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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+ | </ul> | ||
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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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+ | <ul> | ||
+ | <li>Annealing temperature: 55 °C</li> | ||
+ | <li>Bands as expected (3004 bp)</li> | ||
+ | </ul> | ||
+ | </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.