The Apparent Induction of Nitrate Uptake by Chara corallina Cells following Pretreatment with or without Nitrate and Chlorate

Nitrate provision has been found to regulate the capacity forChara corallina cells to take up nitrate. When nitrate was suppliedto N sufficient cells maximum nitrate uptake was reached after8 h. Prolonged treatment of the cells in the absence of N alsoresulted in the apparent ability of these cells to take up nitrate.Chlorate was found to substitute partially for nitrate in the‘induction’ step. The effects on nitrate reductionwere separated from those on nitrate uptake by experiments usingtungstate. Tungstate pretreatment had no effect on NO^–₃uptake ‘induced’ by N starvation, but inhibitedNO^–₃ uptake associated with NO^–₃ pretreatment. Chloridepretreatment similarly had no effect on NO^–₃ uptake ‘induced’by N deprivation, but inhibited NO^–₃ uptake followingNO^–₃ pretreatment. The data suggest that there are atleast two mechanisms responsible for the ‘induction’of nitrate uptake by Chara cells, one associated with NO^–₃reduction and ‘induced’ by CIO^–₃ or NO^–₃and one associated with N deprivation. Key words: Nitrate, Chlorate, Chara corallina, Induction     

Regulation of nitrate uptake into Chara corallina cells via NH+4 stimulation of NO−3 efflux

Abstract. Net NO₃ uptake by NO⁻₃ deficient Chara cells was used to calculate [NO⁻₃]_c assuming that the cytoplasm occupies 10% total volume and that nitrate reduction and storage are negligible (i.e. maximum [NO⁻₃]_c was calculated). A linear relationship was found between NO⁻₃ efflux and [NO⁻₃]_c. There was an initial burst of NO⁻₃ efflux when NH⁺₄ was added, followed by a slower efflux rate which matched influx rate such that net NO⁻₃ uptake was zero. Over 50% of NO⁻₃ that had been taken up in 2 h was lost within the first 5 min of NH⁺₄ addition. The Nernst equation was used to predict the direction of the electrochemical driving force for NO⁻₃ entry. Under the experimental conditions used NO⁻₃ efflux is actively transported. The differential involvement of both NO⁻₃ influx and NO⁻₃ efflux in the regulation of NO⁻₃ uptake is discussed and a model is proposed to account for these results which envisages discrete NO⁻₃ influx and NO⁻₃ efflux carriers.     

Nitrate Transport Characteristics in Hordeum vulgare L. Seedlings using Three Different Tracer Techniques

Deane-Drummond, C. E. and Thayer, J.R. 1986. Nitrate transportcharacteristics in Hordeum vulgare L. seedlings using threedifferent tracer techniques.—J. exp. Bot. 37: 429–439. and have been used to investigate various properties of nitrate uptake and translocation intoHordeum vulgare L seedlings. Short term / influx into seed lings grown in CaSO⁴ was stimulated by after a lag of 2 h. The apparent kinetics of shortterm / influx over the concentration range 0?0–0?7mol m fitted Michaelis-Menten equations The apparent V_max didnot change when seedlings were used that had been pretreatedin 10 or 100 mmol m^–3 and V^max=3.77 and 3?56µmol g^–1 fr. wt. h^–1respectively. The apparent Michaelis constants were also similarand K_m=0?47 and 0?45 mol m^–3 respectively. Longer term pulse chase experiments with the heavy isotope ¹⁵Nhave shown that feeding roots with resulted in the preferential appearance of ¹⁵N labelled aminoacids in the xylem sap. Pulse chase experiments with the radioisotope¹³N have shown that feeding shoots with resulted in a radial pattern of distnbution of labelin the leaf veins, which can be detected using autoradiography. The limitations and advantages of all three techniques are comparedby reference to other known experimental data. Key words: ³⁶Chlorate, ¹³nitrate, ¹⁵nitrate, Hordeum vulgare     

Absence of nitrate reductase activity in San 9789 bleached leaves of barley seedlings (Hordeum vulgare cv. Midas)

Abstract San 9789 (norflurazone) blocks carotenoid synthesis which allows chlorophyll bleaching in the light, and has been used recently as a tool to study phytochrome responses without interference from photosynthetic pigments. By using this herbicide, we have found that nitrate reductase activity and light dependent nitrite reduction were lost simultaneously from achlorophyllous areas of barley leaves, with the green areas of the leaf tip still showing high activities. By contrast nitrate reductase is still present in the roots of herbicide treated plants. We suggest that intact chloroplasts are required for the presence of nitrate reductase in barley leaves.     

Mechanism of nitrate uptake into Chara corallina cells: lack of evidence for obligatory coupling to proton pump and a new NO3−/NO3− exchange model

Abstract. Nitrate uptake into Chara corallina cells at different external pH (pH_o) after different NO₃⁻ pretreatment conditions has been investigated. Following NO₃⁻ pretreatment (0.2 mol m⁻³ NO₃⁻) there was little effect of pH_o on subsequent net NO₃⁻ uptake into Chara cells. After N deprivation (2 mmol m⁻³ NO₃⁻) there was a pronounced effect of pH_o on nitrate uptake, the maximum rate occurring at pH_o 4.7. There was no consistent relationship between OH⁻ efflux and NO₃⁻ uptake in short term experiments (< 1 h). NO₃⁻ efflux was also sensitive to pH_o, the maximum rate occurring at ∼ pH_o 5.0. An inhibitor of the proton pump, DES, immediately stimulated NO₃⁻ uptake into cells pretreated with NO₃⁻ and prevented the time-dependent decrease in NO₃⁻, uptake into Chara cells that had been previously treated with low N (2 mmol m⁻³ NO₃⁻). NO₃⁻ efflux was found to be very sensitive to DES with K_i= 0.7 mmol m⁻³. At the optimum pH_o for NO₃⁻ uptake the effect of DES on membrane potential (ψ_m) were slight, and only apparent after 30 min. The results are interpreted in context of current models relating NO₃⁻ uptake and H⁺ pump activity. A new model for NO₃⁻ uptake is proposed which involves NO₃⁻/NO₃⁻ exchange at steady state.     

Compensatory Changes in Ion Fluxes into Barley (Hordeum vulgare L. cv. Betzes) Seedlings in Response to Differential Root/Shoot Growth Temperature

The effect of growth temperature on the short term influx of⁸⁶Rb⁺/K⁺, ³⁶Cl^–/Cl^–, , ⁴⁵Ca²⁺/Ca²⁺and into barley plants (Hordeum vulgareL. cv. Betzes) has been examined. When barley plants were grownwith a differential root: shoot temperature (15 ?C/25 ?C) therewas a marked stimulation of influx of all ions except Ca²⁺.Q₁₀ measurements were close to 2.0 for all ions except Ca²⁺,where Q₁₀ 1.0 was found. Kinetics of ion influx showed thatthere had been almost complete compensation for the lower growingtemperature over a range of concentrations. The regulation of uptake was affected by growth temperature. On exposure to 15?C efflux/influx fell initially but was restored after 5 d. Sensitivity of net uptake to was increased by growth at a lower temperature. The importance of these observations in relationto application to field experiments and the proposed mechanismfor uptake is discussed. Key words: Growth temperature, Nitrate, Ammonium     

A multichannel microcomputer-based system for continuously measuring and recording ion activities of uptake solutions during ion absorption by roots of intact plants

Abstract. A microcomputer-based system for the measurement of changes of ion activity (H⁺, NO₃⁻, K⁺) in the uptake solutions during ion absorption by roots of intact plants is described. Ion activities are measured by means of ion-specific electrodes in a multichannel programmable voltmeter (data acquisition/control unit) which is activated by means of a microcomputer. Incoming data are stored digitally on tape cassettes or floppy discs via the microcomputer. The speed of sampling and large numbers of samples which can be simultaneously measured and recorded make this an extremely versatile system which might be employed for measuring and recording any number of analogue voltage signals.     

Nitrate Transport into Chara corallina Cells using as an Analogue for Nitrate: III. INTERACTIONS BETWEEN CHLORIDE AND NITRATE TRANSPORT PROCESSES

The effects of Cl^– and pretreatment on ³⁶Cl^–influx and influx into Characorallina cells were examined. Both treatments reduced ³⁶Cl^–influx into C. corallina cells in the acid pH range (4.5–7.0). pretreatment stimulated influx into C. corallina cells, but Cl^– pretreatment hadno effect. There was a direct inhibitory effect of CI on influx into C. corallina cells, but no apparenteffect on net NO uptake. The time course of ³⁶Cl accumulation into cytoplasmic and vacuolarcompartments during incubation of the cells with showed that significant radioactivity appeared in the vacuolarsap after 30 min. There was a linear increase in the percentageof total ³⁶CI which crossed the tonoplast (_c-v). There was noeffect of Cl^– or pretreatment on accumulation of radioactivity in the vacuole. Thin layer chromatography ofthe vacuolar sap showed that after 2 h only one component waspresent which had an R_F which was similar to ³⁶CI^–. Therate of accumulation of ³⁶C1^– in the vacuole could beused to estimate rates of reduction. Key words: Chloride, Chlorate, Chara, Nitrate     

Nitrate Transport into Chara corallina Cells using 36C1O3 as an Analogue for Nitrate: II. COMPARISON WITH 14C METHYLAMINE FLUXES AT DIFFERENT pH0 AND NH+4sol;NO3 INTERACTIONS

³⁶C1O₃/NO₃ influx into Chara cells was found to be sensitiveto pH_o and a maximum was found at pH_o = 4.5. By contrast ¹⁴Cmethylamine influx into Chara showed a maximum at pH_o = 8.5,and at this pH_o influx rates were about 150 times higher thanrates of ³⁶C1O₃/NO₃ influx. However, at pH_o = 4.5, ³⁶C1O₃/NO₃influx rates were, in some cases, comparable with rates of ¹⁴Cmethylamine influx. ³⁶C1O₃/NO₃ influx into Chara cells was stimulatedby Rb ⁺, K⁺, Na ⁺, and NH₄⁺, but not by Cs⁺ or Li ⁺. NO₃ andCl reduced ¹⁴C methylamine influx into Chara by 30%. NH₄⁺ causedvery considerable inhibition of ¹⁴C methylamine influx intoChara, but had no effect on ³⁶C1O₃/NO₃ influx in the presenceof K ⁺. Net NO³ uptake into Chara was completely prevented byNH₄⁺ even at relatively low NH₄⁺ concentrations (25 mmol m ^–3).This latter effect was reversed by diethylstilbestrol (DES).Evidence is presented for the stimulation of NO₃ efflux by NH⁴⁺as the mechanism responsible for the immediate effects of NH₄⁺on net NO₃ uptake into Chara cells. Key words: Chara, ¹⁴C methylamine, ³⁶ClO^–₃, pH     

Nitrate Transport into Chara corallina Cells using 36ClO-3 as an Analogue for Nitrate: I. INTERACTION BETWEEN 36ClO-3 AND NO-3 AND CHARACTERIZATION OF 36CIO-3/NO-3 INFLUX

The use of chlorate as an analogue for NO^–₃ during nitrateuptake into Chara corallina cells has been investigated. NO^–₃inhibits ³⁶C1O^–₃ influx into Chara over the concentrationrange 0–1000 mmol m^–3. Lineweaver-Burke plots ofthe data are characteristic of competitive inhibition by NO^–3in the low concentration range (0–300 mmol m^–3 ClO^–₃)and apparent K_INO3 is 140 mmol m^–3 which is of a similarorder of magnitude as apparent K_mCIO3- 180 mmol m^–3. Athigher substrate concentrations the inhibition by NO^–₃was not characteristic of competitive or uncompetitive inhibition. ³⁶C1O^–₃/NO^–₃ influx was dependent on K⁺ and Ca²⁺in the external medium and inhibited by FCCP. NO^–₃ pretreatmentor N starvation increased subsequent ³⁶C1O^–₃/NO^–₃influx into Chara. A comparison between rates of net NO^–₃uptake and ³⁶C1O^–₃/NO^–₃ influx supported the previoushypothesis that NO^–₃ efflux is an important componentin the determination of overall uptake rates. Key words: Nitrate, Chara, ³⁶CIO^–₃