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Appl. Environ. Microbiol., Aug 1995, 2981-2989, Vol 61, No. 8
J Lampinen, M Virta and M Karp
In this article, we present a new bioluminescent test system for the
screening of chemical compounds with an inhibitory effect on protein
synthesis. The test is based on the measurement of real-time in vivo light
production by Escherichia coli strains expressing different luciferase
genes. The eukaryotic lucGR gene from Pyrophorus plagiophthalamus was found
to be the best of three types of luciferase genes tested. Chemicals with
known inhibitory effects on protein synthesis were used as test chemicals
together with some general toxicants. The incubation of a test chemical
with cells was performed either prior to or after the induction of protein
synthesis, and the difference in the results of the two methods
distinguishes the possible influence on protein synthesis from direct
metabolic inhibition. Using lyophilized bacteria, the test is performed in
less than an hour without any bacterial cultivation, which makes the test
suitable for rapid and sensitive screening of chemicals or environmental
samples. Compared with the standardized 50% inhibitory concentration
calculation method of the bioluminescent cytotoxicity test, the more direct
approach of calculation developed in this study proved to be more
convenient than and as reliable as the standard method.
Copyright © 1995, American Society for Microbiology
Use of Controlled Luciferase Expression To Monitor Chemicals Affecting Protein Synthesis
Department of Biochemistry and Pharmacy, Abo Akademi University, FIN-20521 Abo, Finland, and Department of Biochemistry and Biotechnology, University of Turku, FIN-20520 Turku, Finland
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