Dasgupta Jyotishman, Ananyev Gennady M, Dismukes G Charles
306 Lewis Hall, Department of Chemistry, University of California, Berkeley, CA 94709, USA.
Coord Chem Rev. 2008 Feb;252(3-4):347-360. doi: 10.1016/j.ccr.2007.08.022.
The light-driven steps in the biogenesis and repair of the inorganic core comprising the O(2)-evolving center of oxygenic photosynthesis (photosystem II water-oxidation complex, PSII-WOC) are reviewed. These steps, known collectively as photoactivation, involve the photoassembly of the free inorganic cofactors to the cofactor-depleted PSII-(apo-WOC) driven by light and produce the active O(2)-evolving core comprised of Mn(4)CaO(x)Cl(y). We focus on the functional role of the inorganic components as seen through the competition with non-native cofactors ("inorganic mutants") on water oxidation activity, the rate of the photoassembly reaction, and on structural insights gained from EPR spectroscopy of trapped intermediates formed in the initial steps of the assembly reaction. A chemical mechanism for the initial steps in photoactivation is given that is based on these data. Photoactivation experiments offer the powerful insights gained from replacement of the native cofactors, which together with the recent X-ray structural data for the resting holoenzyme provide a deeper understanding of the chemistry of water oxidation. We also review some new directions in research that photoactivation studies have inspired that look at the evolutionary history of this remarkable catalyst.
本文综述了光合放氧中心(光系统II水氧化复合物,PSII-WOC)无机核心生物合成和修复过程中的光驱动步骤。这些步骤统称为光激活,涉及在光驱动下将游离无机辅因子光组装到辅因子耗尽的PSII(脱辅基WOC)上,并产生由Mn(4)CaO(x)Cl(y)组成的活性放氧核心。我们关注无机成分的功能作用,这可以通过与非天然辅因子(“无机突变体”)在水氧化活性、光组装反应速率方面的竞争以及从组装反应初始步骤中形成的捕获中间体的EPR光谱获得的结构见解来体现。基于这些数据给出了光激活初始步骤的化学机制。光激活实验提供了通过替换天然辅因子获得的有力见解,这些见解与静止全酶的最新X射线结构数据一起,能更深入地理解水氧化的化学过程。我们还综述了光激活研究激发的一些新研究方向,这些研究着眼于这种非凡催化剂的进化历史。