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作 者:侯进慧[1] 陈宏伟[1] 高兆建[1] 蔡侃[1]
机构地区:[1]徐州工程学院,江苏徐州221008
出 处:《生物技术》2010年第4期18-21,共4页Biotechnology
基 金:徐州市科技计划项目(XZZD0924);徐州工程学院引进人才科研启动项目;徐州工程学院科研项目(XKY2008110)资助
摘 要:目的:分析肠杆菌科AcrAB多药外排泵的分子演化规律,为多药耐药性病原菌的防治提供基础数据。方法:从NCBI获得肠杆菌科物种AcrAB多药外排泵相关蛋白和核酸序列,采用分析软件,分析肠杆菌科物种AcrAB多药外排泵相关序列。结果:在肠杆菌科各物种AcrA、AcrB和AcrR与大肠埃希氏菌同源性在55%、75%和43%以上。AcrA保守位点分散,在N端和C端较少,在分子一级结构中段较多。AcrB跨膜序列保守性较高,与质子转移相关的三个位点D407、D408和K940以及稳定这三者结构的T978在肠杆菌科完全保守,其一级结构上相邻位点也保守。AcrR序列整体保守性较低,但HTH区域保守性高。与AcrR结合的回文结构及周围序列保守性高,在"茎"结构中仅存在一个氨基酸的差异。结论:AcrAB多药外排泵在肠杆菌科中广泛存在,有一定的保守性。分析肠杆菌科AcrAB多药外排泵有助于病原菌多药耐药性的防治。Objective:To analyze molecular evolution of Enterobacteriaceae AcrAB multidrug efflux pump,and get primary data for the treatment of multidrug resistance pathogens.Method:NCBI data of protein and nuclear sequences related to Enterobacteriaceae AcrAB multidrug efflux pump were analyzed with protein and nucleotide multiple sequence alignment software.Result:Compared with Escherichia coli,homologous of AcrA,AcrB and AcrR in Enterobacteriaceae are more than 55% ,75% and 43% respectively.AcrA conservative sites are dispersive,with less conservative sequences in N and C terminal and more in middle sequence of primary structure.Transmembrane sequences of AcrB are conservative.Putative proton translocation related sites,D407,D408 and K940 and T978 which acts as a stabilizer between the former three sites are completely conservative,and their flanking sequences are also conservative.AcrR sequence as a whole is less conservative,but its HTH domain is highly conservative.AcrR-binding palindrome and flanking sequence are highly conservative and there is only one site in the middle of stem structure are variable.Conclusion:AcrAB multidrug efflux pump gene generally exists in Enterobacteriaceae and is conservative.Analysis of Enterobacteriaceae AcrAB multidrug efflux pump will promote treatment of pathogen multidrug resistance.
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