The DOI matches its Crossref record; 2 of the 2 references it cites were found in a registry or an index.
Multidrug resistance mechanisms: drug efflux across two membranes
Open accessAbstract
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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Citations
Cites
Antibiotic Resistance Caused by Gram‐Negative Multidrug Efflux Pumps
Nikaido, H. (1998) · Clinical Infectious Diseases · doi:10.1086/514920 · Cited by 348
Self-citationNikaido, H., Basina, M., Nguyen, V., & Rosenberg, E. Y. (1998) · Journal of Bacteriology · doi:10.1128/jb.180.17.4686-4692.1998 · Cited by 224 · cited 2×
“Second, AcrB/MexB can efflux drugs, such as many b-lactams, that do not cross the IM (Nikaido et al., 1998), suggesting that the substrate binding occurs either in the outer leaflet of the lipid bilayer or in the lipid±water interface in the periplasmic domains of these transporters.”
BackgroundSelf-citation
Cited by
Challenges of Antibacterial Discovery
Silver, L. L. (2011) · Clinical Microbiology Reviews · doi:10.1128/cmr.00030-10 · Cited by 1,376
Clinically Relevant Chromosomally Encoded Multidrug Resistance Efflux Pumps in Bacteria
Piddock, L. J. V. (2006) · Clinical Microbiology Reviews · doi:10.1128/cmr.19.2.382-402.2006 · Cited by 1,231
Bacterial Resistance to β-Lactam Antibiotics: Compelling Opportunism, Compelling Opportunity
Fisher, J. F., Meroueh, S. O., & Mobashery, S. (2005) · Chemical Reviews · doi:10.1021/cr030102i · Cited by 913
Molecular Analysis of the Copper-Transporting Efflux System CusCFBA of Escherichia coli
Franke, S., Grass, G., Rensing, C., & Nies, D. H. (2003) · Journal of Bacteriology · doi:10.1128/jb.185.13.3804-3812.2003 · Cited by 538
Contribution of the Mycobacterium tuberculosis MmpL Protein Family to Virulence and Drug Resistance
Domenech, P., Reed, M. B., & Barry, C. E. (2005) · Infection and Immunity · doi:10.1128/iai.73.6.3492-3501.2005 · Cited by 361
Metadata
- Authors
- Zgurskaya, H. I., & Nikaido, H.
- Venue
- Molecular Microbiology
- Publisher
- Wiley
- Published
- 2000-07
- Volume
- 37
- Issue
- 2
- Pages
- 219-225
- ISSN
- 0950-382X (ISSN-L)
- 1365-2958
- OpenAlex
- W2019509230
- Cited by
- 466
- References
- 2
- FWCI
- 15.59
- Type
- journal article
- Language
- en
- Open access
- bronze
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