| Line 27: | Line 27: | ||
</br> | </br> | ||
Transfection of competent cells with the biobricks :</br> | Transfection of competent cells with the biobricks :</br> | ||
| - | + | - pLac</br> | |
| - | + | - mCherry</br> | |
| - | + | - cl Inverter</br> | |
| - | + | - RBS (Elowitz 1999)</br> | |
| - | + | - GFP</br> | |
</br> | </br> | ||
</dl> | </dl> | ||
Preparation of freezable competent cells (M15): 40 alicos of 100µL Test of the competent cells.
Begining of ‘intra-cell ROS concentration’ modelisation. Transfection of competent cells with the biobricks : - pLac - mCherry - cl Inverter - RBS (Elowitz 1999) - GFP First contact with Arduino : the electronic device that will be used as a controler, just as the Cambridge 2010 iGEM team. Culture of the BBs k174000 and K592004/5/6
Failure with the transfections. Other problem with the petri dishes : everything grew, even the WT colonies that should have died because of antibiotics. Maybe the antibiotics are too old since they were used by Grenoble iGEM Team of 2012
Preparation of freezable competent cells (WT)(40 alicos of 100µL) Same transfections than wednesday, with fresh antibiotics. PCRs of pAraBad, mCherry and KillerRed, only pAraBAD worked. Team meeting TODO List : - Find a name - Begin construction of : ->pLac-RBS-YF1-fixJ ->pFixK2-RBS-GFP - glycerol-stock BBs - E-glometer, caracterisation of LED
Little Summary with Keywords
PCRs of mCherry and KR (did not work). Is there a problem with the primers or with the DNA templates? Need to work on that Put the transformed cells on petri dishes with the right antibiotics Receive the TSL230RD photodiodes Begin the test of Arduino (digital output) by turning on and off a LED and using a Graphical User Interface (GUI) to control the intensity Construction of the pQE30::KillerRed vector
Incubated a 50mL overnight culture of E. coli M15[pRep4] cells (Qiagen, Venlo, Netherlands), containing the pQE30::αSNAP vector, in preparation for midiprep.
Construction of the pQE30::KillerRed vector
Midi-prepped pQE30::αSNAP. The DNA sample concentration was only of 10 ng/µL. The experiment has to be re performed.
Incubated a 10mL overnight culture of E. coli M15[pRep4-pQE30::αSNAP] cells, in preparation for miniprep.
- Study the reasons why the PCR of mCherry and KR did not work. - New failure of the petri dishes, everything grew => miniprep the WT and found that there is already something in it. - These WT are not really WT, they can’t be used! We may have switched the real tube of WT with another one. Preculture WT from a glycerol stock to do again the transfection. - Create the first elements of an interface for the electronic part with Processing and Arduino.
Construction of the pQE30::KillerRed vector
Mini-prepped pQE30::αSNAP/pRep4 and got a 98,9 ng/µL DNA sample.
Digested pQE30::αSNAP with BamHI and KpnI restriction enzymes. Separation of the gene of non interest (αSNAP) from the pQE30 vector backbone by gel electrophoresis (1.2 % agarose, 30 min, 135V).
- Add some element on the interface of Processing - Write on computer a code that turn on one led or another according to the toggle that is pushed on the interface and generate a graph according to the intensity of the light represented by the value of a slider.
- Weld electric wires on the Surface Mounted Device (SMD) photodiode to test it on the wordkbench
- Read the datasheet of the photodiode (cf Electronic document) - Learn how to record the signal of the photodiode with Arduino - thanks to a tutorial on this website - Add some element on the interface of Processing - Test the analog input of Arduino - Verification of all the parameters for the non-working PCRs, list of test to perform
- PCR with tests (pQE30, and mCherry 2012) on mCherry-pAraBAD using a new sample of mCherry DNA. The test worked, its seems like the problem comes from the primers, I will perform cross pcr next week. - Gel extraction on KillerRed. Team Meeting
- PCR on KillerRed-Pbad - Weld electric wire on a new SMD photodiode to test it on the wordkbench - because the first one didn't appreciate to have 5V on its output instead of its input. - Test the response of the photodiode for different light powers (irrandiance µw/cm²), sensitivities and frequence scalings (cf oscillogram). - The 50% duty cycle mode may be easier for the algorithm in Arduino than the pulse train mode because each output pulses last 2*1/foutput. - Program Arduino and the Processing interface for the photodiode. Test it. The graph on the interface fits the irrandiance given by the oscilloscope
- MIDIPrep with PQE30 plasmids - PBad-KillerRed overlapping PCR -> failed - Weekly reunion decisions : - Electronics : wait to know what/how/when to measure / Create a "general and easily changeable" program. - Webdesign : still in discussion (‘Areva Style’ with improvements ?)
- New PCR on pBAD_KillerRed to have larger amount of DNA for the Overlapping PCR - Compare the different mode of the photodiode (duration pulse -500ns or duty cycle of 50%) - Use the oscilloscope to know if the program gives the same results - seems to have some difficulties for high frequencies. - Creation of models taking account of the inertia of some quantity : measure of fluorescence with severals half life for the GFP - 2 kind of controls : - On/Off control, it is not bad - PID regulator : it is very bad, don’t achieve to stabilize anything ->We need to develop a predictive control
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