The influence of cytokinins in nitrate regulation of nitrate reductase activity and expression in barley

The responses of nitrate reductase (NR) activity and levels of NR-mRNA to environmental nitrate and exogenous cytokinins are characterised in roots and shoots of barley ( Hordeum vulgare L., cv. Golf), using a chemostate-like culture system for controlling nitrate nutrition. Experiments were mainly performed with split root cultures where nitrate-N was supplied at a constant relative addition rate of 0.09 day⁻¹, and distributed between the subroots in a ratio of 20%:80%. The subroot NR-mRNA level and NR activity, as well as the endogenous level of zeatin riboside (ZR), increased when the local nitrate supply to one of the subroots was increased 4-fold by reversing the nitrate addition ratio (i.e. from 20%:80% to 80%:20%). Also shoot levels of ZR, NR-mRNA and NR activity increased in response to this treatment, even though the total nitrate supply remained unaltered. External supply of ZR at 0.1 μ M caused an approximately 3-fold increase in root ZR levels within 6 h. which is comparable to the nitrate-induced increase in root ZR. External application of ZR. zeatin. isopentenyl adenine or isopentenyl adenosine at 0.1 μ M caused from insignificant to 25% increases in NR-mRNA and activity in roots and up to 100% stimulation in shoots, whereas adenine or adenosine had no effect. No synergistic effects of perturbed nitrate supply and cytokinin application were detected in either roots or shoots. The translocation of nitrate from the root to the shoot was unaffected by application of ZR or switching the nitrate distribution ratio between subroots. The data give arguments for a physiological role of cytokinins in the response of root and shoot NR to environmental nitrate availability. The nature and limitations of the physiological role of cytokinins are discussed.     

The effect of marine bioactive substances (N PRO) and exogenous cytokinins on nitrate reductase activity in Arabidopsis thaliana

We investigated the effect of exogenous cytokinins and marine bioactive substances containing seaweed extracts (marketed by the ROULLIER Group under the trade name N PRO^TM.) on nitrate reductase activity in Arabidopsis . Cytokinins, applied either directly in the growth medium or as a foliar spray, did not significantly influence nitrate reductase activity in extracts from in vitro grown Arabidopsis plants. Conversely, Arabidopsis grown in the presence of or sprayed with N PRO had increased nitrate reductase activity. This stimulatory effect of N PRO was even higher when the plants were grown on low nitrate concentration, suggesting that these marine bioactive substances may be beneficial for plant growth in adverse nutritional conditions.     

Influence of cytokinins and phytochrome on nitrate reductase activity in etiolated leaves of maize

Of the different hormones tested, cytokinins stimulated nitrate-induced nitrate reductase (NR) activity in the dark. The optimal stimulation was obtained at 16 hr and this was sensitive to tungstate, 6-methylpurine and cycloheximide. The cytokinin stimulation of NR activity was further enhanced by brief irradiation with red light, but this effect was not noticed when leaves were exposed to far-red light. Both kinetin and red light, when given together, or given with a darkness interruption, stimulated the NR activity more than with either of them alone.     

Investigation on the role of nodule cytokinins in regulation of nitrate reductase activity ofPhaseolus mungo (L.)

The effects of some nodular cytokinis, zeatin (Z), zeatin riboside (ZR), N⁶ (Δ²-isopentenyl) adenine (IPA), and N⁶ (Δ²-isopentenyI) adenosine (IPAS) on nitrate reductase (E.C 1.9.6.1) activity of root nodules ofPhaseolus mungo were investigated. The cytokinis were also tested for their effect on nitrate uptake by nodules. The results show that IPAS is the most effective of all the four cytokinins tested. Z and IPA, which caused higherin vivo activity than ZR and IPAS, stimulated uptake of nitrate by nodules. The other two (ZR and IPAS) while inhibiting uptake showed greaterin vitro activity than Z and IPA. It may be concluded that some cytokinins, in addition to their direct effects on the enzyme, may increase the substrate availability to it, whereas others may have only an direct effect on the enzyme activation or degradation.     

Viscosity effects on eukaryotic nitrate reductase activity

Rate-limiting processes of catalysis by eukaryotic molybdenum-containing nitrate reductase (NaR, EC 1.7.1.1-3) were investigated using two viscosogens (glycerol and sucrose) and observing their impact on NAD(P)H:NaR activity of corn leaf NaR and recombinant Arabidopsis and yeast NaR. Holo-NaR has two "hinge" sequences between stably folded regions housing its internal electron carriers: 1) Hinge 1 between the molybdenum-containing nitrate reducing module and cytochrome b domain containing heme and 2) Hinge 2 between cytochrome b and cytochrome b reductase (CbR) module containing FAD. Solution viscosity negatively impacted the activity of these holo-NaR forms, which suggests that the rate-limiting events in catalysis were likely to involve large conformational changes that restrict or "gate" internal electron-proton transfers (IET). Little effect of viscosity was observed on recombinant CbR module and methyl viologen nitrate reduction by holo-NaR, suggesting that these activities involved no large conformational changes. To determine whether Hinge 2 is involved in gating the first step in IET, the effects of viscosogen on cytochrome c and ferricyanide reductase activities of holo-NaR and ferricyanide reductase activity of the recombinant molybdenum reductase module (CbR, Hinge 2, and cytochrome b) were analyzed. Solution viscosity negatively impacted these partial activities, as if Hinge 2 were involved in gating IET in both enzyme forms. We concluded that both Hinges 1 and 2 appear to be involved in gating IET steps by restricting the movement of the cytochrome b domain relative to the larger nitrate-reducing and electron-donating modules of NaR.     

Investigation on the role of nodule cytokinins in regulation of nitrate reductase activity ofPhaseolus mungo (L.)

The effects of some nodular cytokinis, zeatin (Z), zeatin riboside (ZR), N⁶ (²-isopentenyl) adenine (IPA), and N⁶ (²-isopentenyI) adenosine (IPAS) on nitrate reductase (E.C 1.9.6.1) activity of root nodules ofPhaseolus mungo were investigated. The cytokinis were also tested for their effect on nitrate uptake by nodules. The results show that IPAS is the most effective of all the four cytokinins tested. Z and IPA, which caused higherin vivo activity than ZR and IPAS, stimulated uptake of nitrate by nodules. The other two (ZR and IPAS) while inhibiting uptake showed greaterin vitro activity than Z and IPA. It may be concluded that some cytokinins, in addition to their direct effects on the enzyme, may increase the substrate availability to it, whereas others may have only an direct effect on the enzyme activation or degradation.Deceased.     

The effect of vanadium on nitrate reductase of Chlorella vulgaris

Added vanadate ions inhibit purified nitrate reductase from Chlorella vulgaris by reacting with the enzyme in a manner rather similar to that of HCN. Thus vanadate, like HCN, forms an inactive complex with the reduced enzyme, and this inactivated enzyme can be reactivated rapidly by adding ferricyanide. The inactive vanadate enzyme complex is less stable than the inactive HCN complex, and the two can be distinguished by the fact that EDTA causes a partial reactivation of the former, but not of the latter. Vanadate can also cause an increase in HCN formation by intact Chlorella vulgaris cells. When these cells were incubated with vanadate, their nitrate reductase was reversibly inactivated, and all of this inactive enzyme could be shown to be the HCN complex rather than the vanadate complex. When HCN and vanadate are both present, the HCN-inactivated enzyme, being more stable, will be formed in preference to the vanadate-inactivated enzyme.Abbreviation EDTA ethylenediamine tetraacetate     

The activation state of nitrate reductase is not always correlated with total nitrate reductase activity in leaves

The relation between nitrate reductase (NR; EC 1.6.6.1) activity, activation state and NR protein in leaves of barley (Hordeum vulgare L.) seedlings was investigated. Maximum NR activity (NRA_max) and NR protein content (Western blotting) were modified by growing plants hydroponically at low (0.3 mM) or high (10 mM) nitrate supply. In addition, plants were kept under short-day (8 h light/16 h dark) or long-day (16 h light/8 h dark) conditions in order to manipulate the concentration of nitrate stored in the leaves during the dark phase, and the concentrations of sugars and amino acids accumulated during the light phase, which are potential signalling compounds. Plants were also grown under phosphate deficiency in order to modify their glucose-6-phosphate content. In high-nitrate/long-day conditions, NRA_max and NR protein were almost constant during the whole light period. Low-nitrate/long-day plants had only about 30% of the NRA_max and NR protein of high-nitrate plants. In low-nitrate/long-day plants, NRA_max and NR protein decreased strongly during the second half of the light phase. The decrease was preceded by a strong decrease in the leaf nitrate content. Short daylength generally led to higher nitrate concentrations in leaves. Under short-day/low-nitrate conditions, NRA_max was slightly higher than under long-day conditions and remained almost constant during the day. This correlated with maintenance of higher nitrate concentrations during the short light period. The NR activation state in the light was very similar in high-nitrate and low-nitrate plants, but dark inactivation was twice as high in the high-nitrate plants. Thus, the low NRA_max in low-nitrate/long-day plants was slightly compensated by a higher activation state of NR. Such a partial compensation of a low NR_max by a higher dark activation state was not observed with phosphate-depleted plants. Total leaf concentrations of sugars, of glutamine and glutamate and of glucose-6-phosphate did not correlate with the NR activation state nor with NRA_max. Received: 24 March 1999 / Accepted: 31 May 1999     

The effect of phosphate and flavin adenine dinucleotide on nitrate reductase activity of some unicellular marine algae

Nitrate reductase (NR) activity was measured in cell-free extracts from seven species of unicellular, marine algae. For most species Tris buffer was not a satisfactory assay buffer unless supplemented with phosphate. With some species (e.g. Brachiomonas submarina Bohlin, Nannochloropsis oculata Droop, Phaeodactylum tricomutum Bohlin) maximum NR activity required the addition of phosphate and flavin adenine dinucleotide (FAD) to assays; with extracts of P. tricornutum, the requirement for FAD increased after partial purification of extracts. Like phosphate, arsenate stimulated NR activity in extracts, but selenate, sulphate, and tungstate were less effective. Addition of manganese to partially purified extracts of P. tricomutum resulted in an inhibition of NR activity which was alleviated by phosphate or EDTA.     

Effect of simazine on nitrate reductase activity in corn

The nutritional and environmental parameters required for eliciting increases in the nitrogen content and growth of corn (Zea mays L.) by non-toxic levels of simazine have been established. Corn seedlings with the endosperm removed 10 days after germination, proved to be a suitable test species. The addition of simazine to the root-zone area of corn plants grown under both sub-optimal temperatures and low nitrate levels, increased the nitrogen content and dry weight of the plants by 20 to 25%. This increase was found to be associated with an effect on nitrate reductase.     

The influence of environmental factors on nitrate reductase activity in freshwater phytoplankton

Water samples were taken from three regions in the Kinneret ecosystem (the Watershed (WS), the National Water Carrier (NWC) and the lake) over a 14 month period and nitrate reductase (NR) activity measured by a simplified assay previously developed for field studies. A complex relationship between NR activity and ambient NO₃ and/or NH₄ concentrations was observed. NR activity was not generally predictable from ambient nutrient concentrations. No correlation between NR activity and the ambient orthophosphate (SRP) concentrations or the dissolved, inorganic N : P atomic ratio was observed, although NR activity appeared to correlate with both NO₃ or NH₄ uptake. Our results suggest that NR activity is related to the N nutritional status of the cells and their nutrient prehistory rather than ambient nutrient concentrations.     

Unusual regulatory nitrate reductase activity in cotyledons of Brassica napus seedlings: enhancement of nitrate reductase activity by ammonium supply

The effect of supplying either nitrate or ammonium on nitrate reductase activity (NRA) was investigated in Brassica napus seedlings. In roots, nitrate reductase activity (NRA) increased as a function of nitrate content in tissues and decreased when ammonium was the sole nitrogen source. Conversely, in the shoots (comprising the cotyledons and hypocotyl), NRA was shown to be independent of nitrate content. Moreover, when ammonium was supplied as the sole nitrogen source, NRA in the shoots was surprisingly higher than under nitrate supply and increased as a function of the tissue ammonium content. Under 15 mM of exogenous ammonium, the NRA was up to 2.5-fold higher than under nitrate supply after 6 d of culture. The NR mRNA accumulation under ammonium nutrition was 2-fold higher than under nitrate supply. The activation state of NR in shoots was especially high compared with roots: from nearly 80% under nitrate supply it reached 94% under ammonium. This high NR activation state under ammonium supply could be the consequence of the slight acidification observed in the shoot tissue. The effect of ammonium on NRA was only observed in cotyledons and when more than 3 mM ammonium was supplied. No such NRA increase was evident in the roots or in foliar discs. Addition of 1 mM nitrate under ammonium nutrition halved NRA and decreased the ammonium content in shoots. Thus, this unusual NRA was restricted to seedling cotyledons when nitrate was lacking in the nitrogen source.     

The effect of L-amino acids on the growth of and nitrate reductase activity in cultured cells of Datura innoxia

A study was carried out of the effect of the 20 protein L-amino acids on the growth and nitrate reductase activity (NRA) of suspensions of Datura innoxia (Mill.) cells. Our intention was to use the information to obtain amino acid resistant cell lines which also had aberrant NRA.Culture growth was measured by the dry weight increase over a 5-day period in the presence or absence of single amino acids (0.05–1 mM). NRA in cells was determined at the beginning and end of a 24-h incubation period in a medium containing 25 mM KNO₃ alone or with 1 mM single amino acids.Ten amino acids inhibited growth and the level of NRA. Of these, only cys, his, met and phe inhibited growth and NRA severely. Arg, ser, thr, try, tyr and val inhibited growth severely but the level of NRA to a lesser extent. Ile, leu and lys inhibited growth but not NRA; ala enhanced growth but had no effect on NRA; asp increased growth and NRA; gly inhibited growth but increased RNA.When a promotory (asp) and an inhibitory (cys or met) amino acid were added to cultures together, growth was inhibited more significantly than when cys or met were added alone. However, NRA was intermediate between that found with asp or either sulfur amino acid alone.In no case could the inhibition of growth and the level of NRA be causally linked unequivocally.     

The effect of gallium nitrate on synoviocyte MMP activity

Gallium, a group IIIa metal salt, has been demonstrated to be an effective immunosuppressive agent. Gallium has also been shown to inhibit the production of inflammatory cytokines, such as IL-1beta, produced by macrophage-like cells in vitro. To further characterize the effects of gallium on the inflammatory process, we examined the effects of gallium nitrate on matrix metalloproteinase (MMP) activity utilizing the rabbit synoviocyte cell line HIG-82. HIG-82 cells were incubated with IL-1beta and TPA, with and without increasing concentrations of gallium nitrate. Conditioned medium was collected and assayed for MMP activity using a synthetic substrate and substrate gel zymography. IL-1beta and TPA alone induced MMP activity in HIG-82 cells. A dose-dependent inhibition of IL-1beta and TPA stimulated MMP activity by gallium nitrate at increasing concentrations was observed. This study demonstrates that gallium nitrate can inhibit the activity of MMPs and may be useful as a modulator of inflammation in arthritis.