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Multidrug efflux systems in Gram-negative bacteria
Moreira, Maria Aparecida Scatamburlo; Souza, Edmar Chartone de; Moraes, Célia Alencar de.
  • Moreira, Maria Aparecida Scatamburlo; Universidade Federal de Viçosa. Instituto de Biotecnologia Aplicada à Agropecuária. Departamento de Mcirobiologia. Laboratório de Microbiologia Industrial. Viçosa. BR
  • Souza, Edmar Chartone de; Universidade Federal de Minas Gerais. Instituto de Ciências Biológicas. Departamento de Biologia. Belo Horizonte. BR
  • Moraes, Célia Alencar de; Universidade Federal de Viçosa. Instituto de Biotecnologia Aplicada à Agropecuária. Departamento de Mcirobiologia. Laboratório de Microbiologia Industrial. Viçosa. BR
Braz. j. microbiol ; 35(1/2): 19-28, Jan.-Jun. 2004. ilus
Article in English | LILACS | ID: lil-388792
RESUMO
Multidrug efflux mechanisms in bacteria contribute significantly to intrinsic and acquired resistance to antimicrobial agents. Genome analysis have confirmed the broad distribution of these systems in Gram-negative as well as in Gram-positive bacteria. Among resistance mechanisms, the multidrug efflux system or pump deserves special attention, since a cell that has acquired it can simultaneously diminish or even suppress the susceptibility to a wide range of antimicrobials. The efflux system is mediated by transport proteins which confer resistance to toxic compounds. In Gram-negative bacteria, a tripartite efflux system is necessary to expel the drug to the outer medium: a protein localized in the cytoplasmic membrane; another in the periplasmatic space (membrane fusion protein - MFP); and a third in the outer membrane (outer membrane factor - OMF). The drug transport is active, and depends either on the energy provided by ATP hydrolysis or is directly driven by the proton motive force. The transport proteins are grouped in families, according to the homology of the amino acid sequences and to similarity of mechanisms. Among Gram-negative bacteria, Escherichia coli and Pseudomonas aeruginosa have most of the hitherto identified and studied multidrug efflux systems.
Subject(s)
Full text: Available Index: LILACS (Americas) Main subject: Carrier Proteins / Gram-Negative Bacteria Type of study: Prognostic study Language: English Journal: Braz. j. microbiol Journal subject: Microbiology Year: 2004 Type: Article Affiliation country: Brazil Institution/Affiliation country: Universidade Federal de Minas Gerais/BR / Universidade Federal de Viçosa/BR

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Full text: Available Index: LILACS (Americas) Main subject: Carrier Proteins / Gram-Negative Bacteria Type of study: Prognostic study Language: English Journal: Braz. j. microbiol Journal subject: Microbiology Year: 2004 Type: Article Affiliation country: Brazil Institution/Affiliation country: Universidade Federal de Minas Gerais/BR / Universidade Federal de Viçosa/BR