articleBiochemistryMay 28, 2003Closed access

The First Direct Characterization of a High-Valent Iron Intermediate in the Reaction of an α-Ketoglutarate-Dependent Dioxygenase:  A High-Spin Fe(IV) Complex in Taurine/α-Ketoglutarate Dioxygenase (TauD) from Escherichia coli

Pennsylvania State University

PubMed
Indexed incrossrefpubmed

Abstract

The Fe(II)- and alpha-ketoglutarate(alphaKG)-dependent dioxygenases have roles in synthesis of collagen and sensing of oxygen in mammals, in acquisition of nutrients and synthesis of antibiotics in microbes, and in repair of alkylated DNA in both. A consensus mechanism for these enzymes, involving (i) addition of O(2) to a five-coordinate, (His)(2)(Asp)-facially coordinated Fe(II) center to which alphaKG is also bound via its C-1 carboxylate and ketone oxygen; (ii) attack of the uncoordinated oxygen of the bound O(2) on the ketone carbonyl of alphaKG to form a bicyclic Fe(IV)-peroxyhemiketal complex; (iii) decarboxylation of this complex concomitantly with formation of an oxo-ferryl (Fe(IV)=O(2)(-))…

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Authors

5

Topics & keywords

Keywords
  • Dioxygenase
  • Chemistry
  • Electron paramagnetic resonance
  • Decarboxylation
  • Substrate (aquarium)
  • Carboxylate
  • Reaction intermediate
  • Hydroxylation
UN Sustainable Development Goals
  • Clean water and sanitation
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