合成 α-苄基 L-谷氨酸的生物催化路线探究和酶筛选

P. Quaedflieg, Lisanne M. H. Jente, Monika Müller, Linda Vermote, Victor Plesciuc, Jan-Metske van der Laan, Lone Nielsen, Martin Schürmann
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引用次数: 0

摘要

我们在此报告了合成受保护氨基酸结构单元 α-苄基 L-谷氨酸的四种生物催化方法。我们对这些途径进行了筛选,以确定具有活性和选择性的酶,并在复试反应中确认了主要的命中物。在第一种方法中,N-Boc L-谷氨酸被蛋白酶 Alcalase 单苄基酯化,产率为 81%;在其他三种方法中,α,γ-二苄基 L-谷氨酸的生物催化 γ 选择性水解、α-苄基 L-谷氨酰胺的选择性酰胺水解以及α-苄基 L-焦谷氨酸的选择性内酰胺水解的产率高达 71%。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Biocatalytic route scouting and enzyme screening toward the synthesis of α-benzyl L-glutamate
We here report four biocatalytic approaches for the synthesis of the protected amino acid building block α-benzyl L-glutamate. Screenings of these routes to identify active and selective enzymes were conducted, and major hits were confirmed in retest reactions. In the first approach, N-Boc L-glutamic acid is mono-benzylesterified by the protease Alcalase with 81% yield; and in the other three approaches, a biocatalytic γ-selective hydrolysis of α,γ-dibenzyl L-glutamate, a selective amide hydrolysis of α-benzyl L-glutamine, and a selective lactam hydrolysis of alpha-benzyl L-pyroglutamate is performed with up to 71% yield.
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