Difference between revisions of "Part:BBa K1906000"
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<partinfo>BBa_K1906000 short</partinfo> | <partinfo>BBa_K1906000 short</partinfo> | ||
− | This protein is a translation elongation factor in bacterium | + | This protein is well known as a translation elongation factor in bacterium Escherichia coli. It can also assemble with phage polymerase domain to form a RNA-dependent-RNA polymerase holoenzyme. It was suggested by XJTLU-CHINA 2016 iGEM team that overexpress of this protein together with EF-Tu are essential for the production of Qbeta replicase holoenzyme. |
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+ | ===Characterlization=== | ||
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+ | <P>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.</P> | ||
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+ | <p>Figure 1 is the SDS-PAGE result comparison between cells that were transformed with these three proteins and beta subunit alone.</P> | ||
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+ | [[File:20161019150339!SDS-TSTU-REP.jpg|500px|thumb|left|Figure 1. SDS-PAGE result comparison between three-protein-expressing cells and beta subunit-expressing cells. Wild-type cells were included as a control group. The gel on the left shows the results of cells that had been induced with 2mM IPTG and the gel on the right shows the results of same groups of cells that had not been induced. The blue arrow indicates the band position of beta subunit.]] | ||
+ | <br><br><br><br><br><br><br><br><br><br><br><br><br><br><br><br><br><br><br> | ||
+ | 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. | ||
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+ | <h1> Improved Part </h1> | ||
+ | <p><b>Improved part:</b> BBa_K2443028 submitted by Lethbridge iGEM 2017</p> | ||
+ | <p><b> Rational behind improvements:</b> BBa_K1906000 encodes exclusively for the coding region of EF-Ts. 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 C-terminal hexahistidine tag with a serine glycine linker for easy purification. We have also optimized EF-Ts 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> | ||
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===Usage and Biology=== | ===Usage and Biology=== | ||
Latest revision as of 01:46, 31 October 2017
Elongation Factor Ts
This protein is well known as a translation elongation factor in bacterium Escherichia coli. It can also assemble with phage polymerase domain to form a RNA-dependent-RNA polymerase holoenzyme. It was suggested by XJTLU-CHINA 2016 iGEM team that overexpress of this protein together with EF-Tu are essential for the production 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_K2443028 submitted by Lethbridge iGEM 2017
Rational behind improvements: BBa_K1906000 encodes exclusively for the coding region of EF-Ts. 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 C-terminal hexahistidine tag with a serine glycine linker for easy purification. We have also optimized EF-Ts 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).
Usage and Biology
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 688
- 1000INCOMPATIBLE WITH RFC[1000]Illegal SapI.rc site found at 487