Micalis Institute, INRA, ChemSyBio, AgroParisTech, Université Paris-Saclay, Jouy-en-Josas, France.
Photochem Photobiol. 2017 Jan;93(1):67-77. doi: 10.1111/php.12702. Epub 2017 Jan 27.
Radical S-adenosyl-L-methionine (SAM) enzymes have emerged as one of the last superfamilies of enzymes discovered to date. Arguably, it is the most versatile group of enzymes involved in at least 85 biochemical transformations. One of the founding members of this enzyme superfamily is the spore photoproduct (SP) lyase, a DNA repair enzyme catalyzing the direct reversal repair of a unique DNA lesion, the so-called spore photoproduct, back into two thymidine residues. Discovered more than 20 years ago in the bacterium Bacillus subtilis, SP lyase has been shown to be widespread in the endospore-forming Firmicutes from the Bacilli and Clostridia classes and to use radical-based chemistry to perform C-C bond breakage, a chemically challenging reaction. This review describes how the work on SP lyase has illuminated a unique strategy for DNA repair and provided major advances in our understanding of the emerging radical SAM superfamily of enzymes, from a biochemical and structural perspective.
激进的 S-腺苷-L-蛋氨酸(SAM)酶已成为迄今为止发现的最后一组超级酶家族之一。可以说,它是涉及至少 85 种生化转化的最通用的酶类之一。该酶超家族的创始成员之一是孢子光产物(SP)裂合酶,这是一种 DNA 修复酶,可催化将独特的 DNA 损伤,即所谓的孢子光产物,直接逆转修复为两个胸腺嘧啶残基。SP 裂合酶在芽孢杆菌属的细菌枯草芽孢杆菌中发现 20 多年来,已被证明广泛存在于芽孢形成的厚壁菌门的芽孢杆菌和梭菌目中,并且利用基于自由基的化学来进行 C-C 键断裂,这是一种具有挑战性的化学反应。这篇综述描述了 SP 裂合酶的工作如何阐明了一种独特的 DNA 修复策略,并从生化和结构的角度提供了对新兴的自由基 SAM 超家族酶的理解的重大进展。