Difference between revisions of "Part:BBa K2443027"

 
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<h1> Improved Part </h1>
 
<h1> Improved Part </h1>
 
<p><b>Original part:</b>BBa_K1906004 submitted by XJTLU-China 2016</p>
 
<p><b>Original part:</b>BBa_K1906004 submitted by XJTLU-China 2016</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 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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<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 cells by putting it under the control of a T7 promoter (BBa_I719005), RBS (BBa_B0034) and double terminator (BBa_B0015). The expected size of EF-Tu is 45 kDa, which corresponds to one of the thick bands seen in lane 9 of the overexpression gel below. Overexpression was performed in BL21DE3 gold cells containing K2443027 in pUC57-kan. Overexpressions were performed according to the protocols and notebook on the 2017 iGEM Lethbridge wiki (https://static.igem.org/mediawiki/2017/2/2c/Protein_Overexpression_.pdf and https://static.igem.org/mediawiki/2017/0/0d/October_.pdf) </p>
  
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https://static.igem.org/mediawiki/parts/f/fd/Lethbridge_oct_15_gel_1.png
  
 
<!-- Add more about the biology of this part here
 
<!-- Add more about the biology of this part here

Latest revision as of 20:19, 1 November 2017


EF-Tu optimized for expression in E. coli

EF-Tu (elongation factor thermo unstable) is a prokaryotic elongation factor which catalyzes the binding of an aminoacyl-tRNA (aa-tRNA) to the ribosome. It is a G-protein, and is involved in the selection and binding of an aa-tRNA to the A-site of the ribosome. As a result of its crucial role in translation, EF-Tu is one of the most abundant and highly conserved proteins in prokaryotes. Codon optimized for use in Escherichia coli and contains an N-terminal hexahistidine tag. Under the regulation of T7 Promoter, RBS and double terminator.

Improved Part

Original part:BBa_K1906004 submitted by XJTLU-China 2016

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 cells by putting it under the control of a T7 promoter (BBa_I719005), RBS (BBa_B0034) and double terminator (BBa_B0015). The expected size of EF-Tu is 45 kDa, which corresponds to one of the thick bands seen in lane 9 of the overexpression gel below. Overexpression was performed in BL21DE3 gold cells containing K2443027 in pUC57-kan. Overexpressions were performed according to the protocols and notebook on the 2017 iGEM Lethbridge wiki (https://static.igem.org/mediawiki/2017/2/2c/Protein_Overexpression_.pdf and https://static.igem.org/mediawiki/2017/0/0d/October_.pdf)

Lethbridge_oct_15_gel_1.png

Sequence and Features


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    COMPATIBLE WITH RFC[12]
  • 21
    COMPATIBLE WITH RFC[21]
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    COMPATIBLE WITH RFC[25]
  • 1000
    COMPATIBLE WITH RFC[1000]