Biotechnology Research Institute, Chinese Academy of Agricultural Sciences, Beijing, China.
PLoS One. 2011 Feb 28;6(2):e17367. doi: 10.1371/journal.pone.0017367.
The nickel resistance determinant ncrABCY was identified in Leptospirillum ferriphilum UBK03. Within this operon, ncrA and ncrC encode two membrane proteins that form an efflux system, and ncrB encodes NcrB, which belongs to an uncharacterized family (DUF156) of proteins. How this determinant is regulated remains unknown. Our data indicate that expression of the nickel resistance determinant is induced by nickel. The promoter of ncrA, designated pncrA, was cloned into the promoter probe vector pPR9TT, and co-transformed with either a wild-type or mutant nickel resistance determinant. The results revealed that ncrB encoded a transcriptional regulator that could regulate the expression of ncrA, ncrB, and ncrC. A GC-rich inverted repeat sequence was identified in the promoter pncrA. Electrophoretic mobility shift assays (EMSAs) and footprinting assays showed that purified NcrB could specifically bind to the inverted repeat sequence of pncrA in vitro; this was confirmed by bacterial one-hybrid analysis. Moreover, this binding was inhibited in the presence of nickel ions. Thus, we classified NcrB as a transcriptional regulator that recognizes the inverted repeat sequence binding motif to regulate the expression of the key nickel resistance gene, ncrA.
镍抗性决定簇 ncrABCY 在 Leptospirillum ferriphilum UBK03 中被鉴定出来。在这个操纵子中,ncrA 和 ncrC 编码两种形成外排系统的膜蛋白,而 ncrB 编码 NcrB,它属于一个未被表征的蛋白家族(DUF156)。该决定簇的调控机制尚不清楚。我们的数据表明,镍抗性决定簇的表达受镍诱导。ncrA 的启动子 pncrA 被克隆到启动子探针载体 pPR9TT 中,并与野生型或突变型镍抗性决定簇共转化。结果表明,ncrB 编码一个转录调节因子,可调节 ncrA、ncrB 和 ncrC 的表达。在 pncrA 启动子中鉴定到一个富含 GC 的反向重复序列。电泳迁移率变动分析(EMSA)和足迹分析表明,纯化的 NcrB 可以在体外特异性结合 pncrA 的反向重复序列;这通过细菌单杂交分析得到了证实。此外,这种结合在镍离子存在下被抑制。因此,我们将 NcrB 归类为一种转录调节因子,它识别反向重复序列结合基序来调节关键的镍抗性基因 ncrA 的表达。