The identification of (E)-2-methylglutaconic acid, a new isoleucine metabolite, in the urine of patients with beta-ketothiolase deficiency, propionic acidaemia and methylmalonic acidaemia

Biomed Mass Spectrom. 1982 Jan;9(1):1-5. doi: 10.1002/bms.1200090102.

Abstract

The identification of (E)-2-methylglutaconic acid, a 'new' metabolite of isoleucine, is described. The substance was detected in urine samples from patients with propionic acidaemia, methylmalonic acidaemia and so-called beta-ketothiolase deficiency; in the majority of cases together with N-tiglylglycine. (E)-2-Methylglutaconic acid is thought to be the end product of the 3-methylcrotonyl-CoA carboxylase-catalysed carboxylation of tiglyl-CoA. Prerequisites for the quantitative gas chromatographic analysis of the unstable 2- (and 3-) methyl-glutaconic acid ditrimethylsilyl ester are given.

MeSH terms

  • Acetyl-CoA C-Acyltransferase / deficiency*
  • Acyl Coenzyme A / metabolism
  • Acyltransferases / deficiency*
  • Amino Acid Metabolism, Inborn Errors / blood
  • Amino Acid Metabolism, Inborn Errors / diet therapy
  • Amino Acid Metabolism, Inborn Errors / urine*
  • Gas Chromatography-Mass Spectrometry
  • Glutarates / chemical synthesis
  • Glutarates / metabolism
  • Glutarates / urine*
  • Glycine / analogs & derivatives
  • Glycine / urine
  • Humans
  • Isoleucine / metabolism*
  • Malonates / blood*
  • Methylmalonic Acid / blood*
  • Methylmalonic Acid / urine
  • Propionates / blood*
  • Propionates / urine
  • Reference Values

Substances

  • Acyl Coenzyme A
  • Glutarates
  • Malonates
  • Propionates
  • Isoleucine
  • tiglylglycine
  • 2-methylglutaconic acid
  • tiglyl-coenzyme A
  • Methylmalonic Acid
  • Acyltransferases
  • Acetyl-CoA C-Acyltransferase
  • Glycine