Hier das Protokol zur Erstellung chemisch kompetenter E. coli Zellen nach Hanahan.

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Protocol

Hanahan Competent Cell Protocol
Leslie Vosshall

**USE STERILE TECHNIQUE AT ALL TIMES
**AFTER STEP 6, WORK ON ICE IN THE COLD ROOM TO INCREASE THE QUALITY
OF THE FINAL CELL PREPARATION.
**PROTOCOL PRODUCES ABOUT 160 X 250ul ALIQUOTS OF COMPETENT CELLS.
PLACE SUFFICIENT 1.7ml MICROCENTRIFUGE TUBES AT –80 DEGREES C. AT THE
BEGINNING OF THE DAY FOR USE IN STEP #15.

  1. Streak out frozen stock of bacteria on an LB (+ antibiotics) plate. Grow overnight at 37 degrees C.
  2. Inoculate a single colony into a 250 ml flask containing:
  3. Grow overnight in a shaker at 37 degrees C.
  4. The next day set up two 2 liter flasks containing 250 ml 2XYT. Into each flask, pipet 2.5 ml of overnight culture.
  5. Grow with shaking until culture reaches an OD600 of ~0.5.
  6. Set up two centrifuge bottles on wet ice and transfer culture to bottles by pouring.
  7. Pellet bacteria by spinning in Sorvall centrifuge in GSA rotor; 5000 r.p.m., 4 degrees C.,10 minutes.
  8. Working in the cold room, with cells on ice as much as possible: Pour out supernatant, then use pipet to remove all residual fluid.
  9. Resuspend each pellet gently in 83 ml RF1. Use 10 ml pipet to gently pipet up and down until all clumps have been resuspended.
  10. Incubate on wet ice in cold room for 1 hour.
  11. Pellet bacteria by spinning in Sorvall centrifuge in GSA rotor; 5000 r.p.m., 4 degrees C., 10 minutes.
  12. Working in the cold room, with cells on ice as much as possible: Pour out supernatant, then use pipet to remove all residual fluid.
  13. Resuspend each pellet gently in 20 ml of RF2. Use 10 ml pipet to gently pipet up and down until all clumps have been resuspended.
  14. Incubate on wet ice in cold room for 15 minutes.
  15. Take microcentrifuge tubes out of –80 degree C freezer and at least 160 tubes with open lids in an ice bucket containing wet ice.
    Dispense 100 ul of cell suspension into each tube. If possible, work with a second person, one person dispensing the cells,
    and the second person sealing tubes as they are filled. Once tubes are sealed, drop them in a Dewar flask containing liquid nitrogen.
    Once all 40 ml of competent cells are dispensed into microcentrifuge tubes, freeze all remaining tubes in liquid nitrogen.
    Collect tubes and store in a paper freezer box with no dividers.
  16. Measure the efficiency of the competent cells by transforming a standard amount of commercial plasmid. Express efficiency
    as colony forming units / microgram of DNA cfu/ug. If you transform 0.1 ng of plasmid DNA and obtain 500 colonies, the efficiency
    of the cells is 5 x 106 cfu/ug.

SOLUTIONS

 
RF1 
                          FW      PER LITER   
100mM Rubidium Chloride   120.9    12.1 g 
50mM  Manganese Chloride  197.9   9.895 g 
30mM  Potassium Acetate   98.14   2.944 g 
10mM  Calcium Chloride    147.0    1.47 g 
15% w/v Glycerol                    150 g 
 
Adjust pH to 5.8 and bring volume to 1 liter. 
Sterilize by filtration. 
 
 
 
RF2 
                         FW      PER 500ML 
10mM  MOPS               209.3    1.05 g   
10mM  Rubidium Chloride  120.9     0.6 g 
75mM  Calcium Chloride   147.0    5.51 g 
15% w/v Glycerol                    75 g 
Bring volume to 500 ml. 
Sterilize by filtration.
 


YT medium (2x)
                                 PER LITER 
Bacto tryptone                       16g
Bacto yeast extract                  10g
NaCl                                  5g
Bring volume to 1 liter.
Sterilize by autoclave.