The S1 to S2 and S2 to S3 state transitions in plant photosystem II: relevance to the functional and structural heterogeneity of the water oxidizing complex

被引:0
|
作者
Pavlou, Andrea [1 ]
Styring, Stenbjorn [1 ]
Mamedov, Fikret [1 ]
机构
[1] Uppsala Univ, Dept Chem Angstrom, Mol Biomimet, POB 523, S-75120 Uppsala, Sweden
关键词
Photosystem II; Water oxidation; S state transitions; Low spin S-2 state; High spin S-2 state; Temperature dependence; Electron paramagnetic resonance; OXYGEN-EVOLVING COMPLEX; ELECTRON-PARAMAGNETIC-RESONANCE; LIQUID-HELIUM TEMPERATURES; NEAR-INFRARED LIGHT; SUBSTRATE WATER; ALCOHOL BINDING; EPR SIGNALS; MN-CLUSTER; S-STATES; OXIDATION;
D O I
10.1007/s11120-024-01096-4
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
In Photosystem II, light-induced water splitting occurs via the S state cycle of the CaMn4O5-cluster. To understand the role of various possible conformations of the CaMn4O5-cluster in this process, the temperature dependence of the S-1 -> S-2 and S-2 -> S-3 state transitions, induced by saturating laser flashes, was studied in spinach photosystem II membrane preparations under different conditions. The S-1 -> S-2 transition temperature dependence was shown to be much dependent on the type of the cryoprotectant and presence of 3.5% methanol, resulting in the variation of transition half-inhibition temperature by 50 K. No similar effect was observed for the S-2 -> S-3 state transition, for which we also show that both the low spin g = 2.0 multiline and high spin g = 4.1 EPR configurations of the S-2 state advance with similar efficiency to the S-3 state, both showing a transition half-inhibition temperature of 240 K. This was further confirmed by following the appearance of the Split S-3 EPR signal. The results are discussed in relevance to the functional and structural heterogeneity of the water oxidizing complex intermediates in photosystem II.
引用
收藏
页码:401 / 411
页数:11
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