Gain of glutaminase function in mutants of the ammonia-specific frog carbamoyl phosphate synthetase

J Biol Chem. 2003 Jul 18;278(29):26722-6. doi: 10.1074/jbc.M303774200. Epub 2003 May 8.

Abstract

Depending on their physiological role, carbamoyl phosphate synthetases (CPSs) use either glutamine or free ammonia as the nitrogen donor for carbamoyl phosphate synthesis. Sequence analysis of known CPSs indicates that, regardless of whether they are ammonia- or glutamine-specific, all CPSs contain the structural equivalent of a triad-type glutamine amidotransferase (GAT) domain. In ammonia-specific CPSs, such as those of rat or human, the catalytic inactivity of the GAT domain can be rationalized by the substitution of the Triad cysteine residue by serine (1). The ammonia-specific CPS of Rana catesbeiana (fCPS) presents an interesting anomaly in that, despite its retention of the entire catalytic triad (2) and almost all other residues conserved in Triad GATs, it is unable to utilize glutamine as a nitrogen-donating substrate (3). Based on our earlier work with the glutamine-utilizing E. coli CPS (eCPS), we have targeted residues Lys258 and Glu261 in the fCPS GAT domain as critical for preventing GAT function. Previously we have shown that substitution of the corresponding residues in eCPS by their fCPS counterparts (Leu --> Lys and Gln --> Glu) resulted in complete loss of GAT function in eCPS (3). To examine the role of these residues in the fCPS GAT component, we have cloned the full-length fCPS gene from R. catesbeiana liver. Here we report the first heterologous expression of an ammonia-specific CPS and show that a single mutation of the frog enzyme, K258L, yields a gain of glutaminase function.

Publication types

  • Comparative Study
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Amino Acid Sequence
  • Animals
  • Base Sequence
  • Carbamoyl-Phosphate Synthase (Ammonia) / chemistry
  • Carbamoyl-Phosphate Synthase (Ammonia) / genetics*
  • Carbamoyl-Phosphate Synthase (Ammonia) / metabolism*
  • Cloning, Molecular
  • DNA, Recombinant / genetics
  • Glutaminase / genetics*
  • Glutaminase / metabolism*
  • Humans
  • Kinetics
  • Mutagenesis, Site-Directed
  • Protein Structure, Tertiary
  • Rana catesbeiana / genetics*
  • Rana catesbeiana / metabolism*
  • Rats
  • Recombinant Proteins / chemistry
  • Recombinant Proteins / genetics
  • Recombinant Proteins / metabolism

Substances

  • DNA, Recombinant
  • Recombinant Proteins
  • Glutaminase
  • Carbamoyl-Phosphate Synthase (Ammonia)