化学
双加氧酶
立体化学
铁
催化作用
部分
氧气输送
血红素
活动站点
酶
催化循环
氧化酶试验
氧化磷酸化
组氨酸
基质(水族馆)
加氧酶
氧气
酶催化
键裂
电子顺磁共振
铁质
氧气储存
氧化还原
光化学
蛋白质结构
构象变化
过氧化物酶
运动发酵单胞菌
作者
Daan Ren,Tai‐Ping Zhou,Jin Xiong,Xueli Hou,Yu‐Hsuan Lee,Jiahai Zhou,Yisong Guo,Binju Wang,Hung‐wen Liu
摘要
Abstract Domain of unknown function 4243 (DUF4243) family proteins are an emerging class of nonheme mononuclear iron enzymes characterized by a distinctive iron-binding motif comprised of four histidine (His) and one Nε-carboxylysine (Kcx) residue. Although predominantly found in fungi, OzmD is the only characterized bacterial member. OzmD catalyzes oxidative rearrangement of an aminopyridone ring into a 1,3-oxazine moiety with concomitant cyanide elimination in the final step of oxazinomycin biosynthesis. Herein, the X-ray crystal structure of OzmD is solved, demonstrating the presence of a conserved 4-His-1-Kcx iron-binding motif similar to other DUF4243 family proteins. Biochemical characterization using a substrate analog carrying a hydroxypyridone ring reveals that OzmD also exhibits intrinsic dioxygenase activity, catalyzing a transformation analogous to those of fungal DUF4243 dioxygenases. Electron paramagnetic resonance and Mössbauer spectroscopic characterization of MinCC, a functionally equivalent homologue of OzmD, reveals that the as-isolated protein predominantly contains ferric iron, which can be reduced to the ferrous state upon binding with either the native substrate or the hydroxy analog under anaerobic conditions. These findings support a unified mechanism in which catalysis begins with single-electron transfer from the substrate to ferric iron, enabling molecular oxygen activation and formation of an alkylperoxide intermediate. Overall reaction mechanisms for substrates bearing aminopyridone and hydroxypyridone rings are proposed based on chemical precedents and computational analyses. These findings reveal that OzmD employs a distinctive FeIII-dependent path for oxygen activation in contrast to the classical FeII-dependent route used by most oxygenases and establish a functional connection between bacterial and fungal DUF4243 enzymes.
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