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 Brewin, B.
Right arrow Articles by Drummond, M.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Brewin, B.
Right arrow Articles by Drummond, M.

 Previous Article  |  Next Article 

Journal of Bacteriology, December 1999, p. 7356-7362, Vol. 181, No. 23
0021-9193/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.

The Basis of Ammonium Release in nifL Mutants of Azotobacter vinelandii

Brett Brewin,dagger Paul Woodley, and Martin Drummond*

Department of Molecular Microbiology, John Innes Centre, Norwich NR4 7UH, United Kingdom

Received 30 June 1999/Accepted 1 September 1999

In Azotobacter vinelandii, nitrogen fixation is regulated at the transcriptional level by an unusual two-component system encoded by nifLA. Certain mutations in nifL result in the bacterium releasing large quantities of ammonium into the medium, and earlier work suggested that this occurs by a mechanism that does not involve NifA, the activator of nif gene transcription. We have investigated a number of possible alternative mechanisms and find no evidence for their involvement in ammonium release. Enhancement of NifA-mediated transcription, on the other hand, by either elimination of nifL or overexpression of nifA, resulted in ammonium release, correlating with enhanced levels of nifH mRNA, raised levels of nitrogenase and acetylene-reducing activity, and increased concentrations of intracellular ammonium. Up to 35 mM ammonium can accumulate in the medium. Where measured, intracellular levels exceeded extracellular levels, indicating that rather than being actively transported, ammonium is lost from the cell passively, possibly by reversal of an NH4+ uptake system. The data also indicate that in the wild type the bulk of NifA is inactivated by NifL during steady-state growth on dinitrogen.


* Corresponding author. Mailing address: Department of Molecular Microbiology, John Innes Centre, Norwich NR4 7UH, United Kingdom. Phone: 44-(0)-1603-452571. Fax: 44-(0)-1603-454970. E-mail: martin.drummond{at}bbsrc.ac.uk.

dagger Present address: Genera Technologies, Newmarket CB8 7NY, United Kingdom.


Journal of Bacteriology, December 1999, p. 7356-7362, Vol. 181, No. 23
0021-9193/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.



This article has been cited by other articles:

  • Mirbod-Donovan, F., Schaller, R., Hung, C.-Y., Xue, J., Reichard, U., Cole, G. T. (2006). Urease Produced by Coccidioides posadasii Contributes to the Virulence of This Respiratory Pathogen. Infect. Immun. 74: 504-515 [Abstract] [Full Text]  
  • Mitra, R., Das, H. K., Dixit, A. (2005). Identification of a Positive Transcription Regulatory Element within the Coding Region of the nifLA Operon in Azotobacter vinelandii. Appl. Environ. Microbiol. 71: 3716-3724 [Abstract] [Full Text]  
  • Martinez-Argudo, I., Little, R., Dixon, R. (2004). A crucial arginine residue is required for a conformational switch in NifL to regulate nitrogen fixation in Azotobacter vinelandii. Proc. Natl. Acad. Sci. USA 101: 16316-16321 [Abstract] [Full Text]