Team:XMU-China/Project Application BlackHole

From 2014.igem.org

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     <span style="font-family: Times New Roman; font-size: 18px;">—S</span><span style="font-family: Times New Roman; font-size: 18px;">uicide by chemotaxis</span>
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     <span style="font-size: 18px;">—Suicide by chemotaxis</span>
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     <span style="font-family: Times New Roman;">T</span><span style="font-family: Times New Roman;">housands of years ago in C</span><span style="font-family: Times New Roman;">hina, people </span><span style="font-family: Times New Roman;">began to preserve food by curing them</span><span style="font-family: Times New Roman;"> which was recorded in</span><span style="font-family: Times New Roman; font-style: italic;"> Qimin Yaoshu</span><span style="font-family: Times New Roman;"> around 540 AD</span><span style="font-family: Times New Roman;"> (</span><span style="font-family: Times New Roman; font-weight: 700;">Figure 1</span><span style="font-family: Times New Roman;">)</span><span style="font-family: Times New Roman;">. Curing is any of various food preservation and flavoring processes of foods such as meat, fish and vegetables, by the addition of</span><span style="font-family: Times New Roman;"> a combination of salt, nitrate</span><span style="font-family: Times New Roman;">s</span><span style="font-family: Times New Roman;">, nitrite or sugar and it is one of the oldest m</span><span style="font-family: Times New Roman;">ethods of preserving food.</span><span style="font-family: Times New Roman; valign: sup;">[1]</span><span style="font-family: Times New Roman;"> T</span><span style="font-family: Times New Roman;">able salt is the primary ingredient used in food curing. Removal of water and addition of salt to meat creates a solute-rich environment where osmotic pressure draws water out of microorganisms, slowing down their growth. Doing this requires a concentration of salt of nearly 20%. </span><span style="font-family: Times New Roman;">It has already been proved that 5% concentration of NaCl could inhibit the growth of </span><span style="font-family: Times New Roman; font-style: italic;">E.coli</span><span style="font-family: Times New Roman;">.</span><span style="font-family: Times New Roman;"> </span><span style="font-family: Times New Roman; valign: sup;">[2]</span><span style="font-family: Times New Roman;"> However, utilizing </span><span style="font-family: Times New Roman;">hyperosmotic pressure</span><span style="font-family: Times New Roman;"> </span><span style="font-family: Times New Roman;">to kill </span>
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     Thousands of years ago in China, people began to preserve food by curing them which was recorded in <em><span style="font-family:times new roman">Qimin Yaoshu</span></em> around 540 AD (<strong>Figure 1</strong>). Curing is any of various food preservation and flavoring processes of foods such as meat, fish and vegetables, by the addition of a combination of salt, nitrates, nitrite or sugar and it is one of the oldest methods of preserving food.<sup>[1]</sup> Table salt is the primary ingredient used in food curing. Removal of water and addition of salt to meat creates a solute-rich environment where osmotic pressure draws water out of microorganisms, slowing down their growth. Doing this requires a concentration of salt of nearly 20%. It has already been proved that 5% concentration of NaCl could inhibit the growth of <em><span style="font-family:times new roman">E.coli</span></em>. <sup>[2]</sup> However, utilizing hyperosmotic pressure to kill <em><span style="font-family:times new roman">E.coli</span></em> haven’t been fully explored in synthetic biology. This year, our team have put efforts on this topic and developed a system that will contribute to biosafety.
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    <span style="font-family: Times New Roman; font-style: italic;">E.coli</span><span style="font-family: Times New Roman;"> haven’t been fully explored</span><span style="font-family: Times New Roman;"> in synthetic biology</span><span style="font-family: Times New Roman;">. T</span><span style="font-family: Times New Roman;">his year, our team have put efforts on this </span><span style="font-family: Times New Roman;">topic </span><span style="font-family: Times New Roman;">and develop</span><span style="font-family: Times New Roman;">ed</span><span style="font-family: Times New Roman;"> a system </span><span style="font-family: Times New Roman;">that</span><span style="font-family: Times New Roman;"> will contribute to biosafety.</span>
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     <span style="font-family: Times New Roman; font-weight: 700;">Circuit design</span>
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     <span style="font-weight: 700;">Circuit design</span>
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     <span style="font-family: Times New Roman; font-style: italic;">E</span><span style="font-family: Times New Roman; font-style: italic;">.c</span><span style="font-family: Times New Roman; font-style: italic;">oli</span><span style="font-family: Times New Roman;"> make</span><span style="font-family: Times New Roman;">s</span><span style="font-family: Times New Roman;"> use of the EnvZ/OmpR system to mediate signal transduction in response to environmental osmolarity changes. EnvZ, a histidine kinase, undergoes trans-autophosphorylation, then the </span><span style="font-family: Times New Roman;">high-</span><span style="font-family: Times New Roman;">energy phosphoryl group is subsequently transferred to OmpR, a response regulator</span><span style="font-family: Times New Roman;">.</span><span style="font-family: Times New Roman;"> </span><span style="font-family: Times New Roman;">In </span><span style="font-family: Times New Roman;">our</span><span style="font-family: Times New Roman;"> system, we </span><span style="font-family: Times New Roman;">involved OmpR-controlled promoter</span><span style="font-family: Times New Roman;"> (</span><span style="font-family: Times New Roman;">pOmp</span><span style="font-family: Times New Roman;">R</span><span style="font-family: Times New Roman;">)</span><span style="font-family: Times New Roman;"> in</span><span style="font-family: Times New Roman;"> (Figure 2)</span><span style="font-family: Times New Roman;">. </span><span style="font-family: Times New Roman;">The expression strength of </span><span style="font-family: Times New Roman;">pOmp</span><span style="font-family: Times New Roman;">R</span><span style="font-family: Times New Roman;"> </span><span style="font-family: Times New Roman;">depends</span><span style="font-family: Times New Roman;"> upon the medium osmolarity. </span><span style="font-family: Times New Roman;">When medium osmolarity is increasing, the EnvZ will phosphorylate more OmpR into phosphorylated OmpR (OmpR-P), </span><span style="font-family: Times New Roman;">resulting</span><span style="font-family: Times New Roman;"> in stronger expression strength of </span><span style="font-family: Times New Roman;">pO</span><span style="font-family: Times New Roman;">mpR.</span><span style="font-family: Times New Roman;"> </span><span style="font-family: Times New Roman;">In our circuitry design, </span><span style="font-family: Times New Roman; font-style: italic;">CheZ</span><span style="font-family: Times New Roman;"> is upstream regulated by </span><span style="font-family: Times New Roman;">pOmp</span><span style="font-family: Times New Roman;">R</span><span style="font-family: Times New Roman;"> (</span><span style="font-family: Times New Roman; font-weight: 700;">Figure 2</span><span style="font-family: Times New Roman;">)</span><span style="font-family: Times New Roman;">.</span>
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     <em><span style="font-family:times new roman">E.coli</span></em> makes use of the EnvZ/OmpR system to mediate signal transduction in response to environmental osmolarity changes. EnvZ, a histidine kinase, undergoes trans-autophosphorylation, then the high-energy phosphoryl group is subsequently transferred to OmpR, a response regulator. In our system, we involved OmpR-controlled promoter (pOmpR) in (<strong>Figure 2</strong>). The expression strength of pOmpR depends upon the medium osmolarity. When medium osmolarity is increasing, the EnvZ will phosphorylate more OmpR into phosphorylated OmpR (OmpR-P), resulting in stronger expression strength of pOmpR. In our circuitry design, <span style="font-family:times new roman"><em>CheZ</em></span> is upstream regulated by pOmpR (Figure 2).
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                     <img width="539" height="302" style="font-family: Times New Roman;" src="http://convert.wenku.baidu.com/rtcs/image?md5sum=d2b20345561baa81eee55b5acd0c2891.docx&l=webapp&ipr={&quot;t&quot;:&quot;img&quot;,&quot;w&quot;:&quot;539.14&quot;,&quot;h&quot;:&quot;302.09&quot;,&quot;dataType&quot;:&quot;png&quot;,&quot;c&quot;:&quot;word\/media\/image2.png&quot;}"/>
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     <span style="font-family: Times New Roman; font-weight: 700;">Characterization of circuit</span>
     <span style="font-family: Times New Roman; font-weight: 700;">Characterization of circuit</span>
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     <span style="font-family: Times New Roman;">We use semi-solid medium culture with gradient concentration of sucrose</span><span style="font-family: Times New Roman;"> to char</span><span style="font-family: Times New Roman;">acterize the device (BBa_K1412010</span><span style="font-family: Times New Roman;">)</span><span style="font-family: Times New Roman;">.</span><span style="font-family: Times New Roman;"> </span><span style="font-family: Times New Roman;">And we assume that </span><span style="font-family: Times New Roman;">the motile ability is proportional to the moving radius.</span><span style="font-family: Times New Roman;"> In t</span><span style="font-family: Times New Roman;">he plot (</span><span style="font-family: Times New Roman; font-weight: 700;">Figure 3</span><span style="font-family: Times New Roman;">), when </span><span style="font-family: Times New Roman;">no sucrose added in, the motile ability is the weakest. The motile ability keeps growing </span><span style="font-family: Times New Roman;">as </span><span style="font-family: Times New Roman;">the concentration of sucrose increase</span><span style="font-family: Times New Roman;">s </span><span style="font-family: Times New Roman;">from 0 to 4%. Then t</span><span style="font-family: Times New Roman;">he motile ability goes </span><span style="font-family: Times New Roman;">down slightly as the sucrose concentration increased from 4% to 10%, but </span><span style="font-family: Times New Roman;">the ability is</span><span style="font-family: Times New Roman;"> still stronger than that at</span><span style="font-family: Times New Roman;"> concentration 0. We can draw a </span><span style="font-family: Times New Roman;">conclusion that our device is working </span><span style="font-family: Times New Roman;">as expectation</span><span style="font-family: Times New Roman;">, the motile ability </span><span style="font-family: Times New Roman;">goes</span><span style="font-family: Times New Roman;"> down</span><span style="font-family: Times New Roman;"> (4%~10%)</span><span style="font-family: Times New Roman;"> because of the inhibition from hyperosmotic pressure.</span>
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     We use semi-solid medium culture with gradient concentration of sucrose to characterize the device (BBa_K1412010). And we assume that the motile ability is proportional to the moving radius. In the plot (<strong>Figure 3</strong>), when no sucrose added in, the motile ability is the weakest. The motile ability keeps growing as the concentration of sucrose increases from 0 to 4%. Then the motile ability goes down slightly as the sucrose concentration increased from 4% to 10%, but the ability is still stronger than that at concentration 0. We can draw a conclusion that our device is working as expectation, the motile ability goes down (4%~10%) because of the inhibition from hyperosmotic pressure.
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     <span style="font-family: Times New Roman;">Based on the characterization, we spotted hyperosmotic pressure spot and reprogrammed</span><span style="font-family: Times New Roman; font-style: italic;"> CL-1</span><span style="font-family: Times New Roman;"> spot on semi-solid medium culture as </span><span style="font-family: Times New Roman; font-weight: 700;">Figure 4 </span><span style="font-family: Times New Roman;">shows. The concentration will decrease</span><span style="font-size: 14px;"> </span><span style="font-family: Times New Roman;">w</span><span style="font-family: Times New Roman;">ith the increase of the distance away from hyperosmotic pressure spot</span><span style="font-family: Times New Roman;">. As osmotic pressure is proportional to the medium concentration. The moving tendency of reprogrammed </span><span style="font-family: Times New Roman; font-style: italic;">CL-1</span><span style="font-family: Times New Roman;"> will orient to the hyperosmotic pressure spot. Even at the inhibiting osmotic pressure, the motile ability is still stronger than that without any inducer. So </span><span style="font-family: Times New Roman;">that </span><span style="font-family: Times New Roman;">reprogrammed </span><span style="font-family: Times New Roman; font-style: italic;">CL-1 </span><span style="font-family: Times New Roman;">may even swim </span><span style="font-family: Times New Roman;">t</span><span style="font-family: Times New Roman;">owards the high-osmotic site and die</span><span style="font-family: Times New Roman;">. The killing mechanism is just like the black hole. When the bacteria move into the “event horizon” </span><span style="font-family: Times New Roman;">w</span><span style="font-family: Times New Roman;">here the osmotic pressure reaches to the critical value named the killing osmotic pressure</span><span style="font-family: Times New Roman;">, the bacteria can’t go out of the border and be killed finally.</span>
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     Based on the characterization, we spotted hyperosmotic pressure spot and reprogrammed <span style="font-family:times new roman"><em>CL-1</em></span> spot on semi-solid medium culture as <strong>Figure 4 </strong>shows. The concentration will decrease with the increase of the distance away from hyperosmotic pressure spot. As osmotic pressure is proportional to the medium concentration. The moving tendency of reprogrammed <span style="font-family:times new roman"><em>CL-1</em></span> will orient to the hyperosmotic pressure spot. Even at the inhibiting osmotic pressure, the motile ability is still stronger than that without any inducer. So that reprogrammed <span style="font-family:times new roman"><em>CL-1</em></span> may even swim towards the high-osmotic site and die. The killing mechanism is just like the black hole. When the bacteria move into the “event horizon” where the osmotic pressure reaches to the critical value named the killing osmotic pressure, the bacteria can’t go out of the border and be killed finally.
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     <span style="font-family: Times New Roman; font-size: 14px;">We </span><span style="font-family: Times New Roman; font-size: 14px;">draw a horizontal line with 10% sucrose and erect line with water, and spotted cells on the cross</span><span style="font-family: Times New Roman; font-size: 14px;"> (</span><span style="font-family: Times New Roman; font-size: 14px; font-weight: 700;">Figure </span><span style="font-family: Times New Roman; font-size: 14px; font-weight: 700;">5</span><span style="font-family: Times New Roman; font-size: 14px;">)</span><span style="font-family: Times New Roman; font-size: 14px;">. Culturing for 48 hours, we observed that reprogrammed E.coli has significant </span><span style="font-family: Times New Roman; font-size: 14px;">orientation</span><span style="font-family: Times New Roman; font-size: 14px;"> to high concentration line. As high concentration sucrose generates high </span><span style="font-family: Times New Roman; font-size: 14px;">hyperosmosis</span><span style="font-family: Times New Roman; font-size: 14px;">, it has proved that CL-1 has the tendency swimming to high </span><span style="font-family: Times New Roman; font-size: 14px;">osmotic</span><span style="font-family: Times New Roman; font-size: 14px;"> pressure.</span>
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     We draw a horizontal line with 10% sucrose and erect line with water, and spotted cells on the cross (<strong>Figure 5</strong>). Culturing for 48 hours, we observed that reprogrammed <span style="font-family:times new roman"><em>E.coli</em></span> has significant orientation to high concentration line. As high concentration sucrose generates high hyperosmosis, it has proved that <span style="font-family:times new roman"><em>CL-1</em></span> has the tendency swimming to high osmotic pressure.
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    <span style="font-family: Times New Roman;">The source</span><span style="font-family: Times New Roman;">s</span><span style="font-family: Times New Roman;"> (such as NaCl and sucrose) to create hyperosmotic pressure</span><span style="font-family: Times New Roman;"> are cheap, </span><span style="font-family: Times New Roman;">accessible</span><span style="font-family: Times New Roman;"> and </span><span style="font-family: Times New Roman;">environmentally friendly</span><span style="font-family: Times New Roman;">, </span><span style="font-family: Times New Roman;">while antibiotics is expensive and have a bad effect on environmental microbiology because of drug resistance.</span><span style="font-family: Times New Roman;"> </span><span style="font-family: Times New Roman;">If our black hole system could be fully developed, </span><span style="font-family: Times New Roman;">it will reduce the barriers to microbiology research especially for the scientists in poor countries.</span>
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The sources (such as NaCl and sucrose) to create hyperosmotic pressure are cheap, accessible and environmentally friendly, while antibiotics is expensive and have a bad effect on environmental microbiology because of drug resistance. If our black hole system could be fully developed, it will reduce the barriers to microbiology research especially for the scientists in poor countries.
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     <span style="font-family: Times New Roman; font-size: 21px; font-weight: 700;">R</span><span style="font-family: Times New Roman; font-size: 21px; font-weight: 700;">eference</span><span style="font-family: Times New Roman; font-size: 21px; font-weight: 700;">s</span>
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Revision as of 21:24, 15 October 2014

side_bar

Black hole

—Suicide by chemotaxis

 

Thousands of years ago in China, people began to preserve food by curing them which was recorded in Qimin Yaoshu around 540 AD (Figure 1). Curing is any of various food preservation and flavoring processes of foods such as meat, fish and vegetables, by the addition of a combination of salt, nitrates, nitrite or sugar and it is one of the oldest methods of preserving food.[1] Table salt is the primary ingredient used in food curing. Removal of water and addition of salt to meat creates a solute-rich environment where osmotic pressure draws water out of microorganisms, slowing down their growth. Doing this requires a concentration of salt of nearly 20%. It has already been proved that 5% concentration of NaCl could inhibit the growth of E.coli. [2] However, utilizing hyperosmotic pressure to kill E.coli haven’t been fully explored in synthetic biology. This year, our team have put efforts on this topic and developed a system that will contribute to biosafety.

 

Figure 1. The production of curing food.

 

Circuit design

E.coli makes use of the EnvZ/OmpR system to mediate signal transduction in response to environmental osmolarity changes. EnvZ, a histidine kinase, undergoes trans-autophosphorylation, then the high-energy phosphoryl group is subsequently transferred to OmpR, a response regulator. In our system, we involved OmpR-controlled promoter (pOmpR) in (Figure 2). The expression strength of pOmpR depends upon the medium osmolarity. When medium osmolarity is increasing, the EnvZ will phosphorylate more OmpR into phosphorylated OmpR (OmpR-P), resulting in stronger expression strength of pOmpR. In our circuitry design, CheZ is upstream regulated by pOmpR (Figure 2).

 

Figure 2. The schematic of osmotic-taxis design.

 

Characterization of circuit

We use semi-solid medium culture with gradient concentration of sucrose to characterize the device (BBa_K1412010). And we assume that the motile ability is proportional to the moving radius. In the plot (Figure 3), when no sucrose added in, the motile ability is the weakest. The motile ability keeps growing as the concentration of sucrose increases from 0 to 4%. Then the motile ability goes down slightly as the sucrose concentration increased from 4% to 10%, but the ability is still stronger than that at concentration 0. We can draw a conclusion that our device is working as expectation, the motile ability goes down (4%~10%) because of the inhibition from hyperosmotic pressure.

 

 

Figure 3. The plot of moving radius versus sucrose concentration. The four curves were measured after 10h, 11h, 12h and 16.5h respectively.


Based on the characterization, we spotted hyperosmotic pressure spot and reprogrammed CL-1 spot on semi-solid medium culture as Figure 4 shows. The concentration will decrease with the increase of the distance away from hyperosmotic pressure spot. As osmotic pressure is proportional to the medium concentration. The moving tendency of reprogrammed CL-1 will orient to the hyperosmotic pressure spot. Even at the inhibiting osmotic pressure, the motile ability is still stronger than that without any inducer. So that reprogrammed CL-1 may even swim towards the high-osmotic site and die. The killing mechanism is just like the black hole. When the bacteria move into the “event horizon” where the osmotic pressure reaches to the critical value named the killing osmotic pressure, the bacteria can’t go out of the border and be killed finally.

 

Figure 4. Schematic of killing bacteria by black hole.

 

We draw a horizontal line with 10% sucrose and erect line with water, and spotted cells on the cross (Figure 5). Culturing for 48 hours, we observed that reprogrammed E.coli has significant orientation to high concentration line. As high concentration sucrose generates high hyperosmosis, it has proved that CL-1 has the tendency swimming to high osmotic pressure.

Figure 5 Drawing horizontal line with 10% sucrose and erect line with water. Spotting cells on the cross. Two plates are parallel experiment.

 

Meaning

The sources (such as NaCl and sucrose) to create hyperosmotic pressure are cheap, accessible and environmentally friendly, while antibiotics is expensive and have a bad effect on environmental microbiology because of drug resistance. If our black hole system could be fully developed, it will reduce the barriers to microbiology research especially for the scientists in poor countries.

 

 

References

1. http://en.wikipedia.org/wiki/Curing_(food_preservation)

2. SUN Z, WANG J, LU M, et al. The Inhibitory Function of NaCl to a Few Common Bacteria [J][J]. Sea-Lake Salt and Chemical Industry, 2007, 1: 004.

http://en.cnki.com.cn/Article_en/CJFDTOTAL-HHYH200701004.htm