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Team:BIT/project biosensors
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| + | <table width="824" border="0" class="bg3"> | ||
| + | <tr> | ||
| + | <td width="608" class="t1">Biosensors</td> | ||
| + | </tr> | ||
| + | |||
| + | <tr> | ||
| + | <td class="t2"><strong>Background</strong></td> | ||
| + | </tr> | ||
| + | <tr> | ||
| + | <td class="t2"> In order to prevent cow mastitis, all the producers of diary products feed the cows with antibiotics. However, excessive residual antibiotics will increase the drug resistance on human body. According to international standards for antibiotics, most dairy farmers use beta-lactams, such as penicillin deviants and cephalosporin which exceed quality standards on their cows. The beta-lactam biosensor is designed for the detection of beta-lactam in dairy products.<br/> | ||
| + | Beta-lactam biosensor is aimed to create a biosensor that can be applied in practical life. It is useful for citizens to know what they drink and what they buy for their little babies are qualified and hygienic. While there are traditional methods to detect beta-lactam antibiotics, such as enzyme-linked immunosorbent assay (ELISA) and ECLIPSE50, all these methods have to rely on laboratories which are equipped with precise instruments. In order to solve the problem, our Beta-lactam biosensor is designed to be used on on-site detection in a few hours by users without special training. | ||
| + | </td> | ||
| + | </tr> | ||
| + | <tr> | ||
| + | <td class="t2"><strong>Device</strong></td> | ||
| + | </tr> | ||
| + | <tr> | ||
| + | <td class="t2"> Beta-Lactam antibiotics have become less effective for the treatment of staphylococcal infections as a result of the bacteria's resistance to Beta-Lactam increases sharply during the past few years. Researches have shown that the resistance is mediated by beta-lactamase (encoded by blaZ) that hydrolyzes penicillin whose transcription is regulated by related regulators (encoded by blaI). The purified repressor(BlaI) of beta-lactamase production has been shown to bind specifically to two regions of dyad symmetry, known as operators, which are located between the divergently transcribed beta-lactamase structural gene(blaZ) and the gene(blaR1) encoding the putative transmembrane sensor protein.<br/> | ||
| + | The bla operon has been found that is induced by beta-lactam.<br> | ||
| + | Hypothesis identified bla as a beta-lactam-sensing operon of beta-lactamase expression, so we designed two devices working in E.coli (DH5α) to build the beta-lactam biosensor.<br> | ||
| + | </td> | ||
| + | </tr> | ||
| + | <tr> | ||
| + | <td class="t3"><img src=" https://static.igem.org/mediawiki/2013/8/8a/BITbeta-lactam_device1.jpg" width="600" height="457"> | ||
| + | </td> | ||
| + | </tr> | ||
| + | <tr> | ||
| + | <td class="t4">Device 1 | ||
| + | </td> | ||
| + | </tr> | ||
| + | <tr> | ||
| + | <td class="t2"> This device will work to detect the concentration of Beta-Lactam in dairy products. At the same time, we designed another two devices to decrease the detection limit. | ||
| + | </td> | ||
| + | </tr> | ||
| + | <tr> | ||
| + | <td class="t3"><img src="https://static.igem.org/mediawiki/2013/8/81/BITbeta-lactam_device2.jpg" width="675" height="500"> | ||
| + | </td> | ||
| + | </tr> | ||
| + | <tr> | ||
| + | <td class="t4">Device 2 | ||
| + | </td> | ||
| + | </tr> | ||
| - | + | <tr> | |
| - | + | <td width="608" class="t1">Tetracycline Detection </td> | |
| - | + | </tr> | |
| - | + | ||
| - | + | <tr> | |
| - | + | <td class="t2"><strong>Device</strong></td> | |
| - | + | </tr> | |
| - | + | <tr> | |
| - | + | <td class="t2"> Our project is centered on creating a working toggle switch which changes between two different states when chemicals are added. We started with a simple switch that utilizes two inhibitor proteins, LacI and TetR, which bind to sites on the pLac and pTet promoters, respectively. When bound to the promoter, it would not start transcription and produce the green protein. However, certain chemicals (tetracycline and IPTG) will prevent the inhibitor from binding to their respective promoters. So, the promoters are unlocked and the green fluorescence protein is produced. | |
| - | + | </td> | |
| - | + | </tr> | |
| - | + | <tr> | |
| - | + | <td class="t3"><img src="https://static.igem.org/mediawiki/2013/8/81/BIT_T1.png" width="600" height="300"> | |
| - | + | </td> | |
| - | + | </tr> | |
| - | + | <tr> | |
| - | + | <td class="t2"> When there is no tetracycline, the pTet promoter is locked, which means no fluorescence will be produced. | |
| - | + | </td> | |
| - | + | </tr> | |
| - | + | <tr> | |
| - | + | <td class="t3"><img src="https://static.igem.org/mediawiki/2013/7/7f/BIT_T2.png" width="600" height="300"> | |
| + | </td> | ||
| + | </tr> | ||
| + | <tr> | ||
| + | <td class="t2"> However, when tetracycline and IPTG are added, the TetR protein combines with the tetracycline. At the same time, the pTet promoter transcripts the the T7polymerase, which binds to the T7 promoter. Because IPTG has activated the LacI, the green fluorescence protein will be produced. Moreover, as the concentration of tetracycline is increasing, the intensity of the fluorescence will increase spontaneously. </td> | ||
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| + | <td width="110"> </td> | ||
| + | <td width="790">Beijing Institute of Technology | 5 South Zhongguancun Street, Haidian DistrictBeijing, China 100081 </td> | ||
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| + | </tr> | ||
| + | <tr> | ||
| + | <td> </td> | ||
| + | <td> E-mail: yifei0114@bit.edu.cn</td> | ||
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| + | <td>Beijing Institute of Technology © 2013<a id="d1" href="http://english.bit.edu.cn/"> Privacy Policy</a></td> | ||
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Revision as of 13:55, 18 September 2013
| Biosensors |
| Background |
| In order to prevent cow mastitis, all the producers of diary products feed the cows with antibiotics. However, excessive residual antibiotics will increase the drug resistance on human body. According to international standards for antibiotics, most dairy farmers use beta-lactams, such as penicillin deviants and cephalosporin which exceed quality standards on their cows. The beta-lactam biosensor is designed for the detection of beta-lactam in dairy products. Beta-lactam biosensor is aimed to create a biosensor that can be applied in practical life. It is useful for citizens to know what they drink and what they buy for their little babies are qualified and hygienic. While there are traditional methods to detect beta-lactam antibiotics, such as enzyme-linked immunosorbent assay (ELISA) and ECLIPSE50, all these methods have to rely on laboratories which are equipped with precise instruments. In order to solve the problem, our Beta-lactam biosensor is designed to be used on on-site detection in a few hours by users without special training. |
| Device |
| Beta-Lactam antibiotics have become less effective for the treatment of staphylococcal infections as a result of the bacteria's resistance to Beta-Lactam increases sharply during the past few years. Researches have shown that the resistance is mediated by beta-lactamase (encoded by blaZ) that hydrolyzes penicillin whose transcription is regulated by related regulators (encoded by blaI). The purified repressor(BlaI) of beta-lactamase production has been shown to bind specifically to two regions of dyad symmetry, known as operators, which are located between the divergently transcribed beta-lactamase structural gene(blaZ) and the gene(blaR1) encoding the putative transmembrane sensor protein. The bla operon has been found that is induced by beta-lactam. Hypothesis identified bla as a beta-lactam-sensing operon of beta-lactamase expression, so we designed two devices working in E.coli (DH5α) to build the beta-lactam biosensor. |
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| Device 1 |
| This device will work to detect the concentration of Beta-Lactam in dairy products. At the same time, we designed another two devices to decrease the detection limit. |
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| Device 2 |
| Tetracycline Detection |
| Device |
| Our project is centered on creating a working toggle switch which changes between two different states when chemicals are added. We started with a simple switch that utilizes two inhibitor proteins, LacI and TetR, which bind to sites on the pLac and pTet promoters, respectively. When bound to the promoter, it would not start transcription and produce the green protein. However, certain chemicals (tetracycline and IPTG) will prevent the inhibitor from binding to their respective promoters. So, the promoters are unlocked and the green fluorescence protein is produced. |
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| When there is no tetracycline, the pTet promoter is locked, which means no fluorescence will be produced. |
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| However, when tetracycline and IPTG are added, the TetR protein combines with the tetracycline. At the same time, the pTet promoter transcripts the the T7polymerase, which binds to the T7 promoter. Because IPTG has activated the LacI, the green fluorescence protein will be produced. Moreover, as the concentration of tetracycline is increasing, the intensity of the fluorescence will increase spontaneously. |
