Team:INSA-Lyon/Parts

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<a href="https://2014.igem.org/Team:INSA-Lyon/Notebook" class="hu-icon"><li class="iconmulti"  style="line-height:40px;  ">NOTEBOOK</li></a>
<a href="https://2014.igem.org/Team:INSA-Lyon/Notebook" class="hu-icon"><li class="iconmulti"  style="line-height:40px;  ">NOTEBOOK</li></a>
<a href="https://2014.igem.org/Team:INSA-Lyon/Parts" class="hu-icon"><li class="iconmulti"  style="line-height:40px;  ">PARTS</li></a>
<a href="https://2014.igem.org/Team:INSA-Lyon/Parts" class="hu-icon"><li class="iconmulti"  style="line-height:40px;  ">PARTS</li></a>
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<a href="https://2014.igem.org/Team:INSA-Lyon/DataPage" class="hu-icon"><li class="iconmulti"  style="line-height:40px;  ">DATA PAGE</li></a>
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Revision as of 18:33, 16 October 2014

Curly'on - IGEM 2014 INSA-LYON

  • 5 biobricks have been constructed, three for Nickel chelation, three for promoter characterization.




    Biobricks for nickel chelation

    The principal of the construction is shown in the figure below.





  • On a pSB1C3 backbone, two essential part have been assembled: a promoter and a reporter coding for CsgA.The promoter in this case is always the same: P70.However, the reporter is different for each construction.

  • The first CsgA is called CsgA WT, the sequence is exactly the same as we found in a wild type CsgA protein except one mutation in order to eliminate one restriction site. The construction is also called CsgA.




  • The second CsgA is based on the same sequence but with a short sequence coding for a his tag(a peptide chain coding six histidines). This construction is called His1.




  • The last CsgA is almost the same but with 2 his tag. This construction is called His2.




  • 5 biobricks have been constructed, three for Nickel chelation, three for promoter characterization.




    Biobrick for promoter characterization

    The principal of the construction is shown in the figure below.





  • On a pKK backbone, two essential parts have been assembled: a promoter and a reporter. The reporter in this case is always the same: gfp. However, the promoter is different for each construction.

  • The first promoter is P70, sequence found in the Resgistry. This construction is called p70::gfp




  • The second promoter is PCurli, obtained from a PCR, sequence coding for the inter-genic regulation for curli production. This construction is called pcurli::gfp.




  • <groupparts>iGEM014 INSA-Lyon</groupparts>