"
Team:Tokyo Tech/Projects/Urea-cooler/construction
From 2011.igem.org
HayashiMaiko (Talk | contribs) |
|||
| (5 intermediate revisions not shown) | |||
| Line 328: | Line 328: | ||
<!-- main contents --> | <!-- main contents --> | ||
<div class="main"> | <div class="main"> | ||
| - | <!-- ############ | + | <!-- ############ Write main contents here ############### --> |
<!-- page title --> | <!-- page title --> | ||
| Line 346: | Line 346: | ||
<h2 id="rocF">3. The <i>rocF</i></h2> | <h2 id="rocF">3. The <i>rocF</i></h2> | ||
| - | <img src="https://static.igem.org/mediawiki/2011/ | + | <img src="https://static.igem.org/mediawiki/2011/e/e7/Urea1.png" alt="rocF" width="800px" /> |
<p> | <p> | ||
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). | 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). | ||
| Line 352: | Line 352: | ||
<h2 id="const1">4. construction of Ptrc-RBS-<i>rocF</i>-Arg box</h2> | <h2 id="const1">4. construction of Ptrc-RBS-<i>rocF</i>-Arg box</h2> | ||
| - | <img src="https://static.igem.org/mediawiki/2011/ | + | <img src="https://static.igem.org/mediawiki/2011/archive/5/54/20111028104906%21Urea2.png" alt="Argbox plus" width="800px" /> |
<p> | <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> | 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> | ||
| Line 358: | Line 358: | ||
<h2 id="const2">5. construction of Ptrc-RBS-<i>rocF</i></h2> | <h2 id="const2">5. construction of Ptrc-RBS-<i>rocF</i></h2> | ||
| - | <img src="https://static.igem.org/mediawiki/2011/ | + | <img src="https://static.igem.org/mediawiki/2011/b/bf/Urea3.png" alt="Argbox minus" width="800px" /> |
<p> | <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> | 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> | ||
Latest revision as of 14:38, 28 October 2011
Construction-Urea
1. Primers
All primers we used in this study were purchased from the Operon.
2. The Arg box
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
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
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
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)
