<th><h3><a href="https://2017.igem.org/Team:Cologne-Duesseldorf/Results">Results</h3></th>

               <th><h3>Achieved</h3></th>

               <td>By decorating the peroxisomes with the v-SNARE Snc1 we successfully secreted their entire contents</td>

               <td>With two different sensors we were able to efficiently measure the pH and the redox potential inside our yeast peroxisomes</td>

               <td>Via fluorescence microscopy we verified that the integration of new membrane proteins into the peroxisomal membrane is possible</td>

               <td>By successfully translocating the required enzymes for the metabolic pathways of Nootkatone and Violacein into the peroxisome and actually synthesizing the latter, we developed a proof of concept for our toolbox</td>

               <td>We successfully implemented a way of customizing the size and number of the peroxisomes into our toolbox</td>

               <td>With a high throughput assay we characterized the import efficiency of different PTS2 sequences</td>

               <td>To get a better understanding of possible problems and pitfalls of our metabolic engineering concepts we extensively modeled the whole nootkatone pathway and the benefits of it being translocated inside our compartment</td>

               <td>For our planned optogenetic experiments we designed an affordable lightbox which can easily be assembled in a short time

               <td>All our excellent results can be combined into a highly variable compartment toolbox for designing artificial compartments based on the peroxisomes in <i>S. cerevisiae</i> with an enormous range of applications