Adaptation of Comamonas testosteroni TA441 to utilization of phenol by spontaneous mutation of the gene for a trans‐acting factor
Open Access
- 1 September 1999
- journal article
- research article
- Published by Wiley in Molecular Microbiology
- Vol. 33 (6) , 1132-1140
- https://doi.org/10.1046/j.1365-2958.1999.01554.x
Abstract
Comamonas testosteroni TA441 adapts to utilization of phenol upon incubation with phenol as the major carbon source. Strain TA441 has a cluster of genes (aphKLMNOPQB) encoding the catabolic enzymes phenol hydroxylase and catechol 2,3‐dioxygenase, and a divergently transcribed regulatory gene (aphR), but these genes are silent until adaptation occurs. We found another regulatory gene (aphS) downstream of aphR. AphS belongs to the GntR family of transcriptional regulators. All adapted strains were found to have mutations in the aphS gene or in the aphR–aphS intervening region. The adapted strains expressed phenol hydroxylase and catechol 2,3‐dioxygenase activity in the presence of phenol. The transcriptional activity of both the aphK and the aphR promoters was elevated in the adapted strains. A strain whose aphS gene was artificially disrupted was found to be able to grow using phenol, and the cells showed high levels of the above‐mentioned transcriptional and enzymatic activities, indicating that adaptation was caused only by the mutation in the aphS gene. Gel retardation analysis revealed that AphS bound to two specific sites in the promoter region between aphK and aphR. These results indicate that the active aphS gene product acts as a trans‐acting factor and represses transcription of the aph genes in strain TA441.Keywords
This publication has 23 references indexed in Scilit:
- Adaptation of Cornamonas testosteroni TAM1 to utilize phenol: organization and regulation of the genes involved in phenol degradatioMicrobiology, 1998
- Activation of the bgl operon by adaptive mutationMolecular Biology and Evolution, 1998
- Localization and organization of phenol degradation genes ofPseudomonas putida strain HMolecular Genetics and Genomics, 1995
- Molecular cloning and sequencing of the phenol hydroxylase gene from Pseudomonas putida BHJournal of Fermentation and Bioengineering, 1995
- Cloning and sequences of the first eight genes of the chromosomally encoded (methyl) phenol degradation pathway from Pseudomonas putida P35XGene, 1994
- Selection, adaptation, and bacterial operonsGenome, 1989
- The gluconate operon gnt of Bacillus subtilis encodes its own transcriptional negative regulator.Proceedings of the National Academy of Sciences, 1987
- Molecular cloning of the plasmid RP4 primase region in a multi-host-range tacP expression vectorGene, 1986
- High frequency mobilization of gram-negative bacterial replicons by the in vitro constructed Tn5-Mob transposonMolecular Genetics and Genomics, 1984
- A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye bindingAnalytical Biochemistry, 1976