Difference between revisions of "Team:Goettingen/Description"

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<h2> Our project </h2>
 
<h2> Our project </h2>
  
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The <b>iGEM team Goettingen 2015</b> is currently developing “<b>Flexosome</b>”  
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The <b>iGEM team Goettingen 2015</b> is currently developing the “<b>Flexosome</b>”.
 
It is our <b>enzymatic penknife</b>: a customizable complex for more efficient and <b>synergistic multi-enzymatic processes</b>. It consists of a <b>scaffoldin, dockerins</b> and  <b>exchangeable enzymes</b>.
 
It is our <b>enzymatic penknife</b>: a customizable complex for more efficient and <b>synergistic multi-enzymatic processes</b>. It consists of a <b>scaffoldin, dockerins</b> and  <b>exchangeable enzymes</b>.
 
The enzymes of interest can be attached to the scaffoldin via the dockerin stations and once attached complete the reactions.
 
The enzymes of interest can be attached to the scaffoldin via the dockerin stations and once attached complete the reactions.
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<h2> The first step</h2>
 
<h2> The first step</h2>
  
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Right now the team is working on a proof of concept. Our first Flexosome will contain <b>phosphatase, esterase</b> and <b>lipase</b> found in metagenomic libraries along with a fluorescent reporter gene. Once our E. coli is able to express and produce this functional Flexosome, this will open the door for more complex and specific applications.
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Right now the team is working on a proof of concept. Our first Flexosome will contain <b>phosphatase, esterase</b> and <b>cellulase</b> found in metagenomic libraries along with RFP, a fluorescent reporter gene. Once our <em>E. coli</em> is able to express and produce this functional Flexosome, this will open the door for more complex and specific applications.
  
 
<h2> The inspiration </h2>
 
<h2> The inspiration </h2>

Revision as of 14:59, 16 September 2015



About our Project

Our project

The iGEM team Goettingen 2015 is currently developing the “Flexosome”. It is our enzymatic penknife: a customizable complex for more efficient and synergistic multi-enzymatic processes. It consists of a scaffoldin, dockerins and exchangeable enzymes. The enzymes of interest can be attached to the scaffoldin via the dockerin stations and once attached complete the reactions.

The first step

Right now the team is working on a proof of concept. Our first Flexosome will contain phosphatase, esterase and cellulase found in metagenomic libraries along with RFP, a fluorescent reporter gene. Once our E. coli is able to express and produce this functional Flexosome, this will open the door for more complex and specific applications.

The inspiration

We studied the natural cellulosome structure, in which different cellulotytic enzymes are assembled into a bigger scaffoldin via dockerin stations, leading to optimized cellulose degradation. The interaction between scaffoldin and dockerins has been proven to be strong and stable, this gave us the ideal platform to design our "Flexosome” device. Traditionally cellulosome engineering is thought for optimization of cellulose degradation, but we don’t have to stop there! A much broader range of enzymes are actively being discovered every year. That is why we intend to combine the scaffoldin protein from cellulolytic bacterium with varying and exchangeable enzymes. The result: a very versatile, stable and innovative tool!

The goal

We want to achieve a protein construct which will be able to ensure a high local concentration of enzymes and catalyse multiple enzymatic processes at one site, making the product of one process the substrate of the next on the scaffoldin. Ultimately, the construct will not only increase efficiency of the reactions but also be fully customisable for any kind of enzymatic process.

References