Team:Bielefeld-CeBiTec/Notebook/Journal/Biosafety/Jul

From 2014.igem.org

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Successful amplifikation of the oligonucleotide containing the flanking sites for the deletion of <i>dadX</i> and purification using the <a href="https://2014.igem.org/Team:Bielefeld-CeBiTec/Notebook/Protocols#DNAPurificationbyCentrifugationgel" target="_blank">gel extraction clean-up kit</a> from Promega.
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Transformation of the oligonucleotide containing the flanking sites for the deletion of <i>dadX</i>. The successful replacement of the constitutive alanine racemase was verified via kanamycin selection and
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<a href="https://2014.igem.org/Team:Bielefeld-CeBiTec/Notebook/Protocols#ColonyPCR" target="_blank">Colony PCR</a> (<a href="https://2014.igem.org/Team:Bielefeld-CeBiTec/Notebook/Primer#dadX_Ec_control1" target="_blank">dadX_Ec_control1</a>, <a href="https://2014.igem.org/Team:Bielefeld-CeBiTec/Notebook/Primer#dadX_Ec_control2" target="_blank">dadX_Ec_control2</a>)
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<li>Annealing temperature: 55 °C</li>
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<li>Bands as expected (3004 bp)</li>
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Resulting in the genotype DH5aplha ∆<i>alr</i> <i>kan:dadX</i>, while the dadX deletion in the KRX strain was not successful.
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Revision as of 02:06, 9 October 2014


July

  • Transformation of the single deletions strains E. coli strains KRX ∆alr and DH5alpha ∆alr with the plasmid pRedET containg the Recombinase using the Genebridge RedET-System protocol.
  • Successful amplifikation of the oligonucleotide containing the flanking sites for the deletion of dadX and purification using the gel extraction clean-up kit from Promega.
  • Transformation of the oligonucleotide containing the flanking sites for the deletion of dadX. The successful replacement of the constitutive alanine racemase was verified via kanamycin selection and Colony PCR (dadX_Ec_control1, dadX_Ec_control2)
    • Annealing temperature: 55 °C
    • Bands as expected (3004 bp)
  • Resulting in the genotype DH5aplha ∆alr kan:dadX, while the dadX deletion in the KRX strain was not successful.