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. 2014 Jan 17;9(1):e85731. doi: 10.1371/journal.pone.0085731

Figure 3. Correlation of the Lrp-sensor output (eYFP) and the plasmid marker E2-Crimson.

Figure 3

(A) Microscopy overlay plot of phase-contrast, eYFP and E2-Crimson signal of an isogenic microcolony of the ΔaceE Δpqo Δpgi sensor strain after 46 h (see Figure 2C). (B) Dot plot displaying eYFP and E2-Crimson signal of single cells of three isogenic microcolonies (triangles, circles, and diamonds) of the ΔaceE Δpqo Δpgi sensor strain.

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