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Team:EPF-Lausanne/LOVTAP Results
From 2009.igem.org
Parts
The biobrick parts (inducible LovTAP, RO1 and RO2) have been produced. We are currently sequencing them to confirm that there are no errors in the insert. You can have more information about these parts here
Characterization of RO1 and RO2
We characterized RO1 and RO2 by culturing cells containing one of the read-out systems under different conditions :
- With TRP
- With ATC
- With both
- Without anything
And at different concentrations.
We had some trouble with the media, as we usually cultured the cells in LB, but it contains some TRP so it pertubated the results. Therefore we had to find a medium in which there was no TRP but on which cells could grow. We did a lot of different tests and we finally settled on a medium containing M9/minimal, amino acids and thiamine. At the beginning we also compared the results between growth on LB or M9 to see the difference.
Here are the final graphics that characterize our two read-out systems. More details can be found in the notebook section.
For RO1 :
So we can see there is a decrease in RFP expression when TRP is added.
For RO2 :
This experiment was done in LB medium. All cells were normalized to an OD's of 0.2 before adding inducers which were put into the liquid culture just before the measurements. The concentration of Tryptophan was 0.9 mg/ml and the concentration of Anhydrous Tetracyclin was of 50 ug/ml.
Here are the result from the machine
Here is an average signal for each condition as we had 4 measurements for each state
A last picture shows the relative difference between the signal from cells with Trp or ATC and the signal from the cells' background fluorescence.
This confirms that our construct responds both to Trp and ATC and shows the characteristics we expected.
Characterization of the entire system
The first result we obtained after an illumination of the entire system was the following :
We can see that our system mimicks the response with TRP, which is exactly what we wanted.
We first did one static measurement of fluorescence. For the + light condition we exposed the cells to the light for 2 hours.
Then we wanted to see the time course of the induction : when is the RFP expressed, how etc.
It appears that this actually happens during the first hour.
