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 Darwin, A. J.
Right arrow Articles by Stewart, V.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Darwin, A. J.
Right arrow Articles by Stewart, V.

 Previous Article  |  Next Article 

Journal of Bacteriology, August 1998, p. 4192-4198, Vol. 180, No. 16
0021-9193/98/$04.00+0
Copyright © 1998, American Society for Microbiology. All rights reserved.

Fnr, NarP, and NarL Regulation of Escherichia coli K-12 napF (Periplasmic Nitrate Reductase) Operon Transcription In Vitro

Andrew J. Darwin,1,dagger Eva C. Ziegelhoffer,2,Dagger Patricia J. Kiley,3 and Valley Stewart1,*

Section of Microbiology, Cornell University, Ithaca, New York 14853,1 and Departments of Bacteriology2 and Biomolecular Chemistry,3 University of Wisconsin, Madison, Wisconsin 53706

Received 16 March 1998/Accepted 17 June 1998

The expression of several Escherichia coli operons is activated by the Fnr protein during anaerobic growth and is further controlled in response to nitrate and nitrite by the homologous response regulators, NarL and NarP. Among these operons, the napF operon, encoding a periplasmic nitrate reductase, has unique features with respect to its Fnr-, NarL-, and NarP-dependent regulation. First, the Fnr-binding site is unusually located compared to the control regions of most other Fnr-activated operons, suggesting different Fnr-RNA polymerase contacts during transcriptional activation. Second, nitrate and nitrite activation is solely dependent on NarP but is antagonized by the NarL protein. In this study, we used DNase I footprint analysis to confirm our previous assignment of the unusual location of the Fnr-binding site in the napF control region. In addition, the in vivo effects of Fnr-positive control mutations on napF operon expression indicate that the napF promoter is atypical with respect to Fnr-mediated activation. The transcriptional regulation of napF was successfully reproduced in vitro by using a supercoiled plasmid template and purified Fnr, NarL, and NarP proteins. These in vitro transcription experiments demonstrate that, in the presence of Fnr, the NarP protein causes efficient transcription activation whereas the NarL protein does not. This suggests that Fnr and NarP may act synergistically to activate napF operon expression. As observed in vivo, this activation by Fnr and NarP is antagonized by the addition of NarL in vitro.


* Corresponding author. Present address: Section of Microbiology, University of California, 156 Hutchison Hall, One Shields Ave., Davis, CA 95616-8665. Phone: (530) 754-7994. Fax: (530) 752-9014. E-mail: vjstewart{at}ucdavis.edu.

dagger Present address: Department of Molecular Microbiology, Washington University School of Medicine, St. Louis, MO 63110-1093.

Dagger Present address: Division of Biology 156-29, California Institute of Technology, Pasadena, CA 91125.


Journal of Bacteriology, August 1998, p. 4192-4198, Vol. 180, No. 16
0021-9193/98/$04.00+0
Copyright © 1998, American Society for Microbiology. All rights reserved.



This article has been cited by other articles:

  • Stewart, V., Bledsoe, P. J., Chen, L.-L., Cai, A. (2009). Catabolite Repression Control of napF (Periplasmic Nitrate Reductase) Operon Expression in Escherichia coli K-12. J. Bacteriol. 191: 996-1005 [Abstract] [Full Text]  
  • Lin, H.-Y., Bledsoe, P. J., Stewart, V. (2007). Activation of yeaR-yoaG Operon Transcription by the Nitrate-Responsive Regulator NarL Is Independent of Oxygen- Responsive Regulator Fnr in Escherichia coli K-12. J. Bacteriol. 189: 7539-7548 [Abstract] [Full Text]  
  • Van Alst, N. E., Picardo, K. F., Iglewski, B. H., Haidaris, C. G. (2007). Nitrate Sensing and Metabolism Modulate Motility, Biofilm Formation, and Virulence in Pseudomonas aeruginosa. Infect. Immun. 75: 3780-3790 [Abstract] [Full Text]  
  • Filenko, N., Spiro, S., Browning, D. F., Squire, D., Overton, T. W., Cole, J., Constantinidou, C. (2007). The NsrR Regulon of Escherichia coli K-12 Includes Genes Encoding the Hybrid Cluster Protein and the Periplasmic, Respiratory Nitrite Reductase. J. Bacteriol. 189: 4410-4417 [Abstract] [Full Text]  
  • Ando, H., Abe, H., Sugimoto, N., Tobe, T. (2007). Maturation of functional type III secretion machinery by activation of anaerobic respiration in enterohaemorrhagic Escherichia coli. Microbiology 153: 464-473 [Abstract] [Full Text]  
  • Seib, K. L., Wu, H.-J., Kidd, S. P., Apicella, M. A., Jennings, M. P., McEwan, A. G. (2006). Defenses against Oxidative Stress in Neisseria gonorrhoeae: a System Tailored for a Challenging Environment. Microbiol. Mol. Biol. Rev. 70: 344-361 [Abstract] [Full Text]  
  • Constantinidou, C., Hobman, J. L., Griffiths, L., Patel, M. D., Penn, C. W., Cole, J. A., Overton, T. W. (2006). A Reassessment of the FNR Regulon and Transcriptomic Analysis of the Effects of Nitrate, Nitrite, NarXL, and NarQP as Escherichia coli K12 Adapts from Aerobic to Anaerobic Growth. J. Biol. Chem. 281: 4802-4815 [Abstract] [Full Text]  
  • Stewart, V., Bledsoe, P. J. (2005). Fnr-, NarP- and NarL-Dependent Regulation of Transcription Initiation from the Haemophilus influenzae Rd napF (Periplasmic Nitrate Reductase) Promoter in Escherichia coli K-12. J. Bacteriol. 187: 6928-6935 [Abstract] [Full Text]  
  • Delgado, M. J., Bonnard, N., Tresierra-Ayala, A., Bedmar, E. J., Muller, P. (2003). The Bradyrhizobium japonicum napEDABC genes encoding the periplasmic nitrate reductase are essential for nitrate respiration. Microbiology 149: 3395-3403 [Abstract] [Full Text]  
  • Gutierrez-Rios, R. M., Rosenblueth, D. A., Loza, J. A., Huerta, A. M., Glasner, J. D., Blattner, F. R., Collado-Vides, J. (2003). Regulatory Network of Escherichia coli: Consistency Between Literature Knowledge and Microarray Profiles. Genome Res 13: 2435-2443 [Abstract] [Full Text]  
  • Stewart, V., Bledsoe, P. J., Williams, S. B. (2003). Dual Overlapping Promoters Control napF (Periplasmic Nitrate Reductase) Operon Expression in Escherichia coli K-12. J. Bacteriol. 185: 5862-5870 [Abstract] [Full Text]  
  • Ellington, M. J. K., Sawers, G., Sears, H. J., Spiro, S., Richardson, D. J., Ferguson, S. J. (2003). Characterization of the expression and activity of the periplasmic nitrate reductase of Paracoccus pantotrophus in chemostat cultures. Microbiology 149: 1533-1540 [Abstract] [Full Text]  
  • Stewart, V., Bledsoe, P. J. (2003). Synthetic lac Operator Substitutions for Studying the Nitrate- and Nitrite-Responsive NarX-NarL and NarQ-NarP Two-Component Regulatory Systems of Escherichia coli K-12. J. Bacteriol. 185: 2104-2111 [Abstract] [Full Text]  
  • Ellington, M. J. K., Richardson, D. J., Ferguson, S. J. (2003). Rhodobacter capsulatus gains a competitive advantage from respiratory nitrate reduction during light-dark transitions. Microbiology 149: 941-948 [Abstract] [Full Text]  
  • Pruss, B. M., Campbell, J. W., Van Dyk, T. K., Zhu, C., Kogan, Y., Matsumura, P. (2003). FlhD/FlhC Is a Regulator of Anaerobic Respiration and the Entner-Doudoroff Pathway through Induction of the Methyl-Accepting Chemotaxis Protein Aer. J. Bacteriol. 185: 534-543 [Abstract] [Full Text]  
  • Gavira, M., Roldan, M. D., Castillo, F., Moreno-Vivian, C. (2002). Regulation of nap Gene Expression and Periplasmic Nitrate Reductase Activity in the Phototrophic Bacterium Rhodobacter sphaeroides DSM158. J. Bacteriol. 184: 1693-1702 [Abstract] [Full Text]  
  • Stewart, V., Lu, Y., Darwin, A. J. (2002). Periplasmic Nitrate Reductase (NapABC Enzyme) Supports Anaerobic Respiration by Escherichia coli K-12. J. Bacteriol. 184: 1314-1323 [Abstract] [Full Text]  
  • Koretke, K. K., Lupas, A. N., Warren, P. V., Rosenberg, M., Brown, J. R. (2000). Evolution of Two-Component Signal Transduction. Mol Biol Evol 17: 1956-1970 [Abstract] [Full Text]  
  • Happe, T., Schütz, K., Böhme, H. (2000). Transcriptional and Mutational Analysis of the Uptake Hydrogenase of the Filamentous Cyanobacterium Anabaena variabilis ATCC 29413. J. Bacteriol. 182: 1624-1631 [Abstract] [Full Text]  
  • Richard, D. J., Sawers, G., Sargent, F., McWalter, L., Boxer, D. H. (1999). Transcriptional regulation in response to oxygen and nitrate of the operons encoding the [NiFe] hydrogenases 1 and 2 of Escherichia coli. Microbiology 145: 2903-2912 [Abstract] [Full Text]