Brocklehurst K R, Hobman J L, Lawley B, Blank L, Marshall S J, Brown N L, Morby A P
School of Biosciences, Cardiff University, UK.
Mol Microbiol. 1999 Feb;31(3):893-902. doi: 10.1046/j.1365-2958.1999.01229.x.
We have identified the promoter/operator region of the zntA gene of Escherichia coli and shown that Zn(II) is the primary inducer of expression of this Zn(II)/Cd(II) export gene. The promoter PzntA shows sequence similarities to the promoters of mercury resistance (mer) operons, including a long spacer region containing an inverted repeat sequence. The gene encoding the transcriptional regulator of PzntA, designated zntR, has been identified from genome sequence data, by expression of the gene product and by insertional inactivation/complementation. The ZntR product is a member of the MerR family of transcriptional regulators and appears to act as a hypersensitive transcriptional switch. A hybrid MerR/ZntR protein has been constructed and indicates that the C-terminal region of ZntR recognizes Zn(II).
我们已鉴定出大肠杆菌zntA基因的启动子/操纵子区域,并证明锌(II)是该锌(II)/镉(II)输出基因表达的主要诱导物。启动子PzntA与汞抗性(mer)操纵子的启动子具有序列相似性,包括一个含有反向重复序列的长间隔区。通过基因组序列数据、基因产物的表达以及插入失活/互补,已鉴定出编码PzntA转录调节因子的基因,命名为zntR。ZntR产物是转录调节因子MerR家族的成员,似乎作为一个超敏转录开关起作用。构建了一种杂交MerR/ZntR蛋白,表明ZntR的C末端区域识别锌(II)。