Multicopper manganese oxidase accessory proteins bind Cu and heme

Cristina N. Butterfield, Lizhi Tao, Kelly N. Chacón, Thomas G. Spiro, Ninian Blackburn, William H. Casey, R. David Britt, Bradley Tebo

Research output: Contribution to journalArticle

15 Citations (Scopus)

Abstract

Multicopper oxidases (MCOs) catalyze the oxidation of a diverse group of metal ions and organic substrates by successive single-electron transfers to O2 via four bound Cu ions. MnxG, which catalyzes MnO2 mineralization by oxidizing both Mn(II) and Mn(III), is unique among multicopper oxidases in that it carries out two energetically distinct electron transfers and is tightly bound to accessory proteins. There are two of these, MnxE and MnxF, both approximately 12 kDa. Although their sequences are similar to those found in the genomes of several Mn-oxidizing Bacillus species, they are dissimilar to those of proteins with known function. Here, MnxE and MnxF are co-expressed independent of MnxG and are found to oligomerize into a higher order stoichiometry, likely a hexamer. They bind copper and heme, which have been characterized by electron paramagnetic resonance (EPR), X-ray absorption spectroscopy (XAS), and UV-visible (UV-vis) spectrophotometry. Cu is found in two distinct type 2 (T2) copper centers, one of which appears to be novel; heme is bound as a low-spin species, implying coordination by two axial ligands. MnxE and MnxF do not oxidize Mn in the absence of MnxG and are the first accessory proteins to be required by an MCO. This may indicate that Cu and heme play roles in electron transfer and/or Cu trafficking.

Original languageEnglish (US)
Pages (from-to)1853-1859
Number of pages7
JournalBiochimica et Biophysica Acta - Proteins and Proteomics
Volume1854
Issue number12
DOIs
StatePublished - Dec 1 2015

Fingerprint

Accessories
Manganese
Heme
Oxidoreductases
Electrons
Copper
X-Ray Absorption Spectroscopy
Ions
Proteins
X ray absorption spectroscopy
Spectrophotometry
Electron Spin Resonance Spectroscopy
Bacilli
Stoichiometry
Bacillus
Metal ions
Paramagnetic resonance
Genes
Metals
Genome

Keywords

  • Electron paramagnetic resonance spectroscopy
  • Metallo-subunit
  • Multicopper oxidase
  • Protein oligomerization
  • Type 2 copper
  • X-ray absorption spectroscopy

ASJC Scopus subject areas

  • Biochemistry
  • Biophysics
  • Analytical Chemistry
  • Molecular Biology

Cite this

Multicopper manganese oxidase accessory proteins bind Cu and heme. / Butterfield, Cristina N.; Tao, Lizhi; Chacón, Kelly N.; Spiro, Thomas G.; Blackburn, Ninian; Casey, William H.; Britt, R. David; Tebo, Bradley.

In: Biochimica et Biophysica Acta - Proteins and Proteomics, Vol. 1854, No. 12, 01.12.2015, p. 1853-1859.

Research output: Contribution to journalArticle

Butterfield, Cristina N. ; Tao, Lizhi ; Chacón, Kelly N. ; Spiro, Thomas G. ; Blackburn, Ninian ; Casey, William H. ; Britt, R. David ; Tebo, Bradley. / Multicopper manganese oxidase accessory proteins bind Cu and heme. In: Biochimica et Biophysica Acta - Proteins and Proteomics. 2015 ; Vol. 1854, No. 12. pp. 1853-1859.
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