TABLE 1.
Effects of pH and salt on fimB-lacZ and fimE-lacZ fusions in WT E. coli compared to effects on isogenic rcsB and rcsC mutants
Fusion and strain | Expression level (Miller units) under indicated growth conditiona
|
|||
---|---|---|---|---|
pH 7.0 | pH 7.0 (+) | pH 5.5 | pH 5.5 (+) | |
fimB-lacZ fusion | ||||
WT | 345 ± 30 | 259 ± 36 | 271 ± 20 | 219 ± 23 |
rcsB | 201 ± 19b | 229 ± 27 | 274 ± 62 | 182 ± 48 |
rcsB/pRcsBc | 329 ± 21 | 315 ± 13 | 297 ± 11 | 231 ± 11 |
rcsC | 305 ± 34 | 235 ± 36 | 284 ± 51 | 238 ± 57 |
fimE-lacZ fusion | ||||
WT | 335 ± 26 | 318 ± 54 | 252 ± 35 | 237 ± 26 |
rcsB | 332 ± 34 | 463 ± 68 | 260 ± 54 | 221 ± 60 |
rcsB/pRcsB | 339 ± 32 | 377 ± 70 | 231 ± 55 | 245 ± 13 |
rcsC | 365 ± 21 | 437 ± 53 | 260 ± 32 | 253 ± 48 |
Values indicate fimB and fimE promoter expression in terms of β-galactosidase activity and are means ± standard deviations from at least three independent experiments. Cells were grown in LB at pH 7.0 or pH 5.5 with the low or high (+) salt and harvested during mid-exponential phase.
Bold denotes that the differential expression is significant (P < 0.05) as determined by Student's t test.
rcsB/pRcsB is the rcsB mutant transformed with pHRcsB, which encodes a His-tagged WT rcsB allele under the control of the lac promoter. Induction, however, was unnecessary.