Team:DTU Denmark

From 2009.igem.org

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     Also check out our Danish website<br><br>
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     Sponsors and acknowledgements<br><br>
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     <a href="http://www.bio.dtu.dk/igem.aspx" CLASS=leftbar>DTU iGEM 2009</a><br>
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     <a href="https://2009.igem.org/Team:DTU_Denmark/sponsors" CLASS=leftbar>- List of sponsors</a><br>
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     <a href="https://2009.igem.org/Team:DTU_Denmark/acknowledgement" CLASS=leftbar>- Acknowledgement</a><br>
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    The people we owe it all to<br><br>
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Also check out our Danish website<br><br>
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     <a href="http://www.bio.dtu.dk/igem.aspx" CLASS=leftbar>List of sponsors</a><br>
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     <a href="http://www.bio.dtu.dk/igem.aspx" target="_blank" CLASS=leftbar>- DTU iGEM 2009</a><br>
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<b>DTU Denmark</b><br><br><br>
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<b>DTU DENMARK</b><br><br>
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<font size="4"><b>Project abstract</b></font><br><br>
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<p align="justify">Welcome to the DTU-DENMARK iGEM team wiki. Here we present everything about our project, the team, how we have contributed to improve the registry of standard biological parts, and much more.
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<font size="3"><b>The Project</b></font><br>
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In <a href="https://2009.igem.org/Team:DTU_Denmark/project"> this project</a> we have<br>
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*Designed and constructed a redox sensing device: The Redoxilator<br>
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*Performed extensive mathematical modelling on the operation of the Redoxilator device<br>
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*Written and submitted a novel biobrick assembly standard based on USER fusion that allows the assembly of several biobricks at once<br>
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*Made a program for the design of primers needed for USER fusion online: PHUSER<br>
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Furthermore we have constructed and submitted <a href="https://2009.igem.org/Team:DTU_Denmark/parts">four very useful biobricks</a> to the registry.
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<font size="3"><b>The Redoxilator</b></font><br>
 
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<p align="justify">By in silico design and computer modelling followed by gene synthesis, we have constructed a molecular NAD/NADH ratio sensing system in Saccharomyces cerevisiae. The sensor works as an inducible transcription factor being active only at certain levels of the NAD/NADH ratios. By the coupling of a yeast optimized fast degradable GFP, the system can be used for in vivo monitoring of NAD/NADH redox poise. A future novel application of the system is heterologous redox coupled protein production in yeast.</p>
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<p align="justify"><font size="3"><b>The Team</b></font><br>
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Our team consists of six students in biotechnology and systems biology engineering, and we are the first team from the Technical University of Denmark. Please check out our <a href="https://2009.igem.org/Team:DTU_Denmark/team">team page</a> to read more about us and our advisors.
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[[Image:regulation.redox.jpg|300px|thumb|center|The redox coupled system]]
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<font size="3"><b>The USER fusion standard</b></font><br>
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<p align="justify"><i>The project has been done by a synthetic biology approach, and genetic components from diverse organisms have been assembled to build a genetic device. Synthetic biology is an increasingly significant area of research that can broadly be defined as an engineering approach to biology, with the goal of designing and implementing new cellular behaviors.</i>
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<p align="justify">Another part of our project is the proposal of a new parts-assembly standard for Biobricks based on USER(TradeMark) cloning. With this technique, not based on restriction enzymes, all parts independent of function can be assembled without leaving any scars from the restriction enzyme digestions.</p>
 
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  <p align="justify"><b>NEWS NEWS NEWS NEWS</b></p><br>
 
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<b>28.09.2009</b><br>
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<font size="3"><strong>Achievements</strong></font><br>
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<p align="justify">The wiki page layout is now settled. Stay tuned for project results!<p>
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<strong>Redox sensing device</strong><br>
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Two novel genes have been designed and synthesized each comprised of 5 genetic elements. Together they function as a device termed the Redoxilator that can sense the internal redox state of a yeast cell, and output a reporter signal. Extensive mathematical modelling was performed to simulate how the construct would operate <i>in vivo</i>.<br>
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<b>25.09.2009</b><br>
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<strong>Biobricks</strong><br>
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<p align="justify">We just received word that Lundbeckfonden has granted us $8000 USD for completion of our project! We owe them our gratitude, and continue our work delighted that thanks to Lundbeckfonden, Otto Mønsteds Fond, and Center for Microbial Biotechnology, we are now 100% funded and ready for iGEM 2009!<p>
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DNA of several new biobricks have been designed and submitted including a yeast optimized GFP reporter protein, a protein degradation sequence and a fast degradable yeast GFP. (Bronze medal)<br>
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We have demonstrated that our USER fusion biobrick works as expected and documented it (silver medal)<br>
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<strong>USER fusion Assembly standard</strong><br>
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A new biobrick assembly standard that allows the rapid construction of multi-part devices have been developed and documented. The assembly standard offers many benefits: All restriction sites are allowed, multiple biobricks can be joined in one step, the result is scar-free making it ideal for protein fusions and more. (Gold medal)<br>
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<strong>USER-fusion primer design software</strong><br>
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A novel and very useful software tool have been developed that can automatically design the optimal primers for USER fusion assembly of 2-9 biobricks, taking several parameters into account.
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Latest revision as of 00:32, 22 October 2009

Wiki banner 967px.png

Welcome to the DTU iGEM wiki!


Sponsors and acknowledgements

- List of sponsors
- Acknowledgement


Also check out our Danish website

- DTU iGEM 2009


DTU DENMARK

Welcome to the DTU-DENMARK iGEM team wiki. Here we present everything about our project, the team, how we have contributed to improve the registry of standard biological parts, and much more.

The Project
In this project we have

  • Designed and constructed a redox sensing device: The Redoxilator
  • Performed extensive mathematical modelling on the operation of the Redoxilator device
  • Written and submitted a novel biobrick assembly standard based on USER fusion that allows the assembly of several biobricks at once
  • Made a program for the design of primers needed for USER fusion online: PHUSER


Furthermore we have constructed and submitted four very useful biobricks to the registry.

The Team
Our team consists of six students in biotechnology and systems biology engineering, and we are the first team from the Technical University of Denmark. Please check out our team page to read more about us and our advisors.

Front figure-v5.png

The project has been done by a synthetic biology approach, and genetic components from diverse organisms have been assembled to build a genetic device. Synthetic biology is an increasingly significant area of research that can broadly be defined as an engineering approach to biology, with the goal of designing and implementing new cellular behaviors.

Achievements

Redox sensing device
Two novel genes have been designed and synthesized each comprised of 5 genetic elements. Together they function as a device termed the Redoxilator that can sense the internal redox state of a yeast cell, and output a reporter signal. Extensive mathematical modelling was performed to simulate how the construct would operate in vivo.

Biobricks
DNA of several new biobricks have been designed and submitted including a yeast optimized GFP reporter protein, a protein degradation sequence and a fast degradable yeast GFP. (Bronze medal)

We have demonstrated that our USER fusion biobrick works as expected and documented it (silver medal)

USER fusion Assembly standard
A new biobrick assembly standard that allows the rapid construction of multi-part devices have been developed and documented. The assembly standard offers many benefits: All restriction sites are allowed, multiple biobricks can be joined in one step, the result is scar-free making it ideal for protein fusions and more. (Gold medal)

USER-fusion primer design software
A novel and very useful software tool have been developed that can automatically design the optimal primers for USER fusion assembly of 2-9 biobricks, taking several parameters into account.

Comments or questions to the team? Please -- Comments of questions to webmaster? Please