Table 2.
PhoPQ regulation of ivi genes
ivi-lac fusion* | β-Galactosidase, units†
|
||
---|---|---|---|
phoP+Q+ | phoP102::Tn10d-Cm | phoQ24 | |
phoP | 110 | 11 | 132 |
spvB | 118 | 14 | 294 |
pmrB | 122 | 31 | 187 |
mgtB | 48 | 9 | 35 |
iviVI-A | 236 | 5 | 563 |
ndk | 18 | 21 | 21 |
Wild-type, PhoP− [phoP102::Tn10d-Cm (7)], and PhoQc [phoQ24, which constitutively activates PhoP-activated genes (8)] strains were grown in Mops media (15), where Mops [3-(N-morpholino)propanesulfonic acid] was replaced with Mes [2-(N-morpholino)ethanesulfonic acid] and buffered to pH 5.5 (50 μM Mg2+). The defects observed in phoP102::Tn10d-Cm may also be attributed to the lack of phoQ.
Numbers given indicate β-galactosidase activities assayed according to Slauch and Silhavy (14). Units are given as (units per OD600 unit × ml of cell suspension) × 103, where 1 unit = 1 μmol of o-nitrophenol formed per min (n = 3, SD < 10%).