Model for the fluorescence induction curve of photoinhibited thylakoids

被引:17
作者
Vavilin, DV
Tyystjärvi, E
Aro, EM
机构
[1] Univ Turku, Dept Biol, Lab Plant Physiol, FIN-20014 Turku, Finland
[2] Moscow MV Lomonosov State Univ, Fac Biol, Dept Biophys, Moscow 119899, Russia
基金
芬兰科学院;
关键词
D O I
10.1016/S0006-3495(98)77539-3
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
The fluorescence induction curve of photoinhibited thylakoids measured in the presence of 3-(3,4-dichlorophenyl)-1,1-dimethyl urea was modeled using an extension of the model of Lavergne and Trissl (Biophys. J. 68:2474-2492), which takes into account the reversible exciton trapping by photosystem II (PSII) reaction centers and exciton exchange between PSII units. The model of Trissl and Lavergne was modified by assuming that PSII consists of photosynthetically active and photoinhibited (inactive in oxygen evolution) units and that the inactive PSII units can efficiently dissipate energy even if they still retain the capacity for the charge separation reaction. Comparison of theoretical and experimental fluorescence induction curves of thylakoids, which had been subjected to strong light in the presence of the uncoupler nigericin, suggests connectivity between the photoinhibited and active PSII units. The model predicts that photoinhibition lowers the yield of radical pair formation in the remaining active PSII centers. However, the kinetics of PSII inactivation in nigericin-treated thylakoids upon exposure to photoinhibitory light ranging from 185 to 2650 mu mol photons m(-2) s(-1) was strictly exponential. This may suggest that photoinhibition occurs independently of the primary electron transfer reactions of PSII or that increased production of harmful substances by photoinhibited PSII units compensates for the protection afforded; by the quenching of excitation energy in photoinhibited centers.
引用
收藏
页码:503 / 512
页数:10
相关论文
共 38 条
[1]   GRANA STACKING AND PROTECTION OF PHOTOSYSTEM-II IN THYLAKOID MEMBRANES OF HIGHER-PLANT LEAVES UNDER SUSTAINED HIGH IRRADIANCE - AN HYPOTHESIS [J].
ANDERSON, JM ;
ARO, EM .
PHOTOSYNTHESIS RESEARCH, 1994, 41 (02) :315-326
[2]   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
[3]   KINETICS OF PHOTOINHIBITION IN HYDROXYLAMINE-EXTRACTED PHOTOSYSTEM-II MEMBRANES - RELEVANCE TO PHOTOACTIVATION AND SITES OF ELECTRON DONATION [J].
BLUBAUGH, DJ ;
CHENIAE, GM .
BIOCHEMISTRY, 1990, 29 (21) :5109-5118
[4]  
Chow W, 1994, Advanves in Molecular and Cell Biology, Vol, V10, P151, DOI DOI 10.1016/S1569-2558(08)60397-5
[5]  
DAU H, 1994, PHOTOCHEM PHOTOBIOL, V60, P1
[6]   CHARACTERIZATION OF TRIPLET-STATES IN ISOLATED PHOTOSYSTEM-II REACTION CENTERS - OXYGEN QUENCHING AS A MECHANISM FOR PHOTODAMAGE [J].
DURRANT, JR ;
GIORGI, LB ;
BARBER, J ;
KLUG, DR ;
PORTER, G .
BIOCHIMICA ET BIOPHYSICA ACTA, 1990, 1017 (02) :167-175
[7]   A SIMPLE-MODEL RELATING PHOTOINHIBITORY FLUORESCENCE QUENCHING IN CHLOROPLASTS TO A POPULATION OF ALTERED PHOTOSYSTEM-II REACTION CENTERS [J].
GIERSCH, C ;
KRAUSE, GH .
PHOTOSYNTHESIS RESEARCH, 1991, 30 (2-3) :115-121
[8]   DEVELOPMENT OF PHOTOSYSTEM-II IN DARK-GROWN CHLAMYDOMONAS-REINHARDTII - A LIGHT-DEPENDENT CONVERSION OF PS-II-BETA, QB-NONREDUCING CENTERS TO THE PS-II-ALPHA, QB-REDUCING FORM [J].
GUENTHER, JE ;
NEMSON, JA ;
MELIS, A .
PHOTOSYNTHESIS RESEARCH, 1990, 24 (01) :35-46
[9]   SINGLET OXYGEN PRODUCTION IN THYLAKOID MEMBRANES DURING PHOTOINHIBITION AS DETECTED BY EPR SPECTROSCOPY [J].
HIDEG, E ;
SPETEA, C ;
VASS, I .
PHOTOSYNTHESIS RESEARCH, 1994, 39 (02) :191-199
[10]   Superoxide radicals are not the main promoters of acceptor-side-induced photoinhibitory damage in spinach thylakoids [J].
Hideg, E ;
Spetea, C ;
Vass, I .
PHOTOSYNTHESIS RESEARCH, 1995, 46 (03) :399-407