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来自光系统II中放氧复合体S0态的振荡锰电子顺磁共振信号。

An oscillating manganese electron paramagnetic resonance signal from the S0 state of the oxygen evolving complex in photosystem II.

作者信息

Ahrling K A, Peterson S, Styring S

机构信息

Department of Biochemistry, Center for Chemistry and Chemical Engineering, Lund University, Sweden.

出版信息

Biochemistry. 1997 Oct 28;36(43):13148-52. doi: 10.1021/bi971815w.

Abstract

Photosynthesis produces the oxygen necessary for all aerobic life. During this process, the manganese-containing oxygen evolving complex (OEC) in photosystem II (PSII), cycles through five oxidation states, S0-S4. One of these, S2, is known to be paramagnetic and gives rise to electron paramagnetic resonance (EPR) signals used to probe the catalytic structure and function of the OEC. The S0 states has long been thought to be paramagnetic. We report here a Mn EPR signal from the previously EPR invisible S0 state. The new signal oscillates with a period of four, indicating that it originates from fully active PSII centers. Although similar to the S2 state multiline signal, the new signal is wider (2200 gauss compared with 1850 gauss in samples produced by flashing), with different peak intensity and separation (82 gauss compared with 89 gauss). These characteristics are consistent with the S0 state EPR signal arising from a coupled MnII-MnIII intermediate. The new signal is more stable than the S2 state signal and its decay in tens of minutes is indicative of it originating from the S0 state. The S0 state signal will provide invaluable information toward the understanding of oxygen evolution in plants.

摘要

光合作用产生所有需氧生命所必需的氧气。在此过程中,光系统II(PSII)中含锰的放氧复合体(OEC)会经历S0 - S4这五种氧化态循环。其中之一的S2态已知具有顺磁性,并产生用于探测OEC催化结构和功能的电子顺磁共振(EPR)信号。长期以来,人们一直认为S0态具有顺磁性。我们在此报告了一种来自先前EPR不可见的S0态的锰EPR信号。新信号以四周期振荡,表明它源自完全活跃的PSII中心。尽管新信号与S2态多线信号相似,但新信号更宽(2200高斯,而闪光产生的样品中为1850高斯),具有不同的峰值强度和间距(82高斯,而闪光产生的样品中为89高斯)。这些特征与由耦合的MnII - MnIII中间体产生的S0态EPR信号一致。新信号比S2态信号更稳定,其在数十分钟内的衰减表明它源自S0态。S0态信号将为理解植物中的氧气释放提供宝贵信息。

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