Resting membrane potential and action potential of Nitella expansa protoplasts

Inside negative membrane potentials were observed for protoplastsobtained from Nitella expansa leaf internodal cells in mediacontaining 1 to 100 mM CaCl₂ using the microelectrode technique.The potential values were less negative than the membrane potentialof intact N. expansa leaf internodal cells. In addition, anaction potential consisting of two components—a fast componentand a slow component—was induced by electrical stimulationfor the protoplasts as well as the intact cells. (Received December 18, 1979; )     

Light-induced hyperpolarization of membrane potential in Nitella flexilis call plasmalemma

Light-induced hyperpolarization of the membrane potential in Nitella flexilis cell plasmalemma was investigated by the clamping method. It is shown that this response is of an excitation character. The equivalent electric diagram used in the work and the electromotive force included on its basis allowed consideration of two possible (from the common point of view) mechanisms of the response: the action of the electrogenic ion pump and membrane specific permeability to a definite ion. The membrane being in the hyperpolarization state is not capable of acting as a bicarbonate electrode. It is suggested that the response under study is defined by the action of the electrogenic pump, the role of which is performed by HCO2(3)-dependent H+-ATPase with the ion channel as an exciting one.     

Nitella fluctuation and instability in the membrane potential near threshold.

Excitation of Nitella internodal cell was investigated as an example of the phase transition in an open system far more thermal equilibrium. The power density spectrum of the membrane potential fluctuation had a bulge in a frequency range lower than 1 Hz at the resting state and a peak at approximately 0.03 Hz at a depolarized state near the threshold. A critical oscillation in the membrane potential was observed when threshold was gradually approached from the resting state. Repetitive firing was observed under a step-current of the superthreshold value. The frequency of spectral peaking, critical oscillation, and repetitive firing agree well with each other. The result suggests that the hard-mode instability occurs in the Nitella internodal cell. The membrane impedance had no peak in the same frequency region as the peak of the voltage spectrum. The spectral peak may be ascribed to be electrogenic pump modulated by the metabolic feedback system in photosynthesis.     

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     

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; )     

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; )     

Dynamic property of membrane formation in a protoplasmic droplet of Nitella

A theory is presented to explain the dynamic characteristics of an electric potential and the resistance of a surface membrane during the formation of a protoplasmic droplet isolated from Nitella. Basic equations are coupled ones for describing ion concentrations near the surface of the droplet, active and passive ion fluxes on the surface, and kinetics of membrane-constituting molecules diffusing from the inside of the protoplasm. The present results give a good explanation of the observed kinetics of electric properties throughout the formative process of surface membranes after the ion concentrations are replaced by lower ones. The results can also explain well the observed data on the steady state. Oscillatory changes in the membrane potential induced by ions strongly adsorbed on the surface membrane are discussed in relation to growth and regeneration phenomena in biological systems such as bean roots and Acetabularia.     

Helicoidal orientation of cellulose microfibrils in Nitella opaca internode cells: ultrastructure and computed theoretical effects of strain reorientation during wall growth

The ultrastructure of the mature internode cell wall of Nitella opaca is described. It is interpreted in terms of a helicoidal array of cellulose microfibrils set in a matrix. A helicoid is a multiple plywood made up of layers of parallel microfibrils. There is a progressive change in direction from ply to ply, giving rise to characteristic arced patterns in oblique sections. A critical tilting test, using an electron microscope fitted with a goniometric stage, showed the expected reversal of direction of the arced pattern. Nitella cell wall is thus more regularly structured than previous studies have shown. From a survey of the cell-wall literature, we show that such arced patterns are common. This indicates that the helicoidal structure may be more widespread than is generally realised, although numerous other cell walls show no signs of it. Nevertheless, there are examples in most major plant taxa, and in several types of cells, including wood tracheids. Most of the examples, however, need confirmation by tilting evidence. There are possible implications for wall morphogenesis. Helicoidal cell walls might arise by selfassembly via a liquid crystalline phase, since it is known that the cholesteric state is itself helicoidal. A computer graphics programme has been developed to plot the expected effects of growth strain on the patterns in oblique sections of helicoids with various original angles between consecutive layers. Herringbone patterns typical of crossed polylamellate texture can be generated in this way, indicating a possible mode of their formation.