Team:HokkaidoU Japan

From 2011.igem.org

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          This year, we aim to make further development of  "Dr. E. coli"; our project of iGEM 2010. Dr. E. coli can inject desired protein molecules into a target eukaryotic cell through a syringe like organelle named Type 3 Secretion  System(T3SS). Pathogenic gram-negative bacterium such as Salmonella  has  T3SS. In nature it is used to inject virulence effector proteins into a target eukaryotic cell. Last year, by injecting GFP into RK13 cells we showed that T3SS works in E. coli.  
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          This year, we are going one step further. Using Dr. E. coli as a "nano  injection system", we are planning to develop a cancer terminator or carry out direct reprogramming of somatic cells; for example we aim to induce differentiation from preadipocyte to insulin-secreting cell.
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          For human practice, we are going to hold a Science Gallery. We will exhibit awesome photographs related with molecular biology in a public place and ask some questions about synthetic biology. We hope to catch the public's interest in current biotechnology and investigate the public's thoughts about synthetic biology.
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You are provided with this team page template with which to start the iGEM season. You may choose to personalize it to fit your team but keep the same "look." Or you may choose to take your team wiki to a different level and design your own wiki. You can find some examples <a href="https://2009.igem.org/Help:Template/Examples">HERE</a>.
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You <strong>MUST</strong> have a team description page, a project abstract, a complete project description, a lab notebook, and a safety page. PLEASE keep all of your pages within your teams namespace.
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Revision as of 03:26, 16 July 2011


This year, we aim to make further development of "Dr. E. coli"; our project of iGEM 2010. Dr. E. coli can inject desired protein molecules into a target eukaryotic cell through a syringe like organelle named Type 3 Secretion System(T3SS). Pathogenic gram-negative bacterium such as Salmonella has T3SS. In nature it is used to inject virulence effector proteins into a target eukaryotic cell. Last year, by injecting GFP into RK13 cells we showed that T3SS works in E. coli. This year, we are going one step further. Using Dr. E. coli as a "nano injection system", we are planning to develop a cancer terminator or carry out direct reprogramming of somatic cells; for example we aim to induce differentiation from preadipocyte to insulin-secreting cell. For human practice, we are going to hold a Science Gallery. We will exhibit awesome photographs related with molecular biology in a public place and ask some questions about synthetic biology. We hope to catch the public's interest in current biotechnology and investigate the public's thoughts about synthetic biology.



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