This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrowReprints and Permissions
Right arrow Copyright Information
Right arrow Books from ASM Press
Right arrow MicrobeWorld
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Ampe, F.
Right arrow Articles by Lindley, N. D.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Ampe, F.
Right arrow Articles by Lindley, N. D.
Agricola
Right arrow Articles by Ampe, F.
Right arrow Articles by Lindley, N. D.

Next Article 

Appl Environ Microbiol, January 1998, p. 1-6, Vol. 64, No. 1
0099-2240/98/$04.00+0
Copyright © 1998, American Society for Microbiology. All rights reserved.

Repression of Phenol Catabolism by Organic Acids in Ralstonia eutropha

Frédéric Ampe,dagger David Léonard, and Nicholas D. Lindley*

Centre de Bioingénierie Gilbert Durand, Unité Mixte de Recherche 5504 du Centre National de la Recherche Scientifique, Laboratoire associé à l'Institut National de Recherche Agronomique, Institut National des Sciences Appliquées, Complexe Scientifique de Rangueil, 31077 Toulouse Cedex 4, France

Received 11 August 1997/Accepted 4 October 1997

During batch growth of Ralstonia eutropha (previously named Alcaligenes eutrophus) on phenol in the presence of acetate, acetate was found to be the preferred substrate; this organic acid was rapidly metabolized, and the specific rate of phenol consumption was considerably decreased, although phenol consumption was not abolished. This decrease corresponded to a drop in phenol hydroxylase and catechol-2,3-dioxygenase specific activities, and the synthesis of the latter was repressed at the transcriptional level. Studies with a mutant not able to consume acetate indicated that the organic acid itself triggers the repression. Other organic acids were also found to repress phenol degradation. One of these, benzoate, was found to completely block the catabolism of phenol (diauxic growth). A mutant unable to metabolize benzoate was also unable to develop on benzoate-phenol mixtures, indicating that the organic acid rather than a metabolite involved in benzoate degradation was responsible for the repression observed.


* Corresponding author. Mailing address: Centre de Bioingénierie Gilbert Durand, Unité Mixte de Recherche 5504 du Centre National de la Recherche Scientifique, Laboratoire associé à l'Institut National de Recherche Agronomique, Institut National des Sciences Appliquées, Complexe Scientifique de Rangueil, 31077 Toulouse Cedex 4, France. Phone: 33 (0)5 61 55 94 89. Fax: 33 (0)5 61 55 94 00. E-mail: lindley{at}insa-tlse.fr.

dagger Present address: ORSTOM-Laboratoire de Biotechnologie et de Microbiologie Tropicale, 34032 Montpellier Cedex 1, France.




This article has been cited by other articles:

  • Moreno, R., Rojo, F. (2008). The Target for the Pseudomonas putida Crc Global Regulator in the Benzoate Degradation Pathway Is the BenR Transcriptional Regulator. J. Bacteriol. 190: 1539-1545 [Abstract] [Full Text]  
  • Arndt, A., Eikmanns, B. J. (2007). The Alcohol Dehydrogenase Gene adhA in Corynebacterium glutamicum Is Subject to Carbon Catabolite Repression. J. Bacteriol. 189: 7408-7416 [Abstract] [Full Text]  
  • Matthews, A., Grimaldi, A., Walker, M., Bartowsky, E., Grbin, P., Jiranek, V. (2004). Lactic Acid Bacteria as a Potential Source of Enzymes for Use in Vinification. Appl. Environ. Microbiol. 70: 5715-5731 [Full Text]  
  • Martinez-Perez, O., Moreno-Ruiz, E., Floriano, B., Santero, E. (2004). Regulation of Tetralin Biodegradation and Identification of Genes Essential for Expression of thn Operons. J. Bacteriol. 186: 6101-6109 [Abstract] [Full Text]  
  • Barragan, M. J. L., Carmona, M., Zamarro, M. T., Thiele, B., Boll, M., Fuchs, G., Garcia, J. L., Diaz, E. (2004). The bzd Gene Cluster, Coding for Anaerobic Benzoate Catabolism, in Azoarcus sp. Strain CIB. J. Bacteriol. 186: 5762-5774 [Abstract] [Full Text]  
  • Ayala-del-Rio, H. L., Callister, S. J., Criddle, C. S., Tiedje, J. M. (2004). Correspondence between Community Structure and Function during Succession in Phenol- and Phenol-plus-Trichloroethene-Fed Sequencing Batch Reactors. Appl. Environ. Microbiol. 70: 4950-4960 [Abstract] [Full Text]  
  • Brzostowicz, P. C., Reams, A. B., Clark, T. J., Neidle, E. L. (2003). Transcriptional Cross-Regulation of the Catechol and Protocatechuate Branches of the {beta}-Ketoadipate Pathway Contributes to Carbon Source-Dependent Expression of the Acinetobacter sp. Strain ADP1 pobA Gene. Appl. Environ. Microbiol. 69: 1598-1606 [Abstract] [Full Text]  
  • Sze, C. C., Bernardo, L. M. D., Shingler, V. (2002). Integration of Global Regulation of Two Aromatic-Responsive {sigma}54-Dependent Systems: a Common Phenotype by Different Mechanisms. J. Bacteriol. 184: 760-770 [Abstract] [Full Text]  
  • Ayoubi, P. J., Harker, A. R. (1998). Whole-Cell Kinetics of Trichloroethylene Degradation by Phenol Hydroxylase in a Ralstonia eutropha JMP134 Derivative. Appl. Environ. Microbiol. 64: 4353-4356 [Abstract] [Full Text]