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. 2002 Jun;184(12):3167–3175. doi: 10.1128/JB.184.12.3167-3175.2002

TABLE 5.

Environmental regulation with σSΔ1-50a

Variable(s) Culture condition β-Galactosidase sp act for lac fusion with the following promoter in the indicated strain:
proU P1
katE
rpoS+ ΔrpoS/pHYD408 rpoS+ ΔrpoS/pHYD408
Temp and growth phase 30°C, log 63 27 110 50
30°C, stationary 536 263 772 586
10°C, log 279 263 1,686 645
Osmolarity No NaCl 63 21 297 65
0.3 M NaCl 275 193 576 333
a

Cultures for β-galactosidase assays were grown in LB medium for experiments involving growth phase (log or mid-exponential phase and 1 h after entry into stationary phase) and temperature as variables and in K-tryptone medium (to mid-exponential phase at 30°C) for those involving osmolarity as the variable. For strain derivatives with the proU P1-lac fusion (on plasmid pHYD275), the medium was supplemented with trimethoprim; for derivatives with plasmid pHYD408, it was supplemented with ampicillin and Ara. Enzyme specific activities are reported in Miller units (22). Strains used were as follows (in the order rpoS+ and ΔrpoS): for proU P1-lac, GJ862 and GJ2778 (each with pHYD275); and for katE-lac, GJ2770 and GJ2782.