Leibniz-Institute of Plant Biochemistry, Department of Bioorganic Chemistry, Weinberg 3, D-06120 Halle, Germany.
Curr Opin Chem Biol. 2013 Apr;17(2):229-35. doi: 10.1016/j.cbpa.2013.02.016. Epub 2013 Mar 18.
Chemospecific and regiospecific modifications of natural products by methyl, prenyl, or C-glycosyl moieties are a challenging and cumbersome task in organic synthesis. Because of the availability of an increasing number of stable and selective transferases and cofactor regeneration processes, enzyme-assisted strategies turn out to be promising alternatives to classical synthesis. Two categories of alkylating enzymes become increasingly relevant for applications: firstly prenyltransferases and terpene synthases (including terpene cyclases), which are used in the production of terpenoids such as artemisinin, or meroterpenoids like alkylated phenolics and indoles, and secondly methyltransferases, which modify flavonoids and alkaloids to yield products with a specific methylation pattern such as 7-O-methylaromadendrin and scopolamine.
通过甲基、异戊烯基或 C-糖基部分对天然产物进行化学特异性和区域特异性修饰,在有机合成中是一项具有挑战性且繁琐的任务。由于越来越多的稳定和选择性转移酶以及辅酶再生过程的出现,酶辅助策略成为经典合成的有前途的替代方法。两类烷基化酶在应用中变得越来越重要:首先是异戊烯基转移酶和萜烯合酶(包括萜烯环化酶),它们用于生产青蒿素等萜类化合物或倍半萜类化合物,如烷基化酚类和吲哚类化合物,其次是甲基转移酶,它修饰类黄酮和生物碱,生成具有特定甲基化模式的产物,如 7-O-甲基莪术二酮和东莨菪碱。