Singlet oxygen formation detected by near-infrared emission from isolated photosystem II reaction centres: Direct correlation between P680 triplet decay and luminescence rise kinetics and its consequences for photoinhibition

Journal of Photochemistry and Photobiology B: Biology

Volumn 48, Issue 2-3, 1999, Pages 89-96

  Telfer, A ^a   Oldham, T C ^a   Phillips, D ^a   Barber, J ^a  

^a IMPERIAL COLLEGE LONDON   (United Kingdom)

Author keywords

D1 D2 Cytb559 complex; Luminescence; P680; Photoinhibition; Transient absorption; Triplet state

Indexed keywords

PHEOPHYTIN; SINGLET OXYGEN; VEGETABLE PROTEIN;

CHEMOLUMINESCENCE; CONFERENCE PAPER; CONTROLLED STUDY; INFRARED SPECTROSCOPY; LUMINESCENCE; NONHUMAN; OXIDATION REDUCTION REACTION; PHOTOCHEMISTRY; PHOTOSYNTHESIS; PHOTOSYSTEM II; PHYTOCHEMISTRY; PRIORITY JOURNAL; PROTEIN DEGRADATION;

EID: 0033081605     PISSN: 10111344     EISSN: None     Source Type: Journal    
DOI: 10.1016/S1011-1344(99)00028-7     Document Type: Conference Paper

References (32)

1. [1] A.N. Macpherson, A. Telfer, J. Barber, T.G. Truscott, Direct detection of singlet oxygen from isolated Photosystem II reaction centres, Biochim. Biophys. Acta 1143 (1993) 301-309.
2. [2] A. Telfer, S. Dhami, S.M. Bishop, D. Phillips, J. Barber, β-Carotene quenches singlet oxygen formed by isolated Photosystem II reaction centres, Biochemistry 33 (1994) 14469-14474.
3. [3] A. Telfer, S.M. Bishop, D. Phillips, J. Barber, Isolated photosynthetic reaction center of photosystem two as a sensitizer for the formation of singlet oxygen, J. Biol. Chem. 269 (1994) 13244-13253.
4. [4] E. Hideg, C. Spetea, I. Vass, Singlet oxygen and free radical production during acceptor-and donor-side-induced photoinhibition. Studies with spin trapping EPR spectroscopy, Biochim. Biophys. Acta 1186 (1994) 143-152.
5. [5] R.J. Cogdell, H.A. Frank, How carotenoids function in photosynthetic bacteria, Biochim. Biophys. Acta 895 (1987) 3-79.
6. [6] Y. Takahashi, Ö. Hansson, P. Mathis, K. Satoh, Primary radical pair in the photosystem II reaction center, Biochim. Biophys. Acta 893 (1987) 49-59.
7. [7] J.R. Durrant, L.B. Giorgi, J. Barber, D.R. Klug, G. Porter, Characterisation of triplet states in isolated Photosystem II reaction centres: oxygen quenching as a mechanism for photodamage, Biochim. Biophys. Acta 1017 (1990) 167-175.
8. [8] D. Zheleva, B. Hankamer, J. Barber, Heterogeneity and pigment composition of isolated PSII reaction centres. Biochemistry 35 (1996) 15074-15079.
9. [9] F. Vacha, D.M. Joseph, J.R. Durrant, A. Telfer, D.R. Klug, G. Porter, J. Barber, Photochemistry and spectroscopy of a five-chlorophyll reaction center of photosystem II isolated by using a Cu affinity column, Proc. Natl. Acad. Sci. USA 92 (1995) 2929-2933.
10. [10] J. De Las Rivas, A. Telfer, J. Barber, Two coupled β-carotene molecules protect P680 from photodamage in isolated Photosystem II reaction centres, Biochim. Biophys. Acta 1142 (1993) 155-164.
11. [11] M.Y. Okamura, K. Satoh, R.A. Isaacson, G. Feher, Evidence of the primary charge separation in the D1D2 complex of photosystem II from spinach: EPR of the triplet state. in: J. Biggins (Ed.), Progress in Photosynthesis Research, vol. 1, Martinus Nijhoff, Dordrecht, 1987, pp. 379-381.
12. [12] P. Mathis, K. Satoh, Ö. Hansson, Kinetic evidence for the function of Z in isolated photosystem II reaction centers, FEBS Lett. 251 (1989) 241-244.
13. [13] A. Telfer, J. Barber, Evidence for the photo-induced oxidation of the primary electron donor P680 in the isolated photosystem II reaction centre, FEBS Lett. 246 (1989) 223-228.
14. [14] W. Kühlbrandt, D.N. Wang, Y. Fujiyoshi, Atomic model of plant light-harvesting complex by electron crystallography, Nature 367 (1994) 614-621.
15. [15] A. Ducruix, F. Reiss-Husson, Preliminary characterisation by X-ray diffraction of crystals of photochemical reaction centers from wild-type Rhodopseudomonas spheroides. Plant Mol. Biol. 193 (1987) 419-421.
16. [16] G. McDermott, S.M. Prince, A.A. Freer, A.M. Hawthornthwaite-Lawless, M.Z. Papiz, R.J. Cogdell, N.W. Isaacs, Crystal-structure of an integral membrane light-harvesting complex from photosynthetic bacteria, Nature 374 (1995) 517-521.
17. [17] E. Hofmann, P.M. Wrench, F.P. Sharples, R.G. Hiller, W. Welte, K. Diederichs, Structural basis of light-harvesting by carotenoids - peridinin-chlorophyll-protein from Amphidinium carterae, Science 272 (1996) 1788-1791.
18. [18] V.V. Klimov, S.I. Allakhverdiev, S. Demeter, A.A. Krasnovsky, Pheophytin reduction in photosystem II of chloroplasts in relation to oxidation-reduction potential of medium, Dokl. Akad. Nauk SSSR 249 (1979) 227-230.
19. [19] A. Telfer, J. De Las Rivas, J. Barber, β-Carotene within the isolated Photosystem II reaction centre: photooxidation and irreversible bleaching of this chromophore by oxidised P680, Biochim. Biophys. Acta 1060 (1991) 106-114.
20. [20] A. Telfer, J. Barber, Role of carotenoid bound to the photosystem II reaction centre. in: P. Mathis (Ed.), Photosynthesis: from Light to Biosphere, vol. IV, Kluwer, Dordrecht, 1995, pp. 15-20.
21. [21] J. Barber, B. Andersson, Too much of a good thing - light can be bad for photosynthesis, Trends Biochem. Sci. 17 (1992) 61-66.
22. A species promote chlorophyll triplet formation, Proc. Natl. Acad. Sci. USA 89 (1992) 1408-1412.
23. [23] A.A. Gorman, M.A.J. Rodgers, Singlet oxygen. in: J.C. Scaiano (Ed.), The Handbook of Organic Photochemistry, vol. 2, CRC Press, Boca Raton, FL, 1989, pp. 229-247.
24. [24] S.Y. Egorov, V.F. Kamalov, N.I. Koroteev, A.A. Krasnovsky Jr., B.N. Toleutaev, S.V. Zinukov, Rise and decay kinetics of photosensitized singlet oxygen luminescence in water. Measurements with nanosecond time-correlated single photon counting technique, Chem. Phys. Lett. 163 (1989) 421-424.
25. [25] F. Wilkinson, W.P. Helman, A.B. Ross, Rate constants for the decay and reactions of the lowest electronically excited singlet-state of molecular-oxygen in solution - an expanded and revised compilation, J. Phys. Chem. Ref. Data 24 (1995) 663-1021.
26. [26] A.A. Gorman, M.A.J. Rodgers, Current perspectives of singlet oxygen detection in biological environments, J. Photochem. Photobiol. B: Biol. 14 (1992) 159-176.
27. [27] I. Yruela, M.S. Churio, T. Gensch, S.E. Braslavsky, A.R. Holzwarth, Optoacoustic and singlet oxygen near-IR emission study of the isolated D1-D2-cyt b-559 reaction centre complex of photosystem II. Protein movement associated with charge separation, J. Phys. Chem. 98 (1994) 12789-12795.
28. [28] L.B. Giorgi, P.J. Nixon, S.A.P. Merry, D.M. Joseph, J.R. Durrant, J. De Las Rivas, J. Barber, G. Porter, D.R. Klug, Comparison of primary charge separation in the Photosystem II reaction center complex isolated from wild type and D1-130 mutants of the cyanobacterium Synechocystis PCC 6803, J. Biol. Chem. 271 (1996) 2093-2101.
29. [29] A.W. Rutherford, K. Satoh, P. Mathis, Reaction center triplet-state in Photosystem-II, Biophys. J. 41 (1983) 40a.
30. [30] H.J. den Blanken, A.J. Hoff, A.P.J.M. Jongenelis, B.A. Diner, High-resolution triplet-minus-singlet absorption difference spectrum of photosystem II particles, FEBS Lett. 157 (1983) 21-27.
31. [31] J. De Las Rivas, B. Crystall, P.J. Booth, J.R. Durrant, S. Ozer, G. Porter, D.R. Klug, J. Barber, Long lived primary radical pair state detected by time resolved fluorescence and absorption spectroscopy in an isolated photosystem two core, Photosynth. Res. 34 (1992) 419-431.
32. [32] J. Sharma, M. Panico, C.A. Shipton, F. Nilsson, H.R. Morris, J. Barber, Primary structure characterisation of the PSII D1 and D2 subunits, J. Biol. Chem. 272 (1997) 33158-33166.