Certain inhibitors have been found to affect the low frequency spectral component of the electrical noise power spectrum in Chara corallina. Application of the ATPase inhibitor N,N'-dicyclohexylcarbodiimide removed the low frequency spectral component, strengthening the case that the component is produced by active proton pumping. Cytocholasin B, which inhibits cyclosis in internodes of C. corallina, removed the low frequency spectral component in a time-dependent fashion which was correlated with the cessation of streaming. The protonophore carbonyl cyanide m-chlorophenylhydrazone did not produce consistent effects on the low frequency spectral component in these cells.In noise analysis, the power spectral density resulting from a signal which is the sum of two or more statistically independent noise generating processes is equal to the sum of the PSDs3 of each of those processes individually. This implies that in membrane noise analysis, inhibition of an electrical noise-producing transport process will remove the portion ofthe power spectrum produced by that particular ion flux. Inhibitors with known properties may therefore be used to study the type of transport process which is responsible for specific spectral characteristics in the noise PSD from a given cell type.In a previous paper (21) we described a low frequency spectral component which appeared to be produced by active proton transport in internodes of Chara corallina at pH values from 5.2 to 9 in the light. We have investigated the nature of this spectral component using various inhibitory compounds, to see whether the identification of the LFSC with active proton transport could be further confirmed or refuted, and to study the interaction between cyclosis and membrane transport in these cells.
MATERIALS AND METHODSThe experimental arrangement for sampling voltage noise signals from internodes of Chara corallina has been described previously (21,22 described by Hope and Walker (4), which will henceforth be referred to as CPW. The CPW was supplemented with the inhibitors listed in Table I. The voltage noise signals were analogto-digital converted and stored on a PDP-1 1/03 computer system, and power spectra computed by means of the fast Fourier transform technique (20,21). In all cases spectra were sampled with the cells under control conditions in CPW, illuminated by a halogen lamp at 30 W/m2, then compared to spectra sampled in the presence of an inhibitor.The inhibitors were not very water soluble, and had to be dissolved either in ethanol or DMSO to make a concentrated stock solution, which was added to the CPW to obtain the desired final concentration ofinhibitor as indicated in Table I. The stock solutions of inhibitors were stored in a freezer at -1 1°C between experiments and were mixed with the CPW just prior to use in an experiment. Table I also indicates the final v/v concentration of organic solvent included in the media. Control experiments in which 0.25% v/v ethanol was added to the CPW did not result in any change in transmem...