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. 2006 Dec 1;189(3):833–843. doi: 10.1128/JB.01530-06

FIG. 3.

FIG. 3.

Arginine-specific activity partitioning in the bacterial culture. Early stationary-phase cultures of each mutant were separated into cellular, vesicular, and medium fractions, and 20-μl samples of each fraction were assayed against an Arg-specific synthetic substrate as per Materials and Methods. The total Rgp activity in the RgpB+ control mutant was set at 100 activity units. Data were obtained from duplicate enzymatic measurements from four independently grown cultures and were normally distributed. Differences in the total arginine-specific activity of each strain against the RgpB+ mutant were statistically analyzed using one-way ANOVA with Bonferroni's correction. Values that were significantly different from the value for the RgpB+ mutant are indicated by asterisks (*, P < 0.05; ***, P < 0.001).