Creation of the logo of the AMU team :
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Plasmids transformation :
Add 20 ng of plasmid to 100 µL of competent cells thawed in ice
Incubate 30-45 min in ice
Thermal shock : put tubes in the Thermomixer at 42°C during 2 min
Incubate 5 min in ice
Add 900 µL of LB
Incubate 1 hour at 37°C with agitation
Spread 100 µL on LB limp (with antibiotic)
To make negative control, follow the same procedure but without add plasmids and spread 300 µL
Ligation transformation:
Add 20 ng of ligation’s product to 100 µL of competent cells thawed in ice
Incubate 30-45 min in ice
Thermal shock : put tubes in the Thermomixer at 42°C during 2 min
Incubate 5 min in ice
Add 900 µL of LB
Incubate 1 hour at 37°C with agitation
Centrifuge 5 min at 5000 rpm
Eliminate 850 µL of medium
Suspend the pellet
Spread 150 µL on LB limp (with antibiotic)
To make negative control, follow the same procedure but without add plasmids and spread 300 µL
Make a culture of your bacteria in LB medium and let it grow until bacteria are in exponential phase
(OD600 = 0.5).
Cells are cold centrifuge 10 min at 3500 rpm.
The pellet is slowly suspended in 80 mL of Tfb1 buffer (300mM KOAc, 0.05M MnCl2, 0.1M KCl, 0.01M
CaCl2, 15% Glycerol (see next section “Preparation of Tbf1 and Tbf2 buffer”).
After another 5 min cold centrifugation at 3500 rpm, the pullet is suspended in 8 mL of Tbf2 Buffer
(0.01mM NaMOPS pH 7, 0.075M CaCl2, 0.01M KCl, 15% Glycerol)
Incubate 15 min in ice. Aliquot 200µL of cell suspension in sterile Eppendorf tubes. The cell
suspension is conserved at -80°C.
For 200 mL of culture:
Preparation of 80 mL of Tbf1 Buffer:
KAc 1M
2.4 mL
MnCl2 0.5M
8 mL
KCl 1 M
8 mL
CaCl2 0.1M
8 mL
Gly 80%
15 mL
H2O
38.6 mL
Preparation of 8 mL of Tbf2 Buffer:
NaMOPS 0.2M
400 µL
CaCl2 0.1M
6 mL
KCl 1 M
8 mL
Gly 80%
1.5 mL
KCl 1M
80 µL
H2O
500 µL
50% glycerol
6.25 mL Glycerol 80%
20 mM EDTA
0.4 mL EDTA 0.5 M
0.05% Bromophenol blue
≈0.05g Bromophenol blue
0.05% Xylene cyanol
≈0.05g xylene cyanol
1% SDS
1 mL SDS 10%
DNA
Between 50 and 100 ng
EcoRI-HF
0.2 µL
PstI
0.2 µL
10X NEBuffer 2
2 µL
100X BSA
0.2 µL
H2O
To 20 µL
Incubate all digest reactions at 37°C for 1 hour and then add 3 µL of SES 4X and migrate 30 min at
150V on a 1% agarose gel.
Upstream part :
Upstream part plasmid
500 ng
EcoRI-HF
1 µL
PstI
1 µL
10X NEBuffer 2
2.5 µL
100X BSA
0.5 µL
H2O
To 50 µL
Downstream part :
Downstream part plasmid
500 ng
Xba I
1 µL
Spe I
1 µL
10X NEBuffer 2
2.5 µL
100X BSA
0.5 µL
H2O
To 50 µL
Destination plasmid:
Destination plasmid
500 ng
EcoRI-HF
1 µL
PstI
1 µL
DpnI
1 µL
10X NEBuffer 2
2.5 µL
100X BSA
0.5 µL
H2O
To 50 µL
Incubate the three restriction digest reactions at 37°C for 10 minutes and then heat inactivate at
80°C for 20 minutes.
Upstream part digestion
2 µL
Dowstream part digestion
2 µL
Destination plasmid
2 µL
10X T4 DNA ligase buffer
2 µL
T4 DNA ligase
1 µL
H2O
11 µL
Incubate at RT for 1 hour.
The sequences are already prepared like BioBrick Assembly, they also have the prefixe and suffixe
This protocol is made to prepare the DNA, digest, ligate and transform it.
1- Resuspend gBlocks Gene fragment to a final concentration of 10 ng/µL in TE or AE
(elution buffer). The tube contain 1000 ng of gBlocks Gene fragment so you have to add
100µL of AE
2- Mix well, a vortex shall be used
Digestion E/P
Digest 100 ng in 50µL
Component
50 µL of reaction
DNA
10 µL
Net buffer 2.1
5 µL
H2O
33 µL
EcoRI
1 µL
Pst I
1 µL
1- Incubate for 45 min at 37°C
2- Incubate 20 min at 80°C (inactivation of restriction enzyme)
Component
50 µL of reaction
DNA
10 µL
Net buffer 2 (10X)
5 µL
BSA (100X)
0.5 µL
H2O
33 µL
EcoRI
1 µL
Pst I
1 µL
Ligation
1- Ligate 50 ng vector with a 3X molar excess of gBlocks Gene fragments in fresh T4 DNA
ligase buffer diluted to 1X and 400 U T4 DNA ligase for a total volume of 20 µL
Component
20 µL of reaction
PSBIC3 (or other vector) at 12.5 ng/µL
2 µL
insert digested (at 37.5 ng/µL)
12 µL
T4 ligase buffer
2 µL
T4 ligase 400U
1 µL
H2O
3 µL
1- Incubate 2h at room temperature
Transformation
1- Add 10 µL of ligation’s product to 100 µL of competent cells thawed in ice (TGI cells)
2- Incubate 45 min in ice
3- Thermal shock: put tubes in the thermomixer at 42°C during 2 min
4- Incubate 5 min in ice
5- Add 900 µL of LB
6- Incubate 1 hour at 37°C with agitation
7- Centrifuge 5 min at 5000 rpm
8- Eliminate 850 µL of supernatant
9- Suspend the pellet in the 150µL of remaining medium
10- Spread 150 µL on LB limp (with antibiotic)
To make negative control, follow the same procedure but without add plasmids and spread 300 µL
