Login / Signup

Bioinformatic Discovery of a Cambialistic Monooxygenase.

Chang LiuMagan M PowellGuodong RaoR David BrittJonathan Rittle
Published in: Journal of the American Chemical Society (2024)
Dinuclear monooxygenases mediate challenging C-H bond oxidation reactions throughout nature. Many of these enzymes are presumed to exclusively utilize diiron cofactors. Herein we report the bioinformatic discovery of an orphan dinuclear monooxygenase that preferentially utilizes a heterobimetallic manganese-iron (Mn/Fe) cofactor to mediate an O 2 -dependent C-H bond hydroxylation reaction. Unlike the structurally similar Mn/Fe-dependent monooxygenase AibH2, the diiron form of this enzyme (SfbO) exhibits a nascent enzymatic activity. This behavior raises the possibility that many other dinuclear monooxygenases may be endowed with the capacity to harness cofactors with a variable metal content.
Keyphrases
  • metal organic framework
  • transition metal
  • small molecule
  • hydrogen peroxide
  • high throughput
  • electron transfer
  • room temperature
  • visible light