TOP10 chemically competent cells

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This protocol is a variant of the Hanahan protocol using CCMB80 buffer for DH10B and TOP10 strains. It builds on Example 2 of the Bloom05 patent as well.

Preparing glassware and media

Detergent is a major inhibitor of competent cell growth and transformation. Glass and plastic must be detergent free for these protocols. The easiest way to do this is to avoid washing glassware, and simply rinse it out. Autoclaving glassware filled 3/4 with DI water is an effective way to remove most detergent residue. Media and buffers should be prepared in detergent free glassware and cultures grown up in detergent free glassware.

Preparing seed stocks

  • streak TOP10 cells on an SOB plate and grow for single colonies at 23 C
    • room temperature works well
  • Pick single colonies into 2 ml of SOB medium and shake overnight at 23 C
    • room temperature works well
  • Add glycerol to 15%
  • Aliquot 1 ml samples to Nunc cryotubes
  • Place tubes into a zip lock bag, immerse bag into a dry ice/ethanol bath for 5 minutes
    • This step may not be necessary
  • Place in -80 freezer indefinitely.

Preparing competent cells

  • Inoculate 250 ml of SOB medium with 1 ml vial of seed stock and grow at 20 C to an OD of 0.5
    • This takes approximately 16 hours. Controlling the temperature makes this a more reproducible process, but is not essential. Room temperature will work.
  • Centrifuge at 3000g / 4C for 10 minutes in a flat bottom centrifuge bottle.
    • Flat bottom centrifuge tubes make the fragile cells much easier to resuspend
  • Gently resuspend in 80 ml of ice cold CCMB80 buffer
  • Incubate on ice 20 minutes
  • Centrifuge again at 4C and resuspend in 20 ml of ice cold CCMB80 buffer.
  • Incubate on ice for 20 minutes
  • Aliquot to chilled screw top 2 ml vials or 50 ul into chilled microtiter plates
  • Store at -80C indefinitely.
    • Flash freezing does not appear to be necessary

CCMB80 buffer:

  • 10 mM KOAc pH 7.0 (10 ml of a 1M stock/l)
  • 80 mM CaCl2.2H2O (11.8 g/l)
  • 20 mM MnCl2.4H2O (4.0 g/l)
  • 10 mM MgCl2.6H2O (2.0 g/l)
  • 10% glycerol (100 ml/l)
  • adjust pH to 6.4 with 0.1N HCl
    • adjusting pH up will precipitate manganese dioxide from Mn containing solutions.
  • sterile filter and store at 4C.

Experimental results:

  • Transform 50 μl of cells with 1 μl of standard pUC19 plasmid (Invitrogen)
  • Hold on ice 0.5 hours
  • Heat shock 60 sec
  • Add 250 μl SOC
  • Incubate at 37 C for 1 hour in 2 ml centrifuge tubes rotated
  • Plate 20 μl on AMP plates using 3.5 mm glass beads

Colony count was 420 on experimental plate. This is 420*15 = 6300 transforms/10 pg or 6.3 x 108 transforms/μg. The control from Invitrogen was 210 colonies under identical conditions, or 3.2 x 108 transforms/μg

6/7/06 results of transformations: