Team:Newcastle University

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Newcastle University

GOLD MEDAL WINNER 2008

Home Team Original Aims Software Modelling Proof of Concept Brick Wet Lab Conclusions


Welcome! This year is Newcastle's first year participating in the iGEM competition! We are a small team of six students, three supervisors, and seven advisors, but we had high ambitions for our first year. Recognizing the problem of antibiotic-resistant bacteria and poor methods of diagnosis in developing countries, we aim to use synthetic biology and bioinformatics to engineer a simple, safe, fast, and reliable biological diagnostic system to identify bacteria.


Overview

We aimed to develop a diagnostic biosensor for detecting pathogens. We wanted this to be cheaply and readily available for deployment in areas with limited medical resources such as refrigeration and sophisticated laboratories. We chose to use Bacillus subtilis as a method of delivery due to its ability to sporulate. The sensor bacteria could then be dried down as spores, which are extremely resilient to environmental conditions, and then could be rehydrated when required.

Gram-positive bacteria communicate using quorum communication peptides. Research has shown that they are extremely strain-specific. We chose to engineer a Bacillus 168 to detect four Gram-positive pathogens through their quorum communication peptides. The output of the system is followed by analysing expression of fluorescent proteins such as mCherry, GFP, CFP and YFP.

Mapping multiple inputs to three output states is a multiplexing problem. The design of the genetic circuitry to do this is non-trivial and is not feasible manually. We therefore chose to use a biological implementation of an artificial neural network (ANN). Our team members wrote designed and implemented a complete suite of tools that allowed the design and simulation of regulatory networks. An essential part of the approach was the use of computational evolution to design circuits with predictable behaviour even when the details of the required topology are unknown in advance. We used the modelling language CellML because of its ability to easily model virtual parts that can be easily assembled into a circuit which can be simulated. We aimed to translate this model into a sequence that could be implemented as BioBricks.

Learn more about our project

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Conceptual overview of the implementation of an ANN in a bacterium.


Achievements

  • We designed and submitted a [http://partsregistry.org/Part:BBa_K104001 working standard BioBrick] for sensing the quorum communication peptide subtilin, that works as expected.
  • Sent information and developed a B. subtilis website to help the Cambridge University team.
  • Developed and documented a new technical standard using CellML for the modelling and simulation of BioBrick parts

Sponsors