Team:UNICAMP-EMSE Brazil/Methodology
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For the reasons explained in the safety proposals, we synthesized the following gene sequences according to assembling standard 23 and in the format of transcriptional units [with RBS ([http://partsregistry.org/Part:BBa_B0030 B0030]) and stop codon, when protein coding: | For the reasons explained in the safety proposals, we synthesized the following gene sequences according to assembling standard 23 and in the format of transcriptional units [with RBS ([http://partsregistry.org/Part:BBa_B0030 B0030]) and stop codon, when protein coding: | ||
<br clear="all"> | <br clear="all"> | ||
- | [[Image:UNICAMP_EMSE_flhdc.jpg|left|100px]] <br><br>flhDC promoter, part [ http://partsregistry.org/wiki/index.php?title=Part:BBa_K554001 BBa_K554001] | + | [[Image:UNICAMP_EMSE_flhdc.jpg|left|100px]] <br><br>flhDC promoter, part [http://partsregistry.org/wiki/index.php?title=Part:BBa_K554001 BBa_K554001] |
- | + | ||
<br clear="all"> | <br clear="all"> | ||
[[Image:UNICAMP_EMSE_soxs.jpg|right|100px]] <br><br><div align=right>SoxS promoter, part [ http://partsregistry.org/wiki/index.php?title=Part:BBa_K554000 BBa_K554000]</div> | [[Image:UNICAMP_EMSE_soxs.jpg|right|100px]] <br><br><div align=right>SoxS promoter, part [ http://partsregistry.org/wiki/index.php?title=Part:BBa_K554000 BBa_K554000]</div> | ||
<br clear="all"> | <br clear="all"> | ||
+ | [[Image:UNICAMP_EMSE_soxr.jpg|left|100px]] <br>RBS+SoxR gene, part [http://partsregistry.org/wiki/index.php?title=Part:BBa_K554003 BBa_K554003] | ||
<br clear="all"> | <br clear="all"> | ||
- | [[Image: | + | [[Image:UNICAMP_EMSE_il10.jpg|right|100px]] <br><br><div align=right>RBS+IL-10 gene, part [ http://partsregistry.org/wiki/index.php?title=Part:BBa_K554004 BBa_K554004]</div> |
+ | <br clear="all"> | ||
+ | [[Image:UNICAMP_EMSE_il12.jpg|left|100px]] <br>RBS+IL-12 gene, part [http://partsregistry.org/wiki/index.php?title=Part:BBa_K554005 BBa_K554005] | ||
+ | <br clear="all"> | ||
+ | [[Image:UNICAMP_EMSE_HlyB.jpg|right|100px]] <br><br><div align=right>RBS+Hemolysin B(HlyB) gene, part [ http://partsregistry.org/wiki/index.php?title=Part:BBa_K554007 BBa_K554007]</div> | ||
+ | <br clear="all"> | ||
+ | [[Image:UNICAMP_EMSE_hlyD.jpg|left|100px]] <br>RBS+Hemolysin D(HlyD) gene, part [http://partsregistry.org/wiki/index.php?title=Part:BBa_K554008 BBa_K554008] | ||
+ | <br clear="all"> | ||
+ | [[Image:UNICAMP_EMSE_TolC.jpg|right|100px]] <br><br><div align=right>RBS+TolC gene, part [ http://partsregistry.org/wiki/index.php?title=Part:BBa_K554009 BBa_K554009]</div> | ||
+ | <br clear="all"> | ||
+ | [[Image:UNICAMP_EMSE_qsecqseb.jpg|left|100px]] <br>RBS+QseB gene+QseC gene, part [http://partsregistry.org/wiki/index.php?title=Part:BBa_K554006 BBa_K554006] | ||
+ | <br clear="all"> | ||
+ | [[Image:UNICAMP_EMSE_hlyA.jpg|right|100px]] <br><br><div align=right>RBS+HlyA coding secretion signal sequence, part [ http://partsregistry.org/wiki/index.php?title=Part:BBa_K554002 BBa_K554002]</div> | ||
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+ | :*'''In our project, we also used the following biobricks from the 2011´s biobrick collection distribution sent by the iGEM headquarters:''' | ||
+ | <br clear="all"> | ||
+ | [[Image:UNICAMP_EMSE_const.jpg|left|100px]] <br><br>Constitutive promoter, part [http://partsregistry.org/Part:BBa_J23119 BBa_J23119] | ||
+ | <br clear="all"> | ||
+ | [[Image:UNICAMP_EMSE_gfp.jpg|right|100px]] <br><br><div align=right>GFP gene, part [ http://partsregistry.org/Part:BBa_E0040 BBa_E0040]</div> | ||
+ | <br clear="all"> | ||
+ | [[Image:UNICAMP_EMSE_term.jpg|left|100px]] <br><br>Double terminator, part [http://partsregistry.org/Part:BBa_B0014 BBa_B0014] | ||
+ | <br clear="all"> | ||
Revision as of 19:20, 28 September 2011
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Creating a great WARRIOR!
In order to create our “Jedi coli” to fight the STRESS WARS, we trained padawan colis to use their power to sense Nitric Oxide (NO) or Adrenaline and produce IL-10 and IL-12, respectively, to defend or bodyConfederation host against inVader bacteria. By the end of the harsh Jedi training, which included hours of cutting and ligation, cloning and transformation, we aimed to develop the following gene constructions:
Work plan:
Our work was divided in three main steps:
- Biobrick assembly;
- Suit the biobrick for shipment (remove them from the original plasmid and insert them on pSB1C3 plasmid);
- Devices construction and testing.
First step: Biobricks Assembly
For the reasons explained in the safety proposals, we synthesized the following gene sequences according to assembling standard 23 and in the format of transcriptional units [with RBS ([http://partsregistry.org/Part:BBa_B0030 B0030]) and stop codon, when protein coding:
flhDC promoter, part [http://partsregistry.org/wiki/index.php?title=Part:BBa_K554001 BBa_K554001]
RBS+SoxR gene, part [http://partsregistry.org/wiki/index.php?title=Part:BBa_K554003 BBa_K554003]
RBS+IL-12 gene, part [http://partsregistry.org/wiki/index.php?title=Part:BBa_K554005 BBa_K554005]
RBS+Hemolysin D(HlyD) gene, part [http://partsregistry.org/wiki/index.php?title=Part:BBa_K554008 BBa_K554008]
RBS+QseB gene+QseC gene, part [http://partsregistry.org/wiki/index.php?title=Part:BBa_K554006 BBa_K554006]
- In our project, we also used the following biobricks from the 2011´s biobrick collection distribution sent by the iGEM headquarters:
Constitutive promoter, part [http://partsregistry.org/Part:BBa_J23119 BBa_J23119]
Double terminator, part [http://partsregistry.org/Part:BBa_B0014 BBa_B0014]