TABLE 3.
Clone | No. colonies
|
Rate of mutation (%) | Titer | ||
---|---|---|---|---|---|
Green | Clear | Mix colored | |||
Clone 1 | 431 | 1 | 2 | 0.7 | 0.18 × 105 |
Clone 2 | 487 | 1 | 1 | 0.4 | 1 × 105 |
Clone 3 | 761 | 8 | 1 | 1.2 | 0.25 × 105 |
Clone 4 | 782 | 8 | 5 | 1.6 | 0.27 × 105 |
Clone 5 | 564 | 3 | 1 | 0.7 | 1.2 × 105 |
Clone 6 | 172 | 2 | 0 | 1.2 | 0.34 × 105 |
Clone 7 | 289 | 1 | 0 | 0.5 | 0.57 × 105 |
Total | 3,486 | 24 | 10 | 0.9 ± 0.4b | (0.54 × 105) ± (0.40 × 105)c |
Viruses from step 2 PG13 cells, which contain a gfp gene, were used to infect D17 cells. Infected D17 cells were selected for hygromycin resistance. Each hygromycin-resistant colony was analyzed under a fluorescence microscope.
The rate of deletion of JZ442+3′ Hyg was 62%, whereas the rate mutation of JZ442 was 1% (24).
The titer of viruses released from JZ442+3′Hyg was (0.86 × 105) ± (0.38 × 105) (24).