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The MtrR repressor binds the DNA sequence between the mtrR and mtrC genes of Neisseria gonorrhoeae.

机译:MtrR阻遏物结合淋病奈瑟氏球菌的mtrR和mtrC基因之间的DNA序列。

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摘要

Gonococcal resistance to antimicrobial hydrophobic agents (HAs) is due to energy-dependent removal of HAs from the bacterial cell by the MtrCDE membrane-associated efflux pump. The mtrR (multiple transferrable resistance Regulator) gene encodes a putative transcriptional repressor protein (MtrR) believed to be responsible for regulation of mtrCDE gene expression. Gel mobility shift and DNase I footprint assays that used a maltose-binding protein (MBP)-MtrR fusion protein demonstrated that the MtrR repressor is capable of specifically binding the DNA sequence between the mtrR and mtrC genes. This binding site was localized to a 26-nucleotide stretch that includes the promoter utilized for mtrCDE transcription and, on the complementary strand, a 22-nucleotide stretch that contains the -35 region of the mtrR promoter. A single transition mutation (A-->G) within the MtrR-binding site decreased the affinity of the target DNA for MtrR and enhanced gonococcal resistance to HAs when introduced into HA-susceptible strain FA19 by transformation. Since this mutation enhanced expression of the mtrCDE gene complex but decreased expression of the mtrR gene, the data are consistent with the notion that MtrR acts as a transcriptional repressor of the mtrCDE efflux pump protein genes.
机译:淋球菌对抗菌疏水剂(HAs)的抵抗力是由于MtrCDE膜相关外排泵从细菌细胞中依赖能量去除HAs所致。 mtrR(多重可转移抗性调节剂)基因编码一种假定的转录阻遏蛋白(MtrR),据信该蛋白负责调控mtrCDE基因的表达。使用麦芽糖结合蛋白(MBP)-MtrR融合蛋白的凝胶迁移率迁移和DNase I足迹分析表明,MtrR阻遏物能够特异性结合mtrR和mtrC基因之间的DNA序列。该结合位点定位于26个核苷酸的延伸片段,该片段包括用于mtrCDE转录的启动子,而在互补链上,包含22个核苷酸的延伸片段,其包含mtrR启动子的-35区。当通过转化引入HA易感株FA19时,MtrR结合位点内的单个过渡突变(A-> G)降低了目标DNA对MtrR的亲和力,并增强了淋球菌对HA的抵抗力。由于该突变增强了mtrCDE基因复合物的表达但降低了mtrR基因的表达,因此数据与MtrR充当mtrCDE外排泵蛋白基因的转录阻遏物的观点一致。

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