Glutathione-Dependent O-Alkyl and O-Aryl Conjugations for Dicapthon and Fenitrothion in Several Insects

Yasuhiko Konno, Takashi Shishido

Research output: Contribution to journalArticle

Abstract

Glutathione-dependent O-alkyl and O-aryl conjugations for 14C-dicapthon (O, O-dimethyl O-2-chloro-4-nitrophenyl phosphorothionate) and 14C-fenitrothion (O, O-dimethyl O-3-methyl-4-nitrophenyl phosphorothionate) were studied in the each cytosolic fraction prepared from the whole bodies of the azuki bean beetle, Callosobruchus chinensis, the chestnut weevil, Curculio dentipes, the green rice leafhopper, Nephotettix cincticeps, the almond moth, Ephestia cautella, the yellow peach moth, Conogethes punctiferalis, and the rice stem borer, Chilo suppressalis. Fenitrothion was degraded almost by O-alkyl conjugation, whereas relatively high ratio of O-aryl conjugation was observed for dicapthon degradation. Particularly in the azuki bean beetle, the green rice leafhopper and the almond moth, O-aryl conjugation was dominant (60–80%). This result is the first evidence that O-aryl conjugation is preferentially occurred for O, O-dimethyl O-aryl phosphorothionates in insects. Malpighian tubes, fat body and midgut prepared from the common cutworm, Spodoptera litura, were also assayed with 14C-dicapthon. Interestingly, the ratios of O-alkyl and O-aryl conjugation were clearly different among the three tissues.

Original languageEnglish
Pages (from-to)430-433
Number of pages4
JournalJournal of Pesticide Science
Volume21
Issue number4
DOIs
Publication statusPublished - 1996 Jan 1
Externally publishedYes

ASJC Scopus subject areas

  • Insect Science
  • Health, Toxicology and Mutagenesis

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