Difference between revisions of "Team:BGU Israel/InterLab"

Line 16: Line 16:
  
  
 +
<div class="container-fluid">
 +
            <div class='row'>
 +
                <div class="col-lg-12 whiteback">
 +
                    <div class="OverviewBox">
 +
                        <div class="row">
 +
                            <div class="col-lg-8">
 +
                                <p class="bigAssHeader">Overview</p>
 +
                                <div class="partOverviewText">
 +
                                    <p>
 +
                                        We have decided to submit 9 new BioBricks this year, which are separated into 2 categories:
 +
                                    </p>
 +
                                    <ol>
 +
                                        <li>
 +
                                            The chassis for our project is based on the <i>Pseudomonas putida</i> bacterium, for its ability to utilize aromatic molecules, mainly focusing on protocatechuate. We have decided to contribute the the iGEM part repository by submitting the genes encoding the enzymes participating in the protocatechuate degradation pathway, in which Protocatechuate, a toxic molecule for most bacteria, is converted to 3-oxoadipate. One of the genes, pcaB, had 4 PstI restriction cut sites and we did not have enough time to introduce silent mutations to the sequence, hence we did not clone and submit it. All 4 other genes were cloned into the pSB1C3 vector and submitted. 
 +
                                        </li>
 +
                                        <li>
 +
                                            Another part of our project involves engineering of the LC-Cutinase protein. We have chosen the LC-Cutinase protein as a target for rational mutagenesis for its PET degrading activity, and using the PROSS algorithm produced 4 mutants.
 +
                                            We have also designed a codon optimized version of the W.T. protein.
 +
                                            We have cloned and submitted all 5 LC-Cutinase variants.
 +
                                        </li>
 +
                                    </ol>
 +
 +
                                </div>
 +
                            </div>
 +
                            <div class="col-lg-4">
 +
                                <img class="partOverviewPic" src="https://static.igem.org/mediawiki/2016/b/b6/BioBrick_overviewBGU.png">
 +
                                <br>
 +
                                <div class='row'>
 +
                                    <div class='col-lg-1'></div>
 +
                                    <div class='col-lg-5'>
 +
                                        <a href="https://2016.igem.org/Team:BGU_ISRAEL/Basic_Part" class="btn btn-primary infobtn" role="button">Basic Parts</a>
 +
                                    </div>
 +
                                    <div class='col-lg-5'>
 +
                                        <a href="https://2016.igem.org/Team:BGU_ISRAEL/ImprovedParts" class="btn btn-primary infobtn" role="button">Improved Parts</a>
 +
                                    </div>
 +
                                </div>
 +
                               
 +
                            </div>
 +
                        </div>
 +
                    </div>
 +
                </div>
 +
            </div>
 +
        </div>
  
  

Revision as of 00:11, 26 July 2018

OriginALS

InterLab

Bronze Medal Criterion #4

Standard Tracks: Participate in the Interlab Measurement Study and/or obtain new, high quality experimental characterization data for an existing BioBrick Part or Device and enter this information on that part's Main Page in the Registry. The part that you are characterizing must NOT be from a 2018 part number range.

For teams participating in the InterLab study, all work must be shown on this page.

Overview

We have decided to submit 9 new BioBricks this year, which are separated into 2 categories:

  1. The chassis for our project is based on the Pseudomonas putida bacterium, for its ability to utilize aromatic molecules, mainly focusing on protocatechuate. We have decided to contribute the the iGEM part repository by submitting the genes encoding the enzymes participating in the protocatechuate degradation pathway, in which Protocatechuate, a toxic molecule for most bacteria, is converted to 3-oxoadipate. One of the genes, pcaB, had 4 PstI restriction cut sites and we did not have enough time to introduce silent mutations to the sequence, hence we did not clone and submit it. All 4 other genes were cloned into the pSB1C3 vector and submitted.
  2. Another part of our project involves engineering of the LC-Cutinase protein. We have chosen the LC-Cutinase protein as a target for rational mutagenesis for its PET degrading activity, and using the PROSS algorithm produced 4 mutants. We have also designed a codon optimized version of the W.T. protein. We have cloned and submitted all 5 LC-Cutinase variants.