Reaction of tryptophan with carbohydrates: identification and quantitative determination of novel beta-carboline alkaloids in food

J Agric Food Chem. 2001 May;49(5):2486-92. doi: 10.1021/jf0014112.

Abstract

The formation of various carbohydrate-derived beta-carbolines was observed when model reactions of tryptophan with glucose were studied by means of HPLC with diode array detection, as well as by means of HPLC-MS. Isolation of these compounds and subsequent characterization by tandem mass spectrometry and NMR spectroscopy led to the identification of diastereomeric 1-(1,3,4,5-tetrahydroxypent-1-yl)-9H-pyrido[3,4-b]indoles (1a/b), 1-(1,4,5-trihydroxypent-1-yl)-9H-pyrido[3,4-b]indoles (2a/b), and E/Z isomers of 1-(1,5-dihydroxypent-3-en-1-yl)-9H-pyrido[3,4-b]indole (3a/b). HPLC-MS was used to prove the presence of these novel beta-carboline alkaloids in various food samples. In addition, quantitative determination of beta-carbolines 1a, 1b, and 2a/b in numerous products was achieved by means of HPLC with fluorometric detection. Concentrations ranged from 12 to 1922 microg/L for 1a and 1b and from 3 to 644 microg/L for 2a/b. The highest concentrations of all carbohydrate-derived beta-carbolines under study were found in ketchup, soy sauce, and fish sauce.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alkaloids
  • Carbolines / chemistry
  • Carbolines / isolation & purification*
  • Chromatography, High Pressure Liquid
  • Food Analysis
  • Glucose / chemistry*
  • Maillard Reaction
  • Mass Spectrometry
  • Spectrophotometry, Ultraviolet
  • Tryptophan / chemistry*

Substances

  • Alkaloids
  • Carbolines
  • Tryptophan
  • Glucose