ACTION POTENTIAL OF NITELLA INTERNODES

The ionic current during a non-propagating action potentialis analysed from the voltage clamp experiments. The shape ofthe action potential of the Nitella internode can be reconstructedfrom the data of the voltage clamp experiments. The N-shapedcurrent-voltage characteristics (I-V curve) of the Nitella membraneis not constant with time as it is in the tunnel diode, butdecays with time, converging finally into a delayed rectificationcurve. The temporal locus of the potential at which each I-Vcurve crosses the voltage axis coincides almost exactly withthe action potential. The membrane resistance which is calculatedfrom the slope of the I-V curve at each intersection with thevoltage axis also changes in parallel to the action potential.Such correlations are found in the Nitella not only in the pondwater, but also in high Na, high Ca or high Mg medium, wherethe shape of the action potential is modified in various ways.It is highly probable that the action potential is a locus ofthe change of the membrane potential so that the net membranecurrent may be maintained at zero after the transient modificationof the membrane structure by stimulation. (Received June 30, 1966; )     

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.     

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.     

Electromotive force of Nitella membrane during excitation

Excitation of the Nitella membrane is analysed by assuming themembrane to be an electromotive force in series with a resistance,both being variables of time and of membrane potential. Duringstep depolarization beyond a threshold, conductance and electromotiveforce increase transiently, finally reaching their respectivesteady state levels. The conductance increase peak is attainedearlier than the peak for electromotive force increase. Wheneverelectromotive force increases beyond the level of clamped membranepotential, the ionic current flows inward. This is consideredto be the origin of the apparent negative resistance characteristicof the excitable membrane. Anodal break response and spontaneousfiring of Nitella membrane are also caused by transient increasesin electromotive force and conductance irrespective of whetherthe membrane potential is being held at its resting level. Thetransient increase in electromotive force reflects changes,like a phase transition, occurring during excitation. (Received May 6, 1968; )     

Oscillations in Extracellular Current, External pH and Membrane Potential and Conductance in the Alkaline Bands of Nitella and Chara

Oscillations with a period of approximately 2 min were observedin the membrane potential of Chara and Nitella upon illuminationof dark-treated cells, as well as in the extracellular currentpattern and pH values. A 2-min oscillation in the membrane potentialwas observed when the voltage electrode was placed close tothe border of an alkaline and acid region. Comparison of resultsfrom Chara and Nitella revealed an identical control mechanismfor external pattern stabilization in the effect of light onmembrane potential and conductance. Vibrating probe experimentsindicated that oscillations in the extracellular current occurredonly at the border of the alkaline band. Ion-specific pH micro-electrodesplaced within the alkaline band detected oscillations associatedwith light reactivation of the banding phenomenon. These resultsindicate that the oscillations represent a localized phenomenoninvolving spatially-dependent time-constants. More evidencefor the spatial dependence of time constants is gained fromsingle active acid regions in Nitella. Using this combinationof techniques, we have established that a light-dependent H⁺transporter is involved in this oscillation. Current-voltagecurves taken during these oscillations and relaxation, afterchanging the light intensity, confirmed this identification. Key words: Oscillation, vibrating probe, pH micro-electrode, time-constant. I/V curve, Chara, Nitella     

The electrogenic ion pump revealed by the external pH effect on the membrane potential of Nitella. Influences of external ions and electric current on the pH effect

The influences of external ions and electric current on thepH effect of the membrane potential of Nitella are described.Results are explained in terms of a pH-dependent electrogenicion pump. The reduction of membrane resistance with a pH rise is attributedto the pump current being potential-dependent. (Received July 9, 1974; )     

The Influence of Temperature on a K+-Channel and on a Carrier-Type Transporter in Nitella

Fisahn, J. and Hansen, U-P. 1986. The influence of temperatureon a K⁺ -channel and on a carrier type transporter in Nilella—J.exp. Bot. 37. 440–460. In Nitella, the effects of temperature on membrane potentialand on resistance consist of several components. The evaluationof their associated time-constants measured in linear(ized)temperature responses at a resting potential of–120 mVprovides an approach to their identification. For changes slowerthan c. 1 s, the temperature effect on membrane potential andresistance does not originate from temperature action on theinvolved transporter, but is mediated by signals from temperaturesensitive metabolic processes. In the case of potential, theseprocesses seem to be identical to those which also mediate thelight effect: pH-regulation, and two direct signals from photosynthesis,as indicated by the similarities of the related time-constants( respectively). The temperature effect on resistance displays only one time-constant of 40 sinmost experiments. The related process is unknown. The non-coincidenceof the time-constants of the effect on potential and on resistanceimplies the involvement of a carrier-type transporter (H+-pumpor cotransporter) in the effect on potential, and of a K+channelin the effect on resistance. The K+-channel is identified bythe reversal potential of the effect on membrane potential measuredin cells depolarized or hyperpolarized by an injected electricalcurrent Under these conditions the temperature effect on resistancedominates the effect on potential. Key words: H⁺-pump, K⁺-channel, kinetic analysis, Nitella, oscillation, pH-regulation, reversal, potential, temperature, time-constants     

Rhythmic change of membrane potential and cyclosis of Nitella internode

The membrane potential of Nitella internode shows a spontaneousrhythmicity. The period depends largely upon temperature andthe length of the cell. Moreover, the period is reversibly prolongedat low temperature and also by treatment with cytochalasin B.We concluded that this bioelectrical rhythm is closely relatedto cytoplasmic streaming. (Received August 11, 1975; )     

The Influence of the Cell Membrane on some Toxicity Effects of Growth Substances in Nitella

When cells of Nitella are placed in a solution of some plantgrowth substances there is a profound increase in the membraneresistance as measured by means of an internal silver/silverchloride micro-electrode. This impedance effect is accompaniedby some marked visible changes within the cell cytoplasm, thesechanges being dependent upon the concentration of undissociatedgrowth substance in the vicinity of the membrane, and upon thepH of the external environment. A detailed study is made of these visible changes and, takinginto account the negatively charged membrane, one possible interpretationof the results is that only undissociated molecules of the growthsubstance may enter the cytoplasm of Nitella from the environment,the diffusion obeying a simple Fick Law relationship. The substances are used in sufficient quantity to kill the Nitellacell, death following the visible effects, and they appear tobe unique in that their toxic effect produces a system of highmembrane impedance.     

Separate Oscillations of the Electrogenic Pump and of a K+ -Channel in Nitella as Revealed by Simultaneous Measurement of Membrane Potential and of Resistance

In Nitella oscillations of membrane potential with periods ofabout 15 min and of about 1 h can be observed. The comparisonof the related changes in resistance and in potential showsthat the 1-h oscillation controls a carrier-type transporter,probably an electrogenic pump with a stoichiometry of 1 H⁺/1ATP. The control loop related to the 1-h oscillation can bestimulated by internal pH as changed by butyrate or procaine.IV-curve studies show that the 15-min oscillation modulatesthe conductivity of a K⁺ -channel. No way has been found toinfluence the spontaneously occurring 15-min oscillation whichprobably is generated in the chioroplasts. The oscillationsseem to provide a means of exerting a selective influence onone transporter. Correspondence to: Institut für Angewandte Physik, NeueUniversität, Haus N61A, D-2300 Kiel, F.R.G. Key words: H⁺-pump, IV-curves, Nitella, oscillations, pH-regulation, potassium channel, stoichiometry     

Rhythmic Excitation in Nitella at Conditions of Voltage Clamp

Rhythmic excitation of Nitella cells initiated in 100 mM NaCloccurred when the voltage across the plasmalemma was fixed notonly at the resting level, but also at different hyperpolarizedlevels. The results presented indicate that the activation ofthe excitable units is not potential-dependent but is insteadchemical, reflecting changes in the ionic status within themembrane. Key words: Nitella, Plasmalemma potential difference, Rhythmic excitation     

Respiration-Dependent Membrane Hyperpolarization in Tonoplast-Free Cells of Nitella axilliformis

Cells of Nitella axilliformis were made tonoplast-free by intracellularperfusion of media containing ethyleneglycol-bis-(ß-aminoethylether)N,N'-tetraaceticacid (EGTA). When the perfusion medium contained ADP as wellas ATP, the membrane hyperpolarized in darkness in a mannersimilar to light-induced hyperpolarization. This light-independenthyperpolarization seems to be due to activation of the electrogenicion pump in the plasma membrane because the hyperpolarized valueof the membrane potential was more negative than the equilibriumpotential for K^$, the most negative ion equilibrium potentialin Nitella. The hyperpolarization was inhibited by the respiratory chaininhibitors NaCN (1 mM), antimycin A (10 µM) and rotenone(10 µM). NaCN slightly decreased the ATP concentrationin the cell perfused with medium containing 1 mM ATP and 1 mMADP; but, even after treatment with NaCN, the cell had about80% of the ATP value for the control. ^* This study is dedicated to the late Professor J. Ashida. (Received June 24, 1982; Accepted October 15, 1982)     

Cycloprodigiosin Hydrochloride Inhibits Acidification of the Plant Vacuole

The effect of cycloprodigiosin hydrochloride (cPrG-HCl), obtainedfrom the marine bacterium Pseudoalteromonas denitnficans, onacidification of the vacuole was studied in Characeae cells.In internodal cells of Nitella, the plasma membrane of whichhad been permeabilized, cPrG-HCl inhibited both ATP- and pyrophosphate-dependentacidification of the vacuole. Application of cPrG-HCl to livinginternodal cells of Chara, induced a significant increase invacuolar pH. The role of cPrG-HCl as a tool for studying thephysiological role of acidic vacuole is discussed. (Received August 26, 1998; Accepted November 17, 1998)     

HYPERPOLARIZING RESPONSE IN NITELLA INTERNODES

The ionic aspect of the hyperpolarizing response in the internodalcell of Nitella is reported in some detail. The response wasobserved by passing a large inward current through the Nitellamembrane, the resistance of which had been decreased by a concentratedalkali metal ion. It was not possible to demonstrate the responsein a concentrated solution of CaCl₂, MgCl₂, BaCl₂, ZnCl₂ orAlCl₂ or AlCl₃. After hundreds of the spontaneous repetitiveaction potentials, which occurred in a single solution of concentratedNaCl or LiCl or caused by an application of 1–2 mM EDTAin the artificial pond water, the Nitella cell showed the hyperpolarizingresponse. Almost the same size of the response was observedfor change in pH of the external KC1 solution from 6.7 to 10.0,but it decreased markedly for pH lower than 4.7. It seems tobe an essential condition for the response to remove the divalentcations from the cell surface, having a concentrated monovalentcation in the external medium. (Received April 22, 1966; )     

REPETITIVE ACTION POTENTIALS IN NITELLA INTERNODES

Typical spontaneous action potentials can be elicited in 10–100mM NaCl or LiCl solution. The period of repetition is 0.5–2seconds and the action potential generally consists of a rapidspike alone. Similar spontaneous action potentials are alsodemonstrated by adding either 1 mM EDTA (pH 6.6) or 2 mM ATP(pH 6.6) to the artificial pond water. In these cases, however,the period of repetition is much longer and the action potentialis of a normal shape, a rapid spike being followed by a slowtransient depolarization. The period of repetition and the sizeof the action potential decrease with the elevation of the vacuolarpotential level. The cause of the spontaneous firing is supposedto be the removal of Ca⁺⁺ from the outer surface of the Nitellamembrane. (Received May 18, 1966; )     

The Influence of H+ on the Membrane Potential and Ion Fluxes of Nitella

The resting membrane potential of the Nitella cell is relatively insensitive to [K]_o, but behaves like a hydrogen electrode. K⁺ and Cl^- effluxes from the cell were measured continuously, while the membrane potential was changed either by means of a negative feedback circuit or by external pH changes. The experiments indicate that P_K and P_Cl are independent of pH but are a function of membrane potential. Slope ion conductances, G_K, G_Cl, and G_Na were calculated from efflux measurements, and their sum was found to be negligible compared to membrane conductance. The possibility that a boundary potential change might be responsible for the membrane potential change was considered but was ruled out by the fact that the peak of the action potential remained at a constant level regardless of pH changes in the external solution. The conductance for H⁺ was estimated by measuring the membrane current change during an external pH change while the membrane potential was clamped at K⁺ equilibrium potential. In the range of external pH 5 to 6, H⁺ chord conductance was substantially equal to the membrane conductance. However, the [H]_i measured by various methods was not such as would be predicted from the [H]_o and the membrane potential using the Nernst equation. In artificial pond water containing DNP, the resting membrane potential decreased; this suggested that some energy-consuming mechanism maintains the membrane potential at the resting level. It is probable that there is a H⁺ extrusion mechanism in the Nitella cell, because the potential difference between the resting potential and the H⁺ equilibrium potential is always maintained notwithstanding a continuous H⁺ inward current which should result from the potential difference.     

Light and Electrical Current Stimulate the Same Feed-back System in Nitella

Slow damped oscillations (period about 1 hr) of membrane potentialin Nitella can be initiated by a change in light intensity aswell as by an injection of electrical current. This observationsupports a model of the involvement of feed-back controlledtransport in pH-regulation. (Received July 16, 1981; Accepted November 30, 1981)     

Cytochalasin Rearranges Cortical Actin of the Alga Nitella into Short, Stable Rods

The cortical cytoplasm of the alga Nitella contains reticulateactin that does not survive perfusion fixation with glutaraldehydeunless prestabilized with the cross-linker 3-maleimidobenzoyl-N-hydroxysuccinimidester (MBS). Cytochalasin D remodels thiscortical actin into short rods which are more stable, survivingaldehyde fixation without MBS pre-treatment. The overall alignmentof these actin rods correlates with that of cortical microtubules(transverse in young cells, random in old cells) but probablydoes not involve one-to-one correspondence. The time course,dose dependence and reversibility of these structural changesbroadly resemble those for streaming inhibition by cytochalasinbut the cortical actin responds to concentrations that do notslow streaming. Because the structural changes concern the corticaland not the subcortical actin, they seem unlikely to directlyinhibit streaming. Formation of cortical rods is not a responseto streaming inhibition per se since it does not occur whentwo other inhibitors of streaming (2,4-dinitrophenol (DNP) andNethyl maleimide (NEM)) are used. NEM, however, resembles MBSin stabilizing the reticulate form of cortical actin even thoughit cannot cross link. ¹Address from July 1995; Department of Biology, Faculty of Science,Osaka University, Machikaneyama 1-1, Tayonaka, Osaka, 560 Japan.     

The Membrane Potential of Enzymatically Isolated Nitella expansa Protoplasts as Compared with their Intact Cells

With the enzymatically isolated Nitella protoplasts, sufficientinsertions of micro-electrodes to make a stable measurementof the membrane potential by the conventional method could notbe made because of an ‘elasticity’ of the outermembrane. We developed an effective method in which a micro-electrodecould be inserted after the outer membrane was punctured bypassing an electrical impulse through the micro-electrode. Inthis method, Ca ions play a crucial role in the ‘punching’and ‘healing’ processes of the protoplast membrane. The effects of the cations K⁺, Na⁺, Ca²⁺ and the anions Cl^–,, , on the membrane potentials of Nitella expansa protoplasts were compared with those of intactcells. The membrane potential of protoplasts was less negativethan that of intact cells when concentrations of Na or K, inthe presence of Ca, were below certain levels which increasedwith increasing Ca concentration; and it tended to become identicalto that of intact cells when Na or K concentrations were beyondthose levels. Beyond those levels for K the membrane potentialsof both protoplasts and intact cells typically seemed to bethe Nernst potentials in the presence of 0•1 to 30 molm^–3 Ca²⁺. However, for Na, the difference in potentialsbetween intact cells and protoplasts decreased at much higherconcentrations than for K. Increase of Ca always gave less negativeprotoplast potentials than those in intact cells. Replacementof Ca by Mg did not change the membrane potential of intactcells, although it was deleterious to protoplasts. The cellwall potential of intact cells was also measured by the micro-electrodetechnique and was revealed as a simple Donnan potential, assumingthe fixed negative charge density of 0•8 equivalent perdm³. The membrane potential of intact cells seems to be a significantreflection of the plasmalemma potential which is thought tobe measured directly in their protoplasts in terms of ionicselectivity and concentration dependency of the ion speciesexamined. In addition, increased sensitivity to calcium in protoplastpotentials compared to intact cells is suggested, though themembrane potential of intact cells seems to be largely preservedin their enzymatically isolated protoplasts. Key words: Membrane potential, protoplasts, Nitella expansa, cell wall potential     

STUDIES ON NITELLA HAVING ARTIFICIAL CELL SAP I. REPLACEMENT OF THE CELL SAP WITH ARTIFICIAL SOLUTIONS

A method for replacing the cell sap of Nitella with an artificialsolution was introduced. The technique, which is a modificationof KAMIYA and KURODA'S (1, 2), is applicable not only for isotonicbut also for hypertonic or hypotonic solutions. Photometricdeterminations of K⁺, Na⁺, Ca⁺⁺ and Cl^– proved that thereplacement of the cell sap with the present method is satisfactory.The internodal cell of Nitella, whose cell sap was replacedwith an isotonic solution with a simple composition such asa mixture of KCl, NaCl and CaCl₂, can be kept living at leastfor several days, sometimes even for more than one month. (Received September 6, 1963; )