AEM
Home Help [Feedback] [For Subscribers] [Archive] [Search] [Contents]
This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Other Versions of this Article:
AEM.01067-06v1
72/11/7418    most recent
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 Aranda-Olmedo, I.
Right arrow Articles by Marqués, S.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Aranda-Olmedo, I.
Right arrow Articles by Marqués, S.
Agricola
Right arrow Articles by Aranda-Olmedo, I.
Right arrow Articles by Marqués, S.
Applied and Environmental Microbiology, November 2006, p. 7418-7421, Vol. 72, No. 11
0099-2240/06/$08.00+0     doi:10.1128/AEM.01067-06
Copyright © 2006, American Society for Microbiology. All Rights Reserved.

SHORT REPORT

Role of the ptsN Gene Product in Catabolite Repression of the Pseudomonas putida TOL Toluene Degradation Pathway in Chemostat Cultures{triangledown}

Isabel Aranda-Olmedo, Patricia Marín, Juan L. Ramos, and Silvia Marqués*

Consejo Superior de Investigaciones Científicas, Estación Experimental del Zaidín, Dept. of Environmental Protection, C/. Profesor Albareda no. 1, Granada E-18008, Spain

Received 9 May 2005/ Accepted 8 August 2006

The Pseudomonas putida KT2440 TOL upper pathway is repressed under nonlimiting conditions in cells growing in chemostat with succinate as a carbon source. We show that the ptsN gene product IIANtr participates in this repression. Crc, involved in yeast extract-dependent repression in batch cultures, did not influence expression when cells were growing in a chemostat with succinate at maximum rate.

* Corresponding author. Mailing address: Consejo Superior de Investigaciones Científicas, Estación Experimental del Zaidín, Dept. of Environmental Protection, C/. Profesor Albareda no. 1, Granada E-18008, Spain. Phone: 34 958 181600, ext. 285. Fax: 34 958 135740. E-mail: silvia.marques{at}eez.csic.es.

{triangledown} Published ahead of print on 22 September 2006.

Applied and Environmental Microbiology, November 2006, p. 7418-7421, Vol. 72, No. 11
0099-2240/06/$08.00+0     doi:10.1128/AEM.01067-06
Copyright © 2006, American Society for Microbiology. All Rights Reserved.



This article has been cited by other articles:



Home Help [Feedback] [For Subscribers] [Archive] [Search] [Contents]
J. Bacteriol. Microbiol. Mol. Biol. Rev. Eukaryot. Cell All ASM Journals

Copyright © 2006 by the American Society for Microbiology. All rights reserved.