Team:Goettingen/Focus Groups

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Focus Groups

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#1 - Selection / Swimming

In this group it´s all about creating a selection system that enables selecting the E. coli clones that are able to swim the fastest. In an extensive literature search we have collected different swimming media and swimming assays and have evaluated them in regards to our goal. The media can differ in various ways from each other and in our case the most important ones are the Agar concentration and the nutrient content. The agar concentration has to be low enough to make swimming possible but high enough to form a semisolid structure and the nutrient content hast to be as low as possible without inhibiting growth too efficient because the E. coli cells will only start to swim when there are no more nutrients in their current place. The low nutrient content is also necessary to observe whether a directed taxis in dependence of our tested molecule occurs. Through all these different experiments we will be able to set up a selection system that is quick, easy to handle and delivers reproducible results.

#2 - Speed Improvement

In this group we focus on the improvement of E. coli swimming abilities. To achieve this, we chose a set of different genes that might be able to improve the swimming speed of E. coli. The expression levels of these genes are then changed and the modified bacteria are tested on swimming agar plates. Such genes include the master regulator of motility and chemotaxis FlhDC but also genes coding for parts of the bacterial flagellum such as motB. Furthermore, we use different E. coli strains for our experiments to identify differences in motility between these.

#3 - Chemoreceptor Library

In this group, the main focus is to first clone the aspartate receptor TAR from E. coli under different strong constitutive promoters into vectors. After examination of effects overexpressing this chemotaxis receptor, the next challenge is to mutagenize this protein to receive a chemoreceptor library. Ideally, the specificity of the receptor becomes altered due to mutation of the ligand binding sites important for chemical binding.

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+In this group it´s all about creating a selection system that enables selecting the E. coli clones that are able to swim the fastest. In an extensive literature search we have collected different swimming media and swimming assays and have evaluated them in regards to our goal. The media can differ in various ways from each other and in our case the most important ones are the Agar concentration and the nutrient content. The agar concentration has to be low enough to make swimming possible but high enough to form a semisolid structure and the nutrient content hast to be as low as possible without inhibiting growth too efficient because the E. coli cells will only start to swim when there are no more nutrients in their current place. The low nutrient content is also necessary to observe whether a directed taxis in dependence of our tested molecule occurs. Through all these different experiments we will be able to set up a selection system that is quick, easy to handle and delivers reproducible results.
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