Difference between revisions of "Team:TCU Taiwan/Composite Part"

 
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     <div id="about">
 
     <div id="about">
 
       <h2 class="title">Parts table</h2>
 
       <h2 class="title">Parts table</h2>
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      <table width="100%" height="50%" border="1">
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        <tr>
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<td>Favorite</td>
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          <th height="34" scope="30">Name</th>
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          <td>Type</td>
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          <td>Description </td>
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          <td>Legth</td>
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        </tr>
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        <tr>
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          <th height="23" scope="30">&hearts;</th>
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          <td><a  href="http://parts.igem.org/Part:BBa_K1727000">BBa_K1727000</a></td>
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          <td>Coding</td>
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          <td><a title="Signiferin is a kind of antimicrobial peptide (AMPs) and it is a stable peptides that have extensive abilities to kill or inhibit the growth of bacteria. Signiferin has demonstrated effectiveness in killing Methicillin-Resistant Staphylococcus aureus (MRSA), and has been proven by the TU-Delft 2013 iGEM team. In order to have more efficient to get Signiferin, we treated signal peptide from S.lividans on the upstream of N-terminal of antimicrobial peptides to facilitate the peptide production." href="">Signiferin with signal peptide</a></td>
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          <td>179 bp</td>
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        </tr>
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        <tr>
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          <th height="27" scope="30">&hearts;</th>
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          <td><a  href="http://parts.igem.org/Part:BBa_K1727001">BBa_K1727001</a></td>
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          <td>Coding</td>
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          <td><a title="Epinecidin-1 is a kind of antimicrobial peptide (AMPs) and it is a stable peptides that have extensive abilities to kill or inhibit the growth of bacteria. They play a role in defense mechanism for Epinephelus coioides to against microbes. Epinecidin-1 use it's chargeability to interact with bacteria cell membrane. Than use hydrophobic region interfere the membrane structure. This leads to cell lysis and bypasses bacterial antibiotic drug-resistance mechanisms. Moreover Epinecidin-1 has ability to help wound healing and has been proven by animal studies." href="">Epinecidin-1 (<I>Epinephelus coioides</I>)</a></td>
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          <td>216 bp</td>
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        </tr>
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        <tr>
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          <th height="28" scope="30">&hearts;</th>
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          <td><a  href="http://parts.igem.org/Part:BBa_K1727002">BBa_K1727002</a></td>
 +
          <td>Coding</td>
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          <td><a title="This signal peptide is comes from the signal of chitinase C which extracted by S.lividans. This signal had been proved that can worked in E.coli and successfully secret target protein to E.coli LB culture medium. After translation process signal peptide will lead mature peptide to the secretion system of E.coli. When the pre-mature peptides go through the periplasmic space, peptidase will identified the cleavage site Ala-Gln-Ala and cut at the double Ala at the signal and mature peptide linkage site. Then separate signal peptide from mature peptide. Finally, secreting out mature peptide into the culture medium." href="">Signal peptide (<I>S.lividans</I> chitinase C)</a></td>
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          <td>93 bp</td> 
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        </tr>
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        <tr>
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          <th width="109" height="29" scope="30">&nbsp;</th>
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          <td width="119"><a  href="http://parts.igem.org/Part:BBa_K1727003">BBa_K1727003</a></td>
 +
          <td>Coding</td>
 +
          <td width="185"><a title="Epinecidin-1 is a kind of antimicrobial peptide (AMPs) and it is a stable peptides that have extensive abilities to kill or inhibit the growth of bacteria. They play a role in defense mechanism for Epinephelus coioides to against microbes. Moreover Epinecidin-1 has ability to help wound healing and has been proven by animal studies. In order to have more efficient to get Epinecidin-1, we treated signal peptide from S.lividans on the upstream of N-terminal of antimicrobial peptides to facilitate the peptide production." href="">Epinecidin-1 with signal peptide</a></td>
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          <td width="218">309 bp</td>
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        </tr>
 +
        <tr>
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          <th height="27" scope="30">&nbsp;</th>
 +
          <td><a  href="http://parts.igem.org/Part:BBa_K1727005">BBa_K1727005</a></td>
 +
          <td>Coding</td>
 +
          <td><a title="Signiferin is a kind of antimicrobial peptide (AMPs) and it is a stable peptides that have extensive abilities to kill or inhibit the growth of bacteria. They play a role in defense mechanism for Crinia signifera to against microbes. Signiferin use it's chargeability to interact with bacteria cell membrane. Than use hydrophobic region interfere the membrane structure. This leads to cell lysis and bypasses bacterial antibiotic drug-resistance mechanisms. Signiferin has demonstrated effectiveness in killing Methicillin-Resistant Staphylococcus aureus (MRSA), and has been proven by the TU-Delft 2013 iGEM team." href="">Signiferin (<I>Crinia signifera</I>)</a></td>
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          <td>275 bp</td>
 +
        </tr>
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 +
<tr>
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          <th height="30" scope="row">&nbsp;</th>
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          <td><a  href="http://parts.igem.org/Part:BBa_K1727007">BBa_K1727007</a></td>
 +
          <td>Composite</td>
 +
          <td><a title="Epinecidin-1 is a kind of antimicrobial peptide (AMPs) and it is a stable peptides that have extensive abilities to kill or inhibit the growth of bacteria. They play a role in defense mechanism for Epinephelus coioides to against microbes. Moreover Epinecidin-1 has ability to help wound healing and has been proven by animal studies. In order to have more efficient to get Epinecidin-1, we treated signal peptide from S.lividans on the upstream of N-terminal of antimicrobial peptides to facilitate the peptide production. This part is built by part:BBa_K1727003.<br>
 +
We used T5 promoter, Lac operator, RBS, terminator on pQE 60 vector. So we can use IPTG induction to get our product." href="">Promoter+<I>Lac</I>&nbsp;operator+RBS+signal&nbsp;peptide<br>+Epinecidin-1+Terminater</a></td>
 +
          <td>216 bp</td>
 +
        </tr>
 +
        <tr>
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          <th height="30" scope="row">&nbsp;</th>
 +
          <td><a  href="http://parts.igem.org/Part:BBa_K1727008">BBa_K1727008</a></td>
 +
          <td>Composite</td>
 +
          <td><a title="Signiferin is a kind of antimicrobial peptide (AMPs) and it is a stable peptides that have extensive abilities to kill or inhibit the growth of bacteria. Signiferin has demonstrated effectiveness in killing Methicillin-Resistant Staphylococcus aureus (MRSA), and has been proven by the TU-Delft 2013 iGEM team. In order to have more efficient to get Signiferin, we treated signal peptide from S.lividans on the upstream of N-terminal of antimicrobial peptides to facilitate the peptide production.<br>
 +
This part is built by part:BBa_K1727000. We used T5 promoter, Lac operator, RBS, terminator on pQE 60 vector. So we can use IPTG induction to get our product." href="">Promoter+<I>Lac</I>&nbsp;operator+RBS+Signal&nbsp;peptide<br>+Signiferin+Terminater</a></td>
 +
          <td>179 bp</td>
 +
        </tr>
 +
 +
      </table>
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 +
    </div>
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</div>
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</div>
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</div>
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</div>
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<div id="st1" class="st">
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<div class="inner">
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<div id="wrrapper">
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    <div id="about">
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      <h2 class="title">Composite parts table</h2>
 
       <table width="100%" height="50%" border="1">
 
       <table width="100%" height="50%" border="1">
 
         <tr>
 
         <tr>
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<div id="about">
 
<div id="about">
 
   
 
   
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<h1><span style="font-family:Calibri;text-align:justify;"><font size="5"><img src="https://static.igem.org/mediawiki/2015/0/06/TCU_Taiwanbba007.png" width="100%" />We used T5 promoter, Lac operator, RBS, terminator on pQE 60 vectors. So we can use IPTG induction to get our product.<br/><br/></font></span></h1>
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<h1><span style="font-family:Calibri;text-align:justify;"><font size="5"><img src="https://static.igem.org/mediawiki/2015/0/06/TCU_Taiwanbba007.png" width="70%" align="center" /></br>We used T5 promoter, Lac operator, RBS, terminator on pQE 60 vectors. So we can use IPTG induction to get our product.<br/><br/></font></span></h1>
  
 
</div>
 
</div>
 
<div id="about">
 
<div id="about">
 
 
 
 
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<h1><span style="font-family:Calibri;text-align:justify;"><font size="5"><img src="https://static.igem.org/mediawiki/2015/d/d6/TCU_Taiwanbba008.png" width="100%" />We used T5 promoter, Lac operator, RBS, terminator on pQE 60 vectors. So we can use IPTG induction to get our product.<br/><br/></font></span></h1>
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<h1><span style="font-family:Calibri;text-align:justify;"><font size="5"><img src="https://static.igem.org/mediawiki/2015/d/d6/TCU_Taiwanbba008.png" width="70%" align="center" /></br>We used T5 promoter, Lac operator, RBS, terminator on pQE 60 vectors. So we can use IPTG induction to get our product.<br/><br/></font></span></h1>
  
 
</div>
 
</div>

Latest revision as of 03:39, 19 September 2015

This year TCU_Taiwan iGEM team had built new standard biological parts for iGEM community. Click on the name of the parts for detailed information.

Composite parts table

Favorite Name Type Description Legth
  BBa_K1727007 Composite Promoter+Lac operator+RBS+signal peptide
+Epinecidin-1+Terminater		 216 bp
  BBa_K1727008 Composite Promoter+Lac operator+RBS+Signal peptide
+Signiferin+Terminater		 179 bp


We used T5 promoter, Lac operator, RBS, terminator on pQE 60 vectors. So we can use IPTG induction to get our product.


We used T5 promoter, Lac operator, RBS, terminator on pQE 60 vectors. So we can use IPTG induction to get our product.



             
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Contact us
 tcutaiwan@gmail.com
No.701, Sec. 3, Zhongyang Rd. Hualien 97004, Taiwan