Team:Toulouse/Project/Fungicides

From 2014.igem.org

(Difference between revisions)
Line 94: Line 94:
<p class="legend">Figure 1: Scheme of the fungicide module</p></center>
<p class="legend">Figure 1: Scheme of the fungicide module</p></center>
-
         <p class="textesimple">The main objective of SubtiTree is to ensure the <b> destruction of the pathogenic fungi </b> inside the tree. In order to achieve this goal, we built a genetic module to produce three different peptides with antifungal activities. This triple therapy minimizes the risk of the introduction of a resistance mechanism.</p> <br>
+
         <p class="textesimple">The main objective of SubtiTree is to ensure the <b> destruction of the pathogenic fungi </b> inside the tree. In order to achieve this goal, we built a genetic module to produce three different peptides with antifungal activities. This triple therapy minimizes the risk of resistance.</p> <br>
  <p class="textesimple">Originally from plants, these peptides have different targets to maximize the lethality on <i>C. platani</i>.</p>
  <p class="textesimple">Originally from plants, these peptides have different targets to maximize the lethality on <i>C. platani</i>.</p>
Line 121: Line 121:
<br>
<br>
<p  class="title2">Secretion</p>
<p  class="title2">Secretion</p>
-
<p  class="texte">In order to export the peptides outside the bacteria, the coding sequence of D4E1 and GAFP-1 was flanked on the N-terminal end with a signal peptide (amyE signal peptide) followed by a pro peptide, cleaved during the secretion process.</p><br>
+
<p  class="texte">In order to export the peptides outside the bacteria, the coding sequences of D4E1 and GAFP-1 were flanked on the N-terminal end with a signal peptide (amyE signal peptide) followed by a pro peptide, cleaved during the secretion process.</p><br>

Revision as of 20:30, 16 October 2014