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Team:Bielefeld-CeBiTec/Results/Pathway
From 2014.igem.org
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<p>We started with the <b>pSB1C3_<i>alsS</i>_<i>ilvC</i>_<i>ilvD</i>_<i>kivD</i></b> construct which is the part <a href="http://parts.igem.org/wiki/index.php?title=Part:BBa_K1465302" target="_blank"> K1465302</a>. Therefore we used the CDS of the NCTU team Formosa 2011/2012 BioBricks <i>alsS</i> (<a href="http://parts.igem.org/Part:BBa_K539627" target="_blank">BBa_K539627</a>), <i>ilvC</i> (<a href="http://parts.igem.org/Part:BBa_K539621" target="_blank">BBa_K539621</a>), <i> | <p>We started with the <b>pSB1C3_<i>alsS</i>_<i>ilvC</i>_<i>ilvD</i>_<i>kivD</i></b> construct which is the part <a href="http://parts.igem.org/wiki/index.php?title=Part:BBa_K1465302" target="_blank"> K1465302</a>. Therefore we used the CDS of the NCTU team Formosa 2011/2012 BioBricks <i>alsS</i> (<a href="http://parts.igem.org/Part:BBa_K539627" target="_blank">BBa_K539627</a>), <i>ilvC</i> (<a href="http://parts.igem.org/Part:BBa_K539621" target="_blank">BBa_K539621</a>), <i> | ||
ilvD</i> (<a href="http://parts.igem.org/Part:BBa_K539626" target="_blank">BBa_K539626</a>) and <i>kivD</i> (<a href="http://parts.igem.org/Part:BBa_K539742" target="_blank">BBa_K539742</a>)</li>. We used the parts of the Parts Kit to combine them by <a href="https://2014.igem.org/Team:Bielefeld-CeBiTec/Notebook/Protocols#Gibson" target="_blank">Gibson Assembly</a>. For this we amplified the various CDS and combined them with a RBS (<a href="http://parts.igem.org/Part:BBa_B0034" target="_blank">BBa_B0034</a>) by a PCR. <br>In the beginning it did not worked with pSB1C3 so we used pSB1K3. <br> When we had pSB1K3_<i>alsS</i>_<i>ilvC</i>_<i>ilvD</i>_<i>kivD</i>, we wanted to reclone it in pSB1C3 and combine it with a promoter. This we wanted to do with <a href="https://2014.igem.org/Team:Bielefeld-CeBiTec/Notebook/Protocols#BioBrick" target="_blank">BioBrick Assembly</a>. Thereby we identified an illegal restriction side in the end of <i>alsS</i> because of the combination with the following RBS. This we removed by PCR amplification and Gibson with new primer (<a href="https://2014.igem.org/Team:Bielefeld-CeBiTec/Notebook/Primer#rv_ilvC_alsS-new" target="_blank">rv_ilvC_alsS-new</a>, <a href="https://2014.igem.org/Team:Bielefeld-CeBiTec/Notebook/Primer#fw_alsS_ilvC-new" target="_blank">fw_alsS_ilvC-new</a>). In this approach we were able to amplify pSB1C3 as backbone, so no recloning was necessary. | ilvD</i> (<a href="http://parts.igem.org/Part:BBa_K539626" target="_blank">BBa_K539626</a>) and <i>kivD</i> (<a href="http://parts.igem.org/Part:BBa_K539742" target="_blank">BBa_K539742</a>)</li>. We used the parts of the Parts Kit to combine them by <a href="https://2014.igem.org/Team:Bielefeld-CeBiTec/Notebook/Protocols#Gibson" target="_blank">Gibson Assembly</a>. For this we amplified the various CDS and combined them with a RBS (<a href="http://parts.igem.org/Part:BBa_B0034" target="_blank">BBa_B0034</a>) by a PCR. <br>In the beginning it did not worked with pSB1C3 so we used pSB1K3. <br> When we had pSB1K3_<i>alsS</i>_<i>ilvC</i>_<i>ilvD</i>_<i>kivD</i>, we wanted to reclone it in pSB1C3 and combine it with a promoter. This we wanted to do with <a href="https://2014.igem.org/Team:Bielefeld-CeBiTec/Notebook/Protocols#BioBrick" target="_blank">BioBrick Assembly</a>. Thereby we identified an illegal restriction side in the end of <i>alsS</i> because of the combination with the following RBS. This we removed by PCR amplification and Gibson with new primer (<a href="https://2014.igem.org/Team:Bielefeld-CeBiTec/Notebook/Primer#rv_ilvC_alsS-new" target="_blank">rv_ilvC_alsS-new</a>, <a href="https://2014.igem.org/Team:Bielefeld-CeBiTec/Notebook/Primer#fw_alsS_ilvC-new" target="_blank">fw_alsS_ilvC-new</a>). In this approach we were able to amplify pSB1C3 as backbone, so no recloning was necessary. | ||
| - | </p><p>Additionally we wanted to combine our part <a href="http://parts.igem.org/wiki/index.php?title=Part:BBa_K1465302" target="_blank"> K1465302</a> with the <i>adhA</i> from <i>Lactococcus lactis</i>. This alcoholdehydrogenase was identified as the best enzyme for the last step in the 2-keto-acid pathway (<a href="#Atsumi2008">Atsumi2008</a>, <a href="#Atsumi2010">Atsumi2010</a>).</p></div></div> | + | </p><p>Additionally we wanted to combine our part <a href="http://parts.igem.org/wiki/index.php?title=Part:BBa_K1465302" target="_blank"> K1465302</a> with the <i>adhA</i> from <i>Lactococcus lactis</i>. This alcoholdehydrogenase was identified as the best enzyme for the last step in the 2-keto-acid pathway (<a href="#Atsumi2008">Atsumi2008</a>, <a href="#Atsumi2010">Atsumi2010</a>). This pathway is responsible for the isobutanol production.</p></div></div> |
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Revision as of 11:43, 17 October 2014
Module III - Isobutanol production
Cloning
Coding sequences
We started with the pSB1C3_alsS_ilvC_ilvD_kivD construct which is the part K1465302. Therefore we used the CDS of the NCTU team Formosa 2011/2012 BioBricks alsS (BBa_K539627), ilvC (BBa_K539621),
ilvD (BBa_K539626) and kivD (BBa_K539742). We used the parts of the Parts Kit to combine them by Gibson Assembly. For this we amplified the various CDS and combined them with a RBS (BBa_B0034) by a PCR.
In the beginning it did not worked with pSB1C3 so we used pSB1K3.
When we had pSB1K3_alsS_ilvC_ilvD_kivD, we wanted to reclone it in pSB1C3 and combine it with a promoter. This we wanted to do with BioBrick Assembly. Thereby we identified an illegal restriction side in the end of alsS because of the combination with the following RBS. This we removed by PCR amplification and Gibson with new primer (rv_ilvC_alsS-new, fw_alsS_ilvC-new). In this approach we were able to amplify pSB1C3 as backbone, so no recloning was necessary.
Additionally we wanted to combine our part K1465302 with the adhA from Lactococcus lactis. This alcoholdehydrogenase was identified as the best enzyme for the last step in the 2-keto-acid pathway (Atsumi2008, Atsumi2010). This pathway is responsible for the isobutanol production.
Constructs with promoter
Expression
Cultivation
Production
Conclusion
References
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Atsumi S, Wu TY, Eckl EM, Hawkins SD, Buelter T, Liao JC. 2010. Engineering the isobutanol biosynthetic pathway in Escherichia coli by comparison three aldehyde reductase/alcohol dehydrogenase genes. In: Appl. Microbiol. Biotechnol 85, 651–657
