Difference between revisions of "Part:BBa K567011"
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− | [https://parts.igem.org/wiki/index.php?title=Part:BBa_K567012 BBa_K567012] | + | tRNA<sup>Asp</sup>-AGG ([https://parts.igem.org/wiki/index.php?title=Part:BBa_K567012 BBa_K567012]) |
− | [https://parts.igem.org/wiki/index.php?title=Part:BBa_K567013 BBa_K567013] | + | tRNA<sup>Asp</sup>-TAG ([https://parts.igem.org/wiki/index.php?title=Part:BBa_K567013 BBa_K567013]) |
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Revision as of 02:56, 6 October 2011
PT7-TDRS
aspartyl aminoacyl tRNA synthetase without anticodon recognition domain under the control of T7 promoter and lac operator. This biobrick is constructed by deleting the anticodon recognition domain of AspRS from E.coli. This modified AspRS can charge Asp to tRNA(Asp)-TAG (BBa_K567013) and tRNA(Asp)-AGG (BBa_K567012).
To deprive AspRS of its anticodon specificity, we analyzed the structure of AspRS and expressed a truncated AspRS without anticodon recognition domain. Our design is shown below. This modified enzyme keeps its ability of aminoacylation while loses its activity of recognizing anticodon of tRNA.
We have used PT7-RFP-6AGG (BBa_K567017) as our Reporter. We have constructed tRNAAsp-AGG and PT7-TDRS (AspRS without anticodon recognition domain, ) (BBa_K567012 and BBa_K567011)as the Modulator. tRNAAsp-AGG, which can recognize rare codon AGG, is under constitutive promoter. Our device works as follows: Without Modulator, RFP with 6 consecutive AGG insertions can hardly be expressed. When Modulator works, tRNAAsp-AGG can be charged with Asp by TDRS. tRNAAsp-AGG recognizes rare codon AGG on the Reporter RFP-6AGG. The ribosome gets through this part of the mRNA more easily. RFP is expressed. Red fluorescence is observed. Our experiment results are shown below.
Related Biobrick:
tRNAAsp-AGG (BBa_K567012)
tRNAAsp-TAG (BBa_K567013)
Sequence and Features
- 10INCOMPATIBLE WITH RFC[10]Illegal EcoRI site found at 1595
Illegal EcoRI site found at 1767
Illegal XbaI site found at 48
Illegal PstI site found at 1152 - 12INCOMPATIBLE WITH RFC[12]Illegal EcoRI site found at 1595
Illegal EcoRI site found at 1767
Illegal NheI site found at 1556
Illegal PstI site found at 1152
Illegal NotI site found at 1620 - 21INCOMPATIBLE WITH RFC[21]Illegal EcoRI site found at 1595
Illegal EcoRI site found at 1767
Illegal BamHI site found at 1589
Illegal XhoI site found at 1629 - 23INCOMPATIBLE WITH RFC[23]Illegal EcoRI site found at 1595
Illegal EcoRI site found at 1767
Illegal XbaI site found at 48
Illegal PstI site found at 1152 - 25INCOMPATIBLE WITH RFC[25]Illegal EcoRI site found at 1595
Illegal EcoRI site found at 1767
Illegal XbaI site found at 48
Illegal PstI site found at 1152 - 1000COMPATIBLE WITH RFC[1000]