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哈帕林多型生物碱生物合成早期结构多样化的分子和遗传基础。

Molecular and genetic basis for early stage structural diversifications in hapalindole-type alkaloid biogenesis.

作者信息

Zhu Qin, Liu Xinyu

机构信息

Department of Chemistry, University of Pittsburgh, 219 Parkman Avenue, Pittsburgh, PA 15260, USA.

出版信息

Chem Commun (Camb). 2017 Mar 2;53(19):2826-2829. doi: 10.1039/c7cc00782e.

Abstract

Heterologous expressions and purifications of all WelU proteins from the welwitindolinone pathways in Hapalosiphon welwitschii UTEX B1830 and IC-52-3 led to the discovery that WelU1 and WelU3 selectively assemble 12-epi-fischerindole U (2) and 12-epi-hapalindole C (1), respectively, from 3-geranyl 3-isocyanovinyl indolenine (4) via an enzymatic cascade featuring the Cope rearrangement, stereoselective aza-Prins cyclization and regioselective carbocation deposition. In combination with the in vitro characterization of WelU1/WelU3-homolog AmbU4 for the biogenesis of 12-epi-hapalindole U, this study provide a unified view on the origin of the early stage structural diversifications in hapalindole-type alkaloid biosynthesis, post common intermediate 4.

摘要

对来自韦氏鞘丝藻UTEX B1830和IC - 52 - 3的韦氏吲哚酮途径中所有WelU蛋白进行异源表达和纯化后发现,WelU1和WelU3分别通过一个具有Cope重排、立体选择性氮杂-Prins环化和区域选择性碳正离子沉积的酶促级联反应,从3 - 香叶基-3 - 异氰基乙烯基吲哚(4)选择性地组装12 - 表 - 费氏吲哚U(2)和12 - 表 - 哈帕林多吲哚C(1)。结合对WelU1/WelU3同源物AmbU4参与12 - 表 - 哈帕林多吲哚U生物合成的体外表征,本研究对哈帕林多型生物碱生物合成中共同中间体4之后早期结构多样化的起源提供了一个统一的观点。

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