Mechanism of Water Delivery to the Active Site of Photosystem II along the S2 to S3 Transition

被引:85
作者
Capone, Matteo [1 ]
Narzi, Daniele [2 ]
Bovi, Daniele [2 ]
Guidoni, Leonardo [2 ]
机构
[1] Univ Roma La Sapienza, Dipartmento Chim, I-00185 Rome, Italy
[2] Univ Aquila, Dipartimento Sci Fis & Chim, I-67100 Laquila, Italy
来源
JOURNAL OF PHYSICAL CHEMISTRY LETTERS | 2016年 / 7卷 / 03期
基金
欧洲研究理事会;
关键词
OXYGEN-EVOLVING COMPLEX; O BOND FORMATION; SUBSTRATE-WATER; MANGANESE COMPLEX; RESOLUTION; EXCHANGE; STATE; OXIDATION; PATHWAYS; DYNAMICS;
D O I
10.1021/acs.jpclett.5b02851
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The two water molecules serving as substrate for the oxygen evolution in Photosystem II are already bound in the S-2 state of the Kok-Joliot's cycle. Nevertheless, an additional water molecule is supposed to bind the duster during the transition between the S-2 and S-3 states, which has been recently revealed to have the Mn4CaO5 catalytic cluster arranged in an open cubane fashion. In this Letter, by means of ab initio calculations, we investigated the possible pathways for the binding of the upcoming water molecule. Upon the four different possibilities checked in our calculations, the binding of the crystallographic water molecule, originally located nearby the Cl- binding site, showed the lowest activation energy barrier. Our findings therefore support the view in which the W2 hydroxyl group and the O5 oxygen act as substrates for the oxygen evolution. Within this framework the role of the open and closed Mn4CaO5 conformers is clarified as well as the exact mechanistic events occurring along the S-2 to S-3 transition.
引用
收藏
页码:592 / 596
页数:5
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