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Updated: Jun 11, 2026

The Use of a β-lactamase-based Conductimetric Biosensor Assay to Detect Biomolecular Interactions
Published on: February 1, 2018
Structural basis for the interaction of lactivicins with serine beta-lactamases
Tom Brown1, Paulette Charlier, Raphaël Herman
1Chemistry Research Laboratory, Department of Chemistry, University of Oxford, Oxford, UK.
Abstract:
Lactivicin (LTV) is a natural non-beta-lactam antibiotic that inhibits penicillin-binding proteins and serine beta-lactamases. A crystal structure of a BS3-LTV complex reveals that, as for its reaction with PBPs, LTV reacts with the nucleophilic serine and that cycloserine and lactone rings of LTV are opened. This structure, together with reported structures of PBP1b with lactivicins, provides a basis for developing improved lactivicin-based gamma-lactam antibiotics.
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