Difference between revisions of "Team:IIT Delhi/Basic Part"

 
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.bgimg-4{
 
.bgimg-4{
 
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background: url("https://static.igem.org/mediawiki/2018/3/3e/T--IIT_Delhi--basic_parts.png") ;
  
 
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     </div>
 
     </div>
 
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   </div>
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<div class="dropdownsakks">
 
         <div class= "borderYtoX">
 
         <div class= "borderYtoX">
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   <a href="https://2018.igem.org/Team:IIT_Delhi/Results" >Results</a>
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   <a href="javascript:void(0)" >Results</a>
 
     </div>
 
     </div>
  
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  <div class="dropdownsakks-content"  style="margin-top: 66px;">
 +
      <a href="https://2018.igem.org/Team:IIT_Delhi/Demonstrate">Demonstrate</a>
 +
      <a href="https://2018.igem.org/Team:IIT_Delhi/InterLab">Interlab</a>
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 +
    </div>
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     </div>
 
     </div>
 
      
 
      
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        <a href="https://2018.igem.org/Team:IIT_Delhi/Results" style="padding-bottom: 15px;padding-top: 15px;" >Results</a>
 
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     <button class="overlayved-btn" onclick="myFunction2()" style="padding-bottom: 15px;">Parts
 
     <button class="overlayved-btn" onclick="myFunction2()" style="padding-bottom: 15px;">Parts
 
       <i class="fa fa-caret-right"></i>   
 
       <i class="fa fa-caret-right"></i>   
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     <a href="https://2018.igem.org/Team:IIT_Delhi/Basic_Part" style="font-size: 15px;font-size: 15px; padding-bottom: 5px; padding: 10px; padding-top: 3px;" >Basic Parts</a>
 
     <a href="https://2018.igem.org/Team:IIT_Delhi/Basic_Part" style="font-size: 15px;font-size: 15px; padding-bottom: 5px; padding: 10px; padding-top: 3px;" >Basic Parts</a>
 
     <a href="https://2018.igem.org/Team:IIT_Delhi/Composite_Part" style="font-size: 15px;font-size: 15px; padding: 10px; padding-bottom: 5px; padding-top: 5px;" >Composite Parts</a>
 
     <a href="https://2018.igem.org/Team:IIT_Delhi/Composite_Part" style="font-size: 15px;font-size: 15px; padding: 10px; padding-bottom: 5px; padding-top: 5px;" >Composite Parts</a>
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    <button class="overlayved-btn" onclick="myFunction6()" style="padding-bottom: 15px;">Results
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    </button>
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    <div class="dropdownsakks-container" id="mydropdownsakks6" style= "font-style: italic;">
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    <a href="https://2018.igem.org/Team:IIT_Delhi/Demonstrate" style="font-size: 15px;font-size: 15px; padding-bottom: 5px; padding: 10px; padding-top: 3px;" >Demonstrate</a>
 +
    <a href="https://2018.igem.org/Team:IIT_Delhi/InterLab" style="font-size: 15px;font-size: 15px; padding: 10px; padding-bottom: 5px; padding-top: 5px;" >Interlab</a>
 
            
 
            
 
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</section>
 
</section>
  
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  <div class="caption">
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    <span class="border" >Text anyone?</span>
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<div style="color: black;background-color:white;text-align:center;padding:50px 80px;text-align: justify;margin: auto;width: 80%;font-size: 60%;line-height: 1.5;">
  
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<div style="color: #777;background-color:white;text-align:center;padding:50px 80px;text-align: justify;">
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<table>
−
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  <tr>
−
  <p style="font-size: 30px; font-family: 'Roboto', sans-serif;font-weight:700;">BBa_K2814001 = pLTL
+
    <th>S. No</th>
−
     <br>
+
    <th>Part Name</th>
−
      </p>
+
    <th>BioBrick</th>
−
      <p style="font-size:20px;font-family: 'Lato', sans-serif;font-weight:400;"> The pLTL (Lac-Tet-Lac) is a hybrid promoter. It is a promoter composed of the operator sequences of pTet and the pLac promoter. There are multiple benefits of using the pLTL promoter.
+
    <th>Description</th>
−
</p>
+
    <th>Part Type</th>
−
   
+
  </tr>
−
      <ul style="font-size:20px;" >
+
  <tr>
−
      <li style="font-family: 'Lato', sans-serif;font-weight:400;">The hybrid pLTL shows almost complete repression on being repressed, and on induction (by IPTG and/or aTc), the hybrid pLTL promoter shows a 1.4-2 times higher expression.</li>
+
    <td>1</td>
−
      <li style="font-family: 'Lato', sans-serif;font-weight:400;">The hybrid pLTL promoter also permits flexible gene expression because it can be utilized under either or both repression controls (LacI and TetR) simultaneously.</li>
+
    <td><a href="http://parts.igem.org/Part:BBa_K2814001"><span style="font-weight: 400;">BBa_K2814001</span></a></td>
−
   
+
    <td>pLTL</td>
−
     </ul>
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     <td>Lac-Tet-Lac Hybrid Promoter</td>
−
<br>
+
    <td>Promoter</td>
−
 
+
  </tr>
−
<p style="font-size: 30px; font-family: 'Roboto', sans-serif;font-weight:700;">BBa_K2814008 = rrnB T1 Terminator + T7Te Terminator
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  <tr>
−
     <br>
+
    <td>2</td>
−
      </p>
+
    <td><a href="http://parts.igem.org/Part:BBa_K2814007">BBa_K2814007</a></td>
−
      <p style="font-size:20px;font-family: 'Lato', sans-serif;font-weight:400;"> Our part is double terminator composed of rrnB T1 Terminator(BBa B0010) and T7 Te Terminator(BBa B0012). Both of these are forward terminators that are extensively used in E. coli.
+
    <td>sfGFP_ssrA</td>
−
</p>
+
    <td>Reporter gene (codon-optimised for E. coli)</td>
−
<br>
+
    <td>Coding Sequence</td>
−
 
+
  </tr>
−
<p style="font-size: 30px; font-family: 'Roboto', sans-serif;font-weight:700;">BBa_K2814009 = mKate2
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  <tr>
−
 
+
    <td>3</td>
−
     <br>
+
    <td><a href="http://parts.igem.org/Part:BBa_K2814008">BBa_K2814008</a></td>
−
      </p>
+
    <td>rrnB T1 Terminator + T7Te Terminator</td>
−
      <p style="font-size:20px;font-family: 'Lato', sans-serif;font-weight:400;"> Mkate2 - mKate2 is a red fluorescent protein derived from Entacmaea quadricolor. It possesses fluorescence with excitation maxima at 588 nm and emission maxima at 588 and 633 nm, mKate2 is almost 3-fold brighter than mKate. mKate2 can be used in   labelling applications along with blue, cyan, green, yellow, and red fluorescent dyes. Its high pH-stability with pKa=5.4 makes it useful for imaging in acidic organelles, such as late and recycling endosomes and lysosomes.
+
    <td>Double Transcriptional Terminator</td>
−
 
+
    <td>Terminator</td>
−
</p>
+
  </tr>
−
<br>
+
  <tr>
−
 
+
    <td>4</td>
−
<p style="font-size: 30px; font-family: 'Roboto', sans-serif;font-weight:700;">BBa_K2814010 = rrnB T1 Terminator
+
    <td><a href="http://parts.igem.org/Part:BBa_K2814009">BBa_K2814009</a></td>
−
 
+
    <td>mKate2</td>
−
     <br>
+
    <td>Reporter gene (codon-optimised for E. coli)</td>
−
      </p>
+
     <td>Coding Sequence</td>
−
     <br>
+
  </tr>
 +
  <tr>
 +
    <td>5</td>
 +
    <td><a href="http://parts.igem.org/Part:BBa_K2814010">BBa_K2814010</a></td>
 +
    <td>rrnB T1 Terminator</td>
 +
    <td>Transcriptional Terminator</td>
 +
     <td>Terminator</td>
 +
  </tr>
 +
  <tr>
 +
    <td>6</td>
 +
    <td><a href="http://parts.igem.org/Part:BBa_K2814011">BBa_K2814011</a></td>
 +
    <td>attP TP901-1</td>
 +
    <td>Attachment site for TP901-1 Integrase</td>
 +
    <td>DNA</td>
 +
  </tr>
 +
  <tr>
 +
    <td>7</td>
 +
    <td><a href="http://parts.igem.org/Part:BBa_K2814012">BBa_K2814012</a></td>
 +
    <td>BxbI Integrase + ssrA(LVA) deg tag</td>
 +
    <td>CDS for Integrase Bxb1</td>
 +
    <td>Coding Sequence</td>
 +
  </tr>
 +
  <tr>
 +
    <td>8</td>
 +
    <td><a href="http://parts.igem.org/Part:BBa_K2814013">BBa_K2814013</a></td>
 +
    <td>attB TP901-1</td>
 +
    <td>Attachment site for TP901-1 Integrase</td>
 +
    <td>DNA</td>
 +
  </tr>
 +
  <tr>
 +
    <td>9</td>
 +
    <td><a href="http://parts.igem.org/Part:BBa_K2814014">BBa_K2814014</a></td>
 +
    <td>complement of B0034, RBS on the antisense strand</td>
 +
     <td>Ribosome Binding Site</td>
 +
    <td>RBS</td>
 +
  </tr>
 +
  <tr>
 +
    <td>10</td>
 +
    <td><a href="http://parts.igem.org/Part:BBa_K2814015">BBa_K2814015</a></td>
 +
    <td>pLac(lambda) hybrid</td>
 +
    <td>Lac-Lambda Hybrid Promoter</td>
 +
    <td>Promoter</td>
 +
  </tr>
 +
  <tr>
 +
    <td>11</td>
 +
    <td><a href="http://parts.igem.org/Part:BBa_K2814017">BBa_K2814017</a></td>
 +
    <td>attP Bxb1</td>
 +
    <td>Attachment site for Bxb1 Integrase</td>
 +
    <td>DNA</td>
 +
   </tr>
 +
  <tr>
 +
    <td>12</td>
 +
    <td><a href="http://parts.igem.org/Part:BBa_K2814018">BBa_K2814018</a></td>
 +
    <td>attB Bxb1</td>
 +
    <td>Attachment site for Bxb1 Integrase</td>
 +
    <td>DNA</td>
 +
  </tr>
 +
  <tr>
 +
    <td>13</td>
 +
    <td><a href="http://parts.igem.org/Part:BBa_K2814019">BBa_K2814019</a></td>
 +
    <td>P7 Promoter</td>
 +
    <td>Constitutive P7 promoter</td>
 +
    <td>Promoter</td>
 +
  </tr>
 +
  <tr>
 +
    <td>14</td>
 +
    <td><a href="http://parts.igem.org/Part:BBa_K2814021">BBa_K2814021</a></td>
 +
    <td>BxbI-Xis + ssrA(LVA) deg tag</td>
 +
    <td>CDS for Recombinase Directionality Factor for Integrase Bxb1</td>
 +
    <td>Coding Sequence</td>
 +
  </tr>
 +
  <tr>
 +
    <td>15</td>
 +
    <td><a href="http://parts.igem.org/Part:BBa_K2814022">BBa_K2814022</a></td>
 +
    <td>attB BxbI (reverse orientation)</td>
 +
     <td>Attachment site for Bxb1 Integrase (Reverse)</td>
 +
    <td>DNA</td>
 +
  </tr>
 +
  <tr>
 +
     <td>16</td>
 +
    <td><a href="http://parts.igem.org/Part:BBa_K2814025">BBa_K2814025</a></td>
 +
    <td>TP901-1 Integrase</td>
 +
    <td>CDS for Integrase TP901-1</td>
 +
    <td>Coding Sequence</td>
 +
  </tr>
 +
</table> 
 
</div>
 
</div>
  
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<div class="bgimg-2">
 
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  <div class="caption">
 
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    <span class="border" >Text anyone?</span>
 
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</div>
 
  
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<div style="position:relative;">
 
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<p style="font-size: 30px; font-family: 'Roboto', sans-serif;font-weight:700;">BBa_K2814007 = sfGFP_ssrA
 
  
  
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     <br>
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     <div style="background-color: white">
−
      </p>
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         <div  style="background-color: #555;color:black;font-size: 35px;text-align: center;font-family: sans-serif;"><h4 style="color: white">Contact us</h4></div>
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      <p style="font-size:20px;font-family: 'Lato', sans-serif;font-weight:400;">Our part consists of sfGFP appended with a ssrA(LVA) deg-tag. It has been codon optimised for E. coli.  This part is useful as it has high intensity as compared to other gfp variants as well as faster degradation rates and shorter reporter lifetimes.
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             <div style="text-align: center;margin-bottom: -136px;"><h4 style="color:black;font-size: 50px;"><u class="fx" style="cursor: pointer;text-align: center">Address</u></h4><p style="text-align: center;margin-bottom: 16px">Undergraduate Laboratory<br>
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</p>
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<p style="font-size:20px;font-family: 'Lato', sans-serif;font-weight:400;">Superfolder GFP is a basic (constitutively fluorescent) green fluorescent protein derived from Aequorea victoria. It has an emission wavelength of 510 nm and excitation wavelength of 485nm. It has a robust folding characteristic. The superfolder mutations also make the folding of GFP tolerant of mutations that would otherwise reduce the folding yield of GFP.
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</p>
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<p style="font-size:20px;font-family: 'Lato', sans-serif;font-weight:400;">Our ssrA degtag is the gfp(LVA) that has a single (A → G) point mutation in nucleotide 349, resulting in an Asp117 → Gly117 (D117G) amino acid change. This point mutation does not appear to change the fluorescence spectrum of gfp(LVA). The LVA tag has been reported to lead to fast protein degradation, degrading GFP with rate -0.018 per minute. This corresponds to in vivo half-lives of mature Gfp(LVA) of approximately 40 min.
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</p>
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<p style="font-size:20px;font-family: 'Lato', sans-serif;font-weight:400;">References</p>
+
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<ol style="font-size: 20px;">
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−
<li style="font-family: 'Lato', sans-serif;font-weight:400;">Pédelacq JD, Cabantous S, Tran T, Terwilliger TC, Waldo GS. Engineering and characterization of a superfolder green fluorescent protein. Nature biotechnology. 2006 Jan;24(1):79.</li>
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+
−
<li style="font-family: 'Lato', sans-serif;font-weight:400;">Andersen, J. B. et al. New unstable variants of green fluorescent protein for studies of transient gene expression in bacteria. Appl. Environ. Microbiol. 64, 2240–6 (1998).
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</li>
+
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+
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+
−
  </ol>
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−
<br>
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−
 
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<p style="font-size: 30px; font-family: 'Roboto', sans-serif;font-weight:700;">BBa_K2814011 = attP TP901-1
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−
 
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    <br>
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      </p>
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      <p style="font-size:20px;font-family: 'Lato', sans-serif;font-weight:400;">AttP TP901-1 - It is the AttP site of TP901-1 integrase (serine based recombinase enzyme). TP901-1 integrase is an enzyme that has been isolated from TP901-1 phage. It is responsible for catalysing site-specific recombination at AttP and AttB sites. The recombination mechanism depends on the orientation of the AttP and AttB sites. These enzymes help the virus integrate its DNA into the bacterial genome. TP901-1 is widely used in the construction of logic gates and modification of DNA sequences.
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</p>
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<br>
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<p style="font-size: 30px; font-family: 'Roboto', sans-serif;font-weight:700;">BBa_K2814012 = BxbI Integrase + ssrA(LVA) deg tag
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+
−
 
+
−
    <br>
+
−
      </p>
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−
      <p style="font-size:20px;font-family: 'Lato', sans-serif;font-weight:400;">BxbI Integrase triggers attP × attB recombination. The product of attP × attB recombination is an integrated prophage flanked by two new recombination sites, attL and attR, each containing half sites derived from attP and attB. In the absence of accessory factors the integrases mediate unidirectional recombination between attP and attB with greater than 80% efficiency. In the presence of a phage-encoded accessory protein, the recombination directionality factor (RDF) the attP × attB recombination is inhibited and the attL × attR recombination is stimulated.
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−
Bxb1 integrase yields approximately two-fold more recombinants  and displays about two fold less damage to the recombination sites than other phage-encoded serine integrases.
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Our BxbI Integrase has a ssrA deg tag attached to it for faster degradation rates.
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</p>
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<br>
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<p style="font-size: 30px; font-family: 'Roboto', sans-serif;font-weight:700;">BBa_K2814013 = attB TP901-1
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    <br>
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      </p>
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      <p style="font-size:20px;font-family: 'Lato', sans-serif;font-weight:400;">AttB TP901-1 -  It is the AttB site of TP901-1 integrase (serine based recombinase enzyme). TP901-1 integrase is an enzyme that has been isolated from TP901-1 phage. It is responsible for catalysing site-specific recombination at AttP and AttB sites. The recombination mechanism depends on the orientation of the AttP and AttB sites. These enzymes help the virus integrate its DNA into the bacterial genome. TP901-1 is widely used in the construction of logic gates and changing DNA sequence.
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<p style="font-size: 30px; font-family: 'Roboto', sans-serif;font-weight:700;">BBa_K2814014 = complement of B0034, RBS on the antisense strand, twin exists
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      <p style="font-size:20px;font-family: 'Lato', sans-serif;font-weight:400;">pLac - Lambda hybrid - is a hybrid promoter consisting of Lac and Lambda operator sites in the core region. This hybrid promoter can be induced in the presence of  IPTG or
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<p style="font-size: 30px; font-family: 'Roboto', sans-serif;font-weight:700;">BBa_K2814017 = attP Bxb1
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      <p style="font-size:20px;font-family: 'Lato', sans-serif;font-weight:400;">AttP Bxb1 - It is the AttP site of Bxb1 integrase (Serine based recombinase). Bxb1 integrase carries out site-specific recombination by catalysing unidirectional recombination to produce AttL and AttR sites from AttP and AttB. This switching capacity allows them to be used in the design of toggle switches.
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      <p style="font-size:20px;font-family: 'Lato', sans-serif;font-weight:400;">AttB Bxb1 - It is the AttB site of Bxb1 integrase (Serine based recombinase). Bxb1 integrase carries out site-specific recombination by catalysing unidirectional recombination to produce AttL and AttR sites from AttP and AttB. This switching capacity allows them to be used in the design of logic gates.
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<p style="font-size: 30px; font-family: 'Roboto', sans-serif;font-weight:700;">BBa_K2814021 = BxbI-Xis  + ssrA(LVA) deg tag------------
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      <p style="font-size:20px;font-family: 'Lato', sans-serif;font-weight:400;">AttB-BxbI (Reverse Orientation) - Contains AttB site of Bxb1 integrase in the reverse orientation (Reverse of  BBa_K2814018). Bxb1 integrase carries out site-specific recombination by catalysing unidirectional recombination to produce AttL and AttR sites from AttP and AttB. This switching capacity allows them to be used in the design of logic gates.
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         <div  style="background-color: #555;font-size: 35px;text-align: center;font-family: sans-serif;"><h4 style="color: white">Contact us</h4></div>
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             <div style="text-align: center;margin-bottom: -136px;"><h4 style="font-size: 50px;"><u class="fx" style="cursor: pointer;text-align: center">Address</u></h4><p style="text-align: center;margin-bottom: 16px">Undergraduate Laboratory<br>
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Department of Biotechnology and Biochemical Engineering, IIT Delhi</p>  
 
Department of Biotechnology and Biochemical Engineering, IIT Delhi</p>  
 
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Latest revision as of 23:40, 17 October 2018

iGEM IIT Delhi

Notebook
Lab Records Medal Criteria
Team
Members Attributions
Collaboration
Human Practices
Human Practices Safety Public Engagement
Modelling
Parts
Basic Parts Composite Parts
Results
Demonstrate Interlab
Project
Overview Design
S. No Part Name BioBrick Description Part Type
1 BBa_K2814001 pLTL Lac-Tet-Lac Hybrid Promoter Promoter
2 BBa_K2814007 sfGFP_ssrA Reporter gene (codon-optimised for E. coli) Coding Sequence
3 BBa_K2814008 rrnB T1 Terminator + T7Te Terminator Double Transcriptional Terminator Terminator
4 BBa_K2814009 mKate2 Reporter gene (codon-optimised for E. coli) Coding Sequence
5 BBa_K2814010 rrnB T1 Terminator Transcriptional Terminator Terminator
6 BBa_K2814011 attP TP901-1 Attachment site for TP901-1 Integrase DNA
7 BBa_K2814012 BxbI Integrase + ssrA(LVA) deg tag CDS for Integrase Bxb1 Coding Sequence
8 BBa_K2814013 attB TP901-1 Attachment site for TP901-1 Integrase DNA
9 BBa_K2814014 complement of B0034, RBS on the antisense strand Ribosome Binding Site RBS
10 BBa_K2814015 pLac(lambda) hybrid Lac-Lambda Hybrid Promoter Promoter
11 BBa_K2814017 attP Bxb1 Attachment site for Bxb1 Integrase DNA
12 BBa_K2814018 attB Bxb1 Attachment site for Bxb1 Integrase DNA
13 BBa_K2814019 P7 Promoter Constitutive P7 promoter Promoter
14 BBa_K2814021 BxbI-Xis + ssrA(LVA) deg tag CDS for Recombinase Directionality Factor for Integrase Bxb1 Coding Sequence
15 BBa_K2814022 attB BxbI (reverse orientation) Attachment site for Bxb1 Integrase (Reverse) DNA
16 BBa_K2814025 TP901-1 Integrase CDS for Integrase TP901-1 Coding Sequence

Contact us

Address

Undergraduate Laboratory
Department of Biotechnology and Biochemical Engineering, IIT Delhi