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Evidence supporting a model of voltage-dependent uptake of auxin into Cucurbita vesicles

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Abstract

The accumulation of [14C]indole-3-acetic acid (IAA), of [3H]tetra-phenyl phosphonium ion as a membrane potential probe, and of [14C]butyric acid as probe for pH gradients was studied with membrane vesicles from etiolated hypocotyls of Cucurbita pepo. Ion gradients (K+, H+) were applied in the presence and absence of specific ionophores e.g. valinomycin or carbonylcyanide m-chlorophenylhydrazone. In all cases tested, the accumulation of [14C]IAA equals neither potential probe nor pH-probe accumulation, but represents. an intermediate between the two. Auxin molecules seem to be taken up as positively charged ions and a pH gradient is required for accumulation. The uptake mechanism thus appears to be a specific, carrier-mediated cotransport of the anion of IAA and no less than two protons. The initial rates of auxin uptake by the saturable influx carrier, of permeation through the membrane, and of efflux by the phytotropin-affected efflux carrier were analysed.

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Abbreviations

BA:

butyric acid

CCCP:

carbonylcyanid-3-chlorophenylhydrazone

CPD:

2-carboxylphenyl-3-phenylpropan-1,3-dion

IAA:

indole-3-acetic acid

IAA:

anion of IAA

IAAH:

undissociated form of IAA

2-NAA:

2-naphthaleneacetic acid

NPA:

1-N-naphthylphthalamic acid

TPP+ :

tetra-phenyl phosphonium ion

References

  • Clark, K.A., Goldsmith, M.H.M. (1986) Roles of transport and binding in the specific pH-dependent accumulation of auxin by zucchini membrane vesicles. In: Plant growth substances 1985, pp. 203–208, Bopp, M., ed. Springer, Berlin Heidelberg New York

    Google Scholar 

  • Depta, H., Hertel, R. (1982) FCCP sensitive association of weak organic acids to membranes from Cucurbita homogenates: evidence for closed and intact membrane vesicles. In: Plasmalemma and tonoplast: Their functions in the plant cell, pp. 137–145, Marmé, D., Marré, E., Hertel, R., eds. Elsevier, Amsterdam

    Google Scholar 

  • Goldsmith, M.H.M. (1982) A saturable site responsible for polar transport of indole-3-acetic acid in sections of maize coleoptiles. Planta 155, 68–75

    Google Scholar 

  • Goldsmith, M.H.M., Rose, R. (1983) Hyperpolarizing corn coleoptile cells with fusicoccin does not increase polar auxin transport. Plant Physiol. 72, s-145

  • Guern, J. (1985) Possible roles of malate transfer through the tonoplast in intracellular pH and tonoplast potential regulation. G. Bot. ital. 119, s-13-20

  • Hasenstein, K.H., Rayle, D. (1984) Cell wall pH and auxin transport. Plant Physiol. 76, 65–67

    Google Scholar 

  • Hertel, R. (1983a) The mechanism of auxin transport as a model for auxin action. Z. Pflanzenphysiol. 112, 53–67

    Google Scholar 

  • Hertel, R. (1983b) Hormonbindung, in-vitro-Transport, Gewebesensitivität: ihre mögliche Bedeutung für die Analyse der Auxinwirkung. Hohenheimer Arbeiten 129, 81–101

    Google Scholar 

  • Hertel, R. (1986) Two comments on auxin transport: the uptake/efflux-mechanism and the problem of adaptation. In: Plant growth substances 1985, pp. 214–217, Bopp, M., ed. Springer, Berlin Heidelberg New York

    Google Scholar 

  • Hertel, R., Lomax, T.L., Briggs, W.R. (1983) Auxin transport in membrane vesicles from Cucurbita pepo L.. Planta 157, 193–201

    Google Scholar 

  • Jacobs, M., Hertel, R. (1978) Auxin binding to subcellular fractions from Cucurbita hypocotyls: evidence for an auxin transport carrier. Planta 141, 1–10

    Google Scholar 

  • Katekar, G.F., Geissler, A.E. (1980) Auxin transport inhibitors. IV. Evidence of a common mode of action for a proposed class of auxin transport inhibitors: the phytotrophins. Plant Physiol. 68, 1190–1195

    Google Scholar 

  • Lomax, T.L. (1986) Active auxin uptake by specific plasma membrane carriers. In: Plant growth substances 1985, pp. 209–213, Bopp, M., ed. Springer, Berlin Heidelberg New York

    Google Scholar 

  • Lomax, T.L., Mehlhorn, R.J., Briggs, W.R. (1985) Determination of osmotic volumes and pH-gradients of plant membrane and lipid vesicles using ESR spectroscopy. Proc. Natl. Acad. Sci. USA 82, 6541–6545

    Google Scholar 

  • Rottenberg, H. (1979) The measurement of membrane potential and pH in cells, organelles and vesicles. Methods Enzymol. 55F, 547–569

    Google Scholar 

  • Rubery, P.H. (1978) Hydrogen ion dependence of carrier-mediated auxin uptake by suspension-cultured crown gall cells. Planta 142, 203–206

    Google Scholar 

  • Rubery, P.H., Sheldrake, A.R. (1974) Carrier-mediated auxin transport. Planta 118, 101–121

    Google Scholar 

  • Sussman, M.R., Goldsmith, M.H.M. (1981) Auxin uptake and action of N-1-naphthylphthalamic acid in corn coleptiles. Planta 150, 15–25

    Google Scholar 

  • Thomson, K.S., Hertel, R., Müller, S., Tavares, J.E. (1973) N-1-Naphthylphthalamic acid and 2,3,5-triiodobenzoic acid. In vitro binding to particulate cell fractions and action on auxin transport in corn coleoptiles. Planta 109, 337–352

    Google Scholar 

  • Walker, N.A. (1980) The transport systems of charophyte giant algae and their integration into modes of behavior. In: Plant membrane transport: Current conceptual issues, pp. 287–300, Spanswick, R.M., Lucas, W.J., Dainty, J. eds. Elsevier, Amsterdam

    Google Scholar 

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Benning, C. Evidence supporting a model of voltage-dependent uptake of auxin into Cucurbita vesicles. Planta 169, 228–237 (1986). https://doi.org/10.1007/BF00392319

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  • DOI: https://doi.org/10.1007/BF00392319

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