Time and spectral resolved phosphorescence of singlet oxygen and pigments in photosystem II particles

被引:26
作者
Dedic, R
Svoboda, A
Psencík, J
Lupínková, L
Komenda, J
Hála, J
机构
[1] Charles Univ Prague, Fac Math & Phys, Dept Chem Phys & Opt, CZ-12116 Prague 2, Czech Republic
[2] Univ S Bohemia, Inst Biol Phys, CZ-37333 Nove Hrady, Czech Republic
[3] Acad Sci Czech Republic, Inst Microbiol, CZ-37981 Trebon, Czech Republic
关键词
singlet oxygen phosphorescence; triplet kinetics; photosystem II particles;
D O I
10.1016/S0022-2313(02)00524-0
中图分类号
O43 [光学];
学科分类号
070207 ; 0803 ;
摘要
Singlet oxygen generated via chlorophyll triplets in photosynthetic systems can destroy basic components of photosynthetic apparatus. In order to study this process a sensitive spectroscopic experimental set-up was built to detect both weak infrared (IR) chlorophyll phosphorescence (between 900 and 1000 nm) and singlet oxygen phosphorescence (at 1270 nm). The spectral and time resolution of the used monochromator and photon counting multiscaler are sufficient to provide two-dimensional matrix of temporally and spectrally resolved IR luminescence data. We have studied IR emission of photosystem 11 particles in D2O and H2O buffer including the effect of the sodium dodecyl sulphate (SDS) detergent. Both sub-microsecond lifetime of chlorophyll triplet states and microsecond lifetime of singlet oxygen were determined. The singlet oxygen lifetime in D2O (of 18 mus) was approximately five times longer than that in H2O, Quantum efficiency of singlet oxygen generation in photosystem 11 particles was significantly lower than that in chlorophyll a in acetone, however, it could be substantially increased by addition of SDS. (C) 2003 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:313 / 317
页数:5
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