Team:Groningen/protocols/Transformation
From 2013.igem.org
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- | The complete mixture should be dissolved in 100ml. First add 50ml | + | The complete mixture should be dissolved in 100ml. First add 50ml milliQ water and mix. When everything is dissolved add MQ water till 100ml. Filter sterilize the complete mixture and store at -20°C |
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Revision as of 19:15, 28 July 2013
B. subtilis transformation
The Losick protocol is used
Day 0: Streak out the Bacillus strain of use and plate this on an LB agar plate o/n at 37°C.Transformation (D-Day):
1. Pick up a nice big colony and drop it in 2ml of completed MC (1x) (see sub1).
2. Grow at 37 °C for 5 hours (longer if the culture is not really turbid).
3. Mix 400µl of culture with DNA* in a fresh tube (i.e. 15ml tubes loosely closed – aeration)
4. Grow the cells at 37°C for an additional 2 hours .
5. Spread the complete 400µl reaction mix on selective antibiotic plates, and incubate at 37°C overnight.
(*usually 1µl. Then 10µl of Quiagen plasmid miniprep or <1µl of chromosomal prep)
Sub1: Competence medium (MC completed)
compound | amount | treatment |
---|---|---|
MQ water | 1.8ml | |
10x MC (Sub2) | 200µl | filter sterilized |
MgSO4 | 6.7µl | autoclaved |
Tryptophan 1% | 10µl | filter sterilized (stored in aluminium foil) |
Sub2: MC 10x
compound | amount 10ml | amount 100ml |
---|---|---|
K2HPO4 | 1.40g | 14.04g |
KH2PO4 | 0.52g | 5.24g |
Glucose | 2g | 20g |
Tri-Na Citrate 300mM (Sub3) |
1ml | 10ml |
Ferric NH4 citrate (Sub4) |
0.1ml | 1ml |
Casein Hydrolysate |
0.1g | 1g |
Potassium Glutamate | 0.2g | 2g |
Sub3: Tri-Na Citrate 300mM
compound | amount |
---|---|
Tri-Na Citrate | 0.88g |
MQ water | 10ml |
Sub4: Ferric NH4 citrate
compound | amount |
---|---|
Ferric NH4 | 0.22g |
MQ water | 10ml |