Journal of Medicinal Chemistry · 2017 · 57 citations · 26 references
Life SciencesMicrobiologyMolecular BiologyEnzymologyStructural BiochemistryStructural BiologyAntibiotic ResistanceAntibiotic Resistance MechanismsBeta-lactam ResistanceCarbapenem ResistanceEnzyme-substrate RecognitionProtein StructureCarbapenem AntibioticsCarbapenem-hydrolyzing EnzymesCarbapenemase EnzymesKlebsiella Pneumoniae CarbapenemaseKlebsiella Pneumoniae ResistanceProduct ReleaseSerine Beta-lactamasesβ-Lactam Antibiotics
Carbapenem-resistant Enterobacteriaceae are resistant to most β-lactam antibiotics due to the production of the Klebsiella pneumoniae carbapenemase (KPC-2) class A β-lactamase. Here, we present the first product complex crystal structures of KPC-2 with β-lactam antibiotics containing hydrolyzed cefotaxime and faropenem. They provide experimental insights into substrate recognition by KPC-2 and its unique cephalosporinase/carbapenemase activity. These structures also represent the first product complexes for a wild-type serine β-lactamase, elucidating the product release mechanism of these enzymes in general.
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