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Ammonium Uptake by Rice Roots (I. Fluxes and Subcellular Distribution of 13NH4+)

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Journal Plant Physiol
Specialty Physiology
Date 1993 Dec 1
PMID 12232017
Citations 37
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Abstract

The time course of 13NH4+ uptake and the distribution of 13NH4+ among plant parts and subcellular compartments was determined for 3-week-old rice (Oryza sativa L. cv M202) plants grown hydroponically in modified Johnson's nutrient solution containing 2,100, or 1000 [mu]M NH4+ (referred to hereafter as G2, G100, or G1000 plants, respectively). At steady state, the influx of 13NH4+ was determined to be 1.31, 5.78, and 10.11 [mu]mol g-1 fresh weight h-1, respectively, for G2, G100, and G1000 plants; efflux was 11, 20, and 29%, respectively, of influx. The NH4+ flux to the vacuole was calculated to be between 1 and 1.4 [mu]mol g-1 fresh weight h-1. By means of 13NH4+ efflux analysis, three kinetically distinct phases (superficial, cell wall, and cytoplasm) were identified, with t1/2 for 13NH4+ exchange of approximately 3 s and 1 and 8 min, respectively. Cytoplasmic [NH4+] was estimated to be 3.72, 20.55, and 38.08 mM for G2, G100, and G1000 plants, respectively. These concentrations were higher than vacuolar [NH4+], yet 72 to 92% of total root NH4+ was located in the vacuole. Distributions of newly absorbed 13NH4+ between plant parts and among the compartments were also examined. During a 30-min period G100 plants metabolized 19% of the influxed 13NH4+. The remainder (81%) was partitioned among the vacuole (20%), cytoplasm (41%), and efflux (20%). Of the metabolized 13N, roughly one-half was translocated to the shoots.

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References
1.
Breteler H, Nissen P . Effect of exogenous and endogenous nitrate concentration on nitrate utilization by dwarf bean. Plant Physiol. 1982; 70(3):754-9. PMC: 1065765. DOI: 10.1104/pp.70.3.754. View

2.
Lavoie N, Vezina L, Margolis H . Absorption and assimilation of nitrate and ammonium ions by jack pine seedlings. Tree Physiol. 1992; 11(2):171-83. DOI: 10.1093/treephys/11.2.171. View

3.
Roberts J, Pang M . Estimation of Ammonium Ion Distribution between Cytoplasm and Vacuole Using Nuclear Magnetic Resonance Spectroscopy. Plant Physiol. 1992; 100(3):1571-4. PMC: 1075822. DOI: 10.1104/pp.100.3.1571. View

4.
Hole D, Emran A, Fares Y, Drew M . Induction of nitrate transport in maize roots, and kinetics of influx, measured with nitrogen-13. Plant Physiol. 1990; 93(2):642-7. PMC: 1062563. DOI: 10.1104/pp.93.2.642. View

5.
Cooper A, Gelbard A, Freed B . Nitrogen-13 as a biochemical tracer. Adv Enzymol Relat Areas Mol Biol. 1985; 57:251-356. DOI: 10.1002/9780470123034.ch4. View