Team:University College London/Module 2/Results


Module 2: Aggregation

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

Congo Red Agar Assay

We have used a congo red agar assay to determine if our curli BioBrick transformed cells have successfully expressed the amyloid fibrins. Congo red is a diazo dye that binds to the curli fibrins, thereby causing cells positive for curlis to appear red when grown on this agar.

As can be seen from plates below, our cells transformed with BBa_K729017 display a red tinge to their colonies, while the untransformed W3110 cells do not. We hence conclude that we have successfully transformed our cells to produce curlis.

Congo Red Agar Assay
Control (W3110) BBa_K729017
UniversityCollegeLondon Curli Congo Red Control.jpg UniversityCollegeLondon Curli Congo Red K729017.jpg

Shear Force Assay

Using a rotary shear device, we have obtained data relating to the shear resistance of our curliated biofilms. Over a 24 hour period, biofilms were allowed to grow on the surface of plastic discs, which were then subjected to shear forces in the rotary shear device. By finding the critical shear radius, the point at which cells start to detach from the plastic discs, we have calculated the critical shear stresses that our biofilms are capable of resisting.

Based on the results we have obtained, we have determined that the biofilms produced by cells transformed with BBa_K729018 have a two-fold shear resistance when compared to the biofilms of the control cell line W3110. This gives corroborating evidence that our curli BioBrick is functioning as intended, as curli generated biofilms are more resistant to shear forces, and detach less readily.

UniversityCollegeLondon Curli Shear Stress.png