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K Regulates Bacteroid-associated Functions of Bradyrhizobium

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Specialty Science
Date 1987 Jul 1
PMID 16593858
Citations 7
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Abstract

Cowpea Bradyrhizobium 32H1 cells, when grown under 0.2% O(2), synthesize nitrogenase, as well as a methylammonium (ammonium) transport system and an electrogenic K(+)/H(+) antiporter. This effect was seen in growth medium containing 8-12 mM K(+) but not with 50 muM K(+). Addition of K(+) to cells growing under low O(2) tensions in low-K(+) medium led to various phenotypic properties associated with bacteroids, including the ability to reduce acetylene, induction of an ammonium transport carrier and the K(+)/H(+) antiporter, and increased synthesis of two heme-biosynthetic enzymes, delta-aminolevulinate synthase and delta-aminolevulinate dehydratase. K(+) addition caused the repression of glutamine synthetase and of capsular polysaccharide synthesis, functions related to the free-living state. A similar pattern of regulation was observed in Bradyrhizobium japonicum. In addition, K(+)-mediated depression in Bradyrhizobium 32H1 was inhibited by exudate of Vigna unguiculata, its host plant. We conclude that K(+) ions, in addition to low O(2) tension, are needed for the expression of several bacteroid-related functions in bradyrhizobia and thus are a major controlling influence in bacteroid development.

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References
1.
Tully R, Terry M . Decreased Exopolysaccharide Synthesis by Anaerobic and Symbiotic Cells of Bradyrhizobium japonicum. Plant Physiol. 1985; 79(2):445-50. PMC: 1074905. DOI: 10.1104/pp.79.2.445. View

2.
Ludwig R . Regulation of Rhizobium nitrogen fixation by the unadenylylated glutamine synthetase I system. Proc Natl Acad Sci U S A. 1980; 77(10):5817-21. PMC: 350162. DOI: 10.1073/pnas.77.10.5817. View

3.
Mort A, Bauer W . Composition of the Capsular and Extracellular Polysaccharides of Rhizobium japonicum: CHANGES WITH CULTURE AGE AND CORRELATIONS WITH BINDING OF SOYBEAN SEED LECTIN TO THE BACTERIA . Plant Physiol. 1980; 66(1):158-63. PMC: 440550. DOI: 10.1104/pp.66.1.158. View

4.
Nadler K, Avissar Y . Heme Synthesis in Soybean Root Nodules: I. On the Role of Bacteroid delta-Aminolevulinic Acid Synthase and delta-Aminolevulinic Acid Dehydrase in the Synthesis of the Heme of Leghemoglobin. Plant Physiol. 1977; 60(3):433-6. PMC: 542631. DOI: 10.1104/pp.60.3.433. View

5.
Shearman C, Rossen L, Johnston A, Downie J . The Rhizobium leguminosarum nodulation gene nodF encodes a polypeptide similar to acyl-carrier protein and is regulated by nodD plus a factor in pea root exudate. EMBO J. 1986; 5(4):647-52. PMC: 1166839. DOI: 10.1002/j.1460-2075.1986.tb04262.x. View