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Sample Data

How Our System Works

Our Favorite New Parts

1. [http://partsregistry.org/Part:BBa_K608408 BBa_K608408] GST
2. [http://partsregistry.org/Part:BBa_K608407 BBa_K608407] Precipitator fused with GST tag

The Precipitator is a new artificially designed LRR protein. It is meant as a protein that binds Nickel ions with Histidines grouped on its surface. The bound Nickel can then precipitate His-tagged proteins. In our "Lab in a Cell" it should function as an adaptor between the plastic surface of pipettes and the His-tagged protein. Please look at our detailed description of the design layout in our modeling section. The sequence was synthesised and cloned into the iGEM vector. The submitted sequence was fully confirmed by sequencing.The Precipitator was fused with the C-terminus of our GST tag in order to extract and further test the construct for its Nickel binding affinity. We successfully cloned it together using the Gibson Assembly and then subsequently pasted it into the iGEM vector. The submitted sequence was partially confirmed by sequencing.

3. [http://partsregistry.org/Part:BBa_K608404 BBa_K608404] IPTG-inducible Promoter with plastic binding domain-tagged GFP

Also new parts

[http://partsregistry.org/Part:BBa_K608101 BBa_K608101] CcaR, green light response regulator

[http://partsregistry.org/Part:BBa_K608102 BBa_K608102] CcaS, green light receptor

Pre-existing Parts

[http://partsregistry.org/Part:BBa_K608151 BBa_K608151] translational unit of pcyA

We designed this composite in order to gain the enzyme pcyA (phycocyanobilin-ferredoxin oxidoreductase),
this design is essential if the part is going be integrated into an assembly of various genes.
The enzyme plays an important role in the production of the PCB chromophore (phycocyanobilin)
which is essential for the green and red light receptor system.
Sequencing confirmed that the part is correct in the pSB1C3 vector.
All physical DNA samples used for this composite come from the [http://partsregistry.org/Main_Page registry of standart biological parts]
For PCB chromophore production the enzyme ho1 (heme oxygenase) in a similar design is needed
because both enzymes are necessary to convert heme into PCB chromophore.

We've Also Characterized the Following Parts

[http://partsregistry.org/Part:BBa_K608351 BBa_K608351] correct temperatursesitive promotor

[http://partsregistry.org/Part:BBa_K608352 BBa_K608352] Bacteriophage Lysis Cassette with RBS

[http://partsregistry.org/Part:BBa_K608002 BBa_K608002] strong Promotor and strong RBS

[http://partsregistry.org/Part:BBa_K608003 BBa_K608003] strong Promotor , medium RBS

[http://partsregistry.org/Part:BBa_K608004 BBa_K608004] strong Promotor , weak RBS

[http://partsregistry.org/Part:BBa_K608005 BBa_K608005] medium Promotor , strong RBS

[http://partsregistry.org/Part:BBa_K608006 BBa_K608006] medium Promotor , medium RBS

[http://partsregistry.org/Part:BBa_K608007 BBa_K608007] medium Promotor , weak RBS

Precipitator

Green light receptor

Lysis cassette

The Concept

The idea behind our lysis cassette was to be able to achieve cell lysis by simply heating the bacteria to 42°C for a short period of time. This was accomplished by combining the biobricks BBa_K098995 (temperature sensitive promoter) and BBa_K124017 (Bacteriophage λ lysis genes). Sequencing of these parts (carried out by GATC Biotech GmbH) showed some fundamental inconsistencies leading to a lot of time spent on fixing them. Currently we are still in the process of correcting the sequences. Therefore the whole planned lysis cassette was not yet sent to the registry.

Part Design

The temperature sensitive promoter ([http://partsregistry.org/Part:BBa_K608351 BBa_K608351])

The bacteriophage λ lysis genes ([http://partsregistry.org/Part:BBa_K608352 BBa_K608352])

Bacteriophage λ lysis genes at work

The temperature sensitive lysis cassette

The much anticipated part that we frustratingly could not clone in time to send to the registry.

Theoretically 28°C - 30°C incubation should repress the lysis genes, while a shift to 42°C would lead to their expression and finally cell lysis.

[File:Freiburg11_LysisCassetteODmeasurement.jpg|900px]

frame|caption|The lysis genes seem to work as expected, though the preliminary results hint that the temperature sensitive promoter might be quite leaky at 30°C. More testing is necessary to be able to propose the exact functionality of the]