Human carbonyl and aldose reductases: new catalytic functions in tetrahydrobiopterin biosynthesis

Biochem Biophys Res Commun. 1991 Mar 29;175(3):738-44. doi: 10.1016/0006-291x(91)91628-p.

Abstract

New catalytic functions of human carbonyl- and aldose reductase in tetrahydrobiopterin biosynthesis are proposed. 6-Pyruvoyl tetrahydropterin, an intermediate in the biosynthesis of tetrahydrobiopterin, was converted to 6-lactoyl tetrahydropterin and 1'-hydroxy-2'-oxopropyl tetrahydropterin by carbonyl reductase under anaerobic condition. 1'-Hydroxy-2'-oxopropyl tetrahydropterin was subsequently metabolized to tetrahydrobiopterin by aldose reductase. Based on these results alternative pathways for the synthesis of tetrahydrobiopterin in patients with genetic defects of sepiapterin reductase are suggested.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alcohol Oxidoreductases / isolation & purification
  • Alcohol Oxidoreductases / metabolism*
  • Aldehyde Reductase / isolation & purification
  • Aldehyde Reductase / metabolism*
  • Aldo-Keto Reductases
  • Biopterins / analogs & derivatives*
  • Biopterins / biosynthesis
  • Brain / enzymology
  • Chromatography, Gel
  • Humans
  • Kinetics

Substances

  • Biopterins
  • Alcohol Oxidoreductases
  • Aldo-Keto Reductases
  • sepiapterin reductase
  • Aldehyde Reductase
  • sapropterin