The internal potential of Neurospora appears to have two components, one (a) which is reduced by anoxia or abolished by respiratory inhibitors such as azide and 2,4-dinitrophenol, and (b) a fraction that remains in the presence of respiratory inhibitors and is sensitive to the external potassium concentration. Under standard conditions 1 ram azide or dinitrophenol diminishes internal potentials from near --200 mv to about --30 mv within 1 minute and at a maximal rate of 20 mv/second. The internal potential usually recovers within 10 minutes after the inhibitor has been removed. The effect of carbon monoxide on the internal potential is similar to that of azide or dinitrophenol, but can be reversed by visible light, specifically of the wavelengths (430 m# and 590 m/z) known to decompose cytochrome-CO complexes in yeast. Respiration and internal potentials vary proportionally with azide concentration, but dinitrophenol at low (3 X 10 -6 M) concentrations enhances oxygen consumption without affecting the internal potential. In the presence of 0. I m~ calcium, the fraction of the internal potential which persists during respiratory inhibition increases (becomes more negative) about 30 mv for each tenfold decrease of external potassium, over the range 10 to 0.1 mM. The surface resistivity of Neurospora, normally about 5000 ohm.era 2, is unchanged by respiratory inhibitors during the period of rapid potential shift.
I N T R O D U C T I O NT h e only proven mechanism for generating bioelectric potentials still remains the passive diffusion of ions down chemical gradients established by cellular metabolism. Yet the recurrent suggestion that metabolism might play a more intimate role has recently received considerable experimental support. K e r n a n (23) found, and others (1,24,28) have confirmed that striated muscle shows considerable hyperpolarization during periods of rapid sodium extrusion. A similar observation has been m a d e on snail ganglion cells (22). T h e electrical polarization of gastric mucosa has resisted attempts at an explanation in terms of ion diffusion (29); so has the post-tetanic hyperpolarization of nonmyelinated nerves (5). T h e notion which has grown out of these experiments 93