Team:Paris Saclay/Notebook/August/6
From 2014.igem.org
(→Lab work) |
m (→Wednesday 6th August) |
||
(15 intermediate revisions not shown) | |||
Line 2: | Line 2: | ||
=Wednesday 6th August= | =Wednesday 6th August= | ||
==Lab work== | ==Lab work== | ||
- | === | + | ===The chassis coli Odor free=== |
====Final stock of MG1655==== | ====Final stock of MG1655==== | ||
''by Romain'' | ''by Romain'' | ||
Line 8: | Line 8: | ||
2 final stocks of the MG1655 made with 1ml of strain and 250µl glycerol 87%, in -80°C. | 2 final stocks of the MG1655 made with 1ml of strain and 250µl glycerol 87%, in -80°C. | ||
- | === | + | ===Salicylate Inducible Suppressing System=== |
====Plasmid DNA Purification==== | ====Plasmid DNA Purification==== | ||
''by Eugene and Fabio'' | ''by Eugene and Fabio'' | ||
Line 16: | Line 16: | ||
[https://2014.igem.org/Team:Paris_Saclay/Protocols/Extraction_of_the_Genomic_DNA_from_Bacteria_by_using_NucleoSpin®_Tissue Protocol] | [https://2014.igem.org/Team:Paris_Saclay/Protocols/Extraction_of_the_Genomic_DNA_from_Bacteria_by_using_NucleoSpin®_Tissue Protocol] | ||
+ | |||
====Digestion==== | ====Digestion==== | ||
''by Eugene and Fabio'' | ''by Eugene and Fabio'' | ||
Line 31: | Line 32: | ||
[https://2014.igem.org/Team:Paris_Saclay/Protocols/BioBrick_Assembly#Digest_reaction BioBrick Assembly - Digest Reaction Protocol] | [https://2014.igem.org/Team:Paris_Saclay/Protocols/BioBrick_Assembly#Digest_reaction BioBrick Assembly - Digest Reaction Protocol] | ||
====Segregate Process by Electrophoresis==== | ====Segregate Process by Electrophoresis==== | ||
+ | |||
+ | [[File:Paris_Saclay_060814_cut_gel.jpg|200px|left]] | ||
+ | |||
''by Eugene and Fabio'' | ''by Eugene and Fabio'' | ||
- | |||
# BBa_B0015 digested by '''EcoRI''' and '''XbaI''' | # BBa_B0015 digested by '''EcoRI''' and '''XbaI''' | ||
+ | # BBa_K1372000 digested by '''EcoRI''' and '''SpeI''' | ||
- | |||
- | |||
- | |||
- | |||
[https://2014.igem.org/Team:Paris_Saclay/Protocols/BioBrick_Assembly#Segregate_process BioBrick Assembly - Segregate Process Protocol] | [https://2014.igem.org/Team:Paris_Saclay/Protocols/BioBrick_Assembly#Segregate_process BioBrick Assembly - Segregate Process Protocol] | ||
- | === | + | ===Lemon scent=== |
- | ====PCR | + | ====PCR Clean-up==== |
''by Pierre & Sean'' | ''by Pierre & Sean'' | ||
Line 51: | Line 51: | ||
[https://2014.igem.org/Team:Paris_Saclay/Protocols/PCR_clean-up Protocol] | [https://2014.igem.org/Team:Paris_Saclay/Protocols/PCR_clean-up Protocol] | ||
- | |||
- | |||
- | |||
- | |||
- | |||
- | |||
- | |||
====PCR digestion==== | ====PCR digestion==== | ||
Line 87: | Line 80: | ||
Then bain-marie at 37°C for one hour. | Then bain-marie at 37°C for one hour. | ||
Finally conduct PCR cleanup for both BioBricks, with 15µl of NE buffer. | Finally conduct PCR cleanup for both BioBricks, with 15µl of NE buffer. | ||
+ | |||
+ | ''We acidentally used PvuI instead of PacI. - SC 6/8/14'' | ||
====PCR pCola plasmide (Geranyl Synthase)==== | ====PCR pCola plasmide (Geranyl Synthase)==== | ||
Line 95: | Line 90: | ||
[https://2014.igem.org/Team:Paris_Saclay/Protocols/PCR_for_the_genomic_DNA_of_bacteria protocol] | [https://2014.igem.org/Team:Paris_Saclay/Protocols/PCR_for_the_genomic_DNA_of_bacteria protocol] | ||
+ | PCR protocol: | ||
+ | 98° --> 2min | ||
+ | |||
+ | 5 PCR cycle: | ||
+ | |||
+ | {| class="wikitable centre" width="50%" | ||
+ | |+ | ||
+ | |- | ||
+ | ! scope=col | time | ||
+ | ! scope=col | 10sec | ||
+ | ! scope=col | 20sec | ||
+ | ! scope=col | 45sec | ||
+ | |- | ||
+ | !temperature | ||
+ | |98° | ||
+ | |(depending on the tube - see the gradient) | ||
+ | |72° | ||
+ | |} | ||
+ | |||
+ | 25 PCR cycle | ||
+ | |||
+ | {| class="wikitable centre" width="50%" | ||
+ | |+ | ||
+ | |- | ||
+ | ! scope=col | time | ||
+ | ! scope=col | 10sec | ||
+ | ! scope=col | 20sec | ||
+ | ! scope=col | 45sec | ||
+ | |- | ||
+ | !temperature | ||
+ | |98° | ||
+ | |72° | ||
+ | |72° | ||
+ | |} | ||
+ | |||
+ | and last step: 72° during 10min | ||
+ | |||
+ | but we don't have any results | ||
====Gel electrophoresis==== | ====Gel electrophoresis==== | ||
Line 101: | Line 134: | ||
Samples used: | Samples used: | ||
- | |||
# '''BBa_K762100''' (2µl) | # '''BBa_K762100''' (2µl) | ||
+ | # '''BBa_K517003''' (2µl) | ||
# '''p cola'''(12µl) | # '''p cola'''(12µl) | ||
Line 111: | Line 144: | ||
Still working on my mission: find more informations about limonene, pinene and citral A and B.I got now a couple of very interessant reviews about limonene and pinene. | Still working on my mission: find more informations about limonene, pinene and citral A and B.I got now a couple of very interessant reviews about limonene and pinene. | ||
+ | ==Photo of the Day== | ||
+ | [[File:Paris Saclay 6_august.jpg|600px|center]] | ||
'''Members present:''' | '''Members present:''' |
Latest revision as of 14:21, 14 October 2014
Contents |
Wednesday 6th August
Lab work
The chassis coli Odor free
Final stock of MG1655
by Romain
2 final stocks of the MG1655 made with 1ml of strain and 250µl glycerol 87%, in -80°C.
Salicylate Inducible Suppressing System
Plasmid DNA Purification
by Eugene and Fabio
- BBa_K1372000 Cl.1
- BBa_K1372000 Cl.2
From Liquid Culture made the 5th August
Digestion
by Eugene and Fabio
In order to place the BBa_B0015 just after the BBa_K1372000, we will start the [http://parts.igem.org/Help:Assembly/3A_Assembly Assembly procedure] again.
- BioBrick BBa_K1372000 (Salicylate promoter + NahR + RNA suppressor) as Part A
- BioBrick BBa_B0015 (Double terminator) as Part B
The enzymes used were:
- EcoRI and SpeI for BBa_K1372000
- EcoRI and XbaI for BBa_B0015
TODO: Illustration of the process
BioBrick Assembly - Digest Reaction Protocol
Segregate Process by Electrophoresis
by Eugene and Fabio
- BBa_B0015 digested by EcoRI and XbaI
- BBa_K1372000 digested by EcoRI and SpeI
BioBrick Assembly - Segregate Process Protocol
Lemon scent
PCR Clean-up
by Pierre & Sean
BioBricks used: BBa_K762100 and BBa_K517003 (PCR perfomed on the 4th August)
PCR digestion
by Pierre & Sean
Protocol
For each BioBrick (Bba_K517003 and BBa_K762100)mix the following into a microcentrifuge tube.
component | volume |
---|---|
H2O | 5.5μl |
PacI | .5μl |
Fast Digest buffer | 4μl |
Cleaned-up PCR content | 30μl |
Then bain-marie at 37°C for one hour. Finally conduct PCR cleanup for both BioBricks, with 15µl of NE buffer.
We acidentally used PvuI instead of PacI. - SC 6/8/14
PCR pCola plasmide (Geranyl Synthase)
by melanie
amplification of geranyl Synthase
PCR protocol: 98° --> 2min
5 PCR cycle:
time | 10sec | 20sec | 45sec |
---|---|---|---|
temperature | 98° | (depending on the tube - see the gradient) | 72° |
25 PCR cycle
time | 10sec | 20sec | 45sec |
---|---|---|---|
temperature | 98° | 72° | 72° |
and last step: 72° during 10min
but we don't have any results
Gel electrophoresis
by Sean,Pierre & Melanie
Samples used:
- BBa_K762100 (2µl)
- BBa_K517003 (2µl)
- p cola(12µl)
Bibliography
By Hoang Vu
Still working on my mission: find more informations about limonene, pinene and citral A and B.I got now a couple of very interessant reviews about limonene and pinene.
Photo of the Day
Members present:
- Instructors and advisors: Alice.
- Students: Eugene, Fabio, Hoang Vu, Juliette, Melanie, Pierre, Romain, Sean and Terry.