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 |
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.