Messinger J, Robblee J H, Bergmann U, Fernandez C, Glatzel P, Visser H, Cinco R M, McFarlane K L, Bellacchio E, Pizarro S A, Cramer S P, Sauer K, Klein M P, Yachandra V K
Melvin Calvin Laboratory, Physical Biosciences Division, Lawrence Berkeley National Laboratory, Berkeley, California 94720, USA.
J Am Chem Soc. 2001 Aug 15;123(32):7804-20. doi: 10.1021/ja004307+.
A key question for the understanding of photosynthetic water oxidation is whether the four oxidizing equivalents necessary to oxidize water to dioxygen are accumulated on the four Mn ions of the oxygen-evolving complex (OEC), or whether some ligand-centered oxidations take place before the formation and release of dioxygen during the S(3) --> [S(4)] --> S(0) transition. Progress in instrumentation and flash sample preparation allowed us to apply Mn Kbeta X-ray emission spectroscopy (Kbeta XES) to this problem for the first time. The Kbeta XES results, in combination with Mn X-ray absorption near-edge structure (XANES) and electron paramagnetic resonance (EPR) data obtained from the same set of samples, show that the S(2) --> S(3) transition, in contrast to the S(0) --> S(1) and S(1) --> S(2) transitions, does not involve a Mn-centered oxidation. On the basis of new structural data from the S(3)-state, manganese mu-oxo bridge radical formation is proposed for the S(2) --> S(3) transition, and three possible mechanisms for the O-O bond formation are presented.
理解光合水氧化的一个关键问题是,将水氧化为二氧所需的四个氧化当量是积累在放氧复合体(OEC)的四个锰离子上,还是在S(3)→[S(4)]→S(0)转变过程中,在二氧形成和释放之前发生了一些以配体为中心的氧化反应。仪器设备和闪光样品制备技术的进步使我们首次能够将锰Kβ X射线发射光谱(Kβ XES)应用于这个问题。Kβ XES结果,结合从同一组样品获得的锰X射线吸收近边结构(XANES)和电子顺磁共振(EPR)数据,表明与S(0)→S(1)和S(1)→S(2)转变不同,S(2)→S(3)转变不涉及以锰为中心的氧化反应。基于S(3)态的新结构数据,提出了S(2)→S(3)转变过程中锰μ-氧桥自由基的形成,并给出了O-O键形成的三种可能机制。