|
|
||||||||
Plant-Microbe Interactions |
Centro de Investigación sobre Fijación de Nitrógeno, Programa de Ingeniería Metabólica, Universidad Nacional Autónoma de México, AP 565-A, Cuernavaca, Morelos, 62271, Mexico1
Author for correspondence: Jaime Mora. Tel: +52 7 3139944. Fax: +52 7 3175094. e-mail: jmora{at}cifn.unam.mx
The isolation and characterization of a Rhizobium etli glutamate auxotroph, TAD12, harbouring a single Tn5 insertion, is reported. This mutant produced no detectable glutamate synthase (GOGAT) activity. The cloning and physical characterization of a 7·2 kb fragment of R. etli DNA harbouring the structural genes gltB and gltD encoding the two GOGAT subunits GltB and GltD is also reported. In comparison with the wild-type strain (CFN42), the GOGAT mutant strain utilized less succinate and glutamate and grew less with this and other amino acids as nitrogen source. R. etli assimilates ammonium by the glutamine synthetase (GS)-GOGAT pathway and a GOGAT mutant prevents the cycling of glutamine by this pathway, something that impairs nitrogen and carbon metabolism and explains the decrease in the amino-nitrogen during exponential growth, with glutamate as nitrogen source. GOGAT activity also has a role in ammonium turnover and in the synthesis of amino acids and proteins, processes that are necessary to sustain cell viability in non-growing conditions. The assimilation of ammonium is important during symbiosis and glutamate constitutes 2040% of the total amino-nitrogen. In symbiosis, the blockage of ammonium assimilation by a GOGAT mutation significantly decreases the amino-nitrogen pool of the bacteroids and may explain why more N2 is fixed in ammonium, excreted to the plant cell, transported to the leaves and stored in the seeds.
Keywords: nitrogen assimilation, carbon metabolism, glutamine turnover, nitrogen fixation, glutamate auxotroph
Abbreviations: GDH, glutamate dehydrogenase; GOGAT, glutamate synthase; GS, glutamine synthetase; MM, minimal media; MSO, methionine sulfone
The GenBank accession number for the sequence reported in this paper is AF107264.
a Present address: Instituto de Biotecnología, Departamento de Bioingeniería, Universidad Nacional Autónoma de México, AP 510-3, Cuernavaca, Morelos, 62250, Mexico.
This article has been cited by other articles:
![]() |
E. J. Patriarca, R. Tate, and M. Iaccarino Key Role of Bacterial NH4+ Metabolism in Rhizobium-Plant Symbiosis Microbiol. Mol. Biol. Rev., June 1, 2002; 66(2): 203 - 222. [Abstract] [Full Text] [PDF] |
||||
| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |
| INT J SYST EVOL MICROBIOL | MICROBIOLOGY | J GEN VIROL |
| J MED MICROBIOL | ALL SGM JOURNALS | |