The light-dependent effect of external pH on the membrane potential of Nitella

In the light the membrane potential of Nitella flexilis andNitella axilliformis was hyperpolarized by raising the externalpH above pH 5.5, at the rate of 30–40 mV/pH below pH 8.This hyperpolarization was largely reduced in the dark. The membrane potential was sensitive to the external pH of mediawith a low potassium concentration, where it was relativelyinsensitive to potassium concentration. In media of a high concentrationwhere it was sensitive to the potassium concentration, the membranebecame insensitive to the external pH. The transition from apH-sensitive to a pH-insensitive state occurred rather abruptlyon increasing the external potassium concentration. (Received September 1, 1972; )     

The effect of external pH on the membrane potential of Nitella and its linkage to metabolism

The membrane potential of Nitella is highly sensitive to externalpH in the neutral region (pH 5.5 to 8) in the light. We foundthat the sensitivity usually was reduced by darkness, metabolicinhibitors (DCMU, DNP) or cooling. Under some circumstancesthe high pH-sensitivity of the membrane potential was observedeven in the dark. However, even in this case, it was reducedby DNP or cooling. These results indicate that the externalpH-dependence of the membrane potential of Nitella is closelylinked to metabolism. (Received May 8, 1973; )     

Effect of intracellular pH on the light-induced potential change and electrogenic activity in tonoplast-free cells of Chora australis

Effects of the intracellular H+ concentration on the membranepotential and membrane resistance of tonoplast-free cells ofChara australis were examined under light and dark conditions.Cells were made tonoplast-free by perfusing the vacuole withmedia containing 5 mM EGTA and 30 mM buffers of various pH values.The electrogenic pump was stopped by removing the intracellularATP. The ATP-dependent part of the membrane potential was largeat pH₁ 6.2 and 6.9, but decreased in both the acidic (pH₁ 5.1,5.7) and alkaline (pH₁ 7.9, 8.7) ranges. Assuming that the putativeelectrogenic H+ pump acts solely as a current source, we estimatedthe current and the work done by the pump. Both the currentand the work were at a maximum at pH₁ 6.9, but decreased tosome extent at pH₁ 7.9–8.7 and decreased greatly at pH₁5.7–5.1. Light caused a significant membrane hyperpolarization at pH₁6.2–7.9, but only a slight hyperpolarization at pH₁ 5.1,5.7 and 8.7. The presence of light-induced hyperpolarizationat pH₁ lower than 6.2 suggests that acidification of the cytoplasmupon illumination does not cause activation of the putativeH+ pump. Membrane resistance was very high at pH₁ 5.1 and 5.7 and verylow at pH₁ 8.7. The very high R_m values at pH₁ 5.1 and 5.6 arebelieved to be related to inhibition of the activity of thepump. (Received June 20, 1979; )     

Action of Mono- and Difluorodinitrobenzene on Induced Electrical Modifications by External pH Changes in Nitella

The action of mono- (FNB) or difluorodinitrobenzene (DFNB) onion permeability is mainly attributed to its interactionwithamino groups of the membrane by dinitrophenylation. Nitella cells were dimtrophenylated at pH 7.3 and the membranepotential and electrical resistance were then measured in acidicor basic solutions. No matter what the pH value was, FNB andDFNB induced a depolarization of the membrane potential andcaused a diminution of resistance. However these effects ofFNB and DFNB were more drastic at alkaline pH and in the presenceof a weak concentration of potassium. Neither the addition of0.1 mM calcium nor the substitution of chlorides by nitratesmodified the DFNB effect. These results are compatible withthe assumption that the DFNB binding to the membrane leads toan augmentation of the negative charges of the membrane bringingabout an increased cation conductance and a modification ofthe affinity of a K⁺/H⁺exchange pump. The transient responseof the membrane potential at the time of dinitrophenylationwas used to roughly estimate the total density of amino groupsof the membrane of Nitella.     

The Role of the Plasma Membrane Proton Pump in Short-term pH Regulation in the Aquatic Liverwort Riccia fluitans L.

The question is raised, to what extent is the plasma membraneproton pump involved in short-term pH regulation of plant cells?For this purpose the cytosolic pH (pH_c) of Riccia fluitans rhizoidand thallus cells has been measured continuously using pH-sensitivemicroelectrodes (Felle and Bertl, 1986a). It is demonstratedthat pH perturbations (light, weak acids, external pH) in bothdirections are completely or at least partly eliminated withinminutes. The pH_c recovery occurs regardless of the activationstate of the proton pump. The proton pump reacts to changesin cytosolic pH as expected, namely with increased proton extrusionto decreased pH_c; however, changes in pump activity (fusicoccin,CCCP, cyanide) do not necessarily result in cytosolic pH shifts.These results suggest that several proton transport mechanisms(including the proton pump) co-operate in the restoration ofa perturbed cytosolic pH. It is concluded, however, that theproton pump, although most important for the energization ofthe plasma membrane, does not regulate cytosolic pH.     

Electrogenic Pump Current and ATP-Dependent H+ Efflux Across the Plasma Membrane of Nitellopsis obtusa

The correlation between the pump current and the ATP-dependentH⁺ efflux was examined in internodal cells of Nitellopsis obtusa.To control the cytoplasmic pH and ATP concentration, the tonoplastwas removed by intracellular perfusion with an EGTA-containingmedium. Two groups of perfused cells were prepared, one with1 mM ATP (+ATP cells) and the other without ATP but with hexokinaseand glucose (–ATP cells). The ATP-dependent H⁺ effluxwas calculated as the difference in H⁺ efflux between the +ATPand –ATP cells. Based on an electrically equivalent circuitmodel of the plasma membrane, the pump current was calculatedfrom the membrane potentials and the membrane resistances ofboth +ATP and –ATP cells. When the membrane potentialwas not too high (–220 mV), the ATP-dependent H⁺ current(19 mA m^–2) was almost equal to the pump current (20 mAm^–2) calculated from the electrical data. This indicatesthat the electrogenic pump current across the plasma membraneof Nitellopsis obtuse was mostly carried by H⁺. But when themembrane potential was high (–280 mV), the H⁺ currentwas lower than the pump current. The possible cause of thisdiscrepancy is discussed. (Received November 5, 1984; Accepted February 28, 1985)     

The Regulation of Proton/Amino Acid Symport in Riccia fluitans L. by Cytosolic pH and Proton Pump Activity

In the aquatic liverwort Riccia fluitans the regulation of theplasma membrane H⁺/amino acid symport has been investigated.Cytosolic pH (pH_c), membrane potential (E_m) and membrane conductancehave been measured and related to transport data, (i) The releaseof [¹⁴C]amino acids is strongly stimulated by cytosolic acidification,induced by the external addition of acetic acid, a decreasein external K⁺, and in the change from light to dark. On average,a decrease in pHc of 0.5 to 0.6 units corresponded with a 4-foldstimulation in amino acid efflux. (ii) External pH changes havefar less effect on substrate transport than the cytosolic pHshifts of the same order. (iii) The inwardly directed positivecurrent, induced by amino acids, is severely inhibited by cytosolicacidification. (iv) Fusicoccin (FC) stimulates amino acid uptakewithout considerable change in proton motive force. (v) Whenthe proton motive force is kept constant, the uptake of aminoacids into Riccia thalli is much lower than when the pump isdeactivated. It is suggested that both the proton pump activityand cytosolic pH are the dominant factors in the regulationof the H⁺/amino acid symport across the plasma membrane of Ricciafluitans, and it is concluded that the proton motive force isnot a reliable quantity to predict and interpret transport kinetics. Key words: Amino acid, cytosolic pH, pH-sensitive electrode, proton motive force, regulation, Riccia fluitans     

Transient light-induced changes in ion channel and proton pump activities in the plasma membrane of tobacco mesophyll protoplasts

Rapid, transient changes of the membrane potential upon lighttransitions are generally observed in microelectrode studies.In a patch-clamp study similar responses to light transitionswere found in current clamp. Corresponding with the changesof membrane potential, light-induced current changes in voltageclamp were observed. This paper evaluates the involvement ofoutward rectifying conductances and plasma membrane bound H⁺-ATpases(proton pump) to these light responses in mesophyll protoplastsof Nicotiana tabacum L. The contribution of K⁺-channels to theseresponses, could be minimized by variation of the holding potentialor addition of the K⁺-channel blocker verapamil. It was concludedthat light transitions modulate both proton pump and K⁺-channelactivity. Effects of light on membrane current were not observedin root cells and chlorophyll-deficient cells, suggesting thatthe response requires photosynthetic activity. However, blockersof photosystems I and II did not affect current changes. Key words: Light, patch-clamp, plasma membrane, tobacco, whole cell     

The effects of bicarbonate ions and external pH on the membrane potential and resistance ofNitella translucens

Summary The effects of bicarbonate ions on the membrane potential and resistance ofNitella translucens are shown to be primarily due to the change in pH produced by the bicarbonate acting as a buffer, and not due to the presence of an electrogenic anion pump. The mechanism by which pH affects the membrane potential is discussed in the context of recent work by other authors on this effect.     

Efflux of photosynthate and acid from developing seed coats of Phaseolus vulgaris L.: a chemiosmotic analysis of pump-driven efflux

Seed coats of Phaseolus vulgaris L. unload photosynthetic products,mineral ions and acid into the apoplastic space surroundingthe embryo. We report measurements, on detached seed coats,of the rates of unloading of photosynthates, ions and acid atdifferent external pH and in the presence of treatments intendedto alter the rate of proton pumping. We also report measurementsof membrane potential difference (PD) and of cytoplasmic pHunder the same conditions, measurements which have allowed usto validate the treatments we used and to investigate functionalrelationships between membrane processes. A chemiosmotic model of the seed-coat cell membrane is proposed,in which sucrose efflux and acid efflux are both driven by theproton pump. Sucrose efflux is proposed to occur by sucrose/protonantiport driven by the proton-motive force (PMF), and acid effluxto occur by pumped protons accompanied by a passive efflux ofanions. We use our measurements to estimate the net efflux ofsucrose on the antiporter and the total efflux of protons onthe pump. We have tested the model by using experimental treatments designedto manipulate the pump rate as the independent variable. Underthese conditions, and assuming the model is correct, the pumprate determines the cytoplasmic pH. Over the range covered byour experiments the net sucrose efflux is dependent on externaland cytoplasmic pH, the latter having the major role. The effluxof acid, under the same treatments, depends primarily on theproton pump rate, and was found to be well fitted by a quadraticfunction of pump rate. This means that, as pump rate increases,an increasing proportion of the pump output is used by acidefflux and a decreasing proportion by sucrose antiport. The membrane PD, although an important component of the PMF,does not appear to function in rate control of net sucrose orof acid efflux, since neither efflux is correlated with membranePD under our treatments which vary the pump rate. The PD correlateswell with external potassium concentration, and seems largelydetermined by the diffusion of potassium ions and anions. Key words: Phaseolus vulgaris L, photosynthate efflux, proton pump, sucrose/proton antiport, seed coat, membrane transport model     

Intracellular pH Regulation in an Acidophilic Unicellular Alga, Cyanidium caldarium: 31P-NMR Determination of Intracellular pH

The intracellular pH of an acidophilic unicellular alga, Cyanidiumcaldarium, was determined as a function of external pH by ³¹Pnuclear magnetic resonance. The algal cells incubated underaerobic conditions or under anaerobic and illuminated conditionsmaintained the intracellular pH in the range from 6.8 to 7.0even when the external pH was changed from 1.2 to 8.4. Underanaerobic and dark conditions, however, the intracellular pHacidified at the acidic pH region of the external medium. Theacidified intracellular pH reversibly returned to neutral eitheron aeration or illumination. The results indicate that, in Cyanidiumcells growing in extremely acidic environments, an active H⁺efflux (H⁺ pump) which depends on metabolic activity (respirationor photosynthesis) is essential to maintain the intracellularpH at a constant physiological level against the passive H⁺leakage due to the steep pH gradient across the cell membrane. (Received March 19, 1986; Accepted July 17, 1986)     

A pH Gradient across the Root

A pH gradient across the intact root of Helianthus annuus hasbeen measured using pH microelectrodes. The results indicatea steady increase in pH from epidermis to protoxylem. Thereis evidence for the activity of a proton extrusion pump in someof the cells. The possibility that the pH gradient may be thebasis of centripetal ion transport across the root is discussed.     

N-Ethylmaleimide Blocks the H+ Pump in the Plasma Membrane of Chara corallina Internodal Cells

The sulfhydryl (SH) modifying reagent N-ethylmaleimide (NEM)was applied to the internodal cells of Chara corallina to studythe role of SH residues in the activity of the plasma membraneH⁺ pump. NEM (1 µM) caused a marked depolarizing shiftof the resting potential by 6410mV (n=7) together with depressionof the conductance peak at around —200 mV, indicatinga marked depression of the H⁺ pump activity. This effect ofNEM was partly reversible, the membrane repolarized and theconductance peak was restored after extracellular washing. TheH⁺ pump inhibitor, dicyclohexylcarbodiimide (DCCD), caused noadditive membrane depolarization and/or depression of the H⁺pump conductance, in the presence of NEM. This suggests thatNEM blocks the H⁺ pump and that SH residues play a pivotal rolein maintaining the H⁺ pump activity in Chara corallina. (Received April 10, 1993; Accepted July 29, 1993)     

A kinetic analysis of the electrogenic pump ofChara corallina: II. Dependence of the pump activity on external pH

Summary The current-voltage curve of theChara membrane was obtained by applying a slow ramp de- and hyperpolarization by use of voltage clamp. By inhibiting the electrogenic pump with 50m DCCD (dicyclohexylcarbodiimide), theI–V curve approached a steady state within 100 min, which gave thei _d -V curve of the passive diffusion channel. Thei _p -V curve of the electrogenic pump channel was obtained by subtracting the latter from the former. With the increase of external pH, thei _d -V curve showed only a slight change, while thei _p -V curve of the pump channel showed almost a parallel shift, in the hyperpolarizing direction, along the voltage axis in the pH range between 6.5 and 7.5. The sigmoidali _p -V curve in this pH range could be simulated satisfactorily with the five-state model reported previously (U. Kishimoto, N. Kami-ike, Y. Takeuchi & T. Ohkawa,J. Membrane Biol. 80:175–183, 1984) as well as with a lumped two-state model presented in this report. The analysis based on these models suggests that the electrogenic pump of theChara membrane is mainly a 2H⁺/1ATP pump. The forward rate constant in the voltage-dependent step increased with the increase of external pH, while the backward one decreased. On the other hand, the forward rate constant in the voltage-independent step remained almost unchanged with the increase of external pH, while the backward one increased markedly. The pump conductance at the resting membrane potential showed either a slight increase or a decrease with the increase of external pH, depending on the sample. Nevertheless, the pump current showed generally a slight increase with the increase of external pH.     

Effects of Intracellular Vanadate on Electrogenesis, Excitability and Cytoplasmic Streaming in Nitellopsis obtusa

Vanadate, which is known to inhibit the plasma membrane H^$-ATPaseof Neurospora, was applied intracellularly to internodal cellsof Nitellopsis by use of the intracellular perfusion technique.It inhibited electrogenesis and H^$-extrusion, evidence thatthe electrogenic pump of the Characeae plasmalemma is the H^$-extrudingone. The concentration of vanadate for the half-maximal inhibitionof the activity of the pump was 5 µM. The membrane potentialand H^$-extrusion occasionally recovered from vanadate inhibitionsfor reasons that are unknown. Membrane excitability, which isdependent on Mg?ATP, was not inhibited by vanadate, which suggeststhat the ATPase involved with membrane excitability differsfrom that of the H^$ pump. Cytoplasmic streaming took place evenwhen the cell was perfused with the medium containing 1 mM vanadate,which indicates that the vanadate-insensitive actomyosin systemis concerned with the motive force generation of the streaming. (Received August 27, 1981; Accepted April 13, 1982)     

The Effect of Darkness on Active and Passive Transport in Chara corallina

In Chara corallina, the membrane potential may stay much morenegative than the equilibrium potential for potassium in thedark, indicating that the proton pump is operative. The highproton conductance which occurs at high external pH, as indicatedby a high membrane conductance and a membrane potential nearthe equilibrium potential for protons, is not seen in the darkat pH 11. This effect is likely to be related to inhibitionof photosynthesis since DCMU has the same effect. The effectis similar but not identical to the effect of a decreased internalpH. Key words: Light, dark, membrane potential, Chara     

Effect of pH on the Membrane Potential and Electrical Resistance of Nitella flexilis in the Presence of Calcium

Effects of pH on the membrane potential and electrical resistanceof Nitella were investigated in a bathing medium with or withoutcalcium. The membrane potential became more negative as theexternal pH was raised, at a faster rate in the presence ofcalcium than in its absence. The value then achieved by thepotential could be reversed by restoring the original pH whilstin a Ca-free medium the cell remained ‘hyperpolarized’.Tenfold changes of the external concentration of potassium broughtabout larger modifications of the membrane potential when thepH of the solution was high and calcium concentration low. Theelectrical resistance was lowest in alkaline and calcium-freesolutions. We conclude that calcium prevents the mediation ofsome changes in the membrane structure by lowering the concentrationof external H⁺ ions, and that the permeability of Nitella topotassium increases with rising pH.     

Effects of Cations on the Cytoplasmic pH of Chara corallina

Smith, F. A. and Gibson, J.–L. 1985. Effects of cationson the cytoplasmic pH of Chara corallina.—J.exp. Bot.36: 1331–1340 Removal of external Ca²⁺ from cells of Chara corallina lowersthe cytoplasmic pH, as determined by the intracellular distributionof the weak acid 5,5–dimethyloxazolidine2–,4–dione(DM0), when the external pH is below about 60. This effect isreversed, at least partially, by addition of the following cationsto Ca²⁺-free solutions: tetraethylammonium (TEA⁺) and Na⁺ at5 or 10 mol m^-3, Li⁺ and Cs⁺ (10 mol m^-3), or Mg²⁺, Mn²⁺ andLa³⁺ (02 or 05 mol m^-3). Under the same conditions, increasesin pH sometimes, but not always, occur in the presence of 10mol m^-3 K⁺ or Rb⁺ The results are discussed in relation to the major transportprocesses that determine pH and the electric potential differenceacross the plasma membrane, namely fluxes of H⁺ and of K⁺. Thesimplest explanation of the effects of the various cations testedin this study is that they primarily affect pHi_c via changesin influx of H⁺ but direct effects on the H⁺ pump or on K⁺ fluxesmay also be involved Key words: Chara corallina, cytoplasmic pH, cations, H⁺transport     

Voltage--Current Characteristics of Chara australis During Changes of pH and Exchange of Ca-Mg in the External Medium

Chara australis was the subject of voltage-clamp experimentsin which external calcium, magnesium, and hydrogen were varied.The voltage clamp was applied across the combined plasmalemma,cytoplasm, and tonoplast of internodal cells. Calcium is necessaryin the batching medium for transient currents to occur duringa depolarizing voltage clamp. Magnesium cannot replace calciumas mediator in this function. Lowering the medium pH appearsto affect more than one variable in the membrane system. Weargue that more than one ion is responsible for the transientcurrent; large increases in membrane current of sodium, potassium,and chloride occur.     

Effects of Osmotic Stress, Ionic Stress and IAA on the Cell-Membrane Resistance of Vigna Hypocotyls

The cell-membrane resistance (R_m) of Vigna hypocotyls was examined,and the effects of osmotic stress, ionic stress and IAA on R_mwere investigated. R_m decreased by 64 to 77% under osmotic stressin the presence of absorbable solutes (40 mM sorbitol, 15 mMKC1, 30 mM sucrose; or 40 mM sorbitol, 15 mM KC1, 30 mM sucroseplus 10^–4 M IAA) or under ionic stress (50 mM NaCl or50 mM KC1). R_m was not changed by perfusion with 10^–4M IAA. Therefore, the hyper-polarizations of the membrane potentialobserved in both cases should be ascribed totally to the activationof the electrogenic proton pump. Although R_m showed an increaseof 1.6 fold when the hypocotyls were subjected to osmotic stress(100 mM sorbitol or 100 mM sorbitol plus 10^–4 M IAA),83.6% or 92.4% of the hyperpolarization of the membrane potential(V_px was also the result of the activation of the pump. Theresults, calculated on the basis of the current source model,support the viewpoint that the hyperpolarization of the cellmembrane potential of Vigna hypocotyls under osmotic stress,ionic stress or in the presence of IAA is an expression of theactivation of the proton pump, and is not caused by an increasein R_m. ¹ Present address: Researchers and Planners of Natural Environment, Yotsugi Bldg. (2F), 1-5-4 Horinouchi, Suginami-Ku, Tokyo,166 Japan ² Present address: Graduate School of Integrated Science, YokohamaCity University, 22-2 Seto, Kanazawa-Ku, Yokohama, 236 Japan (Received February 14, 1991; Accepted July 24, 1991)