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Team:Braunschweig/Results
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| - | The first step of our experimental procedure was the isolation of the methane-degrading soluble methane monooxygenase from the host organism Methylococcus capsulatus. See here how this worked out! | + | The first step of our experimental procedure was the isolation of the methane-degrading soluble methane monooxygenase from the host organism <i>Methylococcus capsulatus</i>. See here how this worked out! |
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Revision as of 12:15, 17 October 2014
Results
In this year’s iGEM project we, the iGEM Team Braunschweig, fought global warming right at the source - the digestive tract of cows. We developed an approach to reduce the emission of the important greenhouse gas methane using a genetically engineered bacterium - E. cowli.
E. cowli uses the enzyme soluble methane monooxygenase (sMMO) isolated from M. capsulatus. We were not only able to express all subunits of sMMO in soluble form but could also prove the activity of the whole enzyme complex in the heterologous host organism E. coli. However, this was not as trivial as it may sound - proper folding required coexpression of molecular chaperones.
Beside the successful expression and proof of activity we developed a practical application for the designed E. cowli to degrade methane before it gets emitted. This application included the immobilization of E. cowli into an alginate matrix resulting in many beneficial and advantageous effects such as a user-friendly dosage, high cost-efficiency, easy production as well as the biodegradability of the product.
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Cloning and Expression
The first step of our experimental procedure was the isolation of the methane-degrading soluble methane monooxygenase from the host organism Methylococcus capsulatus. See here how this worked out!
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Delivery
In order to make E. cowli accessible for future applications we had to find a way of introducing it into the cow’s rumen where it is supposed to degrade methane. Take a look at our unBEADables here!
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Activity
What use would E. cowli be if the methane-degrading enzyme was not active? To prevent this scenario and show the functionality of the complex we had to perform activity assays with our modified bacterium.
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Interlab Study
Although we are not in the Measurement track we participated in the first international Interlab Study and thus helped to characterize the strength of different promoters in collaboration with teams from all over the world.
