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Anthrol还原酶:发现、在生物合成中的作用及在天然产物合成中的应用

Anthrol reductases: discovery, role in biosynthesis and applications in natural product syntheses.

作者信息

Rajput Anshul, Manna Tanaya, Husain Syed Masood

机构信息

Department of Biological and Synthetic Chemistry, Centre of Biomedical Research, SGPGIMS Campus, Raebareli Road, Lucknow 226014, India.

出版信息

Nat Prod Rep. 2023 Oct 18;40(10):1672-1686. doi: 10.1039/d3np00027c.

Abstract

Covering: up to 2023Short-chain dehydrogenase/reductases (SDR) are known to catalyze the regio- and stereoselective reduction of a variety of substrate types. Investigations of the deoxygenation of emodin to chrysophanol has led to the discovery of the anthrol reductase activity of an SDR, MdpC involved in monodictyphenone biosynthesis of and provided access to ()-dihydroanthracenone, a putative biosynthetic intermediate. This facilitated the identification of several MdpC-related enzymes involved in the biosynthesis of aflatoxins B1, cladofulvin, neosartorin, agnestins and bisanthraquinones. Because of their ability to catalyze the reduction of hydroanthraquinone (anthrols) using NADPH, they were named anthrol reductases. This review provides a comprehensive summary of all the anthrol reductases that have been identified and characterized in the last decade along with their role in the biosynthesis of natural products. In addition, the applications of these enzymes towards the chemoenzymatic synthesis of flavoskyrins, modified bisanthraquinones, 3-deoxy anthraquinones, chiral cycloketones and β-halohydrins have been discussed.

摘要

涵盖范围

截至2023年

已知短链脱氢酶/还原酶(SDR)可催化多种底物类型的区域选择性和立体选择性还原反应。对大黄素脱氧生成大黄酚的研究导致发现了一种参与单隔孢菌素生物合成的SDR(MdpC)的蒽酚还原酶活性,并获得了一种假定的生物合成中间体(±)-二氢蒽酮。这有助于鉴定几种与MdpC相关的酶,它们参与黄曲霉毒素B1、枝孢菌素、新萨托菌素、阿格奈斯汀和双蒽醌的生物合成。由于它们能够利用NADPH催化氢化蒽醌(蒽酚)的还原反应,因此被命名为蒽酚还原酶。本综述全面总结了过去十年中已鉴定和表征的所有蒽酚还原酶及其在天然产物生物合成中的作用。此外,还讨论了这些酶在黄酮斯基林、修饰双蒽醌、3-脱氧蒽醌、手性环酮和β-卤代醇的化学酶促合成中的应用。

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