SummaryChromosomeless minicells are formed by misplaced cell fissions near the polar extremities of an Escherichia coli K12 mutant strain. Superhelical λdv DNA can be introduced into minicells by segregation from a λdv-containing derivative of the original mutant. One single-strand break changes the sedimentation constant of such a DNA and hence sedimentation of minicell lysates in neutral and alkaline sucrose gradients enables one accurately to quantitate the numbers of ‘clean’ chain breaks and alkali-labile bonds produced in DNA by γ-irradiation in vivo. Although the total number of single-strand breaks measured in alkali is enhanced three- to fourfold when 60Co γ-rays are delivered to an oxygenated minicell suspension, the fraction which requires an alkaline environment for expression is almost twice as great in minicell samples irradiated in the absence (∼ 35 per cent) as in the presence (∼ 21 per cent) of oxygen.In contrast to chain breaks, alkali-labile bonds do not disappear from DNA of minicells during post-radiation incubation and, therefore, are presumably unsuitable substrates for certain DNA repair enzymes operative in minicells.
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Paterson et al. (1973) studied this question.
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