Abstract

The autonomously replicating plasmid λ dv is a DNA molecule about one-eighth the size of the λ virulent genome from which it was derived. Lambda dv contains only the immunity region of λ and the genes necessary for phage DNA synthesis (see Fig. 1). Cells carrying λ dv appear immune to λ but are lysed by certain hybrid phage such as λimm 21 (in which the immunity region of phage 21 has replaced that of λ ). During λimm 21 infection of λ dv carrier cells, recombinants arise which carry genes originating from the λ dv plasmid (Matsubara and Kaiser, 1968). The majority of these recombinants appear to have added a λ dv unit to the genome of the infecting phage (Kellenberger-Gujer, this volume). The structure of these genomes has permitted an examination of the role of the λN gene product in phage multiplication. Before discussing the regulatory properties of the duplication phage, it will be necessary to describe their genetic structure. THE FORMATION OF DUPLICATION PHAGE Approximately 0.2% of the progeny phage from infection of cells carrying λ dv with phage λimm 21 sus P are P + recombinants. To show that recombination between an infecting phage and the λ dv plasmid can add λ dv to the phage genome, I used λb 538 imm 21 susP 901, a 21% deletion relative to wild-type λ ( λ + ), to infect λ dv carrier strain KM424, anticipating that the 21% deletion would compensate for the addition of λ dv during packaging. The density distribution of P − recombinants from the λb 538 imm 21 susP 901 phage infection of KM424 is given in Fig. 2. This is...

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