School of Biosciences, Cardiff University, Museum Avenue, Cardiff CF10 3AX, UK.
Department of Chemistry, School of Natural Sciences, The University of Manchester, Oxford Road, Manchester M13 9PL, UK.
J Photochem Photobiol B. 2024 Aug;257:112946. doi: 10.1016/j.jphotobiol.2024.112946. Epub 2024 May 29.
The deprotonation of O6 within the S state marks the final deprotonation event before the formation of oxygen‑oxygen bond interactions and eventual production and release of dioxygen. Gaining a thorough understanding of this event, from the proton acceptors involved, to the exfiltration pathways available, is key in determining the nature of the resulting oxygen species, influencing the mechanism through which the first oxygen‑oxygen bond forms. Computational analysis, using BS-DFT methodologies, showed that proton abstraction by the local Glu189 residue provides consistent evidence against this being a viable mechanistic pathway due to the lack of a stable product structure. In contrast, abstraction via W3 shows an increasingly stable oxo-oxo product state between r[O5O6] = 2.1 Å & 1.9 Å. The resulting oxo-oxo state is stabilised through donation of β electron character from O6 to Mn1 and α electron character from O6 to O5. This donation from the O6 lone pair is shown to be a key factor in stabilising the oxo-oxo state, in addition to showing the initiation of first O5-O6 bond.
O6 的去质子化标志着 S 态形成氧氧键相互作用以及最终产生和释放氧气之前的最后一个去质子化事件。深入了解这一事件,包括涉及的质子受体和可用的渗出途径,对于确定生成氧物种的性质、影响第一个氧氧键形成的机制至关重要。使用 BS-DFT 方法的计算分析表明,由于缺乏稳定的产物结构,局部 Glu189 残基的质子提取提供了一致的证据,表明这不是可行的机制途径。相比之下,通过 W3 进行的提取显示在 r[O5O6] = 2.1 Å 和 1.9 Å 之间,氧-氧产物状态越来越稳定。生成的氧-氧状态通过 O6 向 Mn1 的 β 电子特征和 O6 向 O5 的 α 电子特征的捐赠而稳定。这种来自 O6 孤对电子的捐赠被证明是稳定氧-氧状态的关键因素,除了显示第一个 O5-O6 键的启动。