Physiological and biochemical characterization of AnNitA, the Aspergillus nidulans high-affinity nitrite transporter

Eukaryot Cell. 2011 Dec;10(12):1724-32. doi: 10.1128/EC.05199-11. Epub 2011 Oct 21.

Abstract

High-affinity nitrite influx into mycelia of Aspergillus nidulans has been characterized by use of (13)NO(2)(-), giving average K(m) and V(max) values of 48 ± 8 μM and 228 ± 49 nmol mg(-1) dry weight (DW) h(-1), respectively. Kinetic analysis of a plot that included an additional large number of low-concentration fluxes gave an excellent monophasic fit (r(2) = 0.96), with no indication of sigmoidal kinetics. Two-dimensional (2D) and three-dimensional (3D) models of AnNitA are presented, and the possible roles of conserved asparagine residues N122 (transmembrane domain 3 ]Tm 3]), N173 (Tm 4), N214 (Tm 5), and N246 (Tm 6) are discussed.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Sequence
  • Amino Acid Substitution
  • Aspergillus nidulans / growth & development
  • Aspergillus nidulans / metabolism*
  • Cell Membrane / metabolism
  • Conserved Sequence
  • Fungal Proteins / genetics
  • Fungal Proteins / isolation & purification
  • Fungal Proteins / metabolism*
  • Kinetics
  • Membrane Transport Proteins / genetics
  • Membrane Transport Proteins / isolation & purification
  • Membrane Transport Proteins / metabolism*
  • Models, Molecular
  • Molecular Sequence Data
  • Mutagenesis, Site-Directed
  • Nitrites / metabolism*
  • Protein Structure, Secondary
  • Protein Structure, Tertiary

Substances

  • Fungal Proteins
  • Membrane Transport Proteins
  • Nitrites