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Control of electron flow in intact chloroplasts by the intrathylakoid pH, not by the phosphorylation potential

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Abstract

In the presence of nitrite or oxaloacetate, intact chloroplasts evolved oxygen at a significant rate for the initial 1 to 2 min of illumination. Subsequently, oxygen evolution was suppressed progressively. The suppressed oxygen evolution was stimulated strikingly by NH4Cl. The results indicate that coupled electron flow in intact chloroplasts is controlled in the light, and the control is released by NH4Cl. However, at low concentrations, NH4Cl was not an effective uncoupler of photophosphorylation in intact chloroplasts. Intrachloroplast ATP levels and ATP/ADP ratios were not significantly influenced by NH4Cl. In contrast, the quenching of 9-aminoacridine fluorescence, which can be used to indicate the intrathylakoid pH in intact chloroplasts, was reduced drastically even by low concentrations of NH4Cl. This suggests that the chloroplast phosphorylation potential is not in equilibrium with the proton gradient. In coupled chloroplasts, the intrathylakoid pH was lower in the light with nitrite than with oxaloacetate as electron acceptor. Electron flow was also more effectively controlled in chloroplasts illuminated with nitrite than with oxaloacetate. It is concluded that the intrathylakoid pH, not the phosphorylation potential, is a factor in the control of the rate of electron flow in intact chloroplasts.

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Abbreviations

CCCP:

carbonylcyanide-m-chlorophenylhydrazone

OAA:

oxalo-acetate

MES:

2-(N-morpholino)-ethanesulfonic acid

HEPES:

N-2-hyroxyethylpiperazine-N′-2-ethanesulfonic acid

References

  • Avron, M.: The relation of light-induced reactions of isolated chloroplasts to proton concentrations In: Proc. 2nd Int. Congress on Photosynthesis, pp. 861–871, Forti, G., Avron, M., Melandri, A., eds. The Hague: Dr. W. Junck N.V. 1972

    Google Scholar 

  • de Benedetti, E., Forti, G., Garlaschi, F.M., Rosa, L.: On the mechanism of ammonium stimulation of photosynthesis in isolated chloroplasts. Plant Sci. Lett. 7, 85–90 (1976)

    Google Scholar 

  • de Beneditti, E., Garlaschi, F.M.: On the estimation of proton gradient and osmotic volume in chloroplast membranes. J. Bioenerg. 9, 195–201 (1977)

    Google Scholar 

  • Egneus, H., Heber, U., Matthiesen, U., Kirk, M.: Reduction of oxygen by the electron transport chain of chloroplasts during assimilation of carbon dioxide. Biochim. Biophys. Acta 408, 252–268 (1975)

    Google Scholar 

  • Fiolet, J.W., Bakker, E.P., van Dam, K.: The fluorescent properties of acridines in the presence of chloroplasts or liposomes. On the quantitative relationship between the fluorescence quenching and the transmembrane proton gradient. Biochim. Biophys. Acta 368, 432–445 (1974)

    Google Scholar 

  • Heathcote, P., Hall, D.A.: Non-cyclic photophosphorylation in photosystem II and photosystem I. Stoichiometry and photosynthetic control. In: Proc. 3rd Int. Congress on Photosynthesis, pp. 463–471, Avron, M., ed. Amsterdam: Elsevier 1975

    Google Scholar 

  • Heber, U.: Stoichiometry of reduction and phosphorylation during illumination of intact chloroplasts. Biochim. Biophys. Acta. 305, 140–152 (1973)

    Google Scholar 

  • Heber, U., Purczeld, P.: Substrate and product fluxes across the chloroplast envelope during bicarbonate and nitrite reduction. In: Proc. 4th Int. Congress on Photosynthesis, pp. 107–118 Hall, D.O., Coombs, J., Goodwin, T.W., eds. London: The Biochemical Society 1978

    Google Scholar 

  • Jensen, R.G., Bassham, J.A.: Photosynthesis by isolated chloroplasts. Proc. Natl. Acad. Sci. USA 56, 1095–1101 (1966)

    Google Scholar 

  • Kraayenhof, R.: “State 3 - State 4” transition and phosphate potential in “Class 1” spinach chloroplasts. Biochim. Biophys. Acta 180, 213–215 (1969)

    Google Scholar 

  • Mitchell, P.: Chemiosmotic coupling in oxidative and photosynthetic phosphorylation. Biol. Rev. 41, 445–502 (1966)

    Google Scholar 

  • Mitchell, P.: Vectorial chemistry and the molecular mechanics of chemiosmotic coupling. Power transmission by proticity. Biochem. Soc. Trans. 4, 399–430 (1976)

    Google Scholar 

  • Neumann, J., Jagendorf, A.T.: Light-induced pH changes related to phosphorylation by chloroplasts. Arch. Biochem. Biophys. 107, 109–119 (1964)

    Google Scholar 

  • Purczeld, P., Chon, C.J., Portis, A.R., Heldt H.W., Heber, U.: The mechanism of the control of carbon fixation by the pH in the chloroplast stroma. Studies with nitrite-mediated proton transfer across the envelope. Biochim. Biophys. Acta 501, 488–498 (1978)

    Google Scholar 

  • Robinson, S.P., Wiskich, J.T.: Factors affecting the ADP/O ratio in isolated chloroplasts. Biochim. Biophys. Acta 440, 131–146 (1976)

    Google Scholar 

  • Rottenberg, H., Grunwald, T., Avron, M.: Direct determinations of ΔpH in chloroplasts, and its relation to the mechanisms of photoinduced reactions. FEBS Lett. 13, 41–44 (1971)

    Google Scholar 

  • Rumberg, B., Reinwald, E., Schröder, H., Siggel, U.: Correlations between electron transfer, proton translocation and phosphorylation in chloroplasts. In: Progress in Photosynthesis Research, pp. 1374–1382, Metzner, H., ed. Tübingen: Laupp 1969

    Google Scholar 

  • Schuldiner, S., Rottenberg, H., Avron, M.: Determination of ΔpH in chloroplasts. 2. Fluorescent amines as a probe for the determination of ΔpH in chloroplasts. Eur. J. Biochem. 25, 64–70 (1972)

    Google Scholar 

  • Stanley, P.E., Williams, S.G.: Use of the liquid scintillation spectrometer for determining adenosine triphosphate by the luciferase enzyme. Anal. Biochem. 29, 381–392 (1969)

    Google Scholar 

  • Strehler, B.L.: Adenosine-5′-triphosphate and creatine phosphate determination with luciferase. In: Method of Enzymatic Analysis, pp. 2112–2126, Bergmeyer, H.U., ed. Weinheim: Verlag Chemie 1974

    Google Scholar 

  • Tillberg, J., Giersch, C., Heber, U.: CO2 reduction by intact chloroplasts under a diminished proton gradient. Biochim. Biophys. Acta 461, 31–47 (1977)

    Google Scholar 

  • Trebst, A.: Energy conservation in photosynthetic electron transport of chloroplasts. Annu. Rev. Plant Physiol. 25, 423–458 (1974)

    Google Scholar 

  • Walker, D.A.: Plastid and intracellular transport. In: Encyclopedia of Plant Physiol., new Series, Transport in Plants III. pp. 85–136, Berlin, Heidelberg, New York: Springer 1976

    Google Scholar 

  • Werdan, K., Heldt, H.W., Milovancev, M.: The role of pH in the regulation of carbon fixation in the chloroplast stroma. Studies on CO2 fixation in the light and dark. Biochim. Biophys. Acta 396, 276–292 (1975)

    Google Scholar 

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Kobayashi, Y., Inoue, Y., Shibata, K. et al. Control of electron flow in intact chloroplasts by the intrathylakoid pH, not by the phosphorylation potential. Planta 146, 481–486 (1979). https://doi.org/10.1007/BF00380864

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  • DOI: https://doi.org/10.1007/BF00380864

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