Difference between revisions of "Team:Tokyo Tech/Basic Part"

 
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      <h1>Basic Parts</h1>
 
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<h2 class="smalltitle">Best Basic Part: <i>fimB</i> (wild-type) (BBa_K1632010)</h2>
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<ul>
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<li><a href="http://parts.igem.org/Part:BBa_K1632010" target="_brank">BBa_K1632010</a><br><i>fimB</i>(wild-type)</li>
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</ul>
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<p></p>
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<p></p>
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<p class="text">FimB (<a href="http://parts.igem.org/Part:BBa_K1632010" target="_brank">BBa_K1632010</a>) is a Fim recombinase.  This is derived from the wild type MG1655.  FimB invert the <i>fim</i> switch in the [ON] to [OFF] direction and in the [OFF] to [ON] direction (Fig.5-2-0-1.).</p>
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<p class="text">From our experimental results, we confirmed that the FimB protein inverts the <i>fim</i> switch(wild-type) in the [ON] to [OFF] direction and in the [OFF] to [ON] direction with approximately equal probability and works ideally (Fig.5-2-0-2.).  The expression of FimB is controlled by arabinose in PBAD/<i>araC</i>_<i>fimB</i>(wild-type) (<a href="http://parts.igem.org/Part:BBa_K1632012" target="_brank">BBa_K1632012</a>).</p>
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<table width="940px"><tbody><tr><td align="center"><img src="https://static.igem.org/mediawiki/2015/e/e2/Tokyo_Tech_3333333.png" width="60%"></td></tr><tr><td align="center"><h4 class="fig">Fig.5-2-0-1. Design of <i>fim</i> switch (wild-type)</h4></td></tr></tbody></table>
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<p></p>
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<table width="940 px" border="0px"><tr><td width="940px"><div align="center"><img src="https://static.igem.org/mediawiki/2015/1/1a/Tokyo_Tech_arabinose_fimB_result1.png" width="800px"/></td></tr><tr><td width="940px"><h4 align="center" class="fig">Fig. 5-2-0-2. The result of our experiment used <a href="http://parts.igem.org/Part:BBa_K1632007" target="_brank">BBa_K1632007</a>, <a href="http://parts.igem.org/Part:BBa_K1632008" target="_brank">BBa_K1632008</a> and <a href="http://parts.igem.org/Part:BBa_K1632012" target="_brank">BBa_K1632012</a> with flow cytometers.</h4><td></tr></table><p></p>
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<h2 class="smalltitle">0.Tokyo Tech 2015 iGEM Team: The Others Basic Parts</h2>
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<p class="text"></p>
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<table width="900px" border="2" frame="border" style="border-collapse: collapse;"><tbody><tr height="20px" align="center"><th width="20%">Name</th><th width="10%">Type</th><th width="30%">Description</th><th width="20%">Design</th><th width="10%">Length(bp)</th><th width="10%">Experiment</th></tr>
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<tr height="20px"><td width="20%"><a href="http://parts.igem.org/Part:BBa_K1632000" target="_brank">BBa_K1632000</a></td><td width="10%">Regulatory</td><td width="30%"><i>fim</i> switch[default ON](Tokyo_Tech/J23119)</td><td width="20%">Riku Shinohara</td><td width="10%">382</td><td width="10%">Work</td></tr>
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<tr height="20px"><td width="20%"><a href="http://parts.igem.org/Part:BBa_K1632001" target="_brank">BBa_K1632001</a></td><td width="10%">Regulatory</td><td width="30%"><i>fim</i> switch[default ON](Tokyo_Tech/J23119)</td><td width="20%">Riku Shinohara</td><td width="10%">382</td><td width="10%">Work</td></tr>
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<tr height="20px"><td width="20%"><a href="http://parts.igem.org/Part:BBa_K1632004" target="_brank">BBa_K1632004</a></td><td width="10%">Regulatory</td><td width="30%"><i>fim</i> switch[default OFF](wild-type)</td><td width="20%">Riku Shinohara</td><td width="10%">382</td><td width="10%">Work</td></tr>
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<tr height="20px"><td width="20%"><a href="http://parts.igem.org/Part:BBa_K1632005" target="_brank">BBa_K1632005</a></td><td width="10%">Regulatory</td><td width="30%"><i>fim</i> switch[default OFF](wild-type)</td><td width="20%">Riku Shinohara</td><td width="10%">382</td><td width="10%">Work</td></tr>
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<tr height="20px"><td width="20%"><a href="http://parts.igem.org/Part:BBa_K1632006" target="_brank">BBa_K1632006</a></td><td width="10%">Regulatory</td><td width="30%"><i>fim</i> switch[default ON](Tokyo_Tech/R0010)</td><td width="20%">Riku Shinohara</td><td width="10%">597</td><td width="10%"></td></tr>
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<tr height="20px"><td width="20%"><a href="http://parts.igem.org/Part:BBa_K1632010" target="_brank">BBa_K1632010</a></td><td width="10%">Coding</td><td width="30%"><i>fimB</i>(wild-type)</td><td width="20%">Riku Shinohara</td><td width="10%">603</td><td width="10%">Work</td></tr>
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<tr height="20px"><td width="20%"><a href="http://parts.igem.org/Part:BBa_K1632011" target="_brank">BBa_K1632011</a></td><td width="10%">Coding</td><td width="30%"><i>fimE</i>(wild-type)</td><td width="20%">Riku Shinohara</td><td width="10%">597</td><td width="10%">Work</td></tr>
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</tbody></table></div>
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<p></p>
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<h2 class="smalltitle">1. <i>fim</i> switch (wild-type): BBa_K1632004, BBa_K1632005 </h2>
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<p></p>
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<div class="text">
 +
<ul>
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<li><a href="http://parts.igem.org/Part:BBa_K1632004" target="_brank">BBa_K1632004</a><br><i>fim</i> switch[default ON](wild-type)</li>
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<li><a href="http://parts.igem.org/Part:BBa_K1632005" target="_brank">BBa_K1632005</a><br><i>fim</i> switch[default OFF](wild-type)</li>
 +
</ul>
 +
</div>
 +
<p></p>
 +
<p></p>
 +
<p class="text">We are the first team in iGEM to successfully construct both the <i>fim</i> switch[default ON](wild-type) and the <i>fim</i> switch [default OFF](wild-type) and experimented them. These <i>fim</i> switch is derived from a wild type. The <i>fim</i> switch(wild-type) has a sigma 70 promoter which functions constitutively.  We submitted two parts, one in the [default ON] (<a href="http://parts.igem.org/Part:BBa_K1632004" target="_brank">BBa_K1632004</a>) and the other in the [default OFF] (<a href="http://parts.igem.org/Part:BBa_K1632005" target="_brank">BBa_K1632005</a>)(Fig.5-2-1-1). The <i>fim</i> switch (wild-type) is inverted by two recombinases, FimB (<a href="http://parts.igem.org/Part:BBa_K1632010" target="_brank">BBa_K1632010</a>) and FimE (<a href="http://parts.igem.org/Part:BBa_K1632011" target="_brank">BBa_K1632011</a>).  Therefore, we can regulate the expression of the gene downstream of the <i>fim</i> switch (wild-type) by adding the Fim recombinase.  From our results of experiment, they work ideally (Fig.5-2-1-2 and Fig.5-2-1-3).</p>
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<p></p>
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<p></p>
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<p><br><br>
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</p>
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<p></p>
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<p></p>
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<table width="900px"><tbody><tr><td align="center"><img src="https://static.igem.org/mediawiki/2015/e/e2/Tokyo_Tech_3333333.png" width="60%"></td></tr><tr><td align="center"><h4 class="fig">Fig.5-2-1-1. <i>fim</i> switch is inverted by two recombinases, FimB and FimE. These proteins have distinct activities. The FimB protein inverts <i>fim</i> switch in the ON-to-OFF and the OFF-to-ON direction with approximately equal probability</h4></td></tr></tbody></table>
 +
<p></p>
 +
<table width="940 px" border="0px"><tr><td width="940px"><div align="center"><img src="https://static.igem.org/mediawiki/2015/1/1a/Tokyo_Tech_arabinose_fimB_result1.png" width="800px"/></td></tr><tr><td width="940px"><h4 align="center" class="fig">Fig. 5-2-1-2. The result of our assay used <a href="http://parts.igem.org/Part:BBa_K1632007" target="_brank">BBa_K1632007</a>, <a href="http://parts.igem.org/Part:BBa_K1632008" target="_brank">BBa_K1632008</a> and <a href="http://parts.igem.org/Part:BBa_K1632012" target="_brank">BBa_K1632012</a> with flow cytometers.</h4><td></tr></table><p></p>
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 +
<table width="900px" align="center"><tbody><tr><td align="center"><img src="https://static.igem.org/mediawiki/2015/e/e9/Tokyo_Tech_parts2.png" width="60%"></td></tr><tr><td align="center"><h4 class="fig">Fig.5-2-1-3. The result of our assay used <a href="http://parts.igem.org/Part:BBa_K1632007" target="_brank">BBa_K1632007</a>,<a href="http://parts.igem.org/Part:BBa_K1632008" target="_brank">BBa_K1632008</a> and <a href="http://parts.igem.org/Part:BBa_K1632013" target="_brank">BBa_K1632013</a> with flow cytometers</h4></td></tr></tbody></table>
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<p></p>
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<p></p>
 +
<p></p>
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 +
<h2 class="smalltitle">2. <i>fimE</i> (wild-type): BBa_K1632011 </h2>
 +
<p></p>
 +
<div class="text">
 +
<ul>
 +
<li><a href="http://parts.igem.org/Part:BBa_K1632011" target="_brank">BBa_K1632011</a><br><i>fimE</i>(wild-type)</li>
 +
</ul>
 +
</div>
 +
<p></p>
 +
<p></p>
 +
<p class="text">FimE (<a href="http://parts.igem.org/Part:BBa_K1632011" target="_brank">BBa_K1632011</a>) is a Fim recombinase.  This is derived from the wild type MG1655.  FimE invert the <i>fim</i> switch in the [ON] to [OFF] direction.</p>
 +
<p class="text">From our experimental results, we confirmed that the FimE protein inverts the <i>fim</i> switch(wild -type) predominantly in [ON] state to [OFF] state direction.  The expression of FimE is controlled by arabinose in PBAD/<i>araC</i>_<i>fimB</i>(wild-type) (<a href="http://parts.igem.org/Part:BBa_K1632012" target="_brank">BBa_K1632012</a>).  From our experimental results (Fig. 5-2-2-1), they work ideally.</p>
 +
<table width="940px"><tbody><tr><td align="center"><img src="https://static.igem.org/mediawiki/2015/e/e9/Tokyo_Tech_parts2.png" width="60%"></td></tr><tr><td align="center"><h4 class="fig">Fig.5-2-2-1. The result of our assay used <a href="http://parts.igem.org/Part:BBa_K1632007" target="_brank">BBa_K1632007</a>,<a href="http://parts.igem.org/Part:BBa_K1632008" target="_brank">BBa_K1632008</a> and <a href="http://parts.igem.org/Part:BBa_K1632013" target="_brank">BBa_K1632013</a> with flow cytometers</h4></td></tr></tbody></table>
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<p></p>
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<h2 class="smalltitle">3. <i>fim</i> switch (Tokyo_Tech): BBa_K1632000, BBa_K1632001, BBa_K1632006</h2>
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<p></p>
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<div class="text">
 +
<ul>
 +
<li><a href="http://parts.igem.org/Part:BBa_K1632000" target="_brank">BBa_K1632000</a><br><i>fim</i> switch[default ON](Tokyo_Tech/J23119)</li>
 +
<li><a href="http://parts.igem.org/Part:BBa_K1632001" target="_brank">BBa_K1632001</a><br><i>fim</i> switch[default OFF](Tokyo_Tech/J23119)</li>
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<li><a href="http://parts.igem.org/Part:BBa_K1632006" target="_brank">BBa_K1632006</a><br><i>fim</i> switch[default ON](Tokyo_Tech/R0010)</li>
 +
</ul>
 +
</div>
 +
<p></p>
 +
<p class="text">We designed another <i>fim</i> switch with a standardized interchangeable promoter, <i>fim</i> switch (Tokyo_Tech).  A difference between the <i>fim</i> switch (wild-type) and the <i>fim</i> switch (Tokyo_Tech) is that we replaced the sigma 70 promoter to the J23119 promoter" (<a href="http://parts.igem.org/Part:BBa_J23119" target="_brank">BBa_J23119</a>) and two restriction enzyme cut sites are added in each side of the promoter.(Fig.5-2-3-1).  Due to this addition of the restriction enzyme cut sites, we were able to replace the J23119 promoter (<a href="http://parts.igem.org/Part:BBa_J23119" target="_brank">BBa_J23119</a>) in the <i>fim</i> swtich (Tokyo_Tech).  There is an example. <i>fim</i> switch [default ON] (Tokyo_Tech/R0010) (<a href="http://parts.igem.org/Part:BBa_K1632006" target="_brank">BBa_K1632006</a>) is made by removing the J23119 promoter (<a href="http://parts.igem.org/Part:BBa_J23119" target="_brank">BBa_J23119</a>) and inserted Plac promoter (<a href="http://parts.igem.org/Part:BBa_R0010" target="_brank">BBa_R0010</a>) (Fig.5-2-3-2) . </p>
 +
<p></p>
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<table width="940px"><tbody><tr><td align="center"><img src="https://static.igem.org/mediawiki/2015/a/ae/Tokyo_Tech_2222222222.png" width="60%"></td></tr><tr><td align="center"><h4 class="fig">Fig.5-2-3-1. Design of <i>fim</i> switch (Tokyo_Tech)</h4></tr></td></tbody></table>
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<p></p>
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<table width="940px"><tbody><tr><td align="center"><img src="https://static.igem.org/mediawiki/2015/b/b7/Tokyo_Tech_parts10.png" width="60%"></td></tr><tr><td align="center"><h4 class="fig">Fig.5-2-3-2.  Exchange the promoter of <i>fim</i> switch (Tokyo_Tech)</h4></tr></td></tbody></table>
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Latest revision as of 03:13, 19 September 2015

Basic Parts

Best Basic Part: fimB (wild-type) (BBa_K1632010)

FimB (BBa_K1632010) is a Fim recombinase. This is derived from the wild type MG1655. FimB invert the fim switch in the [ON] to [OFF] direction and in the [OFF] to [ON] direction (Fig.5-2-0-1.).

From our experimental results, we confirmed that the FimB protein inverts the fim switch(wild-type) in the [ON] to [OFF] direction and in the [OFF] to [ON] direction with approximately equal probability and works ideally (Fig.5-2-0-2.). The expression of FimB is controlled by arabinose in PBAD/araC_fimB(wild-type) (BBa_K1632012).

Fig.5-2-0-1. Design of fim switch (wild-type)

Fig. 5-2-0-2. The result of our experiment used BBa_K1632007, BBa_K1632008 and BBa_K1632012 with flow cytometers.



0.Tokyo Tech 2015 iGEM Team: The Others Basic Parts

NameTypeDescriptionDesignLength(bp)Experiment
BBa_K1632000Regulatoryfim switch[default ON](Tokyo_Tech/J23119)Riku Shinohara382Work
BBa_K1632001Regulatoryfim switch[default ON](Tokyo_Tech/J23119)Riku Shinohara382Work
BBa_K1632004Regulatoryfim switch[default OFF](wild-type)Riku Shinohara382Work
BBa_K1632005Regulatoryfim switch[default OFF](wild-type)Riku Shinohara382Work
BBa_K1632006Regulatoryfim switch[default ON](Tokyo_Tech/R0010)Riku Shinohara597
BBa_K1632010CodingfimB(wild-type)Riku Shinohara603Work
BBa_K1632011CodingfimE(wild-type)Riku Shinohara597Work

1. fim switch (wild-type): BBa_K1632004, BBa_K1632005

We are the first team in iGEM to successfully construct both the fim switch[default ON](wild-type) and the fim switch [default OFF](wild-type) and experimented them. These fim switch is derived from a wild type. The fim switch(wild-type) has a sigma 70 promoter which functions constitutively. We submitted two parts, one in the [default ON] (BBa_K1632004) and the other in the [default OFF] (BBa_K1632005)(Fig.5-2-1-1). The fim switch (wild-type) is inverted by two recombinases, FimB (BBa_K1632010) and FimE (BBa_K1632011). Therefore, we can regulate the expression of the gene downstream of the fim switch (wild-type) by adding the Fim recombinase. From our results of experiment, they work ideally (Fig.5-2-1-2 and Fig.5-2-1-3).



Fig.5-2-1-1. fim switch is inverted by two recombinases, FimB and FimE. These proteins have distinct activities. The FimB protein inverts fim switch in the ON-to-OFF and the OFF-to-ON direction with approximately equal probability

Fig. 5-2-1-2. The result of our assay used BBa_K1632007, BBa_K1632008 and BBa_K1632012 with flow cytometers.

Fig.5-2-1-3. The result of our assay used BBa_K1632007,BBa_K1632008 and BBa_K1632013 with flow cytometers

2. fimE (wild-type): BBa_K1632011

FimE (BBa_K1632011) is a Fim recombinase. This is derived from the wild type MG1655. FimE invert the fim switch in the [ON] to [OFF] direction.

From our experimental results, we confirmed that the FimE protein inverts the fim switch(wild -type) predominantly in [ON] state to [OFF] state direction. The expression of FimE is controlled by arabinose in PBAD/araC_fimB(wild-type) (BBa_K1632012). From our experimental results (Fig. 5-2-2-1), they work ideally.

Fig.5-2-2-1. The result of our assay used BBa_K1632007,BBa_K1632008 and BBa_K1632013 with flow cytometers

3. fim switch (Tokyo_Tech): BBa_K1632000, BBa_K1632001, BBa_K1632006

We designed another fim switch with a standardized interchangeable promoter, fim switch (Tokyo_Tech). A difference between the fim switch (wild-type) and the fim switch (Tokyo_Tech) is that we replaced the sigma 70 promoter to the J23119 promoter" (BBa_J23119) and two restriction enzyme cut sites are added in each side of the promoter.(Fig.5-2-3-1). Due to this addition of the restriction enzyme cut sites, we were able to replace the J23119 promoter (BBa_J23119) in the fim swtich (Tokyo_Tech). There is an example. fim switch [default ON] (Tokyo_Tech/R0010) (BBa_K1632006) is made by removing the J23119 promoter (BBa_J23119) and inserted Plac promoter (BBa_R0010) (Fig.5-2-3-2) .

Fig.5-2-3-1. Design of fim switch (Tokyo_Tech)

Fig.5-2-3-2. Exchange the promoter of fim switch (Tokyo_Tech)