Part:BBa_K4195070
pirB_i
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(1). RENDR utilizes a split variant of the Tetrahymena thermophila ribozyme by synthetically splitting it into two non-functional fragments (Fig. 1). 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 bound 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 RENDR detection system. For toxin pirB, we designed BBa_K4195143, BBa_K4195144, BBa_K4195147, BBa_K4195148, BBa_K4195158, BBa_K4195159, BBa_K4195162, BBa_K4195163, BBa_K4195170, BBa_K4195171, BBa_K4195174, BBa_K4195175. Other related parts are as followings: BBa_K4195149, BBa_K4195150, BBa_K4195164, BBa_K4195165, BBa_K4195166, BBa_K4195187, BBa_K4195188, BBa_K4195189, BBa_K4195190.
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) <d>9</d>, (2021).
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]
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