Specific enzymatic chlorination of tryptophan and tryptophan derivatives

Adv Exp Med Biol. 1999:467:603-9. doi: 10.1007/978-1-4615-4709-9_75.

Abstract

In the search for an alternative to chemical halogenation reactions using the free halogens, a novel type of halogenating enzymes was detected. In contrast to haloperoxidases, these NADH-dependent halogenases are specific. Tryptophan halogenase which catalyses the regioselective chlorination of tryptophan to 7-chlorotryptophan can also chlorinate tryptamine, tryptophol, indole-3-acetonitrile, and 3-methylindole. However, indole-3-acetonitrile is not chlorinated in the 7-position, but in positions two and three of the indole ring. Chlorination in the 3-position is obviously stereospecific. In addition to tryptophan and indole derivatives, aminophenylpyrrole is also accepted as a substrate for regioselective chlorination. Since the new NADH-dependent halogenases have a fairly broad substrate specificity and catalyse regioselective chlorination reactions they could be a good alternative to chemical halogenation.

MeSH terms

  • Halogens / metabolism*
  • NAD / metabolism
  • Oxidation-Reduction
  • Oxidoreductases / metabolism*
  • Peroxidases / metabolism*
  • Substrate Specificity
  • Tryptophan / analogs & derivatives*
  • Tryptophan / metabolism*

Substances

  • Halogens
  • NAD
  • Tryptophan
  • Oxidoreductases
  • monodechloroaminopyrrolnitrin halogenase
  • tryptophan halogenase
  • Peroxidases