Spectral resolution of the split EPR signals induced by illumination at 5 K from the S1, S3, and S0 states in photosystem II

被引:31
作者
Havelius, Kajsa G. V.
Su, Ji-Hu
Feyziyev, Yashar
Mamedov, Fikret
Styring, Stenbjorn
机构
[1] Angstrin Lab, Dept Photochem & Mol Sci, S-75120 Uppsala, Sweden
[2] Inst Bot, AZ-1073 Baku, Azerbaijan
关键词
D O I
10.1021/bi060698e
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
S-State-dependent split EPR signals that are induced by illumination at cryogenic temperatures ( 5 K) have been measured in spinach photosystem II without interference from the Y-D(center dot) radical in the g similar to 2 region. This allows us to present the first decay-associated spectra for the split signals, which originate from the CaMn4 cluster in magnetic interaction with a nearby radical, presumably Y-Z(center dot). The three split EPR signals that were investigated, "Split S-1", " Split S-3", and Split S-0", all exhibit spectral features at g similar to 2.0 together with surrounding characteristic peaks and troughs. From microwave relaxation studies we can reach conclusions about which parts of the complex spectra belong together. Our analysis strongly indicates that the wings and the middle part of the split spectrum are parts of the same signal, since their decay kinetics in the dark at 5 K and microwave relaxation behavior are indistinguishable. In addition, our decay-associated spectra indicate that the g similar to 2.0 part of the " Split S-1" EPR spectrum contains a contribution from magnetically uncoupled Y-Z(center dot) as judged from the g value and 22 G line width of the EPR signal. The g value, 2.0033-2.0040, suggests that the oxidation of Y-Z at 5 K results in a partially protonated radical. Irrespective of the S state, a small amount of a carotenoid or chlorophyll radical was formed by the illumination. However, this had relaxation and decay characteristics that clearly distinguish this radical from the split signal spectra. In this paper, we present the "clean" spectra from the low-temperature illumination-induced split EPR signals from higher plants, which will provide the basis for further simulation studies.
引用
收藏
页码:9279 / 9290
页数:12
相关论文
共 75 条
[1]   CA2+ DEPLETION MODIFIES THE ELECTRON-TRANSFER ON BOTH DONOR AND ACCEPTOR SIDES IN PHOTOSYSTEM-II FROM SPINACH [J].
ANDREASSON, LE ;
VASS, I ;
STYRING, S .
BIOCHIMICA ET BIOPHYSICA ACTA-BIOENERGETICS, 1995, 1230 (03) :155-164
[2]  
ANDREASSON LE, 1992, BIOCHIM BIOPHYS ACTA, V1100, P177
[3]   COPPER ENZYMES IN ISOLATED CHLOROPLASTS - POLYPHENOLOXIDASE IN BETA-VULGARIS [J].
ARNON, DI .
PLANT PHYSIOLOGY, 1949, 24 (01) :1-15
[4]   Pulsed EPR study of the S'(3) signal in the Ca2+-depleted photosystem II [J].
Astashkin, AV ;
MIno, H ;
Kawamori, A ;
Ono, TA .
CHEMICAL PHYSICS LETTERS, 1997, 272 (5-6) :506-516
[5]   RAPID, LIGHT-INDUCED TRANSIENT IN ELECTRON-PARAMAGNETIC RESONANCE SIGNAL II ACTIVATED UPON INHIBITION OF PHOTOSYNTHETIC OXYGEN EVOLUTION [J].
BABCOCK, GT ;
SAUER, K .
BIOCHIMICA ET BIOPHYSICA ACTA, 1975, 376 (02) :315-328
[6]   Photosystem II: the engine of life [J].
Barber, J .
QUARTERLY REVIEWS OF BIOPHYSICS, 2003, 36 (01) :71-89
[7]   TYROSINE RADICALS ARE INVOLVED IN THE PHOTOSYNTHETIC OXYGEN-EVOLVING SYSTEM [J].
BARRY, BA ;
BABCOCK, GT .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1987, 84 (20) :7099-7103
[8]   MECHANISM OF PHOTOINHIBITION OF PHOTOSYNTHETIC WATER OXIDATION BY CL- DEPLETION AND F- SUBSTITUTION - OXIDATION OF A PROTEIN RESIDUE [J].
BAUMGARTEN, M ;
PHILO, JS ;
DISMUKES, GC .
BIOCHEMISTRY, 1990, 29 (48) :10814-10822
[9]   A HIGHLY RESOLVED, OXYGEN-EVOLVING PHOTOSYSTEM-II PREPARATION FROM SPINACH THYLAKOID MEMBRANES - ELECTRON-PARAMAGNETIC-RES AND ELECTRON-TRANSPORT PROPERTIES [J].
BERTHOLD, DA ;
BABCOCK, GT ;
YOCUM, CF .
FEBS LETTERS, 1981, 134 (02) :231-234
[10]   Hydrogen bonding of redox-active tyrosine Z of photosystem II probed by FTIR difference spectroscopy [J].
Berthomieu, C ;
Hienerwadel, R ;
Boussac, A ;
Breton, J ;
Diner, BA .
BIOCHEMISTRY, 1998, 37 (30) :10547-10554