Difference between revisions of "Part:BBa K2992042"
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<partinfo>BBa_K2992042 short</partinfo> | <partinfo>BBa_K2992042 short</partinfo> | ||
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===Usage and Biology=== | ===Usage and Biology=== | ||
+ | This parts entry represents a promoterless FAST reporter construct. The construct comprises the fluorescent reporter gene FAST [https://parts.igem.org/Part:BBa_K2992000 BBa_K2992000], coupled with 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> | ||
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Revision as of 11:11, 1 October 2019
Promoterless FAST reporter construct
Usage and Biology
This parts entry represents a promoterless FAST reporter construct. The construct comprises the fluorescent reporter gene FAST BBa_K2992000, coupled with 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 155
References
Street et al 2019. Update