GRK  2062 "Molecular Principles of Synthetic Biology"
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Area A: Synthetic Cells and Switches

Research Area A aims at the generation of synthetic cells and synthetic switches.

PojectPIsTopic
A1 Mascher SporoBeads - functionalized B. subtilis endospores for protein display
A2 Leister Introduction of a functional plant photosystem I in a prokaryotic chassis
A3 Simmel Dynamics of synthetic gene circuits in vitro and in vivo
A4 Broedersz Physical principles of DNA organization by interacting nucleoid-associated proteins
A5 Papenfort Synthetic small RNA regulators for tailored gene expression in bacteria

A1 SporoBeads - functionalized B. subtilis endospores for protein display

Studies in expand a very successful iGEM-project and comprise the development of endospores as functionalized biological beads for stably displaying proteins on their surface. SporoBeads could be used in project A2 to optimize some of the proteins involved in photosynthesis. In addition, SporoBeads could be applied in some projects of Area B for the immobilization and/or in vitro chemical modification of synthetic proteins and protein units.

A2 Introduction of a functional plant photosystem I in a prokaryotic chassis

Complex eukaryotes like plants are not accessible to genetic engineering. Therefore, project A2 aims to contribute to a new paradigm in the genetic engineering of plants by outsourcing a complex plant process to a model prokaryote.

A3 Dynamics of synthetic gene circuits in vitro and in vivo

Project A3 aims at the development of synthetic RNA-based regulatory circuits and their quantitative characterization. The circuits will be based on rationally designed riboregulators and the CRISPR interference mechanism. In order to obtain a good quantitative understanding of the regulatory modules and enable further engineering, their performance will be analyzed and compared in quantitative gene expression studies both in bacteria and in a cell-free setting.

A4 Physical principles of DNA organization by interacting nucleoid-associated proteins

Bacteria employ an array of nucleoid associated proteins, which collectively organize chromosome architecture by binding to the DNA in large numbers. This organization depends on how these nucleoid associated protein physically interact with each other and with DNA. We develop theoretical and computational frameworks to study the basic design principles of how nucleoid associated proteins localize on specific regions of the DNA, organize the bacterial chromosome in 3D, and can control DNA functions such as gene activity.

A5 Synthetic small RNA regulators for tailored gene expression in bacteria

RNA is common to all living organisms. Despite its major function as the coding agent for protein synthesis, an increasing number of regulatory roles have been assigned to RNA in prokaryotic and eukaryotic organisms. The natural versatility and the modular architecture of regulatory RNAs make them ideal substrates for bioengineering purposes. In this project, we develop artificial RNA regulators for specific regulatory tasks in bacteria.


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