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作为氧化剂的S-腺苷甲硫氨酸:自由基SAM超家族

S-adenosylmethionine as an oxidant: the radical SAM superfamily.

作者信息

Wang Susan C, Frey Perry A

机构信息

Department of Biochemistry, University of Wisconsin-Madison, 1710 University Avenue, Madison, WI 53726, USA.

出版信息

Trends Biochem Sci. 2007 Mar;32(3):101-10. doi: 10.1016/j.tibs.2007.01.002. Epub 2007 Feb 8.

Abstract

A recently discovered superfamily of enzymes function using chemically novel mechanisms, in which S-adenosylmethionine (SAM) serves as an oxidizing agent in DNA repair and the biosynthesis of vitamins, coenzymes and antibiotics. Members of this superfamily, the radical SAM enzymes, are related by the cysteine motif CxxxCxxC, which nucleates the [4Fe-4S] cluster found in each. A common thread in the novel chemistry of these proteins is the use of a strong reducing agent--a low-potential 4Fe-4S cluster--to generate a powerful oxidizing agent, the 5'-deoxyadenosyl radical, from SAM. Recent results are beginning to determine the unique biochemistry for some of the radical SAM enzymes, for example, lysine 2,3 aminomutase, pyruvate formate lyase activase and biotin synthase.

摘要

最近发现的一个酶超家族利用化学新机制发挥作用,其中S-腺苷甲硫氨酸(SAM)在DNA修复以及维生素、辅酶和抗生素的生物合成中充当氧化剂。这个超家族的成员,即自由基SAM酶,通过半胱氨酸基序CxxxCxxC相互关联,该基序是每个成员中发现的[4Fe-4S]簇的核心。这些蛋白质新化学性质的一个共同特点是利用一种强还原剂——低电位的4Fe-4S簇——从SAM生成一种强大的氧化剂,即5'-脱氧腺苷自由基。最近的研究结果开始确定一些自由基SAM酶的独特生物化学性质,例如赖氨酸2,3氨基变位酶、丙酮酸甲酸裂解酶激活酶和生物素合酶。

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