Table 5.
Host strains | Plating temperature (˚C) | |||||
---|---|---|---|---|---|---|
25 | 30 | 35 | 37 | 39 | 42 | |
594 | 0.5 | 0.9 | 0.9 | 1.0 | 1.0 | 0.4 |
594[pcIpR-P-timm] | <4 × 10-10 | <4 × 10-10 | 0.2 | 0.5 | 0.7 | 1.0 |
594[pcIpR-O-timm] | <4 × 10-10 | <4 × 10-10 | <4 × 10-10 | 9 × 10-7c | 2 × 10-6c | 0.8 |
594[p434’pR-O-timm] | 0.8 | 0.9 | 1.0 | 1.0 | 1.0 | 1.0 |
a: EOP (efficiency of plating) of 1.0 determined for λimmλcI72 on host 594 at 37 ˚C.
b: The CI[Ts] repressor made from the pcIpR plasmids blocks the vegetative growth of an infecting immλ phage as λcI72, at or below ~39 ˚C, as well as the expression of genes O or P, inserted downstream of the pR promoter. Plasmid p434’pR-O-timm has a hybrid cI gene fusion made from λ and 434 cI genes and the resulting repressor does not repress transcription from pR, allowing constitutive O expression at all temperatures [36].
c: Rare min plaques can only be seen under stereo microscope.