- BBa_K1632010
fimB(wild-type)
Difference between revisions of "Team:Tokyo Tech/Basic Part"
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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 | + | <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> |
− | <p class="text">From our experimental results, we confirmed that the FimB protein inverts the <i>fim</i> switch in the ON | + | <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> |
+ | <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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− | + | <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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− | <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- | + | |
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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> | <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> | ||
<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> | <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> | ||
− | <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%"> | + | <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> |
<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> | <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> | ||
<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> | <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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− | <p class="text">We are the first team in iGEM to successfully construct both the <i>fim</i> switch default ON and the <i>fim</i> switch default OFF and experimented them. These <i>fim</i> switch is derived from a wild type | + | <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> |
+ | <p></p> | ||
<p></p> | <p></p> | ||
<p><br><br> | <p><br><br> | ||
</p> | </p> | ||
<p></p> | <p></p> | ||
− | |||
<p></p> | <p></p> | ||
− | <table width="900px"><tbody><tr><td align="center"><img src="https://static.igem.org/mediawiki/2015/ | + | <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> | <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- | + | <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> |
<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> | <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 class="text"> | + | <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> | <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> | ||
<p></p> | <p></p> | ||
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</div> | </div> | ||
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− | <p class="text">We designed <i>fim</i> switch with a standardized interchangeable | + | <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> | <p></p> | ||
− | <table width="940px"><tbody><tr><td align="center"><img src="https://static.igem.org/mediawiki/2015/ | + | <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> |
<p></p> | <p></p> | ||
− | <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 | + | <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> |
<p><br><br></p> | <p><br><br></p> | ||
<div class="text"> | <div class="text"> |
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
Name | Type | Description | Design | Length(bp) | Experiment |
---|---|---|---|---|---|
BBa_K1632000 | Regulatory | fim switch[default ON](Tokyo_Tech/J23119) | Riku Shinohara | 382 | Work |
BBa_K1632001 | Regulatory | fim switch[default ON](Tokyo_Tech/J23119) | Riku Shinohara | 382 | Work |
BBa_K1632004 | Regulatory | fim switch[default OFF](wild-type) | Riku Shinohara | 382 | Work |
BBa_K1632005 | Regulatory | fim switch[default OFF](wild-type) | Riku Shinohara | 382 | Work |
BBa_K1632006 | Regulatory | fim switch[default ON](Tokyo_Tech/R0010) | Riku Shinohara | 597 | |
BBa_K1632010 | Coding | fimB(wild-type) | Riku Shinohara | 603 | Work |
BBa_K1632011 | Coding | fimE(wild-type) | Riku Shinohara | 597 | Work |
1. fim switch (wild-type): BBa_K1632004, BBa_K1632005
- BBa_K1632004
fim switch[default ON](wild-type) - BBa_K1632005
fim switch[default OFF](wild-type)
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
- BBa_K1632011
fimE(wild-type)
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
- BBa_K1632000
fim switch[default ON](Tokyo_Tech/J23119) - BBa_K1632001
fim switch[default OFF](Tokyo_Tech/J23119) - BBa_K1632006
fim switch[default ON](Tokyo_Tech/R0010)
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) |