Bacteriophage P1 pac sites inserted into the chromosome greatly increase packaging and transduction of Escherichia coli genomic DNA

- Up to five Phage P1 DNA packaging sites were inserted into the E. coli chromosome.
- Packaging of markers downstream of a packaging site is increased by more than 10-fold.
- Transduced recombinants can be increased by up to 1000 fold.
- This may be because the host DNA now packaged is far more recombinogenic than normal.

The Escherichia coli bacteriophage P1 packages host chromosome separately from phage DNA, and transfers it to recipient cells at low frequency in a process called generalized transduction. Phage genomes are packaged from concatemers beginning at a specific site, pac. To increase transduction rate, we have inserted pac into the chromosome at up to five equally spaced positions; at least this many are fully tolerated in the absence of P1 infection. A single chromosomal pac greatly increases transduction of downstream markers without decreasing phage yields; 3.5× as much total chromosomal DNA is packaged. Additional insertions decrease phage yield by >90% and also decrease phage DNA synthesis, although less dramatically. Packaging of chromosomal markers near to and downstream of each inserted pac site is, at the same time, increased by greater than 10 fold. Transduction of markers near an inserted pac site can be increased by over 1000-fold, potentially allowing identification of such transductants by screening.