Lactococcus transformation
Back to Protocols
Preparing Electrocompetent Cells
1.  Grow cells overnight in 25ml of GM17 (M17 with 1% glucose). 
2.  Add 1ml of overnight culture into 25ml SGM17 + 2.0% glycine. 
- SGM17 = 25ml M17 + 0.25g glucose + 5g Sucrose + 0.5g glycine). 
 
- SGM17 = 25ml M17 + 0.25g glucose + 5g Sucrose + 0.5g glycine). 
3.  Grow for ~4 hours until OD600 ~ 0.7. 
4.  Chill culture on ice for 10 mins. 
5.  Centrifuge cells for 15 mins at 3000g. 
6.  Gently shake to resuspend pellet in 3ml Electroporation Buffer (0.5M Sucrose, 10% glycerol). 
7.  Centrifuge cells for 15 mins at 3000g. 
8.  Resuspend pellet in 3ml Electroporation Buffer (0.5M Sucrose, 10% glycerol). 
9.  Centrifuge cells for 15 mins at 3000g. 
10.  Resuspend pellet in 500µl Electroporation Buffer (0.5M Sucrose, 10% glycerol). 
11.  Separate into 100µl aliquots and store at -80°C until use. 
 
Electro-Transformation
1.  Add 5µl of DNA and electroporate at 1200 volts (1mm Cuvettes). 
2.  Add 900µl ice cold M17+ and keep on ice for 10 mins. 
- To eah ml of M17 add the following: 0.5M(.17g)Sucrose + 0.5%(15µl)Glucose + 20mM(10µl)MgCl2 + 0.2mM(10µl)CaCl2. 
 
- To eah ml of M17 add the following: 0.5M(.17g)Sucrose + 0.5%(15µl)Glucose + 20mM(10µl)MgCl2 + 0.2mM(10µl)CaCl2. 
3.  Subculture 100µl into 900ul prewarmed M17+ and incubate for 2 hours. 
4.  Plate with appropriate antibiotic.