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Structural consequences of ammonia binding to the manganese center of the photosynthetic oxygen-evolving complex: an X-ray absorption spectroscopy study of isotropic and oriented photosystem II particles.

机译:氨结合到光合作用的放氧复合物的锰中心的结构后果:各向同性和定向光系统II粒子的X射线吸收光谱研究。

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摘要

The structure and orientation of the manganese complex in NH3-treated photosystem II (PS II) membrane particles of spinach are being studied by X-ray absorption spectroscopy. On the basis of earlier work by our group, a structure for the tetranuclear manganese complex of PS II, which consists of two di-mu-oxo-bridged binuclear Mn units linked by a mono-mu-oxo group, has been proposed [Yachandra, V. K., et al. (1993) Science 260, 675-679]. The extended X-ray absorption fine structure (EXAFS) of the complex modified by NH3 binding in the S2-state is suggestive of an increase in the Mn-Mn distance of one of these units from 2.72 +/- 0.02 to 2.87 +/- 0.02 A, whereas the Mn-Mn distance of the second unit seems to be unaffected by NH3 treatment. The elongation of one binuclear center could result from the replacement of one bridging mu-oxo by an amido group. The lengthening of one Mn-Mn distance means that, by NH3 treatment, the distance degeneracy of the 2.7 A Mn-Mn EXAFS interaction is removed. Consequently, the orientation of individual binuclear units with respect to the membrane normal becomes resolvable by EXAFS spectroscopy of partially oriented PS II membrane particles. The angle between the normal of the PS II-containing membrane and the Mn-Mn vector is determined to be 67 degrees +/- 3 degrees for the 2.87 A distance and 55 degrees +/- 4 degrees for the 2.72 A distance. Only small effects on position, shape, and orientation dependence of Mn K-edge spectra result from NH3 treatment, indicating that the Mn oxidation state, the symmetry of the Mn ligand environment, and the orientation of the complex remain essentially unaffected in the annealed NH3 S2-state. Therefore, it seems likely that the angles determined for the ammonia-modified manganese complex are similar to the respective angles of the untreated complex. The structure of the manganese complex and its orientation in the membrane are discussed.
机译:X射线吸收光谱研究了NH3处理的菠菜膜系统II(PS II)膜颗粒中锰配合物的结构和取向。根据我们小组的早期工作,已提出了PS II的四核锰配合物的结构,该结构由两个通过单mu-氧代基团连接的二-mu-氧代桥联的双核Mn单元组成[Yachandra ,VK等。 (1993)Science 260,675-679]。在S2状态下,NH3结合修饰的复合物的扩展X射线吸收精细结构(EXAFS)表明这些单元之一的Mn-Mn距离从2.72 +/- 0.02增加到2.87 +/- 0.02 A,而第二个单元的Mn-Mn距离似乎不受NH3处理的影响。一个双核中心的延长可能是由一个酰胺基取代了一个桥接的mu-oxo。一个Mn-Mn距离的延长意味着通过NH3处理,可以消除2.7 A Mn-Mn EXAFS相互作用的距离简并性。因此,通过部分取向的PS II膜颗粒的EXAFS光谱,可以分辨单个双核单元相对于膜法线的取向。包含PS II的膜的法线与Mn-Mn向量之间的角度对于2.87 A距离确定为67度+/- 3度,对于2.72 A距离确定为55度+/- 4度。 NH3处理仅对Mn K边缘光谱的位置,形状和取向依赖性产生很小的影响,表明在退火的NH3中Mn的氧化态,Mn配体环境的对称性和配合物的取向基本上保持不变S2状态。因此,对于氨改性的锰络合物确定的角度似乎与未处理的络合物的各个角度相似。讨论了锰配合物的结构及其在膜中的取向。

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