Team:University College London/Module 2/Design

From 2012.igem.org

(Difference between revisions)
(Design)
(Design)
Line 10: Line 10:
'''Requirement 1) Cells must express an adhesive element that allow them to bind to plastics.'''
'''Requirement 1) Cells must express an adhesive element that allow them to bind to plastics.'''
-
Curlis are adherent proteins that allow biofilm formation (Szabó et al. 2005). From the reference papers, curlis expressed bind more readily to plastics at 30˚C than 37˚C, a factor that would be ideal if the system were to be applied to the marine environment.
+
Curlis are adherent proteins that allow biofilm <span class="footnote" title="Curlinonspec">formation</span>. From the reference papers, curlis expressed bind more readily to plastics at 30˚C than 37˚C, a factor that would be ideal if the system were to be applied to the marine environment.

Revision as of 16:23, 9 August 2012

Module 2: Aggregation

Description | Design | Construction | Characterisation | Shear Device | Modelling | Results | Conclusions

Design

Module 2 was designed to meet the following requirements

Requirement 1) Cells must express an adhesive element that allow them to bind to plastics.

Curlis are adherent proteins that allow biofilm formation. From the reference papers, curlis expressed bind more readily to plastics at 30˚C than 37˚C, a factor that would be ideal if the system were to be applied to the marine environment.


Requirement 2) The adhesion system must be compatible with the chassis being used.

Curlis are native to E.Coli, and have been previously deliberately expressed (Chirwa et al. 2003). Furthermore, a curli BioBrick already exist in the Parts Registry (K540000), albeit with a cobalt promoter that will be replaced for the purposes of the project. As curlis have not been expressed before in Roseobacter, this is something we wish to investigate.


Requirement 3) The adhesion system must be compatible with the real world environment that the cells would be expected to be exposed to.

Curlis express favourable at temperatures from 26-30˚C, and during the cellular stationary growth phase (Szabó et al. 2005). These conditions correspond well to the marine environment that we hope to target in our project.