Related Experiment Video
Updated: Aug 30, 2026

Synthesis of Masarimycin, a Small Molecule Inhibitor of Gram-Positive Bacterial Growth
Published on: January 7, 2022
Novel mechanism of inhibiting beta-lactamases by sulfonylation using beta-sultams
Michael I Page1, Paul S Hinchliffe, J Matthew Wood
1Department of Chemical and Biological Sciences, The University of Huddersfield, Queensgate, Huddersfield HD1 3DH, UK. m.i.page@hud.ac.uk
Abstract:
Beta-sultams are the sulfonyl analogues of beta-lactams and N-acyl beta-sultams are novel inactivators of the class C beta-lactamase of Enterobacter cloacae P99. The rates of inactivation show a similar pH-rate dependence as that exhibited by the beta-lactam antibiotics and with ESIMS data it is suggested that beta-sultams sulfonylate the active site serine residue to form a sulfonate ester.
Related Concept Videos
Inhibitors of Gram-positive Cell Wall Synthesis
Amines to Sulfonamides: The Hinsberg Test
Generally, a primary amine reacts with the Hinsberg reagent to produce an N-substituted benzenesulfonamide. The electron-withdrawing sulfonyl...
Electrophilic Aromatic Substitution: Sulfonation of Benzene
Inhibitors of Bacterial Protein Synthesis
Phase II Reactions: Sulfation and Conjugation with α-Amino Acids
Mechanism of Antibiotic Resistance in MRSA
