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Hydroxylation of guanine in nucleosides and DNA at the C-8 position by heated glucose and oxygen radical-forming agents.

Abstract
Heated glucose is mutagenic to Salmonella typhimurium TA 100 in the absence of S-9 mix. For identifying unknown mutagens in heated glucose (dry solid, 200 degrees C, 20 min), reaction with isopropylideneguanosine (IPG) was followed by isolation and characterization of the mutagen-IPG adduct. Two adducts, glyoxal-IPG and 8-hydroxy-IPG, were identified in the reaction mixture by this technique. To elucidate the mechanism of this hydroxylation reaction, we investigated the abilities of various agents to hydroxylate deoxyguanosine or guanine base in DNA. Various reducing agents, metals, asbestoses, polyphenols, aminophenols, and X-ray were effective for hydroxylation, and an oxygen radical seems to be the reactive species. For sensitive detection of 8-hydroxyguanine, a monoclonal antibody for it was prepared.
AuthorsH Kasai, S Nishimura
JournalEnvironmental health perspectives (Environ Health Perspect) Vol. 67 Pg. 111-6 (Aug 1986) ISSN: 0091-6765 [Print] United States
PMID3757945 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Antibodies, Monoclonal
  • Free Radicals
  • Mutagens
  • Nucleosides
  • Guanine
  • 8-Hydroxy-2'-Deoxyguanosine
  • DNA
  • Deoxyguanosine
  • Glucose
  • Oxygen
Topics
  • 8-Hydroxy-2'-Deoxyguanosine
  • Antibodies, Monoclonal
  • DNA
  • Deoxyguanosine (analogs & derivatives, immunology)
  • Food Analysis
  • Food Contamination
  • Free Radicals
  • Glucose
  • Guanine
  • Hot Temperature
  • Hydroxylation
  • Mutagens (isolation & purification)
  • Nucleosides
  • Oxygen

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