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. 1972 Jun;110(3):988–991. doi: 10.1128/jb.110.3.988-991.1972

Correlation Between Hydrolysis of the β-Lactam Bond of the Cephalosporin Nucleus and Expulsion of the 3-Substituent

Cynthia H O'Callaghan 1, Susan M Kirby 1, A Morris 1, R E Waller 1, R E Duncombe 1
PMCID: PMC247519  PMID: 4555421

Abstract

The hydrolysis of two cephalosporins by three different β-lactamases has been studied. Each enzyme caused a decrease in ultraviolet absorption, a loss of biological activity, and the release of the leaving group from the 3-position. The changes occurred at the same rate and to the same extent with each enzyme, and it is inferred that the loss of the leaving group is a consequence of, and not a prerequisite for, hydrolysis of the β-lactam ring.

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Selected References

These references are in PubMed. This may not be the complete list of references from this article.

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