Control of Net Uptake of Nutrients by Regulation of Influx in Barley Plants Recovering from Nutrient Deficiency

Rates of influx and net uptake of nitrate, phosphate and sulphatewere measured in intact barley plants, and concurrent effluxwas obtained by difference. Net uptake of these anions variedwidely depending on the nutrient status of the plants, and thedifferences in net uptake could be accounted for almost entirelyby changes in influx. Efflux played only a minor role in regulatingnet uptake of nitrate, phosphate or sulphate during recoveryfrom N-, P-, or S-deficiency. Nitrate influx and short-term ammonium absorption by N-deficientbarley plants were closely correlated, and varied in parallelwith rates of net uptake of nitrate or ammonium by similar plants.Again, it would seem that net uptake of ammonium is controlledpredominantly by changes in the rate of influx.Copyright 1993,1999 Academic Press Hordeum vulgare, barley, nutrient absorption, influx, nitrate, phosphate, sulphate, ammonium     

Effects of sulphate and pH on the plant-availability of phosphate adsorbed on goethite

The adsorption of phosphate on metal (hydr)oxides may be influenced by the pH and by the adsorption of other ions. In this study, the influence of sulphate and pH on phosphate adsorption on goethite and the availability to plants of adsorbed phosphate was examined. Maize plants were grown on suspensions of goethite with adsorbed phosphate, containing the same total amount of phosphate and either 0.11 mM or 2.01 mM sulphate at pH 3.7, 4.6 or 5.5. The uptake of phosphorus by the plants increased with the larger sulphate concentration and decreasing pH. Mean P uptake in the treatment with 2.01 mM sulphate and pH 3.7 was 55 µmol plant^-1, whereas in the treatment with 0.11 mM sulphate and pH 5.5 it was 2 µmol plant^-1. Batch adsorption experiments using³² P and speciation modelling of ion adsorption showed that in the presence of sulphate, the phosphate concentration in solution strongly increased with decreasing pH, due to competitive adsorption between sulphate and phosphate on goethite. Modelled phosphate concentrations in solution in the uptake experiment were all below 0.6 µM and correlated well with the observed P uptake. This correlation indicates that the strong influence of the sulphate concentration and pH on the plant-availability of adsorbed phosphate results from the competition between sulphate and phosphate for adsorption on goethite.     

Growth of Perennial Ryegrass (Lolium perenne L.) Exposed to a Low Concentration of Sulphur Dioxide

The influence of a low concentration of SO₂ on the growth andsulphur status of perennial ryegrass (Lolium perenne L.) cv.S23 was examined in a system of specially designed growth chambers.For plants grown without additions of sulphate to the soil,erposure to ifitered air containing 50 µg m^–3 SO₂alleviated sulphur deficiency that developed during a sequenceof successive harvests, and gave increased yield. The plantshad higher contents of organic and inorganic sulphur than thosegrown with neither sulphate nor SO₂. Plants grown with addedsulphate showed no signs of sulphur deficiency and althoughexposure to SO₂ increased their sulphur content it had no effecton yield. The coefficient of transpiration (g water transpiredg^–1 dry wt. of shoots) was reduced when plants which otherwisehad an inadequate supply of sulphur were exposed to SO₂; forplants with adequate supplies of sulphate, it was similar whetherthey were grown with or without the addition of SO₂ to the air.The results are discussed in relation to other known reactionsof plants to SO₂.     

Suppression of the High Affinity Phosphate Uptake System: A Mechanism of Arsenate Tolerance in Holcus lanatus L.

In Holcus lanatus L. phosphate and arsenate are taken up bythe same transport system. Short-term uptake kinetics of thehigh affinity arsenate transport system were determined in excisedroots of arsenate-tolerant and non-tolerant genotypes. In tolerantplants the V_max of ion uptake in plants grown in phosphate-freemedia was decreased compared to non-tolerant plants, and theaffinity of the uptake system was lower than in the non-tolerantplants. Both the reduction in V_max and the increase in K_m ledto reduced arsenate influx into tolerant roots. When the twogenotypes were grown in nutrient solution containing high levelsof phosphate, there was little change in the uptake kineticsin tolerant plants. In non-tolerant plants, however, there wasa marked decrease in the V_max to the level of the tolerant plantsbut with little change in the K_m. This suggests that the lowrate of arsenate uptake over a wide range of differing rootphosphate status is due to loss of induction of the synthesisof the arsenate (phosphate) carrier. Key words: Arsenate, Holcus lanatus L., phosphate uptake, tolerance mechanisms, uptake mechanisms     

Growth of Lucerne (Medicago sativa L.) Exposed to Sulphur Dioxide

The effect of exposure to sulphur dioxide (0 or 96 µgm^–3 SO₂) on the growth and sulphur content of lucerne(Medicago sativa L.) was examined in a period of 135 d duringwhich the plants were harvested four times. The lucerne wasgrown in pots of soil with and without the addition of sulphateand of nitrate. Evidence of sulphur deficiency, including areduction in the weight, the number and the sulphur contentof shoots, was found in plants grown without added sulphate.Deficiency was alleviated through exposure of plants to SO₂.Apart from reducing shoot weight at one harvest and generallyincreasimg the concentration of sulphur in the shoots, exposureto SO₂ had no significant effect on plants grown with addedsulphate. The yield of shoots was greater, and was reduced toa lesser extent with sulphur deficiency, in plants grown withadded nitrate than in those dependent on rhizobia. Whilst thetranspiration coefficient increased greatly in sulphur-deficientplants, it was reduced where otherwise similarly treated plantswere exposed to SO₂; this treatment did not alter the coefficientin plants with an adequate supply of sulphur from the soil.     

The Effect of Ions on Growth and Leaf Succulence of Atriplex hortensis var. cupreata

When plants of Atriplex hortensis var. cupreata were grown insolutions containing at least 100 mmoll^–1 of various saltsit was found that sodium was the ion most effective in stimulatingleaf succulence, irrespective of whether the anion was chloride,bromide or sulphate. Potassium was the next most effective ion.Magnesium and calcium were without effect. Dry weight productioncould be greatly reduced by sodium and potassium but stimulatedby magnesium. The results are compared with those previouslyreported for C₄ species of Atriplex.     

Uptake and long-distance transport of phosphate,potassium and chloride in relation to internal ion concentrations in barley: evidence of non-allosteric regulation

The extent to which uptake and transport of either phosphate, potassium or chloride are controlled by the concentration of these ions within the root, perhaps through an allosteric mechanism, was investigated with young barley plants in nutrient solution culture. Plants were grown with their roots divided between two containers, such that a single seminal root was continuously supplied with all the required nutrient ions, while the remaining four or five seminal roots were either supplied with the same solution (controls) or, temporarily, a solution lacking a particular nutrient ion (nutrient-deficient treatment). Compared with controls, there was a marked stimulation of uptake and transport of labelled ions by the single root following 24 h or more of nutrient dificiency to the remainder of the root system. This stimulation, which comprised an increased transport to the shoot and, for all ions except Cl^-, increased transport to the remainder of the root system, took place without appreciable change in the concentration of particular ions within the single root. However, nutrient deficiency quickly caused a lower concentration of ions in the shoot and the remaining roots. The results are discussed in relation to various mechanisms, proposed in the literature, by which the coordination of ion uptake and transport may be maintained within the plant. We suggest that under our conditions any putative allosteric control of uptake and transport by root cortical cells was masked by an alternative mechanism, in which ion influx appears to be regulated by ion efflux to the xylem, perhaps controlled by the concentration of particular ions recycled in the phloem to the root from the shoot.     

The Effect of Wind and a Reduced Supply of Phosphorus and Nitrogen on the Growth and Water Relations of Festuca arundinacea Schreb

Festuca arundinaceae was grown at high and low wind-speed attwo levels of either soil phosphorus or soil nitrogen. At increasedwind-speed, mean relative growth rate and leaf extension ratewere reduced when plants were grown with high nutrient concentrationsand further reduced when phosphorus or nitrogen stress was imposedon the plants. Transpiration was increased at high wind-speedexcept under conditions of phosphorus stress, where the ratewas actually decreased. Relationships between water stress,wind and nutrient status are discussed, especially in relationto the possible role of phosphorus stress in causing sclerophylly. Festuca arundinacea Schreb., relative growth rate, water stress, wind, nitrogen, phosphorus, sclerophylly     

Netuptake of sulphate and its transport to the shoot in tobacco plants fumigated with H2S or SO2

In tobacco plants the net uptake of sulphate and its transport to the shoot were determined after cultivation with low, normal, and high sulphate supply. The relative amount of the sulphate taken up that was transported to the shoot was used as a measure of xylem loading. Net uptake of sulphate and its transport to the shoot were low in tobacco plants grown with low sulphate, and high in plants cultivated with high sulphate. Xylem loading, however, was relatively low in tobacco plants grown with high sulphate and relatively high in tobacco plants grown with low sulphate supply. Pre-culture in low sulphate containing nutrient solution also resulted in a high proportion of the absorbed sulphate being transported into the xylem if normal sulphateconcentration was supplied afterwards. Fumigation with H₂S or SO₂ reduced net uptake of sulphate in tobacco plants grown with normal, but not with high sulphate supply. Sulphate transport to the shoots was diminished by H₂S or SO₂ fumigation in tobacco plants grown with normal and high sulphate supply. Also the relative amount of the sulphate taken up that was transported to the shoot was lowered by fumigation with H₂S or SO₂ in tobacco plants grown with normal sulphate supply. Apparently, the diminished sulphate transport to the shoot upon H₂S or SO₂ fumigation can only partially be explained by a smaller sulphate uptake. Sulphur nutrition of tobacco plants also seems to be controlled by xylem loading of sulphate. The possible role of glutathione as a signal regulating sulphur nutrition of tobacco plants upon fumigation with H₂S and SO₂ is discussed.     

Regulation of Sulphate Transport in a Tropical Legume, Macroptilium atropurpureum, cv. Siratro

When young plants of Macroptilium atropurpureum, cv. Siratrowere deprived of external sulphate (-S plants) growth of shootsand roots continued at rates comparable to those in plants wellsupplied with sulphate (control) for 3 d and 5 d respectively.Dilution of internal sulphur therefore took place and redistributionof sulphur occurred between inorganic and organic forms andbetween roots and younger leaves. Even when S-deficiency limitedgrowth, plants contained 16% of their total sulphur as sulphate,but most of this was retained in old leaves and redistributedslowly to growing zones. The capacity for sulphate uptake increased in roots of –Splants very soon after they were deprived of external sulphate;within 24 h the absorption from 0.25 mol m^–3 SO₄^2–was more than five times that of control roots. Maximum increasedcapacity was reached after 2–3 d stress when the V_maxof system 1 was 1948 nmol h^–1g^–1root fr. wt. in–S plants and 337 nmol h^–1g^–1root fr. wt.in controls. The K^mfor system 1 did not change significantlywith S-stress being between 5–8 µM in both setsof plants. Absorption of L-cysteine was not stimulated by S-stress. There was a close, positive relationship between plant growthrate and the rate at which sulphate uptake capacity was enhancedby withholding sulphate from culture solutions. When –S plants were replaced in sulphate-containing solutiontheir capacity for SO₄^2– declined to the control levelwithin 24 h. Very marked repression of capacity was also foundwhen –S plants were treated with L-cysteine, but therewas no immediate effect with methionine. Roots of this species appear to have a very active system fordegrading L-cysteine to sulphate, 30% of the label in ³⁵S-cysteineabsorbed by roots was recovered in ³⁵SO₄^2– after 20 minor 2 h incubation. By contrast, roots had a very weak abilityto reduce sulphate. When part of the root system was in solution lacking sulphatethere was enhanced uptake of sulphate by other parts which themselveswere amply supplied with sulphate. This is seen as an exampleof compensatory absorption. The response to S-stress is specific and there were no positiveinteractions between S-stress and the absorption of phosphate,or P-stress and the uptake of sulphate. The results are discussed in relation to the close control ofsulphate uptake by internal sulphate concentration, redistributionof forms of sulphur during stress and mobility of sulphate inthe phloem. Key words: Kinetics, Amino-S, Sulpholipid, Repression;, Deficiency     

Nutrient Relations of Groundsel (Senecio vulgaris) Infected by Rust (Puccinia lagenophorae) at a Range of Nutrient Concentrations II. Uptake of N, P and K and Shoot-Root Interactions

Groundsel (Senecio vulgaris), healthy or infected with rust,Puccinia lagenophorae, was grown at a range of nutrient concentrationsin sand culture. Specific absorption rates calculated on thebasis of root dry weight (SAR_W) were greater in rusted thancontrol groundsel for nitrogen, potassium and phosphorus. Whilethe magnitudes of these stimulations varied, they occurred acrossthe whole range of nutrient concentrations. By contrast, specificabsorption rate on the basis of root length (SAR_L) were littlechanged by rust at any external nutrient concentration; SAR_Lfor phosphate and potassium were slightly reduced when nutrientswere freely available. Water flux per unit dry root weight and length was stimulatedby rust because transpiration per unit leaf area was more rapidin infected plants after fungal sporulation. However, water-fluxand the rate of uptake of nutrients were correlated only whenexpressed on the basis of root weight and increased transpirationdid not appear to be the mechanism underlying increased rootactivity. Rather, increased SAR_W for N, P and K could very largelybe attributed to increased shoot demand per unit root, whichresulted from the higher shoot: root (S: R) ratios of infectedindividuals. Changes in S: R accounted for 92, 81 and 57% oftotal variation in SAR_W for K, P and N respectively. Greatervalues for SAR_W were possible because specific root length (SRL)increased, producing more functional root per unit root weight.The lack of stimulation in SAR_L in response to rust could beexplained since the higher SRL of infected plants resulted instable values of shoot weight per unit root length, i.e. shootdemand was not increased by infection on this basis. Senecio vulgaris, Puccinia lagenophorae, rust infection, nutrient uptake, water uptake, shoot: root interactions     

Ion Uptake Efficiency of Sunflower Roots

The term ion uptake efficiency is used for the rate of uptake of a particular ion from nutrient solutions holding a standard concentration of that ion (0.5 mM sulphate, 1.5 mM phosphate or 2.0 mM rubidium). The uptake efficiency for rubidium and phosphate in roots of intact sunflower plants depended on the salt status of the plants and on the concentration of the ion under investigation in pretreatment solutions. The effect of pretreatment was a rapid process causing differences of more than 300% in ion uptake efficiency within 1 h, depending on the composition of the pretreatment solution. At concentrations above 0.1 mM the rate of uptake of rubidium in the root was higher than the net potassium uptake necessary for adequate growth. The rate of sulphate uptake was related to potassium uptake but not to phosphate uptake. It is suggested that ion uptake of the roots is regulated by internal factors as well as by direct interactions between the medium and the absorbing surfaces.     

Nutrient-limited growth rates: quantitative benefits of stress responses and some aspects of regulation

Young sunflower plants (Helianthus annuus L.) under stress oflow nitrate or phosphate availability exhibited increases inroot: shoot ratio and in kinetic parameters for uptake. Theyshowed no significant changes in photosynthetic utilizationof either nutrient. Increases in root: shoot ratio were achievedby early and persistent suppression of shoot growth, but notroot growth. Affinity for phosphate uptake, 1/K_m(P), increasedwith phosphate stress, as did affinity for nitrate uptake, 1/K_m(N),with nitrate stress. Maximal uptake rate, V_max, for phosphateuptake increased with phosphorus stress; V_max for nitrate didnot increase with nitrogen stress. Phosphate V_max was relatedstrongly to root nutrient status. Decreases in V_max with plantage were not well explained by changes in age structure of roots.Estimated benefits of acclimatory changes in root: shoot ratioand uptake kinetics ranged up to 2-fold increases in relativegrowth rate, RGR. The relation of RGR to uptake physiology followedpredictions of functional balance moderately well, with somesystematic deviations. Analyses of RGR using growth models implyno significant growth benefit from regulating Vmax, specifically,not from down-regulating it at high nutrient availability. Quantitativebenefits of increases in root: shoot ratio and uptake parametersare predicted to be quite small under common conditions whereinnutrient concentrations are significantly depleted by uptake.The root: shoot response is estimated to confer the smallestbenefit under non-depleting conditions and the largest benefitunder depleting conditions. Even then, the absolute benefitis predicted to be small, possibly excepting the case of heterogeneoussoils. Depleting and non-depleting conditions are addressedwith very different experimental techniques. We note that atheoretical framework is lacking that spans both these cases,other than purely numerical formulations that are not readilyinterpreted. Key words: Nutrient stress, nutrient uptake, nutrient use efficiency, relative growth rate, Helianthus annuus     

Interactive effects of mycorrhization and elevated atmospheric CO2 on sulphur nutrition of young pedunculate oak (Quercus robur L.) trees

Pedunculate oak (Quercus robur L.) was germinated and grown at ambient CO₂ concentration and 650 μmol mol^?1 CO₂ in the presence and absence of the ectomycorrhizal fungus Laccaria laccata for a total of 22 weeks under nonlimiting nutrient conditions. Sulphate uptake, xylem loading and exudation were analysed in excised roots. Despite a relatively high affinity for sulphate (K_M= 1.6 mmol m^?3), the rates of sulphate uptake by excised lateral roots of mycorrhizal oak trees were low as compared to herbaceous plants. Rates of sulphate uptake were similar in mycorrhizal and non-mycorrhizal roots and were not affected by growth of the trees at elevated CO₂. However, the total uptake of sulphate per plant was enhanced by elevated CO₂ and further enhanced by elevated CO₂ and mycorrhization. Sulphate uptake seemed to be closely correlated with biomass accumulation under the conditions applied. The percentage of the sulphate taken up by mycorrhizal oak roots that was loaded into the xylem was an order of magnitude lower than previously observed for herbaceous plants. The rate of xylem loading was enhanced by mycorrhization and, in roots of mycorrhizal trees only, by growth at elevated CO₂. On a whole-plant basis this increase in xylem loading could only partially be explained by the increased growth of the trees. Elevated CO₂ and mycorrhization appeared to increase greatly the sulphate supply of the shoot at the level of xylem loading. For all treatments, calculated rates of sulphate exudation were significantly lower than the corresponding rates of xylem loading of sulphate. Radiolabelled sulphate loaded into the xylem therefore seems to be readily diluted by unlabelled sulphate during xylem transport. Allocation of reduced sulphur from oak leaves was studied by flap-feeding radiolabelled GSH to mature oak leaves. The rate of export of radioactivity from the fed leaves was 4–5 times higher in mycorrhizal oak trees grown at elevated CO₂ than in those grown at ambient CO₂. Export of radiolabel proceeded almost exclusively in a basipetal direction to the roots. From these experiments it can be concluded that, in mycorrhizal oak trees grown at elevated CO₂, the transport of sulphate to the shoot is increased at the level of xylem loading to enable increased sulphate reduction in the leaves. Increased sulphate reduction seems to be required for the enhanced allocation of reduced sulphur to the roots which is observed in trees grown at elevated CO₂. These changes in sulphate and reduced sulphur allocation may be a prerequisite for the positive effect of elevated CO₂ on growth of oak trees previously observed.     

Effect of sulphate deficiency on the plasma membrane polypeptide composition of Brassica napus

Highly purified oilseed rape (Brassica napus) root plasma membranefractions were prepared and their polypeptide patterns analysedby two-dimensional gel electrophoresis. Sulphur starvation enhancesthe sulphate uptake capacity of B. napus roots. The relativeabundance of several polypeptides increased significantly andspecifically after sulphur starvation. Several of them (37,38, 60, and 65 kDa), found in sulphur-starved plants, were moreabundant in a phase-partitioned membrane fraction treated withTriton X-100/KBr, indicating that they are intrinsic polypeptides.One polypeptide (47 kDa) was identified in the in vitro translationproducts of the roots mRNAs as specific for S-starved plants.It was also present among the intrinsic polypeptides specificfor —S plants. These plasma membrane polypeptides mightbe involved in sulphate uptake. Key words: Sulphate, sulphur-starvation, plasma membrane, polypeptides, root, transport     

The Uptake of Phosphate by Plants from Flowing Nutrient Solution: IV. EFFECT OF PHOSPHATE CONCENTRATION ON THE GROWTH OF TRIFOLIUM REPENS L. SUPPLIED WITH NITRATE, OR DEPENDENT UPON SYMBIOTICALLY FIXED NITROGEN

Breeze, V. G. and Hopper, M. J. 1987. The uptake of phosphateby plants from flowing nutrient solution. IV. Effect of phosphateconcentration on the growth of Trifolium repens L. suppliedwith nitrate, or dependent upon symbiotically fixed nitrogen.—J.exp. Bot. 38: 618–630. Nodulated white clover plants were subjected to a range of phosphateconcentrations in flowing solution culture (0.32 to 8.0 mmolm^–3 P) at 41 d from sowing, either supplied with nitrateor dependent on symbiotically-fixed nitrogen. No effect of phosphateconcentration in solution on dry matter production, relativegrowth rate, root/shoot ratio, or water soluble carbohydrateconcentration of the plant tissue was observed after 24 d fromthe start of the experiment, although the plants supplied withnitrate yielded more than the others. Phosphate uptake throughoutthe experimental period was related to the solution concentration,but the source of nitrogen did not affect the phosphorus concentrationsof the shoots. However, the roots of the plants dependent onsymbiotically-fixed nitrogen had higher concentrations of phosphorusthan those supplied with nitrate, but this did not appear tobe due to an increased phosphorus requirement for nitrogen fixation,because the amount fixed was unaffected by the phosphate concentrationin solution. The cation-anion balance showed that plants dependenton nitrogen fixation had no larger requirement for calcium thanplants supplied with nitrate, but a requirement for hydroxylions equivalent to over 130 kg lime per tonne of dry shoot.It is suggested that the enhanced phosphate uptake by plantsdependent on nitrogen fixation is due to this need for a cation-chargebalancing anion. Key words: Phosphate uptake, nitrogen fixation, Trifolium repens L., repens L., cation-anion balance, flowing solution culture     

Nutrient Relations of Groundsel (Senecio vulgaris) Infected by Rust (Puccinia lagenophorae) at a Range of Nutrient Concentrations I. Concentrations, Contents and Distribution of N, P and K

Groundsel (Senecio vulgaris L.), healthy or infected with therust fungus Puccinia lagenophorae was grown in sand and fedwith a complete nutrient medium diluted to give a range of concentrations.Analysis of bulked, dried tissues of the plant showed that undernutrient-rich conditions rust infection resulted in increasedconcentrations of total (Kjeldahl) nitrogen and potassium buthad little effect on phosphorus concentration. Thus, despitereduced dry weight growth, total plant nitrogen contents wereno less in rusted than control plants. Although total contentsof phosphorus and potassium were reduced by rust, effects wereprobably related to loss of these nutrients in fungal spores. Interactions between rust infection and nutrient supply weresignificant but differed between nutrients: rust caused increasednitrogen concentrations only under nutrient-rich conditionsbut increased phosphorus concentrations only when nutrient supplywas limited. Increased concentrations were not confined to infectedtissues. Mechanisms underlying rust-nutrient interactions appearto be complex and to depend inter alia on the partitioning andrecycling of the particular nutrient within the plant. Rust-inducedincreases in potassium concentration occurred under both highand low nutrient conditions but were confined to infected tissues.Potassium accumulation in nutrient deficient conditions wasprobably due to increased transpirational flux into infectedtissues, but under nutrient-rich conditions reduced potassiumexport appeared to assume greater significance. The possible implications of the changed nutrient relationsfor the wider interactions of rust-infected plants in naturalvegetation are discussed. Senecio vulgaris, Puccinia lagenophorae, rust infection, nutrient deficiency, nutrient content, nutrient concentration, nutrient distribution     

Measurement of Endogenous Phosphorus Levels in Relation Flowering in the Long-Day Plant Lemna gibba G3

When Lemna gibba G3 was grown on E medium, a decrease in thephosphate concentration caused a suppression of flowering andlead to a decrease in the phosphorus concentration in the plants.Addition of salicylic acid reversed this inhibition withoutcausing an increase in the phosphorus concentration, while additionof copper or ammonium to Hoagland-type medium inhibited flowering,also without affecting the phosphorus concentration. Plantsgrown under 8 h or 24 h daylengths exhibited a FL% of 0 or about50, respectively, but showed no difference in their phosphorusconcentrations. These results indicate that a high phosphorusconcentration is not always required for flowering in Lemnagibba G3. When plants were grown on a modified E medium in which 1/50strength Hutner’s medium micronutrients were substitutedfor the normal E medium micronutrients, the suppression of floweringcaused by reduced phosphate was completely eliminated. Addingeach micronutrient individually at the normal concentrationto the modified E medium demonstrated that manganese inhibitedflowering in modified E medium with a low phosphate concentration. (Received January 31, 1986; Accepted July 4, 1986)     

Restoration of protein level in detached leaves by supply of sulphate

Summary Young leaves were removed from plants grown at a range of sulphur levels and incubated in solutions with and without sulphate. In the absence of sulphate alcohol-insoluble N in the leaves declined irrespective of sulphur status. Sulphate arrested or reversed the decline in leaves from sulphur-deficient plants but had no such effect on leaves from plants grown with adequate sulphur. The difference in response patterns between deficient and non-deficient plants, induced by sulphate treatment could form the basis for a plant test for sulphur deficiency.     

Influence of glutathione (GSH) on net uptake of sulphate and sulphate transport in tobacco plants

Net uptake of sulphate by the roots, and its transport to theshoot was inhibited in intact tobacco plants by 1 h exposureof its roots to 0.1 or 1.0 mM GSH. The relative amount of sulphatetaken up that was transported to the shoot was not affectedby this treatment. Apparently, sulphate uptake, but not xylemloading of sulphate, was inhibited by GSH. Similar results wereobtained when L-cysteine was used instead of GSH. As L-cysteine,mediated inhibition of sulphate, net uptake was counteractedby exposure of the roots to BSO, GSH synthesis seems to be requiredfor inhibition of sulphate uptake by L-cysteine. However, exposureto 0.1 or 1.0mM GSH did not result In an enhanced GSH levelin roots or shoots. Also the cysteine contents remained unchanged.Small changes in metabolically active pools of GSH or cysteineseem to be responsible for the inhibition of sulphate uptakeand its transport to the shoot. Flap-feeding of GSH to a matureleaf resulted in an inhibition of net uptake of sulphate bythe roots and its transport to the shoot. These findings supportthe hypothesis that GSH produced in the leaves acts as a signalto control sulphur nutrition of plants. Key words: Sulphate transport, sulphate uptake, xylem loading, Nicotiana, Solanaceae, glutathione, cysteine, buthionine sulphoximine