Photosystem II damage induced by chemically generated singlet oxygen in tobacco leaves

被引:49
作者
Hideg, Eva [1 ]
Kos, Peter B. [1 ]
Vass, Imre [1 ]
机构
[1] Biol Res Ctr, Inst Plant Biol, H-6726 Szeged, Hungary
关键词
SYNECHOCYSTIS SP PCC-6803; D1; PROTEIN; OXIDATIVE STRESS; EPR SPECTROSCOPY; LOW-LIGHT; PHOTOINHIBITION; REPAIR; DEGRADATION; PHOTODAMAGE; COMPLEX;
D O I
10.1111/j.1399-3054.2007.00913.x
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
In the present work, we investigated the role of chemically generated singlet oxygen, produced by photodynamic effect of rose bengal, in damaging the PSII complex in tobacco leaves in which protein synthesis-dependent repair was inhibited by infiltration with lincomycin. A 30-min exposure to low-intensity (150 mu mol m(-2) s(-1)) photosynthetically active radiation (PAR) induced singlet oxygen production as detected by quenching of 3-[N-(beta-diethylaminoethyl)- N-dansyl]aminomethyl-2,2,5,5-tetramethyl-2,5-dihydro-1H-pyrrole fluorescence in leaves infiltrated with both lincomycin and rose bengal. This light treatment caused photoinhibition of PSII, as revealed by the marked loss both of the photochemical yield and the amount of D1 protein in PSII reaction center. When rose bengal was not present in the leaves, these symptoms of photodamage were not induced by the same low-intensity PAR. However, when excitation pressure on PSI[ was increased to 1500 mu mol m(-2) s(-1), irreversible photodamage of PSI[ was also observed, showing that the lincomycin treatment applied in vivo was sufficiently inhibiting protein repair. Our results show that singlet oxygen is able to cause oxidative damage in PSII directly, as suggested earlier and argue against its recently hypothesized role exclusive to inhibiting PSI] protein repair (Nishiyama et al. 2006).
引用
收藏
页码:33 / 40
页数:8
相关论文
共 38 条
[1]   Environmental stress inhibits the synthesis de novo of proteins involved in the photodamage-repair cycle of Photosystem II in Synechocystis sp PCC 6803 [J].
Allakhverdiev, SI ;
Murata, N .
BIOCHIMICA ET BIOPHYSICA ACTA-BIOENERGETICS, 2004, 1657 (01) :23-32
[2]   Sources of measurement variation in blood pressure in large-scale epidemiological surveys with follow-up [J].
Andersen, UO ;
Henriksen, JH ;
Jensen, G .
BLOOD PRESSURE, 2002, 11 (06) :357-365
[3]   INVITRO STUDIES ON LIGHT-INDUCED INHIBITION OF PHOTOSYSTEM-II AND D1-PROTEIN DEGRADATION AT LOW-TEMPERATURES [J].
ARO, EM ;
HUNDAL, T ;
CARLBERG, I ;
ANDERSSON, B .
BIOCHIMICA ET BIOPHYSICA ACTA, 1990, 1019 (03) :269-275
[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]   NEW EVIDENCE SUGGESTS THAT THE INITIAL PHOTOINDUCED CLEAVAGE OF THE D1-PROTEIN MAY NOT OCCUR NEAR THE PEST SEQUENCE [J].
BARBATO, R ;
SHIPTON, CA ;
GIACOMETTI, GM ;
BARBER, J .
FEBS LETTERS, 1991, 290 (1-2) :162-166
[6]   Time and spectral resolved phosphorescence of singlet oxygen and pigments in photosystem II particles [J].
Dedic, R ;
Svoboda, A ;
Psencík, J ;
Lupínková, L ;
Komenda, J ;
Hála, J .
JOURNAL OF LUMINESCENCE, 2003, 102 :313-317
[7]   Evidence for the role of the oxygen-evolving manganese complex in photoinhibition of Photosystem II [J].
Hakala, M ;
Tuominen, I ;
Keränen, M ;
Tyystjärvi, T ;
Tyystjärvi, E .
BIOCHIMICA ET BIOPHYSICA ACTA-BIOENERGETICS, 2005, 1706 (1-2) :68-80
[8]   Photoinhibition of photosynthesis in vivo results in singlet oxygen production detection via nitroxide-induced fluorescence quenching in broad bean leaves [J].
Hideg, É ;
Kálai, T ;
Hideg, K ;
Vass, I .
BIOCHEMISTRY, 1998, 37 (33) :11405-11411
[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]  
HIDEG E, 1995, PHOTOCHEM PHOTOBIOL, V62, P949