Don't miss our weekly PhD newsletter | Sign up now Don't miss our weekly PhD newsletter | Sign up now

  *EASTBIO*Structure-function analysis of an adhesin from food-borne E. coli that targets vegetable cell walls


   School of Biology

This project is no longer listed on FindAPhD.com and may not be available.

Click here to search FindAPhD.com for PhD studentship opportunities
  Dr U Schwarz-Linek, Dr N Holden  No more applications being accepted  Competition Funded PhD Project (European/UK Students Only)

About the Project

Background: Our work shows that an adhesin (EcpD) from the food-borne pathogen E. coli O157:H7 targets pectic arabinans in plant cell walls. Although E. coli O157:H7 is primarily found in farmed animals, it can also be transmitted through the food chain in vegetables and so the interaction is important as it represents a specific binding mechanism that cannot occur with animal cells. In nature, EcpD is a surface-expressed protein that requires a chaperone (EcpB, alternatively EcpE) for secretion through the outer membrane of E. coli cells, and when in complex with the main structural protein (EcpA), likely undergoes strand-exchange for polymerization. Based on this information, we have made a series of preliminary constructs to determine the feasibility of protein purification.

Aims & Objectives: The aim of the project is to understand the interaction of EcpD with target arabinans, in order to assess the role it contributes in transmission of E. coli O157:H7 through the food chain. A first objective is to determine the affinity of EcpD for arabinose oligomers and obtain protein structural data. The adhesin is ubiquitous in E. coli isolates and as such a second objective is to carry out a comparative analysis with other EcpD variants to determine how widespread binding is. These objectives will use a combination of biophysical approaches, e.g. isothermal titration calorimetry, surface plasmon resonance, NMR and crystallography, combined with bioinformatics analysis. A third objective is to understand the wider context of E. coli O157:H7 interaction with vegetables in the food chain and the subsequent risks to public health. This part will be carried out with our partner Food Standards Scotland (FSS) reviewing food-borne outbreak and E. coli O157:H7 incidence data.

Training: The supervisors have combined expertise and will provide training in protein science, microbiology, plant cell wall biology for the laboratory work, as well as aspects of bioinformatics. Work with the FSS will involve literature and data surveys and analysis. The work will contribute to reports in this area. Additional training will be provided for translational skills and in bioinformatics, statistical analysis and computational science.


Funding Notes

This project is eligible for the EASTBIO Doctoral Training Partnership: http://www.eastscotbiodtp.ac.uk/

This opportunity is only open to UK nationals (or EU students who have been resident in the UK for 3+ years immediately prior to the programme start date) due to restrictions imposed by the funding body.

Apply by 5.00 pm on 11 December 2017 following the instructions on how to apply at: http://www.eastscotbiodtp.ac.uk/how-apply-0

Informal inquiries to the primary supervisor are very strongly encouraged.


References

Rossez et al., (2014) Escherichia coli common pilus (ECP) targets arabinosyl residues in plant cell walls to mediate adhesion to fresh produce plants. J Biol Chem 289: 34349-34365.
Holden et al., (2015). Plants as alternative hosts for human and animal pathogens. Front. Microbiol. 6. doi: 10.3389/fmicb.2015.00397.
Walden et al. (2015) An internal thioester in a pathogen surface protein mediates covalent host binding eLife 4:e06638 DOI: 10.7554/eLife.06638
Barski et al. (2017) Rift Valley fever phlebovirus NSs protein core domain structure suggests molecular basis for nuclear filaments eLife 6:e29236 DOI: 10.7554/eLife.29236

How good is research at University of St Andrews in Biological Sciences?


Research output data provided by the Research Excellence Framework (REF)

Click here to see the results for all UK universities