The mechanism and substrate specificity of the NADPH:flavin oxidoreductase from Escherichia coli

J Biol Chem. 1995 Dec 22;270(51):30392-400. doi: 10.1074/jbc.270.51.30392.


The NAD(P)H:flavin oxidoreductase from Escherichia coli, Fre, is a monomer of 26.2 kDa that catalyzes the reduction of free flavins by NADPh or NADH. Overexpression in E. coli now allows the preparation of large amounts of pure protein. Structural requirements for recognition of flavins as substrates and not as cofactors were studied by steady-state kinetics with a variety of flavin analogs. The entire isoalloxazine ring was found to be the essential part of the flavin molecule for interaction with the polypeptide chain. Methyl groups at C-7 and C-8 of the isoalloxazine ring and the N-3 of riboflavin also play an important role in that interaction, whereas the ribityl chain of the riboflavin is not required for binding to the protein. On the other hand, the presence of the 2'-OH of the ribityl chain stimulates the NADPH-dependent reaction significantly. Moreover, a study of competitive inhibitors for both substrates demonstrated that Fre follows a sequential ordered mechanism in which NADPH binds first followed by riboflavin. Lumichrome, a very good inhibitor of Fre, may be used to inhibit flavin reductase in E. coli growing cells. As a consequence, it can enhance the antiproliferative effect of hydroxyurea, a cell-specific ribonucleotide reductase inactivator.

Publication types

  • Comparative Study

MeSH terms

  • Cloning, Molecular
  • Escherichia coli / drug effects
  • Escherichia coli / enzymology*
  • Escherichia coli / growth & development
  • FMN Reductase
  • Flavins / metabolism
  • Flavins / pharmacology
  • Hydroxyurea / pharmacology
  • Indicators and Reagents
  • Kinetics
  • NAD / metabolism
  • NADH, NADPH Oxidoreductases / biosynthesis
  • NADH, NADPH Oxidoreductases / metabolism*
  • NADP / metabolism
  • Oxazines / chemical synthesis
  • Oxazines / chemistry
  • Oxazines / metabolism
  • Oxidation-Reduction
  • Plasmids
  • Recombinant Proteins / biosynthesis
  • Recombinant Proteins / metabolism
  • Substrate Specificity


  • Flavins
  • Indicators and Reagents
  • Oxazines
  • Recombinant Proteins
  • NAD
  • 7,8-dimethylalloxazine
  • NADP
  • FMN Reductase
  • NADH, NADPH Oxidoreductases
  • Hydroxyurea