Team:Tec-Monterrey/projectmodeling/construct3
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<h2>PROJECT</h2> | <h2>PROJECT</h2> | ||
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- | + | <p><a href="https://2011.igem.org/Team:Tec-Monterrey/projectoverview">overview</a></p> | |
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<p><a href="https://2011.igem.org/Team:Tec-Monterrey/projectparts">parts</a></p> | <p><a href="https://2011.igem.org/Team:Tec-Monterrey/projectparts">parts</a></p> | ||
<p><a href="https://2011.igem.org/Team:Tec-Monterrey/projectmodeling">genetic frame</a></p> | <p><a href="https://2011.igem.org/Team:Tec-Monterrey/projectmodeling">genetic frame</a></p> | ||
- | <p><a href="https://2011.igem.org/Team:Tec-Monterrey/ | + | <p><a href="https://2011.igem.org/Team:Tec-Monterrey/projectresults/methods">methods</a></p> |
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<p><a href="https://2011.igem.org/Team:Tec-Monterrey/projectresults">results</a></p> | <p><a href="https://2011.igem.org/Team:Tec-Monterrey/projectresults">results</a></p> | ||
+ | <p><a href="https://2011.igem.org/Team:Tec-Monterrey/teamha">human approach</a></p> | ||
<p><a href="https://2011.igem.org/Team:Tec-Monterrey/projectprotocols">protocols</a><p> | <p><a href="https://2011.igem.org/Team:Tec-Monterrey/projectprotocols">protocols</a><p> | ||
+ | <p><a href="https://2011.igem.org/Team:Tec-Monterrey/safetypage">safety</a></p> | ||
+ | <p><a href="https://2011.igem.org/Team:Tec-Monterrey/projectnotebook">notebook</a></p> | ||
<p><a href="https://2011.igem.org/Team:Tec-Monterrey/sampledata">sample data</a></p> | <p><a href="https://2011.igem.org/Team:Tec-Monterrey/sampledata">sample data</a></p> | ||
</div> | </div> | ||
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<p class="textojustif"> | <p class="textojustif"> | ||
- | Our third | + | Our third construct ompA+sacC has the same promoter as the last two (P<sub>BAD</sub> promoter, <a href="http://partsregistry.org/Part:BBa_K206000">BBa_K206000</a>, and its repressor protein araC, <a href="http://partsregistry.org/Part:BBa_I13458">BBa_I13458</a>) We decided to use an already reported part, membrane protein ompA and a signal peptide of lpp (<a href="http://partsregistry.org/Part:BBa_K103006">BBa_K103006</a>). We decided to try out our extracellular invertase “sacC” (<a href="http://partsregistry.org/Part:BBa_K633003">BBa_K633003</a>) cloned out of <i>Zymmomonas Mobilis</i> in our university. The importance behind this part is that it’s a monomeric enzyme, able to produce both glucose and fructose from sucrose, an important approach for inverted sugar. |
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- | Kyono | + | |
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+ | <center><img src="https://static.igem.org/mediawiki/2011/6/66/Referencesimg.png" alt="" name="" width="200" height="50" id="tgo"></center> | ||
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+ | <p class="textojustif"> | ||
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+ | Kyono K, Yanase H, Tonomura K, Kawasaki H and Sakai T. (1995) Cloning and characterization of <i>Zymomonas mobilis</i> genes encoding extracellular levansucrase and invertase. Biosci Biotechnol Biochem. Vol 59 (2):289-293 | ||
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- | Kannan | + | Kannan R, Mukundan G, Ait-Abdelkader N, Augier-Magro V, Baratti J and Gunasekaran P. (1995) Molecular cloning and characterization of the extracellular sucrose gene (sacC) of <i>Zymomonas mobilis</i>” Arch. Microbiol. Vol 163(3):195-204 |
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