Evaluation of cyclohexenoesculetin-beta-D-galactoside and 8-hydroxyquinoline-beta-D-galactoside as substrates for the detection of beta-galactosidase

Author:

James A L1,Perry J D1,Ford M1,Armstrong L1,Gould F K1

Affiliation:

1. Department of Chemical and Life Sciences, University of Northumbria, Newcastle-upon-Tyne, United Kingdom.

Abstract

We describe the synthesis of two new substrates for the detection of beta-galactosidase and evaluate their performance in comparison with that of 5-bromo-4-chloro-3-indolyl-beta-D-galactopyranoside (X-Gal). Of 171 Enterobacteriaceae strains that were able to hydrolyze X-Gal, 166 (97.1%) also hydrolyzed cyclohexenoesculetin-beta-D-galactoside whereas only 96 (56.1%) showed evidence of hydrolysis of 8-hydroxyquinoline-beta-D-galactoside. No false-positive results were observed with either substrate.

Publisher

American Society for Microbiology

Subject

Ecology,Applied Microbiology and Biotechnology,Food Science,Biotechnology

Reference9 articles.

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3. Evaluation of a new agar in Uricult-Trio for rapid detection of Escherichia coli in urine;Dalet F.;J. Clin. Microbiol.,1995

4. Detection of specific bacterial enzymes by high contrast metal chelate formation. I. 8-Hydroxyquinoline ~-D-glucoside, an alternative to aesculin in the differentiation of members of the family Enterobacteriaceae;James A. L.;Zentralbl. Bakteriol. Mikrobiol. Hyg. Ser. A,1987

5. Detection of specific bacterial enzymes by high contrast metal chelate formation. II. Specific detection of Escherichia coli on multipoint inoculated plates using 8-hydroxyquinoline ~-D-glucuronide;James A. L.;Zentralbl. Bakteriol. Mikrobiol. Hyg. Ser. A,1988

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