Difference between revisions of "Part:BBa K2992009"
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===Characterisation=== | ===Characterisation=== | ||
| − | This part was the guide RNA sequence that allowed our CRISPR/Cas9 system to work. This is | + | This part was the guide RNA sequence that allowed our CRISPR/Cas9 system to work. This is the first of two alternative sgRNAs used for the genome-integration stage, we used two different sgRNAs incase one had a higher efficacy than the other. This sgRNA As we integrated our <i> botR </i> in to the genome of <i> C. spororgenes </i>via CRISPR/Cas9 mediated repair which replaced the <i>pyrE</i> gene with our <i> botR </i> expressing modules. sgRNA guides the Cas9 protein to a specific site in the <i> pyrE gene</i>, any bacterium that has not undergone homologous recombination (a double crossover event that replaces <i> pyrE </i> with our <i> botR </i> expressing modules) will be cut by the Cas9 protein and consequentially killed. The use of this part made the integration of parts [https://parts.igem.org/Part:BBa_K2992025 BBa_K2992025], [https://parts.igem.org/Part:BBa_K2992026 BBa_K2992026] and [https://parts.igem.org/Part:BBa_K2992027 BBa_K2992027] in to the <i> C. sporogenes </i> genome possible. See [https://2019.igem.org/Team:Nottingham/Results results page]for more <br><br> |
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<span class='h3bb'>Sequence and Features</span> | <span class='h3bb'>Sequence and Features</span> | ||
Revision as of 18:52, 21 October 2019
Synthetic guide RNA sequence 1 for botR integration
Synthetic guide RNA sequence 1 for the integration of several botR constructs at the pyrE locus of the C. sporogenes genome
Usage and Biology
Synthetic guide RNA sequence 1 for the use of CRISPR-Cas9 for genomic integration of various botR constructs in the generation of our volatile reporter strains for predicting neurotoxin production following food manufacture. Genomic integration of these constructs was at the pyrE locus of C. sporogenes.
Characterisation
This part was the guide RNA sequence that allowed our CRISPR/Cas9 system to work. This is the first of two alternative sgRNAs used for the genome-integration stage, we used two different sgRNAs incase one had a higher efficacy than the other. This sgRNA As we integrated our botR in to the genome of C. spororgenes via CRISPR/Cas9 mediated repair which replaced the pyrE gene with our botR expressing modules. sgRNA guides the Cas9 protein to a specific site in the pyrE gene, any bacterium that has not undergone homologous recombination (a double crossover event that replaces pyrE with our botR expressing modules) will be cut by the Cas9 protein and consequentially killed. The use of this part made the integration of parts BBa_K2992025, BBa_K2992026 and BBa_K2992027 in to the C. sporogenes genome possible. See results pagefor more
Sequence and Features
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000COMPATIBLE WITH RFC[1000]
References
Raffestin, S., Dupuy, B., Marvaud, J. and Popoff, M. (2004). BotR/A and TetR are alternative RNA polymerase sigma factors controlling the expression of the neurotoxin and associated protein genes in Clostridium botulinum type A and Clostridium tetani. Molecular Microbiology, 55(1), pp.235-249.
Zhang, Z., Korkeala, H., Dahlsten, E., Sahala, E., Heap, J., Minton, N. and Lindström, M. (2013). Two-Component Signal Transduction System CBO0787/CBO0786 Represses Transcription from Botulinum Neurotoxin Promoters in Clostridium botulinum ATCC 3502. PLoS Pathogens, 9(3), p.e1003252.