TABLE 2.
Strain | Relevant genotype | Final OD650 in NB containing paraquat atb:
|
||
---|---|---|---|---|
0 μM | 40 μM | 80 μM | ||
DM7226 | Wild type | 0.97 ± <0.01 | 0.92 ± 0.01 | 0.92 ± 0.03 |
DM7225 | yggX | 0.98 ± 0.01 | 0.74 ± 0.12 | 0.25 ± 0.01 |
DM7644 | cyaY | 1.03 ± 0.01 | 0.93 ± 0.02 | 0.74 ± 0.06 |
DM7307 | apbC | 0.97 ± 0.01 | 0.73 ± 0.04 | 0.62 ± 0.01 |
DM7642 | apbC cyaY | 1.00 ± 0.01 | 0.37 ± 0.01 | 0.33 ± 0.01 |
DN7306 | yggX apbC | 0.98 ± <0.01 | 0.35 ± 0.01 | 0.32 ± <0.01 |
DM7643 | yggX cyaY | 1.00 ± 0.01 | 0.34 ± 0.01 | 0.31 ± 0.02 |
DM7641 | yggX apbC cyaY | 1.00 ± 0.01 | 0.22 ± 0.01 | 0.19 ± 0.01 |
Overnight cultures grown in rich media were subcultured with 150 μl added to 5 ml nutrient broth (NB) containing 0, 40, or 80 μM paraquat as indicated. Cultures were incubated with shaking at 37°C, and growth was monitored by measurement of optical density at 650 nm (OD650) with a Bausch and Lomb Spectronic 20. The final OD650 reported was after 24 h, since absorbance for all strains had reached a plateau by that time. In all cases, loci indicated for relevant genotypes were inactivated by insertion.
Values reflect the averages (±standard deviations) of two independent cultures.