The redox state of activated bleomycin

J Biol Chem. 1985 Dec 15;260(29):15406-9.

Abstract

Activated bleomycin appears to have two more oxidizing equivalents than the Fe(III).bleomycin to which it spontaneously decays. Activated bleomycin reacts with NADH and thio-NADH, two-electron reductants, and with KI, a one-electron reductant, to yield Fe(III).bleomycin. The observed stoichiometries were 0.85 +/- 0.07 eq of thio-NADH oxidized or 1.5 +/- 0.25 eq of KI oxidized per mole of activated bleomycin. None of these reactions requires the presence of a redox mediator, as does the reduction of Fe(III).bleomycin by NADH or thio-NADH. The oxidations of both pyridine nucleotide coenzymes and of KI are inhibited by DNA, the usual bleomycin target.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Bleomycin*
  • Chemical Phenomena
  • Chemistry
  • Electron Spin Resonance Spectroscopy
  • Methylphenazonium Methosulfate / pharmacology
  • NAD / analogs & derivatives
  • NAD / metabolism
  • Oxidation-Reduction
  • Time Factors

Substances

  • NAD
  • Bleomycin
  • Methylphenazonium Methosulfate
  • thionicotinamide adenine dinucleotide