Difference between revisions of "Team:Uppsala/Human Practices"

 
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{{Uppsala/javascript/scroll-button}}
 
{{Uppsala/javascript/scroll-button}}
 
{{Uppsala/javascript/redirect_js}}
 
{{Uppsala/javascript/redirect_js}}
 +
{{Uppsala/buttons}}
  
 
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<html>
 
     <head>
 
     <head>
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        <style>
 
  
 +
        <style type="text/css">
  
  
         
+
  .parallax {
           
+
                /* The image used */
           
+
                background-image: url("https://static.igem.org/mediawiki/2018/5/58/T--Uppsala--HP_banner.jpg"); 
              
+
             }
       
+
 
      
+
 
.btn-group button {
+
h1#first-header {
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+
     margin-top: 0px;
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+
}
    padding: 10px 24px; /* Some padding */
+
 
    cursor: pointer; /* Pointer/hand icon */
+
 
    font-size: 26px;
+
.vidi-img{
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+
width:70%;
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 +
}
 +
 
 +
 
 +
 
 +
/* .btn-group button {
 +
  background-color: #8B1A32;
 +
  color: #f9f9f9; /* White text */
 +
  padding: 10px 24px; /* Some padding */
 +
  cursor: pointer; /* Pointer/hand icon */
 +
  font-size: 26px;
 +
  border-radius: 4px;
 
text-align: center;
 
text-align: center;
  
 
transition: all 0.5s;
 
transition: all 0.5s;
font-family: "raleway";
+
font-family: “raleway”;
  
  
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.btn-group span {
 
.btn-group span {
  cursor: pointer;
+
cursor: pointer;
  display: inline-block;
+
display: inline-block;
  position: relative;
+
position: relative;
  transition: 0.5s;
+
transition: 0.5s;
 
}
 
}
  
 
.btn-group span:after {
 
.btn-group span:after {
  content: '\00bb';
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content: \00bb’;
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+
position: absolute;
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opacity: 0;
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+
top: 0;
  right: -20px;
+
right: -20px;
  transition: 0.5s;
+
transition: 0.5s;
 
}
 
}
  
/* Have added button:hover*/
+
/* Have added button:hover */
 
.btn-group button:hover span {
 
.btn-group button:hover span {
  padding-right: 25px;
+
padding-right: 25px;
 
}
 
}
  
/* Have added button:hover*/
+
/* Have added button:hover */
 
.btn-group button:hover span:after {
 
.btn-group button:hover span:after {
  opacity: 1;
+
opacity: 1;
  right: 0;
+
right: 0; */
 
}
 
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         </style>
 
         </style>
 
     </head>
 
     </head>
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<body>                           
 +
                             
 +
<div class="svg-wrapper" id="Project_Description">
  
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    <body>
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                <li class="toclevel tocsection"><a href="#Project_Description" class="scroll"> <span id="whereYouAre"> Human Practice  </span> </a>
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              <h1>UnaG Reporter</h1>
 
  
  
  
  
                 <p>One of the biobrick parts submitted by the 2016 Uppsala team was <a href="http://parts.igem.org/wiki/index.php?title=Part:BBa_K2003011"><b>UnaG combined with a histidine tag and a flexible linker</b></a> for extraction in affinity chromatography. We decided to use this part as our reporter system when we read about it. Mammalian intestines naturally have small amounts of bilirubin in them and also have a limited amount of oxygen present [1] (which is necessary for chromoprotein maturation [2]). we thought this could be a useful reporter.  It also came with a flexible linker, which could be used to potentially connect this reporter system with another output molecule that might be usable to act as a secondary reporter to help detect our target nematodes. 
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                <h1 id="first-header"> Integrated Human Practice </h1>
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<p>When designing our project, we aimed to create something that could truly be appreciated in the field. We therefore explored the needs and concerns of the various stakeholders of our chosen problem in multiple ways. Each of these interactions has shaped our rather vague initial idea. Our idea of creating a smart bacteria for diagnostics.   </p>
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While observing this part's sequence however, we found that there was an error and no histidine tag would be expressed due to the start codon being placed after the histidine tag.  In addition, this part would also express less or no UnaG at all due to the RBS now having a significant amount of space between it and the start codon.  We decided to incorporate this biobrick part into a custom composite part by moving the start codon to its proper location and then proving that the histidine tag works by extracting and purifying the protein via affinity chromatography.  In addition, we conducted a fluorescent bilirubin test and used a plate reader to determine if our new part expressed more UnaG than the 2016 part.  </p>
 
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                <p>However extraction of this protein poses some difficulty.  UnaG, many other chromoproteins, is a membrane protein [3] and therefore needs special conditions to purify. Under "<b><i>find out more</i></b>" we will show how we successfully extracted and purified UnaG from BL21 E. coli cells expressing our custom made plasmid. 
 
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<h2> Vidilab </h2>
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<p> Vidilab (a veterinary diagnostics company) was consulted at multiple points in our project. From the very beginning, when we didn’t even have a project, to the very end of our lab period in august we talked with both management (the CEO, Bitte Ljungström) and researchers at the company (Alice Anlind, Sara Hägglund Ljungström). From these discussions, we learnt about the major issues of the field and how large the need was for a new diagnostic tool for small strongyles. In the end this was the reason why we decided to take up the fight against these parasites. </p>
  
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<p> Initially, our project focused mainly on small strongyles and <i>in vitro</i> diagnosis of the encysted larvae. From the literature we learnt that small strongyles formes cysts containing hundreds of individual worms in the intestinal tract of horses. It was these cysts that we initially planned to detect and isolate from horse tissue and co-culture them with bacteria.</p>
  
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<p> Vidilab was kind enough to provide access to horse tissue with encysted larvae. The cysts we received did not correspond with what we initially expected due to our previous research. Because of this, we decided to focus on detection of the worms rather than the cysts. But as we knew, free floating small strongyles do not put the horse into significant danger. Instead we decided only to focus on providing farmers with better information about their horses’ wellbeing. Thanks to Vidilab we also knew that the usage of anthelmintics is leading towards resistance development in the strongyle population, turning them into a threat to the equine industry and horses’ physical health. By administering more accurate treatments, the resistance development rate among the strongyles could possibly be decreased.</p>
  
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<p>During our second visit to Vidilab they also informed us about the difficulties with detecting large strongyles since all current techniques are based on egg counting in grass samples. After some consideration we outlined a strategy to battle this problem as well. First of all we wanted to investigate the need for a better preventative tool for large strongyle infections. In order to gather data we worked on a market analysis based on a survey that we spread among horse owners in Sweden. Secondly, we wanted to try and see if a similar system as we outlined for the small strongyles could work with large strongyles present in grass, hence we made an analysis of the visibility of fluorescent proteins in grass sampling. </p>
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<p style="text-align:center;"><strong>Figure 1.</strong> Some of our team members during a visit at Vidilab</p>   
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<h2> Interviews </h2>
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<h3> Horse Owners </h3>
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<p> We used every opportunity we had at our disposal to discuss our project with horse owners. From these discussions we learned about the best ways of isolating samples and about the difficulty of isolating urine from a horse. We therefore moved on to investigating detection methods in feces. These interviews also gave us the idea to start investigating on a larger scale to what extent the horse owners are aware of issues related to strongyle infections &mdash; and the idea of conducting a market analysis was born. </p>
  
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<h3> Veterinarians </h3>
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<p> We contacted different veterinarians in the beginning of the project to see what their experience with strongyles was. The overall view was that they did not know about horses becoming ill from a large amount of small strongyles, but they mostly spoke of the negative effects with large strongyles. These results pushed us to investigate more about large strongyle infections.
  
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<h2> Multinational Market Research </h2>
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<p> Before we could start with our project we first needed to look into whether there was a market for our diagnostic tool and whether we could shape the potential product to an existing niche. We were interested in the actual state of urgency of the disease along with potential concerns for the future, though as can be seen from the above mentioned communication we had been receiving some conflicting information. Some sources would state that strongyle infections are of relatively small concern &ndash; while others would see it as a large issue. To analyse this further we conducted a market analysis based on a survey that was distributed not only in Sweden but also abroad. This confirmed that the needs of the horse owners regarding large and small strongyles was consistent with Vidilabs needs, indicating that the majority of each stakeholder had the same view of the current situation. This was noticeable in the concern regarding small strongyles, contradicting some of our skeptical sources. In addition, we used the opportunity to gather data about how a GMO based diagnostic tool would be perceived among horse owners. </p>
  
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<p> Also, to advocate our stance that the amount of treatments can be optimized, we needed to know the mean amount of treatments performed on each horse per year. We received this data as part of our market analysis. Our predictive model simulating the extent of strongyle infection depending on the amount of anthelmintic treatments suggests that the current situation can indeed be optimized. Fewer treatments than the average today would decrease the risk of developing anthelmintic resistance and still keep the horses healthy. </p>
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<p> The market analysis gave us insight into the horse-owners perspective and it resulted in the objective data that we needed to draw our conclusions. We used the data from the survey to confirm our project strategy and to build our different models. </p>
  
  
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                <p>The survey was translated into 10 different languages, making it a truly international feat (see table 1). </p>
  
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  <p> <strong> Table 1. </strong> The table shows the translated versions of the survey with highest amount of answers. </p>
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            <td width="auto" align="left">Swedish</td>
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            <td> 370 </td>
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                 <p>The purpose of this experiment was to determine if fluorescent eukaryotic chromoproteins could be used as a reporter in horse manure. One of these proteins, amilGFP (green fluorescent protein) was chosen because it gave us a opportunity to work with a reporter system developed by earlier iGEM teams of Uppsala, namely those of 2011, 2012 and 2013. To test whether amilGFP was viable or not as a reporter system we decided to run some tests to see if amilGFP could be detected in horse manure, and later, to what extent using a plate reader (fluorescence spectrophotometer) with varying concentrations of amilGFP in liquid culture in horse manure.</p>
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                <p> To read the complete market analysis, click the button below. </p>
  
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<h1 id="Ethics"> Ethics </h1>
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<p>The purpose of our project was to combat the systematic overuse of anthelmintics and thus also address the growing resistance against such compounds [1]. Resistance may arise from multiple factors, like that of mass treatment, under-dosing and not varying the drugs used [2]. These factors may sound familiar, because this is not unlike how resistance against antibiotics arise in bacteria [3]. </p>
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                            <p>The resistance against anthelmintics might also be a problem for humans in the future which increases the motivation for a new diagnosis and/or treatment approach [4]. This is “good” news since the organism used in our project (namely <i>E. coli</i>) are inherent to the microbiome of humans and horses alike. We believe that a new, specific and potentially eco-friendly method of diagnosis or treatment would have a positive outcome on society as a whole. This could lower the degree of stress and potential suffering for animals that get infected as well as for their human owners.</p>
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<h1>Grass Sample Analysis</h1>
 
  
<h2>Design, Experiment & Result</h2>
 
                <p>The purpose of the grass sample analysis was to research the possibility of a future second worm buster, targeting large strongyles. Due to the life cycle of large strongyles, they need to be detected in the grass to prevent ingestion by horses. To see if GFP(<b>Figure 1</b>)/RFP(<b>Figure 2</b>) (common chromoproteins) are visible on the tops of grass using a UV lamp, we spread colonies from transformed <i>E. coli</i> expressing these proteins onto grass. The top portion of blades of grass were used due to large strongyle larvae commonly residing there, waiting to be eaten by their unsuspecting hosts. 
 
  
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Our results (<b>Figure 1</b> and <b>Figure 2</b>) were promising which broadened our potential market with the worm buster technology.</p>
 
  
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                <p> There are however some concerns in the public about <i>E. coli</i> being pathogenic or a transmitter of disease. It’s often the incidence when <i>E. coli</i> contaminated meat for consumption gets coverage in news media. It is thus a challenge when conveying a complex topic to the public which demands some scientific knowledge, especially in biology and this is something our Human Practise group has been challenged with throughout the project. The risks of using <i>E. coli</i> and its given traits for this project are discussed further throughout the text. </p>
                 
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                <h2> GMO, Welcomed by the Public </h2>
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                <p> By authoring and distributing a survey to horse owners we could see that the majority of respondents in Sweden had positive attitudes (83.2 %, 368 respondents) towards a GMO-type of diagnosis method. The survey also showed a public fear of growing anthelmintics resistance against blood worms (strongyles) (77.3% of 370 respondents ranked their fear as 4 or 5 were 5 being the most concerned). </p>
                 <p><strong>Figure 1:</strong> Grass samples that have been spread with bacteria cultures expressing GFP. </p>
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                <p> The <i>E. coli</i> (BL-21, DH5-alpha) that was used in the lab has a biosafety level of 1, which is the lowest possible on a scale of 4 [7]. This means that <i>E. coli</i> is safe to work with in the course laboratories we were provided with by Uppsala University [8]. </p>
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                <p> Nothing that is considered toxic or harmful was genetically introduced (UnaG, amilGFP) into our E.coli. However, for cultivation and selection purposes used in common synthetic biology practical work, antibiotic resistance was also introduced which presents a risk in the potential spread of antibiotic resistance (Chloramphenicol, Ampicillin, Tetracycline), if these plasmids were to spread into the environment. This was avoided to a large degree by following standard lab practise with specific guidelines regarding waste disposal of GMOs.  </p>
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                <p> The ability for proliferation of GMOs and organisms in general is determined by their fitness. As a rule of thumb regarding the spread of GMOs in the environment, fitness is greatly reduced for most lab strains of microorganisms since they have been modified in numerous ways to make them easy to work with. These are not adaptations that are suitable for their natural environment, giving them a negative fitness contribution [9]. Regarding the risks associated with nematodes, you can look at the separate  <a href="https://2018.igem.org/Safety/Final_Safety_Form">safety form</a> and select Uppsala from the menu. </p>
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                <p> This was the first time a team tried to see if this is an applicable solution to diagnose parasitic infections caused by nematodes in equines; it is thus a long way from a potentially finalized product. If a product would surface in the future, further risk assessments must be evaluated to see if an engineered product would be deemed safe to be orally ingested by a living host. Since an enteric diagnostic system based on bacteria is a novel approach there is little to be found in the literature about its applied effects.  In addition to internal reviews, it is common for an external entity (like a government) to perform reviews on the product, especially if the product is classified as a GMO. This is necessary to ensure that the product is safe before letting it hit the market.</p>
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                <h1 id="Burn"> Understanding Your Limits - a Burnout Guidebook </h1>
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                 <p>Mental health awareness is being brought into the spotlight in society, yet talking about it is still a taboo in many settings. For instance, in a project that you truly care for, the risks and warning signs might go by unrecognized. It is an art to find balance at work but in our opinion it is an essential part of success in the long run. Therefore, the Uppsala iGEM team has chosen to acknowledge the importance of understanding one’s limits by writing a guide-book on the topic.</p>
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                 <p>The premise and purpose of the guidebook is that many iGEM teams in retrospect have admitted that the work environment during the iGEM competition oftentimes becomes stressful. Factors such as level of experience, responsibilities, ambitions and deadlines drive projects forward but at the same time easily lead to feelings of being overwhelmed and an increases risk of burning out. Though we’re speaking mainly of the iGEM competition here, the topic of stress at work is universally applicable. Therefore we wanted to address this topic by creating material that anyone who seeks guidance can relate to and use. We tried to make our guidebook as universal as possible to people both inside and outside of academia.</p>
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                <p> In this little book we have compiled some general background about stress, exhaustion, and burnout in order to explain the issue and show that these topics deserve your attention. This is followed by suggestions of some preventive measures that we have found suitable. Some parts of the book might be a repetition of old truths but we try to mix it up with a mix of unique advice and mindfulness exercises. </p>
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                <p>In the guidebook you can also find some statistics about stress levels in different iGEM teams over the years. This is a preview of the iGEM work environment report that the iGEM Uppsala association is working on based on the survey described further down.</p>
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                <p> Also, check out the chapter “The Importance of Authenticity in Organization” from the guidebook written by iGEM Lund’s 2018 team.  They have also been focusing on improving the work environment, but instead of more general stress management techniques their guidebook is directed towards hands-on approaches for increasing efficiency through organization of work. </p>
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                <p> Our hope is that we will encourage people not to overlook the importance of their well-being, and to have a healthier relationship with their work. We hope to give back to the iGEM community for all the wonderful experiences that we’ve had, and we hope that future iGEM teams especially will take note of the advice in “Understanding your Limits - a Burnout Guidebook”.  iGEM is a giving platform for young brilliant people to do truly amazing things. </p>
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<p> Since brilliant people (usually) don't retire after participating in iGEM, it’s important to take care of yourselves.  The world needs you.</p>
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                <p><strong>Figure 2:</strong> Grass samples that have been spread with bacteria cultures expressing RFP. </p>
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<h2 id="References"> References </h2>
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                <p> <b>[1] </b> Salgado JA, Santos C de P, Salgado JA, Santos C de P. 2016. Overview of anthelmintic resistance of gastrointestinal nematodes of small ruminants in Brazil. Revista Brasileira de Parasitologia Veterinária 25: 3–17. <br>
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                <b>[2]</b> Shalaby HA. 2013. Anthelmintics Resistance; How to Overcome it? Iranian Journal of Parasitology 8: 18–32.<br>
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                <b>[3]</b> Grenni P, Ancona V, Barra Caracciolo A. 2018. Ecological effects of antibiotics on natural ecosystems: A review. Microchemical Journal 136: 25–39.<br>
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                <b>[4] </b>Vercruysse J, Albonico M, Behnke JM, Kotze AC, Prichard RK, McCarthy JS, Montresor A, Levecke B. 2011. Is anthelmintic resistance a concern for the control of human soil-transmitted helminths? International Journal for Parasitology: Drugs and Drug Resistance 1: 14–27.<br>
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                <b>[5] </b>Genetically Modified Organisms. WWW-document: <a href="https://www.efsa.europa.eu/en/topics/topic/genetically-modified-organisms">https://www.efsa.europa.eu/en/topics/topic/genetically-modified-organisms</a>. Retrieved 2018-10-04. <br>
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                <b>[6]</b> Papademetriou T. 2014. Restrictions on Genetically Modified Organisms: European Union | Law Library of Congress. <a href="http://www.loc.gov/law/help/restrictions-on-gmos/eu.php">http://www.loc.gov/law/help/restrictions-on-gmos/eu.php</a>. Retrieved 2018-10-04.<br>
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                <b>[7]</b> University © Stanford, Stanford, Complaints C 94305 C. Biosafety Levels for Biological Agents – Stanford Environmental Health &#38; Safety. WWW-document: <a href="https://ehs.stanford.edu/reference/biosafety-levels-biological-agents">https://ehs.stanford.edu/reference/biosafety-levels-biological-agents</a>. Retrieved 2018-10-04.<br>
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                <b>[8]</b> Wallin U. GMO - Uppsala University, Sweden. WWW-dokument: http://www.bmc.uu.se/Environment+%26+Safety/Waste/gmo/.Retrieved 2018-10-04. <br>
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                <b>[9]</b> Qiu J. 2013. Genetically modified crops pass benefits to weeds: herbicide resistance and other genetic modifications could confer an advantage on plants in the wild. Nature 500: 389–390.</p>
  
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<h1>Refereces</h1>
 
  
<p><strong>[1]</strong> Bowen R. Microbial Life in the Digestive Tract. online: http://www.vivo.colostate.edu/hbooks/pathphys/digestion/basics/gi_bugs.html. Accessed October 12, 2018.<br><br>
 
  
<strong>[2]</strong> Engineering a palette of eukaryotic chromoproteins for bacterial synthetic biology | Journal of Biological Engineering | Full Text. online: https://jbioleng.biomedcentral.com/articles/10.1186/s13036-018-0100-0. Accessed October 12, 2018. <br><br>
 
 
<strong>[3]</strong> Kumagai A, Ando R, Miyatake H, Greimel P, Kobayashi T, Hirabayashi Y, Shimogori T, Miyawaki A. 2013. A Bilirubin-Inducible Fluorescent Protein from Eel Muscle. Cell 153: 1602–1611.</p>
 
  
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Latest revision as of 15:59, 3 December 2018