Difference between revisions of "Team:Xiamen City/Partnership"

 
Line 184: Line 184:
 
                             <li><p>We will acquire useful patent protection tools for our gene-edited wine yeast, with which
 
                             <li><p>We will acquire useful patent protection tools for our gene-edited wine yeast, with which
 
                                 we may and further values to in commercialization;</p></li>
 
                                 we may and further values to in commercialization;</p></li>
                             <li><p>Commercialization opportunities for team VI Patent, if the partnership succeeds between
+
                             <li><p>Commercialization opportunities for team VIPatent, if the partnership succeeds between
 
                                 us and VIPatent, this model could be proliferated fast to other iGEM teams, enhancing the
 
                                 us and VIPatent, this model could be proliferated fast to other iGEM teams, enhancing the
 
                                 impact of team VIpatent;</p></li>
 
                                 impact of team VIpatent;</p></li>

Latest revision as of 04:20, 19 October 2021

Partnership

Background of Partnership

VIPatent (Shanghai_Metro) is also a 2021 iGEM high school team. They focuses on developing a quick, effective and affordable strain patent protection solution, whose mechanism is designed based on the type IV secretion system (T6SS) of Gram-negative bacteria which would take effects on both eukaryotic cells and bacterial cells. Since our CRISPR-Cas 9-edited wine yeast is of huge commercial values and originally-designed, we consider that it is necessary to protect its patent. After an in-depth communication with the team VIPatent, we found out that their idea would be feasible. Thus, we decided to develop partnership with this wonderful team. We designed a specific partnered experiment plan with team VIPatent together, which is shown as follows:

Overview of VIPatent Project (Strain Patent Protection Principles)

  • Originally-designed plasmids are transformed to E. Coli (DH5a) to realize patent protection;

  • Options of originally-designed plasmids could be Pus232-ike2-tke2 or Pus232-ike4-tke4;

  • Pus232 is extracted from E.Coli; gene ike and tke are extracted from Pseudomonas putida;

  • Gene tke secretes toxin while gene ike produces protein immune to that toxin;

  • The promoter of gene ike is inducible, indicating that only with the induction of a specific ligand, will gene ike be expressed;

  • The promoter of gene tke is constitutive, indicating that its toxic protein expresses at any time.

How to Protect the Patent of our Gene-edited Yeast through Partnership?

  • Extract gene ike-2-tke2 or ike4-tke4 from originally-designed plasmids;

  • Amplify the extracted genes by PCR;

  • Produce homologous recombination template by CRISPR, and then integrate the extracted genes to the genome of our yeast ; (Since the effector of gene tke and immune factor of gene ike are commonly used, it is unnecessary to re-design them)

  • After the gene editing, put our yeast in a certain ligand to realize patent protection.

Mutual Benefits for us and Team VIPatent

  • We will acquire useful patent protection tools for our gene-edited wine yeast, with which we may and further values to in commercialization;

  • Commercialization opportunities for team VIPatent, if the partnership succeeds between us and VIPatent, this model could be proliferated fast to other iGEM teams, enhancing the impact of team VIpatent;

  • Demonstration of iGEM spirit-creating a mutually-beneficial, open, and collaborated platform for synthetic biology and related projects.