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]