Team:Tokyo Tech/Projects/Urea-cooler/construction

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<h1> Construction-Urea </h1>
<h1> Construction-Urea </h1>
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<p><h2 id="primers">1. Primers</h2>All primers we used in this study were purchased from the Operon.<br /><br />
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<h2 id="primers">1. Primers</h2>
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<h2 id="arg box">2. The Arg box</h2><img src="https://static.igem.org/mediawiki/2011/0/07/For3_fig9.png" alt="Argbox" width="800px" /><br />The arg operator capable of binding the arginine repressor(Arg box) was amplified by PCR using the MG1655 as a template(①). The resulting fragment was ligated into Topo vector(②). To add restriction site, this was also amplified by PCR using a forward primer with EcoRI and XbaI sites, a reverse primer with SpeI and PstI sites(③).<br /><br />
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<p>
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<h2 id="rocF">3. The <i>rocF</i></h2><img src="https://static.igem.org/mediawiki/2011/9/9a/For3_fig11.png" alt="rocF" width="800px" /><br />The <i>rocF</i> gene coding for arginage was amplified by PCR using a forward primer with an NcoI site, a reverse primer with SpeI and PstI sites, and the Bacillus subtilis as a template(④). The resulting fragment was cut with NcoI and PstI and ligated into pTrc99A backbone vector including trc promoter and RBS(⑤).<br /><br />
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All primers we used in this study were purchased from the Operon.
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<h2 id="const1">4. construction of Ptrc-RBS-<i>rocF</i>-Arg box</h2><img src="https://static.igem.org/mediawiki/2011/3/3a/3K3.png" alt="Argbox plus" width="800px" /><br />We cut Arg box(③) with XbaI and PstI and ligated into pTrc99A backbone vector including <i>rocF</i>(⑤) which were cut with SpeI and PstI(⑥). Then We amplified Ptrc-RBS-rocF-Arg box by PCR using a forward primer with EcoRI and XbaI sites, a reverse primer with SpeI and PstI sites(⑦). The resulting fragment was ligated into pSB3K3.(BBa_K649402)<br /><br />
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</p>
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<h2 id="const2">5. construction of Ptrc-RBS-<i>rocF</i></h2><img src="https://static.igem.org/mediawiki/2011/0/0a/RocF3.png" alt="Argbox minus" width="800px" /><br />We amplified Ptrc-RBS-<i>rocF</i> by PCR using a forward primer with EcoRI and XbaI sites, a reverse primer with SpeI and PstI sites, and using ⑤ as a template(⑧). The resulting fragment was ligated into pSB3K3.(BBa_K649301)
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<h2 id="arg box">2. The Arg box</h2>
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<img src="https://static.igem.org/mediawiki/2011/0/07/For3_fig9.png" alt="Argbox" width="800px" />
 +
<p>
 +
The arg operator capable of binding the arginine repressor(Arg box) was amplified by PCR using the MG1655 as a template(1). The resulting fragment was ligated into Topo vector(2). To add restriction site, this was also amplified by PCR using a forward primer with EcoRI and XbaI sites, a reverse primer with SpeI and PstI sites(3).
 +
</p>
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<h2 id="rocF">3. The <i>rocF</i></h2>
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<img src="https://static.igem.org/mediawiki/2011/e/e7/Urea1.png" alt="rocF" width="800px" />
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<p>
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The <i>rocF</i> gene coding for arginage was amplified by PCR using a forward primer with an NcoI site, a reverse primer with SpeI and PstI sites, and the Bacillus subtilis as a template(4). The resulting fragment was cut with NcoI and PstI and ligated into pTrc99A backbone vector including trc promoter and RBS(5).
 +
</p>
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<h2 id="const1">4. construction of Ptrc-RBS-<i>rocF</i>-Arg box</h2>
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<img src="https://static.igem.org/mediawiki/2011/archive/5/54/20111028104906%21Urea2.png" alt="Argbox plus" width="800px" />
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<p>
 +
We cut Arg box(3) with XbaI and PstI and ligated into pTrc99A backbone vector including <i>rocF</i>(5) which were cut with SpeI and PstI(6). Then we amplified Ptrc-RBS-<i>rocF</i>-Arg box by PCR using a forward primer with EcoRI and XbaI sites, a reverse primer with SpeI and PstI sites(7). The resulting fragment was ligated into pSB3K3.<a href="http://partsregistry.org/wiki/index.php?title=Part:BBa_K649402">(BBa_K649402)</a>
 +
</p>
 +
<h2 id="const2">5. construction of Ptrc-RBS-<i>rocF</i></h2>
 +
<img src="https://static.igem.org/mediawiki/2011/b/bf/Urea3.png" alt="Argbox minus" width="800px" />
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<p>
 +
We amplified Ptrc-RBS-<i>rocF</i> by PCR using a forward primer with EcoRI and XbaI sites, a reverse primer with SpeI and PstI sites, and using 5 as a template(8). The resulting fragment was ligated into pSB3K3.<a href="http://partsregistry.org/wiki/index.php?title=Part:BBa_K649301">(BBa_K649301)</a>
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Latest revision as of 14:38, 28 October 2011

Tokyo Tech 2011

Construction-Urea

1. Primers

All primers we used in this study were purchased from the Operon.

2. The Arg box

Argbox

The arg operator capable of binding the arginine repressor(Arg box) was amplified by PCR using the MG1655 as a template(1). The resulting fragment was ligated into Topo vector(2). To add restriction site, this was also amplified by PCR using a forward primer with EcoRI and XbaI sites, a reverse primer with SpeI and PstI sites(3).

3. The rocF

rocF

The rocF gene coding for arginage was amplified by PCR using a forward primer with an NcoI site, a reverse primer with SpeI and PstI sites, and the Bacillus subtilis as a template(4). The resulting fragment was cut with NcoI and PstI and ligated into pTrc99A backbone vector including trc promoter and RBS(5).

4. construction of Ptrc-RBS-rocF-Arg box

Argbox plus

We cut Arg box(3) with XbaI and PstI and ligated into pTrc99A backbone vector including rocF(5) which were cut with SpeI and PstI(6). Then we amplified Ptrc-RBS-rocF-Arg box by PCR using a forward primer with EcoRI and XbaI sites, a reverse primer with SpeI and PstI sites(7). The resulting fragment was ligated into pSB3K3.(BBa_K649402)

5. construction of Ptrc-RBS-rocF

Argbox minus

We amplified Ptrc-RBS-rocF by PCR using a forward primer with EcoRI and XbaI sites, a reverse primer with SpeI and PstI sites, and using 5 as a template(8). The resulting fragment was ligated into pSB3K3.(BBa_K649301)

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