Difference between revisions of "Part:BBa K4195180"
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===Biology=== | ===Biology=== | ||
− | This sequence is a conserved region of toxin gene ''pirB'' | + | This sequence is a conserved region of toxin gene ''pirB'' (''1''). It’s used as the detection target of RENDR system.<br/> |
'''Ribozyme ENabled Detection of RNA (RENDR)'''<br/> | '''Ribozyme ENabled Detection of RNA (RENDR)'''<br/> | ||
RENDR is a high-performing, plug-and-play RNA-sensing platform. RENDR utilizes a split variant of the ''Tetrahymena thermophila'' ribozyme by synthetically splitting it into two non-functional fragments. Two fragments are each appended with designed RNA guide sequences, which can interact with the RNA input of interest. The split ribozyme is then inserted within a desired gene output. When binded with the RNA input, two transcribed split ribozyme fragments are triggered to self-splice and thus the intact transcript of the protein output will form.<br/> | RENDR is a high-performing, plug-and-play RNA-sensing platform. RENDR utilizes a split variant of the ''Tetrahymena thermophila'' ribozyme by synthetically splitting it into two non-functional fragments. Two fragments are each appended with designed RNA guide sequences, which can interact with the RNA input of interest. The split ribozyme is then inserted within a desired gene output. When binded with the RNA input, two transcribed split ribozyme fragments are triggered to self-splice and thus the intact transcript of the protein output will form.<br/> | ||
[[File:T--XMU-China--RENDR.png|400px]]<br/> | [[File:T--XMU-China--RENDR.png|400px]]<br/> | ||
'''Fig. 1 Schematic illustration of RENDR.'''<br/> | '''Fig. 1 Schematic illustration of RENDR.'''<br/> | ||
+ | |||
===Usage and Design=== | ===Usage and Design=== | ||
This part is used as the target of the detection system <partinfo>BBa_K4195187</partinfo>、<partinfo>BBa_K4195188</partinfo>、<partinfo>BBa_K4195189</partinfo> and <partinfo>BBa_K4195190</partinfo>. We build the circuit similar as <partinfo>BBa_K4195178</partinfo>. <br/> | This part is used as the target of the detection system <partinfo>BBa_K4195187</partinfo>、<partinfo>BBa_K4195188</partinfo>、<partinfo>BBa_K4195189</partinfo> and <partinfo>BBa_K4195190</partinfo>. We build the circuit similar as <partinfo>BBa_K4195178</partinfo>. <br/> |
Latest revision as of 15:19, 12 October 2022
Biology
This sequence is a conserved region of toxin gene pirB (1). It’s used as the detection target of RENDR system.
Ribozyme ENabled Detection of RNA (RENDR)
RENDR is a high-performing, plug-and-play RNA-sensing platform. RENDR utilizes a split variant of the Tetrahymena thermophila ribozyme by synthetically splitting it into two non-functional fragments. Two fragments are each appended with designed RNA guide sequences, which can interact with the RNA input of interest. The split ribozyme is then inserted within a desired gene output. When binded with the RNA input, two transcribed split ribozyme fragments are triggered to self-splice and thus the intact transcript of the protein output will form.
Fig. 1 Schematic illustration of RENDR.
Usage and Design
This part is used as the target of the detection system BBa_K4195187、BBa_K4195188、BBa_K4195189 and BBa_K4195190. We build the circuit similar as BBa_K4195178.
Reference
1. J. M. S. Lazarte et al. Passive Immunization with Recombinant Antibody VLRB-PirA(vp)/PirB(vp)-Enriched Feeds against Vibrio parahaemolyticus Infection in Litopenaeus vannamei Shrimp. Vaccines (Basel). 9, (2021).
Sequence and Features
- 10COMPATIBLE WITH RFC[10]
- 12INCOMPATIBLE WITH RFC[12]Illegal NheI site found at 207
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000COMPATIBLE WITH RFC[1000]