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Team:Bielefeld-Germany/Project/Appoach
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|T7 promoter region | |T7 promoter region | ||
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|His-Tag-sequence | |His-Tag-sequence | ||
| - | | | + | |Mating factor alpha 1 |
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| - | | | + | |Chloramphenicol resistance |
| - | | | + | |Histidine auxotrophic complementation |
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Revision as of 19:46, 24 September 2012
Contents |
The conventional methods of sewage treatment plants to take care of waste water are insufficient. This is, because the most common micro contaminants like synthetic estrogen, Bisphenol A, Dicolfenac etc. are very difficult to break down.
The goal of Bielefeld’s iGEM team is to develop a biological filter-system using immobilized laccases to purify municipal and industrial waste water from these synthetic estrogens and other aromatic compounds. Laccases are copper-containing oxidase enzymes found in many organisms. One of their properties is the ability to break down a wide range of aromatic and phenolic compounds. For this purpose, genes of various bacterial and eukaryotic laccases will be isolated and expressed in Escherichia coli and Pichia pastoris. The choice of the expression-system depends on the glycosylation status of the enzyme.
Isolation and generating of new BioBricks
The first step of our project is to isolate the specific gene sequences and to generate new BioBricks for the iGEM competition. The laccases of the following organisms are isolated:
bacterial laccases:
- Escherichia coli
- Bacillus halodurans
- Bacillus pumilus
- Streptomyces griseus
- Streptomyces lavendulae
- Thermus thermophilus
- Xanthomonas campestris
Eukaryota laccases:
- Arabidopsis thaliana
- Trametes versicolor
- Trametes villosa
For more information about the organisms click here.
The additional and essential BioBricks and characteristics, which are used to design our functional plasmids and a new shuttle-vector-system are shown in the following table:
Parts of the E. coli expression vector and the P. pastoris shuttle vector
| Plasmid characteristics | Shuttle vector characteristics |
|---|---|
| T7 promoter region | AOX1 promoter |
| His-Tag-sequence | Mating factor alpha 1 |
| Chloramphenicol resistance | Histidine auxotrophic complementation |
Which expression system is used is determined by the folding and glycosylation of the individual laccase. The resulting genetically modified organisms produce the laccases for our approach. Further down the line, these laccases are isolated and purified.
Determining activity and potential of the different laccases
| The next step to generate a efficient filter system is to characterize the purified laccases. To identify the potential of a laccase, the enzyme is examined on its activity and potential to degrade several substances. The degradation potential of the manufactured laccases is investigated for representative substances from different chemical areas, such as analgetics, endocrine substances, pesticides, poly aromatic hydrocarbons and bleaching agents.
In this case we analyze the specific laccase at its efficiency of degradation at different parameters like temperature, pH, and buffer-systems. A great concern of our team is to guarantee the safety of the generated filter system. Besides the degradation potential, a very important aspect to us is the analysis of the degraded substances, to make sure that the degradation result of the individual laccase does not generate toxic or dangerous substances. This is realized by HPLC-massspectorscopy. With this knowledge we want to identify the laccase which shows the highest potential for a safe and highly-functional filter system. |  |
Immobilization and the final development of the filter
The last step to realize our project is to immobilize the produced lacasses with the highest potentials. To generate a filter-system with a high yield of active and immobilized enzymes, different approaches are tested. On the one hand we try to immobilize the enzymes with a chemical immobilization protocol to bind the laccases covalently on specific silica-beads, and on the other hand we try to generate a natural immobilization protocol by fusing the laccases to natural binding domains, such as the cellulose-binding-domain, the keratin-binding-domain or the chitin-binding-domain. By generating the new natural immobilization protocol three different cellulose-binding-domains of the organisms Cellulomonas fimi, Clostridium josui and Clostridium cellulovorans are inverstigated. At first the binding-domains are linked to GFP (Green fluorescent Protein) to examine the strength of the bonding and the binding-capacity. In the end the domains will be connected to the lacasses.
The goal of the iGEM-Team Bielefeld is to generate a functional filter system with a high efficiency to degrade a high number of different micro contaminants. This filter system will be able to reduce the environmental pollution and improve the quality of the waterbody for the safety of animals and mankind.
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