Difference between revisions of "Team:SJTU-BioX-Shanghai/Description"

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<h2> Project Description </h2>
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<p>This year, we will engineer a recombinant cyanobacteria to achieve “biodesalination”, which means to extract sodium chloride from seawater through biological membranes. There are already some methods to convert saltwater into freshwater, such as distillation and reverse osmosis. However, the high energy consumption of these technologies has limited their application. Therefore the development of an innovative, low-energy biological desalination process, by biological membranes of cyanobacteria, would be very attractive. Many cyanobacteria possess salt-tolerance mechanisms, among which sodium export is the most important one. Halorhodopsin is a light-driven inward-directed chloride pump from halobacteria. We will functionally express it in cyanobacteria to drive influx of chloride together with sodium, thus conferring cyanobacteria the ability to absorb salts to a significant degree.</p>
 
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<p>Cyanobacteria have several characteristics which make them an ideal organism for biodesalination: fast-growing、photoautotrophy、amenable to genetic transformation and able to grow over a wide range of salt concentrations et al. The cultivation of engineered cyanobacteria is proposed to comprise two phases: growth phase and desalination phase.</p>
<p>Tell us about your project, describe what moves you and why this is something important for your team.</p>
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<p>Cyanobateria should grow to reach a high density before beginning to express chloride pump halorhodopsin and absorb salts into the cells. What’s more, inhibition of photosynthetic ATP should be achieved to halt sodium export. Therefore an inducible dark –sensing promoter, is vital to the achievement of biosesalination. Based on an idea of previous iGEM teams, We are modifying the promoter of cpcG2 to obtain a “dark-sensing” promoter. The “dark-sensing” promoter is a combination of the promoter of cpcG2 and a constitutive promoter. Green light induces CpcR to bind to a region of cpcG2, thus inhibiting RNA polymerase binding to the constituve promoter. Therefore darkness will allow the transcription of downstream gene. This is the principle of the “dark-sening” promoter.</p>
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<h5>What should this page contain?</h5>
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<li> A clear and concise description of your project.</li>
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<li>A detailed explanation of why your team chose to work on this particular project.</li>
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<li>References and sources to document your research.</li>
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<li>Use illustrations and other visual resources to explain your project.</li>
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<h4>Advice on writing your Project Description</h4>
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We encourage you to put up a lot of information and content on your wiki, but we also encourage you to include summaries as much as possible. If you think of the sections in your project description as the sections in a publication, you should try to be consist, accurate and unambiguous in your achievements.  
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Judges like to read your wiki and know exactly what you have achieved. This is how you should think about these sections; from the point of view of the judge evaluating you at the end of the year.
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<h4>References</h4>
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<p>iGEM teams are encouraged to record references you use during the course of your research. They should be posted somewhere on your wiki so that judges and other visitors can see how you though about your project and what works inspired you.</p>
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<h4>Inspiration</h4>
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<p>See how other teams have described and presented their projects: </p>
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<li><a href="https://2014.igem.org/Team:Imperial/Project"> Imperial</a></li>
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<li><a href="https://2014.igem.org/Team:UC_Davis/Project_Overview"> UC Davis</a></li>
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<li><a href="https://2014.igem.org/Team:SYSU-Software/Overview">SYSU Software</a></li>
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</ul>
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Revision as of 05:19, 13 July 2015



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This year, we will engineer a recombinant cyanobacteria to achieve “biodesalination”, which means to extract sodium chloride from seawater through biological membranes. There are already some methods to convert saltwater into freshwater, such as distillation and reverse osmosis. However, the high energy consumption of these technologies has limited their application. Therefore the development of an innovative, low-energy biological desalination process, by biological membranes of cyanobacteria, would be very attractive. Many cyanobacteria possess salt-tolerance mechanisms, among which sodium export is the most important one. Halorhodopsin is a light-driven inward-directed chloride pump from halobacteria. We will functionally express it in cyanobacteria to drive influx of chloride together with sodium, thus conferring cyanobacteria the ability to absorb salts to a significant degree.

Cyanobacteria have several characteristics which make them an ideal organism for biodesalination: fast-growing、photoautotrophy、amenable to genetic transformation and able to grow over a wide range of salt concentrations et al. The cultivation of engineered cyanobacteria is proposed to comprise two phases: growth phase and desalination phase.

Cyanobateria should grow to reach a high density before beginning to express chloride pump halorhodopsin and absorb salts into the cells. What’s more, inhibition of photosynthetic ATP should be achieved to halt sodium export. Therefore an inducible dark –sensing promoter, is vital to the achievement of biosesalination. Based on an idea of previous iGEM teams, We are modifying the promoter of cpcG2 to obtain a “dark-sensing” promoter. The “dark-sensing” promoter is a combination of the promoter of cpcG2 and a constitutive promoter. Green light induces CpcR to bind to a region of cpcG2, thus inhibiting RNA polymerase binding to the constituve promoter. Therefore darkness will allow the transcription of downstream gene. This is the principle of the “dark-sening” promoter.