Conserved small protein associates with the multidrug efflux pump AcrB and differentially affects antibiotic resistance

被引:166
作者
Hobbs, Errett C. [1 ]
Yin, Xuefeng [1 ,2 ]
Paul, Brian J. [1 ]
Astarita, Jillian L. [1 ]
Storz, Gisela [1 ]
机构
[1] Eunice Kennedy Shriver Natl Inst Child Hlth & Hum, Cell Biol & Metab Program, Bethesda, MD 20892 USA
[2] Peking Univ, Hlth Sci Ctr, Beijing 100191, Peoples R China
关键词
multidrug resistance; resistance-nodulation-division; RND superfamily; ESCHERICHIA-COLI; TRANSPORTER ACRB; SUBSTRATE PATH; BINDING POCKET; MEMBRANE; MECHANISM; SYSTEM; GENES; RNA; PROMOTER;
D O I
10.1073/pnas.1210093109
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The AcrAB-TolC multidrug efflux pump confers resistance to a wide variety of antibiotics and other compounds in Escherichia coli. Here we show that AcrZ (formerly named YbhT), a 49-amino-acid inner membrane protein, associates with the AcrAB-TolC complex. Co-purification of AcrZ with AcrB, in the absence of both AcrA and TolC, two-hybrid assays and suppressor mutations indicate that this interaction occurs through the inner membrane protein AcrB. The highly conserved acrZ gene is coregulated with acrAB through induction by the MarA, Rob, and SoxS transcription regulators. In addition, mutants lacking AcrZ are sensitive to many, but not all, of the antibiotics transported by AcrAB-TolC. This differential antibiotic sensitivity suggests that AcrZ may enhance the ability of the AcrAB-TolC pump to export certain classes of substrates.
引用
收藏
页码:16696 / 16701
页数:6
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