Difference between revisions of "Team:Berlin/Project/Strategy"

 
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    <div class="row">       
 
    <div class="row">       
 
      <div class="col-xs-3 submenue-project" style="text-align:left;">
 
      <div class="col-xs-3 submenue-project" style="text-align:left;">
        <a href="https://2015.igem.org/Team:Berlin/Project" class="sub-link-project"> 1.What´s the Problem?</a><br/><br/>
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        <a href="https://2015.igem.org/Team:Berlin/Project" class="sub-link-project"> 1. What's the problem?</a><br/><br/>
      <a href="https://2015.igem.org/Team:Berlin/Project/Activities" class="sub-link-project"> 2. How does it work?</a><br/><br/>
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      <a href="https://2015.igem.org/Team:Berlin/Project/Strategy" class="sub-link-project"> 2. How does it work?</a><br/><br/>
        <a href="https://2015.igem.org/Team:Berlin/Project/Detailed-Description" class="sub-link-project">3. The Wastewater Treatment Plant</a><br/><br/>
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        <a href="https://2015.igem.org/Team:Berlin/Project/Plant" class="sub-link-project">3. The Wastewater Treatment Plant</a><br/><br/>
        <a href="https://2015.igem.org/Team:Berlin/Project/Results" class="sub-link-project">4. Implementation of our Product</a><br/><br/>
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        <a href="https://2015.igem.org/Team:Berlin/Project/Implementation" class="sub-link-project">4. Implementation of our Product</a><br/><br/>
        <a href="https://2015.igem.org/Team:Berlin/Project/Summary" class="sub-link-project">5. Properties of the Enzymatic Flagellulose</a><br/><br/>
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        <a href="https://2015.igem.org/Team:Berlin/Project/property" class="sub-link-project">5. Properties of Enzymatic Flagellulose</a><br/><br/>
        <a href="https://2015.igem.org/Team:Berlin/Project/Journal" class="sub-link-project">6. Results</a><br/><br/>
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        <a href="https://2015.igem.org/Team:Berlin/Project/results" class="sub-link-project">6. Results</a><br/><br/>
     
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<a href="https://2015.igem.org/Team:Berlin/Modeling" class="sub-link-project">7. Modeling</a><br/><br/>
        <br/>
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      <br/>
 
      </div>
 
      </div>
 
 
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      <div class="project-headline-float">
 
      <div class="project-headline-float">
      <h4 class="blue-text project-headline"><font face="Arial,Helvetica">2. How does it work?</h4></font>
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      <h4 class="blue-text project-headline"><FONT FACE="Arial">2. How does it work?</h4></FONT>
 
      </div>
 
      </div>
 
                     <p>
 
                     <p>
<strong>
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Our team is approaching this complex problem by means of synthetic biology using natural  
 
Our team is approaching this complex problem by means of synthetic biology using natural  
 
products produced by microorganisms to design the Enzymatic Flagellulose, a molecular  
 
products produced by microorganisms to design the Enzymatic Flagellulose, a molecular  
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<br/><br/>
 
<br/><br/>
  
The Enzymatic Flagellulose Flagellins from structure to function:<br/>  
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<strong>The Enzymatic Flagellulose Flagellins from structure to function:</strong><br/>  
 
Although flagella are an assembly of multiple proteins, the flagellum filament is mostly made of  
 
Although flagella are an assembly of multiple proteins, the flagellum filament is mostly made of  
 
one single protein called flagellin. Flagellin proteins consist of four domains (D0-D3). While the  
 
one single protein called flagellin. Flagellin proteins consist of four domains (D0-D3). While the  
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sequence to structure. Trends Microbiol. 2006 Apr;14(4):151-5. Epub 2006 Mar 15. PubMed  
 
sequence to structure. Trends Microbiol. 2006 Apr;14(4):151-5. Epub 2006 Mar 15. PubMed  
 
PMID: 16540320).<br/>
 
PMID: 16540320).<br/>
This allows us to modify the D3 domain for our purposes by making use of the Synthetic  
+
This allows us to modify the D3 domain for our purposes by making use of Synthetic  
 
Biology. We designed a flagellin gene (fliC_MCS) with gBLOCKS and introduced specific  
 
Biology. We designed a flagellin gene (fliC_MCS) with gBLOCKS and introduced specific  
 
codons at certain regions of the D3 domain that are supposed to code for the tRNA that will  
 
codons at certain regions of the D3 domain that are supposed to code for the tRNA that will  
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region of the D3 domain instead of a methionine due to the reason that we do not add methionine  
 
region of the D3 domain instead of a methionine due to the reason that we do not add methionine  
 
to the medium, and the bacterium basically is forced to use HPG. Under mild conditions HPG  
 
to the medium, and the bacterium basically is forced to use HPG. Under mild conditions HPG  
then reacts to specifically modified arginine residues that we are going to introduce in our  
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then reacts with the Azide group in the residue of the noncanonical amino acid Azidohomoalanine that we will  introduce specifically to our enzymes. <br/>
enzymes. <br/>
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Below, you will find the detailed reaction of the degradation of PET by the cutinase  
 
Below, you will find the detailed reaction of the degradation of PET by the cutinase  
 
which has been worked out by the iGEM Team University of California in 2012: <br/>
 
which has been worked out by the iGEM Team University of California in 2012: <br/>
 
<img src="https://static.igem.org/mediawiki/2015/f/f6/Degradation_of_PET_by_cutinase_UC-Davis.png"/><br/>
 
<img src="https://static.igem.org/mediawiki/2015/f/f6/Degradation_of_PET_by_cutinase_UC-Davis.png"/><br/>
Fig. 5: Degradation of PET by cutinase https://2012.igem.org/Team:UC_Davis/Project/Catalyst <br/><br/>
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<strong>Fig. 5: Degradation of PET by cutinase <a href="https://2012.igem.org/Team:UC_Davis/Project/Catalyst">2012.igem.org/Team:UC_Davis</a> </strong><br/><br/>
  
As shown here, the PET is degraded into a component which can be transformed into an  
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As shown here, PET is decomposed to a component which can be transformed into an  
intermediate of the citrate cycle and terephthalic acid which’s degradation is still too little known  
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intermediate of the citrate cycle and terephthalic acid which’s degradation is still too little known.<br/><br/>
about.<br/><br/>
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The Cutinase is an α-β enzyme, which has the typical triad structure Ser 120, His 188 and Asp  
 
The Cutinase is an α-β enzyme, which has the typical triad structure Ser 120, His 188 and Asp  
175. So the active side is composed of three amino acids. The active serine is not buried under  
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175. So the active site is composed of three amino acids. The active serine is not buried under  
 
surface loops, so it is accessible to solvents. It is composed of a central β-sheet of five parallel  
 
surface loops, so it is accessible to solvents. It is composed of a central β-sheet of five parallel  
strands  covered by five helixes on either side of the sheet (Martinez et al., 1992, Fusarium  
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strands  covered by five helices on either side of the sheet (Martinez et al., 1992, Fusarium  
 
solani cutinase is a lipolytic enzyme with a catalytic serine accessible to solvent). Cutinases are  
 
solani cutinase is a lipolytic enzyme with a catalytic serine accessible to solvent). Cutinases are  
 
able to hydrolyze the ester-linkage within certain plastics, as Polyethlyeneterephtalate (PET)  
 
able to hydrolyze the ester-linkage within certain plastics, as Polyethlyeneterephtalate (PET)  
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pHs (Faiz et al., 2007, Determination and Characterization of Thermostable Esterolytic Activity  
 
pHs (Faiz et al., 2007, Determination and Characterization of Thermostable Esterolytic Activity  
 
from a Novel Thermophilic Bacterium Anoxybacillus genensis A4). Cutinase is an enzyme that  
 
from a Novel Thermophilic Bacterium Anoxybacillus genensis A4). Cutinase is an enzyme that  
once brought to the periplasmic space a leakage occurs that helps to secrete into extracellular  
+
once brought to the periplasmic space a leakage occurs that helps to secrete into the extracellular  
 
matrix. There are several methods to identify the activity of cutinases. One is to incubate small  
 
matrix. There are several methods to identify the activity of cutinases. One is to incubate small  
 
parts of PET within the enzyme, afterwards an analysis by scanning electron microscopy shows  
 
parts of PET within the enzyme, afterwards an analysis by scanning electron microscopy shows  
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solani ist toxic to E.coli, since our expression is performed in E.coli this cutinase is overruled as  
 
solani ist toxic to E.coli, since our expression is performed in E.coli this cutinase is overruled as  
 
well. We decided to use the LC cutinase 2012, since it works at 25°C as good as at 60°C.
 
well. We decided to use the LC cutinase 2012, since it works at 25°C as good as at 60°C.
 +
<br/><br/>
 +
<h5>The following animation visualizes the concept of our modular filter unit</h5>
 +
<iframe src="//player.vimeo.com/video/142793057?byline=0&amp;portrait=0&amp;color=0ecd28" width="700" height="394" frameborder="0" webkitallowfullscreen mozallowfullscreen allowfullscreen><br/>
 +
This animation was developed by Tobias Rosenberg who is an science interested and very talented graphic designer
 +
          <br/>
 
<p/>
 
<p/>
 
    </div>
 
    </div>

Latest revision as of 18:07, 18 October 2015

2. How does it work?

Our team is approaching this complex problem by means of synthetic biology using natural products produced by microorganisms to design the Enzymatic Flagellulose, a molecular filtering machine.
Our filter consists of a surface made up of cellulose (produced by Acetobacter xylinum) to which bacterial flagella will be immobilized via a cellulose-binding domain. In this case, cellulose itself does not provide any functionality besides acting as a biocompatible carrier. Additionally, it is easy to grow and is a non-plastic material. The single flagellum subunits, also known as flagellin, will be interlinked with plastic degrading enzymes.
Using flagella as a scaffold for enzymes has two major advantages. Firstly, this system enables the creation of a three-dimensional reactive nanostructure that has an increased specific surface with highly catalytic activity. Secondly, flagella may be constructed consisting of various different active sites, which will enable the combination of multiple enzymatic steps in close proximity.



The Enzymatic Flagellulose Flagellins from structure to function:
Although flagella are an assembly of multiple proteins, the flagellum filament is mostly made of one single protein called flagellin. Flagellin proteins consist of four domains (D0-D3). While the D0 and D1 domains are well conserved, the D2 and D3 domains are highly variable in sequence and length (1: Beatson SA, Minamino T, Pallen MJ. Variation in bacterial flagellins: from sequence to structure. Trends Microbiol. 2006 Apr;14(4):151-5. Epub 2006 Mar 15. PubMed PMID: 16540320).
This allows us to modify the D3 domain for our purposes by making use of Synthetic Biology. We designed a flagellin gene (fliC_MCS) with gBLOCKS and introduced specific codons at certain regions of the D3 domain that are supposed to code for the tRNA that will deliver L-Homopropargylglycine (HPG; a non-canonical amino acid). When this gene is introduced into a methionine auxotrophic strain, the bacterium builds in HPG at the certain region of the D3 domain instead of a methionine due to the reason that we do not add methionine to the medium, and the bacterium basically is forced to use HPG. Under mild conditions HPG then reacts with the Azide group in the residue of the noncanonical amino acid Azidohomoalanine that we will introduce specifically to our enzymes.
Below, you will find the detailed reaction of the degradation of PET by the cutinase which has been worked out by the iGEM Team University of California in 2012:

Fig. 5: Degradation of PET by cutinase 2012.igem.org/Team:UC_Davis

As shown here, PET is decomposed to a component which can be transformed into an intermediate of the citrate cycle and terephthalic acid which’s degradation is still too little known.

The Cutinase is an α-β enzyme, which has the typical triad structure Ser 120, His 188 and Asp 175. So the active site is composed of three amino acids. The active serine is not buried under surface loops, so it is accessible to solvents. It is composed of a central β-sheet of five parallel strands covered by five helices on either side of the sheet (Martinez et al., 1992, Fusarium solani cutinase is a lipolytic enzyme with a catalytic serine accessible to solvent). Cutinases are able to hydrolyze the ester-linkage within certain plastics, as Polyethlyeneterephtalate (PET) (C10H804)n.
It could be shown that esterases have a stable pH range from 4,0-8,0, so from acidic to neutral pHs (Faiz et al., 2007, Determination and Characterization of Thermostable Esterolytic Activity from a Novel Thermophilic Bacterium Anoxybacillus genensis A4). Cutinase is an enzyme that once brought to the periplasmic space a leakage occurs that helps to secrete into the extracellular matrix. There are several methods to identify the activity of cutinases. One is to incubate small parts of PET within the enzyme, afterwards an analysis by scanning electron microscopy shows the rising porosity of the plastic. Another way is the p-nitrophenol butyrate (pNPB) assay. pNPB, which is a monomer similar to PET, is degraded. Thereby the absorbance at 405 nm increases. There are different cutinases available for our purpose. Cutinase Hic from Humicola insolens has a temperature optimum at 80°C, which is too high. The cutinase FsC from Fusarium solani ist toxic to E.coli, since our expression is performed in E.coli this cutinase is overruled as well. We decided to use the LC cutinase 2012, since it works at 25°C as good as at 60°C.

The following animation visualizes the concept of our modular filter unit