Difference between revisions of "Team:DTU-Denmark/Description"

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                         <h1>Title<p class="lead">leader under the title, short introduction. Ubique moderatius efficiantur eum et, dico oporteat recusabo ius cu, pro id modus sadipscing. Maluisset patrioque eum ad, mel eius doctus accommodare eu, minimum deleniti repudiandae mel ea. Noster nostrud diceret sea no. Eos an nullam molestiae signiferumque, vel ne laudem ignota oblique. Duo te luptatum percipitur signiferumque, at dicunt iriure dolorem his.</p></h1>
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                         <h1>TITLE<p class="lead">leader under the title, short introduction. Ubique moderatius efficiantur eum et, dico oporteat recusabo ius cu, pro id modus sadipscing. Maluisset patrioque eum ad, mel eius doctus accommodare eu, minimum deleniti repudiandae mel ea. Noster nostrud diceret sea no. Eos an nullam molestiae signiferumque, vel ne laudem ignota oblique. Duo te luptatum percipitur signiferumque, at dicunt iriure dolorem his.</p></h1>
 
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             <p>Has ut facer debitis, quo eu agam purto. In eum justo aeterno. Sea ut atqui efficiantur, mandamus deseruisse at est, erat natum cum eu. Quot numquam in vel. Salutatus euripidis moderatius qui ex, eu tempor volumus vituperatoribus has, ius ea ullum facer corrumpit.
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            </p><p>
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             </p>
 
             </p>
 
         </div> <!-- /overview-->
 
         </div> <!-- /overview-->
       
 
 
          
 
          
 
         <div><a class="anchor" id="section-2"></a>
 
         <div><a class="anchor" id="section-2"></a>
         <h2 class="h2">Medal Requirements</h2>
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         <h2 class="h2">Project Description</h2>
           
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        <h3 class="h3">Background</h3>
            <h3 class="h3">Bronze</h3>
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            <div class="grid-row">
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                <div class="col-md-1 col-sm-1 col-xs-1">
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                    <p><p class="check">&#10003;</p> Tryout blblblblblb</p>
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                </div>
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                <div class="col-md-9 col-sm-10 col-xs-12">
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                    <p>We <a href="https://igem.org/Team.cgi?team_id=2117">registered</a> for iGEM, have a great summer, and attend the Giant Jamboree.</p>
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                </div>
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            </div> <!-- /grid-row -->
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            <div class="grid-row">
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                <div class="col-md-3 col-sm-2 col-xs-12">
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                    <p>&#10003; Register and attend</p>
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                </div>
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                <div class="col-md-9 col-sm-10 col-xs-12">
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                    <p>We <a href="https://igem.org/Team.cgi?team_id=2117">registered</a> for iGEM, have a great summer, and attend the Giant Jamboree.</p>
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                </div>
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            </div> <!-- /grid-row -->
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            <div class="grid-row">
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                <div class="col-md-3 col-sm-2 col-xs-12">
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                    <p>&#10003; Deliverables</p>
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                </div>
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                <div class="col-md-9 col-sm-10 col-xs-12">
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                    <p>Meet all deliverables on the Requirements page (section 3).</p>
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                </div>
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            </div> <!-- /grid-row -->
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            <div class="grid-row">
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                <div class="col-md-3 col-sm-2 col-xs-12">
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                    <p>&#10003; Attribution</p>
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                </div>
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                <div class="col-md-9 col-sm-10 col-xs-12">
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                    <p>Create a page on your team wiki with clear attribution of each aspect of your project. This page must clearly attribute work done by the students and distinguish it from work done by others, including host labs, advisors, instructors, sponsors, professional website designers, artists, and commercial services.</p>
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                </div>
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            </div> <!-- /grid-row -->
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            <div class="grid-row">
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                <div class="col-md-3 col-sm-2 col-xs-12">
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                    <p>&#10003; Part</p>
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                </div>
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                <div class="col-md-9 col-sm-10 col-xs-12">
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                    <p>Document at least one new standard BioBrick Part or Device central to your project and submit this part to the iGEM Registry (submissions must adhere to the iGEM Registry guidelines). You may also document a new application of a BioBrick part from a previous iGEM year, adding that documentation to the part main page.</p>
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                </div>
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            </div> <!-- /grid-row -->
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+
           
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            <h3 class="h3">Silver</h3>
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            <div class="grid-row">
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                <div class="col-md-3 col-sm-2 col-xs-12">
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                    <p>&#10003; Validated Part</p>
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                </div>
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                <div class="col-md-9 col-sm-10 col-xs-12">
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                    <p>Experimentally validate that at least one new BioBrick Part or Device of your own design and construction works as expected. Document the characterization of this part in the Main Page section of that Part’s/Device’s Registry entry. Submit this new part to the iGEM Parts Registry. This working part must be different from the part documented in bronze medal criterion #4.</p>
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                </div>
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            </div> <!-- /grid-row -->
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            <div class="grid-row">
+
                <div class="col-md-3 col-sm-2 col-xs-12">
+
                    <p>&#10003; Collaboration</p>
+
                </div>
+
                <div class="col-md-9 col-sm-10 col-xs-12">
+
                    <p>Convince the judges you have helped any registered iGEM team from high school, a different track, another university, or another institution in a significant way by, for example, mentoring a new team, characterizing a part, debugging a construct, modeling/simulating their system or helping validate a software/hardware solution to a synbio problem.</p>
+
                </div>
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            </div> <!-- /grid-row -->
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            <div class="grid-row">
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                <div class="col-md-3 col-sm-2 col-xs-12">
+
                    <p>&#10003; Human Practices</p>
+
                </div>
+
                <div class="col-md-9 col-sm-10 col-xs-12">
+
                    <p>iGEM projects involve important questions beyond the lab bench, for example relating to (but not limited to) ethics, sustainability, social justice, safety, security, and intellectual property rights. Demonstrate how your team has identified, investigated, and addressed one or more of these issues in the context of your project. Your activity could center around education, public engagement, public policy issues, public perception, or other activities (see the human practices hub for more information and examples of previous teams' exemplary work).</p>
+
                </div>
+
            </div> <!-- /grid-row -->
+
           
+
           
+
           
+
            <h3 class="h3">Gold</h3>
+
            <div class="grid-row">
+
                <div class="col-md-3 col-sm-2 col-xs-12">
+
                    <p>&#10003; Integrated Human Practices</p>
+
                </div>
+
                <div class="col-md-9 col-sm-10 col-xs-12">
+
                    <p>Expand on your silver medal activity by demonstrating how you have integrated the investigated issues into the design and/or execution of your project.</p>
+
                </div>
+
            </div> <!-- /grid-row -->
+
            <div class="grid-row">
+
                <div class="col-md-3 col-sm-2 col-xs-12">
+
                    <p>&#10003; Improve a previous part</p>
+
                </div>
+
                <div class="col-md-9 col-sm-10 col-xs-12">
+
                    <p>Improve the function OR characterization of an existing BioBrick Part or Device and enter this information in the Registry. Please see the Registry help page on how to document a contribution to an existing part. This part must NOT be from your 2016 part number range.</p>
+
                </div>
+
            </div> <!-- /grid-row -->
+
            <div class="grid-row">
+
                <div class="col-md-3 col-sm-2 col-xs-12">
+
                    <p>&#10003; Proof of concept</p>
+
                </div>
+
                <div class="col-md-9 col-sm-10 col-xs-12">
+
                    <p>Demonstrate a functional proof of concept of your project. Your proof of concept must consist of a BioBrick device; a single BioBrick part cannot constitute a proof of concept. (biological materials may not be taken outside the lab).</p>
+
                </div>
+
            </div> <!-- /grid-row -->
+
            <div class="grid-row">
+
                <div class="col-md-3 col-sm-2  col-xs-12">
+
                    <p>&#10007; Demonstrate your work</p>
+
                </div>
+
                <div class="col-md-9 col-sm-10 col-xs-12">
+
                    <p>Show your project working under real-world conditions. To achieve this criterion, you should demonstrate your whole system, or a functional proof of concept working under simulated conditions in the lab (biological materials may not be taken outside the lab).</p>
+
                </div>
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            </div> <!-- /grid-row -->
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        </div>
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        <div><a class="anchor" id="section-3"></a>
+
        <h2 class="h2">Section 3</h2>
+
 
             <p>
 
             <p>
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+
In Denmark today, less than half the waste produced is recycled,
            </p>
+
which means that more than 3.5 million tons get burned off each year.  
        </div>
+
We have abundant waste streams from the industry such as glycerol from
 
+
biodiesel production, byproducts from rapeseed production, used cooking
        <div><a class="anchor" id="section-4"></a>
+
oil and ordinary household waste.
         <h2 class="h2">Section 4</h2>
+
</p>
 +
<p>
 +
Cell factories are becoming an increasing factor in the industry today,
 +
where different microorganisms are utilized to produce various compounds
 +
from therapeutics, organic acids, food additives etc. Currently however,  
 +
the sustainability of these industrial processes is limited by the narrow
 +
substrate range of the organisms used. The most common feeds in use are
 +
simple carbohydrates such as glucose produced by enzymatic hydrolysis from
 +
edible plants such as maize, rice and wheat.
 +
</p>
 +
<p>
 +
It is widely established that the dimorphic yeast <i>Yarrowia lipolytica</i>  
 +
grows well on a broad range of substrates such as alcohols, fatty acids,
 +
glycerol as well as on simple sugars in complex mixtures, whereas the
 +
conventional and widely used yeast <i>Saccharomyces cerevisiae</i> only
 +
grows well on a very limited amount of substrates such as glucose.
 +
Furthermore, the protein modification and secretion systems of <i>Y. lipolytica</i>
 +
gives rise to a higher potential as a cell factory for production of a
 +
variety of therapeutics, food additives etc. Both of the species are fast growing,
 +
which contributes to the final efficiency as cell factories.
 +
</p>
 +
<p>
 +
Nonetheless, <i>Y. lipolytica</i> has not been applied in industry as widely
 +
as <i>S. cerevisiae</i> due to lack of tools for genetic engineering and as
 +
genetic manipulation has been tedious and time consuming.
 +
</p>
 +
         <h3 class="h3">Aim</h3>
 
             <p>
 
             <p>
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+
This project aims to develop the chassis for a versatile and efficient cell factory
 +
that can transform abundant waste streams into valuable products.
 
             </p>
 
             </p>
        </div>
 
  
        <div><a class="anchor" id="section-5"></a>
+
<h3 class="h3">Methods</h3>
        <h2 class="h2">Section 5</h2>
+
<ol>
            <p>
+
<li>Substrate screening</li>
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+
<p>
            </p>
+
To confirm the ability of <i>Y. lipolytica</i> for efficient utilization of an impure mixture of compounds, various waste streams will be investigated as a substrate. We chose mixtures of fats, present in biodiesel waste or vegetation waters from rapeseed oil production, as well as sugars, which are present in molasses or brewery waste. In order to demonstrate the versatility of  <i>Y. lipolytica</i>, we are going even further and ferment homogenized household waste.
        </div>
+
</p>
 +
 
 +
<li>Product</li>
 +
<p>
 +
As a proof of concept we aim to demonstrate the production of both an extracellular heterologous protein and an engineered metabolite, and show how a valuable product can be produced by our cell factory utilizing waste streams.
 +
We will implement a codon optimized version of the human proinsulin gene along with a native <i>Y. lipolytica</i> promoter and secretion signal into <i>Y. lipolytica</i>.
 +
Using an already constructed plasmid with <i>S. cerevisiae</i> optimized genes from the bacterium <i>Erwinia uredovora</i> encoding four enzymes, we will implement the biosynthesis pathway of beta-carotene in <i>Y. lipolytica</i> by using the <a href="http://parts.igem.org/Part:BBa_K152005"> K152005 biobrick</a>.
 +
</p>
 +
 
 +
<li>Molecular toolbox</li>
 +
<p>
 +
This project tries to solve the lack of the well-proven tools for <i>Y. lipolytica</i>. We will develop a standardized genetic toolbox, including CRISPR/Cas9-mediated genome editing. The molecular toolbox will bring new opportunities such as an introduction of new pathways, adjusting waste utilization and targeting genetic manipulations.  
 +
</p>
 +
</ol>
  
        <div><a class="anchor" id="section-6"></a>
 
        <h2 class="h2">Section 6</h2>
 
            <p>
 
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            </p>
 
 
         </div>
 
         </div>
 
+
       
         <div><a class="anchor" id="section-7"></a>
+
         <div><a class="anchor" id="section-3"></a>
         <h2 class="h2">Section 7</h2>
+
         <h2 class="h2">Reference tryout</h2>
 
             <p>
 
             <p>
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+
            Has ut facer debitis, quo eu agam purto. In eum justo aeterno. Sea ut atqui efficiantur, mandamus deseruisse at est, erat natum cum eu. Quot numquam in vel. Salutatus euripidis moderatius qui ex, eu tempor volumus vituperatoribus has, ius ea ullum facer corrumpit [<a href="#references">1,4</a>]. Has ut facer debitis, quo eu agam purto. In eum justo aeterno. Sea ut atqui efficiantur, mandamus deseruisse at est, erat natum cum eu. Quot numquam in vel. Salutatus euripidis moderatius qui ex, eu tempor volumus vituperatoribus has, ius ea ullum facer corrumpit.
 +
            </p><p>
 +
            Has ut facer debitis, quo eu agam purto. In eum justo aeterno. Sea ut atqui efficiantur, mandamus deseruisse at est, erat natum cum eu. Quot numquam in vel. Salutatus euripidis moderatius qui ex, eu tempor volumus vituperatoribus has, ius ea ullum facer corrumpit.<sup><a href="#references">2,3</a></sup> Has ut facer debitis, quo eu agam purto. In eum justo aeterno. Sea ut atqui efficiantur, mandamus deseruisse at est, erat natum cum eu. Quot numquam in vel. Salutatus euripidis moderatius qui ex, eu tempor volumus vituperatoribus has, ius ea ullum facer corrumpit.
 +
           
 +
            </p><p>
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             </p>
 
             </p>
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        </div>
 +
       
 +
        <div><a class="anchor" id="references"></a>
 +
        <h2 class="h2">References</h2>
 +
            <ol>
 +
                <li>reference 1</li>
 +
                <li>reference 2</li>
 +
            </ol>
 
         </div>
 
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             <li><a href="#section-2">Section 2</a></li>
 
             <li><a href="#section-2">Section 2</a></li>
 
             <li><a href="#section-3">Section 3</a></li>
 
             <li><a href="#section-3">Section 3</a></li>
             <li><a href="#section-4">Section 4</a></li>
+
             <li><a href="#references">References</a></li>
             <li><a href="#section-5">Section 5</a></li>
+
              
            <li><a href="#section-6">Section 6</a></li>
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            <li><a href="#section-7">Section 7</a></li>
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Project Description

Background

In Denmark today, less than half the waste produced is recycled, which means that more than 3.5 million tons get burned off each year. We have abundant waste streams from the industry such as glycerol from biodiesel production, byproducts from rapeseed production, used cooking oil and ordinary household waste.

Cell factories are becoming an increasing factor in the industry today, where different microorganisms are utilized to produce various compounds from therapeutics, organic acids, food additives etc. Currently however, the sustainability of these industrial processes is limited by the narrow substrate range of the organisms used. The most common feeds in use are simple carbohydrates such as glucose produced by enzymatic hydrolysis from edible plants such as maize, rice and wheat.

It is widely established that the dimorphic yeast Yarrowia lipolytica grows well on a broad range of substrates such as alcohols, fatty acids, glycerol as well as on simple sugars in complex mixtures, whereas the conventional and widely used yeast Saccharomyces cerevisiae only grows well on a very limited amount of substrates such as glucose. Furthermore, the protein modification and secretion systems of Y. lipolytica gives rise to a higher potential as a cell factory for production of a variety of therapeutics, food additives etc. Both of the species are fast growing, which contributes to the final efficiency as cell factories.

Nonetheless, Y. lipolytica has not been applied in industry as widely as S. cerevisiae due to lack of tools for genetic engineering and as genetic manipulation has been tedious and time consuming.

Aim

This project aims to develop the chassis for a versatile and efficient cell factory that can transform abundant waste streams into valuable products.

Methods

  1. Substrate screening
  2. To confirm the ability of Y. lipolytica for efficient utilization of an impure mixture of compounds, various waste streams will be investigated as a substrate. We chose mixtures of fats, present in biodiesel waste or vegetation waters from rapeseed oil production, as well as sugars, which are present in molasses or brewery waste. In order to demonstrate the versatility of Y. lipolytica, we are going even further and ferment homogenized household waste.

  3. Product
  4. As a proof of concept we aim to demonstrate the production of both an extracellular heterologous protein and an engineered metabolite, and show how a valuable product can be produced by our cell factory utilizing waste streams. We will implement a codon optimized version of the human proinsulin gene along with a native Y. lipolytica promoter and secretion signal into Y. lipolytica. Using an already constructed plasmid with S. cerevisiae optimized genes from the bacterium Erwinia uredovora encoding four enzymes, we will implement the biosynthesis pathway of beta-carotene in Y. lipolytica by using the K152005 biobrick.

  5. Molecular toolbox
  6. This project tries to solve the lack of the well-proven tools for Y. lipolytica. We will develop a standardized genetic toolbox, including CRISPR/Cas9-mediated genome editing. The molecular toolbox will bring new opportunities such as an introduction of new pathways, adjusting waste utilization and targeting genetic manipulations.

Reference tryout

Has ut facer debitis, quo eu agam purto. In eum justo aeterno. Sea ut atqui efficiantur, mandamus deseruisse at est, erat natum cum eu. Quot numquam in vel. Salutatus euripidis moderatius qui ex, eu tempor volumus vituperatoribus has, ius ea ullum facer corrumpit [1,4]. Has ut facer debitis, quo eu agam purto. In eum justo aeterno. Sea ut atqui efficiantur, mandamus deseruisse at est, erat natum cum eu. Quot numquam in vel. Salutatus euripidis moderatius qui ex, eu tempor volumus vituperatoribus has, ius ea ullum facer corrumpit.

Has ut facer debitis, quo eu agam purto. In eum justo aeterno. Sea ut atqui efficiantur, mandamus deseruisse at est, erat natum cum eu. Quot numquam in vel. Salutatus euripidis moderatius qui ex, eu tempor volumus vituperatoribus has, ius ea ullum facer corrumpit.2,3 Has ut facer debitis, quo eu agam purto. In eum justo aeterno. Sea ut atqui efficiantur, mandamus deseruisse at est, erat natum cum eu. Quot numquam in vel. Salutatus euripidis moderatius qui ex, eu tempor volumus vituperatoribus has, ius ea ullum facer corrumpit.

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References

  1. reference 1
  2. reference 2

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