Use of repair-deficient strains of Escherichia coli and liver microsomes to detect and characterise DNA damage caused by pyrrolizidine alkaloids heliotrine and monocrotaline

Mutat Res. 1975 Jun;28(3):331-6. doi: 10.1016/0027-5107(75)90227-4.

Abstract

E. coli WP2 and its repair-deficient derivatives were treated with the pyrrolizidine alkaloids, heliotrine and monocrotaline in the presence of a liver microsomal fraction. The doubly repair-deficient strains WP100 uvrA recA and CM611 uvrA exrA showed considerable killing. The singly repair-deficient strains WP2 uvrA, CM561 exrA and CM571 recA showed slight killing. In strains WP2 and WP2 uvrA induced reversion to Trp+ was not detected with either monocrotaline or mitomycin C. These results are entirely consistent with liver activation converting pyrrolizidine alkaloids into bifunctional alkylating agents.

MeSH terms

  • Animals
  • DNA Repair / drug effects*
  • Escherichia coli / drug effects*
  • Escherichia coli / metabolism
  • Genotype
  • Male
  • Microsomes, Liver / metabolism*
  • Mitomycins / pharmacology
  • Mutagens
  • Mutation
  • Pyrrolizidine Alkaloids / pharmacology*
  • Rats

Substances

  • Mitomycins
  • Mutagens
  • Pyrrolizidine Alkaloids
  • heliotrine