2017.igem.org/Team:Potsdam

No Sidebar - Escape Velocity by HTML5 UP

Eerste titel

Link to the Abstract

Project Description
IGEM-Potsdam 2017

Bringing enzymes closer together for increased reaction efficiency by using DNA scaffolds In fields like biotechnology, synthetic biology and in medical applications it becomes increasingly important to produce more and more complex substrates efficiently. For this reason, a high product yield is always sought after.
A relatively straight forward method to achieve this is a close proximity between cooperating enzymes, this so called metabolic channeling (MC) has already been widely observed in natural processes1 like the proteasome for molecular degradation.
To achieve this artificially, we propose two approaches:

1. MC using dCas9

2. MC by Liquid-liquid-phase separation

The first method centers on the usage of a low copy plasmid and a high copy plasmid.

The low copy plasmid contains coding regions for dCas9, sgRNA-aptamer-fusions and enzyme-RNA-binding-protein-fusions (RBPs corresponding to the aptamers). There will also be a slightly altered version with a direct dCas9-enzyme-fusion and no aptamers or RBPs.
The high copy plasmid contains many repeated target regions for the sgRNAs.
After successful transformation of the plasmids the sgRNA-aptamer-fusions will bind to the scaffold DNA directed by dCas9. The enzymes will then be attached to the aptamers with the connected RBPs. Through this arrangement the enzymes will be immobilized on the scaffold close together which should lead to increased efficiency.
The second method revolves around Liquid-liquid-phase separation, a process naturally occurring in cells2.Through this process, proteins aggregate together to form droplets or membrane-less bodies in the cytoplasm or nucleoplasm. Examples are stress granules or cajal bodies. The formation of droplets has already been studied by attaching YFP fluorescent protein to DDX43, a protein known for aggregation. There are also indicators for this to happen in bacteria4.
To use this mechanism for improvement of enzyme efficiency, the YFP-coding region will be replaced by the coding region of the desired enzymes and expressed in yeast (due to the size of the droplets).

In both approaches we will introduce the auxin pathway and compare auxin output with and without metabolic channeling.


1 Lester J. Reed (1973), Multienzyme Complexes, Clayton Foundation Biochemical Institute and Department of Chemistry, University of Texas at Austin, 40-46
2 Anthony A. Hyman et al. (2014), Liquid-Liquid Phase Separation in Biology, Max Planck Institute of Molecular Cell Biology and Genetics Dresden and Max Planck Institute for the Physics of Complex Systems, Dresden, 39-58
3 Nott et al. (2015), Phase Transition of a Disordered Nuage Protein Generates Environmentally Responsive Membraneless Organelles, Mol. Cell, 57, 936-947 4 Yuan A. H., Hochschild A. (2017).A bacterial global regulator forms a prion. Science355, 198–201
Derde titel