于IS 1087 的插入,IS 1087 是IS cnrY 基因中的> 2 插入元素家族。

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