Team:Paris Saclay/Notebook/August/26
From 2013.igem.org
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|name | |name | ||
| fnr(repressor) | | fnr(repressor) | ||
- | | fnr | + | | fnr nirB clone 6 |
- | | fnr | + | | fnr nark clone 6 |
- | | fnr | + | | fnr nirB clone 7 |
- | | fnr | + | | fnr narG clone 6 |
- | | fnr | + | | fnr narG clone 7 |
- | | fnr | + | | fnr nark Digested SPE I |
- | | fnr | + | | fnr narB Digested SPE I |
- | | fnr | + | | fnr narG Digested SPE I |
|- | |- | ||
|conc. | |conc. |
Revision as of 08:39, 9 September 2013
Contents |
Notebook : August 26
summary
- started the Restriction digestion and ligation to get the BioBrick fnr into plasmid PSB1C3 by using restrictin ensyme EcoRI and PstI.
- Sent an E-mail to M. Nesbeth from UCL for requesting the Biobrick BBa_K239005 which was created by iGEM UCL team in 2009
- Designed oligonucleotides for the gene coding for BphR2 (regulator, sensitive for PCBs), Transcriptional regulator of Pseudomonas oleovorans /pseudoalcaligenes group
lab work
- A.aero/anaerobic regulation system
- 1.BioBrick promotor fnr(repressor and activator) in plasmid PSB1C3
- Digestion for promoter fnr(repressor and activator) in PSB1C3
- 2 enzymes SPE I and PST I
- For promoter fnr(repressor) :
DNA | 14µl |
SPE I | 2µl |
PST I | 2µl |
H2O | 0µl |
buffer | 2µl |
total | 20µl |
- For promoter fnr(activator)nirB clone 6:
DNA | 14µl |
SPE I | 2µl |
PST I | 2µl |
H2O | 0µl |
buffer | 2µl |
total | 20µl |
- For promoter fnr(activator)nark clone 6 :
DNA | 4µl |
SPE I | 2µl |
PST I | 2µl |
H2O | 10µl |
buffer | 2µl |
total | 20µl |
- For promoter fnr(activator)nirB clone 7 :
DNA | 14µl |
SPE I | 2µl |
PST I | 2µl |
H2O | 0µl |
buffer | 2µl |
total | 20µl |
- For promoter fnr(activator)narG clone 6 :
DNA | 7µl |
SPE I | 2µl |
PST I | 2µl |
H2O | 7µl |
buffer | 2µl |
total | 20µl |
- For promoter fnr(activator)narG clone 7 :
DNA | 14µl |
SPE I | 2µl |
PST I | 2µl |
H2O | 0µl |
buffer | 2µl |
total | 20µl |
- For promoter fnr(activator)nark Digested SPE I :
DNA | 9µl |
SPE I | 0µl |
PST I | 2µl |
H2O | 7µl |
buffer | 2µl |
total | 20µl |
- For promoter fnr(activator)narB Digested SPE I :
DNA | 13µl |
SPE I | 0µl |
PST I | 2µl |
H2O | 3µl |
buffer | 2µl |
total | 20µl |
- For promoter fnr(activator)narG Digested SPE I :
DNA | 10µl |
SPE I | 0µl |
PST I | 2µl |
H2O | 6µl |
buffer | 2µl |
total | 20µl |
- Incubate at 37°C for 30 mins.
- Then we performed a precipitation by ethanol in order to inactivate the enzymes for those 9 digestion.
Protocol : Ethanl precipitation
- Degestion product quantification
- We used the nano drop to measure the DNA in 260nm and we found its concentration
name | fnr(repressor) | fnr nirB clone 6 | fnr nark clone 6 | fnr nirB clone 7 | fnr narG clone 6 | fnr narG clone 7 | fnr nark Digested SPE I | fnr narB Digested SPE I | fnr narG Digested SPE I |
conc. | 91.8ng/µl | 46.0ng/µl | 19.8ng/µl | 61.6ng/µl | 13.4ng/µl | 103.9ng/µl | 15.1ng/µl | 16.1ng/µl | 17.1ng/µl |
|}
A - Aerobic/Anaerobic regulation system / B - PCB sensing system
1 - Gibson assembly.
- RBS_BphR2_part1, BphR2_part2 and plasmid PSB1C3
- FNR_part1, FNR part1 and plasmid PSB1C3
- RBS_FNR part1, FNR_part2 and plasmid PSB1C3
Sample Volume:
|
These 3 mixture is incubated at 50°C for up to one hour. Transformation and spread in 6 LB plates with Chlorenphenicol . Incubate at 37°C over night.
- Ligation
- After 3h of digestion, we mixed the digestion products:
PCR product | 30µl |
PSB1C3 | 4µl |
Ligation buffer | 2µl |
H2O | 14µl |
- B.PCBs sensor system
- 1.BioBrick BphR2(regulator) in plasmid PSB1C3
- 1.BioBrick BphR2(regulator) in plasmid PSB1C3
- Using software gene manager to find the oligopeptide for amplification of BphR2.
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