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. 2007 Jul 20;189(19):7159–7163. doi: 10.1128/JB.00705-07

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
a

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.

b

Bold denotes that the differential expression is significant (P < 0.05) as determined by Student's t test.

c

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.