Difference between revisions of "Part:BBa K567013"
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This part acts as a stop codon suppressor tRNA. It can be charged with Asp. | This part acts as a stop codon suppressor tRNA. It can be charged with Asp. | ||
− | 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 | + | We have used P''bla''-Luc-TAG ([https://parts.igem.org/wiki/index.php?title=Part:BBa_K567003 BBa_K567003]) as our Reporter. The amount of luciferase produced is reflected using the bioluminescence emitted during the luciferin reaction. Our results demonstrate that TAG insertion into luciferase blocks luciferase production, which was shown in the control group. In the experimental group, with the help of PT7-TDRS([https://parts.igem.org/wiki/index.php?title=Part:BBa_K567011 BBa_K567011]) and tRNA<sup>Asp</sup>-TAG([https://parts.igem.org/wiki/index.php?title=Part:BBa_K567013 BBa_K567013]),luciferase was produced and bioluminescence was emitted during the luciferin reaction. These results proved that '''Stop-Codon Switch can turn on protein expression.''' |
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+ | [[image:11SJTU_stop_02.jpg|thumb|600px|center|''Fig.1'' Functional Analysis of Stop-Codon Switch. ER2566 cannot produce luciferase with Pbla-Luc-TAG ([https://parts.igem.org/wiki/index.php?title=Part:BBa_K567003 BBa_K567003]) only. When PT7-TDRS ([https://parts.igem.org/wiki/index.php?title=Part:BBa_K567011 BBa_K567011]) and tRNA<sup>Asp</sup>-TAG ([https://parts.igem.org/wiki/index.php?title=Part:BBa_K567013 BBa_K567013]) are also transformed into the cell, luciferase is produced. The results proved Stop-Codon Switch as a strict molecular switch without background noise.]] | ||
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Related Biobrick: | Related Biobrick: |
Latest revision as of 02:21, 29 October 2011
tRNA(Asp)-TAG
tRNA(Asp) with its anticodon mutated to CUA (base pairing stop codon UAG) and under the control of aspV promoter. This biobrick is constructed first by cloning the tRNA(Asp) from aspV in E.coli, then the anticodon region is site-directed mutated.
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 (BBa_K567003) as our Reporter. The amount of luciferase produced is reflected using the bioluminescence emitted during the luciferin reaction. Our results demonstrate that TAG insertion into luciferase blocks luciferase production, which was shown in the control group. In the experimental group, with the help of PT7-TDRS(BBa_K567011) and tRNAAsp-TAG(BBa_K567013),luciferase was produced and bioluminescence was emitted during the luciferin reaction. These results proved that Stop-Codon Switch can turn on protein expression.
Related Biobrick:
PT7-TDRS (BBa_K567011)
Sequence and Features
- 10INCOMPATIBLE WITH RFC[10]Illegal EcoRI site found at 281
- 12INCOMPATIBLE WITH RFC[12]Illegal EcoRI site found at 281
- 21INCOMPATIBLE WITH RFC[21]Illegal EcoRI site found at 281
- 23INCOMPATIBLE WITH RFC[23]Illegal EcoRI site found at 281
- 25INCOMPATIBLE WITH RFC[25]Illegal EcoRI site found at 281
- 1000COMPATIBLE WITH RFC[1000]