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离子载体型聚醚类抗生素 lasalocid 的生物合成机制:聚醚骨架的酶法构建。

Biosynthetic machinery of ionophore polyether lasalocid: enzymatic construction of polyether skeleton.

机构信息

Division of Chemistry, Graduate School of Science, Hokkaido University, Sapporo 060-0810, Japan.

出版信息

Curr Opin Chem Biol. 2013 Aug;17(4):555-61. doi: 10.1016/j.cbpa.2013.06.004. Epub 2013 Jun 21.

Abstract

Diversity of natural polycyclic polyethers originated from very simple yet versatile strategy consisting of epoxidation of linear polyene followed by epoxide opening cascade. To understand two-step enzymatic transformations at molecular basis, a flavin containing monooxygenase (EPX) Lsd18 and an epoxide hydrolase (EH) Lsd19 were selected as model enzymes for extensive investigation on substrate specificity, catalytic mechanism, cofactor requirement and crystal structure. This pioneering study on prototypical lasalocid EPX and EH provides insight into detailed mechanism of ionophore polyether assembly machinery and clarified remaining issues for polyether biosynthesis.

摘要

天然多环聚醚的多样性源于非常简单但多功能的策略,包括线性多烯的环氧化,然后是环氧化物开环级联。为了从分子基础上理解两步酶促转化,选择了一种含有黄素的单加氧酶 (EPX) Lsd18 和一种环氧化物水解酶 (EH) Lsd19 作为模型酶,对底物特异性、催化机制、辅因子要求和晶体结构进行了广泛研究。这项关于原型 lasalocid EPX 和 EH 的开创性研究深入了解了离子载体聚醚组装机制的详细机制,并澄清了聚醚生物合成中剩余的问题。

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