Team:Utah State/Results

From 2012.igem.org

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This year Utah State iGEM team has created 64 different spider silk BioBrick parts and has submitted 10 of these parts to the registry.  We are the first iGEM team to create a collection of BioBrick parts and demonstrated that spider silk can be produced from these parts. Furthermore, from this work we have successfully demonstrated that the methods of standard assembly can be used to create these functioning spider silk BioBricks.  
This year Utah State iGEM team has created 64 different spider silk BioBrick parts and has submitted 10 of these parts to the registry.  We are the first iGEM team to create a collection of BioBrick parts and demonstrated that spider silk can be produced from these parts. Furthermore, from this work we have successfully demonstrated that the methods of standard assembly can be used to create these functioning spider silk BioBricks.  
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The figure below shows the 64 different spider silk BioBricks that we have created. All the 64 parts are in pSB1C3 so different parts can be assembled together to create different repeating spider silk units. An example of this would be to take the part ‘patgB8’ (which is an 8 x B unit with a promoter and rbs) and combine it with ‘B6HT’ (6 x B unit with 10 Histag) to produce ‘patgB14HT’.  
The figure below shows the 64 different spider silk BioBricks that we have created. All the 64 parts are in pSB1C3 so different parts can be assembled together to create different repeating spider silk units. An example of this would be to take the part ‘patgB8’ (which is an 8 x B unit with a promoter and rbs) and combine it with ‘B6HT’ (6 x B unit with 10 Histag) to produce ‘patgB14HT’.  
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<p align="center"><img src="https://static.igem.org/mediawiki/2012/5/54/PatgF1gfp_map.PNG" alt="usu_silk" width="300" height="100"></p>
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<p align="center"><img src="https://static.igem.org/mediawiki/2012/5/54/PatgF1gfp_map.PNG" alt="usu_silk" width="350"></p>
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The bacterial cells harboring the patgF1GFP plasmid was spread on LB plates containing chloramphenicol and isopropyl-β-D-1-thiogalactopyranoside (IPTG). The figure below shows that the GFP construct is functional and expressing both spider silk (F1) and GFP.
The bacterial cells harboring the patgF1GFP plasmid was spread on LB plates containing chloramphenicol and isopropyl-β-D-1-thiogalactopyranoside (IPTG). The figure below shows that the GFP construct is functional and expressing both spider silk (F1) and GFP.
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<p align="center"><img src="https://static.igem.org/mediawiki/2012/c/cc/Gfp_plates.png" alt="usu_silk" width="700" height="354"></p>
<p align="center"><img src="https://static.igem.org/mediawiki/2012/c/cc/Gfp_plates.png" alt="usu_silk" width="700" height="354"></p>
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Revision as of 23:08, 3 October 2012

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