Difference between revisions of "Part:BBa K567025"
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<partinfo>BBa_K567025 short</partinfo> | <partinfo>BBa_K567025 short</partinfo> | ||
− | This part is constructed based on PT7-Luc-8AGG ([https://parts.igem.org/wiki/index.php?title=Part:BBa_K567007 BBa_K567007]). The | + | This part is constructed based on PT7-Luc-8AGG ([https://parts.igem.org/wiki/index.php?title=Part:BBa_K567007 BBa_K567007]). The tDNA<sup>Arg</sup> and luciferase gene into T7 operon so that both genes can be transcribed. tRNA<sup>Arg</sup> can be correctly processed and become matured. Luciferase mRNA will be further translated into protein. The induced tRNA<sup>Arg</sup> can facilitate the translation of luciferase-8AGG, achieving positive feedback. |
The transcription of this part is under the control of T7 promoter and ''lac'' operator. RNA expression is induced by 0.5mM IPTG when the OD600 of the culture reaches 0.3. | The transcription of this part is under the control of T7 promoter and ''lac'' operator. RNA expression is induced by 0.5mM IPTG when the OD600 of the culture reaches 0.3. | ||
Revision as of 01:28, 29 October 2011
PT7-Luc-8AGG-tRNA(Arg)
This part is constructed based on PT7-Luc-8AGG (BBa_K567007). The tDNAArg and luciferase gene into T7 operon so that both genes can be transcribed. tRNAArg can be correctly processed and become matured. Luciferase mRNA will be further translated into protein. The induced tRNAArg can facilitate the translation of luciferase-8AGG, achieving positive feedback. The transcription of this part is under the control of T7 promoter and lac operator. RNA expression is induced by 0.5mM IPTG when the OD600 of the culture reaches 0.3.
Sequence and Features
Assembly Compatibility:
- 10INCOMPATIBLE WITH RFC[10]Illegal XbaI site found at 48
Illegal PstI site found at 1941 - 12INCOMPATIBLE WITH RFC[12]Illegal PstI site found at 1941
- 21COMPATIBLE WITH RFC[21]
- 23INCOMPATIBLE WITH RFC[23]Illegal XbaI site found at 48
Illegal PstI site found at 1941 - 25INCOMPATIBLE WITH RFC[25]Illegal XbaI site found at 48
Illegal PstI site found at 1941 - 1000INCOMPATIBLE WITH RFC[1000]Illegal SapI.rc site found at 929