Alanine, not ammonia, is excreted from N 2 -fixing soybean nodule bacteroids

Symbiotic nitrogen fixation, the process whereby nitrogen-fixing bacteria enter into associations with plants, provides the major source of nitrogen for the biosphere. Nitrogenase, a bacterial enzyme, catalyzes the reduction of atmospheric dinitrogen to ammonium. In rhizobia-leguminous plant symbios...

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Veröffentlicht in:Proceedings of the National Academy of Sciences - PNAS 1998-09, Vol.95 (20), p.12038-12042
Hauptverfasser: Waters, James K., Hughes, Bobby L., Purcell, Larry C., Gerhardt, Klaus O., Mawhinney, Thomas P., Emerich, David W.
Format: Artikel
Sprache:eng
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Zusammenfassung:Symbiotic nitrogen fixation, the process whereby nitrogen-fixing bacteria enter into associations with plants, provides the major source of nitrogen for the biosphere. Nitrogenase, a bacterial enzyme, catalyzes the reduction of atmospheric dinitrogen to ammonium. In rhizobia-leguminous plant symbioses, the current model of nitrogen transfer from the symbiotic form of the bacteria, called a bacteroid, to the plant is that nitrogenase-generated ammonia diffuses across the bacteroid membrane and is assimilated into amino acids outside of the bacteroid. We purified soybean nodule bacteroids by a procedure that removed contaminating plant proteins and found that alanine was the major nitrogen-containing compound excreted. Bacteroids incubated in the presence of 15 N 2 excreted alanine highly enriched in 15 N. The ammonium in these assays neither accumulated significantly nor was enriched in 15 N. The results demonstrate that a transport mechanism rather than diffusion functions at this critical step of nitrogen transfer from the bacteroids to the plant host. Alanine may serve only as a transport species, but this would permit physiological separation of the transport of fixed nitrogen from other nitrogen metabolic functions commonly mediated through glutamate.
ISSN:0027-8424
1091-6490
DOI:10.1073/pnas.95.20.12038