Composite

Part:BBa_K4195180

Designed by: Xiaoping Yu   Group: iGEM22_XMU-China   (2022-09-27)
Revision as of 15:08, 12 October 2022 by Elabo (Talk | contribs) (Usage and Design)

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.
T--XMU-China--RENDR.png
Fig. 1 Schematic illustration of RENDR.

Usage and Design

This part is used as the target of the detection system BBa_K4195187BBa_K4195188BBa_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).

[edit]
Categories
Parameters
None