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| {{:Team:FHS_Frederick_MD/Header}} | | {{:Team:FHS_Frederick_MD/Header}} |
- | | + | =Overview= |
- | <!-- *** What falls between these lines is the Alert Box! You can remove it from your pages once you have read and understood the alert ***
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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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- | <li>a team description</li>
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- | <li>project description</li>
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- | <li>safety information (did your team take a safety training course? were you supervised in the lab?)</li>
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- | <li>team attribution (who did what part of your project?)</li>
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- | ===Team===
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| [[File:Tshirts.jpg|right|500px]] | | [[File:Tshirts.jpg|right|500px]] |
- | We are interested in creating a microbial fuel cell that utilizes anaerobic bacteria to produce electricity. In order to optimize the growth conditions in the fuel cell, a fluorescent protein marker will be added so to visualize bacterial growth. We plan to implement an oxygen-sensitive promoter to induce expression of the glowing gene. This should ensure that bacteria only grow under anaerobic conditions. This would lead to the creation of a genetic construct that can be deposited back into the “toolbox” parts repository for iGEM. | + | We are interested in creating a [[Team:FHS_Frederick_MD/Microbial_Fuel_Cells|microbial fuel cell]] that utilizes the facultative anaerobic bacteria, ''Shewanella oneidensis'', to produce [[Team:FHS_Frederick_MD/Renewable_Energy|renewable energy]] and [[Team:FHS_Frederick_MD/Clean_Water|clean water]]. |
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- | ===Goals===
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- | ===Gene Design===
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- | (Kyle and Jonathon, briefly summarize how NirB and LOV work together.)
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- | ===Methods===
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- | (This is Dillon's domain.)
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- | ====3A Assembly====
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- | We used the 3A, or 3 antibody, assembly kit in order to transform E.coli with two genes, the LOV gene and the NirB gene. These genes will allow for further work with Schwenella bacteria in the anaerobic microbial fuel cell. We then used the mini-prep components of the kit to purify our plasmid. We verified the plasmid's presence through electrophoresis and further sequence analysis.
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- | ===Results/Conclusions===
| + | In order to optimize the growth conditions in the anaerobic chamber of the fuel cell, a fluorescent protein marker will be added so to visualize bacterial growth under different conditions. |
- | What did you achieve over the course of your semester?
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| + | We plan to accomplish this using the [[Team:FHS_Frederick_MD/NirB_Promoter|NirB oxygen-sensitive promoter]] to induce expression of the glowing gene only when oxygen is scarce. Furthermore, we must engineer a fluorescent [[Team:FHS_Frederick_MD/LOV_Domain|LOV domain]], which is optimized for expression in ''S. oneidensis'' and capable of fluorescence under anaerobic conditions. |
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- | ===Sponsors===
| + | This genetic construct will help us ensure that the bacteria are actually growing under anaerobic conditions. This would lead to the creation of a BioBrick that can be deposited back into the “toolbox” parts repository for future iGEM teams. |
- | {| cellpadding="20"
| + | {{:Team:FHS_Frederick_MD/Footer}} |
- | |width="30%"| [[File:NEB_Logo.jpg|link=http://neb.com|175px]]
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- | |width="30%"| [[File:BNBL_Logo.jpg|link=http://bnbi.org|175px]]
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- | |width="30%"| [[File:ABT_Logo.jpg|link=http://arsbiotechnica.org|175px]]
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- | |-
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- | |style="vertical-align:top;"| [http://neb.org New England Biolabs] provided our team with many of the enzymes and reagents we needed to for this project.
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- | |style="vertical-align:top;"| [http://bnbi.org The Battelle National Biodefense Institute] helped cover our iGEM registration costs.
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- | |style="vertical-align:top;"| [http://arsbiotechnica.org Ars Biotechnica] is a nonprofit profit organization established by our mentors to help Frederick and other high schools build and maintain synthetic biology labs.
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- | |}
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Overview
We are interested in creating a microbial fuel cell that utilizes the facultative anaerobic bacteria, Shewanella oneidensis, to produce renewable energy and clean water.
In order to optimize the growth conditions in the anaerobic chamber of the fuel cell, a fluorescent protein marker will be added so to visualize bacterial growth under different conditions.
We plan to accomplish this using the NirB oxygen-sensitive promoter to induce expression of the glowing gene only when oxygen is scarce. Furthermore, we must engineer a fluorescent LOV domain, which is optimized for expression in S. oneidensis and capable of fluorescence under anaerobic conditions.
This genetic construct will help us ensure that the bacteria are actually growing under anaerobic conditions. This would lead to the creation of a BioBrick that can be deposited back into the “toolbox” parts repository for future iGEM teams.
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