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 Peekhaus, N.
Right arrow Articles by Conway, T.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Peekhaus, N.
Right arrow Articles by Conway, T.

 Previous Article  |  Next Article 

J Bacteriol, April 1998, p. 1777-1785, Vol. 180, No. 7
0021-9193/98/$04.00+0
Copyright © 1998, American Society for Microbiology. All rights reserved.

Positive and Negative Transcriptional Regulation of the Escherichia coli Gluconate Regulon Gene gntT by GntR and the Cyclic AMP (cAMP)-cAMP Receptor Protein Complex

Norbert Peekhaus* and T. Conway

Department of Microbiology, The Ohio State University, Columbus, Ohio 43210-1292

Received 1 December 1997/Accepted 26 January 1998

The gntT gene of Escherichia coli is specifically induced by gluconate and repressed via catabolite repression. Thus, gluconate is both an inducer and a repressor of gntT expression since gluconate is a catabolite-repressing sugar. In a gntR deletion mutant, the expression of a chromosomal gntT::lacZ fusion is both high and constitutive, confirming that GntR is the negative regulator of gntT. Indeed, GntR binds to two consensus gnt operator sites; one overlaps the -10 region of the gntT promoter, and the other is centered at +120 with respect to the transcriptional start site. The binding of GntR to these sites was proven in vitro by gel redardation assays and in vivo by site-directed mutagenesis of the binding sites. Binding of GntR to the operators is eliminated by gluconate and also by 6-phosphogluconate at a 10-fold-higher concentration. Interestingly, when gntR deletion strains are grown in the presence of gluconate, there is a twofold decrease in gntT expression which is independent of catabolite repression and binding of GntR to the operator sites. This novel response of gntR mutants to the inducer is termed ultrarepression. Transcription of gntT is activated by binding of the cyclic AMP (cAMP)-cAMP receptor protein (CRP) complex to a CRP binding site positioned at -71 upstream of the gntT transcription start site.


* Corresponding author. Mailing address: Department of Microbiology, 484 West 12th Ave., 376 BioSci, The Ohio State University, Columbus, OH 43210-1292. Phone: (614) 688-3520. Fax: (614) 292-8120. E-mail: peekhaus.1{at}osu.edu.




This article has been cited by other articles:

  • Aguilera, L., Campos, E., Gimenez, R., Badia, J., Aguilar, J., Baldoma, L. (2008). Dual Role of LldR in Regulation of the lldPRD Operon, Involved in L-Lactate Metabolism in Escherichia coli. J. Bacteriol. 190: 2997-3005 [Abstract] [Full Text]  
  • del Castillo, T., Duque, E., Ramos, J. L. (2008). A Set of Activators and Repressors Control Peripheral Glucose Pathways in Pseudomonas putida To Yield a Common Central Intermediate. J. Bacteriol. 190: 2331-2339 [Abstract] [Full Text]  
  • Cameron, A. D. S., Redfield, R. J. (2006). Non-canonical CRP sites control competence regulons in Escherichia coli and many other {gamma}-proteobacteria. Nucleic Acids Res 34: 6001-6014 [Abstract] [Full Text]  
  • Tsuge, S., Nakayama, T., Terashima, S., Ochiai, H., Furutani, A., Oku, T., Tsuno, K., Kubo, Y., Kaku, H. (2006). Gene Involved in Transcriptional Activation of the hrp Regulatory Gene hrpG in Xanthomonas oryzae pv. oryzae. J. Bacteriol. 188: 4158-4162 [Abstract] [Full Text]  
  • Letek, M., Valbuena, N., Ramos, A., Ordonez, E., Gil, J. A., Mateos, L. M. (2006). Characterization and Use of Catabolite-Repressed Promoters from Gluconate Genes in Corynebacterium glutamicum. J. Bacteriol. 188: 409-423 [Abstract] [Full Text]  
  • Fineran, P. C., Everson, L., Slater, H., Salmond, G. P. C. (2005). A GntR family transcriptional regulator (PigT) controls gluconate-mediated repression and defines a new, independent pathway for regulation of the tripyrrole antibiotic, prodigiosin, in Serratia. Microbiology 151: 3833-3845 [Abstract] [Full Text]  
  • Murray, E. L., Conway, T. (2005). Multiple Regulators Control Expression of the Entner-Doudoroff Aldolase (Eda) of Escherichia coli. J. Bacteriol. 187: 991-1000 [Abstract] [Full Text]  
  • Bates Utz, C., Nguyen, A. B., Smalley, D. J., Anderson, A. B., Conway, T. (2004). GntP Is the Escherichia coli Fructuronic Acid Transporter and Belongs to the UxuR Regulon. J. Bacteriol. 186: 7690-7696 [Abstract] [Full Text]  
  • Bausch, C., Ramsey, M., Conway, T. (2004). Transcriptional Organization and Regulation of the L-Idonic Acid Pathway (GntII System) in Escherichia coli. J. Bacteriol. 186: 1388-1397 [Abstract] [Full Text]  
  • Tsunedomi, R., Izu, H., Kawai, T., Matsushita, K., Ferenci, T., Yamada, M. (2003). The Activator of GntII Genes for Gluconate Metabolism, GntH, Exerts Negative Control of GntR-Regulated GntI Genes in Escherichia coli. J. Bacteriol. 185: 1783-1795 [Abstract] [Full Text]  
  • van Nimwegen, E., Zavolan, M., Rajewsky, N., Siggia, E. D. (2002). Probabilistic clustering of sequences: Inferring new bacterial regulons by comparative genomics. Proc. Natl. Acad. Sci. USA 99: 7323-7328 [Abstract] [Full Text]  
  • Mitsui, R., Sakai, Y., Yasueda, H., Kato, N. (2000). A Novel Operon Encoding Formaldehyde Fixation: the Ribulose Monophosphate Pathway in the Gram-Positive Facultative Methylotrophic Bacterium Mycobacterium gastri MB19. J. Bacteriol. 182: 944-948 [Abstract] [Full Text]  
  • Peekhaus, N., Conway, T. (1998). What's for Dinner?: Entner-Doudoroff Metabolism in Escherichia coli. J. Bacteriol. 180: 3495-3502 [Full Text]  
  • Bausch, C., Peekhaus, N., Utz, C., Blais, T., Murray, E., Lowary, T., Conway, T. (1998). Sequence Analysis of the GntII (Subsidiary) System for Gluconate Metabolism Reveals a Novel Pathway for L-Idonic Acid Catabolism in Escherichia coli. J. Bacteriol. 180: 3704-3710 [Abstract] [Full Text]