Excretion of ammonium by a nifL mutant of Azotobacter vinelandii fixing nitrogen

Author:

Bali A1,Blanco G1,Hill S1,Kennedy C1

Affiliation:

1. Nitrogen Fixation Laboratory, University of Sussex, Brighton, United Kingdom.

Abstract

A mutation in the gene upstream of nifA in Azotobacter vinelandii was introduced into the chromosome to replace the corresponding wild-type region. The resulting mutant, MV376, produced nitrogenase constitutively in the presence of 15 mM ammonium. When introduced into a nifH-lacZ fusion strain, the mutation permitted beta-galactosidase production in the presence of ammonium. The gene upstream of nifA is therefore designated nifL because of its similarity to the Klebsiella pneumoniae nifL gene in proximity to nifA, in mutant phenotype, and in amino acid sequence of the gene product. The A. vinelandii nifL mutant MV376 excreted significant quantities of ammonium (approximately 10 mM) during diazotrophic growth. In contrast, ammonium excretion during diazotrophy was much lower in a K. pneumoniae nifL deletion mutant (maximum, 0.15 mM) but significantly higher than in NifL+ K. pneumoniae. The expression of the A. vinelandii nifA gene, unlike that of K. pneumoniae, was not repressed by ammonium.

Publisher

American Society for Microbiology

Subject

Ecology,Applied Microbiology and Biotechnology,Food Science,Biotechnology

Reference49 articles.

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3. Bergersen F. J. 1980. Methods for evaluating biological nitrogen fixation. John Wiley & Sons Ltd. London.

4. Genetic analysis of Azotobacter vinelandii mutant strains unable to fix nitrogen;Bishop P. E.;J. Bacteriol.,1977

5. Genetics and molecular biology of alternative nitrogen fixation systems. Annu;Bishop P. E.;Rev. Plant Physiol. Plant Mol. Biol.,1990

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