Leys David, Scrutton Nigel S
SYNBIOCHEM, Manchester Institute of Biotechnology, School of Chemistry, The University of Manchester, Manchester M1 7DN, United Kingdom.
Curr Opin Struct Biol. 2016 Dec;41:19-26. doi: 10.1016/j.sbi.2016.05.014. Epub 2016 Jun 3.
Flavins are arguably one of the most versatile cofactors by virtue of the reactivity of the isoalloxazine ring system. A varied catalogue of reactions for the diverse family of flavoenzymes has been reported, leading to unifying concepts in (long-range) electron transfer, oxygen activation, photochemistry and substrate redox reactions. Recent examples of unprecedented flavin chemistry have been reported that uncover hidden depths of the flavoenzyme chemical repertoire. These include ring expansion of flavin through prenylation and formation of the superoxidized flavin-N5 oxide species. These and other new flavin based species are reviewed here and suggest further exciting discoveries await the flavoenzymology field.
鉴于异咯嗪环系统的反应活性,黄素可以说是用途最为广泛的辅因子之一。已报道了各种黄素酶的一系列不同反应,从而形成了(远距离)电子转移、氧活化、光化学和底物氧化还原反应的统一概念。最近报道了前所未有的黄素化学实例,揭示了黄素酶化学库中隐藏的深度。这些实例包括通过异戊烯基化使黄素发生环扩张以及形成超氧化黄素 - N5氧化物物种。本文对这些以及其他基于黄素的新物种进行了综述,并表明黄素酶学领域还会有更多令人兴奋的发现。