Difference between revisions of "Team:Bielefeld-CeBiTec/Organisms"

 
(13 intermediate revisions by 4 users not shown)
Line 4: Line 4:
  
 
<head>
 
<head>
 +
 +
<style>
 +
.liste2 {
 +
          list-style-position: inside;
 +
          list-style-type: none;
 +
          }
 +
</style>
 +
 
<script>
 
<script>
 
$("#notebook").addClass("navbar-active");
 
$("#notebook").addClass("navbar-active");
Line 16: Line 24:
 
<div class="jumbotron-text">
 
<div class="jumbotron-text">
 
<h1 style="margin-bottom: 0px">Organisms</h1>
 
<h1 style="margin-bottom: 0px">Organisms</h1>
<p>...</p>
+
<p>The favorite pets of a synthetic biologist</p>
 
</div>
 
</div>
 
</div>
 
</div>
  
<div>  
+
  <div class="Subtitle" id="Ecoli">
    <h2><i>Escherichia coli</i></h2>
+
          <h2><i>Escherichia coli</i></h2>
 +
  </div>
 
      
 
      
     <p> We used following strains of <i>E. coli</i> during our project:</p>
+
 
 +
<div class="row">
 +
     <div class="col-md-4">
 +
        <img src="https://static.igem.org/mediawiki/2015/d/d6/Bielefeld-CeBiTec_Ecoli.jpg" width="300px"></a>
 +
    </div>
 +
   
 +
    <div class="col-md-8">         
 +
      <p> We used the following <i>E. coli</i> strains during our project:</p>
 
     <ul>
 
     <ul>
     <li> KRX </li>
+
     <li> KRX (Source: Promega)</li>
 
         <ul>  
 
         <ul>  
 
             <li>  Genotype: [F´, traD36, ΔompP, proA+B+, lacIq, Δ(lacZ)M15] ΔompT, endA1, recA1, gyrA96 (Nalr), thi-1, hsdR17 (rk–, mk+), e14– (McrA–), relA1, supE44, Δ(lac-proAB), Δ(rhaBAD)::T7 RNA polymerase.</li>
 
             <li>  Genotype: [F´, traD36, ΔompP, proA+B+, lacIq, Δ(lacZ)M15] ΔompT, endA1, recA1, gyrA96 (Nalr), thi-1, hsdR17 (rk–, mk+), e14– (McrA–), relA1, supE44, Δ(lac-proAB), Δ(rhaBAD)::T7 RNA polymerase.</li>
 
          
 
          
 
         </ul>
 
         </ul>
     <li> ER2566 (T7 Express Competent <i>E. coli</i>) </li>
+
     <li> ER2566 (T7 Express Competent E. coli (High Efficiency), source: New England Biolabs) </li>
 
         <ul>
 
         <ul>
 
         <li> Genotype: F- λ- fhuA2 [lon] ompT lacZ::T7 gene 1 gal sulA11 Δ(mcrC-mrr)114::IS10 R(mcr-73::miniTn10-TetS)2 R(zgb-210::Tn10)(TetS) endA1 [dcm] </li>
 
         <li> Genotype: F- λ- fhuA2 [lon] ompT lacZ::T7 gene 1 gal sulA11 Δ(mcrC-mrr)114::IS10 R(mcr-73::miniTn10-TetS)2 R(zgb-210::Tn10)(TetS) endA1 [dcm] </li>
 
         </ul>
 
         </ul>
    <li> </li>
 
       
 
       
 
 
     </ul>
 
     </ul>
 +
    <p> Some other strains were used just once to investigate their performance in <i>in vitro</i> cell-free protein synthesis:</p>
 +
 
 +
        <ul>
 +
    <li> Rosetta-gami 2 (Source: Novagen, part of  Merck KGaA) </li>
 +
              <ul>
 +
       
 +
        <li> Genotype: Δ(ara-leu)7697 ΔlacX74 ΔphoA PvuII phoR araD139 ahpC galE galK rpsL F′[lac+ lacIq pro] gor522::Tn10 trxB pRARE2 (CamR, StrR, TetR)</li>
 +
        </ul>
 +
    <li> BL21 (DE3) (Source: New England Biolabs)</li>
 +
            <ul>
 +
            <li>  Genotype: fhuA2 [lon] ompT gal (λ DE3) [dcm] ∆hsdS λ DE3 = λ sBamHIo ∆EcoRI-B int::(lacI::PlacUV5::T7 gene1) i21 ∆nin5</li>
 +
            </ul>
 +
  </ul>   
 +
</div>
 
</div>
 
</div>
 +
      <div class="Subtitle">
 +
          <h2><i>Bacillus subtilis</i></h2>
 +
  </div>
 
      
 
      
     <h2> <i>Bacillus subtilis</i></h2>
+
  <div class="row">
     <p> In our project we used <i>B. subtilis</i> strain 168 with genotype <i>trpC2</i>. You can find further information about the origin of this strain in <a href="#Zeigler2008">Zeigler et al.</a></p>
+
     <div class="col-md-4">
 +
      <img src="https://static.igem.org/mediawiki/2015/1/11/Bielefeld-CeBiTec_Bacillus_subtilis.jpg" width="300px"></a>
 +
       
 +
    </div>
 +
     <div class="col-md-8">         
 +
      <p> In our project we used <i>B. subtilis</i> strain 168 with genotype <i>trpC2</i> for the GABA operon sequence. You can find further information about the origin of this strain in <a href="#Zeigler2008">Zeigler et al.</a></p>
 +
       
 +
    </div>
 +
  </div>
 +
 
 
      
 
      
 +
 +
    <div class="Subtitle">
 +
          <h2><i>Agrobacterium tumefaciens</i></h2>
 +
  </div>
 
      
 
      
    <h2> <i>Agrobacterium tumefaciens</i></h2>
+
  <div class="row">
     <p> We isolated some sequence from <i>A. tumefaciens</i> C58.1. For detailed information about this organism please be referred to <a href="#Wood2001">Wood et al. 2001</a>. </p>
+
    <div class="col-md-4">
 +
      <img src="https://static.igem.org/mediawiki/2015/e/e5/Bielefeld-CeBiTec_Agrobacterium-tumefaciens.png" width="300px"></a>
 +
       
 +
    </div>
 +
     <div class="col-md-8">         
 +
      <p> We isolated the blc-operon from <i>A. tumefaciens</i> C58.1. For detailed information about this organism please be referred to <a href="#Wood2001">Wood et al. 2001</a>. </p>
 +
       
 +
    </div>
 +
  </div>
 +
 
 +
 
 
      
 
      
 
   <h2> References </h2>
 
   <h2> References </h2>
Line 61: Line 114:
 
      
 
      
 
      
 
      
   
+
 
 
     </div>
 
     </div>
 
      
 
      

Latest revision as of 11:03, 18 September 2015

iGEM Bielefeld 2015


Organisms

The favorite pets of a synthetic biologist

Escherichia coli

We used the following E. coli strains during our project:

  • KRX (Source: Promega)
    • Genotype: [F´, traD36, ΔompP, proA+B+, lacIq, Δ(lacZ)M15] ΔompT, endA1, recA1, gyrA96 (Nalr), thi-1, hsdR17 (rk–, mk+), e14– (McrA–), relA1, supE44, Δ(lac-proAB), Δ(rhaBAD)::T7 RNA polymerase.
  • ER2566 (T7 Express Competent E. coli (High Efficiency), source: New England Biolabs)
    • Genotype: F- λ- fhuA2 [lon] ompT lacZ::T7 gene 1 gal sulA11 Δ(mcrC-mrr)114::IS10 R(mcr-73::miniTn10-TetS)2 R(zgb-210::Tn10)(TetS) endA1 [dcm]

Some other strains were used just once to investigate their performance in in vitro cell-free protein synthesis:

  • Rosetta-gami 2 (Source: Novagen, part of Merck KGaA)
    • Genotype: Δ(ara-leu)7697 ΔlacX74 ΔphoA PvuII phoR araD139 ahpC galE galK rpsL F′[lac+ lacIq pro] gor522::Tn10 trxB pRARE2 (CamR, StrR, TetR)
  • BL21 (DE3) (Source: New England Biolabs)
    • Genotype: fhuA2 [lon] ompT gal (λ DE3) [dcm] ∆hsdS λ DE3 = λ sBamHIo ∆EcoRI-B int::(lacI::PlacUV5::T7 gene1) i21 ∆nin5

Bacillus subtilis

In our project we used B. subtilis strain 168 with genotype trpC2 for the GABA operon sequence. You can find further information about the origin of this strain in Zeigler et al.

Agrobacterium tumefaciens

We isolated the blc-operon from A. tumefaciens C58.1. For detailed information about this organism please be referred to Wood et al. 2001.

References

Wood, D. W.; Setubal, J. C.; Kaul, R.; Monks, D. E.; Kitajima, J. P.; Okura, V. K. et al. (2001): The genome of the natural genetic engineer Agrobacterium tumefaciens C58. In: Science (New York, N.Y.) 294 (5550), S. 2317–2323. DOI: 10.1126/science.1066804.

Zeigler, Daniel R.; Prágai, Zoltán; Rodriguez, Sabrina; Chevreux, Bastien; Muffler, Andrea; Albert, Thomas et al. (2008): The origins of 168, W23, and other Bacillus subtilis legacy strains. In: Journal of bacteriology 190 (21), S. 6983–6995. DOI: 10.1128/JB.00722-08.