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大肠杆菌镍铁氢化酶 1 可催化非天然黄素还原:通过老黄酶 Ene-还原酶证明烯烃加氢反应*。

E. coli Nickel-Iron Hydrogenase 1 Catalyses Non-native Reduction of Flavins: Demonstration for Alkene Hydrogenation by Old Yellow Enzyme Ene-reductases*.

机构信息

Department of Chemistry, University of Oxford, Inorganic Chemistry Laboratory, South Parks Rd, Oxford, OX1 3QR, United Kingdom.

Department of Biotechnology, Delft University of Technology, Van der Maasweg 9, 2629, HZ, Delft, The Netherlands.

出版信息

Angew Chem Int Ed Engl. 2021 Jun 14;60(25):13824-13828. doi: 10.1002/anie.202101186. Epub 2021 May 11.

Abstract

A new activity for the [NiFe] uptake hydrogenase 1 of Escherichia coli (Hyd1) is presented. Direct reduction of biological flavin cofactors FMN and FAD is achieved using H as a simple, completely atom-economical reductant. The robust nature of Hyd1 is exploited for flavin reduction across a broad range of temperatures (25-70 °C) and extended reaction times. The utility of this system as a simple, easy to implement FMNH or FADH regenerating system is then demonstrated by supplying reduced flavin to Old Yellow Enzyme "ene-reductases" to support asymmetric alkene reductions with up to 100 % conversion. Hyd1 turnover frequencies up to 20.4 min and total turnover numbers up to 20 200 were recorded during flavin recycling.

摘要

本文介绍了一种新的活性

大肠杆菌[NiFe]摄取氢化酶 1(Hyd1)。使用 H 作为一种简单、完全原子经济的还原剂,直接还原生物黄素辅因子 FMN 和 FAD。Hyd1 的稳健性被利用来在广泛的温度(25-70°C)和延长的反应时间范围内进行黄素还原。通过向 Old Yellow Enzyme“ene-还原酶”提供还原型黄素,该系统作为一种简单、易于实施的 FMNH 或 FADH 再生系统的实用性得到了证明,支持不对称烯烃还原,转化率高达 100%。在黄素循环过程中,Hyd1 的周转率高达 20.4 min-1,总周转率高达 20 200。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4c9e/8252551/b37c39656ef2/ANIE-60-13824-g007.jpg

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