Difference between revisions of "Part:BBa K567013:Experience"

 
(Applications of BBa_K567013)
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This experience page is provided so that any user may enter their experience using this part.<BR>Please enter
 
This experience page is provided so that any user may enter their experience using this part.<BR>Please enter
 
how you used this part and how it worked out.
 
how you used this part and how it worked out.
  
===Applications of BBa_K567013===
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===Construction of BBa_K567013===
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This biobrick is constructed first by cloning the tRNA<sup>Asp</sup> from ''AspV'' in ''E.coli'', then the anticodon region is site-directed mutated. This part is constructed on the backbone plasmid pACYC184.
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===Characterization of BBa_K567013===
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This part acts as a stop codon suppressor tRNA. It can be charged with Asp.
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We have used P''bla''-Luc-TAG as our Reporter. The amount of luciferase produced is reflected using the bioluminescence emitted during the luciferin reaction. Our results demonstrate that this part can suppress TAG insertion into luciferase. In the experimental group, with the help of BBa_K567011 PT7-TDRS (Favorite Part), luciferase-TAG was produced and bioluminescence was emitted during the luciferin reaction. '''These results proved that this tRNA<sup>Asp</sup> can effectively suppress stop codon.
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[[image:11SJTU-stop-codon_switch.jpg|frame|center|fig. Functional Analysis of Stop-Codon Switch. ER2566 cannot produce luciferase with BBa_K567003 Pbla-Luc-TAG only. When BBa_K567011 PT7-TDRS (Favorite Part) and BBa_K567013 tRNA<sup>Asp</sup>-TAG (Favorite Part) are also transformed into the cell, luciferase is produced. The results proved Stop-Codon Switch as a strict molecular switch without background noise.This tRNA<sup>Asp</sup> is part of the Stop-Codon Switch]]
  
 
===User Reviews===
 
===User Reviews===

Revision as of 08:21, 5 October 2011

This experience page is provided so that any user may enter their experience using this part.
Please enter how you used this part and how it worked out.

Construction of BBa_K567013

This biobrick is constructed first by cloning the tRNAAsp from AspV in E.coli, then the anticodon region is site-directed mutated. This part is constructed on the backbone plasmid pACYC184.

Characterization of BBa_K567013

This part acts as a stop codon suppressor tRNA. It can be charged with Asp.

We have used Pbla-Luc-TAG as our Reporter. The amount of luciferase produced is reflected using the bioluminescence emitted during the luciferin reaction. Our results demonstrate that this part can suppress TAG insertion into luciferase. In the experimental group, with the help of BBa_K567011 PT7-TDRS (Favorite Part), luciferase-TAG was produced and bioluminescence was emitted during the luciferin reaction. These results proved that this tRNAAsp can effectively suppress stop codon.

fig. Functional Analysis of Stop-Codon Switch. ER2566 cannot produce luciferase with BBa_K567003 Pbla-Luc-TAG only. When BBa_K567011 PT7-TDRS (Favorite Part) and BBa_K567013 tRNAAsp-TAG (Favorite Part) are also transformed into the cell, luciferase is produced. The results proved Stop-Codon Switch as a strict molecular switch without background noise.This tRNAAsp is part of the Stop-Codon Switch

User Reviews

UNIQbf57c61c3b756557-partinfo-00000000-QINU UNIQbf57c61c3b756557-partinfo-00000001-QINU