Evidence for the role of the oxygen-evolving manganese complex in photoinhibition of Photosystem II

被引:324
作者
Hakala, M [1 ]
Tuominen, I [1 ]
Keränen, M [1 ]
Tyystjärvi, T [1 ]
Tyystjärvi, E [1 ]
机构
[1] Univ Turku, Lab Plant Physiol & Mol BIol, Dept Biol, FI-20014 Turku, Finland
来源
BIOCHIMICA ET BIOPHYSICA ACTA-BIOENERGETICS | 2005年 / 1706卷 / 1-2期
基金
芬兰科学院;
关键词
photoinhibition; photosystem II; manganese; action spectrum;
D O I
10.1016/j.bbabio.2004.09.001
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Photoinhibition of PSII occurs at the same quantum efficiency from very low to very high light, which raises a question about how important is the rate of photosynthetic electron transfer in photoinhibition. We modulated electron transfer rate and light intensity independently of each other in lincomycin-treated pea leaves and in isolated thylakoids, in order to elucidate the specific effects of light and PSII electron transport on photoinhibition. Major changes in the rate of electron transport caused only small changes in the rate of photoinhibition, suggesting the existence of a significant photoinhibitory pathway that contains an electron-transfer-independent phase. We compared the action spectrum of photoinhibition with absorption spectra of PSII components that could function as photoreceptors of the electron-transfer-independent phase of photoinhibition and found that the absorption spectra of Mn(III) and Mn(IV) compounds resemble the action spectrum of photoinhibition, showing a steep decrease from UV-C to blue light and a low visible-light tail. Our results show that the release of a Mn ion to the thylakoid lumen is the earliest detectable step of both UV- and visible-light-induced photo inhibition. After Mn release from the oxygen-evolving complex, oxidative damage to the PSII reaction center occurs because the Mn-depleted oxygen-evolving complex cannot reduce P-680(+) normally. (C) 2004 Elsevier B.V. All rights reserved.
引用
收藏
页码:68 / 80
页数:13
相关论文
共 46 条
[1]   Photoinhibition - a historical perspective [J].
Adir, N ;
Zer, H ;
Shochat, S ;
Ohad, I .
PHOTOSYNTHESIS RESEARCH, 2003, 76 (1-3) :343-370
[2]   Unifying model for the photoinactivation of Photosystem II in vivo under steady-state photosynthesis [J].
Anderson, JM ;
Park, YI ;
Soon, WS .
PHOTOSYNTHESIS RESEARCH, 1998, 56 (01) :1-13
[3]  
Andersson B, 2001, ADV PHOTOSYNTH, V11, P377
[4]   PHOTOINHIBITION OF PHOTOSYSTEM-2 - INACTIVATION, PROTEIN DAMAGE AND TURNOVER [J].
ARO, EM ;
VIRGIN, I ;
ANDERSSON, B .
BIOCHIMICA ET BIOPHYSICA ACTA, 1993, 1143 (02) :113-134
[5]   Two new terpyridine dimanganese complexes:: A manganese(III,III) complex with a single unsupported oxo bridge and a manganese(III,IV) complex with a dioxo bridge.: Synthesis, structure, and redox properties [J].
Baffert, C ;
Collomb, MN ;
Deronzier, A ;
Pécaut, J ;
Limburg, J ;
Crabtree, RH ;
Brudvig, GW .
INORGANIC CHEMISTRY, 2002, 41 (06) :1404-1411
[6]   DEGRADATION OF THE DI-PROTEIN OF PHOTOSYSTEM-II REACTION-CENTER BY ULTRAVIOLET-B RADIATION REQUIRES THE PRESENCE OF FUNCTIONAL MANGANESE ON THE DONOR SIDE [J].
BARBATO, R ;
FRIZZO, A ;
FRISO, G ;
RIGONI, F ;
GIACOMETTI, GM .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1995, 227 (03) :723-729
[7]  
Bensasson R.V., 1983, Flash photolysis and pulse radiolysis
[8]   ELECTROCHEMICAL AND SPECTROSCOPIC STUDIES OF MANGANESE(II), MANGANESE(III), AND MANGANESE(IV) GLUCONATE COMPLEXES .1. FORMULAS AND OXIDATION-REDUCTION STOICHIOMETRY [J].
BODINI, ME ;
WILLIS, LA ;
RIECHEL, TL ;
SAWYER, DT .
INORGANIC CHEMISTRY, 1976, 15 (07) :1538-1543
[9]   CHEMICAL ACTINOMETRY IN THE VISIBLE (475-NM-610 NM) BY MESO-DIPHENYLHELIANTHRENE [J].
BRAUER, HD ;
SCHMIDT, R ;
GAUGLITZ, G ;
HUBIG, S .
PHOTOCHEMISTRY AND PHOTOBIOLOGY, 1983, 37 (06) :595-598
[10]   STUDIES ON THE PHOTOACTIVATION OF THE WATER-OXIDIZING ENZYME .2. CHARACTERIZATION OF WEAK LIGHT PHOTOINHIBITION OF PSII AND ITS LIGHT-INDUCED RECOVERY [J].
CALLAHAN, FE ;
BECKER, DW ;
CHENIAE, GM .
PLANT PHYSIOLOGY, 1986, 82 (01) :261-269