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Characterization of a novel IMP-28 metallo-?-lactamase from a Spanish Klebsiella oxytoca clinical isolate.


ABSTRACT: An isolate of Klebsiella oxytoca carrying a novel IMP metallo-?-lactamase was discovered in Madrid, Spain. The bla(IMP-28) gene is part of a chromosomally located class I integron. The IMP-28 k(cat)/K(m) values for ampicillin, ceftazidime, and cefepime and, to a lesser extent, imipenem and meropenem, are clearly lower than those of IMP-1. The His306Gln mutation may induce important modifications of the L3 loop and thus of substrate accessibility and hydrolysis and be the main reason for this behavior.

SUBMITTER: Perez-Llarena FJ 

PROVIDER: S-EPMC3421603 | biostudies-literature | 2012 Aug

REPOSITORIES: biostudies-literature

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Characterization of a novel IMP-28 metallo-β-lactamase from a Spanish Klebsiella oxytoca clinical isolate.

Pérez-Llarena Francisco José FJ   Fernández Ana A   Zamorano Laura L   Kerff Frédéric F   Beceiro Alejandro A   Aracil Belén B   Cercenado Emilia E   Miro Elisenda E   Oliver Antonio A   Oteo Jesús J   Navarro Ferran F   Bou Germán G  

Antimicrobial agents and chemotherapy 20120605 8


An isolate of Klebsiella oxytoca carrying a novel IMP metallo-β-lactamase was discovered in Madrid, Spain. The bla(IMP-28) gene is part of a chromosomally located class I integron. The IMP-28 k(cat)/K(m) values for ampicillin, ceftazidime, and cefepime and, to a lesser extent, imipenem and meropenem, are clearly lower than those of IMP-1. The His306Gln mutation may induce important modifications of the L3 loop and thus of substrate accessibility and hydrolysis and be the main reason for this beh  ...[more]

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