This is beta-galactosidase activity in cultures that have been transferred from LB (= rich medium) to M9 salts plus a tiny bit of casamino acids (starvation medium). Transfer was at time=0.
All cells carried the
ppdA::lacZ fusion on the same plasmid. The black line is cells that are
sxy+ and
crp+. The blue line cells are
sxy-, and the red line cells are
crp-.
It's clear that beta-gal activity increased similarly in all three cultures. As seen for the cultures in rich medium (previous post), the
crp- cells had slightly lower activity, while the
sxy+ and
sxy- cells had almost identical activity.
So I conclude that the treatments I've tried so far have not changed the Sxy-dependent activity of the
ppdA promoter.
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