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SynBiol-DynHet SIGNED

Diversity in Synthetic Biological Systems

Total Cost €

0

EC-Contrib. €

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Partnership

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Project "SynBiol-DynHet" data sheet

The following table provides information about the project.

Coordinator
LUDWIG-MAXIMILIANS-UNIVERSITAET MUENCHEN 

Organization address
address: GESCHWISTER SCHOLL PLATZ 1
city: MUENCHEN
postcode: 80539
website: www.uni-muenchen.de

contact info
title: n.a.
name: n.a.
surname: n.a.
function: n.a.
email: n.a.
telephone: n.a.
fax: n.a.

 Coordinator Country Germany [DE]
 Total cost 159˙460 €
 EC max contribution 159˙460 € (100%)
 Programme 1. H2020-EU.1.3.2. (Nurturing excellence by means of cross-border and cross-sector mobility)
 Code Call H2020-MSCA-IF-2014
 Funding Scheme MSCA-IF-EF-ST
 Starting year 2015
 Duration (year-month-day) from 2015-09-01   to  2017-08-31

 Partnership

Take a look of project's partnership.

# participants  country  role  EC contrib. [€] 
1    LUDWIG-MAXIMILIANS-UNIVERSITAET MUENCHEN DE (MUENCHEN) coordinator 159˙460.00

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 Project objective

One key problem in the investigation of living systems is their complexity. Synthetic biologists can create artificially designed biological systems, whose design reduces the complexity, and can thus address simplified and specific questions. Theoretical investigations of these systems help to understand these questions, for example by evaluating whether a simple model already predicts the features shown in experiments.

This proposal provides a step towards understanding living systems by theoretically studying diversity in microbial populations. The aim is to investigate both spatial diversity, such as barriers, as well as agents with different traits within a population. This will be done with the goal of answering important ecological as well as microbiological questions. In terms of the ecology, this work will address how spatial barriers, or the presence of diverse agents, can influence the formation of biodiversity and cooperation. In its engagement with microbiology, it will investigate a microbial population's reactions to randomly distributed antibiotic drugs, and the ability to tolerate these antibiotics. With the development of new experimental procedures that allow closer investigations of both these issues, an improved theoretical description is now required alongside such advances.

I will investigate all questions in close collaboration with synthetic biology experiments. This project will allow me to combine my background in the theory of condensed matter and chemistry to work on living systems research, before obtaining an independent researcher position in the field of biological physics.

 Publications

year authors and title journal last update
List of publications.
2017 Marianne Bauer, Isabella R. Graf, Vudtiwat Ngampruetikorn, Greg J. Stephens, Erwin Frey
Exploiting ecology in drug pulse sequences in favour of population reduction
published pages: e1005747, ISSN: 0040-5809, DOI: 10.1371/journal.pcbi.1005747
PLOS Computational Biology 13/9 2019-06-18

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The information about "SYNBIOL-DYNHET" are provided by the European Opendata Portal: CORDIS opendata.

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