Axial ligation of the high-potential heme center in an Arabidopsis cytochrome b561

FEBS Lett. 2011 Feb 4;585(3):545-8. doi: 10.1016/j.febslet.2011.01.006. Epub 2011 Jan 12.

Abstract

Arabidopsis has four putative, di-heme cytochrome b561 proteins, including one localized in the tonoplast (TCytb). From a comparative electron paramagnetic resonance (EPR), UV-Vis absorption and resonance Raman study, on wild type, H83A/H156A-TCytb and H83L/H156L-TCytb double mutants, it follows that the H83 and H156 residues are binding one of the two hemes. These measurements show that the high-potential heme site is situated at the cytoplasmic side of the membrane and allow the unambiguous differentiation between two models on the heme localization in cytochrome b561 proteins.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Substitution
  • Arabidopsis / enzymology*
  • Arabidopsis Proteins / chemistry*
  • Cytochrome b Group / chemistry*
  • Electron Spin Resonance Spectroscopy
  • Heme / chemistry*
  • Histidine / chemistry
  • Models, Molecular
  • Mutagenesis, Site-Directed
  • Mutant Proteins / chemistry
  • Oxidation-Reduction
  • Recombinant Proteins / chemistry
  • Spectrophotometry
  • Spectrum Analysis, Raman
  • Vacuoles / enzymology

Substances

  • Arabidopsis Proteins
  • Cytochrome b Group
  • Mutant Proteins
  • Recombinant Proteins
  • cytochrome b561
  • Heme
  • Histidine