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. Author manuscript; available in PMC: 2014 Jul 21.
Published in final edited form as: Mol Microbiol. 2007 Nov 19;66(6):1459–1473. doi: 10.1111/j.1365-2958.2007.06008.x

Table 2.

Quantitative analysis of WspR–YFP cluster formation in various strains grown on agar surfaces.

Strain Percentage of cells with WspR–YFP localized in clustersa Total cells scored
wspR–yfp 29.7 (±2.9) 692
Δ wspF wspR–yfp 59.8 (±11.8) 493
Δ wspA wspR–yfp 0.22 (±0.3) 253
Δ wspF ΔwspA wspR–yfp 1.32 (±1.2) 270
Δ wspF wspR[E253A]–yfp 74.95 (±1.9) 290
ΔwspA wspR–yfp/pJN105 0.5 (±0.7) 299
ΔwspA wspR–yfp/pWspA 37.6 (±4.3) 280
ΔwspF ΔwspA wspR–yfp/pJN105 0.3 (±0.4) 190
ΔwspF ΔwspA wspR–yfp/pWspA 58.1 (±4.6) 414
a

WspR–YFP clustering was scored based on the presence of a well-defined fluorescent spot in cells. This evaluation was based on the measurement of maximum and average signal intensities of single cells as described in the Experimental procedures. After calculating ratios of maximum to average signal intensities, a ratio value corresponding to presence of a well-defined spot was used as a threshold to sort the cells. At least two independent experiments were performed. Average values are given for the percentage of cells that scored above the ratio threshold value. Standard deviations are indicated in parentheses. Cells were grown on LB medium solidified with 2.5% agar as described in Experimental procedures.