Team:SJTU-BioX-Shanghai/Project/Subproject1-1
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Sylvia ruan (Talk | contribs) (→Design) |
Sylvia ruan (Talk | contribs) (→Design) |
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This rare tRNA<sup>Arg</sup> can be charged with Arg by native '''Arginyl-tRNA Synthetase(ArgRS)''' in E.coli. | This rare tRNA<sup>Arg</sup> can be charged with Arg by native '''Arginyl-tRNA Synthetase(ArgRS)''' in E.coli. | ||
- | [[image:11SJTU_Rare_03.jpg|center|Over expressed tRNA | + | [[image:11SJTU_Rare_03.jpg|center|Over expressed tRNA(Arg)-AGG is charged by native Arginyl-tRNA Synthetase(ArgRS)]] |
'''RFP-6AGG''': we have inserted 6 AGG codons after the start codon ATG in the RFP gene. | '''RFP-6AGG''': we have inserted 6 AGG codons after the start codon ATG in the RFP gene. |
Revision as of 17:00, 28 October 2011
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Rare tRNA AmountDesignIn this part we have overexpressed rare tRNAArg-AGG in the cell. The rare tRNA can recognize AGG codon on the mRNA. tRNAArg-AGG: 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: we have inserted 6 AGG codons after the start codon ATG in the RFP gene. ActionWhen 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.
ResultRFP 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.
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