Difference between revisions of "Part:BBa K567001"
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PT7-Luc-3x4AGG(30bp+111bp) ([https://parts.igem.org/wiki/index.php?title=Part:BBa_K567027 BBa_K567027]) | PT7-Luc-3x4AGG(30bp+111bp) ([https://parts.igem.org/wiki/index.php?title=Part:BBa_K567027 BBa_K567027]) | ||
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Revision as of 02:36, 29 October 2011
lacI-Ptrc-tRNA(Arg)
The tRNA(Arg) is under the control of promoter trc. tRNA(Arg) expression is induced by 0.5mM IPTG when the OD600 of the culture reaches 0.3.
Design
In this part we have overexpressed rare tRNAArg-AGG in the cell. The rare tRNA can recognize AGG codon on the mRNA.
tRNAArg-AGG(BBa_K567001): tRNAArg-AGG is over expressed under the control of trc promoter (induced by IPTG).
This rare tRNAArg can be charged with Arg by native Arginyl-tRNA Synthetase(ArgRS) in E.coli.
RFP-6AGG(BBa_K567017): we have inserted 6 AGG codons after the start codon ATG in the RFP gene.
Action
When rare tRNAArg-AGG is not over-expressed, RFP expression is hindered. When tRNAArg-AGG is over-expressed, this tRNA can recognize the AGG codon on the mRNA so a large amount of RFP is produced.
Result
RFP has been largely produced in cells overexpressing tRNAArg. No RFP can be observed in cells without rare tRNA overexpression.
We have successfully controlled protein expression by controlling rare tRNA amount.
Reference
Ulrich Deuschlel., et al., Promoters of Escherichia coli: a hierarchy of in vivo strength indicates alternate structures The EMBO Journal vol.5 no. 11 pp.2987-2994, 1986
Related Biobrick
Pbla-Luc-2AGG (BBa_K567004)
Pbla-Luc-4AGG (BBa_K567005)
Pbla-Luc-6AGG (BBa_K567006)
Pbla-Luc-8AGG (BBa_K567007)
PT7-Luc-2AGG (BBa_K567008)
PT7-Luc-4AGG (BBa_K567009)
PT7-Luc-6AGG (BBa_K567019)
PT7-Luc-8AGG (BBa_K567010)
PT7-Luc-2x4AGG(111bp) (BBa_K567021)
PT7-RFP-6AGG (BBa_K567017)
PT7-Luc-2x4AGG(30bp) (BBa_K567026)
PT7-Luc-3x4AGG(30bp+111bp) (BBa_K567027)
Sequence and Features
- 10INCOMPATIBLE WITH RFC[10]Illegal PstI site found at 1845
- 12INCOMPATIBLE WITH RFC[12]Illegal PstI site found at 1845
- 21COMPATIBLE WITH RFC[21]
- 23INCOMPATIBLE WITH RFC[23]Illegal PstI site found at 1845
- 25INCOMPATIBLE WITH RFC[25]Illegal PstI site found at 1845
- 1000INCOMPATIBLE WITH RFC[1000]Illegal BsaI site found at 2026