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Team:XMU-China/timedelay
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Revision as of 21:23, 25 September 2012
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Time Delay
1. OverviewFor the lengths of our genetic circuits are not the same, based on quorum sensing system we had studied last year, we considered that the time of genetic expressions of each circuit is different because of the different lengths and strength of ribosome binding sites. So we constructed circuits with five grades strength of ribosome binding sites, including 0.01, 0.6 and 1.0. After induced by arabinose, the duration of response time for GFP expression increases as the strength of RBS declines, bringing about a time-course display.
2. Review of last year
Last year, we had developed a series of devices which program a bacteria population to maintain at different cell densities. [1]We had designed and characterized the genetic circuit to establish a bacterial ‘population-control’ device in E. coli based on the well-known quorum-sensing system from Vibrio fischeri, which autonomously regulates the density of an E. coli population. The cell density however was influenced by the expression levels of a killer gene (ccdB) in our device. As such, we had successfully controlled the expression levels of ccdB by using RBSes of different strength and mutated luxR promoters (lux pr). This circuit incorporated a mechanism for programmed death in respond to changes in the environment.
Figure 1. The mechanism graph of iccdB last year
3. Constructions this year
Figure 2. The construction devices of time delay system
Based on our last year’s project, for convenience of testing the results of time delay device, we chose GFP instead of ccdB as our reporter. On the other hand, because of the basal expression of Plac is very strong, we decided to use arabinose to induce PBAD promoter to activate our device. Meanwhile, to accomplish the aim of time delay, which means we should make the GFP produce in different period of time, we decided to change the RBS’s strength of luxI expression system. RBSes of different strengths will cause the speed of quorum sensing effect, which will lead to the delay of GFP production time.
Figure 3. The mechanism graph of time delay system
4.1 Optimization of inducer concentration
We can find that the curve with 0.1mM arabinose has a higher fluorescence. So we chose the 0.1 mM arabinose for the following fluorescence tests.
4.2 Fluorescent test of the time delay devices
Figure 5. Fluorescence curves of TD1.0 induced by 0.1 mM arabinose and TD1.0 without arabinose.
Figure 6. Fluorescence curves of TD0.01 induced by 0.1 mM arabinose and TD0.01 without arabinose.
Figure 7. Fluorescence curves of TD0.6 induced by 0.1 mM arabinose and TD0.6 without arabinose
Figure 8. Fluorescence curves of the induced TD0.01, TD0.6, TD1.0 and the control BL21(DE3)
Figure 9. Experimentally measured the average time of the three cultures’ fluorescence up to 5000 after induction, it shows that the stronger RBS circuit contains, the less time it takes.
Compared with the groups absence of arabinose, the fluorescence of induction groups were much higher. On the other hand, we could find even the circuit with RBS0.01, the most insensitive one, also expressed green fluorescence protein without arabinose, which means basal expressing phenomenon. According to figure 5, when the three cultures induced by the same concentration of arabinose, the fluorescence of TD1.0 was the highest, TD0.6 was middle and TD0.01 was the lowest. Finally, as shown in figure 8, the fluorescence of the circuits with different RBSes also reached a certain level in different time. It fit the goal of time delay.
