Mechanism and function of the outer membrane channel TolC in multidrug resistance and physiology of enterobacteria

被引:174
作者
Zgurskaya, Helen I. [1 ]
Krishnamoorthy, Ganesh [1 ]
Ntreh, Abigail [1 ]
Lu, Shuo [1 ]
机构
[1] Univ Oklahoma, Dept Chem & Biochem, Norman, OK 73019 USA
基金
美国国家卫生研究院;
关键词
multidrug efflux; outer membrane permeability; acid tolerance; enterobacterial virulence; oxidative stress; HEAT-STABLE ENTEROTOXIN; ESCHERICHIA-COLI; EFFLUX PUMP; DRUG EFFLUX; CRYSTAL-STRUCTURE; PROTEIN TOLC; PSEUDOMONAS-AERUGINOSA; SUSCEPTIBILITY PROFILES; TRANSPORT MECHANISM; VIBRIO-CHOLERAE;
D O I
10.3389/fmicb.2011.00189
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
TolC is an archetypal member of the outer membrane efflux protein (OEP) family. These proteins are involved in export of small molecules and toxins across the outer membrane of Gram-negative bacteria. Genomes of some bacteria such as Pseudomonas species contain multiple copies of OEPs. In contrast, enterobacteria contain a single tolC gene, the product of which functions with multiple transporters. Inactivation of tolC has a major impact on enterobacterial physiology and virulence. Recent studies suggest that the role of TolC in physiology of enterobacteria is very broad and affects almost all aspects of cell adaptation to adverse environments. We review the current state of understanding TolC structure and present an integrated view of TolC function in enterobacteria. We propose that seemingly unrelated phenotypes of tolC mutants are linked together by a single most common condition an oxidative damage to membranes.
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页数:13
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