Skip to main content
Log in

Redox-state of intactNitella cells: dependency on intracellular pH and photosynthesis

  • Original Papers
  • Published:
Protoplasma Aims and scope Submit manuscript

Summary

The present paper describes the construction and properties of a Pt/Ir-semi-microelectrode and its application as a redoxsensitive electrode in intact cells of the giant algaNitella. For compartmental analysis of the stationary redox-state voltage (ERED), a value reflecting the interaction of the dominant redox couples with a Pt/Ir-electrode, the redox-sensitive electrode was inserted into the vacuole of leaf cells or cytoplasm enriched fragments (CEF) fromNitella internodal cells. After correction for the membrane voltage, measured with a second, conventional voltage electrode, ERED values of+237±93mVand+419±51 mV with respect to a normal H+-electrode were obtained for cytoplasm and vacuole, respectively. The redox-state of the cell culture medium was+604 mV. The steady state ERED in the cytoplasm can be perturbed by experimental treatments: indirect acidification of the cytoplasm by an external pH jump from 7.5 to 5.8 and direct acidification, by acid loading with 5 mM butyrate, both resulted in a positive shift of ERED, i.e., to an increase in cytoplasmic oxidation. At the same time the membrane depolarized electrically following the external pH jump, but hyperpolarized in response to acid loading. The data demonstrate the direct dependence of cytoplasmic redox state on intracellular pH, probably due to enhanced oxidation of protonated redox couples favoured by mass action. The electrical membrane voltage changes were not correlated with the shift in cytoplasmic ERED. This demonstrated that redox energy does not determine the electrical membrane voltage. Cytoplasmic ERED was also affected by photosynthesis. When CEFs were transferred from light to dark, or exposed to 10μM 3-(3,4-dichlorophenyl)-1,l-dimethylurea (DCMU), ERED shifted negatively (more reduced) by 6.4±4.5mV or 4.2±2mV, respectively. These data compare favourably with biochemical estimates of cytoplasmic pyridin nucleotides which also show an increase in cytoplasmic reduction in the dark. Therefore, it is unlikely that diffusable reducing equivalents are supplied to the cytoplasm from photosynthetically-active chloroplasts to act as secondary messengers.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

Abbreviations

EM :

transmembrane voltage

ERED :

redox-state voltage

E0 :

midpoint-redox-voltage

APW:

artificial pond water

CEF:

cytoplasm enriched fragment

References

  • Beilby MJ (1989) Electrophysiology of giant algal cells. Methods Enzymol 174: 403–443

    Google Scholar 

  • —, Shepherd VA (1989) Cytoplasm-enriched fragments ofChara: structure and electrophysiology. Protoplasma 48: 150–163

    Google Scholar 

  • Bertl A, Slayman CL (1990) Cation-selective channels in the vacuolar membrane ofSaccharomyces: dependence on calcium, redoxstate, and voltage. Proc Natl Acad Sci USA 87: 7824–7828

    Google Scholar 

  • Brügger M, Fischer-Schliebs E, Lüttge U (1992) Einfluß verschiedener SH-Reagenzien auf die Plasmalemma-H+-ATPase aus Maiswurzeln. In: Haschke H-P, Schnarrenberg C (eds) Botanikertagung 1992, Berlin. Akademie-Verlag, Berlin, p 350

    Google Scholar 

  • Cater DB, Philips AF, Silver IA (1957) Apparatus and techniques for measurements of oxidation-reduction potentials, pH and oxygen tension in vivo. Proc R Soc Lond [Biol] 146: 289–297

    Google Scholar 

  • Coleman HA (1986) Chloride currents inChara —a patch clamp study. J Membrane Biol 93: 41–49

    Google Scholar 

  • Elzenga JTM, Staal M, Prins HBA (1989) ATPase activity of isolated plasmalemma vesicles of leaves ofElodea are affected by thiole reagents and NADH/NAD ratio. Physiol Plant 76: 379–385

    Google Scholar 

  • Heineke D, Riens B, Grosse H, Hoferichter P, Peter U, Flügge U-I, Heldt HW (1991) Redox transfer across the inner chloroplast envelope membrane. Plant Physiol 95: 1131–1137

    Google Scholar 

  • Kochian LV, Lucas WJ (1982) Potassium transport in corn roots. I. Resolution of kinetics into a saturable and linear component. Plant Physiol 70: 1723–1731

    Google Scholar 

  • Lichtner F, Lucas WJ, Spanswick RM (1981) Effect of sulfhydryl reagents on the biophysical properties of the plasmalemma ofChora corallina. Plant Physiol 68: 899–904

    Google Scholar 

  • Lucas WJ, Alexander JM (1980) Sulfhydryl group involvement in plasmalemma transport of HCO3 and OH inChara corallina. Plant Physiol 65: 274–280

    Google Scholar 

  • Mahler HR, Cordes EH (1967) Biological chemistry. Harper®ow, New York

    Google Scholar 

  • Malbon CC, George ST, Moxham CP (1987) Intramolecular disulfide bridges: avenues to receptor activation? Trends Biochem Sci 12: 172–175

    Google Scholar 

  • Mimura T, Kirino Y (1984) Changes in cytoplasmic pH measured by31P-NMR in cells ofNitettopsis obtusa. Plant Cell Physiol 25: 813–820

    Google Scholar 

  • Møller IM, Lin W (1986) Membrane-bound NAD(P)H dehydrogenase in higher plant cells. Annu Rev Plant Physiol 37: 309–334

    Google Scholar 

  • Okihara K, Kiyosawa K (1988) Ion composition of theChara internode. Plant Cell Physiol 29: 21–25

    Google Scholar 

  • Puppi A, Dely M, Prager P (1976) Comparison of the redox-states of different tissues and types of acetylcholine effect. Acta Biochim Biophys Acad Sci Hung 11: 63–73

    Google Scholar 

  • — — — (1980) Redox agents affecting drug actions. Gen Pharmacol 1: 409–418

    Google Scholar 

  • Reid RJ, Smith FA (1988) Measurement of the cytoplasmic pH ofChara corallina using double-barreled pH microelectrodes. J Exp Bot 39: 1421–1432

    Google Scholar 

  • Roth Z, Chayen N, Dickstein S (1983) The involvement of intra-cellular redox-state and pH in the metabolic control of stimulus-response coupling. Int Rev Cytol 85: 39–61

    Google Scholar 

  • Rubinstein B, Stern AI (1991) The role of the plasma membrane redox activity in light effects in plants. J Bioenerg Biomembr 23: 393–408

    Google Scholar 

  • Sanders D (1990) Kinetic modeling of plant and fungal transport systems. Annu Rev Plant Physiol Plant Mol Biol 41: 77–107

    Google Scholar 

  • —, Miller AJ (1986) Measurements of cytoplasmic calcium activity with ion-selective microelectrodes. In: Trewavas AJ (ed) Molecular and cellular aspects of calcium in plant development. Plenum, London, pp 149–156

    Google Scholar 

  • —, Hansen U-P, Slayman CL (1981) Role of the plasma membrane proton pump in pH regulation in non-animal cells. Proc Natl Acad Sci USA 78: 5903–5907

    Google Scholar 

  • Serrano EE, Zeiger E, Hagiwara S (1988) Red light stimulates an electrogenic proton pump inVicia guard cell protoplasts. Proc Natl Acad Sci USA 85: 436–440

    Google Scholar 

  • Spalding EP, Slayman CI, Goldsmith MHM, Gradmann D, Berti A (1992) Ion channels inArabidopsis plasma membrane. Transport characteristics and involvement in light induced voltage changes. Plant Physiol 99: 96–102

    Google Scholar 

  • Takeshige K, Mitsumori F, Tazawa M, Mimura T (1992) Role of cytoplasmic inorganic phosphate in light-induced activation of H+-pumps in the plasma membrane and tonoplast ofChara corallina. Planta 186: 466–472

    Google Scholar 

  • Tazawa M, Kishimoto U, Kikuyama M (1974) Potassium, sodium, and chloride in the protoplasm of Characeae. Plant Cell Physiol 15: 103–110

    Google Scholar 

  • Thaler M, Simonis W, Schönknecht G (1992) Light-dependent changes of the cytoplasmic H+ and Clactivity in the green algaEremosphaera viridis. Plant Physiol 99: 103–110

    Google Scholar 

  • Thiel G, MacRobbie EAC, Hanke DE (1990) Raising the intra-cellular level of inositol 1,4,5-trisphosphate changes plasma membrane ion transport in characean algae. EMBO J 9: 1737–1741

    Google Scholar 

  • Walz D (1979) Thermodynamics of oxidation-reduction reactions and its application to bioenergetics. Biochim Biophys Acta 505: 279–353

    Google Scholar 

  • Winter U, Kirts GO (1990) Salinity response of a freshwater charophyte,Chara vulgaris. Plant Cell Environ 13: 123–134

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Thiel, G. Redox-state of intactNitella cells: dependency on intracellular pH and photosynthesis. Protoplasma 179, 26–33 (1994). https://doi.org/10.1007/BF01360734

Download citation

  • Received:

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF01360734

Keywords

Navigation