TABLE 8.
Synthesis of DNA by dnaE(Ts) strains incubated at 40°Ca
Genotype of strain | Dilution | Vol (ml) | Total amt of DNA (μg) in culture after incubation at 40°C for:
|
N/N0b | |||||
---|---|---|---|---|---|---|---|---|---|
0 h | 1.5 h | 2.5 h | 3 h | 4 h | 4.5 h | ||||
dnaE74 | 1:10 | 50 | 279 | 1,250 | |||||
1:10 | 10 | 80.7 | 221 | 324 | 417 | 3.6 | |||
1:1,000 | 25 | 1.06 | 7.4 | 0.0063 | |||||
1:1,000 | 100 | 4.25 | 32.6 | 0.0044 | |||||
dnaE486 | 1:10 | 10 | 463 | 834 | 1.08 | ||||
1:100 | 50 | 46 | 247 | 0.0058 | |||||
1:1,000 | 100 | 4.6 | 38.9 | 0.001 | |||||
dnaE74 cydA | 1:10 | 10 | 25.8 | 211 | 5 | ||||
1:100 | 50 | 12.9 | 143 | 5.7 | |||||
1:1,000 | 100 | 2.6 | 25.0 | 5.7 | |||||
1:100 | 50 | 9.8 | 31.6 | 45 | 86.6 | 5.7c |
Cultures were grown overnight to a concentration of ≈5 × 109 cells/ml for the dnaE74 strain or 2 × 109 to 3 × 109 cells/ml for the dnaE74 cydA strain, collected, resuspended in LB medium, diluted, and incubated in different volumes of prewarmed medium for different times. Cultures were harvested, washed with 1× SSC, and extracted first with cold perchloric acid and then with hot perchloric acid. The perchloric acid extracts were analyzed by the diphenylamine method of Burton (9).
N, viable count after incubation for 4 h, unless indicated otherwise; N0, viable count at zero time.
The viable count after incubation was determined after incubation for 4.5 h.