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