Detection of an intermediate of photosynthetic water oxidation

被引:99
作者
Clausen, J [1 ]
Junge, W [1 ]
机构
[1] Univ Osnabruck, Dept Biol Chem, Div Biophys, D-49069 Osnabruck, Germany
基金
美国国家卫生研究院;
关键词
D O I
10.1038/nature02676
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The oxygen that we breathe is produced by photosystem II of cyanobacteria and plants. The catalytic centre, a Mn4Ca cluster, accumulates four oxidizing equivalents before oxygen is formed, seemingly in a single reaction step1-8 2H(2)O(<--)(-->) O-2 = 4H(+) + 4e(-). The energy and cycling of this reaction derives solely from light. No intermediate oxidation product of water has been detected so far. Here, we shifted the equilibrium of the terminal reaction backward by increasing the oxygen pressure and monitoring ( by absorption transients in the near-ultraviolet spectrum) the electron transfer from bound water into the catalytic centre. A tenfold increase of ambient oxygen pressure (2.3 bar) half-suppressed the full progression to oxygen. The remaining electron transfer at saturating pressure ( 30 bar) was compatible with the formation of a stabilized intermediate. The abstraction of four electrons from water was probably split into at least two electron transfers: mildly endergonic from the centre's highest oxidation state to an intermediate, and exergonic from the intermediate to oxygen. There is little leeway for photosynthetic organisms to push the atmospheric oxygen concentration much above the present level.
引用
收藏
页码:480 / 483
页数:4
相关论文
共 30 条
[1]  
BABCOCK GT, 1976, FEBS LETT, V61, P286
[2]   Photosystem II: the engine of life [J].
Barber, J .
QUARTERLY REVIEWS OF BIOPHYSICS, 2003, 36 (01) :71-89
[3]   ACTIVE AND RESTING STATES OF THE O-12-EVOLVING COMPLEX OF PHOTOSYSTEM-II [J].
BECK, WF ;
DEPAULA, JC ;
BRUDVIG, GW .
BIOCHEMISTRY, 1985, 24 (12) :3035-3043
[4]   Time-resolved oxygen production by PSII: chasing chemical intermediates [J].
Clausen, J ;
Debus, RJ ;
Junge, W .
BIOCHIMICA ET BIOPHYSICA ACTA-BIOENERGETICS, 2004, 1655 (1-3) :184-194
[5]   Photosynthetic water oxidation in Synechocystis sp PCC6803:: mutations D1-E189K, R and Q are without influence on electron transfer at the donor side of photosystem II [J].
Clausen, J ;
Winkler, S ;
Hays, AMA ;
Hundelt, M ;
Debus, RJ ;
Junge, W .
BIOCHIMICA ET BIOPHYSICA ACTA-BIOENERGETICS, 2001, 1506 (03) :224-235
[6]   KINETICS OF MANGANESE REDOX TRANSITIONS IN THE OXYGEN-EVOLVING APPARATUS OF PHOTOSYNTHESIS [J].
DEKKER, JP ;
PLIJTER, JJ ;
OUWEHAND, L ;
VANGORKOM, HJ .
BIOCHIMICA ET BIOPHYSICA ACTA, 1984, 767 (01) :176-179
[7]  
DEKKER JP, 1992, MANGANESE REDOX ENZY, P85
[8]   Architecture of the photosynthetic oxygen-evolving center [J].
Ferreira, KN ;
Iverson, TM ;
Maghlaoui, K ;
Barber, J ;
Iwata, S .
SCIENCE, 2004, 303 (5665) :1831-1838
[9]   Photosynthetic oxygen evolution: H/D isotope effects and the coupling between electron and proton transfer during the redox reactions at the oxidizing side of Photosystem II [J].
Haumann, M ;
Bogershausen, O ;
Cherepanov, D ;
Ahlbrink, R ;
Junge, W .
PHOTOSYNTHESIS RESEARCH, 1997, 51 (03) :193-208
[10]   Photosystem II of green plants. Oxidation and deprotonation of the same component (histidine?) on S-1(*)double right arrow S-2* in chloride-depleted centers as on S-2 double right arrow S-3 in controls [J].
Haumann, M ;
Drevenstedt, W ;
Hundelt, M ;
Junge, W .
BIOCHIMICA ET BIOPHYSICA ACTA-BIOENERGETICS, 1996, 1273 (03) :237-250