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Glass microelectrode measurements of sieve tube membrane potentials in internode discs and petiole strips of tomato (Solanum lycopersicum L.)

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Summary

In tissue slices of tomato (Solanum lycopersicum L.) sieve tube membrane potentials (Em) were measured by use of glass microelectrodes. In internode discs, the potential differences (pd) of phloem cells near the cut surface fell into two distinct categories with average values of −66 and −109 mV. More distant from the cut surface the values decreased to averages of −71 and −140 mV. These pds were associated with phloem parenchyma cells and sieve tube/companion cell complexes, respectively. In petiole strips, pds were recorded from cells which were identified by iontophoretic injection of fluorescent dye. Averages in two different bathing media, were −140/−146mV, −149/−152mV, and −70/−68mV for sieve tubes, companion cells, and phloem parenchyma cells, respectively. The membrane potentials recorded from sieve tubes were transiently reduced upon sucrose addition. Reduction by CCCP and KCN was more permanent. Sieve tube Ems recovered more slowly from potassium than from sucrose-induced depolarizations. Light/ dark (L/D) responses were minute (±3 mV). The limitations of the present experimentation are evaluated with special reference to the question as whether the recorded Ems represent sieve tube membrane potentials occurring in the intact plant.

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Abbreviations

CCCP:

carbonyl cyanide m-chlorophenylhydrazone

D:

dark(ness)

Em :

membrane potential

L:

light

LYCH:

Lucifer yellow CH

pd:

potential difference

SE:

standard error

References

  • Behnke H-D (1975) Companion cells and transfer cells. Structure, function, development of transfer cell. In: Aronoff S et al (eds) Phloem transport. Plenum Press, New York London, pp 153–175

    Google Scholar 

  • Cheeseman JM, Pickard BG (1977) Electrical characteristics of cells from leaves ofLycopersicon. Can J Bot 55: 497–510

    Google Scholar 

  • Contardi PJ, Davis RF (1978) Membrane potential inPhaeoceros laevis. Plant Physiol 61: 164–169

    Google Scholar 

  • Daie J (1987) Sucrose uptake in isolated phloem of celery is a single saturable transport system. Planta 171: 474–482

    Google Scholar 

  • Delrot S, Bonnemain J-L (1985) Mechanism and control of phloem transport. Physiol Vég 23: 199–220

    Google Scholar 

  • Erwee MG, Goodwin PB, van Bel AJE (1985) Cell-cell communication in the leaves ofCommelina cyanea and other plants. Plant Cell Environ 8: 173–178

    Google Scholar 

  • Evert RF, Eschrich W, Heyser W (1978) Leaf structure in relation to solute transport and phloem loading inZea mays L. Planta 138: 279–294

    Google Scholar 

  • Fensom DS (1975) Work with isolated phloem strands. In: Zimmermann MH, Milburn JA (eds) Transport in plants, vol 1, phloem transport. Springer, Berlin Heidelberg New York, pp 223–244 [Pirson A, Zimmermann MH (eds) Encyclopedia of plant physiology, new series, vol 1]

    Google Scholar 

  • Fisher DG, Evert RF (1982) Studies in the leaf ofAmaranthus retroflexus (Amaranthaceae): ultrastructure, plasmodesmatal frequency and solute concentration in relation to phloem loading. Planta 155: 377–387

    Google Scholar 

  • Fromm J, Eschrich W (1988) Transport processess in stimulated and non-stimulated leaves ofMimosa pudica. II. Energesis and transmission of seismic stimulations. Trees 2: 18–24

    Google Scholar 

  • Giaquinta RT (1977) Possible role of pH gradient and membrane ATPase in the loading of sucrose into the sieve tubes. Nature 264: 369–370

    Google Scholar 

  • —, (1983) Phloem loading of sucrose. Annu Rev Plant Physiol 34: 347–387

    Google Scholar 

  • Gifford RM, Evans LT (1981) Photosynthesis, carbon partitioning, and yield. Annu Rev Plant Physiol 32: 485–509

    Google Scholar 

  • Goodwin PB (1983) Molecular size limit for movement in the symplast of theElodea leaf. Planta 57: 124–130

    Google Scholar 

  • —, Erwee MG (1985) Intercellular transport studied by micro-injection. In: Robards AW (ed) Botanical microscopy. Oxford University Press, Oxford, pp 335–358

    Google Scholar 

  • Gradmann D, Mayer W-E (1977) Membrane potentials and ion permeabilities in flexor cells of the laminar pulvini ofPhaseolus coccineus L. Planta 137: 19–24

    Google Scholar 

  • Komor E (1983) Phloem loading and unloading. Prog Bot 45: 68–75

    Google Scholar 

  • —, Ohrlich G (1986) Sugar-proton symport: from single cells to phloem loading. In: Cronshaw J et al (eds) Phloem transport. Alan R Liss, New York, pp 53–65

    Google Scholar 

  • Malek F, Baker DA (1977) Proton co-transport of sugars in the phloem loading. Planta 135: 297–299

    Google Scholar 

  • — — (1978) Effect of fusicoccin on proton co-transport of sugars in the phloem loading ofRicinus communis L. Plant Sci Lett 11: 233–239

    Google Scholar 

  • Milburn JA (1975) Pressure Flow. In: Zimmermann MH, Milburn JA (eds) Transport in plants, vol 1, phloem transport. Springer, Berlin Heidelberg New York, pp 328–353 [Pirson A, Zimmermann MH (eds) Encyclopedia of plant physiology, new series, vol 1]

    Google Scholar 

  • Overall RL, Gunning BES (1982) Intercellular communication inAzolla roots. II. Electrical coupling. Protoplasma 111: 151–160

    Google Scholar 

  • Palevitz BA, Hepler PK (1985) Changes in dye coupling of stomatal cells ofAllium andCommelina demonstrated by microinjection of Lucifer yellow. Planta 164: 473–479

    Google Scholar 

  • Prins HBA, Harper JR, Higinbotham N (1980) Membrane potentials ofVallisneria leaf cells and their relation to photosynthesis. Plant Physiol 65: 1–5

    Google Scholar 

  • Samejima M, Sibaoka T (1983) Identification of the excitable cells in the petiole ofMimosa pudica by intracellular injection of procion yellow. Plant Cell Physiol 24: 33–39

    Google Scholar 

  • Sibaoka T (1962) Excitable cells inMimosa. Science 137: 226

    Google Scholar 

  • Stewart WW (1981) Lucifer dyes-highly fluorescent dyes for biological tracing. Nature 292: 17–21

    Google Scholar 

  • Tucker EB (1982) Translocation in the staminal hair ofSetcreasea purpurea. I. A study of cell ultrastructure and cell to cell passage of molecular probes. Protoplasma 113: 193–202

    Google Scholar 

  • van Bel AJE, Koops AJ (1985) Uptake of14C-sucrose in isolated minor vein networks ofCommelina benghalensis L. Planta 164: 362–369

    Google Scholar 

  • van der Schoot C, van Bel AJE (1989) Architecture of the internodal xylem of tomato (Solatnum lycopersicum L.) with reference to longitudinal and lateral transfer. Am J Bot (in press)

  • Wright JP, Fisher DB (1981) Measurement of the sieve tube membrane potential. Plant Physiol 67: 845–848

    Google Scholar 

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van der Schoot, C., van Bel, A.J.E. Glass microelectrode measurements of sieve tube membrane potentials in internode discs and petiole strips of tomato (Solanum lycopersicum L.). Protoplasma 149, 144–154 (1989). https://doi.org/10.1007/BF01322986

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  • DOI: https://doi.org/10.1007/BF01322986

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