With the aid of temperature shift experiments, the ts mutants of temperate bacteriophage N15 were divided into two groups, early and late ones. Phage DNA replication is normal in late mutants at elevated temperature both in the vegetative and prophage states, whereas such replication is disturbed under the same condition in both states in early mutants. This disturbance results in the intensive curing of early mutant lysogens under nonpermissive conditions. Prophage N15 DNA sediments in sucrose gradients separately from bacterial DNA. The conclusion is drawn that prophage N15 is not incorporated into the bacterial chromosome. Some other properties of phage N15 and its DNA are described.
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