NosX function connects to nitrous oxide (N2O) reduction by affecting the Cu(Z) center of NosZ and its activity in vivo

FEBS Lett. 2005 Aug 29;579(21):4605-9. doi: 10.1016/j.febslet.2005.07.023.

Abstract

The effect of loss of the 34-kDa periplasmic NosX protein on the properties of N2O reductase was investigated with an N2O-respiration negative, double mutant of the paralogous genes nosX and nirX of Paracoccus denitrificans. In spite of absence of whole-cell N2O-reducing activity, the purified reductase was catalytically active, which attributes NosX a physiological role in sustaining the reaction cycle. N2O reductase exhibited the spectroscopic features of Cu(A) and the redox-inert, paramagnetic state, Cu(Z)*, of the catalytic center. Cu(Z)*, hitherto considered the result of spontaneous reaction of the reductase with dioxygen, attains cellular significance.

MeSH terms

  • Bacterial Proteins / chemistry*
  • Bacterial Proteins / genetics
  • Bacterial Proteins / metabolism*
  • Copper / chemistry*
  • Electron Spin Resonance Spectroscopy
  • Membrane Proteins / genetics
  • Membrane Proteins / metabolism
  • Nitrous Oxide / chemistry*
  • Oxidation-Reduction
  • Oxidoreductases / chemistry*
  • Oxidoreductases / metabolism
  • Paracoccus denitrificans / metabolism
  • Protein Conformation

Substances

  • Bacterial Proteins
  • Membrane Proteins
  • NirX protein, Paracoccus denitrificans
  • Copper
  • Oxidoreductases
  • nitrous oxide reductase
  • Nitrous Oxide