Acridine dyes and other DNA-intercalating agents induce the luminescence system of luminous bacteria and their dark variants.
- 1 June 1981
- journal article
- research article
- Published by Proceedings of the National Academy of Sciences in Proceedings of the National Academy of Sciences
- Vol. 78 (6) , 3338-3342
- https://doi.org/10.1073/pnas.78.6.3338
Abstract
Acridine dyes and other DNA-intercalating agents such as ethidium bromide, theophylline and caffeine induce luminescence in dark variants (K variants) of different luminous species of bacteria (i.e., Photobacterium phosphoreum, P. leiognathi and Beneckea harveyi) and in their wild-type luminous cells, prior to induction. The increase in luminescence appears 10-20 min after the addition of these agents and is inhibited by chloramphenicol or rifampicin. Addition of these agents affects the synthesis of both luciferase and aldehyde-synthesizing enzymes. These agents, through their intercalation into DNA, may cause configurational changes resulting in derepressed transcription of the luminescence operon.Keywords
This publication has 12 references indexed in Scilit:
- A new, sensitive and simple bioluminescence test for mutagenic compoundsMutation Research/Environmental Mutagenesis and Related Subjects, 1980
- Genetic effects of acridine compoundsMutation Research/Reviews in Genetic Toxicology, 1979
- Bacterial bioluminescence: its control and ecological significance.1979
- BACTERIAL BIOLUMINESCENCEAnnual Review of Microbiology, 1977
- Autoinduction of bacterial luciferaseArchiv für Mikrobiologie, 1977
- CaffeineMutation Research/Reviews in Genetic Toxicology, 1977
- An adenosine 3′,5′-monophosphate-requiring mutant of the luminous bacteria Beneckea harveyiBiochimica et Biophysica Acta (BBA) - General Subjects, 1975
- Differential Inhibition of Catabolite-sensitive Enzyme Induction by Intercalating DyesNature New Biology, 1973
- Cyclic adenosine‐3′, 5′‐monophosphate and the inhibition of ribonucleic acid synthesis by proflavineFEBS Letters, 1971
- A stable, inexpensive, solid-state photomultiplier photometerAnalytical Biochemistry, 1971