TABLE 2.
Expression of cnrCBA-lacZ in various AE126 mutant strainsa
Megaplasmid | In trans | 0 mM Ni2+
|
0.5 mM Ni2+
|
||
---|---|---|---|---|---|
β-Galactosidase activityb before induction | Increase in β-galactosidase activityc | β-Galactosidase activity before induction | Increase in β-galactosidase activity | ||
pMOL28d | Φ(cnrHp-lacZ) | 11.1 ± 3.7 | 0 | 10.8 ± 8.6 | 0 |
Φ(cnrYp-lacZ) | 6.43 ± 1.49 | 8.76 | 0.06 ± 0.01 | 39 | |
Φ(cnrCp-lacZ) | 0.87 ± 0.52 | 1.26 | 0 | 15 | |
pMOL28-2, Φ(cnrCBA-lacZ) | None | 62.2 ± 6.8 | 0 | 64 ± 5 | 86.4 |
nccYXH | 40.0 ± 4.5 | 0 | 46.1 ± 4.7 | 0 | |
pMOL28-5e Φ(cnrCBA-lacZ) Ω(cnrHC::pECD581) | None | 121 ± 5 | 0 | 102.6 ± 0.4 | 90.7 |
pMOL28-3, Φ(cnrCBA-lacZ) ΔcnrYXH | None | 28.1 ± 2.5 | 0 | 26.6 ± 1.0 | 0 |
cnrYXH | 36.0 ± 5.1 | 0 | 48.5 ± 1.8 | 24.8 | |
cnrY | 39.9 ± 3.3 | 0 | 33.2 ± 3.3 | 0 | |
cnrX | 34.6 ± 6.0 | 0 | 36.7 ± 3.7 | 0 | |
cnrH | 937 ± 106 | 0 | 770 ± 52 | 0 | |
cnrYX | 31.6 ± 3.6 | 0 | 35.0 ± 4.8 | 0 | |
cnrYH | 1,650 ± 93 | 0 | 1,590 ± 140 | 0 | |
cnrXH | 900 ± 195 | 0 | 1,025 ± 320 | 0 | |
cnrY1(Con) cnrXH | 1,350 ± 60 | 0 | 1,380 ± 97 | 0 | |
nccYXH | 39.9 ± 4.2 | 0 | 47.9 ± 1.3 | 0 | |
pMOL28-4, Φ(cnrCBA-lacZ) cnrY1(Con) | None | 1,025 ± 107 | 0 | 1,095 ± 88 | 0 |
cnrYXH | 63.1 ± 5.9 | 18.4 | 61.3 ± 1.2 | 44.5 | |
cnrY | 114 ± 4 | 0 | 97 ± 2 | 26.0 | |
cnrX | 687 ± 53 | 0 | 896 ± 19 | 0 | |
cnrH | 678 ± 97 | 0 | 785 ± 64 | 0 | |
cnrYX | 151 ± 9 | 0 | 155 ± 19 | 0 | |
cnrYH | 1,010 ± 68 | 0 | 1,050 ± 176 | 0 | |
cnrXH | 1,226 ± 254 | 0 | 1,190 ± 176 | 0 | |
cnrY1(Con) cnrXH | 1,180 ± 55 | 0 | 1,450 ± 123 | 0 | |
nccYXH | 53.0 ± 6.3 | 0 | 59.1 ± 5.3 | 0 |
Ni2+ (0.5 or 0 mM) was added to cells of various Ralstonia strains which were growing in the early exponential phase (0 h). The β-galactosidase activity was determined for at least 3 h and plotted against time.
Means ± standard deviations. Values are units per milligram (dry weight). If no increase occurred, the mean values of all data points of the respective experiment are given.
Values are units per hour per milligram (dry weight).
The lacZ gene is under control of a cnr promoter on a pVDZ′2 plasmid complementing in trans.
Carries an insertion of pLO2 flanked by the duplicated region at bp 2100 to 2400. This separates cnrYXH from cnrCBA (Fig. 1).