Team:Tec-Monterrey/projectmodeling/construct3
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- | 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. | + | 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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