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. 2008 Nov 28;283(48):33455–33464. doi: 10.1074/jbc.M807380200

TABLE 1.

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.

Protein fusion 1 Protein fusion 2 β-Galactosidase activity
Miller units
1 T25-σ70 T18 63
2 T25-σ70 E. coli Crl-T18 60
3 T25-σ70 S. enterica Crl-T18 62
4 T25-σ70 E. coli Rsd-T18 1022
5 T25-σs T18 60
6 T25-σs E. coli Crl-T18 696
7 T25-σs S. enterica Crl-T18 698
8 T25-σs E. coli Rsd-T18 72