Iron Fenton oxidation of 2'-deoxyguanosine in physiological bicarbonate buffer yields products consistent with the reactive oxygen species carbonate radical anion not the hydroxyl radical

Chem Commun (Camb). 2020 Aug 25;56(68):9779-9782. doi: 10.1039/d0cc04138f.

Abstract

Product analysis from the iron Fenton oxidation of 2'-deoxyguanosine found reactions in bicarbonate buffer yield 8-oxo-2'-deoxyguanosine and spiroiminodihyantoin consistent with CO3˙-. Reactions in phosphate buffer furnished high yields of sugar oxidation products consistent with HO˙. These observations change the view of DNA oxidation products from the iron-Fenton reaction.

MeSH terms

  • Anions / chemistry
  • Bicarbonates / chemistry*
  • Carbonates / chemistry*
  • Deoxyadenosines / chemistry
  • Deoxyguanosine / chemistry*
  • Free Radicals / chemistry
  • Free Radicals / metabolism*
  • Hydrogen Peroxide / chemistry*
  • Hydroxyl Radical / chemistry
  • Iron / chemistry*
  • Oxidation-Reduction
  • Reactive Oxygen Species / metabolism*

Substances

  • Anions
  • Bicarbonates
  • Carbonates
  • Deoxyadenosines
  • Fenton's reagent
  • Free Radicals
  • Reactive Oxygen Species
  • Hydroxyl Radical
  • 2'-deoxy-7,8-dihydro-8-oxoadenosine
  • Hydrogen Peroxide
  • Iron
  • Deoxyguanosine