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一种通过原位UDP-葡萄糖循环高效化学酶法生产小分子糖苷的方法。

An efficient chemoenzymatic production of small molecule glucosides with in situ UDP-glucose recycling.

作者信息

Masada Sayaka, Kawase Yoji, Nagatoshi Mai, Oguchi Yukie, Terasaka Kazuyoshi, Mizukami Hajime

机构信息

Department of Pharmacognosy, Graduate School of Pharmaceutical Sciences, Nagoya City University, Nagoya 467-8603, Japan.

出版信息

FEBS Lett. 2007 May 29;581(13):2562-6. doi: 10.1016/j.febslet.2007.04.074. Epub 2007 May 8.

Abstract

A one-pot system for efficient enzymatic synthesis of curcumin glucosides is described. The method couples the activities of two recombinant enzymes, UDP-glucose: curcumin glucosyltransferase from Catharanthus roseus (CaUGT2) and sucrose synthase from Arabidopsis thaliana (AtSUS1). UDP, a product inhibitor of UDP-glucosyltransferase, was removed from the system and used for regeneration of UDP-glucose by the second enzyme, AtSUS1. The productivity was increased several-fold and UDP-glucose initially added to the reaction mixture could be reduced to one-tenth of the normal level. The concept of enhancing glucosylation efficiency by coupling a UDP-glucose regeneration system with glucosyltransferases should be applicable to enzymatic production of a wide range of glucosides.

摘要

本文描述了一种用于高效酶促合成姜黄素葡萄糖苷的一锅法系统。该方法结合了两种重组酶的活性,即来自长春花的UDP-葡萄糖:姜黄素葡萄糖基转移酶(CaUGT2)和来自拟南芥的蔗糖合酶(AtSUS1)。UDP是UDP-葡萄糖基转移酶的产物抑制剂,被从系统中去除,并被第二种酶AtSUS1用于UDP-葡萄糖的再生。生产率提高了几倍,最初添加到反应混合物中的UDP-葡萄糖可以减少到正常水平的十分之一。通过将UDP-葡萄糖再生系统与葡萄糖基转移酶相结合来提高糖基化效率的概念应该适用于多种糖苷的酶促生产。

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