Table 1.
Integrated prophages in DH5Δlac
|
||||
---|---|---|---|---|
λincCrepA-lacZ | λincCrepAincA-lacZ | |||
lacZ activity (Miller units)* | 14 ± 1.2 | 28 ± 2.6 | 13 ± 1.3 | 25 ± 0.36 |
Number of prophages (iterons) | 1 (5) | 2 (10) | 1 (14) | 2 (28) |
Phage yield by ter assay† | <103 | 7 × 105 | <103 | 7 × 105 |
Relative repA mRNA‡ | 1 | 1.5 ± 0.10 | 1.4 ± 0.26 | 1.5 ± 0.25 |
Transformants with pSP102 | 7 × 103 | 4 × 103 | 5 × 103§ | <10 |
Transformants with pVM11¶ | 7 × 103 | 4 × 103 | <10 | <10 |
The activity was measured from log phase cultures grown in L broth (30) and units were used to estimate prophage numbers. The units may not be compared between the two prophages because a transcription terminator in incA and a damaged par promoter precedes lacZ in the incA carrying prophage (unpublished results).
The assay helps to discriminate between mono- and poly-lysogens (13).
RNA was measured by primer extension exactly as described for Fig. 3 by using aliquots from the same culture used for measuring lacZ activity.
As opposed to overnight for others, these colonies appeared after 48 hr at 37°C.
pVM11 is ΔrepAΔincA whereas pSP102 is ΔincA only.