Difference between revisions of "Part:BBa K2992041"
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<partinfo>BBa_K2992041 short</partinfo> | <partinfo>BBa_K2992041 short</partinfo> | ||
− | 5-UTR containing RBS for ha33 gene from <i>C. botulinum</i>. | + | 5-UTR containing RBS for <i>ha33</i> gene from <i>C. botulinum</i>. |
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===Usage and Biology=== | ===Usage and Biology=== | ||
+ | This parts entry represents the 5’-UTR containing the RBS for the hemagglutinin component of the botulinum neurotoxin complex from <i>C. botulinum</i>. Since <i>ha33</i> is natural constituent of the BotR regulon, we chose this promoter to control the expression of our FAST reporter construct thus linking reporter fluorescence with botulinum neurotoxin production. In doing so, we hoped to generate our surrogate host strain as a model for predicting neurotoxin production in foodstuffs following food manufacturing processes. <br><br> | ||
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+ | ===Characterisation=== | ||
+ | Data incoming. | ||
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<partinfo>BBa_K2992041 SequenceAndFeatures</partinfo> | <partinfo>BBa_K2992041 SequenceAndFeatures</partinfo> | ||
+ | ===References=== | ||
+ | Dupuy, B. et al., 2006. Regulation of toxin and bacteriocin gene expression in Clostridium by interchangeable RNA polymerase sigma factors. Molecular Microbiology, 60(4), pp.1044–1057. | ||
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+ | 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. | ||
<!-- Uncomment this to enable Functional Parameter display | <!-- Uncomment this to enable Functional Parameter display |
Latest revision as of 13:56, 21 October 2019
5-UTR containing RBS for ha33 gene from C. botulinum
5-UTR containing RBS for ha33 gene from C. botulinum.
Usage and Biology
This parts entry represents the 5’-UTR containing the RBS for the hemagglutinin component of the botulinum neurotoxin complex from C. botulinum. Since ha33 is natural constituent of the BotR regulon, we chose this promoter to control the expression of our FAST reporter construct thus linking reporter fluorescence with botulinum neurotoxin production. In doing so, we hoped to generate our surrogate host strain as a model for predicting neurotoxin production in foodstuffs following food manufacturing processes.
Characterisation
Data incoming.
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
Dupuy, B. et al., 2006. Regulation of toxin and bacteriocin gene expression in Clostridium by interchangeable RNA polymerase sigma factors. Molecular Microbiology, 60(4), pp.1044–1057.
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.