Streptococcus Transformation: Difference between revisions

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PreDec2022>EricMiller
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PreDec2022>EricMiller
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# Preheat a microcentrifuge tube of 270ul CTM pH 7.8 to 37 degrees using the hot block.  
# Preheat a microcentrifuge tube of 270ul CTM pH 7.8 to 37 degrees using the hot block.  
# Add CSP-1 peptide to this tube to 100 ng/ml eventual final concentration. This is then adding 30ng of CSP-1, as our final volume will eventually be 300ul.
# Add CSP-1 peptide to this tube to 100 ng/ml eventual final concentration. This is then adding 30ng of CSP-1, as our final volume will eventually be 300ul.
# Add DNA  
# Add DNA to 1 ug/ml final concentration.
# Add 30ul of grown cells (a 1:10 dilution).
# Add 30ul of grown cells (a 1:10 dilution).
# Vortex
# Vortex

Revision as of 13:36, 8 July 2021

Reagents Needed

  • CTM (Complete Transformation Medium) pH 7.1
  • CTM pH 7.9
  • CSP-1 peptide (in the -80 freezer) or CSP-2 peptide (which we do not have). Talk to Eric if you are not working with a D39 derivative.

Complete Transformation Medium

  • 3g Trypic Soy Broth
  • 0.1g yeast extract
  • Fill up to 100ml water and autoclave
  • Add to a final concentration filter sterilized 1mM CaCl2 and filter sterilized 0.2% BSA (Bovine Serum Albumin)

Competence Protocol

  1. Freshly grow up single colonies on a blood TSA plate of the strain to be transformed.
  2. Select one colony and grow in 3ml CTM pH 6.8 until OD 0.3, which is 0.39 Absorbance
  3. Preheat a microcentrifuge tube of 270ul CTM pH 7.8 to 37 degrees using the hot block.
  4. Add CSP-1 peptide to this tube to 100 ng/ml eventual final concentration. This is then adding 30ng of CSP-1, as our final volume will eventually be 300ul.
  5. Add DNA to 1 ug/ml final concentration.
  6. Add 30ul of grown cells (a 1:10 dilution).
  7. Vortex
  8. Incubate at 37 degrees using the hot block for 60 minutes.
  9. Plate cells on a blood TSA plate that has appropriate antibiotics in it.

Competence Protocol with CRISPR

  • As above, but add the editing construct at a final concentration of 2.5ug/ul
  • Incubate at 37 degrees using the hot block for 20 minutes.
  • Add the CRISPR targeting construct at a final concentration of 2.5ug/ul, and vortex.
  • Incubate at 37 degrees using the hot block for 40 minutes.