BACTH analysis of Crl-σ interactions The table lists measured
β-galactosidase activities in BTH101 cya cells carrying pKT25
derivatives encoding a T25-σ70 or a T25-σs
fusion protein and pUT18 derivatives encoding Crl-T18 and Rsd-T18 fusions.
Cells were grown on MacConkey maltose plates containing 100 μg/ml
ampicillin, 50 μg/ml kanamycin, and 0.5 mm isopropyl
1-thio-β-d-galactopyranoside at 30°C before measuring
β-galactosidase activities. No difference in activity was detected
between E. coli Crl-T18 and S. enterica Crl-T18.