Difference between revisions of "Team:Pasteur Paris/Kill"

 
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         <div id="index" class="block">
 
         <div id="index" class="block">
 
             <div id="indexContent">
 
             <div id="indexContent">
                <p><a href="#Our" class="link">Our Kill-Switch</a></p>
+
              <p><a href="#Background" class="link">Background</a></p>
                 <p><a href="#Modified" class="link">Modified Cryodeath</a></p>
+
                 <p><a href="#Solution" class="link">Our Solution</a></p>
 
                 <p><a href="#Results" class="link">Results</a></p>
 
                 <p><a href="#Results" class="link">Results</a></p>
 
                 <p><a href="#References" class="link">References</a></p>
 
                 <p><a href="#References" class="link">References</a></p>
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         </div>
 
         </div>
 
         <div id="MainContent">
 
         <div id="MainContent">
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            <div class="block title"><h1 id="Background">BACKGROUND</h1></div>
 
             <div class="block full"><p><i>When we first designed our project, it soon came to our mind that we had to ensure the containment of our bacteria from the environment. The best way to do that, apart from the physical containment performed by the  <a href="https://2018.igem.org/Team:Pasteur_Paris/Membrane">porous membrane</a>, was to implement our bacterial interface with a kill-switch. </i></p></div>
 
             <div class="block full"><p><i>When we first designed our project, it soon came to our mind that we had to ensure the containment of our bacteria from the environment. The best way to do that, apart from the physical containment performed by the  <a href="https://2018.igem.org/Team:Pasteur_Paris/Membrane">porous membrane</a>, was to implement our bacterial interface with a kill-switch. </i></p></div>
 
 
             <div class="block title"><h3 style="text-align: left;">What is a kill-switch? </h3></div>
 
             <div class="block title"><h3 style="text-align: left;">What is a kill-switch? </h3></div>
 
             <div class="block full">
 
             <div class="block full">
                 <p>A kill-switch is, literally, something that tells a bacterium whether to live or die, depending on specific environmental conditions. These switches are of many kinds and have been increasingly used in recent years, with the rapid development of synthetic biology [1]. They mainly work by introducing in the bacteria gene constructs that block important genes or express toxins when exposed to a specific environmental condition. We realized an educational video destined to explain to the public audience the principle of a kill-switch.  This video can be found <a href="https://2018.igem.org/Team:Pasteur_Paris/Public_Engagement">here</a>.</p>
+
                 <p>A kill-switch is, literally, something that tells a bacterium whether to live or die, depending on specific environmental conditions. With the rapid development of synthetic biology, these switches are of many kinds and have been increasingly used in recent years <sup>[1]</sup>. They mainly work by introducing in the bacteria gene constructs that block important genes or express toxins when exposed to a specific environmental condition. We realized an educational video destined to explain to the public audience the principle of a kill-switch.  This video can be found <a href="https://2018.igem.org/Team:Pasteur_Paris/Public_Engagement">here</a>.</p>
 
             </div>
 
             </div>
 +
            <div class="block separator-mark"></div>
  
 +
            <div class="block title"><h1 id="Solution">OUR SOLUTION</h1></div>
 
             <div class="block title"><h3 style="text-align: left;" id="Our">Our kill-switch</h3></div>
 
             <div class="block title"><h3 style="text-align: left;" id="Our">Our kill-switch</h3></div>
 
             <div class="block full">
 
             <div class="block full">
                 <p>Our interface is eventually destined to “cohabit” in a human body. We want to make sure that the bacteria we create cannot develop outside of the space we put it in. Thus, our kill-switch makes sure that when the environmental conditions of the inner human body are not met, the bacteria die. </p>
+
                 <p>Our interface is eventually destined to “cohabit” in a human body. We want to make sure that the bacteria we create cannot develop outside of the space we put them in. Thus, our kill-switch makes sure that when the environmental conditions of the inner human body are not met, the bacteria die. </p>
                 <p>Reviewing the literature led us to come across a very interesting article presenting the cryodeath kill-switch, invented by Finn Stirling in 2017, which is triggered by temperatures under 37°C [2]. For obvious reasons, this kill switch sounded like a perfect fit to our application. Contacting Finn comforted us in that choice, and we had the chance to exchange a lot, not only concerning the kill switch but on our project in general. After reviewing the original sequence, we modified it so that it would become a biobrick, and we removed what was unnecessary to us, leading to the making of our biobrick <a href="https://2018.igem.org/Team:Pasteur_Paris/Composite_Part">BBa_K2616002.</a></p>
+
                 <p>Reviewing the literature led us to come across a very interesting article presenting the cryodeath kill-switch, invented by Finn Stirling in 2017, which is triggered by temperatures under 37°C <sup>[2]</sup>. For obvious reasons, this kill switch sounded like a perfect fit for our application. Contacting Finn comforted us in that choice, and we had the chance to exchange a lot, not only concerning the kill switch but on our project in general. After reviewing the original sequence, we modified it so that it would become a biobrick, and we removed what was unnecessary to us, leading to the making of our biobrick <a href="http://parts.igem.org/Part:BBa_K2616002" style="font-weight: bold ; color:#85196a;" target="__blank">BBa_K2616002.</a></p>
 
             </div>
 
             </div>
  
 
             <div class="block title"><h3 style="text-align: left;" id="Modified">The modified cryodeath kill-switch</h3></div>
 
             <div class="block title"><h3 style="text-align: left;" id="Modified">The modified cryodeath kill-switch</h3></div>
 
             <div class="block full">
 
             <div class="block full">
                 <p>The kill-switch functions by the means of the toxin/antitoxin couple CcdB/CcdA. The toxin targets and inhibits the GyrA subunit of DNA gyrase, an essential bacterial enzyme that catalyzes the super-coiling of double stranded closed circular DNA [3]. </p>
+
                 <p>The kill-switch functions by the means of the toxin/antitoxin couple CcdB/CcdA. The toxin targets and inhibits the GyrA subunit of DNA gyrase, an essential bacterial enzyme that catalyzes the super-coiling of double-stranded closed circular DNA <sup>[3]</sup>. </p>
                 <p>In the kill-switch, the transcription of CcdB and CcdA are regulated by two different promoters. CcdA is expressed by the constitutive promoter P<sub>lac</sub>, which ensures a constant low production of antitoxin [4]. On the contrary, the toxin CcdB is expressed by the promoter PcspA. This promoter was originally discovered upstream of the Cold Shock Protein A in many bacteria, as a way to cope with environmental stress [5]. This promoter ensures a very low transcription rate at 37°C, but it increases drastically below 22°C. </p>
+
                 <p>In the kill-switch, the transcription of CcdB and CcdA are regulated by two different promoters. CcdA is expressed by the constitutive promoter P<sub>lac</sub>, which ensures a constant low production of antitoxin <sup>[4]</sup>. On the contrary, the toxin CcdB is expressed by the promoter PcspA. This promoter was originally discovered upstream of the Cold Shock Protein A (CspA) in many bacteria, as a way to cope with environmental stress. Indeed, when the temperature drops below 37°C, the promoter PcspA increases the level of expression of CspA gradually <sup>[5]</sup>. This promoter ensures a very low transcription rate at 37°C, but it increases drastically below 22°C. </p>
                 <p>Overall, at 37°C, the quantity of antitoxin CcdA is high enough to cope with the leaky low level of toxin produced. However, if the bacteria happen to be in an environment at a lower temperature, the toxin promoter is not repressed anymore, the quantity of toxin becomes too important, and the bacteria is not able to grow (see figure 1). This allows us to make sure that our genetically modified organisms will not spread out in an open environment.  </p>
+
                 <p>Overall, at 37°C, the quantity of antitoxin CcdA is high enough to cope with the leaky low level of toxin produced. However, if the bacteria happen to be in an environment at a lower temperature, the toxin promoter is not repressed anymore, the quantity of toxin becomes too important, and the bacteria is not able to grow (Figure 1). This allows us to make sure that our genetically modified organisms will not spread out in an open environment.  </p>
                 <img src="https://static.igem.org/mediawiki/2018/4/4d/T--Pasteur_Paris--KillSwitchFunctioning.svg">
+
<br>
 +
                 <img src="https://static.igem.org/mediawiki/2018/f/fd/T--Pasteur_Paris--kill-switch-functioning.png">
 
                 <div class="legend"><b>Figure 1: </b>Functioning of the cryodeath kill-switch at 37°C and at 22°C.</div>
 
                 <div class="legend"><b>Figure 1: </b>Functioning of the cryodeath kill-switch at 37°C and at 22°C.</div>
 
             </div>
 
             </div>
 +
            <div class="block separator-mark"></div>
  
             <div class="block title"><h3 style="text-align: left;" id="Results">Results</h3></div>
+
             <div class="block title"><h1 id="Results">RESULTS</h1></div>
 
             <div class="block full">
 
             <div class="block full">
                <p>To test the efficiency of our kill-switch, we decided to culture BL21 pLysS  <i>E. coli</i> transformed with it at several temperatures (15°C, 20°C, 25°C and 37°C). The growth was followed by measuring the optical density at 600 nm every 30 minutes for 6 hours, followed by two additional points at 18 hours and at 72 hours. Each experiment was done in a triplicate and the standard deviations were calculated for every point. On figure 2, we show that the bacteria transformed with the kill-switch showed no measurable growth at 15°C and at 20°C during the 72 hours of the experiment, whereas the control population grew normally.</p>
+
<i><p>Achievements:<br></i>
                <p>At 25°C, the kill-switch population grew more slowly than the control for the first 18 hours, but the growth eventually started to reach normal values at 72 hours. </p>
+
<ul style="text-align: left;list-style: disc;">
                <p>Finally, at 37°C there was no difference in the growth of the kill-switch population compared to the control bacteria. </p>
+
<li>Successfully cloned the biobrick <a href="http://parts.igem.org/Part:BBa_K2616002"style="font-weight: bold ; color:#85196a;"target="_blank"> Bba_K2616002</a> coding for toxin/antitoxin (CcdB/CcdA) system in pSB1C3, creating a <b>new part</b>.</li>
                <img src="https://static.igem.org/mediawiki/2018/1/1b/T--Pasteur_Paris--kill-switch-graph-no-title.png">
+
<li>Successfully sequenced  <a href="http://parts.igem.org/Part:BBa_K2616002"style="font-weight: bold ; color:#85196a;"target="_blank"> BBa_K2616002</a> in pSB1C3 and sent it to iGEM registry.</li>
                <div class="legend"><b>Figure 2: </b>Effect of different temperatures on the growth of Cryodeath kill-switch transformed BL21 <i>E. Coli</i></div>
+
<li>Successfully observed <b>normal growth</b> of our engineered bacteria at 25°C and 37°C and <b>absence of growth</b> at 18°C and 20°C, showing the <b>efficiency of the kill switch</b>.</li>
            </div>
+
</ul><br></p>
            <div class="block separator"></div>
+
<p><i>Next steps:</i><br>
            <div class="block full">
+
<ul style="text-align: left;list-style: disc;">
                <p>To conclude, the cryodeath kill-switch is a highly efficient way to prevent bacterial growth below 22°C. In the original design by Finn Sterling, the kill-switch was introduced in the genome of <i>E. coli</i> bacteria using lambda red recombineering. We successfully managed to modify this design, clone it into a plasmid and making it a novel composite biobrick, while keeping its efficiency. </p>
+
<li>Find a system that kills bacteria when released in the environment rather than just stopping their growth.</li>
 +
</ul>
 +
</p></p>
 
             </div>
 
             </div>
 +
            <div><p style="text-align: center;"> Visit the <a href="https://2018.igem.org/Team:Pasteur_Paris/Results"style="font-weight: bold ; color:#85196a;" target="__blank">RESULTS page </a> to get more information</p></div>
 +
 +
           
  
  
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             <div class="block title"><h1 id="References">REFERENCES</h1></div>
 
             <div class="block title"><h1 id="References">REFERENCES</h1></div>
 
             <div class="block full">
 
             <div class="block full">
                 <ul style="text-align: left;">
+
                 <ul style="text-align: left;list-style: disc;">
 
                     <li style="list-style-type: decimal;">“Kill switches limit modified microbes,” Nature, vol. 528, no. 7581, pp. 166–167, Dec. 2015.<br><br></li>
 
                     <li style="list-style-type: decimal;">“Kill switches limit modified microbes,” Nature, vol. 528, no. 7581, pp. 166–167, Dec. 2015.<br><br></li>
 
                     <li style="list-style-type: decimal;">F. Stirling et al., “Rational Design of Evolutionarily Stable Microbial Kill Switches,” Mol. Cell, vol. 68, no. 4, p. 686–697.e3, Nov. 2017.<br><br></li>
 
                     <li style="list-style-type: decimal;">F. Stirling et al., “Rational Design of Evolutionarily Stable Microbial Kill Switches,” Mol. Cell, vol. 68, no. 4, p. 686–697.e3, Nov. 2017.<br><br></li>
 
                     <li style="list-style-type: decimal;">R. J. Reece and A. Maxwell, “DNA Gyrase: Structure and Function,” Crit. Rev. Biochem. Mol. Biol., vol. 26, no. 3–4, pp. 335–375, Jan. 1991.<br><br></li>
 
                     <li style="list-style-type: decimal;">R. J. Reece and A. Maxwell, “DNA Gyrase: Structure and Function,” Crit. Rev. Biochem. Mol. Biol., vol. 26, no. 3–4, pp. 335–375, Jan. 1991.<br><br></li>
                     <li style="list-style-type: decimal;">T. P. Malan and W. R. McClure, “Dual promoter control of the <i> Escherichia coli </i> lactose operon.,” Cell, vol. 39, no. 1, pp. 173–80, Nov. 1984.<br><br></li>
+
                     <li style="list-style-type: decimal;">T. P. Malan and W. R. McClure, “Dual promoter control of the <i> E. coli </i> lactose operon.,” Cell, vol. 39, no. 1, pp. 173–80, Nov. 1984.<br><br></li>
 
                     <li style="list-style-type: decimal;">R. Keto-Timonen, N. Hietala, E. Palonen, A. Hakakorpi, M. Lindström, and H. Korkeala, “Cold Shock Proteins: A Minireview with Special Emphasis on Csp-family of Enteropathogenic Yersinia,” Front. Microbiol., vol. 7, Jul. 2016.<br><br></li>
 
                     <li style="list-style-type: decimal;">R. Keto-Timonen, N. Hietala, E. Palonen, A. Hakakorpi, M. Lindström, and H. Korkeala, “Cold Shock Proteins: A Minireview with Special Emphasis on Csp-family of Enteropathogenic Yersinia,” Front. Microbiol., vol. 7, Jul. 2016.<br><br></li>
 
                                        
 
                                        

Latest revision as of 14:50, 10 November 2018

""

BACKGROUND

When we first designed our project, it soon came to our mind that we had to ensure the containment of our bacteria from the environment. The best way to do that, apart from the physical containment performed by the porous membrane, was to implement our bacterial interface with a kill-switch.

What is a kill-switch?

A kill-switch is, literally, something that tells a bacterium whether to live or die, depending on specific environmental conditions. With the rapid development of synthetic biology, these switches are of many kinds and have been increasingly used in recent years [1]. They mainly work by introducing in the bacteria gene constructs that block important genes or express toxins when exposed to a specific environmental condition. We realized an educational video destined to explain to the public audience the principle of a kill-switch. This video can be found here.

OUR SOLUTION

Our kill-switch

Our interface is eventually destined to “cohabit” in a human body. We want to make sure that the bacteria we create cannot develop outside of the space we put them in. Thus, our kill-switch makes sure that when the environmental conditions of the inner human body are not met, the bacteria die.

Reviewing the literature led us to come across a very interesting article presenting the cryodeath kill-switch, invented by Finn Stirling in 2017, which is triggered by temperatures under 37°C [2]. For obvious reasons, this kill switch sounded like a perfect fit for our application. Contacting Finn comforted us in that choice, and we had the chance to exchange a lot, not only concerning the kill switch but on our project in general. After reviewing the original sequence, we modified it so that it would become a biobrick, and we removed what was unnecessary to us, leading to the making of our biobrick BBa_K2616002.

The modified cryodeath kill-switch

The kill-switch functions by the means of the toxin/antitoxin couple CcdB/CcdA. The toxin targets and inhibits the GyrA subunit of DNA gyrase, an essential bacterial enzyme that catalyzes the super-coiling of double-stranded closed circular DNA [3].

In the kill-switch, the transcription of CcdB and CcdA are regulated by two different promoters. CcdA is expressed by the constitutive promoter Plac, which ensures a constant low production of antitoxin [4]. On the contrary, the toxin CcdB is expressed by the promoter PcspA. This promoter was originally discovered upstream of the Cold Shock Protein A (CspA) in many bacteria, as a way to cope with environmental stress. Indeed, when the temperature drops below 37°C, the promoter PcspA increases the level of expression of CspA gradually [5]. This promoter ensures a very low transcription rate at 37°C, but it increases drastically below 22°C.

Overall, at 37°C, the quantity of antitoxin CcdA is high enough to cope with the leaky low level of toxin produced. However, if the bacteria happen to be in an environment at a lower temperature, the toxin promoter is not repressed anymore, the quantity of toxin becomes too important, and the bacteria is not able to grow (Figure 1). This allows us to make sure that our genetically modified organisms will not spread out in an open environment.


Figure 1: Functioning of the cryodeath kill-switch at 37°C and at 22°C.

RESULTS

Achievements:

  • Successfully cloned the biobrick Bba_K2616002 coding for toxin/antitoxin (CcdB/CcdA) system in pSB1C3, creating a new part.
  • Successfully sequenced BBa_K2616002 in pSB1C3 and sent it to iGEM registry.
  • Successfully observed normal growth of our engineered bacteria at 25°C and 37°C and absence of growth at 18°C and 20°C, showing the efficiency of the kill switch.

Next steps:

  • Find a system that kills bacteria when released in the environment rather than just stopping their growth.

Visit the RESULTS page to get more information

REFERENCES

  • “Kill switches limit modified microbes,” Nature, vol. 528, no. 7581, pp. 166–167, Dec. 2015.

  • F. Stirling et al., “Rational Design of Evolutionarily Stable Microbial Kill Switches,” Mol. Cell, vol. 68, no. 4, p. 686–697.e3, Nov. 2017.

  • R. J. Reece and A. Maxwell, “DNA Gyrase: Structure and Function,” Crit. Rev. Biochem. Mol. Biol., vol. 26, no. 3–4, pp. 335–375, Jan. 1991.

  • T. P. Malan and W. R. McClure, “Dual promoter control of the E. coli lactose operon.,” Cell, vol. 39, no. 1, pp. 173–80, Nov. 1984.

  • R. Keto-Timonen, N. Hietala, E. Palonen, A. Hakakorpi, M. Lindström, and H. Korkeala, “Cold Shock Proteins: A Minireview with Special Emphasis on Csp-family of Enteropathogenic Yersinia,” Front. Microbiol., vol. 7, Jul. 2016.