Multiplicity Reactivation of 5-Iodouracil-Substituted, Nonviable Bacteriophage T4 td 8

Abstract

Nonviable, 5-iodouracil (IUra)-substituted bacteriophage T4 td 8 can be multiplicity reactivated. The data indicate that two nonviable, IUra-substituted T4 td 8 phage can complement each other intracellularly to produce viable progeny. Phage particles in lysates of T4 td 8-infected Escherichia coli BT − , prepared in the presence of varying mole fractions of IUra plus thymine, were examined by infecting with low and high dilutions of lysate. The yields of multiplicity reactivable particles were identical, regardless of the mole fractions of IUra present in the growth media. However, the yields of viable phage, measured at low multiplicities of infection, decreased with increasing mole fraction of IUra. The results are consistent with the hypothesis that the lethal effect of IUra is a consequence of its incorporation into DNA. Further, the IUra-induced lesion cannot involve genetic damage that shuts off expression at a single region of the genome.