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首页> 外文期刊>Angewandte Chemie >E. coli Nickel-Iron Hydrogenase 1 Catalyses Non-native Reduction of Flavins: Demonstration for Alkene Hydrogenation by Old Yellow Enzyme Ene-reductases**
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E. coli Nickel-Iron Hydrogenase 1 Catalyses Non-native Reduction of Flavins: Demonstration for Alkene Hydrogenation by Old Yellow Enzyme Ene-reductases**

机译:大肠杆菌镍 - 铁氢酶1催化黄酮的非天然还原:通过旧黄色酶烯烯烯烃的烯烃氢化的演示**

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摘要

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-2 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 degrees C) and extended reaction times. The utility of this system as a simple, easy to implement FMNH2 or FADH(2) 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(-1) and total turnover numbers up to 20 200 were recorded during flavin recycling.
机译:本文报道了一种新的大肠杆菌(Hyd1)摄取氢化酶1的活性。利用H-2作为简单、完全原子经济的还原剂,可直接还原生物黄素辅因子FMN和FAD。Hyd1的强大特性可用于在广泛的温度范围(25-70摄氏度)和延长的反应时间内减少黄素。该系统作为一个简单、易于实现的FMNH2或FADH(2)再生系统的实用性,然后通过向旧的黄色酶“烯还原酶”提供还原黄素来证明,以支持高达100%转化率的不对称烯烃还原。在黄素回收过程中,记录的Hyd1周转频率高达20.4分钟(-1),总周转次数高达20 200次。

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