Difference between revisions of "Part:BBa K4195179"
 
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__NOTOC__
 
__NOTOC__
 
===Biology===
 
===Biology===
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This sequence is a conserved region of toxin gene ''pirA''.[1] It’s used as the detection target of RENDR system.<br/>
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This sequence is a conserved region of toxin gene ''pirA''<i>(1)</i>. 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 RENDR detection system. For toxin pirA, we designed <partinfo>BBa_K4195141</partinfo>, <partinfo>BBa_K4195142</partinfo>, <partinfo>BBa_K4195145</partinfo>, <partinfo>BBa_K4195146</partinfo>, <partinfo>BBa_K4195156</partinfo>, <partinfo>BBa_K4195157</partinfo>, <partinfo>BBa_K4195160</partinfo>, <partinfo>BBa_K4195161</partinfo>, <partinfo>BBa_K4195168</partinfo>, <partinfo>BBa_K4195169</partinfo>, <partinfo>BBa_K4195172</partinfo>, <partinfo>BBa_K4195173</partinfo>. Other related parts are as followings: <partinfo>BBa_K4195151</partinfo>, <partinfo>BBa_K4195183</partinfo>, <partinfo>BBa_K4195184</partinfo>, <partinfo>BBa_K4195185</partinfo>, <partinfo>BBa_K4195186</partinfo>.<br/>
 
This part is used as the target of the RENDR detection system. For toxin pirA, we designed <partinfo>BBa_K4195141</partinfo>, <partinfo>BBa_K4195142</partinfo>, <partinfo>BBa_K4195145</partinfo>, <partinfo>BBa_K4195146</partinfo>, <partinfo>BBa_K4195156</partinfo>, <partinfo>BBa_K4195157</partinfo>, <partinfo>BBa_K4195160</partinfo>, <partinfo>BBa_K4195161</partinfo>, <partinfo>BBa_K4195168</partinfo>, <partinfo>BBa_K4195169</partinfo>, <partinfo>BBa_K4195172</partinfo>, <partinfo>BBa_K4195173</partinfo>. Other related parts are as followings: <partinfo>BBa_K4195151</partinfo>, <partinfo>BBa_K4195183</partinfo>, <partinfo>BBa_K4195184</partinfo>, <partinfo>BBa_K4195185</partinfo>, <partinfo>BBa_K4195186</partinfo>.<br/>
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Reference<br/>
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====Reference====
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[1] Lazarte, J., Kim, Y. R., Lee, J. S., Chun, J. H., Kim, S. W., Jung, J. W., Kim, J., Kayansamruaj, P., Thompson, K. D., Kim, H., & Jung, T. S. (2021). Passive Immunization with Recombinant Antibody VLRB-PirAvp/PirBvp-Enriched Feeds against Vibrio parahaemolyticus Infection in Litopenaeus vannamei Shrimp. Vaccines, 9(1), 55. https://doi.org/10.3390/vaccines9010055
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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).
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<span class='h3bb'>Sequence and Features</span>
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<partinfo>BBa_K4195179 SequenceAndFeatures</partinfo>

Latest revision as of 15:17, 12 October 2022

Biology

This sequence is a conserved region of toxin gene pirA(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 RENDR detection system. For toxin pirA, we designed BBa_K4195141, BBa_K4195142, BBa_K4195145, BBa_K4195146, BBa_K4195156, BBa_K4195157, BBa_K4195160, BBa_K4195161, BBa_K4195168, BBa_K4195169, BBa_K4195172, BBa_K4195173. Other related parts are as followings: BBa_K4195151, BBa_K4195183, BBa_K4195184, BBa_K4195185, BBa_K4195186.

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


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    INCOMPATIBLE WITH RFC[12]
    Illegal NheI site found at 205
  • 21
    COMPATIBLE WITH RFC[21]
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    COMPATIBLE WITH RFC[25]
  • 1000
    COMPATIBLE WITH RFC[1000]