Abstract
It is well known that two photosystems, I and II, are needed to transfer electrons from H2O to NADP+ in oxygenic photosynthesis. Each photosystem consists of several components: (a) the light-harvesting antenna (L-HA) system, (b) the reaction center (RC) complex, and (c) the polypeptides and other co-factors involved in electron and proton transport. First, we present a mini review on the heterogeneity which has been identified with the electron acceptor side of Photosystem II (PS II) including (a) L-HA system: the PS IIα and PS IIβ units, (b) RC complex containing electron acceptor Q1 or Q2; and (c) electron acceptor complex: QA (having two different redox potentials QL and QH) and QB (QB-type; Q'B type; and non-QB type); additional components such as iron (Q-400), U (Em,7=−450 mV) and Q-318 (or Aq) are also mentioned. Furthermore, we summarize the current ideas on the so-called inactive (those that transfer electrons to the plastoquinone pool rather slowly) and active reaction centers. Second, we discuss the bearing of the first section on the ratio of the PS II reaction center (RC-II) and the PS I reaction center (RC-I). Third, we review recent results that relate the inactive and active RC-II, obtained by the use of quinones DMQ and DCBQ, with the fluorescence transient at room temperature and in heated spinach and soybean thylakoids. These data show that inactive RC-II can be easily monitored by the OID phase of fluorescence transient and that heating converts active into inactive centers.
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Abbreviations
- DCBQ:
-
2,5 or 2,6 dichloro-p-benzoquinone
- DMQ:
-
dimethylquinone
- QA :
-
primary plastoquinone electron acceptor of photosystem II
- QB :
-
secondary plastoquinone electron acceptor of photosystem II
- IODP:
-
successive fluorescence levels during time course of chlorophyll a fluorescence: O for origin, I for inflection, D for dip or plateau, and P for peak
References
Albertsson P-Å and Yu S-G (1988) Heterogeneity among Photosystem IIα. Isolation of thylakoid membrane vesicles with different functional antennae size of Photosystem IIα. Biochim Biophys Acta 936: 215–221
Andréasson L-E and Vänngård T (1988) Electron transport in Photosystem I and II. Ann Rev Plant Physiol Plant Mol Biol 39: 379–411
Black MT, Brearley TH and Horton P (1986) Heterogeneity in chloroplast photosystem II. Photosynth Res 8: 193–207
Bouges-Bocquet B (1973) Electron transfer between the two photosystms in spinach chloroplasts. Biochim Biophys Acta 314: 250–256
Brettel K, Schlodder E and Witt HT (1985) Evidence for only one stable electron acceptor in the reaction center of Photosystem II in spinach chloroplasts. Photobiochem Photobiophys 9: 205–213
Briantais J-M, Cornic G and Hodges M (1988) The modification of Chlorophyll fluorescence of Chlamydomonas reinhardtii by photoinhibition and chloramphenicol addition suggests a form of photosystem II less susceptible to degradation. FEBS Lett 236: 226–230
Bukhov NG, Sabat SC and Mohanty P (1990) Analysis of chlorophyll a fluorescence changes in weak light in heattreated Amaranthus chloroplasts. Photosynth Res 23: 81–87
Cao J and Govindjee (1989) Chlorophyll a fluorescence transient as an indicator of active and inactive Photosystem II in thylakoid membranes. Biochim Biophys Acta 1015: 180–188
Chow WS, Anderson JM and Hope AB (1988) Variable stoichiometries of Photosystem II to Photosystem I reaction centers. Photosynth Res 17: 277–281
Chow WS, Hope AB and Anderson JM (1989) Oxygen per flash from leaf disks quantifies Photosystem II. Biochim Biophys Acta 973: 105–108
Cylla RA and Whitmarsh J (1989) Inactive Photosystem II complexes in leaves: turnover rate and quantitiation. Plant Physiol 90: 765–772
Chylla RA, Garab B and Whitmarsh J (1987) Evidence for slow turnover in a fraction of Photosystem II complexes in thylakoid membranes. Biochim Biophys Acta 894: 562–571
Cramer WA and Butler WL (1960) Potentiometric titrations of the fluorescence yield of spinach chloroplasts. Biochim Biophys Acta 172: 503–510
Debus RJ, Barry BA, Sithole I, Babcock GT and McIntosh I (1988) Directed mutagenesis indicates that the donor to P680+ in Photosystem II is tyrosine-161 of the D1 polypeptide. Biochemistry 27: 9071–9074
Delrieu M-J and Rosengard F (1988) Characterization of two types of oxygen-evolving Photosystem II reaction center by the flash-induced oxygen and fluorescence yield. Biochim Biophys Acta 936: 39–49
Demeter S and Govindjee (1989) Thermoluminescence in plants. Physiologia Plantarum 75: 121–130
Diner BA (1986) The reaction center of Photosystem II. In: Staehlin LA and Arntzen CJ (eds) Encyclopedia of Plant Physiology; Photosynthesis III (NS), Vol 19, pp 442–436. Springer-Verlag, Berlin
Diner B and Delosme R (1983) Oxidation-reduction properties of the electron acceptors of Photosystem II. I. Redox titration of the flash-induced caroteroid band shift, of C550 and of the variable fluorescence yield in spinach chloroplasts. Biochim Biophys Acta 722: 443–459
Eckert JH and Renger C (1980) Photochemistry of the reaction centers of system II under repetitive flash group excitation in isolated chloroplasts. Photochem Photobiol 31: 501–511
Evans MCW and Ford RC (1986) Evidence for two tightly bound iron quinones in the electron acceptor complex of Photosystem II. FEBS Lett 195: 290–294
Evans MCW, Atkinson YE and Ford RC (1985) Redox characterization of the Photosystem II electron acceptors. Evidence for two electron carriers between pheophytin and Q. Biochim Biophys Acta 806: 247–254
Govindjee (1984) Photosystem II: the oxygen evolving system of photosynthesis. In: Sybesma C (ed) Advances in Photosynthesis Research, Vol I, pp 227–238. Martinus Nijhoff/Dr W Junk, the Hague
Govindjee and Govindjee R (1975) Introduction to Photosynthesis. In: Govindjee (ed) Bioenergetics of Photosynthesis, pp 1–50. Academic Press, New York
Govindjee and Wasielewski M (1989) Photosystem II: from a femtosecond to a millisecond. In: Briggs GE (ed) Photosynthesis, C.S. French International Symposium. Alan Liss Publishers, N.Y., pp 71–103
Govindjee, Amesz J and Fork DC (eds) (1986) Light Emission by Plants and Bacteria. Academic Press, Orlando FL
Graan T and Ort DR (1986) Detection of oxygen-evolving Photosystem II centers inactive in plastoquinone reduction. Biochim Biophys Acta 852: 320–330
Guenther JE and Melis A (1989) The physiological significance of photosystem II heterogeneity in chloroplasts. Photosynth Res 23: 105–109
Guenther JE, Nemson JA and Melis A (1988) Photosystem II stoichiometry and chlorophyll antenna size in Dunaliella salina (green algae). Biochim Biophys Acta 934: 108–117
Guenther JE, Nemson JA and Melis A (1990) Development of Photosystem II in dark grown Chlamydomonas reinhardtii. A light dependent conversion of PS IIβ. QB-nonreducing centers to the PS IIα, QB reducing form. Photosynth Res 24: 35–46
Hansson Ö and Wydrzynski T (1990) Current perceptions in Photosystem II. Photosynth Res 23: 131–162
Hodges M and Barber J (1986) Analysis of chlorophyll fluorescence induction kinetics exhibited by DCMU-inhibited thylakoids and the origin of α and β centers. Biochim Biophys Acta 848: 239–246
Horton P (1981) The effect of redox potential on the kinetics of fluorescence induction in pea chloroplasts. I. Removal of the slow phase. Biochim Biophys Acta 635: 105–110
Horton P and Croze E (1979) Characterization of two quenchers of chlorophyll fluorescence with different midpoint oxidation-reduction potentials in chloroplasts. Biochim Biophys Acta 545: 188–201
Ikegami I and Katoh S (1973) Studies on chlorophyll fluorescence in chloroplasts II: Effect of ferricyanide on the induction of fluorescence in the presence of 3-(3,4-dichlorophenyl)-1, 1-dimethylurea. Plant Cell Physiol 14: 829–836
Joliot P and Joliot A (1977) Evidence for a double hit process in Photosystem II based on fluorescence studies. Biochim Biophys Acta 462: 559–574
Joliot P and Joliot A (1979) Comparative study of the fluorescence yield and of the C550 absorbance change at room-temperature. Biochim Biophys Acta 546: 93–105
Joliot P and Joliot A (1981a) A Photosystem II electron acceptor which is not a plastoquinone. FEBS Lett 134: 155–158
Joliot P and Joliot A (1981b) Characterization of Photosystem II centers by polarographic, spectroscopic and fluorescence methods. In: Akoyunoglou G (ed) Photosynthesis, Proc. 5th Int. Congress Photosynthesis, Vol 3, pp 885–899. Balaban Int. Science, Philadelphia, PA
Joliot P and Joliot A (1983) Electron transfer on the acceptor side of Photosystem II. In: Inoue Y, Crofts AR, Govindjee, Murata N, Renger G and Satoh K (eds) The Oxygen Evolving System of Photosynthesis, pp 359–368. Academic Press, Japan, Tokyo
Jursinic P and Dennenberg RJ (1988a) Enhanced oxygen yields caused by double turnovers of Photosystem II induced by dichlorobenzoquinone. Biochim Biophys Acta 934: 177–185
Jursinic P and Dennenberg R (1988b) Thylakoid Photosystem II activity supported by the non-quinone acceptor Q400 and an ancillary acceptor Aq. Biochim Biophys Acta 935: 225–235
Jursinic P and Dennenberg R (1989) Measurement of stoichiometry of Photosystem II to Photosystem I reaction centers. Photosynth Res 21: 197–200
Jursinic P, Govindjee and Wraight CA (1978) Membrane potential and mircosecond to millisecond delayed light emission after a single excitation flash in isolated chloroplasts. Photochem Photobiol 27: 61–71
Kobayashi M, Watanabe T, Nakazato M, Ikegami I, Hiyama T, Matsunaga T and Murata N (1988) Chlorophyll a/P700 and pheophytin a/P680 stoichiometries in higher plants and cyanobacteria determined by HPLC analysis. Biochim Biophys Acta 936: 81–89
Lavergne J (1982a) Two types of primary acceptors in chloroplast's Photosystem II. I. Different recombination properties. Photobiochem Photobiophys 3: 257–271
Lavergne J (1982b) Two types of primary acceptors in chloroplast's Photosystem II. II. Reduction in two successive photoacts. Photobiochem Photobiophys 3: 273–285
Lavergne J (1987) Optical difference spectra of the S-state transitions in the photosynthetic oxygen evolving complex. Biochim Biophys Acta 894: 91–107
Mathis P and Rutherford AW (1987) The primary reactions of Photosystems I and II of algae and higher plants. In: Amesz J (ed) Photosynthesis, New Comprehensive Biochemistry, Vol 15, pp 63–96. Elsevier, Amsterdam
Meiburg RF, vanGorkom HJ and vanDorssen RJ (1984) Non-electrogenic charge recombination in photosystem II as a source of submillisecond luminescence. Biochim Biophys Acta 765: 295–300
Melis A (1985) Functional properties of PS IIβ in spinach chloroplasts. Biochim Biophys Acta 808: 334–342
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
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
Melis A and Homann PH (1976) Heterogeneity of the photochemical centers in System II of chloroplasts. Photochem Photobiol 23: 343–350
Melis A and Schreiber U (1979) The kinetic relationship between the C-550 absorbance change, the reduction of Q (A320) and the variable fluorescence yield change in chloroplasts at room temperature. Biochim Biophys Acta 547: 47–57
Melis A, Guenther GE, Morrissey PJ and Ghirardi ML (1988) Photosystem II heterogeneity in chloroplasts. In: Lichtenthaler HK (ed) Applications of Chlorophyll Fluroescence, pp 33–43. Kluwer Academic Publishers, Dordrecht
Munday JCM Jr and Govindjee (1969) Light-induced changes in the fluorescence yield of chlorophyll a in vivo III. The dip and the peak in the fluorescence transient of Chlorella pyrenoidosa. Biophysic J 9: 1–21
Myers J and Graham JR (1983) On the ratio of photosynethetic reaction centers RC2/RC1 in Chlorella. Plant Physiol 71: 440–442
Ort DR and Whitmarsh J (1990) Inactive Photosystem II centers: a resolution of discrepencies in Photosystem II quantitation. Photosynth Res 23: 101–104
Owens TG (1986) Photosystem II heterogeneity in the marine diatom Phaeodactylum tricornutum. Photochem Photobiol 43: 535–544
Petrouleas V and Diner B (1986) Identification of Q400, a high potential electron acceptor of Photosystem II, (as) the iron of the quinone-iron acceptor complex. Biochim Biophys Acta 849: 264–275
Rutherford AW and Heathcote P (1985) Primary photochemistry in Photosystem I. Photosynth Res 6: 295–316
Rutherford AW and Zimmermann JJ (1984) A new EPR signal attributed to the primary plastoquinone acceptor in photosystem II. Biochim Biophys Acta 767: 168–175
Sundby CA, Melis A, Maenpaa P and Anderson B (1986) Temperature-dependent changes in the antenna size of Photosystem II. Reversible conversion of Photosystem IIα to Photosystem IIβ. Biochim Biophys Acta 851: 475–483
Thielen APGM and vanGorkom HJ (1981a) Redox potential of electron acceptors in PS IIα and PS IIβ. FEBS Lett 129: 205–209
Thielen APGM and vanGorkom HJ (1981b) Electron transport properties of Photosystems IIα and IIβ. In: Akoyunoglou G (ed) Photosynthesis, Proceedings of the 5th International Congress, Vol II, pp 57–64. Balaban International Services, Philadelphia, PA
Thielen APGM and vanGorkom HJ (1981c) Quantum efficiency and antenna size of Photosystem IIα, IIβ and I in tobacco chloroplasts. Biochim Biophys Acta 635: 111–120
vanGorkom HJ (1985) Electron transfer in Photosystem II. Photosynth Res 6: 97–112
Velthuys BR (1987) The Photosystem two Reaction Center. In: Barber J (ed) The Light Reactions, pp 341–377. Elsevier Science Publishers B.V. (Biomedical Division), Amsterdam
Velthuys BR and Amesz J (1974) Charge accumulation at the reducing side of system II of Photosynthesis. Biochim Biophys Acta 333: 85–94
Vermaas WFJ and Govindjee (1981) The acceptor side of Photosystem II in Photosynthesis. Photochem Photobiol 34: 775–793
Whitmarsh J and Ort DR (1984) Stoichiometries of electron transport complexes in spinach chloroplasts. Arch Biochem 231: 378–389
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Govindjee Photosystem II heterogeneity: the acceptor side. Photosynth Res 25, 151–160 (1990). https://doi.org/10.1007/BF00033157
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DOI: https://doi.org/10.1007/BF00033157