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. Author manuscript; available in PMC: 2014 Jan 1.
Published in final edited form as: Mol Microbiol. 2012 Nov 19;87(1):94–111. doi: 10.1111/mmi.12085

Fig. 2. Resections and alterations of the CepR2 binding site.

Fig. 2

The dyad symmetrical CepR2 binding site is indicated using inverted arrows. All sequences shown were part of bcam0191-lacZ fusions. B. cenocepacia sequences are capitalized while vector sequences are shown in lower case. Vector sequences that fortuitously match the original DNA sequence are capitalized. Site-directed mutations of the CepR2 binding site are underlined.β-galactosidase specific activities were determined for cells cultured for 12 hours in the presence or absence of OHL. The values shown are the means and standard deviations (error bars) of three independent experiments.