Multidrug resistance mechanisms: drug efflux across two membranes

被引:360
作者
Zgurskaya, HI [1 ]
Nikaido, H [1 ]
机构
[1] Univ Calif Berkeley, Dept Mol & Cell Biol, Berkeley, CA 94720 USA
关键词
D O I
10.1046/j.1365-2958.2000.01926.x
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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.
引用
收藏
页码:219 / 225
页数:7
相关论文
共 51 条
[11]   Membrane topology of the xenobiotic-exporting subunit, MexB, of the MexA,B-OprM extrusion pump in Pseudomonas aeruginosa [J].
Guan, L ;
Ehrmann, M ;
Yoneyama, H ;
Nakae, T .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (15) :10517-10522
[12]   RESISTANCE OF NEISSERIA-GONORRHOEAE TO ANTIMICROBIAL HYDROPHOBIC AGENTS IS MODULATED BY THE MTRRCDE EFFLUX SYSTEM [J].
HAGMAN, KE ;
PAN, WB ;
SPRATT, BG ;
BALTHAZAR, JT ;
JUDD, RC ;
SHAFER, WM .
MICROBIOLOGY-SGM, 1995, 141 :611-622
[13]   HEMOLYSIN SECRETION FROM ESCHERICHIA-COLI [J].
HOLLAND, IB ;
KENNY, B ;
BLIGHT, M .
BIOCHIMIE, 1990, 72 (2-3) :131-141
[14]   Alignment and structure prediction of divergent protein families: Periplasmic and outer membrane proteins of bacterial efflux pumps [J].
Johnson, JM ;
Church, GM .
JOURNAL OF MOLECULAR BIOLOGY, 1999, 287 (03) :695-715
[15]   Carbapenem activities against Pseudomonas aeruginosa:: Respective contributions of OprD and efflux systems [J].
Köhler, T ;
Michea-Hamzehpour, M ;
Epp, SF ;
Pechere, JC .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1999, 43 (02) :424-427
[16]   Structure of TolC, the outer membrane component of the bacterial type I efflux system, derived from two-dimensional crystals [J].
Koronakis, V ;
Li, J ;
Koronakis, E ;
Stauffer, K .
MOLECULAR MICROBIOLOGY, 1997, 23 (03) :617-626
[17]   Four cholesterol-sensing proteins [J].
Lange, Y ;
Steck, TL .
CURRENT OPINION IN STRUCTURAL BIOLOGY, 1998, 8 (04) :435-439
[18]   Protein secretion in Gram-negative bacteria: Assembly of the three components of ABC protein-mediated exporters is ordered and promoted by substrate binding [J].
Letoffe, S ;
Delepelaire, P ;
Wandersman, C .
EMBO JOURNAL, 1996, 15 (21) :5804-5811
[19]   ROLE OF MEXA-MEXB-OPRM IN ANTIBIOTIC EFFLUX IN PSEUDOMONAS-AERUGINOSA [J].
LI, XZ ;
NIKAIDO, H ;
POOLE, K .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1995, 39 (09) :1948-1953
[20]   ROLE OF EFFLUX PUMP(S) IN INTRINSIC RESISTANCE OF PSEUDOMONAS-AERUGINOSA - RESISTANCE TO TETRACYCLINE, CHLORAMPHENICOL, AND NORFLOXACIN [J].
LI, XZ ;
LIVERMORE, DM ;
NIKAIDO, H .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1994, 38 (08) :1732-1741