MECHANISMS OF SOLUTE EFFLUX FROM SEED COATS - WHOLE-CELL K-FABA L( CURRENTS IN TRANSFER CELL PROTOPLASTS DERIVED FROM COATS OF DEVELOPING SEEDS OF VICIA)

Citation
Wh. Zhang et al., MECHANISMS OF SOLUTE EFFLUX FROM SEED COATS - WHOLE-CELL K-FABA L( CURRENTS IN TRANSFER CELL PROTOPLASTS DERIVED FROM COATS OF DEVELOPING SEEDS OF VICIA), Journal of Experimental Botany, 48(313), 1997, pp. 1565-1572
Citations number
33
Categorie Soggetti
Plant Sciences
ISSN journal
00220957
Volume
48
Issue
313
Year of publication
1997
Pages
1565 - 1572
Database
ISI
SICI code
0022-0957(1997)48:313<1565:MOSEFS>2.0.ZU;2-M
Abstract
In developing seed of Vicia faba L., solutes imported through the phlo em of the coats move symplastically from the sieve elements to a speci alized set of cells (the thin-walled parenchyma transfer cells) for re lease to the seed apoplast. Potassium (K+) is the predominant cation r eleased from the seed coats. To elucidate the mechanisms of K+ efflux from seed coat to seed apoplast, whole-cell currents across the plasma membranes of protoplasts of thin-walled parenchyma transfer cells wer e measured using the whole-cell patch-clamp technique. Membrane depola rization elicited a time-dependent and an instantaneous outward curren t. The reversal potential (E-R) of the time-dependent outward current was close to the potassium equilibrium potential (E-K) and it shifted in the same direction as E, upon changing the external K+ concentratio n, indicating that this current was largely carried by an efflux of K. The activation of the time-dependent outward K+ current could be wel l fitted by two exponential components plus a constant. The instantane ous outward current could also be carried by K+ efflux as suggested by ion substitution experiments. These K+ outward rectifier currents eli cited by membrane depolarization are probably too small to represent t he mechanism for the normal K+ efflux from seed coat cells. Membrane h yperpolarization more negative than -80 mV activated a time-dependent inward current. K+ influx was responsible for the inward current as th e current reversed at membrane voltage close to E-K and shifted in the same direction as E-K when external [K+] was varied. Activation of th is K+ inward rectifier current was well fitted with two exponential co mponents plus a constant. A regulating function for this current is su ggested.