User:Federico Castro M/Notebook/Spatial Patterns/2008/09/17

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Proposed Procedure

  • Status: Pending for aproval
  • Issues: None

I want to recover the repressilator for latter use in the Spatial Patterns project for the iGEM. This part is escential for the develpment of the project.

The whole procedure should be easy. I await for approval for this procedure.

Biobrick to be extracted.

  • BBa_I5611 available at well 14O at iGEM 2007 Parts Kit Plate 1 in plasmid pSB1A2.

The following protocol is proposed for biobrick recovery from the iGEM page [1]

  1. Puncture a hole through the foil with a pipette tip into the well that corresponds to the Biobrick™-standard part that you want
  2. Add 15 uL of diH2O (deionized water)
  3. Take 1uL DNA and transform into your desired competent cells, plate out on a plate with the correct antibiotic* and grow overnight. Your goal here is to obtain single colonies.

I intend to use the following protocol for transforming the biobricks into competent cells.

  1. Thaw 25 - 200 μl TB buffer cells on ice. Do not use glass tubes, which adsorb DNA.
  2. Add DNA, pipette gently to mix (keep volume of DNA less than 5% of the cell volume)
  3. Incubate on ice for 30 minutes
    • Note: If you are in a rush, you can shorten this incubation time to 5-10 min.
  4. Incubate cells for 30 seconds at 42°C.
  5. Incubate cells on ice for 2 min.
  6. Add 4 volumes of room temperature SOC (not critical)
  7. Incubate for 1 hour at 37°C on shaker.
    • Note: Can also save some time here by reducing incubation to ~45 min.
    • Note: Step can be eliminated if plating on Amp plates, but not most other antibiotics
  8. Spread 100-300 μl onto a plate made with appropriate antibiotic.
  9. Grow overnight at 37°C.

Before the procedure I would need to prepare solid plates with Ampicillin (The vector of the biobrick has a region that confers the bacteria qith Ampicilin resistance). It seems that the proper concentration of Ampicillin is 50 μg/mL.[2]