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. Author manuscript; available in PMC: 2013 May 1.
Published in final edited form as: Mol Microbiol. 2013 Jan 11;87(4):802–817. doi: 10.1111/mmi.12132

Fig. 2. Comparison of RcGTA recipient capability of QS mutant strains with their ability to adsorb RcGTA particles.

Fig. 2

A. Ability of WT, ΔgtaI, ΔgtaR, ΔgtaRI, and ΔgtaI supplemented with C16-acyl-HSL strains to be transduced by RcGTA containing a Rifampicin resistance marker.

B. RcGTA adsorption ability of strains (values are presented as a percentage of the number of RifR transductants obtained in the unabsorbed control where no cells were added to the reaction mixture, indicated by %NC).

C. Western blot of adsorption assay filtrate probed with RcGTA capsid protein antiserum. Error bars represent the standard deviation between samples (n ≥ 3). Statistical analysis was done by One-Way ANOVA, given in Tables S3 and S4.