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首页> 外文期刊>Science >Crystal Structure of Pentalenene Synthase: Mechanistic Insights on Terpenoid Cyclization Reactions in Biology
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Crystal Structure of Pentalenene Synthase: Mechanistic Insights on Terpenoid Cyclization Reactions in Biology

机译:戊烯合酶的晶体结构:生物萜类环化反应的机理见解。

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The crystal structure of pentalenene synthase at 2.6 angstrom resolution reveals critical active site features responsible for the cyclization of famesyl diphosphate into the tricyclic hydrocarbon pentalenene. Metal-triggered substrate ionization initiates catalysis, and the α-barrel active site serves as a template to channel and stabilize the conformations of reactive carbocation intermediates through a complex cyclization cascade. The core active site structure of the enzyme may be preserved among the greater family of terpenoid synthases, possibly implying divergence from a common ancestral synthase to satisfy biological requirements for increasingly diverse natural products.
机译:戊烯烯合酶在2.6埃分辨率下的晶体结构揭示了关键的活性位点特征,这些特征是将法美基二磷酸环化为三环烃戊烯中的责任。金属触发的底物电离可引发催化作用,而α-桶活性位点可作为模板,通过复杂的环化级联作用引导并稳定反应性碳正离子中间体的构象。该酶的核心活性位点结构可以保留在较大的萜类合酶家族中,这可能暗示与普通祖先合酶有差异,以满足日益多样化的天然产物的生物学需求。

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