Functional and structural study on chelator-induced suppression of S2/S1 FTIR spectrum in photosynthetic oxygen-evolving complex

被引:7
作者
Kimura, Y [1 ]
Ono, T [1 ]
机构
[1] Inst Phys & Chem Res, Riken Photodynam Res Ctr, Lab Photobiol 1, Aoba Ku, Sendai, Miyagi 9800845, Japan
关键词
FTIR; chelator; oxygen evolution; calcium; carboxylate;
D O I
10.1016/S0162-0134(03)00282-4
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
Chelating agents have been shown to induce characteristic changes in the light-minus-dark Fourier transform infrared (FTIR) difference spectrum for the S-2/S-1 difference in the oxygen-evolving complex (OEC). Addition of various ethylenediamine-N,N,N',N'-tetraacetic acid (EDTA)-type chelators, such as EDTA, O,O'-bis(2-aminoethyl)ethyleneglycol-N,N,N',N'-tetraacetic acid (EGTA), trans-1,2-diaminocyclohexane-N,N,N',N'-tetraacetic acid (CyDTA), or N-(2-hydroxyethyl)ethylenediamine-N,N',N'-triacetic acid (HEDTA), to Ca2+-depleted PS 11 membranes resulted in the suppression of typical S-2/S-1, vibrational features, including the symmetric (1365(+)/1404(-) cm(-1)) and the asymmetric (1587(+)/1566(-) cm(-1)) carboxylate stretching vibrations, as well as the amide I and 11 modes of the backbone polypeptides. In contrast, the addition of ethylenediamine-N,N'-diacetic acid (EDDA) showed less inhibitory effects. The effects of the chelators depended on the number of the carboxylate groups; chelators with more than two carboxymethyl groups were effective in altering the FTIR spectrum. The bridging structure that connects the two nitrogen atoms also influenced the inhibitory effects. However. the effects were not necessarily correlated with the stability constants of the chelators to Mn2+. The vibrational modes that were suppressed by EDTA were almost completely restored by subsequent washing with Chelex-treated Ca2+-free buffer medium, indicating that the spectral changes are attributable to the reversible association of chelators with the Ca2+-depleted OEC. Nevertheless, prolonged incubation with chelators led to the impairment of the O-2-evolving capability, with differences in the effectiveness, in the order that is consistent with that for the suppression effects on FTIR spectra. Chelators with carboxylate and/or carboxymethyl groups bound to a single nitrogen [nitrilotri acetic acid (NTA) and iminodiacetic acid (IDA)] or carbon (citric acid) were relatively ineffective for the suppression. A chelator that includes four phosphate groups, ethylenediamine-N,N,N',N'-tetrakis(methylenephosphonic) acid (EDTPO), also showed suppression effects on both the carboxylate and amide modes. Based on these findings, a possible mode of interaction between the chelators and the Mn cluster is discussed. (C) 2003 Elsevier Inc. All rights reserved.
引用
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页码:231 / 239
页数:9
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