Abstract
Photosystem II (PS II) is the engine for essentially all life on our planet and its beginning 2.5 billion years ago was the ‘big bang of evolution.’ It produces reducing equivalents for making organic compounds on an enormous scale and at the same time provides us with an oxygenic atmosphere and protection against UV radiation (in the form of the ozone layer). In 1967, when I began my career in photosynthesis research, little was known about PS II. The Zscheme had been formulated [Hill and Bendall (1960) Nature 186: 136–137] and Boardman and Anderson [(1964) Nature 203: 166–167] had isolated PS II as a discrete biochemical entity. PS II was known not only to be the source of oxygen but of variable chlorophyll fluorescence [Duysens and Sweers (1963) In: Studies on Microalgae and Photosynthetic Bacteria, pp. 353–372. University of Tokyo Press, Tokyo] and delayed chlorophyll fluorescence [Arnold and Davidson (1954) J Gen Physiol 37: 677–684]. P680 had just been discovered [Döring et al. (1967) Z Naturforsch 22b: 639–644]. No wonder the ‘black box of PS II’ was described at that time by Bessel Kok and George Cheniae [Current Topics in Bioenergetics 1: 1–47 (1966)] as the ‘inner sanctum of photosynthesis.’ What a change in our level of understanding of PS II since then! The contributions of many talented scientists have unraveled the mechanisms and structural basis of PS II function and we are now very close to revealing the molecular details of the remarkable and thermodynamically demanding reaction which it catalyzes, namely the splitting of water into its elemental constituents. It has been a privilege to be involved in this journey.
Access this chapter
Tax calculation will be finalised at checkout
Purchases are for personal use only
Preview
Unable to display preview. Download preview PDF.
References
Adir N, Zer H, Shochat I and Ohad I (2003) Photoinhibition — a historical perspective. Photosynth Res 76: 343–370
Albertsson PA (2001) A quantitative model of the domain structure of the photosynthetic membrane. Trends Plant Sci (TIPS) 6: 349–353
Albertsson PA (2003) The contribution of photosynthetic pigments to the development of biochemical separation methods: 1900–1980. Photosynth Res 76: 217–225
Allen JF (2002) Plastoquinone redox control of chloroplast thylakoid protein phosphorylation and distribution of excitation energy between photosystems: discovery, background, implications. Photosynth Res 73: 139–148
Anderson JM (2002) Changing concepts about the distribution of Photosystems I and II between grana-appressed and stroma-exposed thylakoid membranes. Photosynth Res 73: 157–164
Anderson JM and Andersson B (1981) Lateral organization of the chlorophyll-protein complexes of spinach thylakoids. In: Akoyunoglou G (ed) Photosynthesis, Vol III, Structure and Molecular Organisation of the Photosynthetic Apparatus, pp 23–31. Balaban International Science Services, Philadelphia, Pennsylvania
Andersson B (1978) Separation of chloroplast lamella fragments by phase partition, including the isolation of inside-out vesicles. PhD thesis. Lund, Sweden
Andersson B and Anderson JM (1980) Lateral heterogeneity in the distribution of the chlorophyll-protein complexes of the thylakoid membranes of spinach chloroplasts. Biochim Biophys Acta 593: 427–440
Arnold WA and Azzi J (1971) Electric field and chloroplast membranes. In: Manson LA (ed) Biomembranes, Vol 2, pp 189–191. Plenum Press, New York
Arnold WA and Davidson JB (1954) The identity of the fluorescence and delayed light emission spectra in Chlorella. J Gen Physiol 37: 677–684
Arnold WA and Davidson JB (1963) The decay of delayed light at short times. In: Kok B and Jagendorf AT (eds) Photosynthetic Mechanisms of Green Plants, pp 689–700. National Academy of Sciences-National Research Council, Washington DC
Arnold WA and Sherwood H (1957) Are chloroplasts semiconductors? Proc Natl Acad Sci USA 43: 105–114
Arnon DI (1992) Conceptual evolution in photosynthesis: the quest for a common denominator. In: Barber J, Guerroro MG and Medrano H (eds) Trends in Photosynthesis Research, pp 13–25. Intercept, Andover, UK
Arnon DI and Barber J (1990) Photoreduction of NADP+ by isolated reaction centers of Photosystem II: requirement for plastocyanin. Proc Natl Acad Sci USA 87: 5930–5934
Arnon DI and Tang GMS (1989) Photoreduction of NADP+ by a choloroplast Photosystem II preparation: effect of light intensity. FEBS Lett 25: 253–256
Barbato R, Friso G, Rigoni F, Dalla Vecchia F and Giacometti GM (1992) Structural changes and lateral redistribution of Photosystem II during donor side photoinhibition of thylakoids. J Cell Biol 119: 325–335
Barber J (1972a) A method of estimating the magnitude of the light-induced electrical potential across the thylakoid membrane. FEBS Lett 20: 251–254
Barber J (1972b) Stimulation of millisecond delayed light emission by KCl and NaCl gradients as a means of investigating the ionic permeability properties of the thylakoid membrane. Biochim Biophys Acta 275: 105–116
Barber J (1976) Ionic regulation in intact chloroplasts and its effect on primary photosynthetic processes. In: Barber J (ed) The Intact Chloroplast, Vol 1, Topics in Photosynthesis, pp 89–134. Elsevier, Amsterdam
Barber J (1979) Energy transfer and its dependence on membrane properties. In: Chlorophyll Organisation and Energy Transfer in Photosynthesis. Ciba Foundation Symp. London, Meeting No. 61 (Special Issue), pp 283–304. Elsevier, Amsterdam
Barber J (1980a) An explanation for the relationship between salt-induced thylakoid stacking and chlorophyll fluorescence changes associated with changes in spillover of energy from Photosystem II to Photosystem I. FEBS Lett 118: 1–10
Barber J (1980b) Membrane surface charges and potentials in relation to photosynthesis. Biochim Biophys Acta 594: 253–308
Barber J (1982) Influence of surface charges on thylakoid structure and function. Ann Rev Plant Physiol 33: 261–295
Barber J (1994) Molecular basis of the vulnerability of Photosystem II to damage by light. Aust J Plant Physiol 22: 201–208
Barber J (2001) P680: what is it and where is it? Bioelectrochemistry 55: 135–138
Barber J (2002) Photosystem II: a multisubunit membrane protein that oxidizes water. Curr Opin Struct Biol 12: 523–530
Barber J (2003) Photosystem II: the engine of life. Biophys Quart Rev 36: 71–89
Barber J and Archer MD (2001) P680, the primary electron donor of PS II. Photochem Photobiol A Chemistry 142: 97–106
Barber J and Chow WS (1979) A mechanism for controlling the stacking and unstacking of chloroplast thylakoid membranes. FEBS Lett 105: 5–10
Barber J and Kraan GPB (1970) Salt induced light emission from chloroplasts. Biochim Biophys Acta 197: 49–95
Barber J and Searle GFW (1978) Cation induced increase in chlorophyll fluorescence yield and the effect of electrical charge. FEBS Lett 92: 5–8
Barber J and Searle GFW (1979) Double layer theory and the effect of pH on cation-induced chlorophyll fluorescence. FEBS Lett 103: 241–245
Barber J, Mills JD and Nicholson J (1974a) Studies with cation specific ionophores show that within the intact chloroplast Mg2+ acts as the main exchange cation for H+-pumping. FEBS Lett 49: 106–109
Barber J, Telfer A, Mills JD and Barber J (1974b) Slow chlorophyll fluorescence changes in isolated intact chloroplasts. Evidence for cation control. In: Avron M (ed) Proceedings III International Congress Photosynthesis, pp 53–63. Elsevier, Amsterdam
Barber J, Telfer A and Nicolson J (1974c) Evidence for divalent cation movement within isolated whole chloroplasts from studies with ionophore A23187. Biochim Biophys Acta 357: 161–165
Barber J, Mills JD and Love A (1977a) Electrical diffuse layers and their influence on photosynthetic processes. FEBS Lett 74: 174–181
Barber J, Mauro S and Lannoye R (1977b) The relationship between the yield factors for prompt and delayed fluorescence. FEBS Lett 80: 449–454
Barber J, Rubin BT and Chow WS (1981) Theoretical aspects of cation induced chlorophyll fluorescence and thylakoid stacking changes. In: Akoyunoglou G (ed) Photosynthesis, Vol I, Photophysical Processes — Membrane Energization, pp 397–405. Balaban International Science Services, Philadelphia, Pennsylvania
Barber J, Chapman DJ and Telfer A (1987) Characterisation of a photosystem two reaction centre isolated from the chloroplasts of Pisum sativum. FEBS Lett 220: 67–73
Barter LM, Durrant JR and Klug DR (2003) A quantitative structure-function relationship for Photosystem II reaction center: supermolecular behaviour in natural photosynthesis. Proc Natl Acad Sci USA 100: 946–951
Bassi R, Ghiretti-Magaldhi A, Tognon G, Giacometti GM and Miller KR (1989) Two dimensional crystals of the Photosystem II reaction center complex from higher plants. Eur J Cell Biol 50: 84–93
Berthold DA, Babcock GT and Yocum CF (1981) A highly resolved, oxygen-evolving Photosystem II preparation from spinach thylakoid membranes: EPR and electron transport properties. FEBS Lett 134: 231–234
Bibby TS, Nield J and Barber J (2001a) Iron deficiency induces formation of an antenna ring around trimeric Photosystem I in cyanobacteria. Nature 412: 743–745
Bibby TS, Nield J and Barber J (2001b) 3D model and characterization of the iron stress induced CP43′-PS I supercomplex isolated from the cyanobacteria Synechocystis PCC 6803. J Biol Chem 276: 43246–43252
Bibby TS, Nield J, Partensky F and Barber J (2001c) Oxyphotobacteria: antennae ring around Photosystem I. Nature 413: 590
Bibby TS, Mary I, Nield J, Partensky F and Barber J (2003a) Low-light-adapted Prochlorococcus species possess specific antenna for each photosystem. Nature 424: 1051–1054
Bibby TS, Nield J, Chen M, Larkum AWA and Barber J (2003b) Structure of a Photosystem II supercomplex isolated from Prochloron didemni retaining its chlorophyll a/b light-harvesting system. Proc Natl Acad Sci USA 100: 9050–9054
Boardman NK and Anderson JM (1964) Isolation from spinach chloroplasts of particles containing different proportions of chlorophyll a and chlorophyll b and their possible role in the light reactions of photosynthesis. Nature 203: 166–167
Boekema EJ, Hankamer B, Bald D, Kruip J, Nield J, Boonstra AF, Barber J and Rögner M (1995) Supramolecular structure of the photosynthetic complex from green plants and cyanobacteria. Proc Natl Acad Sci USA 92: 175–179
Boekema EJ, Hifney A, Yakusheveska AE, Piotrowski M, Keegstra W, Berry S, Michel K-P, Pistorius EK and Kruip J (2001) A giant chlorophyll-protein complex induced by iron deficiency in cyanobacteria. Nature 412: 745–748
Bonaventura C and Myers J (1969) Fluorescence and oxygen evolution from Chlorella pyrenoidosa. Biochim Biophys Acta 189: 366–383
Briantais J-M, Vernotte C, Picaud M and Krause GH (1979) A quantitative study of the slow decline of chlorophyll a fluorescence in isolated chloroplasts. Biochim Biophys Acta 548: 128–138
Brody SS (2002) Fluorescence lifetime, yield, energy transfer and spectrum in photosynthesis, 1950–1960. Photosynth Res 73: 127–132
Chapman DJ, Gounaris K and Barber J (1988) Electron transport properties of the isolated D1-D2-cytochrome b559 Photosystem two reaction centre. Biochim Biophys Acta 933: 423–431
Chow WS and Barber J (1980) Further studies of the relationship between cation-induced chlorophyll fluorescence and thylakoid membrane stacking changes. Biochim Biophys Acta 593: 149–157
Crystal B, Booth PJ, Klug DR, Barber J and Porter G (1989) Resolution of a long lived fluorescence component from D1-D2-cytochrome b559 reaction centres. FEBS Lett 249: 75–78
Debus RJ (2001) Amino acid residues that modulate the properties of tyrosine YZ and the manganese cluster in the water oxidizing complex of Photosystem II. Biochim Biophys Acta 1503: 164–186
Dekker JP and van Grondelle R (2000) Primary charge separation in Photosystem II. Photosynth Res 63: 195–208
De Grooth BG and van Gorkom HJ (1981) External electric field effect on prompt and delayed fluorescence in chloroplasts. Biochim Biophys Acta 635: 445–456
Diner BA (2001) Amino acid residues involved in the coordination and assembly of the Mn cluster of PS II. Proton-coupled electron transport of the redox-active tyrosines and its relationship to water oxidation. Biochim Biophys Acta 1503: 147–163
Diner BA, Schlodder E, Nixon PJ, Coleman WJ, Rappaport F, Lavergne J, Vermaas WFJ and Chisholm DA (2001) Site directed mutations at D1-His189 and D2His197 of PS II in Synechocystis PCC 6803: sites of primary charge separation and cation and triplet stabilization. Biochemistry 40: 9265–9281
Döring G, Stiehl H and Witt HT (1967) A second chlorophyll reaction in the electron chain of photosynthesis. Z Naturforsch 22b: 639–644
Durrant JR, Giorgi LB, Barber J, Klug DR and Porter G (1990) Characterisation of triplet states in isolated Photosystem II reaction centres: oxygen quenching as a mechanism for photodamage. Biochim Biophys Acta 1017: 167–175
Durrant JR, Klug DR, Kwa SLS, van Grondelle R, Porter G and Dekker JP (1995) A multimer model for P680, the primary electron donor of Photosystem II. Proc Natl Acad Sci USA 92: 4798–4802
Duysens LNM and Sweers HE (1963) Mechanism of two photochemical reactions in algae as studied by means of fluorescence. In: Ashida J (ed) Studies on Microalgae and Photosynthetic Bacteria, pp 353–372. University of Tokyo Press, Tokyo
Ellenson JL and Sauer K (1976) The electrophotoluminescence of chloroplasts. Photochem Photobiol 23: 113–123
Ferreira KN, Iverson TM, Maghlaoui K, Barber J and Iwata S (2004) Architecture of the photosynthetic oxygen-evolving center. Science 303: 1831–1837
Gounaris K, Chapman DJ, Booth P, Crystall B, Giorgi LB, Klug DR, Porter G and Barber J (1990) Comparison of the D1/D2/cyt b559 reaction centre complex of photosystem two isolated by two different methods. FEBS Lett 265: 88–92
Govindjee (1995) Sixty-three years since Kautsky: chlorophyll a fluorescence. Aust J Plant Physiol 22: 131–161
Govindjee and Papageorgiou G (1971) Chlorophyll fluorescence and photosynthesis: fluorescence transients. In: Giese AC (ed) Photophysiology, Vol VI, pp 1–46. Academic Press, New York
Hankamer B, Barber J and Boekema EJ (1997a) Structure and membrane organization of PS II in green plants. Annu Rev Plant Phys Mol Biol 48: 641–671
Hankamer B, Nield J, Zheleva D, Boekema EJ, Jansson S and Barber J (1997b) Isolation and biochemical characterization of monomeric and dimeric PS II complexes from spinach and their relevance to the organization of Photosystem II in vivo. Eur J Biochem 243: 422–429
Hankamer B, Morris EP and Barber J (1999) Cryoelectron microscopy of photosystem two shows that CP43 and CP47 are located on opposite sides of the D1/D2 reaction centre proteins. Nature Struct Biol 6: 560–564
Hankamer B, Morris EP, Nield J, Gerle C and Barber J (2001a) Three dimensional structure of Photosystem II core dimer of higher plants determined by electron microscopy. J Struct Biol 135: 262–269
Hankamer B, Morris EP, Nield J, Carne A and Barber J (2001b) Subunit positioning and transmembrane helix organization in the core dimer of Photosystem II. FEBS Lett 504: 142–151
Henderson R and Unwin PNT (1975) Three-dimensional model of purple membrane obtained by electron microscopy. Nature 257: 28–32
Hill R and Bendall F (1960) Function of two cytochrome components in chloroplasts: a working hypothesis. Nature 186: 136–137
Hipkins MF and Barber J (1974) Estimation of the activation energy for millisecond delayed fluorescence from uncoupled chloroplasts. FEBS Lett 42: 289–292
Hoganson CW and Babcock GT (1997) A metalloradical mechanism for the generation of oxygen from water in photosynthesis. Science 277: 1953–1956
Holzenburg A, Bewley MC, Wilson FH, Nicolson WV and Ford RC (1993) Three-dimensional structure of Photosystem II. Nature 363: 470–472
Homann P (1969) Cation effects on the fluorescence of isolated chloroplasts. Plant Physiol 44: 932–936
Hu Q, Miyashita H, Iwasaki I, Kurano N, Miyachi S, Iwaki M and Itoh S (1998) A Photosystem I reaction center driven by chlorophyll d in oxygenic photosynthesis. Proc Natl Acad Sci USA 95: 13319–13323
Ikeuchi M, Shukla VK, Pakrasi HB and Inoue Y (1995) Directed inactivation of the pcbI gene does not affect Photosystem II in cyanobacterium Synechocystis sp. PPP 6803. Mol Gen Genet 249: 622–628
Jackson JB and Crofts AR (1969) The high energy state in chromatophores from Rhodopseudomonas sphaeroides. FEBS Lett 4: 185–189
Jagendorf AT and Uribe E (1966) ATP formation caused by acid-base transition of spinach chloroplasts. Proc Natl Acad Sci USA 55: 170–177
Joliot A and Joliot P (1964) Étude cinétique de la réaction photochimique libérant l’oxygène au cours de la photosynthèse. CR Acad Sci Paris 258: 4622–4625
Joliot P and Joliot A (2003) Excitation transfer between photosynthetic units: the 1964 experiment. Photosynth Res 76: 241–245
Kamiya N and Shen JR (2003) Crystal structure of oxygen-evolving Photosystem II from Thermosynechococcus vulcanus at 3.7Å resolution. Proc Natl Acad Sci USA 100: 98–102
Kautsky H, Appel N and Amann H (1960) Chlorophyll Fluorescenz und Kohlensäure Assimilation XIII. Die Fluorescenz Kurve und die Photochemie der Pflanze. Biochem Z 332: 277–292
Klug DR, Durrant JR and Barber J (1998) The entanglement of excitation energy transfer and electron transfer in the reaction centre of Photosystem II. Phil Trans R Soc London A 356: 449–464
Kok B and Cheniae G (1966) Kinetics and intermediates of the oxygen evolution step in photosynthesis In: Sanadi R (ed) Current Topics in Bioenergetics, Vol 1, pp 1–47. Academic Press, New York
Krause GH (1974) Changes in chlorophyll fluorescence in relation to light-dependent cation transfer across thylakoid membranes. Biochim Biophys Acta 333: 301–313
Krause GH, Vernotte C and Briantais J-M (1982) Photoinduced quenching of chlorophyll fluorescence in intact chloroplasts and algae, resolution into two components. Biochim Biophys Acta 679: 116–124
Krauß N, Schubert W-D, Klukas O, Fromme P, Witt HT and Saenger W (1996) Photosystem I at 4Å resolution represents the first structural model of a joint photosynthetic reaction centre and core antenna system. Nat Struct Biol 3: 965–973
Kühlbrandt W, Wang DN and Fujiyoshi Y (1994) Atomic model for plant light harvesting complex by electron crystallography. Nature 367: 614–621
Kunster P, Guardiola A, Takahashi Y and Rochaix JD (1995) A mutant strain of Chlamydomonas reinhardtii lacking the chloroplast Photosystem II psbI gene grows photoautotrophically. J Biol Chem 270: 9651–9654
Lavorel J (1959) Induction of fluorescence in quinone poisoned Chlorella. Plant Physiol 34: 204–209
Lavorel J (1968) Sur une relation entre fluorescence et luminescence dans les systemes photosynthetiques. Biochim Biophys Acta 153: 727–730
Lyon MK, Marr KM and Furcinitti PS (1993) Formation and characterization of two-dimensional crystals of Photosystem II. J Struct Biol 110: 133–140
Malkin S and Kok B (1966) Fluorescence induction studies in isolated chloroplast. I. Number of components involved in the reaction and quantum yields. Biochim Biophys Acta 126: 413–432
Marder JB, Chapman DJ, Telfer A, Nixon PJ and Barber J (1987) Identification of psbA and psbD gene products, D1 and D2, as reaction centre proteins of Photosystem 2. Plant Mol Biol 8: 325–333
Mayes SR, Cook KM, Self SJ, Zhang ZH and Barber J (1991) Deletion of the gene encoding the PS II 33 kDa protein from Synechocystis PCC 6803 does not inactivate water-splitting but increases vulnerability to photoinhibition. Biochim Biophys Acta 1060: 1–12
Mayes SR, Dubbs JM, Vass I, Hideg E, Nagy L and Barber J (1993) Further characterization of the psbH locus of Synechocystis sp. PCC 6803: inactivation of psbH impairs QA and QB electron transport in photosystem 2. Biochemistry 32: 1454–1465
Mayne BC and Clayton RK (1966) Luminescence of chlorophyll in spinach chloroplasts induced by acid-base transitions. Proc Natl Acad Sci USA 55: 494–497
McTavish H, Picorel R and Seibert M (1989) Stabilization of isolated Photosystem II reaction center complex in the dark and in the light using polyethylene glycol and an oxygen-scrubbing system. Plant Physiol 89: 452–456
Mills JD and Barber J (1975) Energy-dependent cation induced control of chlorophyll a fluorescence in isolated intact chloroplasts. Arch Biochem Biophys 170: 306–314
Mimuro M (2002) Visualization of excitation energy transfer processes in plants and algae. Photosynth Res 73: 133–138
Mitchell P (1966) Chemiosmotic coupling in oxidative and photosynthetic phosphorylation. Biol Rev Cambridge Phil Soc 41: 445–502
Miyashita H, Ikemoto H, Kurano N, Adachi K, Chihara M and Miyachi S (1996) Chlorophyll d as a major pigment. Nature 383: 402
Mohanty P, Braun BZ and Govindjee (1973) Light-induced slow changes in chlorophyll a fluorescence in isolated chloroplasts: effects of magnesium and phenazine methosulfate. Biochim Biophys Acta 292: 459–476
Morris EP, Hankamer B, Zheleva D, Friso G and Barber J (1997) The 3D structure of a Photosystem II core complex determined by electron crystallography. Structure 5: 837–849
Munday JC and Govindjee (1969) Light-induced changes in the fluorescence yield of chlorophyll-a in vivo III. The dip and the peak in fluorescence transients of Chorella pyrenoidosa. Biophys J 9: 1–21
Murakami S and Packer L (1971) The role of cations in the organization of chloroplast membranes. Arch Biochem Biophys 146: 337–347
Murata N (1969) Control of excitation energy transfer in photosynthesis I. Light-induced change of chlorophyll a fluorescence. Biochim Biophys Acta 172: 242–251
Nakatani HY and Barber J (1980) Further studies of thylakoid membrane surface charges by particle electrophoresis. Biochim Biophys Acta 591: 82–91
Nakazato K, Toyoshima C, Enami I and Inoue Y (1996) Two-dimensional crystallization and cryo electron microscopy of Photosystem II. J Mol Biol 257: 225–232
Nanba O and Satoh K (1987) Isolation of a Photosystem II reaction center consisting of D1 and D2 polypeptides and cytochrome b559. Proc Natl Acad Sci USA 84: 109–112
Nield J, Orlova E, Morris E, Gowen B, van Heel M and Barber J (2000a) 3D map of plant Photosystem II supercomplex obtained by cryoelectron microscopy and single particle analysis. Nat Struct Biol 7: 44–47
Nield J, Funk C and Barber J (2000b) Supermolecular structure of Photosystem two and location of the PsbS protein. Phil Trans R Soc London B 355: 1337–1344
Nield J, Balsera M, Dr Las Rivas J and Barber J (2002) 3D cryo-EM study of the extrinsic domains of the oxygen evolving complex of spinach. Assignment of the PsbO protein. J Biol Chem 277: 15006–15012
Ojakian GK and Satir P (1974) Particle movements in chloroplast membranes: quantitative measurements of membrane fluidity by freeze-fracture technique. Proc Natl Acad Sci USA 21: 2052–2054
Olson JM and Blankenship RE (2004) Thinking about the evolution of photosynthesis. Photosynth Res 80: 373–386
Park R and Sane PV (1971) Distribution of function and structure in chloroplast lamellae. Annu Rev Plant Physiol 22: 395–430
Pecoraro VL, Baldwin MJ, Hsieh W-Y and Law NA (1998) A proposal for water oxidation in Photosystem II. Pure Appl Chem 70: 925–929
Peter GF and Thornber JP (1991) Biochemical composition and organization of higher plant Photosystem II light harvesting pigment-proteins. J Biol Chem 266: 16745–16754
Porter G, Tredwell CJ, Searle GFW and Barber J (1978) Picosecond time resolved energy transfer in Porphyridium cruentum Part I. In the intact alga. Biochim Biophys Acta 501: 232–245
Prokhorenko VI and Holzwarth AR (2000) Primary processes and structure of Photosystem II reaction center: a photon echo study. J Phys Chem 104: 11563–11578
Renger G (2003) Apparatus and mechanism of photosynthetic oxygen evolution: a personal perspective. Photosynth Res 76: 269–288
Rhee KH (1998) Three dimensional structure of Photosystem II reaction center by electron cryo-microscopy. PhD thesis. University of Frankfurt, Germany
Rhee KH, Morris EP, Zheleva D, Hankamer B, Kühlbrandt W and Barber J (1997) Two dimensional structure of plant Photosystem II at 8Å resolution. Nature 389: 522–526
Rhee KH, Morris EP, Barber J and Kühlbrandt W (1998) Three dimensional structure of the Photosystem II reaction centre at 8Å resolution. Nature 396: 283–286
Rubin B and Barber J (1980) The role of membrane surface charge in the control of photosynthetic processes and involvement of electrostatic screening. Biochim Biophys Acta 592: 87–102
Rutherford AW, Govindjee and Inoue Y (1984) Charge accumulation and photochemistry in leaves studied by thermoluminescence and delayed light emission. Proc Natl Acad Sci USA 81: 1107–1111
Sane PV, Goodchild DJ and Park RB (1970) Characterization of chloroplast Photosystems 1 and 2 separated by a non-detergent method. Biochim Biophys Acta 218: 162–178
Satoh K (2003) The identification of the Photosystem II reaction center: a personal story. Photosynth Res 76: 233–240
Schubert W-D, Klukas O, Saenger W, Witt HT, Fromme P and Krauß N (1998) A common ancestor for oxygenic and anoxygenic photosynthetic systems — a comparison based on the structural model of Photosystem I. J Mol Biol 280: 297–314
Seibert M (1995) Reflections on the nature and function of the Photosystem II reaction centre. Aust J Plant Physiol 22: 161–166
Seibert M and Wasielewski MR (2003) The isolated Photosystem II reaction center: first attempts to directly measure the kinetics of primary charge separation. Photosynth Res 76: 263–268
Seibert M, DeWit M and Staehelin LA (1987) Structural localization of the oxygen evolving apparatus to multimeric (tetrameric) particles on the lumenal surface of freeze-etched photosynthetic membranes. J Cell Biol 105: 2257–2265
Seibert M, Picorel R, Rubin AB and Connolly JS (1988) Spectral, photophysical, and stability properties of isolated Photosystem II reaction center. Plant Physiol 87: 303–306
Siegbahn PEM (2002) Quantum chemical studies of manganese centers in biology. Curr Opin Chem Biol 6: 227–235
Staehelin LA (1976) Reversible particle movements associated with unstacking and restacking of chloroplast membranes. J Cell Biol 71: 136–158
Staehelin LA (2003) Chloroplast structure: from chlorophyll granules to supra-molecular architecture of thylakoid membranes. Photosynth Res 76: 185–196
Staehelin LA, Armond PA and Miller KR (1976) Chloroplast membrane organization at the supramolecular level and its functional implications. Brookhaven Symp Biol 28: 278–315
Strehler B and Arnold W(1951) Light production from green plants. J Gen Physiol 34: 809–820
Svensson B, Etchebest C, Tuffrey P, van Kan P, Smith J, Styring S (1996) A model for the Photosystem II reaction center core including the structure of the primary donor P680. Biochemistry 35: 14486–14502
Telfer A, Bishop SM, Phillips D and Barber J (1994) Isolated photosynthetic reaction center of Photosystem II as a sensitizer for the formation of singlet oxygen: detection and quantum yield determination using a chemical trapping technique. J Biol Chem 269: 13244–13253
Vass I (2003) The history of photosynthetic thermoluminescence. Photosynth Res 76: 303–318
Vass I and Inoue Y (1992) Thermoluminescence in the study of Photosystem II. In: Barber J (ed) Topics in Photosynthesis, Vol 11, pp 259–294. Elsevier, Amsterdam
Vrettos JS, Limburg J and Brudvig GW (2001) Mechanism of photosynthetic water oxidation; combining biophysical studies of PS II with inorganic model chemistry. Biochim Biophys Acta 1503: 229–245
Wakoo N, Yokoi N, Isoyama N, Hiraishi A, Shimada K, Kobayashi M, Kise H, Iwaki M, Itoh S, Takaichi S and Sakurai Y (1996) Discovery of natural photosynthesis using Zn-containing bacteriochlorophyll in an aerobic bacterium Acidiphilium rubrum. Plant Cell Physiol 37: 889–893
Wasielewski M, Johnson DG, Preston C, Govindjee and Seibert M (1989) Determination of the primary charge separation rate in isolated Photosystem II reaction centers with 500 fs-time resolution. Proc Natl Acad Sci USA 86: 524–528
Witt HT (2004) Steps on the way to building blocks, topologies, crystals and X-ray structural analysis of Photosystems I and II of water-oxidizing photosynthesis. Photosynth Res 80: 85–107
Wraight CA and Crofts AR (1970) Energy-dependent quenching of chlorophyll a fluorescence in isolated chloroplasts. Eur J Biochem 17: 319–327
Wraight CA and Crofts AR (1971) Delayed fluorescence and the high energy state of chloroplasts. Eur J Biochem 19: 386–397
Zhang ZH, Mayes SR, Vass I, Nagy L and Barber J (1993) Characterisation of the psbK locus of Synechocystis sp. PCC 6803 in terms of PS II function. Photosynth Res 38: 369–377
Zheleva D, Sharma J, Panico M, Morris HR and Barber J (1998) Isolation and characterization of monomeric and dimeric CP47-RC PS II complexes. J Biol Chem 273: 16122–16127
Zouni A, Jordan R, Schlodder E, Fromme P and Witt HT (2000) First Photosystem II crystals capable of water oxidation. Biochim Biophys Acta 1457: 103–105
Zouni A, Witt HT, Kern J, Fromme P, Krauß N, Saenger W and Orth P (2001) Crystal structure of Photosystem II form Synechococcus elongatus at 3.8Å resolution. Nature 409: 739–743
Author information
Authors and Affiliations
Editor information
Editors and Affiliations
Rights and permissions
Copyright information
© 2005 Springer
About this chapter
Cite this chapter
Barber, J. (2005). Engine of life and big bang of evolution: a personal perspective. In: Govindjee, Beatty, J.T., Gest, H., Allen, J.F. (eds) Discoveries in Photosynthesis. Advances in Photosynthesis and Respiration, vol 20. Springer, Dordrecht. https://doi.org/10.1007/1-4020-3324-9_28
Download citation
DOI: https://doi.org/10.1007/1-4020-3324-9_28
Received:
Accepted:
Publisher Name: Springer, Dordrecht
Print ISBN: 978-1-4020-3323-0
Online ISBN: 978-1-4020-3324-7
eBook Packages: Biomedical and Life SciencesBiomedical and Life Sciences (R0)