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Heterogeneity of Photosystem I reaction centers in barley leaves as related to the donation from stromal reductants

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Abstract

The light-response curves of P700 oxidation and time-resolved kinetics of P700+ dark re-reduction were studied in barley leaves using absorbance changes at 820 nm. Leaves were exposed to 45 °C and treated with either diuron or diuron plus methyl viologen (MV) to prevent linear electron flow from PS II to PSI and ferredoxin-dependent cyclic electron flow around PSI. Under those conditions, P700+ could accept electrons solely from soluble stromal reductants. P700 was oxidized under weak far-red light in leaves treated with diuron plus MV, while identical illumination was nearly ineffective in diuron-treated leaves in the absence of MV. When heat-exposed leaves were briefly illuminated with strong far-red light, which completely oxidized P700, the kinetics of P700+ dark reduction was fitted by a single exponential term with half-time of about 40 ms. However, two first-order kinetic components of electron flow to P700+ (fast and slow) were found after prolonged leaf irradiation. The light-induced modulation of the kinetics of P700+ dark reduction was reversed following dark adaptation. The fast component (half time of 80–90 ms) was 1.5 larger than the slow one (half time of about 1 s). No kinetic competition occurred between two pathways of electron donation to P700+ from stromal reductants. This suggests the presence of two different populations of PSI.

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References

  • Albertsson P-Å (1995) The structure and function of the chloroplast membrane - a model for the domain organization. Photosynth Res 46: 141–149

    Article  CAS  Google Scholar 

  • Arnon DI and Chain R (1975) Regulation of ferredoxin-catalysed photosynthetic photophosphorylation. Proc Natl Acad Sci USA 72: 4961–4965

    Article  PubMed  CAS  Google Scholar 

  • Asada K, Heber U and Schreiber U (1992) Pool size of electrons that can be donated to P700+, as determined in intact leaves: donated to P700+ from stromal components via the intersystem chain. Plant Cell Physiol 33: 927–932

    CAS  Google Scholar 

  • Asada K, Heber U and Schreiber U (1993) Electron flow to the intersystem chain from stromal components and cyclic electron flow in maize chloroplasts, as detected in intact leaves by monitoring redox changes of P700 and chlorophyll fluorescence. Plant Cell Physiol 34: 39–50

    CAS  Google Scholar 

  • Bendall DS and Manasse RS (1995) Cyclic photophosphorylation and electron transport. Biochim Biophys Acta 1229: 23–38

    Article  Google Scholar 

  • Bennoun P (1994) Chlororespiration revisited: mitochondrialplastid interactions in Chlamidomonas. Biochim Biophys Acta 1186: 59–66

    Article  CAS  Google Scholar 

  • Buchanan BB (1980) Role of light in the regulation of chloroplast enzymes. Annu Rev Plant Physiol 31: 341–374

    Article  CAS  Google Scholar 

  • Bukhov NG, Wiese C, Neimanis S and Heber U (1999) Heat sensitivity of chloroplasts and leaves: Leakage of protons from thylakoids and reversible activation of cyclic electron transport. Photosynth Res 59: 81–93

    Article  CAS  Google Scholar 

  • Bukhov NG, Samson G and Carpentier R (2000) Nonphotosynthetic reduction of the intersystem electron transport chain of chloroplasts following heat stress. Steady state rate. Photochem Photobiol 72: 351–359

    Article  PubMed  CAS  Google Scholar 

  • Cleland RE and Bendall DS (1992) Photosystem I cyclic electron transport: Measurement of ferredoxin-plastoquinone reductase activity. Photosynth Res 34: 409–418

    Article  CAS  Google Scholar 

  • Corneille S, Cournac L, Guedeney G, Havaux M and Peltier G (1998) Reduction of the plastoquinone pool by exogenous NADH and NADPH in higher plant chloroplasts. Characterization of a NAD(P)H-plastoquinone oxidoreductase activity. Biochim Biophys Acta 1361: 59–69

    Google Scholar 

  • Feild TS, Nedbal L and Ort DR (1998) Non-photochemical reduction of the plastoquinone pool in sunflower leaves originates from chlororespiration. Plant Physiol 116: 1209–1218

    Article  PubMed  CAS  Google Scholar 

  • Groom Q, Kramer DM, Crofts AR and Ort DR (1993) The nonphotochemical reduction of plastoquinone in leaves. Photosynth Res 36: 205–215

    Article  CAS  Google Scholar 

  • Harbinson J and Hedley CL (1989) The kinetics of P700+ reduction in leaves: a novel in situ probe of thylakoid functioning. Plant Cell Environ 10: 131–140

    Google Scholar 

  • Havaux M (1996) Short-term responses of Photosystem I to heat stress. Induction of a PS II-independent electron transport through PS I fed by stromal components. Photosynth Res 47: 85–97

    Article  CAS  Google Scholar 

  • Kobayashi Y and Heber U (1994) Rates of vectorial proton transport supported by cyclic electron flow during oxygen reduction by illuminated intact chloroplasts. Photosynth Res 41: 419–428

    Article  CAS  Google Scholar 

  • Peltier G, Ravenel J and Verméglio A (1987) Inhibition of a respiratory activity by short saturating flashes in Chlamidomonas: Evidence for a chlororespiration. Biochim Biophys Acta 893: 83–90

    Article  CAS  Google Scholar 

  • Ravenel J, Peltier G and Havaux M (1994) The cyclic electron pathways around Photosystem I in Chlamydomonas reinhardtii as determined in vivo by photoacoustic measurements of energy storage. Planta 193: 251–259

    Article  CAS  Google Scholar 

  • Sazanov LA, Burrows P and Nixon P (1996) Detection and characterization of a complex I-like NADH-specific dehydrogenase from pea thylakoids. Trans Biochem Soc London 24: 739–743

    CAS  Google Scholar 

  • Sazanov L, Burrows P and Nixon P (1998) The chloroplast Ndh complex mediates the dark reduction of the plastoquinone pool in response to heat stress in tobacco leaves. FEBS Lett 429: 115–118

    Article  PubMed  CAS  Google Scholar 

  • Schreiber U, Klughammer C and Neubauer C (1988) Measuring P700 absorbance changes around 830 nm with a new type of pulse modulated system. Z Naturforsch 43c: 686–698

    Google Scholar 

  • Shikanai T, Endo T, Hashimoto T, Y. Yamada Y, Asada K and Yokota A (1998) Directed disruption of the tobacco ndhB gene impairs cyclic electron flow around Photosystem I. Proc Natl Acad Sci USA 95: 9705–9709

    Article  PubMed  CAS  Google Scholar 

  • Sparla F, Tedeschi G and Trost P (1996) NAD(P)H:(quinoneacceptor) oxidoreductase of tobacco leaves is a flavin mononucleotide-containing flavoenzyme. Plant Physiol 112: 249–258

    PubMed  CAS  Google Scholar 

  • Witt HT (1971) Coupling of quanta, electrons, fields, ions and phosphorylation in the functional membrane of photosynthesis. Results by pulse spectrophotometric methods. Quart Rev Biophys 4: 365–477

    Article  CAS  Google Scholar 

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Correspondence to Robert Carpentier.

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Bukhov, N., Carpentier, R. & Samson, G. Heterogeneity of Photosystem I reaction centers in barley leaves as related to the donation from stromal reductants. Photosynthesis Research 70, 273–279 (2001). https://doi.org/10.1023/A:1014741814581

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