Thiosulfate-induced formation of SoxB and SoxG.
P. pantotrophus was cultivated in mineral medium (400
ml) with 10 mM sodium succinate plus 10 mM glucose in a 1-liter baffled
Erlenmeyer flask. After the cells reached the stationary phase at an
optical density at 436 nm of 6.35, sodium thiosulfate (20 mM) was
added. Cells (0.7 ml) were collected by centrifugation, resuspended
with 150 μl of SDS sample buffer, and incubated at 60 and 100°C for
5 min each. Cell debris was removed by centrifugation, and the
supernatant was diluted with four aliquots of sample buffer. From this
preparation, 20 μg of protein was subjected to SDS-PAGE.
Immunoblotting was performed as described in Materials and Methods.
Signal intensity was quantified using the Scion Image software. ○,
oxygen uptake rate; ●, pH; ▪, SoxG; □, SoxB.