Literature DB >> 2126509

Evolution of enzymatic mechanisms of resistance among beta-lactam antibiotics.

L Gutmann1, M D Kitzis, J F Acar.   

Abstract

Resistance to third-generation cephalosporins occurs as a result of either the production of high concentrations of chromosomal cephalosporinase or, increasingly, the presence of broad-spectrum plasmid-mediated beta-lactamases. Both cases represent the response of bacteria in the hospital setting to the selection pressure brought to bear by the use of these antibiotics. Continued evolution of the plasmid-mediated enzymes is occurring as new antibiotics are introduced, probably reflecting the process that began when the first beta-lactamase apparently evolved from the penicillin-binding proteins. beta-Lactamase inhibitors offer one approach to dealing with the evolution of resistance to previously beta-lactamase-stable antibiotics.

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Year:  1990        PMID: 2126509

Source DB:  PubMed          Journal:  J Int Med Res        ISSN: 0300-0605            Impact factor:   1.671


  3 in total

1.  In vitro activity of the trinem sanfetrinem (GV104326) against gram-positive organisms.

Authors:  K V Singh; T M Coque; B E Murray
Journal:  Antimicrob Agents Chemother       Date:  1996-09       Impact factor: 5.191

2.  In vitro activity of the tribactam GV104326 against gram-positive, gram-negative, and anaerobic bacteria.

Authors:  E Di Modugno; I Erbetti; L Ferrari; G Galassi; S M Hammond; L Xerri
Journal:  Antimicrob Agents Chemother       Date:  1994-10       Impact factor: 5.191

3.  Critical hydrogen bonding by serine 235 for cephalosporinase activity of TEM-1 beta-lactamase.

Authors:  U Imtiaz; E K Manavathu; S A Lerner; S Mobashery
Journal:  Antimicrob Agents Chemother       Date:  1993-11       Impact factor: 5.191

  3 in total

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