Active-site structure of a β-hydroxylase in antibiotic biosynthesis

J Am Chem Soc. 2011 May 11;133(18):6938-41. doi: 10.1021/ja201822v. Epub 2011 Apr 20.

Abstract

X-ray absorption and resonance Raman spectroscopies show that CmlA, the β-hydroxylase of the chloramphenicol biosynthetic pathway, contains a (μ-oxo)-(μ-1,3-carboxylato)diiron(III) cluster with 6-coordinate iron centers and 3 - 4 His ligands. This active site is found within a unique β-lactamase fold and is distinct from those of soluble methane monooxygenase and related enzymes that utilize a highly conserved diiron cluster with a 2-His-4-carboxylate ligand set within a 4-helix bundle motif. These structural differences may have an impact on the nature of the activated oxygen species of the reaction cycle.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Absorptiometry, Photon
  • Amino Acid Motifs
  • Anti-Bacterial Agents / biosynthesis*
  • Catalytic Domain
  • Chloramphenicol / biosynthesis*
  • Mixed Function Oxygenases / chemistry*
  • Protein Conformation
  • Spectrum Analysis, Raman

Substances

  • Anti-Bacterial Agents
  • Chloramphenicol
  • Mixed Function Oxygenases