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Effect of photosystem II reaction center closure on nanosecond fluorescence relaxation kinetics

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Abstract

The fluorescence decay of chlorophyll in spinach thylakoids was measured as a function of the degree of closure of Photosystem II reaction centers, which was set for the flowed sample by varying either the preillumination by actinic light or the exposure of the sample to the exciting pulsed laser light. Three exponential kinetic components originating in Photosystem II were fitted to the decays; a fourth component arising from Photosystem I was determined to be negligible at the emission wavelength of 685 nm at which the fluorescence decays were measured. Both the lifetimes and the amplitudes of the components vary with reaction center closure. A fast (170–330 ps) component reflects the trapping kinetics of open Photosystem II reaction centers capable of reducing the plastoquinone pool; its amplitude decreases gradually with trap closure, which is incompatible with the concept of photosynthetic unit connectivity where excitation energy which encounters a closed trap can find a different, possibly open one. For a connected system, the amplitude of the fast fluorescence component is expected to remain constant. The slow component (1.7–3.0 ns) is virtually absent when the reaction centers are open, and its growth is attributable to the appearance of closed centers. The middle component (0.4–1.7 ns) with approximately constant amplitude may originate from centers that are not functionally linked to the plastoquinone pool. To explain the continuous increase in the lifetimes of all three components upon reaction center closure, we propose that the transmembrane electric field generated by photosynthetic turnover modulates the trapping kinetics in Photosystem II and thereby affects the excited state lifetime in the antenna in the trap-limited case.

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Abbreviations

DCMU:

3-(3,4-dichlorophenyl)-1,1-dimethylurea

HEPES:

4-(2-hydroxyethyl)-1-piperazineethane sulfonic acid

PQ:

plastoquinone

PSI and PSII:

Photosystem I and II

QA and QB :

primary and secondary quinone acceptor of PSII

References

  • Arnon, DI (1949) Copper enzymes in isolated chloroplasts. Polyphenoloxidase in Beta vulgaris. Plant Physiol 24: 1–15

    Google Scholar 

  • Black, MT, Brearley, TH and Horton, P (1986) Heterogeneity in chloroplast Photosystem II. Photosynth Res 8: 193–207

    Google Scholar 

  • Bonaventura, C and Myers, J (1969) Fluorescence and oxygen evolution from Chlorella pyrenoidosa. Biochim Biophys Acta 189: 366–383

    PubMed  Google Scholar 

  • Boxer SG, Lockhart DJ and Takiff L (1988) Nature of excited states in bacterial photosynthesis: Stark effect and phosphorescence. Biophys J 53: 205a

  • Butler, WL, Magde, D and Behrens, SJ (1983) Fluorescence lifetimes in the bipartite model of the photosynthetic apparatus with α,β heterogeneity in Photosystem II. Proc Natl Acad Sci USA 80: 7510–7514

    Google Scholar 

  • Chylla, RA, Garab, G and Whitmarsh, J (1987) Evidence for slow turnover in a fraction of Photosystem II complexes in thylakoid membranes. Biochim Biophys Acta 89: 562–571

    Google Scholar 

  • Dutton PL, Alegria G and Gunner MR (1988) The possible existence of a charge transfer state which precedes the formation of (BChl)2 + BPh- in Rb. sphaeroides reaction centers. Biophys J 53: 66a

  • Duysens, LNM (1986) Introduction to (bacterio)chlorophyll emission: a historical perspective. In: Govindjee, Amesz, J and Fork, DC (eds) Light Emission by Plants and Bacteria, pp 3–28. Academic Press, New York

    Google Scholar 

  • Duysens, LNM and Sweers, HE (1963) Mechanism of two photochemical reactions in algae as studied by means of fluorescence. In: Japanese Society of Plant Physiologists (eds) Microalgae and Photosynthetic Bacteria, pp 353–372. University of Tokyo Press, Tokyo

    Google Scholar 

  • Geacintov, NE and Breton, J (1987) Energy transfer and fluorescence mechanisms in photosynthetic membranes. CRC Critical Reviews in Plant Sciences 5: 1–44

    Google Scholar 

  • Geacintov, NE, Breton, J, France, L, Deprez, J and Dobek, A (1987) Laser flash-induced non-sigmoidal fluorescence induction curves in chloroplasts. In: Biggins, J (ed) Progress in Photosynthesis Research, Vol I, pp 107–110. Martinus Nijhoff Publishers, Dordrecht

    Google Scholar 

  • Gulotty, RJ, Fleming, GR and Alberte, RS (1982) Low-intensity picosecond fluorescence kinetics and excitation dynamics in barley chloroplasts. Biochim Biophys Acta 682: 322–331

    Google Scholar 

  • Gulotty, RJ, Mets, L, Alberte, RS and Fleming, GR (1985) Picosecond fluorescence study of photosynthetic mutants of Chlamydomonas reinhardii: origin of the fluorescence decay kinetics of chloroplasts. Photochem Photobiol 41: 487–496

    PubMed  Google Scholar 

  • Haehnel, W, Holzwarth, A and Wendler, J (1983) Picosecond fluorescence kinetics and energy transfer in the antenna chlorophylls of green algae. Photochem Photobiol 37: 435–443

    Google Scholar 

  • Haehnel, W, Nairn, JA, Reisberg, P and Sauer, K (1982) Picosecond fluorescence kinetics and energy transfer in chloroplasts and algae. Biochim Biophys Acta 680: 161–173

    Google Scholar 

  • Hodges, M and Moya, I (1986) Time-resolved chlorophyll fluorescence studies of photosynthetic membranes: resolution and characterisation of four kinetic components. Biochim Biophys Acta 849: 193–202

    Google Scholar 

  • Hodges, M and Moya, I (1987) Modification of room-temperature picosecond chlorophyll fluorescence kinetics in Photosystem-II-enriched particles by photochemistry. Biochim Biophys Acta 892: 42–47

    Google Scholar 

  • Holzwarth, AR (1987) Picosecond fluorescence spectroscopy and energy transfer in photosynthetic antenna pigments. In: Barber, J (ed) Topics in Photosynthesis, Vol 8, pp 95–157. Elsevier, Amsterdam

    Google Scholar 

  • Holzwarth, AR, Wendler, J and Haehnel, W (1985) Time-resolved picosecond fluorescence spectra of the antenna chlorophylls in Chlorella vulgaris. Biochim Biophys Acta 807: 155–167

    Google Scholar 

  • Horvath, G, Droppa, M and Melis, A (1984) Herbicide action on Photosystem II in spinach chloroplasts: concentration effect on PS IIα and PS IIβ. Photobiochem Photobiophys 7: 249–256

    Google Scholar 

  • Joliot, A and Joliot, P (1964) Étude cinetique de la réaction photochimique libérant l'oxygène au cours de la photosynthèse. C R Acad Sci 258: 4622–4625

    Google Scholar 

  • Karukstis, KK and Sauer, K (1983) Fluorescence decay kinetics of chlorophyll in photosynthetic membranes. J Cell Biochem 23: 131–158

    PubMed  Google Scholar 

  • Knutson, JR, Beechem, JM and Brand, L (1983) Simultaneous analysis of multiple fluorescence decay curves: a global approach. Chem Phys Lett 102: 501–507

    Article  Google Scholar 

  • Lam, E, Baltimore, B, Ortiz, W, Chollar, S, Melis, A and Malkin, R (1983) Characterization of a resolved oxygen-evolving Photosystem II preparation from spinach thylakoids. Biochim Biophys Acta 724: 201–211

    Google Scholar 

  • Ley, AC and Mauzerall, DC (1986) The extent of energy transfer among Photosystem II reaction centers in Chlorella. Biochim Biophys Acta 850: 234–248

    Google Scholar 

  • Melis, A (1985) Functional properties of Photosystem IIβ in spinach chloroplasts. Biochim Biophys Acta 808: 334–342

    Google Scholar 

  • Melis, A and Duysens, LNM (1979) Biphasic energy conversion kinetics and absorbance difference spectra of Photosystem II of chloroplasts. Evidence for two different Photosystem II reaction centers. Photochem Photobiol 29: 373–382

    Google Scholar 

  • Melis, A and Homann, PH (1975) Kinetic analysis of the fluorescence induction in 3-(3,4-dichlorophenyl)-1,1-dimethylurea poisoned chloroplasts. Photochem Photobiol 21: 431–437

    Google Scholar 

  • Moya, I, Hodges, M and Barbet, J-C (1986) Modification of room-temperature picosecond chlorophyll fluorescence kinetics in green algae by Photosystem II trap closure. FEBS Lett 198: 256–262

    Article  Google Scholar 

  • Murata, N (1969) Control of excitation energy transfer in photosynthesis. I. Light-induced change of chlorophyll a fluorescence in Porphyridium cruentum. Biochim Biophys Acta 172: 242–251

    PubMed  Google Scholar 

  • Owens, TG, Webb, SP, Mets, L, Alberte, RS and Fleming, GR (1987) Antenna size dependence of fluorescence decay in the core antenna of Photosystem I: Estimates of charge separation and energy transfer rates. Proc Natl Acad Sci USA 84: 1532–1536

    PubMed  Google Scholar 

  • Pearlstein, RM (1982) Exciton migration and trapping in photosynthesis. Photochem Photobiol 35: 835–844

    Google Scholar 

  • Popovic, ZD, Kovacs, GJ, Vincett, PS, Alegria, G and Dutton, PL (1986) Electric-field dependence of the quantum yield in reaction centers of photosynthetic bacteria. Biochim Biophys Acta 851: 38–48

    Google Scholar 

  • Schatz, GH, Brock, H and Holzwarth, AR (1987) Picosecond kinetics of fluorescence and absorbance changes in Photosystem II particles excited at low photon density. Proc Natl Acad Sci USA 84: 8414–8418

    Google Scholar 

  • Schatz, GH and Holzwarth, AR (1986) Mechanisms of chlorophyll fluorescence revisited: prompt or delayed emission from photosystem II with closed reaction centers? Photosynth Res 10: 309–318

    Google Scholar 

  • Trissl, H-W, Breton, J, Deprez, J and Leibl, W (1987) Primary electrogenic reactions of Photosystem II as probed by the light-gradient method. Biochim Biophys Acta 893: 305–319

    Google Scholar 

  • Wendler, J and Holzwarth, AR (1987) State transitions in the green alga Scenedesmus obliquus probed by time-resolved chlorophyll fluorescence spectroscopy and global data analysis. Biophys J 52: 717–728

    Google Scholar 

  • Witt, HT (1955) Experimente zum Primärprozess der Photosynthese. Z Electrochem 59: 981–986

    Google Scholar 

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Keuper, H.J.K., Sauer, K. Effect of photosystem II reaction center closure on nanosecond fluorescence relaxation kinetics. Photosynth Res 20, 85–103 (1989). https://doi.org/10.1007/BF00028623

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