Difference between revisions of "Part:BBa K1906004"
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<h1> Improved Part </h1> | <h1> Improved Part </h1> | ||
<p><b>Improved part:</b> BBa_K2443027 submitted by Lethbridge iGEM 2017</p> | <p><b>Improved part:</b> BBa_K2443027 submitted by Lethbridge iGEM 2017</p> | ||
− | <p><b> Rational behind improvements:</b> BBa_K1906004 encodes exclusively for the coding region of EF-Tu. In order to improve it and incorporate it into our Next vivo system we have codon optimized for use in E. coli and attached a N-terminal hexahistidine tag with a serine glycine linker for easy purification. We have also optimized EF-Tu to be overexpressed in BL21 DE3 gold cells by putting it under the control of a T7 promoter (BBa_I719005), RBS (BBa_B0034) and double terminator (BBa_B0015). </p> | + | <p><b> Rational behind improvements:</b> BBa_K1906004 encodes exclusively for the coding region of EF-Tu. In order to improve it and incorporate it into our Next vivo system we have codon optimized for use in E. coli and attached a N-terminal hexahistidine tag with a serine glycine linker for easy purification. We have also optimized EF-Tu to be overexpressed in BL21-Gold (DE3) gold cells by putting it under the control of a T7 promoter (BBa_I719005), RBS (BBa_B0034) and double terminator (BBa_B0015). </p> |
Latest revision as of 02:06, 31 October 2017
Elongation Factor Tu
This protein is well known as a translation elongation factor in bacterium Escherichia coli. It can also assemble with phage polymerase domain to form an RNA-dependent-RNA polymerase. It was suggested by XJTLU-CHINA 2016 iGEM team that over-expression of this protein together with EF-TS are essential for the production of beta subunit of Qbeta replicase holoenzyme.
Characterlization
It was quite surprising that plasmids that carry beta subunit genes don't lead to a heavy production of the protein upon the induction. However, this situation can be improved when EF-Ts and EF-Tu are co-expressed with beta subunit.
Figure 1 is the SDS-PAGE result comparison between cells that were transformed with these three proteins and beta subunit alone.
It can be clearly seen that cells transformed with beta subunit alone had no detectable level of protein expression. However, the expression of beta subunit can be greatly restored when plasmids that carry EF-Tu and EF-Ts are transformed into the cells.
Improved Part
Improved part: BBa_K2443027 submitted by Lethbridge iGEM 2017
Rational behind improvements: BBa_K1906004 encodes exclusively for the coding region of EF-Tu. In order to improve it and incorporate it into our Next vivo system we have codon optimized for use in E. coli and attached a N-terminal hexahistidine tag with a serine glycine linker for easy purification. We have also optimized EF-Tu to be overexpressed in BL21-Gold (DE3) gold cells by putting it under the control of a T7 promoter (BBa_I719005), RBS (BBa_B0034) and double terminator (BBa_B0015).
Sequence and Features
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25INCOMPATIBLE WITH RFC[25]Illegal AgeI site found at 280
Illegal AgeI site found at 685 - 1000INCOMPATIBLE WITH RFC[1000]Illegal SapI.rc site found at 430