As part of our chasis characterisation process, we have decided to model B. subtilis motility. In order to do this, the approach illustrated below was taken. The first phase of modelling involved data collection using microscopy techniques and cell tracking. Collected data was then analysed using algorithms which enabled us to extract distributions of parameters as defined in our model.
Materials
We used the Zeiss Axiovert 200 inverted microscope and Improvision Volocity acquisition software. This system offers a full incubation chamber with temperature control and a highly sensitive 1300x1000 pixel camera for fast low-light imaging. Video images are captured into memory by the system at a basal video frame rate of 16.3Hz. This can be further increased to 27.9Hz by performing x4 binning.
A short video of swimming B. subtilis is shown:
Method
In order to choose suitable tracking software, we generated a synthetic video and applied tracking algorithms to the data. We then assessed the reliability, validity and errors associated with the various tracking methods. We chose manual tracking as our method of tracking due to its high reliability and acceptable error.
[http://openwetware.org/wiki/IGEM:IMPERIAL/2008/New/Motility/Validation >>> Details >>>]
We manually tracked motile B. subtilis, obtaining two-dimensional coordinate data points which describes by the trajectory of the cells. The open source tracking software can be found [http://rsbweb.nih.gov/ij/plugins/track/track.html here].
The coordinate data obtained was then fed into algorithms to model cell trajectory and motility. Algorithms used to extract motility data and fit cell trajectory data to models can be found in the appendices
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