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Effect of the Pool Size of Stromal Reductants on the Alternative Pathway of Electron Transfer to Photosystem I in Chloroplasts of Intact Leaves

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Abstract

The effect of elevated temperature on electron flow to plastoquinone pool and to PSI from sources alternative to PSII was studied in barley (Hordeum vulgare L.) and maize (Zea mays L.) leaves. Alternative electron flow was characterized by measuring variable fluorescence of chlorophyll and absorption changes at 830 nm that reflect redox changes of P700, the primary electron donor of PSI. The treatment of leaves with elevated temperature resulted in a transient increase in variable fluorescence after cessation of actinic light. This increase was absent in leaves treated with methyl viologen (MV). The kinetics of P700+ reduction in barley and maize leaves treated with DCMU and MV exhibited two exponential components. The rate of both components markedly increased with temperature of the heat pretreatment of leaves when the reduction of P700+ was measured after short (1 s) illumination of leaves. The acceleration of both kinetic components of P700+ reduction by high-temperature treatment was much less pronounced when P700+ reduction rate was measured after illumination of leaves for 1 min. Since the treatment of leaves with DCMU and MV inhibited both the electron flow to PSI from PSII and ferredoxin-dependent cycling of electrons around PSI, the accelerated reduction of P700+ indicated that high temperature treatment activated electron flow to PSII from reductants localized in the chloroplast stroma. We conclude that the lesser extent of activation of this process by elevated temperature after prolonged illumination of heat-inhibited leaves is caused by depletion of the pool stromal reductants in light due to photoinduced electron transfer from these reductants to oxygen.

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REFERENCES

  1. Stitt, M., Limitation of Photosynthesis by Carbon Metabolism: 1. Evidence for Excess Electron Transport Capacity in Leaves Carrying out Photosynthesis in Saturating Light and CO2, Plant Physiol., 1986, vol. 81, pp. 1115–1122.

    Google Scholar 

  2. Baker, N.R., A Possible Role for Photosystem II in Environmental Perturbations of Photosynthesis, Physiol. Plant., 1991, vol. 81, pp. 563–570.

    Google Scholar 

  3. Bukhov, N.G. and Mohanty, P., Elevated Temperature Stress Effects on Photosystems: Characterization and Evaluation of the Nature of Heat Induced Impairments, Concepts in Photobiology, Photosynthesis and Photomorphogenesis, Singhal, G.S. et al., Eds., New Delhi: Narosa Publ. House, 1999, pp. 617–648.

    Google Scholar 

  4. Krause, G.H. and Behrend, U., ?pH-Dependent Chlorophyll Fluorescence Quenching Indicating a Mechanism of Protection against Photoinhibition of Chloroplasts, FEBS Lett., 1986, vol. 200, pp. 298–302.

    Google Scholar 

  5. Poulson, M., Samson, G., and Whitmarsh, J., Evidence that Cytochrome b-559 Protects Photosystem II against Photoinhibition, Biochemistry, 1995, vol. 34, pp. 10932–10938.

    Google Scholar 

  6. Cleland, R.E. and Bendall, D.S., Photosystem I Cyclic Electron Transport: Measurement of Ferredoxin-Plastoquinone Reductase Activity, Photosynth. Res., 1992, vol. 34, pp. 409–418.

    Google Scholar 

  7. Arnon, D.I. and Chain, R., Regulation of Ferredoxin-Catalyzed Photosynthetic Photophosphorylations, Proc. Natl. Acad. Sci. USA, 1975, vol. 72, pp. 4961–4965.

    Google Scholar 

  8. Badger, M.R., Photosynthetic Oxygen Exchange, Annu. Rev. Plant Physiol., 1985, vol. 36, pp. 27–53.

    Google Scholar 

  9. Albertsson, P.-Å., The Structure and Function of the Chloroplast Photosynthetic Membrane-a Model for the Domain Organization, Photosynth. Res., 1995, vol. 46, pp. 141–149.

    Google Scholar 

  10. Feild, T.S., Nedbal, L., and Ort, D.R., Non-Photochemical Reduction of the Plastoquinone Pool in Sunflower Leaves Originated from Chlororespiration, Plant Physiol., 1998, vol. 116, pp. 1209–1218.

    Google Scholar 

  11. Funk, E., Schafer, E., and Steinmuller, K., Characterization of the Complex I-Homologous NAD(P)H-Plaslastoquinone-Oxidoreductase (NDH-Complex) of Maize Chloroplasts, J. Plant Physiol., 1999, vol. 154, pp. 16–23.

    Google Scholar 

  12. Groom, Q., Kramer, D.M., Crofts, A.R., and Ort, D.R., The Non-Photochemical Reduction of Plastoquinone in Leaves, Photosynth. Res., 1993, vol. 36, pp. 205–215.

    Google Scholar 

  13. Havaux, M., Short-Term Responses of Photosystem II to Heat Stress. Induction of a PS II-Independent Electron Transport through PS I Fed by Stromal Components, Photosynth. Res., 1996, vol. 47, pp. 85–97.

    Google Scholar 

  14. Bukhov, N.G., Wiese, C., Neimanis, S., and Heber, U., Heat Sensitivity of Chloroplasts and Leaves: Leakage of Protons from Thylakoids and Reversible Activation of Cyclic Electron Transport, Photosynth. Res., 1999, vol. 59, pp. 81–93.

    Google Scholar 

  15. Egorova, E.A. and Bukhov, N.G., Effect of Elevared Temperatures on the Activities of Alternative Pathways of Photosynthetic Electron Transport in Intact Barley and Maize, Fiziol. Rast. (Moscow), 2002, vol. 49, pp. 645–655 (Russ. J. Plant Physiol., Engl. Transl.).

    Google Scholar 

  16. Fujii, T., Yokoyama, E., Inoue, K., and Sakurai, H., The Sites of Electron Donation of Photosystem I to Methyl Viologen, Biochim. Biophys. Acta, 1990, vol. 1015, pp. 41–48.

    Google Scholar 

  17. Schreiber, U., Schliwa, U., and Bilger, W., Continuous Recording of Photochemical and Non-Photochemical Chlorophyll Fluorescence Quenching with a New Type of Modulation Fluorometer, Photosynth. Res., 1986, vol. 10, pp. 51–62.

    Google Scholar 

  18. Schreiber, U., Klughammer, C., and Neubauer, C., Measuring P700 Absorbance Changes around 830 nm with a New Type of Pulse Modulated System, Z. Naturforsch., 1988, vol. 43c, pp. 686–698.

    Google Scholar 

  19. Diner, B.A., Dependence of the Deactivation Reactions of Photosystem II on the Redox State of Plastoquinone Pool A Varied under Anaerobic Conditions. Equilibria on the Acceptor Side of Photosystem II, Biochim. Biophys. Acta, 1977, vol. 460, pp. 247–258.

    Google Scholar 

  20. Egorova, E.A., Bukhov, N.G., Krendeleva, T.E., and Rubin, A.B., Heterogeneity of Quinone Acceptor Reduction in Intact Barley Leaves, Dokl. Akad. Nauk, 2001, vol. 377, pp. 1–4.

    Google Scholar 

  21. Bennoun, P., Réoxidation du quencher de fluorescence “Q” en présence de 3-(3,4-Dichlorophényl)-1,1-Diméthylurea, Biochim. Biophys. Acta, 1970, vol. 216, pp. 357–363.

    Google Scholar 

  22. Bukhov, N.G., Samsom, G., and Carpentier, R., Non-Photosynthetic Reduction of the Intersystem Electron Transport Chain of Chloroplasts Following Heat Stress: The Pool Size of Stromal Reductants, Photochem. Photobiol., 2001, vol. 74, pp. 438–443.

    Google Scholar 

  23. Sazanov, L., Burrows, P., and Nixon, P., The Chloroplast NDH Complex Mediates the Dark Reduction of the Plastoquinone Pool in Response to Heat Stress in Tobacco Leaves, FEBS Lett., 1998, vol. 429, pp. 115–118.

    Google Scholar 

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Egorova, E.A., Bukhov, N.G., Heber, U. et al. Effect of the Pool Size of Stromal Reductants on the Alternative Pathway of Electron Transfer to Photosystem I in Chloroplasts of Intact Leaves. Russian Journal of Plant Physiology 50, 431–440 (2003). https://doi.org/10.1023/A:1024700202498

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