Kinetic and structural characterization of an intermediate in the biomineralization of bacterioferritin

FEBS Lett. 1993 Oct 25;333(1-2):197-202. doi: 10.1016/0014-5793(93)80404-i.

Abstract

The mechanism by which iron-storage proteins take up and oxidise iron(II) is not understood. We show by rapid-kinetic and EPR measurements that iron uptake, in vitro, by a bacterial iron-storage protein, bacterioferritin, involves at least three kinetically distinguishable phases: phase 1, the binding of Fe(II) ions, probably at a dimeric iron ferroxidase centre; phase 2, oxidation of the Fe(II) dimer and production of mononuclear Fe(III); and phase 3, iron core formation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Bacterial Proteins / chemistry
  • Bacterial Proteins / metabolism
  • Cytochrome b Group / chemistry
  • Cytochrome b Group / metabolism*
  • Electron Spin Resonance Spectroscopy
  • Escherichia coli
  • Ferritins / chemistry
  • Ferritins / metabolism*
  • Iron / metabolism
  • Kinetics

Substances

  • Bacterial Proteins
  • Cytochrome b Group
  • Ferritins
  • bacterioferritin
  • Iron