Monday, April 6, 2015

Check Out Our Microbe's Moves: An Analysis of Our Soil Microbe's Motility

This past week in lab, Austin and I discovered another feature about our little microbe. We used the soft agar deep test to determine if our microbe is motile or not. For the experiment, we used a motile control (E. coli) and an immotile control (S. aureus). However, the E. coli sample did not behave properly because the results indicated that the sample was immotile, which is not true. As seen in the picture below, our microbe was very motile and moved all throughout the agar, which was determined by the cloudiness of the sample. A thick layer of microbes also developed on top of the agar.
Soft agar deep test results
So what makes bacteria motile or immotile? The main structural feature that allows microbes to be motile is the presence of flagella, which can vary in number and arrangement. As we studied in cell and molecular biology, flagella are anchored to cells by a hook that attaches to the basal body. A rotary motor unit does the actual whipping of the tale and can vary in speeds from 200 to 1000 revolutions per second, which is crazy fast!
There are advantages for microbes to evolve to be motile. The presence of flagella allows bacteria to swim towards nutrients and dodge harmful substances. They can also swim to new areas and colonize. Many bacteria are motile, however, some bacteria are immotile and have evolved to stay that way. A reason for remaining immotile is dependent on the types of fluid the bacteria travel through. Flagella are not useful when moving through viscous media and microbes that live in these environments do not want to be motile.

Each week in lab, we are continuously getting closer to identifying our microbe. To ensure the accuracy of our endospore verification test from last week's lab, we reran the experiment. The results ended up being the same but this time the controls produced the expected results. Below is a new picture of our endospore results.
Results from endospore verification redo
Hopefully next week, we will be able to narrow down the possible identifications of our microbe.
Check back next week for an update from Mills!
-Anne



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