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A bifunctional monocyclic beta-lactam cross-links across the active site of beta-lactamase
R Ahluwalia1, R A Day, J Nauss
1Department of Chemistry, University of Cincinnati, OH 45221-0172.
Biochemical and Biophysical Research Communications
|January 17, 1995
Abstract:
A 4-alkoxy-2-azetidinone behaves as a bifunctional active site-directed inhibitor of the class A beta-lactamase from Bacillus cereus 569/H. It cross-links SER 70 and LYS 234 as it binds in a approximately 1:1 ratio. The cross-linked enzyme is irreversibly inhibited while the secondary structure is partially stabilized under conditions when the native enzyme is otherwise converted to a form with no detectable secondary structure by circular dichroism.