Purification, crystallization and X-ray diffraction analyses of the T-elongatus PSII core dimer with strontium replacing calcium in the oxygen-evolving complex

被引:32
作者
Kargul, Joanna
Maghlaoul, Karim
Murray, James W.
Deak, Zsuzsanna
Boussac, Alain
Rutherford, A. William
Vass, Imre
Barber, James [1 ]
机构
[1] Univ London Imperial Coll Sci Technol & Med, Fac Nat Sci, Wolfson Labs, Div Mol Biosci, London SW7 2AZ, England
[2] Hungarian Acad Sci, Inst Plant Biol, Biol Res Ctr, H-6701 Szeged, Hungary
[3] CEA Saclay, URA CNRS 2096, Serv Bioenerget, F-91191 Gif Sur Yvette, France
来源
BIOCHIMICA ET BIOPHYSICA ACTA-BIOENERGETICS | 2007年 / 1767卷 / 06期
基金
英国生物技术与生命科学研究理事会;
关键词
photosynthesis; photosystem II structure; strontium replacement; X-ray crystallography; fluorescence decay and imaging; water splitting;
D O I
10.1016/j.bbabio.2007.01.007
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
The core complex of photosystem II (PSII) was purified from therm ophillic cyanobaterium Thermosynechococcus elongatus grown in Sr2+-containing and Ca2+-free medium. Functional in vivo incorporation of Sr2+ into the oxygen-evolving complex (OEC) was confirmed by EPR analysis of the isolated and highly purified SrPSII complex in agreement with the previous study of Boussac et at. [J. Biol. Chem. 279 (2004) 22809-22819]. Three-dimensional crystals of SrPSII complex were obtained which diffracted to 3.9 A and belonged to the orthorhombic space group P2(1)2(1)2(1) with unit cell dimensions of a= 133.6 angstrom, b=236.6 angstrom, c=307.8 angstrom. Anomalous diffraction data collected at the Sr K-X-ray absorption edge identified a novel Sr2+-binding site which, within the resolution of these data (6.5 angstrom), is consistent with the positioning of Ca2+ in the recent crystallographic models of PSII [Ferreira et al. Science 303 (2004) 1831-1838, Loll et al. Nature 438 (2005) 1040-1044]. Fluorescence measurements on SrPSII crystals confirmed that crystallized SrPSII was active in transferring electrons from the OEC to the acceptor site of the reaction centre. However, SrPSII showed altered functional properties of its modified OEC in comparison with that of the CaPSII counterpart: slowdown of the Q(A)-to-Q(B) electron transfer and stabilized S(2)Q(A)(-) charge recombination. Crown Copyright (c) 2007 Published by Elsevier B.V All rights reserved.
引用
收藏
页码:404 / 413
页数:10
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