The utilization of alanine, glutamic acid, and serine as amino acid substrates for glycine N-acyltransferase

J Biochem Mol Toxicol. 2000;14(2):102-9. doi: 10.1002/(sici)1099-0461(2000)14:2<102::aid-jbt6>3.0.co;2-h.

Abstract

The conjugation of benzoyl-CoA with the aliphatic and acidic amino acids by glycine N-acyltransferase, as well as the amides of the latter group, was investigated. Bovine and human liver benzoyl-amino acid conjugation were investigated using electrospray ionization tandem mass spectrometry (ESI-MS-MS). Bovine glycine N-acyltransferase catalyzed conjugation of benzoyl-CoA with Gly (Km(Gly) = 6.2 mM), Asn (Km(Asn) = 129 mM), Gln (Km(Gln) = 353 mM), Ala (Km(Ala) = 1573 mM), Glu (Km(Glu) = 1148 mM) as well as Ser in a sequential mechanism. In the case of the human form, conjugation with Gly (Km(Gly) = 6.4 mM), Ala (Km(Ala) = 997 mM), and Glu was detected. The presence of these alternative conjugates did not inhibit bovine glycine N-acyltransferase activity significantly. Considering the relatively low levels at which these conjugates are formed, it is unlikely that they will have a significant contribution to acyl-amino acid conjugation under normal conditions in vivo. However, their cumulative contribution to acyl-amino acid conjugation under metabolic disease states may prove to have a useful contribution to detoxification of elevated acyl-CoAs.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acyltransferases / isolation & purification
  • Acyltransferases / metabolism*
  • Alanine / metabolism*
  • Animals
  • Cattle
  • Glutamic Acid / metabolism*
  • Glycine / metabolism*
  • Humans
  • Kinetics
  • Serine / metabolism*

Substances

  • Glutamic Acid
  • Serine
  • Acyltransferases
  • glycine acyltransferase
  • Alanine
  • Glycine