Difference between revisions of "Team:ASIJ Tokyo/Parts"

 
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           <a class="dropdown-toggle" data-toggle="dropdown" href="">Project<span class="caret"></span></a>
 
           <a class="dropdown-toggle" data-toggle="dropdown" href="">Project<span class="caret"></span></a>
 
           <ul class="dropdown-menu">
 
           <ul class="dropdown-menu">
−
             <li><a href="https://2016.igem.org/Team:ASIJ_Tokyo/ASIJProjectDescription">Project Description + Abstract</a></li>
+
             <li><a href="https://2016.igem.org/Team:ASIJ_Tokyo/Description">Project Description + Abstract</a></li>
 
             <li><a href="https://2016.igem.org/Team:ASIJ_Tokyo/Experiments">Experiments</a></li>
 
             <li><a href="https://2016.igem.org/Team:ASIJ_Tokyo/Experiments">Experiments</a></li>
 
             <li><a href="https://2016.igem.org/Team:ASIJ_Tokyo/Results">Results</a></li>
 
             <li><a href="https://2016.igem.org/Team:ASIJ_Tokyo/Results">Results</a></li>
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         <li><a href="https://2016.igem.org/Team:ASIJ_Tokyo/Attributions">Attributions</a></li>
 
         <li><a href="https://2016.igem.org/Team:ASIJ_Tokyo/Attributions">Attributions</a></li>
 
         <li><a href="https://2016.igem.org/Team:ASIJ_Tokyo/Parts">Parts</a></li>     
 
         <li><a href="https://2016.igem.org/Team:ASIJ_Tokyo/Parts">Parts</a></li>     
−
 
+
        <li><a href="https://2016.igem.org/Team:ASIJ_Tokyo/Human_Practices">Human Practices</a></li> 
 
       </ul>
 
       </ul>
  
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<br>
 
<br>
 
<h3><strong>Tags</strong></h3>
 
<h3><strong>Tags</strong></h3>
−
<li>N-OsmY: Fusion proteins with an N-terminal osmY have been shown to successfully secrete proteins of interest out of <i>E. Coli</i></li>
+
<li>N-OsmY
−
<li>C-Myc: This C-terminal tag would allow the PETase construct to be more easily detected by Western blot assays for expression </li>
+
      <ul>
 +
          <li>Fusion proteins with an N-terminal osmY have been shown to successfully secrete proteins of interest out of <i>E. Coli</i></li>
 +
      </ul>
 +
</li>
 +
<li>C-Myc
 +
    <ul>
 +
      <li>This C-terminal tag would allow the PETase construct to be more easily detected by Western blot assays for expression </li>
 +
    </ul>
 +
</li>
 
<br>
 
<br>
 
<h3><strong>Others</strong></h3>
 
<h3><strong>Others</strong></h3>
−
<li>PETase sequence: gene that coded for the PET hydrolase</li>
+
<li>PETase sequence
−
<li>Plasmid backbone: the pSB1C3 backbone is recommended </li>
+
<ul>
−
<li>High efficiency <i>E. Coli</i> cells: hosted the PETase constructs</li>
+
      <li>Gene that coded for the PET hydrolase</li>
 +
</ul>
 +
</li>
 +
<li>Plasmid backbone
 +
<ul>
 +
    <li>The pSB1C3 backbone is recommended</li>
 +
</ul>
 +
</li>
 +
<li>High efficiency <i>E. Coli</i> cells
 +
<ul>
 +
    <li>Hosted the PETase constructs</li>
 +
</ul>
 +
</li>
 
<br>
 
<br>
 
<h3><strong>Parts Submitted</strong></h3>
 
<h3><strong>Parts Submitted</strong></h3>
−
<li>BBa_K1885001
+
<li>Gibson-assembled pSB1C3 with novel fusion osmY-PETase A1 (BBa_K1885001)
 
     <ul>
 
     <ul>
−
          <li>This part offers efficiency in the initial step in the bioremediation of polyethylene terephthalate (PET): the production of metabolizable monomers (ethylene glycol and terephthalate) through hydrolysis. PETase catalyzes the hydrolysis of PET into terephthalate and ethylene glycol monomers. The N-terminal osmY protein and its signal peptide fused to PETase, with serine-glycine peptide’s repeating intervention, serves to secrete PETase out of the cell (this reacts with PET in the cell's local environment). The Anderson promoter, with a relative strength of 1 that precedes the fusion protein in the plasmid, serves to constitutively express the fusion PETase, enhancing the degradation of environmental PET. This part utilizes the pSB1C3 backbone and confers resistance to chloramphenicol.</li>
+
          <li>This part offers efficiency in the initial step in the bioremediation of polyethylene terephthalate (PET): the production of metabolizable monomers (ethylene glycol and terephthalate) through hydrolysis. PETase catalyzes the hydrolysis of PET into terephthalate and ethylene glycol monomers. The N-terminal osmY protein and its signal peptide fused to PETase, with serine-glycine peptide’s repeating intervention, serves to secrete PETase out of the cell (this reacts with PET in the cell's local environment). The Anderson promoter, with a relative strength of 1 that precedes the fusion protein in the plasmid, serves to constitutively express the fusion PETase, enhancing the degradation of environmental PET. This part utilizes the pSB1C3 backbone and confers resistance to chloramphenicol.</li>
 
     </ul>
 
     </ul>
 
</li>
 
</li>
−
<li>BBa_K1885002
+
<li>Gibson-assembled pSB1C3 with novel fusion osmY-PETase A0.58 (BBa_K1885002)
 
     <ul>
 
     <ul>
 
           <li>This part offers efficiency in the initial step in the bioremediation of polyethylene terephthalate (PET): the production of metabolizable monomers (ethylene glycol and terephthalate) through hydrolysis. PETase catalyzes the hydrolysis of PET into terephthalate and ethylene glycol monomers. The N-terminal osmY protein and its signal peptide fused to PETase, with serine-glycine peptide’s repeating intervention, serves to secrete PETase out of the cell (this reacts with PET in the cell's local environment). The Anderson promoter, with a relative strength of 0.58 that precedes the fusion protein in the plasmid, serves to constitutively express the fusion PETase, enhancing the degradation of environmental PET. This part utilizes the pSB1C3 backbone and confers resistance to chloramphenicol.</li>
 
           <li>This part offers efficiency in the initial step in the bioremediation of polyethylene terephthalate (PET): the production of metabolizable monomers (ethylene glycol and terephthalate) through hydrolysis. PETase catalyzes the hydrolysis of PET into terephthalate and ethylene glycol monomers. The N-terminal osmY protein and its signal peptide fused to PETase, with serine-glycine peptide’s repeating intervention, serves to secrete PETase out of the cell (this reacts with PET in the cell's local environment). The Anderson promoter, with a relative strength of 0.58 that precedes the fusion protein in the plasmid, serves to constitutively express the fusion PETase, enhancing the degradation of environmental PET. This part utilizes the pSB1C3 backbone and confers resistance to chloramphenicol.</li>
 
     </ul>
 
     </ul>
 
</li>
 
</li>
−
<li>BBa_K1885005
+
<li>Gibson-assembled pSB1C3 with novel fusion osmY-PETase A0.33 (BBa_K1885005)
 
     <ul>
 
     <ul>
 
           <li>This part offers efficiency in the initial step in the bioremediation of polyethylene terephthalate (PET): the production of metabolizable monomers (ethylene glycol and terephthalate) through hydrolysis. PETase catalyzes the hydrolysis of PET into terephthalate and ethylene glycol monomers. The N-terminal osmY protein and its signal peptide fused to PETase, with serine-glycine peptide’s repeating intervention, serves to secrete PETase out of the cell (this reacts with PET in the cell's local environment). The Anderson promoter, with a relative strength of 0.33 that precedes the fusion protein in the plasmid, serves to constitutively express the fusion PETase, enhancing the degradation of environmental PET. This part utilizes the pSB1C3 backbone and confers resistance to chloramphenicol.</li>
 
           <li>This part offers efficiency in the initial step in the bioremediation of polyethylene terephthalate (PET): the production of metabolizable monomers (ethylene glycol and terephthalate) through hydrolysis. PETase catalyzes the hydrolysis of PET into terephthalate and ethylene glycol monomers. The N-terminal osmY protein and its signal peptide fused to PETase, with serine-glycine peptide’s repeating intervention, serves to secrete PETase out of the cell (this reacts with PET in the cell's local environment). The Anderson promoter, with a relative strength of 0.33 that precedes the fusion protein in the plasmid, serves to constitutively express the fusion PETase, enhancing the degradation of environmental PET. This part utilizes the pSB1C3 backbone and confers resistance to chloramphenicol.</li>

Latest revision as of 23:32, 19 October 2016

The BIG TEMPLATE : RESPONSIVE and FREE

Parts


Anderson Promoters

  • Relative Strength: weak (0.33) BBa_J23110
    • Selected as a relatively weak promoter against which to compare the expression of the PETase construct
  • Relative Strength: moderate (0.58) BBa_J23111
    • Selected as a relatively moderately strong promoter against which to compare the expression of the PETase construct
  • Relative Strength: strong (1) BBa_J23100
    • Selected as a relatively strong promoter against which to compare the expression of the PETase construct

    • Tags

  • N-OsmY
    • Fusion proteins with an N-terminal osmY have been shown to successfully secrete proteins of interest out of E. Coli
  • C-Myc
    • This C-terminal tag would allow the PETase construct to be more easily detected by Western blot assays for expression

    • Others

  • PETase sequence
    • Gene that coded for the PET hydrolase
  • Plasmid backbone
    • The pSB1C3 backbone is recommended
  • High efficiency E. Coli cells
    • Hosted the PETase constructs

    • Parts Submitted

  • Gibson-assembled pSB1C3 with novel fusion osmY-PETase A1 (BBa_K1885001)
    • This part offers efficiency in the initial step in the bioremediation of polyethylene terephthalate (PET): the production of metabolizable monomers (ethylene glycol and terephthalate) through hydrolysis. PETase catalyzes the hydrolysis of PET into terephthalate and ethylene glycol monomers. The N-terminal osmY protein and its signal peptide fused to PETase, with serine-glycine peptide’s repeating intervention, serves to secrete PETase out of the cell (this reacts with PET in the cell's local environment). The Anderson promoter, with a relative strength of 1 that precedes the fusion protein in the plasmid, serves to constitutively express the fusion PETase, enhancing the degradation of environmental PET. This part utilizes the pSB1C3 backbone and confers resistance to chloramphenicol.
  • Gibson-assembled pSB1C3 with novel fusion osmY-PETase A0.58 (BBa_K1885002)
    • This part offers efficiency in the initial step in the bioremediation of polyethylene terephthalate (PET): the production of metabolizable monomers (ethylene glycol and terephthalate) through hydrolysis. PETase catalyzes the hydrolysis of PET into terephthalate and ethylene glycol monomers. The N-terminal osmY protein and its signal peptide fused to PETase, with serine-glycine peptide’s repeating intervention, serves to secrete PETase out of the cell (this reacts with PET in the cell's local environment). The Anderson promoter, with a relative strength of 0.58 that precedes the fusion protein in the plasmid, serves to constitutively express the fusion PETase, enhancing the degradation of environmental PET. This part utilizes the pSB1C3 backbone and confers resistance to chloramphenicol.
  • Gibson-assembled pSB1C3 with novel fusion osmY-PETase A0.33 (BBa_K1885005)
    • This part offers efficiency in the initial step in the bioremediation of polyethylene terephthalate (PET): the production of metabolizable monomers (ethylene glycol and terephthalate) through hydrolysis. PETase catalyzes the hydrolysis of PET into terephthalate and ethylene glycol monomers. The N-terminal osmY protein and its signal peptide fused to PETase, with serine-glycine peptide’s repeating intervention, serves to secrete PETase out of the cell (this reacts with PET in the cell's local environment). The Anderson promoter, with a relative strength of 0.33 that precedes the fusion protein in the plasmid, serves to constitutively express the fusion PETase, enhancing the degradation of environmental PET. This part utilizes the pSB1C3 backbone and confers resistance to chloramphenicol.