Mesoplasma florum:Electroporation

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Transformation of Mesoplasma florum by electroporation
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Transformation of ''Mesoplasma florum'' by electroporation
Materials
Materials
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* overnight culture of Mesoplasma florum in ATCC 1161 medium
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* overnight culture of ''Mesoplasma florum'' in ATCC 1161 medium
* chilled mycoplasma electroporation buffer
* chilled mycoplasma electroporation buffer
** 8 mM HEPES pH 7.4
** 8 mM HEPES pH 7.4
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* Add 200 μl of chilled 1161 medium from a 2 ml tube, mix with the pipet
* Add 200 μl of chilled 1161 medium from a 2 ml tube, mix with the pipet
* Transfer the cuvette contents back into the same tube
* Transfer the cuvette contents back into the same tube
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** transfer may be easier with gel loading tip to reach into the gap
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** transfer may be easier with a gel loading tip to reach into the gap
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* Place the 2 ml tubes into the 30° incubator for outgrowth for 2 hours
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* Place the 2 ml tubes into the 30° incubator for outgrowth for 2-3 hours
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** cells can be held at 4° following outgrowth
* Plate 100 μl aliquots on selective plates
* Plate 100 μl aliquots on selective plates
* Transfer 100 μl aliquots into 10 ml of selective medium
* Transfer 100 μl aliquots into 10 ml of selective medium

Revision as of 21:06, 5 September 2007

Transformation of Mesoplasma florum by electroporation

Materials

  • overnight culture of Mesoplasma florum in ATCC 1161 medium
  • chilled mycoplasma electroporation buffer
    • 8 mM HEPES pH 7.4
    • 272 mM sucrose
  • chilled 1 mm electroporation cuvettes
  • chilled ATCC 1161 medium aliquots of 1 ml in 2 ml tubes
  • Selective medium or plates
    • Tetracycline resistance from TetM is higher than 100 μg/ml
    • Untransformed cells grow poorly at 4 μg/ml
    • Selective plates are at 10 μg/ml


Protocol

  • chill the centrifuge to 4°
  • spin down 10 ml of overnight culture at 8000g for 5 minutes, remove the supernatent
  • resuspend the pellet in the remaining liquid by vigorous vortexing
  • add 10 ml of chilled electroporation buffer and mix
  • spin down again, remove supernatent
  • resuspend the pellet in the remaining liquid
  • add 0.5 ml of chilled electroporation buffer, mix
  • hold the cells on ice
  • Aliquot 50 μl of cells into chilled eppendorfs
  • Add 1 μl of DNA for transformation
  • Mix and transfer to a chilled 1 mm gap electroporation cuvette
  • Pulse the cuvette at 1.75 KV twice, with a 5 second delay
  • Add 200 μl of chilled 1161 medium from a 2 ml tube, mix with the pipet
  • Transfer the cuvette contents back into the same tube
    • transfer may be easier with a gel loading tip to reach into the gap
  • Place the 2 ml tubes into the 30° incubator for outgrowth for 2-3 hours
    • cells can be held at 4° following outgrowth
  • Plate 100 μl aliquots on selective plates
  • Transfer 100 μl aliquots into 10 ml of selective medium
  • grow plates and medium at 30° for colonies or color change
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