An oxyl/oxo mechanism for oxygen-oxygen coupling in PSII revealed by an x-ray free-electron laser.
Michihiro SugaFusamichi AkitaKeitaro YamashitaYoshiki NakajimaGo UenoHongjie LiTakahiro YamaneKunio HirataYasufumi UmenaShinichiro YonekuraLong-Jiang YuHironori MurakamiTakashi NomuraTetsunari KimuraMinoru KuboSeiki BabaTakashi KumasakaKensure TonoMakina YabashiHiroshi IsobeKizashi YamaguchiMasaki YamamotoHideo AgoJian Ren ShenPublished in: Science (New York, N.Y.) (2019)
Photosynthetic water oxidation is catalyzed by the Mn4CaO5 cluster of photosystem II (PSII) with linear progression through five S-state intermediates (S0 to S4). To reveal the mechanism of water oxidation, we analyzed structures of PSII in the S1, S2, and S3 states by x-ray free-electron laser serial crystallography. No insertion of water was found in S2, but flipping of D1 Glu189 upon transition to S3 leads to the opening of a water channel and provides a space for incorporation of an additional oxygen ligand, resulting in an open cubane Mn4CaO6 cluster with an oxyl/oxo bridge. Structural changes of PSII between the different S states reveal cooperative action of substrate water access, proton release, and dioxygen formation in photosynthetic water oxidation.