Literature DB >> 10931319

Multidrug resistance mechanisms: drug efflux across two membranes.

H I Zgurskaya1, H Nikaido.   

Abstract

A set of multidrug efflux systems enables Gram-negative bacteria to survive in a hostile environment. This review focuses on the structural features and the mechanism of major efflux pumps of Gram-negative bacteria, which expel from the cells a remarkably broad range of antimicrobial compounds and produce the characteristic intrinsic resistance of these bacteria to antibiotics, detergents, dyes and organic solvents. Each efflux pump consists of three components: the inner membrane transporter, the outer membrane channel and the periplasmic lipoprotein. Similar to the multidrug transporters from eukaryotic cells and Gram-positive bacteria, the inner membrane transporters from Gram-negative bacteria recognize and expel their substrates often from within the phospholipid bilayer. This efflux occurs without drug accumulation in the periplasm, implying that substrates are pumped out across the two membranes directly into the medium. Recent data suggest that the molecular mechanism of the drug extrusion across a two-membrane envelope of Gram-negative bacteria may involve the formation of the membrane adhesion sites between the inner and the outer membranes. The periplasmic components of these pumps are proposed to cause a close membrane apposition as the complexes are assembled for the transport.

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Year:  2000        PMID: 10931319     DOI: 10.1046/j.1365-2958.2000.01926.x

Source DB:  PubMed          Journal:  Mol Microbiol        ISSN: 0950-382X            Impact factor:   3.501


  147 in total

Review 1.  Chunnel vision. Export and efflux through bacterial channel-tunnels.

Authors:  C Andersen; C Hughes; V Koronakis
Journal:  EMBO Rep       Date:  2000-10       Impact factor: 8.807

2.  Resistance-nodulation-cell division-type efflux pump involved in aminoglycoside resistance in Acinetobacter baumannii strain BM4454.

Authors:  S Magnet; P Courvalin; T Lambert
Journal:  Antimicrob Agents Chemother       Date:  2001-12       Impact factor: 5.191

3.  Coarse-grained simulations of conformational changes in the multidrug efflux transporter AcrB.

Authors:  Yead Jewel; Jin Liu; Prashanta Dutta
Journal:  Mol Biosyst       Date:  2017-09-26

4.  Sequential mechanism of assembly of multidrug efflux pump AcrAB-TolC.

Authors:  Elena B Tikhonova; Yoichi Yamada; Helen I Zgurskaya
Journal:  Chem Biol       Date:  2011-04-22

5.  Amino acid residues essential for function of the MexF efflux pump protein of Pseudomonas aeruginosa.

Authors:  Julio Ramos Aires; Jean-Claude Pechère; Christian Van Delden; Thilo Köhler
Journal:  Antimicrob Agents Chemother       Date:  2002-07       Impact factor: 5.191

6.  The Escherichia coli multidrug transporter MdfA catalyzes both electrogenic and electroneutral transport reactions.

Authors:  Oded Lewinson; Julia Adler; Gerrit J Poelarends; Piotr Mazurkiewicz; Arnold J M Driessen; Eitan Bibi
Journal:  Proc Natl Acad Sci U S A       Date:  2003-02-10       Impact factor: 11.205

Review 7.  Interactions among strategies associated with bacterial infection: pathogenicity, epidemicity, and antibiotic resistance.

Authors:  José L Martínez; Fernando Baquero
Journal:  Clin Microbiol Rev       Date:  2002-10       Impact factor: 26.132

8.  Efflux of cytoplasmically acting antibiotics from gram-negative bacteria: periplasmic substrate capture by multicomponent efflux pumps inferred from their cooperative action with single-component transporters.

Authors:  Michael Palmer
Journal:  J Bacteriol       Date:  2003-09       Impact factor: 3.490

9.  Stress-based identification and classification of antibacterial agents: second-generation Escherichia coli reporter strains and optimization of detection.

Authors:  Elyse Shapiro; François Baneyx
Journal:  Antimicrob Agents Chemother       Date:  2002-08       Impact factor: 5.191

10.  Aminoglycosides are captured from both periplasm and cytoplasm by the AcrD multidrug efflux transporter of Escherichia coli.

Authors:  Julio Ramos Aires; Hiroshi Nikaido
Journal:  J Bacteriol       Date:  2005-03       Impact factor: 3.490

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