Team:Paris/Protocols Competent Bacteria
From 2009.igem.org
(Difference between revisions)
Christophe.R (Talk | contribs) (→2nd Protocol for competent bacteria) |
Christophe.R (Talk | contribs) (→Solution for competent bacteria (by RbCl)) |
||
Line 52: | Line 52: | ||
===Solution for competent bacteria (by RbCl)=== | ===Solution for competent bacteria (by RbCl)=== | ||
*Tampon I (250ml) | *Tampon I (250ml) | ||
- | ** | + | **Potassium acetate (C<sub>2</sub>H<sub>3</sub>KO<sub>2</sub> 30mM pH 5,8 0,733g |
**RbCl 100mM 3,02g | **RbCl 100mM 3,02g | ||
**CaCl<sub>2</sub> 10mM 0,3741g | **CaCl<sub>2</sub> 10mM 0,3741g | ||
Line 58: | Line 58: | ||
**Glycerol 15% ~37,5ml | **Glycerol 15% ~37,5ml | ||
**QSP 250ml H<sub>2</sub>O ~218,5ml | **QSP 250ml H<sub>2</sub>O ~218,5ml | ||
- | **Ajuster le pH à 5,8 avec de l'acide acétique glacial. Attention si le pH descend en dessous de 5,8 il faut refaire la solution. | + | **Acetic acid (CH<sub>3</sub>COOH)Ajuster le pH à 5,8 avec de l'acide acétique glacial. Attention si le pH descend en dessous de 5,8 il faut refaire la solution. |
**Stériliser par filtration | **Stériliser par filtration | ||
+ | |||
*Tampon II (125ml) | *Tampon II (125ml) |
Revision as of 19:32, 9 August 2009
Contents |
Protocol to make competent bacteria (iGEM2007)
Prepare CaCl2 0.1M
- Add 7,351g of CaCl2.2 H2O (FM 147,02) in 500 mL H2O
- dissolve the CaCl2 by mixing the suspension with the help of a magnetic stirrer
- Filter the solution with a cell-culture unit of filtration
- Aliquotes the filtered solution: 25mL in a 50 mL Falcon. Storage at +4°C
Steps
- Use non competent bacteria (ex: MG1655) stocked in 1.5 mL LB (20% Glycerol): put a sterile tip in the 1.5 mL stock tube and then place it in a 50 mL Falcon with 5 ml LB medium.
Over Night culture at 37°C / 200 rpm - 1/100 dilution in LB medium QSP 50 mL in an erlenmeyer of 250 mL
- Culture at 37°C / 200 rpm untill OD600 reach 0.6
- Fast cooling at +4°C by gently shaking the erlen in ice
- Use pre-cooled centrifuge at +4°C. Centrifuge 50 mL of the culture in 50 mL falcon: +4°C / 5 min / 4000 rpm
- Discard supernatant by inverting the tube, and resuspend the pellet with 1 mL of cold CaCl2 and mix gently the suspension by up and down
- Add cold CaCl2 QSP 20 mL and incubate 30 min / +4°C
- Centrifuge the suspension : +4°C / 5 min / 4000 rpm
- Discard supernatant by inverting the tube, and resuspend the pellet with 1 mL of cold CaCl2 and mix gently the suspension by up and down
- Transform or freeze the competent cells. Freeze the competent cells in 50 µL aliquots in the 0.1M CaCl2 medium with 15% glycerol.
- After transformation, prepare a Glycerol Stock
2nd Protocol for competent bacteria
- Inoculate 50/5 ml of LB with fresh colony or dilution of an overnight culture
- Grow up to OD600 0.5-0.8
- Leave on ice 10min
- Spin 40/2 ml of cell suspension, 5min at 4000rpm, 4°C/minispin 2min at 5000rpm, 4°C
- Resuspend the pellet in 20/1 ml CaCl2 50mM (1/2 of initial Vol)
- Leave on ice 10min
- Spin 40/2 ml of resuspension, 5min at 4000rpm, 4°C/minispin 2min at 5000rpm, 4°C
- Resuspend the pellet in 2ml/100µl CaCl2 50mM (1/20 of initial Vol)
- Leave on ice overnight before stock at -80°C
Protocol for competent bacteria by RbCl
Solution for competent bacteria (by RbCl)
- Tampon I (250ml)
- Potassium acetate (C2H3KO2 30mM pH 5,8 0,733g
- RbCl 100mM 3,02g
- CaCl2 10mM 0,3741g
- MnCl250mM 2,5g
- Glycerol 15% ~37,5ml
- QSP 250ml H2O ~218,5ml
- Acetic acid (CH3COOH)Ajuster le pH à 5,8 avec de l'acide acétique glacial. Attention si le pH descend en dessous de 5,8 il faut refaire la solution.
- Stériliser par filtration
- Tampon II (125ml)
- MOPS 10mM pH 6.5 0,2382g
- RbCl 10mM 0,150g
- CaCl2 10mM 1,37gg
- Glycerol 15% ~18,75ml
- QSP 1250ml H2O ~106.25ml
- Ajuster le pH à 6.5 avec du KOH 1M
- Stérilisation par filtration