Difference between revisions of "Part:BBa K2992044"
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<partinfo>BBa_K2992044 short</partinfo> | <partinfo>BBa_K2992044 short</partinfo> | ||
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===Usage and Biology=== | ===Usage and Biology=== | ||
+ | This parts entry represents a FAST reporter construct under the regulatory control of P<i>ntnH</i> for the non-toxic non-haemagglutinin <i>ntnH</i> gene of <i>C. botulinum</i>. The construct comprises the strong clostridial promoter P<i>ntnH</i> [https://parts.igem.org/Part:BBa_K2992001 BBa_K2992001] and its associated 5’-UTR containing the RBS [https://parts.igem.org/Part:BBa_K2992015 BBa_K2992015] driving the expression of the fluorescent reporter gene FAST [https://parts.igem.org/Part:BBa_K2992000 BBa_K2992000]. Transcriptional terminator occurs through the activity of the strong clostridial terminator T<i>Fad</i> [https://parts.igem.org/Part:BBa_K2284012 BBa_K2284012]. FAST is one of the few fluorescent reporters available for effective use in anaerobic organisms. FAST is derived from Halorhodospira halophila and has been codon optimised for fluorescence studies in the genus Clostridium. In our project we couple FAST with the natural promoters of the BotR regulon 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> | ||
+ | <!-- --> | ||
+ | ===Characterisation=== | ||
+ | Data incoming. | ||
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<span class='h3bb'>Sequence and Features</span> | <span class='h3bb'>Sequence and Features</span> | ||
<partinfo>BBa_K2992044 SequenceAndFeatures</partinfo> | <partinfo>BBa_K2992044 SequenceAndFeatures</partinfo> | ||
+ | ===References=== | ||
+ | Heap modular | ||
+ | Street et al 2019. Update | ||
<!-- Uncomment this to enable Functional Parameter display | <!-- Uncomment this to enable Functional Parameter display |
Revision as of 12:14, 1 October 2019
FAST reporter construct with PntnH 5-UTR+RBS.
Usage and Biology
This parts entry represents a FAST reporter construct under the regulatory control of PntnH for the non-toxic non-haemagglutinin ntnH gene of C. botulinum. The construct comprises the strong clostridial promoter PntnH BBa_K2992001 and its associated 5’-UTR containing the RBS BBa_K2992015 driving the expression of the fluorescent reporter gene FAST BBa_K2992000. Transcriptional terminator occurs through the activity of the strong clostridial terminator TFad BBa_K2284012. FAST is one of the few fluorescent reporters available for effective use in anaerobic organisms. FAST is derived from Halorhodospira halophila and has been codon optimised for fluorescence studies in the genus Clostridium. In our project we couple FAST with the natural promoters of the BotR regulon 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]
- 1000INCOMPATIBLE WITH RFC[1000]Illegal BsaI.rc site found at 330
References
Heap modular Street et al 2019. Update