Team:CAPS Kansas/Safety

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<link rel="alternate" type="application/atom+xml" title="2014hs.igem.org Atom feed" href="/wiki/index.php?title=Special:RecentChanges&amp;feed=atom" /> <title>Team:BV CAPS Kansas Team Page Code Testing 2 - 2014hs.igem.org</title>
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    <ul>
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                    <li class='selected'        ><a href="https://2014hs.igem.org/Team:CAPS_Kansas">
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                    <li class='selected'        ><a href="https://2014hs.igem.org/Team:CAPS_Kansas">Page</a></li>
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                 <li class='new'><a href="https://2014hs.igem.org/wiki/index.php?title=Talk:Team:CAPS_Kansas/Safety&amp;action=edit&amp;redlink=1">Discussion</a></li>
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  History</a></li>
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iGEM</b></a>
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                  <li ><a href="https://static.igem.org/mediawiki/2014hs/b/bd/CAPS_iGEM_Slideshow_2014.pdf">
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  2014</a></li>
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                  <li ><a href="https://static.igem.org/mediawiki/2014hs/6/66/IGEM_2012_Slideshow.pdf">
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  2012</a></li>
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            <li ><a href="https://2014hs.igem.org/Team:CAPS_Kansas/Gallery">
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Glycolysis Poem</a></li>
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                 <li ><a href="https://2014hs.igem.org/Team:CAPS_Kansas/Gallery">
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                 <li ><a href="https://2014hs.igem.org/Team:CAPS_Kansas/Gallery">Glycolysis Poem</a></li>
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title="Safety"><b>Safety</b></a></li>
title="Safety"><b>Safety</b></a></li>
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         <li ><a href="https://2014hs.igem.org/Team:CAPS_Kansas/Project" title="Project"><b>
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         <li ><a href="https://2014hs.igem.org/Team:CAPS_Kansas/Project" title="Project"><b>Project</b></a>
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Project</b></a>
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           <ul>
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             <li ><a href="https://2014hs.igem.org/Team:CAPS_Kansas/Project">
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             <li ><a href="https://2014hs.igem.org/Team:CAPS_Kansas/Project">Project Overview</a></li>
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Project Overview</a></li>
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             <li ><a href="https://2014hs.igem.org/Team:CAPS_Kansas/Project/Problems">Problems</a></li>
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             <li ><a href="https://2014hs.igem.org/Team:CAPS_Kansas/Project/Problems">
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             <li ><a href="https://2014hs.igem.org/Team:CAPS_Kansas/Solutions">Solutions</a></li>
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Problems</a></li>
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             <li ><a href="https://2014hs.igem.org/Team:CAPS_Kansas/Project/Notebook">Notebook</a></li>
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             <li ><a href="https://2014hs.igem.org/Team:CAPS_Kansas/Project/Methods">Methods</a></li>
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Solutions</a></li>
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             <li ><a href="https://2014hs.igem.org/Team:CAPS_Kansas/Project/Achievements">Achievements</a></li>
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             <li ><a href="https://2014hs.igem.org/Team:CAPS_Kansas/Project/Notebook">
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             <li ><a href="https://2014hs.igem.org/Team:CAPS_Kansas/Project/References">References</a></li>
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Notebook</a></li>
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             <li ><a href="https://2014hs.igem.org/Team:CAPS_Kansas/Project/Future">Future</a></li>
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Methods</a></li>
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Achievements</a></li>
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References</a></li>
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Future</a></li>
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           </ul>
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         <li ><a href="https://2014hs.igem.org/Team:CAPS_Kansas/Team" title="Team"><b>
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         <li ><a href="https://2014hs.igem.org/Team:CAPS_Kansas/Team" title="Team"><b>Team</b></a></li>
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Team</b></a></li>
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         <li ><a href="https://2014hs.igem.org/Team:CAPS_Kansas" title="Home"><b>
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         <li ><a href="https://2014hs.igem.org/Team:CAPS_Kansas" title="Home"><b>Home</b></a></li>
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Home</b></a></li>
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<h2>BV CAPS iGEM Tweets</h2>
<h2>BV CAPS iGEM Tweets</h2>
</center>
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<a class="twitter-timeline" href="https://twitter.com/CAPSiGEM" data-widget-id="342763142138454016">
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<a class="twitter-timeline" href="https://twitter.com/CAPSiGEM" data-widget-id="342763142138454016">Tweets by @CAPSiGEM</a>
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Tweets by @CAPSiGEM</a>
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<script charset="utf-8" src="http://widgets.twimg.com/j/2/widget.js"></script>
<script charset="utf-8" src="http://widgets.twimg.com/j/2/widget.js"></script>
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<h1> Safety </h1>
<h1> Safety </h1>
-
Here at CAPS, we make safety our number one priority when we plan and  
+
Here at CAPS, we make safety our number one priority when we plan and execute our experiments. Situational awareness and communication is essential for any success. When using cyanobacteria or chemicals, we always work in sterilized environment. It’s important not to contaminate our sample with ourselves or surroundings and not to contaminate us with our sample! At all times, we wear our personal protection equipment (PPE) which consists of disposable gloves, lab coats, and eye protection. We follow a safety handling protocol suggested by one of our mentors to safely and efficiently handle cyanobacteria. A mentor or qualified adult is always present to be an extra set of eyes. We know what we are going to do before we set foot in the lab.<br>  
-
execute our experiments. Situational awareness and communication is  
+
-
essential for any success. When using cyanobacteria or chemicals, we always  
+
-
work in sterilized environment. It’s important not to contaminate our sample  
+
-
with ourselves or surroundings and not to contaminate us with our sample! At  
+
-
all times, we wear our personal protection equipment (PPE) which consists of  
+
-
disposable gloves, lab coats, and eye protection. We follow a safety  
+
-
handling protocol suggested by one of our mentors to safely and efficiently  
+
-
handle cyanobacteria. A mentor or qualified adult is always present to be an  
+
-
extra set of eyes. We know what we are going to do before we set foot in the  
+
-
lab.<br>  
+
<br><b>Researcher Safety</b><br><br>
<br><b>Researcher Safety</b><br><br>
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Everyone on the team obtained laboratory <a href="https://static.igem.org/mediawiki/2014hs/1/1c/CAPS_Bioscience_Lab_Safety_Manual.pdf">
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Everyone on the team obtained laboratory <a href="https://static.igem.org/mediawiki/2014hs/1/1c/CAPS_Bioscience_Lab_Safety_Manual.pdf">safety training</a> through the Machinery of Life/Foundations of Molecular Medicine and Bioengineering CAPS Class and had experience with bacterial culture (in E.coli) and genetic transformation (inserting pGLO into E. coli) prior to beginning the project. <br><br>
-
safety training</a> through the Machinery of Life/Foundations of Molecular  
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During the work, our team took the following safety precautions<ol>
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Medicine and Bioengineering CAPS Class and had experience with bacterial  
+
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culture (in E.coli) and genetic transformation (inserting pGLO into E. coli)  
+
-
prior to beginning the project. <br><br>
+
-
During the work, our team took the following safety precautions<ol>
+
<li>Lab coats, gloves and goggles were worn at all times. </li>
<li>Lab coats, gloves and goggles were worn at all times. </li>
<li>We were supervised in both the CAPS lab and at Dr. Fenton’s lab down KU Med. </li>
<li>We were supervised in both the CAPS lab and at Dr. Fenton’s lab down KU Med. </li>
<li>All equipment (both disposable and autoclaved) was sterile. </li>
<li>All equipment (both disposable and autoclaved) was sterile. </li>
-
<li>The bench and other work surfaces were sterilized with water and bleach  
+
<li>The bench and other work surfaces were sterilized with water and bleach before and after lab work. </li>
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before and after lab work. </li>
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<li>Because cyanobacteria can pose a risk if ingested, there was no food or drink in the lab. </li>
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<li>Because cyanobacteria can pose a risk if ingested, there was no food or  
+
-
drink in the lab. </li>
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<li>There were no lit burners or other fire during lab work.  </ol><br>
<li>There were no lit burners or other fire during lab work.  </ol><br>
<b>Organism and Part Safety</b><br><br>
<b>Organism and Part Safety</b><br><br>
-
Because our project utilizes the mixotrophic cyanobacteria <i>Synechocytis  
+
Because our project utilizes the mixotrophic cyanobacteria <i>Synechocytis PCC6803</i> and E. coli (two BSL-1 organisms) safety risks may initially appear to be minimal, almost nonexistent. Neither of our organisms are pathogenic. However, upon closer examination, our project contains elements that call for considerable thought towards safety. <br><br>
-
PCC6803</i> and E. coli (two BSL-1 organisms) safety risks may initially  
+
First, we recognize that cyanobacteria are autotrophs and require little other than water and light to survive. Therefore, if we did not practice sterile technique, it would be possible for cyanobacteria to be dripped or spilled and survive. <br><br>
-
appear to be minimal, almost nonexistent. Neither of our organisms are  
+
Cyanobacteria produce enzyme-inhibiting toxin that can affect the nervous system, immune system, and liver. These toxins have killed waterfowl and marine mammals that drank from algal bloom-contaminated water. However, the worst cyantoxins, cyclic petides, alkaloids, and ketides are not produced by our chassis, <i>Synechocytis 6803</i>. <br><br>
-
pathogenic. However, upon closer examination, our project contains elements  
+
Alkanes are biologically inactive and impose a small but present risk. Many of the alkanes that are gases or liquids at room temperature (most notably, ethane, methane, propane and butane) are flammable. These gaseous alkanes are not toxic and would only pose a danger if we breathed them in such high concentrations (which would have to be twelve to sixteen percent) that we suffered from oxygen deficiency. <br><br>
-
that call for considerable thought towards safety. <br><br>
+
-
First, we recognize that cyanobacteria are autotrophs and require little  
+
-
other than water and light to survive. Therefore, if we did not practice  
+
-
sterile technique, it would be possible for cyanobacteria to be dripped or  
+
-
spilled and survive. <br><br>
+
-
Cyanobacteria produce enzyme-inhibiting toxin that can affect the nervous  
+
-
system, immune system, and liver. These toxins have killed waterfowl and  
+
-
marine mammals that drank from algal bloom-contaminated water. However, the  
+
-
worst cyantoxins, cyclic petides, alkaloids, and ketides are not produced by  
+
-
our chassis, <i>Synechocytis 6803</i>. <br><br>
+
-
Alkanes are biologically inactive and impose a small but present risk. Many  
+
-
of the alkanes that are gases or liquids at room temperature (most notably,  
+
-
ethane, methane, propane and butane) are flammable. These gaseous alkanes  
+
-
are not toxic and would only pose a danger if we breathed them in such high  
+
-
concentrations (which would have to be twelve to sixteen percent) that we  
+
-
suffered from oxygen deficiency. <br><br>
+
<b>Environmental Safety </b><br><br>
<b>Environmental Safety </b><br><br>
-
However, the main risk deals not with toxins themselves but with the  
+
However, the main risk deals not with toxins themselves but with the dangerous of cyanobacteria to the environment and the risks our altered Synechocytis PCC6803 might pose to the ecosystem. Besides the inherent risk of introducing any genetically modified organism into the world outside the laboratory, we recognize that our Synechocytis 6803, like any cyanobacteria, could become the culprit in an algal bloom. Per iGem safety suggestions, we consider the worst-case scenario.<br><br><br> <center><img src="https://static.igem.org/mediawiki/2014hs/0/0f/Hab.jpg" width="400"></center><br><br><br>
-
dangerous of cyanobacteria to the environment and the risks our altered  
+
Harmful algal blooms (HABs) are essentially proliferations (often as dense as millions of bacteria per milliliter) of cyanobacteria in salt or freshwater. The water may appear entirely green and become so turgid that animals that hunt by sight cannot see more than a centimeter or two. The cyanobacteria may consume all the oxygen in the water, leaving none for other organisms, and when they die, they sink to the bottom of the body of water, and can suffocate organisms there. Though some algal blooms can be natural (for example, those that are believed to be related to El Nino) many are the direct result of human eunutrition. Runoff from fertilizers puts high levels of phosphates and nitrogen into water, creating an ideal environment for cyanobacteria growth. <br><br>
-
Synechocytis PCC6803 might pose to the ecosystem. Besides the inherent risk  
+
If our alkane-producing cyanobacteria were to be the culprit in an algal bloom, the effects might be worse than if an unaltered cyanobacteria proliferated in the bloom. Because alkanes are a major component of gasoline and diesel, the effects might be similar to an oil spill. Furthermore, certain bacteria and archea are able to metabolize alkanes, possibly leading to an out-of-control proliferation of these organisms. <br><br>
-
of introducing any genetically modified organism into the world outside the  
+
-
laboratory, we recognize that our Synechocytis 6803, like any cyanobacteria,  
+
-
could become the culprit in an algal bloom. Per iGem safety suggestions, we  
+
-
consider the worst-case scenario.<br><br><br> <center><img src="https://static.igem.org/mediawiki/2014hs/0/0f/Hab.jpg" width="400"></center><br><br><br>
+
-
    Harmful algal blooms (HABs) are essentially proliferations (often as dense  
+
-
as millions of bacteria per milliliter) of cyanobacteria in salt or  
+
-
freshwater. The water may appear entirely green and become so turgid that  
+
-
animals that hunt by sight cannot see more than a centimeter or two. The  
+
-
cyanobacteria may consume all the oxygen in the water, leaving none for  
+
-
other organisms, and when they die, they sink to the bottom of the body of  
+
-
water, and can suffocate organisms there. Though some algal blooms can be  
+
-
natural (for example, those that are believed to be related to El Nino) many  
+
-
are the direct result of human eunutrition. Runoff from fertilizers puts  
+
-
high levels of phosphates and nitrogen into water, creating an ideal  
+
-
environment for cyanobacteria growth. <br><br>
+
-
If our alkane-producing cyanobacteria were to be the culprit in an algal  
+
-
bloom, the effects might be worse than if an unaltered cyanobacteria  
+
-
proliferated in the bloom. Because alkanes are a major component of gasoline  
+
-
and diesel, the effects might be similar to an oil spill. Furthermore,  
+
-
certain bacteria and archea are able to metabolize alkanes, possibly leading  
+
-
to an out-of-control proliferation of these organisms. <br><br>
+
<b>Ethical Safety</b><br><br>
<b>Ethical Safety</b><br><br>
-
We recognize that our yeast pyruvate kinase gene was isolated by Dr. Fenton  
+
We recognize that our yeast pyruvate kinase gene was isolated by Dr. Fenton and that we only get to use it per his permission. Accordingly, we have kept him informed on our work with it and the possibility of this gene becoming readily available in the Standard Registry of Biological Parts.  
-
and that we only get to use it per his permission. Accordingly, we have kept  
+
-
him informed on our work with it and the possibility of this gene becoming  
+
-
readily available in the Standard Registry of Biological Parts.  
+
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  "></li><li><a style="color:#000000 "
href="https://2014hs.igem.org/Team:CAPS_Kansas/Outreach">
href="https://2014hs.igem.org/Team:CAPS_Kansas/Outreach">
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Outreach</a> </li></ul>
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Outreach</a> </li></ul>
<li style="float:left ;margin:0 10px"><a
<li style="float:left ;margin:0 10px"><a
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Latest revision as of 01:23, 21 June 2014

Team:BV CAPS Kansas Team Page Code Testing 2 - 2014hs.igem.org

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Safety

Here at CAPS, we make safety our number one priority when we plan and execute our experiments. Situational awareness and communication is essential for any success. When using cyanobacteria or chemicals, we always work in sterilized environment. It’s important not to contaminate our sample with ourselves or surroundings and not to contaminate us with our sample! At all times, we wear our personal protection equipment (PPE) which consists of disposable gloves, lab coats, and eye protection. We follow a safety handling protocol suggested by one of our mentors to safely and efficiently handle cyanobacteria. A mentor or qualified adult is always present to be an extra set of eyes. We know what we are going to do before we set foot in the lab.

Researcher Safety

Everyone on the team obtained laboratory safety training through the Machinery of Life/Foundations of Molecular Medicine and Bioengineering CAPS Class and had experience with bacterial culture (in E.coli) and genetic transformation (inserting pGLO into E. coli) prior to beginning the project.

During the work, our team took the following safety precautions
  1. Lab coats, gloves and goggles were worn at all times.
  2. We were supervised in both the CAPS lab and at Dr. Fenton’s lab down KU Med.
  3. All equipment (both disposable and autoclaved) was sterile.
  4. The bench and other work surfaces were sterilized with water and bleach before and after lab work.
  5. Because cyanobacteria can pose a risk if ingested, there was no food or drink in the lab.
  6. There were no lit burners or other fire during lab work.

Organism and Part Safety

Because our project utilizes the mixotrophic cyanobacteria Synechocytis PCC6803 and E. coli (two BSL-1 organisms) safety risks may initially appear to be minimal, almost nonexistent. Neither of our organisms are pathogenic. However, upon closer examination, our project contains elements that call for considerable thought towards safety.

First, we recognize that cyanobacteria are autotrophs and require little other than water and light to survive. Therefore, if we did not practice sterile technique, it would be possible for cyanobacteria to be dripped or spilled and survive.

Cyanobacteria produce enzyme-inhibiting toxin that can affect the nervous system, immune system, and liver. These toxins have killed waterfowl and marine mammals that drank from algal bloom-contaminated water. However, the worst cyantoxins, cyclic petides, alkaloids, and ketides are not produced by our chassis, Synechocytis 6803.

Alkanes are biologically inactive and impose a small but present risk. Many of the alkanes that are gases or liquids at room temperature (most notably, ethane, methane, propane and butane) are flammable. These gaseous alkanes are not toxic and would only pose a danger if we breathed them in such high concentrations (which would have to be twelve to sixteen percent) that we suffered from oxygen deficiency.

Environmental Safety

However, the main risk deals not with toxins themselves but with the dangerous of cyanobacteria to the environment and the risks our altered Synechocytis PCC6803 might pose to the ecosystem. Besides the inherent risk of introducing any genetically modified organism into the world outside the laboratory, we recognize that our Synechocytis 6803, like any cyanobacteria, could become the culprit in an algal bloom. Per iGem safety suggestions, we consider the worst-case scenario.





Harmful algal blooms (HABs) are essentially proliferations (often as dense as millions of bacteria per milliliter) of cyanobacteria in salt or freshwater. The water may appear entirely green and become so turgid that animals that hunt by sight cannot see more than a centimeter or two. The cyanobacteria may consume all the oxygen in the water, leaving none for other organisms, and when they die, they sink to the bottom of the body of water, and can suffocate organisms there. Though some algal blooms can be natural (for example, those that are believed to be related to El Nino) many are the direct result of human eunutrition. Runoff from fertilizers puts high levels of phosphates and nitrogen into water, creating an ideal environment for cyanobacteria growth.

If our alkane-producing cyanobacteria were to be the culprit in an algal bloom, the effects might be worse than if an unaltered cyanobacteria proliferated in the bloom. Because alkanes are a major component of gasoline and diesel, the effects might be similar to an oil spill. Furthermore, certain bacteria and archea are able to metabolize alkanes, possibly leading to an out-of-control proliferation of these organisms.

Ethical Safety

We recognize that our yeast pyruvate kinase gene was isolated by Dr. Fenton and that we only get to use it per his permission. Accordingly, we have kept him informed on our work with it and the possibility of this gene becoming readily available in the Standard Registry of Biological Parts.

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