Assay for drug discovery: Synthesis and testing of nitrocefin analogues for use as β-lactamase substrates

Anal Biochem. 2015 Oct 1:486:75-7. doi: 10.1016/j.ab.2015.06.032. Epub 2015 Jul 2.

Abstract

We report on the synthesis of three nitrocefin analogues and their evaluation as substrates for the detection of β-lactamase activity. These compounds are hydrolyzed by all four Ambler classes of β-lactamases. Kinetic parameters were determined with eight different β-lactamases, including VIM-2, NDM-1, KPC-2, and SPM-1. The compounds do not inhibit the growth of clinically important antibiotic-resistant gram-negative bacteria in vitro. These chromogenic compounds have a distinct absorbance spectrum and turn purple when hydrolyzed by β-lactamases. One of these compounds, UW154, is easier to synthesize from commercial starting materials than nitrocefin and should be significantly less expensive to produce.

Keywords: Antibiotic resistance detection; Chromogenic cephalosporin; Nitrocefin analogues; β-Lactamase.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Biocatalysis
  • Cephalosporins / chemical synthesis*
  • Cephalosporins / chemistry
  • Cephalosporins / metabolism*
  • Chemistry Techniques, Synthetic
  • Drug Evaluation, Preclinical
  • Hydrolysis
  • Kinetics
  • beta-Lactamases / metabolism*

Substances

  • Cephalosporins
  • beta-Lactamases
  • nitrocefin