Cellular compartmentation of ureide biogenesis in root nodules of cowpea (Vigna unguiculata (L.) Walp.)

Cowpea (Vigna unguiculata (L.) Walp.) nodules have been investigated by means of cytochemical and immunocytochemical procedures at the ultrastructural level in order to assess the role of the uninfected cells in ureide biogenesis. Uricase activity in the nodules was shown by cytochemical methods to be localized exclusively in the numberous large peroxisomes confined to the uninfected cells; the small peroxisomes in the infected cells did not stain for uricase. Uricase was also localized in the peroxisomes of uninfected cells by immunogold techniques employing polyclonal antibodies against nodule-specific uricase of soybean. There was no labeling above background of any structures in the infected cells. The results indicate that the uninfected cells are essential for ureide biogenesis in cowpea. Although tubular endoplasmic reticulum, the presumptive site of allantoinase, increases greatly in the uninfected cells during nodule development, it virtually disappears as the nodules mature. The inconsistency between the disappearance of the tubular endoplasmic reticulum from older nodules and the high allantoinase activity reported for older plants remains to be explained.Abbreviations DAB 3,3-diaminobenzidine - ER endoplasmic reticulum - GARG goat anti-rabbit immunoglobulin G - IgG immunoglobulin G - kDa knodalton - Mr apparent molecular mass - SDS-PAGE sodium dodecyl sulfate-polyacrylamide gel electrophoresis     

Symbiotic nitrogen fixation and physiological performance of bean (Phaseolus vulgaris L.) plants as affected by Rhizobium inoculum position and bean rugose mosaic virus infection

Bean (Phaseolus vulgaris L. var. Tacarigua) plants were grownin sterilized Leonard jars under controlled conditions. Beforesowing, 1 g of gamma irradiated peat containing the Rhizobiumtropici strain CIAT899 was placed at either 2 or 10 cm belowthe sand surface. Mechanical infection of bean rugose mosaicvirus (BRMV) was carried out in 3-d-old seedlings. Thus, theearly events of nodulation occurred before the arrival of virusparticles to roots. Rhizobium inoculation at 2 cm deep resultedin the formation of nodule clusters close to the crown, in contrastto the homogeneous nodulation along the roots observed in plantsinoculated with Rhizobium at a depth of 10 cm. The uniform arrangementof nodules on the roots enhanced the plant shoot biomass, althoughthe total nodule mass per plant did not differ between Rhizobiuminoculation treatments. Nodules located on deeper roots resultedin higher ureide concentrations in shoots and leaves and inreduced carbohydrate concentrations in leaves. In healthy plants,nodules formed on deeper roots had higher allantoinase activityand a greater carbohydrate concentration when compared to thatof nodules located close to the crown. Deeper nodules had ureideconcentrations similar to those of upper nodules, probably asa consequence of increased translocation of N-compounds to aerialorgans. A similar pattern of nodule formation and response toinoculum position was observed in BRMV-infected plants at allharvests. However, virus infection resulted in reduced totalnodule mass, shoot biomass, total leaf area and induced transitoryalterations in the ureide, -amino-N and carbohydrate concentrationin the different plant compartments. The effect of BRMV infectionon plant parameters was more evident during the vegetative stagesof growth. Nevertheless, the magnitude of the effect was alwaysmore pronounced in plants inoculated with Rhizobium at a depthof 2 cm compared to those Inoculated at 10 cm due to a greateractivity of deeper nodules despite virus infection. Deeper nodulesin BRMV-infected plants showed higher carbohydrate concentrationas well as higher allantoinase and uricase activity than thosedeveloped close to the crown, at all harvests. This observationwas further supported by ultrastructural analysis of virus-infectednodules, since virus replication took place in cells containingbacteroids of upper and lower nodules, but only in the interstitialcells of the latter. BRMV infection did not hinder the allantoinaseactivity and the chlorophyll content of uppermost mature leavesregardless of inoculum position. At the flowering and fruitingstages, healthy and BRMV-infected plants did not differ withregard to any of the tested parameters. Only inoculum positionhad an effect. The nearly normal functioning of the symbioticprocess at these stages of growth was attributed to the formationof a new generation of nodules in BRMV-infected plants subjectedto each of the Rhlzobium inoculation treatments. Key words: Bean rugose mosaic virus, symbiotic nitrogen fixation, bean, Rhizobium inoculum position, nodule ultrastructure     

Ultrastructural localization of urate oxidase in nodules of Sesbania exaltata,Glycine max,and Medicago sativa

Summary The localization of urate oxidase (=uricase, E.C. 1.7.3.3) was determined cytochemically in nodules of Sesbania exaltata (Raf.) Cory, soybean (Glycine max [L.] Merr.) and alfalfa (Medicago sativa [L.]), using the precipitation of peroxide (produced during the oxidation of urate) by cerium chloride. Cerium perhydroxide reaction product was noted only in the microbodies, a localization consistent with biochemical fractionation studies on urate oxidase. Urate oxidase was present not only in the uninfected cells of the cortical tissue, but also in both infected and interstitial cells in the central tissue, suggesting that at least this enzyme of ureide metabolism is not confined to interstitial cells. Urate oxidase cytochemistry of nodules from alfalfa (Medicago sativa L.), an amide producer, also resulted in microbody staining but the microbodies were infrequently noted in cell profiles.     

Organic Acid Metabolism in Cellular Organelles of Vigna cylindrica (Mitorisasage) Cotyledons

In starchy cotyledons of Vigna cylindrica (L.) Skeels (Mitorisasage)during seed germination, the enzymes of the glyoxylate cyclewere located in the matrix of mitochondria. Glyoxysomes wereabsent. The glyoxylate cycle in the mitochondria supplies organicacids to the tricarboxylic acid cycle. In mitochondria, isocitratelyase activity was much higher than malate synthase activity.Part of the glyoxylate thus produced in mitochondria may benonenzymatically converted to formate by H₂O₂ and the formatethen converted to CO₂ by peroxidase or by formic dehydrogenase.The activity of superoxide dismutase, which supplies H₂O₂, washigher in mitochondria than in peroxisomes. The remaining glyoxylatein mitochondria is possibly converted to glycine by alanine-glyoxylateaminotransferase or transported to peroxisomes which lackedisocitrate lyase activity but had high malate synthase activity.In peroxisomes, glyoxylate may be also produced from urate,as is suggested by the fairly high activities of uricase, allantoinaseand allantoicase. Judging from the enzyme distribution, Vignaperoxisomes should be capable of producing malate, oxalacetate,citrate, isocitrate and a-ketoglutarate. ¹Present address: Department of Horticulture, College of Agricultureand Animal Science, Yeugnam University, Gyeongsan 632, Korea. (Received May 27, 1987; Accepted October 7, 1987)     

Evidence for sugar signalling in the regulation of asparagine synthetase gene expressed in Phaseolus vulgaris roots and nodules

A cDNA clone, designated as PvNAS2, encoding asparagine amidotransferase(asparagine synthetase) was isolated from nodule tissue of commonbean (Phaseolus vulgaris cv. Negro Jamapa). Southern blot analysisindicated that asparagine synthetase in bean is encoded by asmall gene family. Northern analysis of RNAs from various plantorgans demonstrated that PvNAS2 is highly expressed in roots,followed by nodules in which it is mainly induced during theearly days of nitrogen fixation. Investigations with the PvNAS2promoter gusA fusion revealed that the expression of PvNAS2in roots is confined to vascular bundles and meristematic tissues,while in root nodules its expression is solely localized tovascular traces and outer cortical cells encompassing the centralnitrogen-fixing zone, but never detected in either infectedor non-infected cells located in the central region of the nodule.PvNAS2 is down-regulated when carbon availability is reducedin nodules, and the addition of sugars to the plants, mainlyglucose, boosted its induction, leading to the increased asparagineproduction. In contrast to PvNAS2 expression and the concomitantasparagine synthesis, glucose supplement resulted in the reductionof ureide content in nodules. Studies with glucose analoguesas well as hexokinase inhibitors suggested a role for hexokinasein the sugar-sensing mechanism that regulates PvNAS2 expressionin roots. In light of the above results, it is proposed that,in bean, low carbon availability in nodules prompts the down-regulationof the asparagine synthetase enzyme and concomitantly asparagineproduction. Thereby a favourable environment is created forthe efficient transfer of the amido group of glutamine for thesynthesis of purines, and then ureide generation. Key words: Asparagine and ureide synthesis, asparagine synthetase, nodules, Phaseolus vulgaris, sugar signalling     

N2Fixation Response to Drought in Common Bean (Phaseolus vulgarisL.)

Nitrogen fixation activity in common bean is generally thoughtto be low and sensitive to soil drying and, consequently, droughtcan have important negative effects on N accumulation and yieldpotential. The objectives of this research were to examine theresponse of N₂fixation to drought stress in common bean, andto test the hypothesis that drought sensitivity of N₂fixationin common bean is linked to ureide levels in the plants. Twoglasshouse experiments were conducted to compare the responsesof leaf transpiration and acetylene reduction activity (ARA)to soil water contents. ARA decrease during soil dehydrationwas found to lag behind the decline in transpiration. This indicatesthat ARA is relatively less sensitive to soil dehydration comparedto leaf gas exchange. Further, in comparing two cultivars therewas no consistent difference in the relative response of ARAand transpiration to soil drying. The ureide concentrationsmeasured in common bean plants were low, ranging from 0.1 to1.0 mmol l^-1in xylem sap exudates. Ureide concentrations inthe sap exudate varied significantly among the two genotypeseven though there was no difference in ARA response to drought.It was concluded that in common bean, the lower sensitivityof N₂fixation to drought compared to leaf gas exchange couldbe related to low ureide concentrations in petioles and xylemsap.Copyright 1998 Annals of Botany Company Phaseolus vulgaris,nitrogen fixation, drought stress, nodules, ureides.     

Differentiation of Photorespiratory Activity between Mesophyll and Bundle Sheath Cells of C4 Plants II. Peroxisomes of Panicum miliaceum L.

Peroxisomes were isolated by sucrose density gradient centrifugationfrom mesophyll and bundle sheath protoplasts of a C₄ plant,Panicum miliaceum L. The equilibrium density in the gradientwas 1.25 for bundle sheath peroxisomes and 1.23 for mesophyllperoxisomes, the former density being similar to that of peroxisomesof wheat mesophyll protoplasts. Photorespiratory and other microbody enzymes were assayed forthe peroxisomes of P. miliaceum to detect possible differentiationat an enzyme level. The specific activities of photorespiratoryenzymes, except for hydroxypyruvate reductase, in bundle sheathperoxisomes were 40–60% of those in wheat peroxisomes,when compared on a protein basis, and only 20–30% in mesophyllperoxisomes. However, peroxisomes from both cell types containedsignificant levels of all the enzymes involved in the photorespiratoryglycolate pathway, when compared with castor bean glyoxysomes.The activity of hydroxypyruvate reductase in the peroxisomesof P. miliaceum was comparable to or higher than that in wheatperoxisomes. Two ß-oxidation enzymes and urate oxidasewere detected in the peroxisomes in a similar level to thatin wheat peroxisomes. These results suggest that the peroxisomes of mesophyll andbundle sheath cells of P. miliaceum are essentially similarto those of C₃ plants, and that they cannot be differentiatedexcept for a difference in equilibrium density in a sucrosegradient. (Received December 24, 1984; Accepted April 9, 1985)     

Transport and Partitioning of CO(2) Fixed by Root Nodules of Ureide and Amide Producing Legumes

Nodulated and denodulated roots of adzuki bean (Vigna angularis), soybean (Glycine max), and alfalfa (Medicago sativa) were exposed to ¹⁴CO₂ to investigate the contribution of nodule CO₂ fixation to assimilation and transport of fixed nitrogen. The distribution of radioactivity in xylem sap and partitioning of carbon fixed by nodules to the whole plant were measured. Radioactivity in the xylem sap of nodulated soybean and adzuki bean was located primarily (70 to 87%) in the acid fraction while the basic (amino acid) fraction contained 10 to 22%. In contrast, radioactivity in the xylem sap of nodulated alfalfa was primarily in amino acids with about 20% in organic acids. Total ureide concentration was 8.1, 4.7, and 0.0 micromoles per milliliter xylem sap for soybean, adzuki bean, and alfalfa, respectively. While the major nitrogen transport products in soybeans and adzuki beans are ureides, this class of metabolites contained less than 20% of the total radioactivity. When nodules of plants were removed, radioactivity in xylem sap decreased by 90% or more. Pulse-chase experiments indicated that CO₂ fixed by nodules was rapidly transported to shoots and incorporated into acid stable constituents. The data are consistent with a role for nodule CO₂ fixation providing carbon for the assimilation and transport of fixed nitrogen in amide-based legumes. In contrast, CO₂ fixation by nodules of ureide transporting legumes appears to contribute little to assimilation and transport of fixed nitrogen.     

Cellular and subcellular organization of pathways of ammonia assimilation and ureide synthesis in nodules of cowpea (Vigna unguiculata L. Walp)

Fractionation of cell organelles of nitrogen-fixing nodules of cowpea (Vigna unguiculata L. Walp) by discontinuous and continuous sucrose density centrifugation indicated that starch-containing plastids possessed the complete pathway for purine nucleotide synthesis together with significant activities of some other enzymes associated with the provision of substrates in purine synthesis; triosephosphate isomerase (EC 5.3.1.1), NADH-glutamate synthase (EC 2.6.1.53), aspartate aminotransferase (EC 2.6.1.1), phosphoglycerate oxidoreductase (EC 1.1.1.95), and methylene tetrahydrofolate oxidoreductase (EC 1.5.1.5). Enzymes of purine oxidation, xanthine oxidoreductase (EC 1.2.3.2), and urate oxidase (EC 1.7.3.3) were recovered in the soluble fraction; glutamine synthetase (EC 6.3.1.2) occurred in bacteroids and in the cytosol. Intact, infected (bacteroid-containing) and uninfected cells were prepared by enzymatic maceration of the central zone of the nodule and partially separated by centrifugation on discontinuous sucrose gradients. Glutamine synthetase was largely restricted to infected cells whereas plastid enzymes, de novo purine synthesis, and urate oxidase were present in both cell types. Although the levels of all enzymes assayed were higher in infected cells, both cell types possessed the necessary enzyme complement for ureide formation. A model for the cellular and subcellular organization of nitrogen metabolism and the transport of nitrogenous solutes in cowpea nodules is proposed.     

Transport of Nitrate and Calcium into Legume Root Nodules

Nitrate transport into nodulated plants of soybean (Glycinemax), cowpea (Vigna unguiculata) and faba bean (Vicia faba)was investigated. Nitrate entering the root system of soybeandid not pass out of the vascular system into nodular tissuesin detectable quantities. On the other hand, nitrate could passfrom soil through the outer surface of nodules but did not penetratethe infected tissue. Similarly, nitrate was restricted to corticaltissues of cowpea and faba bean. Thus, nitrate cannot inhibitnitrogen fixation as a result of reduction to nitrite by nitratereductase within the bacteroid zone. These results are, however,consistent with an effect of nitrate on an oxygen diffusionresistance located in the nodule cortex. Unlike nitrate, measurable quantities of ⁴⁵calcium were transportedvia the xylem into infected and cortical tissues of soybeannodules: it also passed from the soil into the free space ofthe nodule cortex. Key words: Nitrate, legume nodules, calcium     

Peroxisomes of soybean (Glycine max) root nodule vascular parenchyma cells contain a "nodule—specific" urate oxidase

The cortex of soybean ( Glycine max L. cv. Centennial) nodules contain an organellerich layer of vascular parenchyma tissue, which encircles the elaborate vascular tissue of the nodule. Peroxisomes with small, electron-opaque nucleoids are found in the vascular parenchyma cells. Positive cytochemical staining for catalase (EC 1.11.1.6) confirms their morphological identification as peroxisomes. Activities of both glycolate oxidase (EC 1.1.3.1) and urate oxidase (EC 1.7.3.3) were detected cytochemically in these peroxisomes. Nodule-specific urate oxidase was localized principally in the nucleoid region of these vascular parenchyma peroxisomes, as indicated by immunogold labelling using antibodies against nodulin-35, the nodule-specific urate oxidase. The density of urate oxidase immunogold labelling in the vascular parenchyma peroxisome nucleoid is similar to that of the more well-characterized interstitial cell peroxisomes of the infected zone. These results show that the induction of nodule-specific urate oxidase may be induced in tissue outside of the infected zone.     

Biochemical, electrophoretic and immunological characterization of peroxisomal enzymes in three soybean organs

Biochemical, electrophoretic and immunological studies were made among peroxisomal enzymes in three organs of soybean [Glycine max (L.) Merr. cv. Centennial] to compare the enzyme distribution and characteristics of specialized peroxisomes in one species. Leaves, nodules and etiolated cotyledons were compared with regard to several enzymes localized solely in their peroxisomes: catalase (EC 1.11.1.6), malate synthase (EC 4.1.3.2), glycolate oxidase (EC 1.1.3.1), and urate oxidase (EC 1.7.3.3). Catalase activity was found in all tissue extracts. Electrophoresis on native polyacrylamide gels indicated that leaf catalase migrated more anodally than nodule or cotyledon catalase as shown by both activity staining and Western blotting. Malate synthase activity and immunologically detectable protein were present only in the cotyledon extracts. Western blots of denaturing (lithium dodecyl sulfate) gels probed with anti-cotton malate synthase antiserum, reveal a single subunit of 63 kDa in both cotton and soybean cotyledons. Glycolic acid oxidase activity was present in all three organs, but ca 20-fold lower (per mg protein) in both nodule and cotyledon extracts compared to leaf extracts. Electrophoresis followed by activity staining on native gels indicated one enzyme form with the same mobility in nodule, cotyledon and leaf preparations. Urate oxidase activity was found in nodule extracts only. Native gel electrophoresis showed a single band of activity. Novel electrophoretic systems had to be developed to resolve the urate oxidase and glycolate oxidase activities; both of these enzymes moved cathodally in the gel system employed while most other proteins moved anodally. This multifaceted study of enzymes located within three specialized types of peroxisomes in a single species has not been undertaken previously, and the results indicate that previous comparisons between the enzyme content of specialized peroxisomes from different organisms are mostly consistent with that for a single species, soybean.     

Alterations in Apoplastic and Total Solute Concentrations in Soybean Nodules Resulting from Treatments Known to Affect Gas Diffusion

Ureide concentration in the cortical apoplast of soybean (Glycinemax(L.) Merr.) nodules increases rapidly in response to noduleexcision. The objective here was to determine if changes inapoplastic ureide may be related to the control of resistanceto gas diffusion which is thought to be localized in the nodulecortex. Following decapitation of shoots, nitrogenase activity(acetylene reduction) and ureide concentration in total noduleextracts declined over a period of several hours. Apoplasticureide concentration relative to total nodule ureide was elevatedunder these conditions, but the treatment effect was small comparedto non-decapitated controls. Decapitation also caused a significantdecline in the concentrations of sucrose, glucose, and D-pinitolin nodules. However, the decline in carbohydrates was similarin the nodule cortex and the nodule as a whole, suggesting thatthe carbohydrate changes are not related to a cortex-localizedmechanism. Non-invasive treatments involving increases or decreasesin oxygen concentration supplied to nodulated roots caused rapiddecreases in respiration of nodulated roots and in ureide concentrationin total nodule extracts, but did not cause major changes inapoplastic ureide concentrations. The combined results indicatethat apoplastic ureide is probably not involved in the regulationof resistance to gas diffusion. The rapid decline in noduleureide concentrations in response to changing oxygen supplydocuments the sensitivity of ureide synthesis and/or transportto alterations in nodule respiration and/or nitrogenase activity Key words: Glycine max, Pisum sativum, ureide, carbohydrates     

Polyamines in Nodules from Various Plant-Microbe Symbiotic Associations

Polyamine compositions of root or stem nodules collected fromvarieties of nitrogen-fixing leguminous (22 species) and non-leguminous(5 species) plants were investigated. Relatively high concentrationsof homospermidine were observed in root or stem nodules of allthe leguminous plants. Based on the ratio of homospermidineto spermidine, legume nodules were generally characterized intotwo major groupes; one containing almost equal amounts of homospermidineand spermidine, and the other a high homospermidine/spermidineratio. Root nodules from pigeon pea (Cajanus cajan L. Millsp)was the only exception which exhibited very low homospermidine/spermidineratio. Amongst the legumes, nodules of adzuki bean (Vigna angularis),siratro (Macroptilium atropurpureum DC. Urb.), pea (Pisum sativumL.), and hairly vetch (Vicia hirsuta S.F. Gray) were rich indiamine putrescine. Such characters of nodule polyamine compositionwere inherent characteristics of each legume species, and notrelated to the type of infected rhizobia (Rhizobium or Bradyrhizobium).In contrast to herbaceous leguminous plants, nonleguminous woodyplants, which symbiotically associate with actinomycete Frankiaspecies, contained little polyamines in their root nodules.Root nodules of non-leguminous Parasponia andersonii infectedby bradyrhizobia were found to contain large quantities of putrescineand homospermidine. No significant differences in polyaminecomposition were observed between root and stem nodules bothin Aeschynomene indica and Sesbania rostrata. (Received June 13, 1994; Accepted August 17, 1994)     

Gibberellin A3 Causes a Decrease in the Accumulation of mRNA for ACC Oxidase and in the Activity of the Enzyme in Azuki Bean (Vigna angularis) Epicotyls

Differential screening, aimed at the isolation of cDNA clonesof mRNAs whose accumulation is influenced by GA₃, resulted inthe isolation of a cDNA clone of an mRNA whose level was decreasedby GA₃ in segments of epicotyls of Vigna angularis. The putativeprotein encoded by this cDNA resembled the 1-aminocyclopropane-l-carbox-ylateoxidases (ACC oxidases) identified in other plant species (about80% homology at the amino acid level). Thus, the correspondinggene was designated AB-ACO1 (azuki bean ACC oxidase). GA₃ alsodecreased the activity of ACC oxidase in azuki bean epicotyls,but it did not decrease the rate of ethylene evolution. In fact,GA₃ increased the rate of ethylene evolution and the level ofACC. Thus, GA₃ seemed to increase the production of ethyleneby promoting the synthesis of ACC. (Received January 10, 1997; Accepted July 31, 1997)     

The Fine Structure of some Dry Seed Tissues Observed after Completely Anhydrous Chemical Fixation

Completely anhydrous fixation with acrolein vapour or osmiumtetroxide vapour was applied to tissues of air-dry seeds: thecoleoptile of wheat (Trilicum aestivum), and plumule and radicleof mung bean (Vigna radiata). Great shrinkage of cells and organelleswas noted, but all the usual organelles could be identified,except for Golgi bodies and (in most cases) ribosomes. The endoplasmicreticulum was very abundant and endoplasmic reticulum tubuleswere closely associated with the storage organelles, namelylipid bodies in the wheat coleoptile, and protein bodies inthe mung bean embryo axis. Aqueous fixation resulted in considerabledistortion of cellular structure. Triticum aestivum L., wheat, Vigna radiata L., mung bean, seed, fine structure, anhydrous fixation     

Expression of antisense nodulin-35 RNA in Vigna aconitifolia transgenic root nodules retards peroxisome development and affects nitrogen availability to the plant

A nodulin-35 (N-35) cDNA encoding nodule-specific uricase (EC 1.7.3.3.) was isolated from a Vigna aconitifolia (mothbean) root nodule cDNA library. Sequence analysis of Vigna uricase (VN-35) cDNA revealed 90% homology to that of soybean. The VN-35 cDNA was inserted in the antisense orientation downstream of the CaMV—35S promoter, and transgenic hairy roots were formed on Vigna plants using Agrobacterium rhizogenes . Infection with Bradyrhizobium (cowpea) gave rise to root nodules on transgenic hairy roots supported by the wild-type shoot. Expression of antisense VN-35 RNA was detected in transgenic nodules on individual roots using polymerase chain reaction (PCR). The nodules expressing antisense VN-35 RNA were smaller in size and showed lower uricase activity than nodules formed on the hairy roots transformed with a binary vector containing β-glucuronidase (GUS) gene (used as control), and the plants exhibited nitrogen deficiency symptoms. Ultrastructural analysis and immunogold labeling with antibody against soybean N-35 revealed that the growth of peroxisomes was retarded in transgenic nodules expressing antisense VN-35 RNA. These data suggest that a reduction in ureide biosynthesis limits the availability of symbiotically reduced nitrogen to the plant. The nodules of tropical legumes appear to be specialized in nitrogen assimilation and are developmentally controlled to produce and transport ureides.     

Effect of Nitrogen on Nitrate Reductase Activity in the Nodules and Leaves of Summer Moong (Vigna radiata)

The relation of the in vivo nitrate reductase (NR) activityto growth period was studied in the nodules and the leaves ofthe summer moong (Vigna radiata). The maximum NR activity wasobserved 31 days after sowing (DAS) in the leaves and 28 DASin the case of the nodules. In a pot experiment, the effectof the various nitrogen concentrations, namely 0, 3, 6, 9 and12 mg kg^–1 was studied on NR activity at three growthstages. The maximum NR activity was observed at 6 mg kg^–1N during the pre-flowering stage (26 DAS). Though the noduleshave higher NR activity, its expression was limited by substrateavailability. The NR activity in the leaf could be used as anindex of NR activity in the nodules. Nitrate reductase, nitrogen, nitrate, moong, Vigna radiata     

Uptake hydrogenase in Rhizobium and nodule leghemoglobin in cow pea miscellany hosts

Two effective strains of green gram rhizobia S24 (slow growing and Hup⁺) and M11 (fast growing and Hup^-) were tested for leghemoglobin production in nodules and effectivity on six species of cow pea miscellany hosts. Both strains nodulate green gram [Vigna radiata (L.) (Wilczek)], black gram [Vigna mungo (L.) (Hepper)], cow pea [Vigna unguiqulata (L.)], moth bean [Vigna aconitifolia (Jacq.) (Marechel)], Cluster bean [Cyamopsis tetragonoloba (L.) (Taub.)] and pigeon pea [Cajanus cajan (L.)]. In all these hosts, nodules formed by strain M11 contained 1.5 to 2 times more leghemoglobin than the nodules formed by strain S24. Gel electrophoresis of nodule contents of different host species showed a high concentration of a fast-moving ferricoxy leghemoglobin in the nodules of plants inoculated with strain M11 as compared to that of strain S24. Strain M11, however, was relatively less effective than strain S24 on black gram, cow pea and moth bean and was at par with the later on green gram, cluster bean and pigeon pea. Hydrogen recycling ability of the strain S24 was observed in nodules of all the host species. The effective functioning of strain S24 at low levels of leghemoglobin suggests an involvement of recycling hydrogenase in maintaining an appropriate oxidation-reduction potential in nodules.Abbreviations Lb Leghemoglobin - Cvr cultivar     

The Effects of Temperature on Vegetative and Early Reproductive Growth of a Cold-Tolerant and a Cold-Sensitive Line of Phaseolus vulgaris L. 2. Nodular Uricase, Allantoinase, Xylem transport of N and Assimilation in Shoot Tissues

The activities of nodular uricase and allantoinase, the compositionof bleeding sap N, estimated rates of xylary N translocationand ureide assimilation in shoot tissues were compared in acold-tolerant (194) and sensitive (Seafarer, SF) line of nodulatedPhaseolus vulgaris grown under three different temperature regimes.Uricase activity increased with increasing growth temperatureand was generally greater in nodules of 194 than in SF at anyparticularly temperature. Extractable allantoinase activity,on the other hand, was highest in nodules from plants grownat the coolest temperature (15/10 C day/night) and there waslittle or no difference in activity between the lines. There was little difference in sap composition between linesor amongst temperature treatments. Ureides contributed between80–91 percent of the total sap N in both lines grown at25/15 or 20/15 C with a slightly lower per cent (65–84)when grown at 15/10 C. Estimated rates of N translocation werehigher in 194 than SF at the coolest growth temperature. Increasesin rates of N translocation between successive harvests of eitherline were often correlated with increases in total N accumulationand also an accumulation of ureides in stems plus petioles butnot leaves. Generally leaves assimilated all of the ureidesinto other compounds at all growth temperatures. Nodules andshoots of either line did not accumulate ureides at 15/10 C.194 Accumulated greater amounts of ureides in stems and petiolesthan SF when grown at the two warmer temperatures. The resultsare discussed in relation to the ability of 194 to fix greateramounts of N than SF at suboptimal growth temperatures. Phaseolus vulgaris, common bean, uricase, allantoinase, sap composition, ureide assimilation, low temperature stress