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 Zeng, X.
Right arrow Articles by Switzer, R. L.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Zeng, X.
Right arrow Articles by Switzer, R. L.

 Previous Article  |  Next Article 

Journal of Bacteriology, April 2000, p. 1916-1922, Vol. 182, No. 7
0021-9193/00/$04.00+0
Copyright © 2000, American Society for Microbiology. All rights reserved.

Purification and Characterization of the DeoR Repressor of Bacillus subtilis

Xianmin Zeng,1 Hans H. Saxild,1,* and Robert L. Switzer2

Department of Microbiology, Technical University of Denmark, DK-2800 Lyngby, Denmark,1 and Department of Biochemistry, University of Illinois, Urbana, Illinois2

Received 24 September 1999/Accepted 13 December 1999

Transcription of the Bacillus subtilis dra-nupC-pdp operon is repressed by the DeoR repressor protein. The DeoR repressor with an N-terminal His tag was overproduced with a plasmid under control of a phage T5 promoter in Escherichia coli and was purified to near homogeneity by one affinity chromatography step. Gel filtration experimental results showed that native DeoR has a mass of 280 kDa and appears to exist as an octamer. Binding of DeoR to the operator DNA of the dra-nupC-pdp operon was characterized by using an electrophoretic gel mobility shift assay. An apparent dissociation constant of 22 nM was determined for binding of DeoR to operator DNA, and the binding curve indicated that the binding of DeoR to the operator DNA was cooperative. In the presence of low-molecular-weight effector deoxyribose-5-phosphate, the dissociation constant was higher than 1,280 nM. The dissociation constant remained unchanged in the presence of deoxyribose-1-phosphate. DNase I footprinting exhibited a protected region that extends over more than 43 bp, covering a palindrome together with a direct repeat to one half of the palindrome and the nucleotides between them.


* Corresponding author. Mailing address: Department of Microbiology, Technical University of Denmark, Building 301, DK-2800 Lyngby, Denmark. Phone: 45 25 24 95. Fax: 45 88 26 60. E-mail: imhhs{at}pop.dtu.dk.


Journal of Bacteriology, April 2000, p. 1916-1922, Vol. 182, No. 7
0021-9193/00/$04.00+0
Copyright © 2000, American Society for Microbiology. All rights reserved.



This article has been cited by other articles:

  • Dietrich, C., Nato, A., Bost, B., Le Marechal, P., Guyonvarch, A. (2009). Regulation of ldh expression during biotin-limited growth of Corynebacterium glutamicum. Microbiology 155: 1360-1375 [Abstract] [Full Text]  
  • Bai, G., Gazdik, M. A., Schaak, D. D., McDonough, K. A. (2007). The Mycobacterium bovis BCG Cyclic AMP Receptor-Like Protein Is a Functional DNA Binding Protein In Vitro and In Vivo, but Its Activity Differs from That of Its M. tuberculosis Ortholog, Rv3676. Infect. Immun. 75: 5509-5517 [Abstract] [Full Text]  
  • Engels, V., Wendisch, V. F. (2007). The DeoR-Type Regulator SugR Represses Expression of ptsG in Corynebacterium glutamicum. J. Bacteriol. 189: 2955-2966 [Abstract] [Full Text]  
  • Martin, M. G., Magni, C., de Mendoza, D., Lopez, P. (2005). CitI, a Transcription Factor Involved in Regulation of Citrate Metabolism in Lactic Acid Bacteria. J. Bacteriol. 187: 5146-5155 [Abstract] [Full Text]  
  • Arias-Barrau, E., Olivera, E. R., Luengo, J. M., Fernandez, C., Galan, B., Garcia, J. L., Diaz, E., Minambres, B. (2004). The Homogentisate Pathway: a Central Catabolic Pathway Involved in the Degradation of L-Phenylalanine, L-Tyrosine, and 3-Hydroxyphenylacetate in Pseudomonas putida. J. Bacteriol. 186: 5062-5077 [Abstract] [Full Text]  
  • Lopez-Rubio, J. J., Padmanabhan, S., Lazaro, J. M., Salas, M., Murillo, F. J., Elias-Arnanz, M. (2004). Operator Design and Mechanism for CarA Repressor-mediated Down-regulation of the Photoinducible carB Operon in Myxococcus xanthus. J. Biol. Chem. 279: 28945-28953 [Abstract] [Full Text]  
  • Chhabra, S. R., Shockley, K. R., Conners, S. B., Scott, K. L., Wolfinger, R. D., Kelly, R. M. (2003). Carbohydrate-induced Differential Gene Expression Patterns in the Hyperthermophilic Bacterium Thermotoga maritima. J. Biol. Chem. 278: 7540-7552 [Abstract] [Full Text]  
  • Yebra, M. J., Perez-Martinez, G. (2002). Cross-talk between the L-sorbose and D-sorbitol (D-glucitol) metabolic pathways in Lactobacillus casei. Microbiology 148: 2351-2359 [Abstract] [Full Text]  
  • Popp, R., Kohl, T., Patz, P., Trautwein, G., Gerischer, U. (2002). Differential DNA Binding of Transcriptional Regulator PcaU from Acinetobacter sp. Strain ADP1. J. Bacteriol. 184: 1988-1997 [Abstract] [Full Text]  
  • Lopez-Rubio, J. J., Elias-Arnanz, M., Padmanabhan, S., Murillo, F. J. (2002). A Repressor-Antirepressor Pair Links Two Loci Controlling Light-induced Carotenogenesis in Myxococcus xanthus. J. Biol. Chem. 277: 7262-7270 [Abstract] [Full Text]  
  • Zeng, X., Galinier, A., Saxild, H. H. (2000). Catabolite repression of dra-nupC-pdp operon expression in Bacillus subtilis. Microbiology 146: 2901-2908 [Abstract] [Full Text]