Description

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1.3.2 mazEF System Assay

Since MazE resuscitates E. coli after MazF expression inhibits cell growth and translation, MazF inhibits cell growth and translation after MazE expression, it was suggested that using maze system can regulate cell growth and translation.

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1.4 Discussion

We learned the appropriate Arabinose concentration, 0.02%, to induce MazF. This assay firstly shows that in one cell, MazE resuscitates E. coli after MazF expression inhibits cell growth and translation, then, MazF inhibits cell growth and translation after MazE expression. It is suggested that using maze system regulate cell growth and translation. In conclusion, we can indicate, as the function of TA system, not Kill Switch but a regulator of systems. It will be useful for information processing.

2. Improvement of Prhl

2.1. "Background”for our improvement of Prhl

We simulated our final genetic circuits and found that the circuits did not work, because Prhl activity was too weak compared to Plux. (see the Model page and the AHL Only Assay page). We therefore considered using the improved Prhl (BBa_K1529310, BBa_K1529300) established by iGEM 2014 Tokyo_Tech, but we noticed that they were inappropriate for two reasons: crosstalk to C12 and type of rhlR (written below). Then, we decided to improve wild type Prhl(BBa_R0071).

2.2. Summary of the experiment

By introducing a single point mutation into wild type Prhl (BBa_R0071) by PCR, we obtained 198 Prhl mutants and obtained the Prhl mutants of which promoter activity was stronger than wild type Prhl(BBa_R0071), and named it Prhl(Noticeable Mutant) (BBa_K1949060), hereafter referred to as Prhl(NM), which suited our goal.

2.3. Results

The SN ratio of Prhl(NM)(BBa_K1949060) was higher than that of Prhl(LR)), Prhl(LR)(BBa_1529310)and Prhl(NM)(BBa_K1949060) did not crosstalk to C12 unlike Prhl(LR).

2.4. Discussion

Many iGEM teams used AHL and probably this tendency continues. When you use AHL, you will find that promoter strength is quite different depending on the type of AHL and it bothers you to design genetic circuits, for example, including Plux and Prhl. Prhl(NM) (BBa_K1949060) has almost as same strong activity as Plux. Furthermore, Prhl(NM) (BBa_K1949060) has higher specificity to C4 than Prhl(LR)(BBa_1529310). Prhl(NM) (BBa_K1949060) can be said that it expands the possibility of using various combination promoters depending on AHL.

3. Characterization of rhlR

3.1. "Background”for our Characterization of rhlR

When we used two type of rhlR, one was LVA-tagged and the other was normal, we found that gap introduced with rhlR barely expressed but gfp introduced with rhlR-LVA expressed greatly. We decided to find this cause.

3.2. Summary of the experiment

Measure RFU of GFP of the E. coli containing (a) Pcon-rbs-rhlR-LVA (pSB6A1), Prhl(LR)-rbs-gfp (pSB3K3), (b) Pcon-rbs-rhlR (pSB6A1), Prhl(LR)-rbs-gfp (pSB3K3), (c) Pcon-rbs-rhlR-LVA (pSB6A1), Prhl(RL)-rbs-gfp (pSB3K3) or (d)Pcon-rbs-rhlR(pSB6A1), Prhl(RL)-rbs-gfp (pSB3K3). And we found that gfp expresses much if it introduced with rhlR-LVA even though using stronger Prhl than wild type Prhl(BBa_R0071). Thls is because that RhlR, which represses Prhl without C4, tagged LVA is prone to be degraded and the concentration of RhlR in a cell decreases then the repression becomes weak.

3.3. Results

The level of GFP expression of (a)~(d) are shown below.

3.4. Discussion

The expression level of the gene under Prhl depends on not only Prhl activity but also the type of the rhlR. In other words, this characterize shows that the combinations of Prhl and rhlR can control the expression level of the gene under Prhl. It gives you more choices which Prhl and rhlR you use.