Lambda cI autoinducing loop family

Leakiness of the autoinducing loops

To estimate the rate in which single cells are activated by too much leakage of cI protein we measured the fluorescence in uninduced cells with a flow cytometer. To measure the activation we used a construct with the PRM promoter producing GFP with an LVA tag to make dynamic measurement possible.

Flowcytometry-data of the cI autoinducing loop with no tag (BBa_K607022) after 4 hours of incubation
Figure 1. A dotplot of uninduced cells carrying the pSB1K3 plasmid with the biobrick BBa_K607022 and the plasmid pSB1A3 with an input(PBAD controlling cI) as well as the output (PRM controlling GFP-LVA).	Number  % of total Mean fluorescence Visible 50000 100 --- Fluorescent 9180 18,36 11419 Non-Fluorescent 34424 68 5974
Two populations are visible on the dotplot. We seperated both populations on the histogram to show that the major peak of nonfluorescent cells overlaps the minor peak of fluorescenting cells.

Flowcytometry-data of the cI autoinducing loop with a DAS tag (BBa_K607017) after 4 hours of incubation
Figure 2. A dotplot of uninduced cells carrying the pSB1K3 plasmid with the biobrick BBa_K607017 and the plasmid pSB1A3 with an input(PBAD controlling cI) as well as the output (PRM controlling GFP-LVA).	Number  % of total Mean fluorescence Visible 50000 100 --- Fluorescent 5793 11,58 17336 Non-Fluorescent 43237 86,47 16276
Two populations are visible on the dotplot. We seperated both populations on the histogram to show that the major peak of nonfluorescent cells overlaps the minor peak of fluorescenting cells.

Flowcytometry-data of the cI autoinducing loop with a LVA tag (BBa_K607011) after 4 hours of incubation
Figure 3. A dotplot of uninduced cells carrying the pSB1K3 plasmid with the biobrick BBa_K607011 and the plasmid pSB1A3 with an input(PBAD controlling cI) as well as the output (PRM controlling GFP-LVA).	Number  % of total Mean fluorescence Visible 50000 100 --- Fluorescent 1119 2,23 6445 Non-Fluorescent 41686 83,37 2955
Only one population is visible on the dotplot. The histogram was obtained in the same fashion as in figure 1 to show that there are cultures with activated cI loops and cultures without.

These measurements indicate activation and by this bimodal behavior of cells containing BBa_K607022 and BBa_K607017. But no activation of BBa_K607011 and several other constructs. In these measurements we used GFP-LVA. The degradation seems to be about as fast as the production so only faint signals are visible. We decided to repeat the measurement with similar constructs but with GFP instead of GFP-LVA as an output.

	no-tag	DAS	LVA
RBS 0,07	BBa_K607019	BBa_K607014	BBa_K607010
RBS 0,3	BBa_K607020	BBa_K607016	BBa_K607011
RBS 0,6	BBa_K607021	BBa_K607017	BBa_K607012
RBS 1	BBa_K607022	BBa_K607018	BBa_K607013
Figure 4. Flow cytometer data taken at different time-points during exponential growth of cells carrying different cI autoinducing loops.

This result shows that both, tag and RBS, used for the expression of the transcription factor have a huge impact on the bimodal behavior of the autoinducing loop. All loops that contain a LVA-tag tag are inactive if not induced. Those without any tag are mostly active even without induction while those with a DAS-tag show a bimodal behavior. Especially the cells carrying the plasmids with a strong RBS in the autoinducing loop look promising.

Figure 5. BBa_K607022 This autoinducing loop does exhibit heterogenity when non-induced. Two populations are visible - a population that is not producing GFP and a population that is producing GFP is observed. After 4 hours of incubation approximately 87,82% of the visible cells are fluorescent while 9,24% are not fluorescent. That means that the loop is induced in some of the cells through a leaky promoter. Changing the promoter to a less leaky version might make it a good candidate for an inducible and robust bistable switch.

Figure 6. BBa_K607018 This autoinducing loop does exhibit heterogenity when non-induced. Two populations are visible - a population that is not producing GFP and a population that is producing GFP is observed. After 4 hours of incubation approximately 36,45% of the visible cells are fluorescent while 61,88% are not fluorescent. That means that the loop is induced in some of the cells through a leaky promoter. Changing the promoter to a less leaky version might make it a good candidate for an inducible bistable switch.

Figure 7. BBa_K607013 This autoinducing loop does not exhibit heterogenity when non-induced. Only the population that is not producing GFP is observed. After 4 hours of incubation approximately only 1,03% of the visible cells are fluorescent while 93,91% are not fluorescent. That means that the loop is not induced through a leaky promoter and is a good candidate for an inducible bistable switch.

Induction of the autoinducing loops

In the future it should be tried to activate the autoinducing loops by expression of cI-LVA controlled by the arabinose induced promoter pBAD.