ISSN:
1432-2048
Keywords:
Current-voltage (I–V) relationship
;
Fusicoccin action
;
H+ pump
;
Membrane potential
;
Potassium channel (voltage gated)
;
Tetraethylammonium chloride
;
Vicia (fusicoccin action)
;
Voltage clamp
Source:
Springer Online Journal Archives 1860-2000
Topics:
Biology
Notes:
Abstract Fusicoccin commonly is thought to promote secondary solute transport via an increase in electrical driving force which follows the enhancement of primary, “electrogenic” H+ extrusion by the plant plasma membrane H+-ATPase. However, previous electrical studies ofVicia faba L. guard cells in FC (Blatt, 1988, Planta174, 187) demonstrated, in addition to a limited rise in pump current, appreciable declines in membrane conductance near and positive to the free-running membrane potential (V m). Much of the current at these potentials could have been carried by outward-rectifying K+ channels which were progressively inactivated in FC. We have examined this possibility in electrical studies, using whole-cell currents measured under voltage clamp to quantitate steadystate and kinetic characteristics of the K+ channels both before and during exposure to FC; channels block in tetraethylammonium chloride was exploited to assess changes in background ‘leak’ currents. The cells showed little evidence of primary pump activity, a fact which further simplified analyses. Under these conditions, outward-directed K+ channel current contributed to charge balance maintainingV m, and adding 10 μM FC on average depolarized (positive-going)V m. Steady-state current-voltage relations revealed changes both in K+ channel and in leak currents underlying the voltage response. Changes in the leak were variable, but on average the leak equilibrium potential was shifted (+)19 mV and leak conductance declined by 21% over 30–40 min in FC. Potassium currents were inactivated irreversibly and with halftimes (current maxima) of 6.2–10.7 min. Inactivation was voltage-dependent, so that the activation (“gating”) potential for the current was shifted, positive-going, with time in FC. Channel gating kinetics, inferred from the macroscopic currents, were also affected; current rise at positive potentials accelerated 4.5-fold and more, but in a manner apparently independent of voltage and extracellular potassium concentration. Current decay at negative potentials was quickened, also. These results identify the outward-rectifying K+ channels as one site of action for FC at a higher plant cell membrane; they complete the link introduced in the preceding paper between K+ channel current, K+(86Rb+) flux and irreversible cation uptake in the toxin. The data also offer some insights toward a kinetic description of channel gating. Finally, they provide a vehicle for interpreting FC-induced changes in K+ and net H+ flux, and in membrane potential without the necessity for postulating gross changes in H+ pumping.
Type of Medium:
Electronic Resource
URL:
http://dx.doi.org/10.1007/BF00963821
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