Haritha Adhikarla, Sagar Korripally Prem, Tiwari Anand, Kiranmayi Patnala, Rodrigue Agnes, Mohan Pamarthi Maruthi, Singh Surya Satyanarayana
Department of Biochemistry, Osmania University, Hyderabad, India.
J Bacteriol. 2009 Oct;191(19):5976-87. doi: 10.1128/JB.00465-09. Epub 2009 Jul 31.
We report here the identification and characterization of mrdH, a novel chromosomal metal resistance determinant, located in the genomic island 55 of Pseudomonas putida KT2440. It encodes for MrdH, a predicted protein of approximately 40 kDa with a chimeric domain organization derived from the RcnA and RND (for resistance-nodulation-cell division) metal efflux proteins. The metal resistance function of mrdH was identified by the ability to confer nickel resistance upon its complementation into rcnA mutant (a nickel- and cobalt-sensitive mutant) of Escherichia coli. However, the disruption of mrdH in P. putida resulted in an increased sensitivity to cadmium and zinc apart from nickel. Expression studies using quantitative reverse transcription-PCR showed the induction of mrdH by cadmium, nickel, zinc, and cobalt. In association with mrdH, we also identified a conserved hypothetical gene mreA whose encoded protein showed significant homology to NreA and NreA-like proteins. Expression of the mreA gene in rcnA mutant of E. coli enhanced its cadmium and nickel resistance. Transcriptional studies showed that both mrdH and mreA underwent parallel changes in gene expression. The mobile genetic elements Tn4652 and IS1246, flanking mrdH and mreA were found to be induced by cadmium, nickel, and zinc, but not by cobalt. This study is the first report of a single-component metal efflux transporter, mrdH, showing chimeric domain organization, a broad substrate spectrum, and a location amid metal-inducible mobile genetic elements.
我们在此报告对mrdH的鉴定与特性分析,mrdH是一种新型的染色体金属抗性决定因子,位于恶臭假单胞菌KT2440的基因组岛55中。它编码MrdH,这是一种预测分子量约为40 kDa的蛋白质,具有源自RcnA和RND(抗性-结瘤-细胞分裂)金属外排蛋白的嵌合结构域组织。mrdH的金属抗性功能通过其互补到大肠杆菌的rcnA突变体(对镍和钴敏感的突变体)中赋予镍抗性的能力得以鉴定。然而,恶臭假单胞菌中mrdH的缺失除了导致对镍敏感外,还增加了对镉和锌的敏感性。使用定量逆转录PCR进行的表达研究表明,镉、镍、锌和钴可诱导mrdH表达。与mrdH相关,我们还鉴定了一个保守的假定基因mreA,其编码的蛋白质与NreA和NreA样蛋白具有显著同源性。mreA基因在大肠杆菌rcnA突变体中的表达增强了其对镉和镍的抗性。转录研究表明,mrdH和mreA的基因表达发生平行变化。发现位于mrdH和mreA侧翼的移动遗传元件Tn4652和IS1246可被镉、镍和锌诱导,但不能被钴诱导。本研究首次报道了一种单组分金属外排转运蛋白mrdH,其具有嵌合结构域组织、广泛的底物谱,且位于金属诱导的移动遗传元件之中。