Radical SAM enzymes: Nature's choice for radical reactions.

Joan B Broderick, William E Broderick, Brian M Hoffman

Journal: FEBS letters 2023;597(1):92-101

PMID: 36251330

Abstract

Enzymes that use a [4Fe-4S] cluster plus S-adenosyl-l-methionine (SAM) to initiate radical reactions (radical SAM) form the largest enzyme superfamily, with over half a million members across the tree of life. This review summarizes recent work revealing the radical SAM reaction pathway, which ultimately liberates the 5'-deoxyadenosyl (5'-dAdo•) radical to perform extremely diverse, highly regio- and stereo-specific, transformations. Most surprising was the discovery of an organometallic intermediate Ω exhibiting an Fe-C5'-adenosyl bond. Ω liberates 5'-dAdo• through homolysis of the Fe-C5' bond, in analogy to Co-C5' bond homolysis in B , previously viewed as biology's paradigmatic radical generator. The 5'-dAdo• has been trapped and characterized in radical SAM enzymes via a recently discovered photoreactivity of the [4Fe-4S] /SAM complex, and has been confirmed as a catalytically active intermediate in enzyme catalysis. The regioselective SAM S-C bond cleavage to produce 5'-dAdo• originates in the Jahn-Teller effect. The simplicity of SAM as a radical precursor, and the exquisite control of 5'-dAdo• reactivity in radical SAM enzymes, may be why radical SAM enzymes pervade the tree of life, while B enzymes are only a few.

© 2022 Federation of European Biochemical Societies.

Address: Department of Chemistry & Biochemistry, Montana State University, Bozeman, MT, USA.; Department of Chemistry, Northwestern University, Evanston, IL, USA.
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