Mechanism of Metallo-β-Lactamase Inhibition by Oxacephalosporin Antibiotic


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Metallo-β-lactamases is a family of bacterial zinc-dependent enzymes that hydrolyze β-lactam antibiotics and are responsible for the bacterial resistance to them. As a result of the reaction, the slowly hydrolyzed substrate moxalactam undergoes not only chemical transformations in the structure of the β-lactam ring but a negatively charged fragment is also released on the periphery of the molecule, resulting in the formation of an intermediate firmly bound to the active site. In the paper, we present the results of the calculations of the mechanism of this process by a combined quantum mechanics/molecular mechanics approach.

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M. Khrenova

Department of Chemistry

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Email: wasabiko@lcc.chem.msu.ru
俄罗斯联邦, Moscow, 119991

A. Kulakova

Department of Chemistry

Email: wasabiko@lcc.chem.msu.ru
俄罗斯联邦, Moscow, 119991

B. Grigorenko

Department of Chemistry

Email: wasabiko@lcc.chem.msu.ru
俄罗斯联邦, Moscow, 119991

A. Nemukhin

Department of Chemistry

Email: wasabiko@lcc.chem.msu.ru
俄罗斯联邦, Moscow, 119991

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