Mechanism of inactivation of beta-lactamases by novel 6-methylidene penems elucidated using electrospray ionization mass spectrometry

J Med Chem. 2004 Jul 1;47(14):3674-88. doi: 10.1021/jm049903j.

Abstract

The reactions of 6-methylidene penems 4-7 with beta-lactamases (TEM-1, SHV-1, Amp-C) were characterized by electrospray ionization mass spectrometry (ESI-MS). The kinetics of the reactions were monitored, demonstrating that only one penem molecule reacts to form an acyl-enzyme complex. For penem 5, the ESI-MS/MS spectrum of the hydrolysis product produced in the reaction was identical to the spectrum generated from a synthesized dihydro[1,4]thiazepine 10, confirming the rearrangement of the penem ring system to a seven-membered dihydro[1,4]thiazepine structure. Gas-phase ESI-MS/MS fragmentation data were rationalized due to tautomerization between imine and enamine substructures. ESI-MS/MS analysis of the T-6 trypsin-digested fragments of TEM-1 and SHV-1 demonstrated that the penems were only attached to Ser-70 of these class A beta-lactamases and that the penem ring structures were rearranged to seven-membered dihydro[1,4]thiazepines.

MeSH terms

  • Bacterial Proteins / chemistry
  • Binding Sites
  • Hydrolysis
  • Spectrometry, Mass, Electrospray Ionization
  • beta-Lactamase Inhibitors
  • beta-Lactamases / chemistry*
  • beta-Lactams / chemical synthesis
  • beta-Lactams / chemistry*

Substances

  • Bacterial Proteins
  • beta-Lactamase Inhibitors
  • beta-Lactams
  • beta-lactamase PIT-2
  • AmpC beta-lactamases
  • beta-Lactamases
  • beta-lactamase TEM-1
  • carbapenemase