Skip to main content
. Author manuscript; available in PMC: 2020 Apr 14.
Published in final edited form as: Nat Chem Biol. 2019 Oct 14;15(11):1102–1109. doi: 10.1038/s41589-019-0372-9

Figure 6.

Figure 6

Experimental estimation of the phase difference maps. (a) Kymograph of a P2N2 consortium with windows indicating the relative positions of two example subpopulations used to calculate phase difference maps (n=5 independent experiments). The paired subpopulation windows are 167μm wide, and 67μm apart. (b) Average total fluorescence as a function of phase for the two subpopulations in the windows shown in (a). Here Δϕi represents the phase difference at the peak of the ith cycle. The phase differences are decreasing and the two subpopulations reach synchrony at the 6th cycle. (c) The mapping of phase differences (|Δϕi+1| as a function of |Δϕi |) for different architectures (light symbols) was computed using the data presented in Fig. 2il and Supplementary Fig. 3eh. We obtained mean phase difference maps for each consortium type by averaging groups of 10 phase differences sequentially, separately for consortia with (blue curve) and without (red curve) a positive feedback loop. On average, phase differences shrink for consortia with the positive feedback, as the blue curve lies below the diagonal. In contrast, phase differences grow for consortia without the positive feedback, as the red curve is mostly above the diagonal. Error bars represent standard error.