Difference between revisions of "Team:Paris Saclay/Notebook/August/4"
(→Water contamination) |
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Line 32: | Line 32: | ||
We can conclude that all BBa_K1707008 clones are OK | We can conclude that all BBa_K1707008 clones are OK | ||
+ | |||
We make a glycerol stock of #1 and #2 | We make a glycerol stock of #1 and #2 | ||
− | ===Electrophoresis=== | + | ===Electrophoresis Verification=== |
''by Pauline and Coralie'' | ''by Pauline and Coralie'' | ||
Line 59: | Line 60: | ||
* BBa_K1707012 | * BBa_K1707012 | ||
− | SpeI + Pst | + | SpeI + Pst: |
− | === | + | * BBa_R0051 x2 |
− | '' by | + | * BBa_K1707013 |
+ | * BBa_K1707019 | ||
+ | * BBa_K1707000 | ||
+ | |||
+ | XbaI + EcoRI: | ||
+ | * BBa_I13602 | ||
+ | |||
+ | EcoRI + SpeI: | ||
+ | * BBa_K1707004 | ||
+ | |||
+ | |||
+ | Mix: | ||
+ | * 1 µL Enzyme 1 | ||
+ | * 1 µL Enzyme 2 | ||
+ | * 2 µL Buffer FastDigest 10x | ||
+ | * 6 µL H2O | ||
+ | * 10 µL Plasmide | ||
+ | |||
+ | |||
+ | ===Purification agarose gel=== | ||
+ | ''by Coralie and Audrey'' | ||
Biobricks: | Biobricks: | ||
− | * | + | * BBa_K1707011 |
− | * | + | * BBa_K1707004 |
+ | * BBa_E0022 | ||
+ | * BBa_E0422 | ||
+ | * BBa_K1707012 | ||
+ | * BBa_I13602 | ||
− | + | Agarose gel 1% | |
+ | |||
+ | Migration 100 V | ||
+ | |||
+ | We can conclude that I13602 isn't digested | ||
+ | |||
+ | |||
+ | ===Purification=== | ||
+ | ''by Pauline'' | ||
+ | |||
+ | Biobricks: | ||
+ | * BBa_K1707011 | ||
+ | * BBa_K1707004 | ||
+ | * BBa_E0022 | ||
+ | * BBa_E0422 | ||
+ | * BBa_K1707012 | ||
+ | * BBa_R0051 | ||
+ | * BBa_K1707013 | ||
+ | * BBa_K1707019 | ||
+ | * BBa_K1707000 | ||
+ | * BBa_K1707004 | ||
− | |||
===Soil experiment=== | ===Soil experiment=== | ||
Line 81: | Line 125: | ||
Water + concentrate cells solution 10 fold dilution | Water + concentrate cells solution 10 fold dilution | ||
Water + concentrate cells solution 100 fold dilution | Water + concentrate cells solution 100 fold dilution | ||
− | + | ||
+ | |||
+ | J0: we take 100µL of each water and put it on plates with specific antibiotic: | ||
* MacConkey + Spectinomycin | * MacConkey + Spectinomycin | ||
* MacConkey + Tetracyclin | * MacConkey + Tetracyclin | ||
* MacConkey + Chloramphenicol | * MacConkey + Chloramphenicol | ||
− | And | + | |
+ | And only MacConkey for the Water + LB | ||
+ | |||
+ | Incubation ON, 37°C | ||
====Soil==== | ====Soil==== | ||
− | Observation of plates ( | + | Observation of plates (03/08/2015): |
− | + | Less contamination on plates with MCK+Sorbitol thant MCK+Lactose. | |
− | + | ||
− | + | ||
− | + | ||
− | We | + | We choose to only use MCK+Sorbitol now |
− | + | ||
− | + | ||
− | |||
− | |||
− | |||
− | + | ===Low Budget Challenge=== | |
+ | ''by Coralie'' | ||
+ | |||
+ | Observation of plates (03/08/2015): | ||
+ | We can saw a little bit of colony. We can suppose that the initial culture wasn't enough in growing phase. | ||
+ | |||
+ | We try another time, with the same protocol than the 03/08/2015 but a fresh culture of bacteria. | ||
− | |||
− | |||
− | |||
− | |||
− | |||
− | |||
− | |||
− | |||
− | |||
− | |||
− | |||
− | |||
Revision as of 09:33, 10 August 2015
Contents
Tuesday 4th August
Lab Work
Plasmid extraction
by Pauline
Biobricks:
- BBa_K1707008 #1 to #6
- BBa_I13600 #1 and #2
With the Macherey-Nagel Extraction kit
Digestion Verification
by Pauline and Coralie
Biobricks: BBa_K1707008 #1 to #6
Mix:
- 2 µL Plasmid
- 0,5 µL XbaI
- 0,5 µL PstI
- 1 µL Buffer FastDigest 10x
- 6 µL H2O
Incubation 2h, 37°C
Electrophoresis
by Pauline
Agarose gel 1% Migration 90V
We can conclude that all BBa_K1707008 clones are OK
We make a glycerol stock of #1 and #2
Electrophoresis Verification
by Pauline and Coralie
Agarose gel, 1%
Migration 100V
We can conclude that:
- BBa_K1707021: #2, #3, #4 and #6 are OK
- BBa_K1707011: #1 to #6 are OK
- BBa_K1707004: #1 to #6 are OK
We make glycerol stock of them.
Digestion
by Coralie
XbaI + PstI:
- BBa_K1707011
- BBa_K1707004 x2
- BBa_E0022
- BBa_E0422
- BBa_K1707012
SpeI + Pst:
- BBa_R0051 x2
- BBa_K1707013
- BBa_K1707019
- BBa_K1707000
XbaI + EcoRI:
- BBa_I13602
EcoRI + SpeI:
- BBa_K1707004
Mix:
- 1 µL Enzyme 1
- 1 µL Enzyme 2
- 2 µL Buffer FastDigest 10x
- 6 µL H2O
- 10 µL Plasmide
Purification agarose gel
by Coralie and Audrey
Biobricks:
- BBa_K1707011
- BBa_K1707004
- BBa_E0022
- BBa_E0422
- BBa_K1707012
- BBa_I13602
Agarose gel 1%
Migration 100 V
We can conclude that I13602 isn't digested
Purification
by Pauline
Biobricks:
- BBa_K1707011
- BBa_K1707004
- BBa_E0022
- BBa_E0422
- BBa_K1707012
- BBa_R0051
- BBa_K1707013
- BBa_K1707019
- BBa_K1707000
- BBa_K1707004
Soil experiment
by Coralie
Water
Sea Water separate in 5mL in 50mL Falcon Fresh water separate in 5mL in 50mL Falcon Contamination with 1mL Water + LB Water + concentrate cells solution Water + concentrate cells solution 10 fold dilution Water + concentrate cells solution 100 fold dilution
J0: we take 100µL of each water and put it on plates with specific antibiotic:
- MacConkey + Spectinomycin
- MacConkey + Tetracyclin
- MacConkey + Chloramphenicol
And only MacConkey for the Water + LB
Incubation ON, 37°C
Soil
Observation of plates (03/08/2015):
Less contamination on plates with MCK+Sorbitol thant MCK+Lactose.
We choose to only use MCK+Sorbitol now
Low Budget Challenge
by Coralie
Observation of plates (03/08/2015): We can saw a little bit of colony. We can suppose that the initial culture wasn't enough in growing phase.
We try another time, with the same protocol than the 03/08/2015 but a fresh culture of bacteria.
Member present:
- Instructors: Claire
- Students: Coralie, Audrey and Pauline