Difference between revisions of "Team:Newcastle/Design"

 
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                         Hydroponics
 
                         Hydroponics
 
                     </a>
 
                     </a>
                     <a href="#construct" class="smoothscroll btn btn--stroke">
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              Naringenin Operon
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                    </a>
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                    <a href="#operon" class="smoothscroll btn btn--stroke">
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              Improved Operon
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                    </a>
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                    <a href="#primers" class="smoothscroll btn btn--stroke">
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              Primer construction
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                    </a>
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                 </div>
 
                 </div>
  
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     </section> <!-- end s-about -->
 
     </section> <!-- end s-about -->
 
    <!-- services
 
    ================================================== -->
 
    <section id='construct' class="s-services">
 
<div class="row section-header has-bottom-sep" data-aos="fade-up">
 
            <div class="col-full">
 
                <h3 class="subhead">Naringenin Operon</h3>
 
                <h1 class="display-1">DESIGN</h1>
 
</div>
 
        </div> <!-- end section-header -->
 
 
        <div class="row about-desc" data-aos="fade-up">
 
            <div class="col-full">
 
<p class="about-para"> In order to produce the flavonoid naringenin, construction of a naringenin operon that would be synthesised from the sequence in the iGEM parts registry to gblocks by IDT was required. This operon was based on that used by the TU Darmstadt 2014 iGEM team, allowing the production of naringenin to attract nitrogen fixing bacteria. It contains the genes for four enzymes: 4 – Coumaryl ligase, Tyrosine ammonia lyase, Chalcone isomerase and Chalcone synthase. Each of these genes will contain a strong ribosome binding site. This construct will be under the control of a J23100 constitutive promoter to observe its expression in <i>Escherichia coli</i> as a proof of concept. Once biosynthesis under the control of J23100 is achieved, the construct future experiments would test this under a T7 promoter in E. coli. Parts for biosynthesis in the final chassis organism, root-colonising <i>Pseudomonas fluorescens</i>, will be constructed in the plasmid backbone pSB1C3.</p>
 
 
</div>
 
        </div> <!-- end project-desc -->
 
 
<div class="row services-list block-1-2 block-tab-full">
 
 
            <div class="col-block service-item" data-aos="fade-up">
 
                <div class="service-icon">
 
                    <i class="icon-paint-brush"></i>
 
                </div>
 
                <div class="service-text">
 
                    <img src="https://static.igem.org/mediawiki/2018/e/e8/T--Newcastle--j23100plasmid.jpeg">
 
                    <p style="text-align:center"><br> The naringenin biosynthetic operon under control of a J23100 promoter created in Benchling.</p>
 
               
 
  </div>
 
            </div>
 
 
            <div class="col-block service-item" data-aos="fade-up">
 
                <div class="service-icon">
 
                    <i class="icon-paint-brush"></i>
 
                </div>
 
                <div class="service-text">
 
                    <img src="https://static.igem.org/mediawiki/2018/d/d6/T--Newcastle--t7plasmid.jpeg">
 
                    <p style="text-align:center"><br>The naringenin biosynthetic operon under control of a T7 promoter created in Benchling.</p>
 
                   
 
                   
 
                </div>
 
            </div>
 
<div class="row services-list block-1-2 block-tab-full">
 
 
            <div class="col-block service-item" data-aos="fade-up">
 
                <div class="service-icon">
 
                    <i class="icon-paint-brush"></i>
 
                </div>
 
                <div class="service-text">
 
                    <img src="https://static.igem.org/mediawiki/2018/0/09/T--Newcastle--SBOLJ231002.jpeg">
 
                    <p style="text-align:center"><br> The naringenin biosynthetic operon construct under control of a J23100 promoter created in SBOL.</p>
 
               
 
  </div>
 
            </div>
 
  <div class="col-block service-item" data-aos="fade-up">
 
                <div class="service-icon">
 
                    <i class="icon-paint-brush"></i>
 
                </div>
 
                <div class="service-text">
 
                    <img src="https://static.igem.org/mediawiki/2018/7/7e/T--Newcastle--SBOLT72.jpeg">
 
                    <p style="text-align:center"><br>The naringenin biosynthetic operon contruct under control of a T7 promoter created in SBOL.</p>
 
                   
 
                   
 
                </div>
 
            </div>
 
 
 
        </div>        <!-- end services-list -->
 
 
    </section> <!-- end s-services --> 
 
                   
 
 
    <!-- about
 
    ================================================== -->
 
    <section id='operon' class="s-about">
 
<div class="row section-header has-bottom-sep" data-aos="fade-up">
 
            <div class="col-full">
 
                <h3 class="subhead subhead--dark">Improved Naringenin Operon based on Pathway Modelling</h3>
 
                <h1 class="display-1 display-1--light">DESIGN</h1>
 
</div>
 
        </div> <!-- end section-header -->
 
 
        <div class="row about-desc" data-aos="fade-up">
 
            <div class="col-full">
 
<p class="about-para"> Results of the modelling showed that weaker expression of the first two genes and 10 fold stronger expression of the last two genes would reduce the build-up of malonyl CoA and optimise naringenin synthesis. Therefore we found two synthetic promoters: BG28 and BG51 and an additional <i>E. coli</i> his operon terminator to be placed after the first two genes. These will allow enhanced naringenin production in future experiments, as BG28 is a weak promoter for the first two genes and BG51 is a strong promoter for the last two.</p>
 
 
</div>
 
            </div> <!-- end project-desc -->
 
 
<div class="row services-list block-1-2 block-tab-full">
 
 
            <div class="col-block service-item" data-aos="fade-up">
 
                <div class="service-icon">
 
                    <i class="icon-paint-brush"></i>
 
                    <img src="https://static.igem.org/mediawiki/2018/e/ed/T--Newcastle--BGplasmid.jpeg">
 
                </div>
 
                <div class="service-text">
 
                    <p style="text-align:center"><br>The naringenin biosynthetic operon under control of synthetic promoters BG28 and BG51 created in Benchling.</p>
 
 
</div>
 
            </div>
 
 
            <div class="col-block service-item" data-aos="fade-up">
 
                <div class="service-icon">
 
                    <i class="icon-paint-brush"></i>
 
                </div>
 
                <div class="service-text">
 
                    <img src="https://static.igem.org/mediawiki/2018/c/c8/T--Newcastle--BGcloseup.jpeg">
 
                    <p style="text-align:center"><br>A close up of the synthetic promoters BG28 and BG51 placement in the operon, created in Benchling.</p>
 
           
 
</div>
 
            </div>
 
<div class="row services-list block-1-2 block-tab-full">
 
 
            <div class="col-block service-item" data-aos="fade-up">
 
                <div class="service-icon">
 
                    <i class="icon-paint-brush"></i>
 
                </div>
 
                <div class="service-text">
 
                    <img src="https://static.igem.org/mediawiki/2018/8/85/T--Newcastle--SBOLBG28BG512.jpeg">
 
                    <p style="text-align:center"><br> The naringenin biosynthetic operon contruct under control of a BG28 and BG51 promoters and an additional his operon terminator created in SBOL.</p>
 
               
 
  </div>
 
            </div>
 
 
    <!--    </div>        end about-list -->
 
 
    </section> <!-- end s-about -->
 
   
 
<!-- services
 
    ================================================== -->
 
    <section id='primers' class="s-services">
 
<div class="row section-header has-bottom-sep" data-aos="fade-up">
 
            <div class="col-full">
 
                <h3 class="subhead">Primers</h3>
 
                <h1 class="display-1">DESIGN</h1>
 
</div>
 
        </div> <!-- end section-header -->
 
 
        <div class="row about-desc" data-aos="fade-up">
 
            <div class="col-full">
 
<p class="about-para"> Primers were designed in Benchling for amplification and detection of the 4 gblocks and the pSB1C3 backbone.</p>
 
 
<table style="width:100%">
 
  <tr>
 
    <th>Primer name</th>
 
    <th>Sequence</th>
 
    <th>Tm</th>
 
    <th>Ta Q5</th>
 
    <th>Amplified product(bp)</th>
 
    <th>Shown to work</th>
 
    <th>Description</th>
 
  </tr>
 
  <tr>
 
    <td>pSB1C3F</td>
 
    <td>tactagtagcggccgctgc</td>
 
    <td>70</td>
 
    <td>71</td>
 
    <td>2070</td>
 
    <td>6/8/18</td>
 
    <td>To amplify pSB1C3 backbone</td>
 
  </tr>
 
<tr>
 
    <td>pSB1C3R</td>
 
    <td>ctctagaagcggccgcga</td>
 
    <td>70</td>
 
    <td>71</td>
 
    <td>2070</td>
 
    <td>6/8/18</td>
 
    <td>To amplify pSB1C3 backbone</td>
 
  </tr>
 
<tr>
 
    <td>4CLF</td>
 
    <td>ccaaatcgccgccaattttc</td>
 
    <td>59</td>
 
    <td>56</td>
 
    <td>1686</td>
 
    <td>6/9/18</td>
 
    <td>To detect 4CL part</td>
 
  </tr>
 
<tr>
 
    <td>4CLR</td>
 
    <td>cgtcgtcgttttgaagtggt</td>
 
    <td>59.07</td>
 
    <td>56</td>
 
    <td>1686</td>
 
    <td>28/9/18</td>
 
    <td>To detect 4CL part</td>
 
  </tr>
 
<tr>
 
    <td>TALF</td>
 
    <td>gaatgtccgaacgctacagg</td>
 
    <td>58.72</td>
 
    <td>55</td>
 
    <td>1649</td>
 
    <td>28/9/18</td>
 
    <td>To detect TAL part</td>
 
  </tr>
 
<tr>
 
    <td>TALR</td>
 
    <td>tcggaattgagcaggtcgat</td>
 
    <td>59.18</td>
 
    <td>56</td>
 
    <td>1649</td>
 
    <td>28/9/18</td>
 
    <td>To detect TAL part</td>
 
  </tr>
 
 
</table>
 
 
</div>
 
        </div> <!-- end project-desc -->
 
  
 
     <!-- Java Script
 
     <!-- Java Script

Latest revision as of 09:19, 15 October 2018

Alternative Roots/Design

Alternative Roots

Design

Hydroponics

DESIGN

Once the project idea was finalised, the team began looking for cheap, efficient and standardised methods for growing plants in iGEM. The hope was that such an item existed that would meet these specifications as well as being a closed container to prevent contamination and also providing a high throughput of plants. It was soon established that such an item did not exist to meet our specifications. Therefore, to combat this issue, it was decided that the best way forward would be to design our own hydroponics system. This would allow us to grow large amounts of Arabidopsis in a controlled setting for the purposes of our project. Several team members were assigned to this “sub-project”.

Before getting hands-on in building the system, the team as a whole established a few design parameters. For example, the system needed to be cheap and easy to build from scratch. This is so future iGEM teams are able to construct the system for their own needs and even build upon our design, as necessary. Additionally, the system must be versatile, open-source and easily adapted for various conditions such as light intensity and wavelength. By adopting such an open and adaptable design the intention is that the end-user is able to effortlessly match the system to their needs, without getting entangled in streams of code.

Several weeks were spent modifying the design until a design was found that met all the above criteria, the specifications of the design can be seen below.

UP TO
1344
SEEDS CAN BE GROWN
IN HYDROPONICS
APPROXIMATELY
70
KWH OF POWER ANNUALLY
USED TO POWER SYSTEM
PROVIDES UP TO
1700
LUX OF LIGHT
TO GROW SEEDS
CONTAINS
120
INDIVIDUALLY ADDRESSABLE
LOW-POWER LED'S