Abstract
Recombination between F42lac and λplac5 is typically 20- to 50-fold more efficient than recombination between chromosomal lac and λplac5. This enhancement of recombination requires trans-acting factors located in the promoter-distal and promoter-proximal regions of the main traY-to-traI (traZ) operon. By testing the ability of deletion mutants of tra to support enhanced recombination, we have identified traY as the only essential gene from thepromoter-proximal region of tra. The possibility of a direct role for the traJ gene product has been ruled out. We also report that traI is the only gene from the promoter-distal end of the traY to traI operon that is required for recombination enhancement. Of the two proposed domains of traI, we conclude that the oriT-nicking activity is essential, whereas the helicase activity is largely dispensable. The possibility of a third traI activity is also discussed.
Original language | English (US) |
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Pages (from-to) | 1027-1034 |
Number of pages | 8 |
Journal | Journal of bacteriology |
Volume | 173 |
Issue number | 3 |
DOIs | |
State | Published - 1991 |
All Science Journal Classification (ASJC) codes
- Microbiology
- Molecular Biology