| Literature DB >> 24301580 |
C W Hoganson1, N Lydakis-Simantiris, X S Tang, C Tommos, K Warncke, G T Babcock, B A Diner, J McCracken, S Styring.
Abstract
Recent magnetic-resonance work on YŻ suggests that this species exhibits considerable motional flexibility in its functional site and that its phenol oxygen is not involved in a well-ordered hydrogen-bond interaction (Tang et al., submitted; Tommos et al., in press). Both of these observations are inconsistent with a simple electron-transfer function for this radical in photosynthetic water oxidation. By considering the roles of catalytically active amino acid radicals in other enzymes and recent data on the water-oxidation process in Photosystem II, we rationalize these observations by suggesting that YŻ functions to abstract hydrogen atoms from aquo- and hydroxy-bound managanese ions in the (Mn)4 cluster on each S-state transition. The hydrogen-atom abstraction process may occur either by sequential or concerted kinetic pathways. Within this model, the (Mn)4/YZ center forms a single catalytic center that comprises the Oxygen Evolving Complex in Photosystem II.Entities:
Year: 1995 PMID: 24301580 DOI: 10.1007/BF00020428
Source DB: PubMed Journal: Photosynth Res ISSN: 0166-8595 Impact factor: 3.573