Augustus Anne Marie, Celaya Teresa, Husain Fasahath, Humbard Matthew, Misra Rajeev
Department of Chemistry and Biochemistry, Arizona State University, Tempe, Arizona 85287, USA.
J Bacteriol. 2004 Mar;186(6):1851-60. doi: 10.1128/JB.186.6.1851-1860.2004.
The TolC protein of Escherichia coli, through its interaction with AcrA and AcrB, is thought to form a continuous protein channel that expels inhibitors from the cell. Consequently, tolC null mutations display a hypersensitive phenotype. Here we report the isolation and characterization of tolC missense mutations that direct the synthesis of mutant TolC proteins partially disabled in their efflux role. All alterations, consisting of single amino acid substitutions, were localized within the periplasmic alpha-helical domain. In two mutants carrying an I106N or S350F substitution, the hypersensitivity phenotype may be in part due to aberrant TolC assembly. However, two other alterations, R367H and R390C, disrupted efflux function by affecting interactions among the helices surrounding TolC's periplasmic tunnel. Curiously, these two TolC mutants were sensitive to a large antibiotic, vancomycin, and exhibited a Dex(+) phenotype. These novel phenotypes of TolC(R367H) and TolC(R390C) were likely the result of a general influx of molecules through a constitutively open tunnel aperture, which normally widens only when TolC interacts with other proteins during substrate translocation. An intragenic suppressor alteration (T140A) was isolated from antibiotic-resistant revertants of the hypersensitive TolC(R367H) mutant. T140A also reversed, either fully (R390C) or partially (I106N and S350F), the hypersensitivity phenotype of other TolC mutants. Our data suggest that this global suppressor phenotype of T140A is the result of impeded antibiotic influx caused by tapering of the tunnel passage rather than by correcting individual mutational defects. Two extragenic suppressors of TolC(R367H), mapping in the regulatory region of acrAB, uncoupled the AcrR-mediated repression of the acrAB genes. The resulting overexpression of AcrAB reduced the hypersensitivity phenotype of all the TolC mutants. Similar results were obtained when the chromosomal acrR gene was deleted or the acrAB genes were expressed from a plasmid. Unlike the case for the intragenic suppressor T140A, the overexpression of AcrAB diminished hypersensitivity towards only erythromycin and novobiocin, which are substrates of the TolC-AcrAB efflux pump, but not towards vancomycin, which is not a substrate of this pump. This showed that the two types of suppressors produced their effects by fundamentally different means, as the intragenic suppressor decreased the general influx while extragenic suppressors increased the efflux of TolC-AcrAB pump-specific antibiotics.
大肠杆菌的TolC蛋白通过与AcrA和AcrB相互作用,被认为形成了一个连续的蛋白质通道,将抑制剂排出细胞。因此,tolC无效突变表现出超敏表型。在此,我们报告了tolC错义突变的分离和表征,这些突变指导合成在其外排作用中部分失活的突变TolC蛋白。所有改变均由单个氨基酸取代组成,位于周质α-螺旋结构域内。在两个携带I106N或S350F取代的突变体中,超敏表型可能部分归因于异常的TolC组装。然而,另外两个改变,R367H和R390C,通过影响TolC周质通道周围螺旋之间的相互作用破坏了外排功能。奇怪的是,这两个TolC突变体对一种大的抗生素万古霉素敏感,并表现出Dex(+)表型。TolC(R367H)和TolC(R390C)的这些新表型可能是由于分子通过组成性开放的通道孔径普遍流入的结果,该通道孔径通常仅在底物转运期间TolC与其他蛋白质相互作用时才会变宽。从超敏TolC(R367H)突变体的抗生素抗性回复子中分离出一个基因内抑制改变(T140A)。T140A也完全(R390C)或部分(I106N和S350F)逆转了其他TolC突变体的超敏表型。我们的数据表明,T140A的这种全局抑制表型是通道变窄导致抗生素流入受阻的结果,而不是纠正个体突变缺陷的结果。TolC(R367H)的两个基因外抑制子,定位在acrAB的调控区域,解除了AcrR介导的对acrAB基因的抑制。由此产生的AcrAB过表达降低了所有TolC突变体的超敏表型。当染色体acrR基因被删除或acrAB基因从质粒表达时,也获得了类似的结果。与基因内抑制子T140A的情况不同,AcrAB的过表达仅降低了对红霉素和新生霉素的超敏性,它们是TolC-AcrAB外排泵的底物,但对万古霉素没有降低超敏性,万古霉素不是该泵的底物。这表明这两种类型的抑制子通过根本不同的方式产生其作用,因为基因内抑制子减少了普遍流入,而基因外抑制子增加了TolC-AcrAB泵特异性抗生素的外排。