This Article
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 Geanacopoulos, M.
Right arrow Articles by Adhya, S.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Geanacopoulos, M.
Right arrow Articles by Adhya, S.

 Previous Article  |  Next Article 

J. Bacteriol., Jan 1997, 228-234, Vol 179, No. 1
Copyright © 1997, American Society for Microbiology

Functional characterization of roles of GalR and GalS as regulators of the gal regulon

M Geanacopoulos and S Adhya
Laboratory of Molecular Biology, National Cancer Institute, National Institutes of Health, Bethesda, Maryland 20892-4255, USA.

An isorepressor of the gal regulon in Escherichia coli, GalS, has been purified to homogeneity. In vitro DNase I protection experiments indicated that among operators of the gal regulon, GalS binds most strongly to the external operator of the mgl operon, which encodes the high-affinity beta-methylgalactoside galactose transport system, and with less affinity to the operators controlling expression of the gal operon, which codes for enzymes of galactose metabolism. GalS has even less affinity for the external operator of galP, which codes for galactose permease, the major low-affinity galactose transporter in the cell. This order of affinities is the reverse of that of GalR, which binds most strongly to the operator of galP and most weakly to that of mgl. Our results also show that GalS, like its homolog, GalR, is a dimeric protein which in binding to the bipartite operators of the gal operon selectively represses its P1 promoter. Consistent with the fact that GalR is the exclusive regulator of the low-affinity galactose transporter, galactose permease, and that the major role of GalS is in regulating expression of the high-affinity galactose transporter encoded by the mgl operon, we found that the DNA binding of GalS is 15- fold more sensitive than that of GalR to galactose.


This article has been cited by other articles:

  • Semsey, S., Krishna, S., Erdossy, J., Horvath, P., Orosz, L., Sneppen, K., Adhya, S. (2009). Dominant Negative Autoregulation Limits Steady-State Repression Levels in Gene Networks. J. Bacteriol. 191: 4487-4491 [Abstract] [Full Text]  
  • Desai, T. A., Rodionov, D. A., Gelfand, M. S., Alm, E. J., Rao, C. V. (2009). Engineering transcription factors with novel DNA-binding specificity using comparative genomics. Nucleic Acids Res 37: 2493-2503 [Abstract] [Full Text]  
  • El Qaidi, S., Plumbridge, J. (2008). Switching Control of Expression of ptsG from the Mlc Regulon to the NagC Regulon. J. Bacteriol. 190: 4677-4686 [Abstract] [Full Text]  
  • Kolesov, G., Wunderlich, Z., Laikova, O. N., Gelfand, M. S., Mirny, L. A. (2007). How gene order is influenced by the biophysics of transcription regulation. Proc. Natl. Acad. Sci. USA 104: 13948-13953 [Abstract] [Full Text]  
  • Liu, M., Tolstorukov, M., Zhurkin, V., Garges, S., Adhya, S. (2004). A mutant spacer sequence between -35 and -10 elements makes the Plac promoter hyperactive and cAMP receptor protein-independent. Proc. Natl. Acad. Sci. USA 101: 6911-6916 [Abstract] [Full Text]  
  • Soupene, E., van Heeswijk, W. C., Plumbridge, J., Stewart, V., Bertenthal, D., Lee, H., Prasad, G., Paliy, O., Charernnoppakul, P., Kustu, S. (2003). Physiological Studies of Escherichia coli Strain MG1655: Growth Defects and Apparent Cross-Regulation of Gene Expression. J. Bacteriol. 185: 5611-5626 [Abstract] [Full Text]  
  • Plumbridge, J. (2001). DNA binding sites for the Mlc and NagC proteins: regulation of nagE, encoding the N-acetylglucosamine-specific transporter in Escherichia coli. Nucleic Acids Res 29: 506-514 [Abstract] [Full Text]  
  • Geanacopoulos, M., Vasmatzis, G., Lewis, D. E.A., Roy, S., Lee, B., Adhya, S. (1999). GalR mutants defective in repressosome formation. Genes Dev. 13: 1251-1262 [Abstract] [Full Text]  
  • Berlyn, M. K. B. (1998). Linkage Map of Escherichia coli K-12, Edition 10: The Traditional Map. Microbiol. Mol. Biol. Rev. 62: 814-984 [Abstract] [Full Text]  
  • Nieto, C., Espinosa, M., Puyet, A. (1997). The Maltose/Maltodextrin Regulon of Streptococcus pneumoniae. DIFFERENTIAL PROMOTER REGULATION BY THE TRANSCRIPTIONAL REPRESSOR MalR. J. Biol. Chem. 272: 30860-30865 [Abstract] [Full Text]