Difference between revisions of "Team:East Chapel Hill"

 
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          <h2>Developing the Fluoride Riboswitch as a Technology to Combat Excess Fluoride in Water</h2>
 
          <h3>East Chapel Hill High School 2017 iGEM Team</h3>
 
 
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          <h2>Developing the Fluoride Riboswitch as a Technology to Combat Excess Fluoride in Water</h2>
 
          <h3>East Chapel Hill High School 2017 iGEM Team</h3>
 
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          <h2>Developing the Fluoride Riboswitch as a Technology to Combat Excess Fluoride in Water</h2>
 
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          <h2>Developing the Fluoride Riboswitch as a Technology to Combat Excess Fluoride in Water</h2>
 
          <h3>East Chapel Hill High School 2017 iGEM Team</h3>
 
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          <h2>Developing the Fluoride Riboswitch as a Technology to Combat Excess Fluoride in Water</h2>
 
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<h1><p2>Improving the Efficacy of Riboswitch Based Sensor for Visual Detection of Fluoride in Water</h1></p2>
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<h1><p2>Improving the Efficacy of Riboswitch Based Sensor for Visual Detection of Excess Fluoride in Water</h1></p2>
 
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<p2> Fluoride, in appropriate quantities, has been recognized as beneficial for protecting tooth enamel from decay. However, a significant problem arises when excess amounts of fluoride infiltrate drinking water. High fluoride concentrations can result in dental fluorosis, which is characterized in children by hypomineralization of the enamel. To address this challenge by efficiently detecting fluoride in water, we aim to develop a fluoride biosensor using previously characterized fluoride riboswitches. Last year, we have developed an operon that, when fluoride binds, activates the riboswitch resulting in transcription of the chloramphenicol acetyltransferase gene. Thus, when fluoride is present, bacterial growth can be observed in the presence of chloramphenicol. However, this system was only able to detect high fluoride concentrations. To improve the efficacy and reduce the detection threshold, we used restriction enzymes to test various promoters and riboswitch sequences. We found that two of the new sequences promoted higher bacterial growth.   
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<p2> Scientists around the world have recognized fluoride as a markedly beneficial resource for protecting tooth enamel from decay. However, excess fluoride can also have an adverse effect on human health. A significant problem arises when excess amounts of fluoride infiltrate drinking water. High fluoride concentrations can have devastating impacts on dental health, especially those of children, and eventually lead to hypomineralization and dental fluorosis.  
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To address this challenge, we aim to first develop an efficient, user-friendly, and cost-sensitive fluoride biosensor using previously characterized fluoride riboswitches. Last year, we developed an operon whose riboswitch was only activated when bound to fluoride. This fluoride-specific activation allowed for selective transcription of the chloramphenicol acetyltransferase (CAT) gene. Bacteria that can express the CAT gene have a resistance to the chloramphenicol antibiotic, and can survive in the presence of chloramphenicol. Consequently, the presence of fluoride allows for bacterial growth in the presence of chloramphenicol. However, this system was not able to detect concentrations low enough to prove useful in realistic applications. This summer, we focused on testing various promoters and riboswitch sequences to reduce the detection threshold and improve the efficacy of our previous operon.   
 
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Latest revision as of 02:27, 18 October 2018

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Improving the Efficacy of Riboswitch Based Sensor for Visual Detection of Excess Fluoride in Water


Scientists around the world have recognized fluoride as a markedly beneficial resource for protecting tooth enamel from decay. However, excess fluoride can also have an adverse effect on human health. A significant problem arises when excess amounts of fluoride infiltrate drinking water. High fluoride concentrations can have devastating impacts on dental health, especially those of children, and eventually lead to hypomineralization and dental fluorosis.

To address this challenge, we aim to first develop an efficient, user-friendly, and cost-sensitive fluoride biosensor using previously characterized fluoride riboswitches. Last year, we developed an operon whose riboswitch was only activated when bound to fluoride. This fluoride-specific activation allowed for selective transcription of the chloramphenicol acetyltransferase (CAT) gene. Bacteria that can express the CAT gene have a resistance to the chloramphenicol antibiotic, and can survive in the presence of chloramphenicol. Consequently, the presence of fluoride allows for bacterial growth in the presence of chloramphenicol. However, this system was not able to detect concentrations low enough to prove useful in realistic applications. This summer, we focused on testing various promoters and riboswitch sequences to reduce the detection threshold and improve the efficacy of our previous operon.