Abstract
Uptake of 3H-labelled (±)-abscisic acid (ABA) into isolated barley (Hordeum vulgare L.) epidermal cell protoplasts (ECP) was followed over a range of pH values and ABA concentrations. The present results show that ABA uptake is not always linearly correlated with the external concentration of undissociated ABA (ABAH). At pH 7.25, ABA uptake exhibited saturation kinetics with an apparent K m value of 75 mmol·m−3 to tal ABA. This saturable transport component was inhibited by pretreating the protoplasts with 1 mol·m−3 p-chloromercuribenzenesulfonic acid at pH 8.0, conditions that minimized the uptake of this acid sulfhydryl reagent. Moreover, the rate of (±)-[3]HABA uptake was reduced by addition of 0.1 mol·m−3 (±)-ABA to 41%, whereas the same concentration of (±)-ABA was approximately half as effective (46% of the inhibitory effect). Thus, it was concluded that only (±)-ABA competes for an ABA carrier that is located in the epidermal cell plasma membrane. The permeability of the epidermal cell plasma membrane was studied by performing a Collander analysis. At pH 6 the overall plasma-membrane permeability of epidermal cells was similar to that of guard cells but was about two times higher than that of mesophyll cells.
Similar content being viewed by others
Abbreviations
- ABA:
-
abscisic acid
- ABA− :
-
anion of ABA
- ABAH:
-
undissociated ABA
- 2,4-D:
-
2,4-dichlorophenoxyacetic acid
- DMO:
-
5,5-dimethyloxazolidine-2,4-dione
- ECP:
-
deepidermal cell protoplast
- Kr :
-
partition coefficient
- Mr :
-
relative molecular mass
- NEM:
-
N-ethylmaleimide
- PCMBS:
-
p-chloromercuriben zenesulfonic acid
- Ps :
-
permeability coefficient
References
Astle, M.C., Rubery, P.H. (1980) A study of abscisic acid uptake by apical and proximal root segments of Phaseolus coccineus L. Planta 150, 312–320
Baier, M. (1990) Transport und Verteilung von Abscisinsäure im Blatt. Die Rolle der Schließzellen. Ph.D. thesis, University of Würzburg
Baier, M., Hartung, W. (1988) Movement of abscisic acid across the plasmalemma and the tonoplast of guard cells of Valerianella locusta. Bot. Acta 101, 332–337
Baier, M., Gimmler, H., Hartung, W. (1990) The permeability of the guard cell plasma membrane and tonoplast. J. Exp. Bot. 41, 351–358
Collander, R. (1954) The permeability of Nitella cells to non-electrolytes. Physiol. Plant. 7, 420–445
Daeter, W., Hartung, W. (1990) Compartmentation and transport of abscisic acid in mesophyll cells of intact leaves of Valerianella locusta. J. Plant Physiol. 136, 306–312
Dietz, K.-J., Schramm, M., Betz, M., Busch, H., Dürr, C., Martinoia, E. (1992) Characterization of the epidermis from barley primary leaves. I. Isolation of epidermal protoplasts. Planta 187, 425–430
Gimmler, H., Hartung, W. (1988) Low permeability of the plasma membrane of Dunaliella parva for solutes. J. Plant Physiol. 133, 165–172
Gimmler, H., Heilmann, B., Demmig, B., Hartung, W. (1981) The permeability coefficients of the plasmalemma and the chloroplast envelope of spinach mesophyll cells for phytohormones. Z. Naturforsch. 36c, 672–678
Guy, M., Reinhold, L., Rahat, M., Seiden, A. (1981) Protonation and light synergistically convert plasmalemma sugar carrier system in mesophyll protoplasts to its fully activated form. Plant Physiol. 67, 1146–1150
Hartung, W., Slovik, S. (1991) Physicochemical properties of plant growth regulators and plant tissues determine their distribution and redistribution: stomatal regulation by abscisic acid in leaves. New Phytol. 119, 361–382
Hartung, W., Radin, J.W., Hendrix, D.L. (1988) Abscisic acid movement into the apoplastic solution of water-stressed cotton leaves. Plant Physiol. 86, 908–913
Hartung, W., Slovik, S., Baier, M. (1990) pH changes and redistribution of ABA within the leaf under stress. In: Importance of root to shoot communication in the responses to environmental stress (Monograph 21), pp. 215–236, Davies, W.J., Jeffcoat, B., ededs. British Society for Plant Growth Regulation
Heilmann, B., Hartung, W., Gimmler, H. (1980) The distribution of abscisic acid between chloroplasts and cytoplasm of leaf cells and the permeability of the chloroplast envelope for abscisic acid. Z. Pflanzenphysiol. 97, 67–78
Höfler, K., Stiegler, A. (1930) Permeabilitätsverteilung in verschiedenen Geweben der Pflanze. Protoplasma 9, 469–512
Kaiser, W.M., Hartung, W. (1981) Uptake and release of abscisic acid by isolated photoautotrophic mesophyll cell, depending on pH gradients. Plant Physiol. 68, 202–206
Milborrow, B.V., Rubery, P.H. (1985) The specifity of the carriermediated uptake of ABA by root segments of Phaseolus coccineus L. J. Exp. Bot. 36, 807–822
Riordan, J.F., Valle, B.L. (1972) Reactions with N-ethylmaleimide and p-mercuribenzoate. Methods Enzymol. 25, 449–456
Rubery, P.H. (1979) The effects of 2,4-dinitrophenol and chemical modifying reagents on auxin transport by suspension-cultured crown gall cells. Planta 144, 173–178
Slovik, S., Baier, M., Hartung, W. (1992) Compartmental distribution and redistribution of abscisic acid in intact leaves. I. Mathematical formulation. Planta 187, 14–25
Url, W. (1952) Unterschiede der Plasmapermeabilität in den Gewebeschichten krautiger Stengel. Physiol. Plant. 5, 135–144
Webb, J.L. (1966) Enzyme and metabolic inhibitors, vol. 3, pp. 361–362, Academic Press, London New York
Windsor, M.L., Milborrow, B.V., McFarlane, I.J. (1992) The uptake of (+)-S- and (−)-R-abscisic acid b suspension cultured cells of hopbush (Dodonaea viscosa). Plant Physiol. 100, 54–62
Author information
Authors and Affiliations
Additional information
We are grateful to Barbara Dierich for expert technical assistance, to Prof. H. Gimmler (Lehrstuhl für Botanik I, Universität Würzburg, FRG) for helpful discussions and to the Deutsche Forschungsgemeinschaft (SFB 251, TP 3) for financial support.
Rights and permissions
About this article
Cite this article
Daeter, W., Hartung, W. The permeability of the epidermal cell plasma membrane of barley leaves to abscisic acid. Planta 191, 41–47 (1993). https://doi.org/10.1007/BF00240894
Received:
Accepted:
Issue Date:
DOI: https://doi.org/10.1007/BF00240894