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Mechanistic Investigation of Oxidative Decarboxylation Catalyzed by Two Iron(II)- and 2-Oxoglutarate-Dependent Enzymes.

Jhih-Liang HuangYijie TangCheng-Ping YuDev SanyalXinglin JiaXinyu LiuYisong GuoWei-Chen Chang
Published in: Biochemistry (2018)
Two non-heme iron enzymes, IsnB and AmbI3, catalyze a novel decarboxylation-assisted olefination to produce indole vinyl isonitrile, an important building block for many natural products. Compared to other reactions catalyzed by this enzyme family, decarboxylation-assisted olefination represents an attractive biosynthetic route and a mechanistically unexplored pathway in constructing a C═C bond. Using mechanistic probes, transient state kinetics, reactive intermediate trapping, spectroscopic characterizations, and product analysis, we propose that both IsnB and AmbI3 initiate stereoselective olefination via a benzylic C-H bond activation by an Fe(IV)-oxo intermediate, and the reaction likely proceeds through a radical- or carbocation-induced decarboxylation to complete C═C bond installation.
Keyphrases
  • room temperature
  • small molecule
  • molecular docking
  • high glucose
  • transition metal
  • iron deficiency
  • diabetic rats
  • electron transfer
  • living cells
  • oxidative stress
  • cerebral ischemia
  • stress induced