Team:SDU-Denmark/Tour33
From 2013.igem.org
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<h2>Design</h2> | <h2>Design</h2> | ||
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- | <a class="popupImg alignRight" style="width:250px" target="_blank" href="https://static.igem.org/mediawiki/2013/c/c0/SDU2013_BBa_K1088016_-_Hvid_midt.png" title=""> | + | <a class="popupImg alignRight" style="width:250px" target="_blank" href="https://static.igem.org/mediawiki/2013/c/c0/SDU2013_BBa_K1088016_-_Hvid_midt.png" title="BioBrick BBa_K1088016 - pSB1K3-<i>araC</i>-pBAD-<i>HRT2</i>-terminator. Device made to express the prenyltransferase, HRT2."> |
- | <img src="https://static.igem.org/mediawiki/2013/ | + | <img src="https://static.igem.org/mediawiki/2013/e/ee/SDU2013_Small_BBa_K1088016_-_Hvid_midt.png" style="width:250px" /> |
- | BioBrick BBa_K1088016 - | + | BioBrick BBa_K1088016 - pSB1K3-<i>araC</i>-<i>HRT2</i>-terminator. Device made to express the prenyltransferase, HRT2. |
</a> | </a> | ||
- | + | <h4>The micro system of modern rubber production</h4> | |
<p> | <p> | ||
- | The most important step in the synthesis of natural rubber is the polymerization of isoprene catalyzed by HRT2. Our model showed that the reactions catalysed by Dxs and IspG are the rate limiting steps in the MEP pathway. Therefore it was decided that these would be the sites of our intervention in the pathway with the purpose of increasing the amount of IPP and DMAPP. | + | |
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+ | <span class="intro">The most important step</span> in the synthesis of natural rubber is the polymerization of isoprene catalyzed by HRT2. Our model showed that the reactions catalysed by Dxs and IspG are the rate limiting steps in the MEP pathway. Therefore it was decided that these would be the sites of our intervention in the pathway with the purpose of increasing the amount of IPP and DMAPP. | ||
</p><p> | </p><p> | ||
Our production system will be composed of two plasmids: one expressing HRT2 and one overexpressing Dxs and IspG. | Our production system will be composed of two plasmids: one expressing HRT2 and one overexpressing Dxs and IspG. | ||
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- | <a class="popupImg alignRight" style="width:250px" target="_blank" href="https://static.igem.org/mediawiki/2013/0/0e/SDU2013_BBa_K1088015_-_Hvid_midt.png" title=""> | + | |
- | <img src="https://static.igem.org/mediawiki/2013/ | + | |
- | Biobrick BBa_K1088015 - pSB1C3-lacI-dxs-ispG. Device made to increase the IPP and DMAPP levels | + | <span class="intro"><a class="dialogLink" href="http://parts.igem.org/Part:BBa_K1088016">Device expressing HRT2</a> - (pSB1K3-<span class="specialWord">araC</span>-Para-<span class="specialWord">HRT2</span>)</span><br> |
+ | The expression of the device responds to arabinose under glucose scarce conditions; arabinose binds to AraC and relieves the transcription inhibition brought forth by this protein. | ||
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+ | <a class="popupImg alignRight" style="width:250px" target="_blank" href="https://static.igem.org/mediawiki/2013/0/0e/SDU2013_BBa_K1088015_-_Hvid_midt.png" title="Biobrick BBa_K1088015 - pSB1C3-<i>lacI</i>-<i>dxs</i>-<i>ispG</i>. Device made to increase the IPP and DMAPP levels."> | ||
+ | <img src="https://static.igem.org/mediawiki/2013/1/11/SDU2013_Small_BBa_K1088015_-_Hvid_midt.png" style="width:250px" /> | ||
+ | Biobrick BBa_K1088015 - pSB1C3-<i>lacI</i>-<i>dxs</i>-<i>ispG</i>. Device made to increase the IPP and DMAPP levels. | ||
</a> | </a> | ||
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+ | It contains an arabinose promoter, a ribosomal binding site, the <span class="specialWord">E. coli</span> codon-optimized HRT2 gene of <span class="specialWord">Hevea brasiliensis</span>, and a terminator. The backbone is the pSB1K3 plasmid, which carries kanamycin resistance. | ||
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</p> | </p> | ||
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- | The device responds to allolactose and IPTG through LacI relieved inhibition. It contains a lactose promoter, a ribosomal binding site, the B. subtilis derived dxs gene, and the E. coli derived ispG gene. The backbone is the pSB1C3 plasmid, which carries chloramphenicol resistance. | + | |
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+ | <span class="intro"><a class="dialogLink" href="http://parts.igem.org/Part:BBa_K1088015">Device expressing Dxs and IspG</a> - pSB1C3-<span class="specialWord">lacI</span>-Plac-<span class="specialWord">dxs-ispG</span></span><br> | ||
+ | The device responds to allolactose and IPTG through LacI relieved inhibition. It contains a lactose promoter, a ribosomal binding site, the <span class="specialWord">B. subtilis</span> derived <span class="specialWord">dxs</span> gene, and the <span class="specialWord">E. coli</span> derived <span class="specialWord">ispG</span> gene. The backbone is the pSB1C3 plasmid, which carries chloramphenicol resistance. | ||
</p> | </p> | ||
<br><br><br><br><br> | <br><br><br><br><br> | ||
Links to our two devices on parts registry<br> | Links to our two devices on parts registry<br> | ||
- | <a href="http://parts.igem.org/Part:BBa_K1088015 | + | <a class="dialogLink" href="http://parts.igem.org/Part:BBa_K1088015">BBa_K1088015</a><br> |
- | <a href="http://parts.igem.org/Part:BBa_K1088016 | + | <a class="dialogLink" href="http://parts.igem.org/Part:BBa_K1088016">BBa_K1088016</a><br> |
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</html> | </html> | ||
{{:Team:SDU-Denmark/core/footer}} | {{:Team:SDU-Denmark/core/footer}} |
Latest revision as of 01:11, 29 October 2013
Design
BioBrick BBa_K1088016 - pSB1K3-araC-HRT2-terminator. Device made to express the prenyltransferase, HRT2.The micro system of modern rubber production
The most important step in the synthesis of natural rubber is the polymerization of isoprene catalyzed by HRT2. Our model showed that the reactions catalysed by Dxs and IspG are the rate limiting steps in the MEP pathway. Therefore it was decided that these would be the sites of our intervention in the pathway with the purpose of increasing the amount of IPP and DMAPP.
Our production system will be composed of two plasmids: one expressing HRT2 and one overexpressing Dxs and IspG.
Device expressing HRT2 - (pSB1K3-araC-Para-HRT2)
The expression of the device responds to arabinose under glucose scarce conditions; arabinose binds to AraC and relieves the transcription inhibition brought forth by this protein.
Biobrick BBa_K1088015 - pSB1C3-lacI-dxs-ispG. Device made to increase the IPP and DMAPP levels.
It contains an arabinose promoter, a ribosomal binding site, the E. coli codon-optimized HRT2 gene of Hevea brasiliensis, and a terminator. The backbone is the pSB1K3 plasmid, which carries kanamycin resistance.
Device expressing Dxs and IspG - pSB1C3-lacI-Plac-dxs-ispG
The device responds to allolactose and IPTG through LacI relieved inhibition. It contains a lactose promoter, a ribosomal binding site, the B. subtilis derived dxs gene, and the E. coli derived ispG gene. The backbone is the pSB1C3 plasmid, which carries chloramphenicol resistance.
Links to our two devices on parts registry
BBa_K1088015
BBa_K1088016