Abstract

The replication defective transducing phage λp lac5 O29 P 3 carries a portion of the E. coli lac operon in the b 2 region of the lambda phage. This lac operon segment contains the lac promoter, the lac operator, and the β-galactosidase z gene, but does not contain the lac repressor i gene. The z gene can be expressed from both the inserted lac promoter and the phage promoter. When E. coli strain 594 ( z −, i +) or JC6256 (Δ lac ) is infected by λp lac5 O29 P 3 in the absence of additional cyclic AMP, β-galactosidase synthesis is shown to be expressed from the phage promoter. When 594 ( λ +) or JC6256 ( λ +) is infected by λp lac5 O29 P 3 in the presence of additional cyclic AMP and IPTG, β-galactosidase synthesis is shown to be expressed from the inserted lac promoter. The ability to separate the phage promoter from the inserted lac promoter for β-galactosidase expression will simplify the interpretation whenever λp lac 5 is used.

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