Reversible Formation of Alkyl Radicals at [Fe<inf>4</inf>S<inf>4</inf>] Clusters and Its Implications for Selectivity in Radical SAM Enzymes
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nihms-1619142.pdf
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Accepted version
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906.49 KB
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Author(s)
Brown, Alexandra C.
Suess, Daniel Leif Migdow
Date Issued
2020
Journal
Journal of the American Chemical Society
Publisher
American Chemical Society (ACS)
Version
Author's final manuscript
Abstract
Copyright © 2020 American Chemical Society. All kingdoms of life use the transient 5′-deoxyadenosyl radical (5′-dAdoâ ) to initiate a wide range of difficult chemical reactions. Because of its high reactivity, the 5′-dAdo•must be generated in a controlled manner to abstract a specific H atom and avoid unproductive reactions. In radical S-Adenosylmethionine (SAM) enzymes, the 5′-dAdo•is formed upon reduction of SAM by an [Fe4S4] cluster. An organometallic precursor featuring an Fe-C bond between the [Fe4S4] cluster and the 5′-dAdo group was recently characterized and shown to be competent for substrate radical generation, presumably via Fe-C bond homolysis. Such reactivity is without precedent for Fe-S clusters. Here, we show that synthetic [Fe4S4]-Alkyl clusters undergo Fe-C bond homolysis when the alkylated Fe site has a suitable coordination number, thereby providing support for the intermediacy of organometallic species in radical SAM enzymes. Addition of pyridine donors to [(IMes)3Fe4S4-R]+ clusters (R = alkyl or benzyl; IMes = 1,3-dimesitylimidazol-2-ylidene) generates Râ , ultimately forming R-R coupled hydrocarbons. This process is facile at room temperature and allows for the generation of highly reactive radicals including primary carbon radicals. Mechanistic studies, including use of the 5-hexenyl radical clock, demonstrate that Fe-C bond homolysis occurs reversibly. Using these experimental insights and kinetic simulations, we evaluate the circumstances in which an organometallic intermediate can direct the 5′-dAdo•toward productive H-Atom abstraction. Our findings demonstrate that reversible homolysis of even weak M-C bonds is a feasible protective mechanism for the 5′-dAdo•that can allow selective X-H bond activation in both radical SAM and adenosylcobalamin enzymes.
MIT Department
Massachusetts Institute of Technology. Department of Chemistry
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DOI of Published Version
https://doi.org/10.1021/jacs.0c05590
