The upper part of a nodulated soybean root hydroponically cultured in a glass bottle was monitored using a computer microscope under controlled environmental conditions, and the diameter of individual nodules was measured from 10-24 d after planting. The diameter of a root nodule attached to the primary root increased from 1 mm to 6 mm for 2 weeks under nitrogen-free conditions. The increase in diameter of the nodules was almost completely stopped after 1 d of supplying 5 mM nitrate, and was due to the cessation of nodule cell expansion. However, nodule growth quickly returned to the normal growth rate following withdrawal of nitrate from the solution. The reversible depression of nodule growth by nitrate was similar to the restriction of photoassimilate supply by continuous dark treatment for 2 d followed by normal light/dark conditions. In addition, the inhibitory effect of nitrate was partially alleviated by the addition of 3% (w/v) sucrose to the medium. Plant leaves were exposed to (11)C or (14)C-labelled carbon dioxide to investigate the effects of 5 mM nitrate on the translocation and distribution of photosynthates to nodules and roots. Supplying 5 mM nitrate stimulated the translocation rate and the distribution of labelled C in nitrate-fed parts of the roots. However, the (14)C partitioning to nodules decreased from 9% to 4% of total (14)C under conditions of 5 mM nitrate supply. These results indicate that the decrease in photoassimilate supply to nodules may be involved in the quick and reversible nitrate inhibition of soybean nodule growth.

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The application of combined nitrogen, especially nitrate, to soybean plants is known to strongly inhibit nodule formation, growth and nitrogen fixation. In the present study, we measured the effects of supplying 5 mM nitrate on the growth of nodules, primary root, and lateral roots under light at 28 °C or dark at 18 °C conditions. Photographs of the nodulated roots were periodically taken by a digital camera at 1-h intervals, and the size of the nodules was measured with newly developed computer software. Nodule growth was depressed approximately 7 h after the addition of nitrate under light conditions. The nodule growth rate under dark conditions was almost half that under light conditions, and nodule growth was further suppressed by the addition of 5 mM nitrate. Similar results were observed for the extending growth rate of the primary root as those for nodule growth supplied with 5 mM nitrate under light/dark conditions. In contrast, the growth of lateral roots was promoted by the addition of 5 mM nitrate. The 2D-PAGE profiles of nodule protein showed similar patterns between the 0 and 5 mM nitrate treatments, which suggested that metabolic integrity may be maintained with the 5 mM nitrate treatment. Further studies are required to confirm whether light or temperature condition may give the primary effect on the growth of nodules and roots.

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Nitrate is one of the major sources of nitrogen for higher plants and is taken up from the soil by active transporters coupled with H ϩ across the plasma membrane (PM) of root cells. Nitrate uptake systems have been classified into two groups: low-affinity transport systems (LATS) and high-affinity transport systems (HATS). The LATS contribute to nitrate uptake at high nitrate concentrations above 1 mM whereas the HATS operate at micromolar concentrations of external nitrate and display MichaelisMenten kinetics saturating at 0.2-0.5 mM nitrate. The HATS are further divided into two categories: constitutive HATS (cHATS) and inducible HATS (iHATS), which are significantly affected by the supply of external nitrate. Many studies of the molecular basis of nitrate uptake reveal the existence of two gene families, namely the NRT1 and NRT2 families, which potentially encode for LATS and HATS respectively. NRT2 genes are identified in a variety of organisms including fungi, certain yeasts, green algae, and higher plants ( Unkles et al. 1991;Quesada et al. 1994;Trueman et al. 1996;Pérez et al. 1997;Quesada et al. 1997;Amarasinghe et al. 1998;Zhuo et al., 1999;Araki and Hasegawa 2006;Tsujimoto et al. 2007). In most species, NRT2 genes are members of a multigene family: for example, seven Arabidopsis genes (AtNRT2.1-AtNRT2.7) and four rice genes (OsNRT2.1-OsNRT2.4) have been found in their genomes (Orsel et al. 2002; Araki and Hasegawa 2007), and at least four NRT2 genes (HvNRT2.1-HvNRT2.4) exist in barley (Vidmar 2000a). Amino acid sequences deduced from these genes indicate that the NRT2 proteins are typically 480-510 amino acids in length and predicted to be integral to membranes with 12 transmembrane helices (Forde 2000).It has been well documented that iHATS activity is strongly induced by nitrate supply, and is down-regulated by the accumulation of nitrate assimilation products, especially ammonium and glutamine (Crawford and Glass 1998). In several plant species, it has been shown that a particular member of the NRT2 gene family (e.g., NpNRT2.1 for Nicotiana plumbaginifolia, AtNRT2.1 for Arabidopsis, HvNRT2.1 for barley) contribute to iHATS, because those transcript levels are highly correlated with changes in iHATS activity in such species (Krapp et al. 1998;Lejay et al. 1999;Zhuo et al. 1999;Vidmar et al. 2000a Abstract A high affinity transport system (HATS) for nitrate in plants is operated by a two-component NRT2/NAR2 transport system. However, the regulation and localization of NRT2 and NAR2 at protein level are largely unknown and especially so in crop plant species. In this study with barley (Hordeum vulgare), membrane localization, protein expression in the roots, and a direct protein-protein interaction of HvNRT2 and HvNAR2 proteins were investigated. Immunochemical analysis showed that both HvNRT2 and HvNAR2 proteins were co-localized in the plasma membrane of the roots. Expression of HvNRT2 and HvNAR2 proteins was more strongly induced by treatment with higher concentrations of external nitrate, while H...

The ammonium produced by nitrogen fixation in the bacteroid is rapidly excreted to cytosol of infected cell of soybean nodules and then assimilated into glutamine and glutamic acid, by glutamine synthetase/glutamate synthase pathway. Most of the nitrogen is further assimilated into ureides, allantoin, and allantoic acid, via purine synthesis, and they are transported through xylem to the shoots. Nitrate absorbed in the roots is reduced by nitrate reductase and nitrite reductase to ammonia either in the roots or leaves. The ammonia is also assimilated by glutamine synthetase/glutamate synthase pathway, and mainly transported by asparagine, and not ureides. The nitrogen transported into leaves is readily utilized for protein synthesis, and then, some of them are decomposed and retransported to roots, apical shoots, and pods via phloem mainly in the form of asparagine.

The effects of deep placement (supplied at 20 cm depth from soil surface below plants) of 100 kg N ha−1 of N fertilizers, urea, coated urea or calcium cyanamide (lime nitrogen) on the growth, nitrogen fixation activity, nitrogen absorption rate and seed yield of soybean (Glycine max L. Merr.) plants were examined by comparing them with control plots without deep placement of N fertilizer in sandy dune field. In addition, three different inoculation methods of bradyrhizobia were used for each N treatment: (1) transplantation of 10‐day‐old seedling in a paper pot with vermiculite inoculated with Bradyrhizobium japonicum USDA110, (2) direct transplantation of inoculated 10‐day‐old seedlings, and (3) transplantation of 10‐day‐old seedlings in a non‐inoculated paper pot. The deep placement of N fertilizers, especially calcium cyanamide and coated urea, markedly increased the growth and total N accumulation in shoot, roots and nodules, which resulted in an increase in seed yield. Daily N2 fixation activity and N absorption rate were estimated by relative abundance of ureide‐N analysed from the concentration of N constituents (ureide‐N, amide‐N and nitrate‐N) in root bleeding xylem sap and increase in total N accumulation in whole plants at R1, R3, R5 and R7 stages. The total amount of N2 fixation was about 50 % higher in the plants with calcium cyanamide and coated urea deep placements compared with control plants. Deep placement of slow release fertilizers kept nodule dry weight higher in the maturing stage of seed, possibly through abundant supply of photoassimilate to the nodules by supporting leaf area and activity until late reproductive stages. The results indicate that deep placement of calcium cyanamide or coated urea enhances N2 fixation activity, which ultimately increases the seed yield. The promotive effect was observed with the seedlings transplanted in paper pot with inoculum of bradyrhizobia within any treatments, although nodulation by indigenous rhizobia was observed in the plants transplanted with non‐inoculated paper pot.