Difference between revisions of "Team:Glasgow/BacillusSubtilis"

Challenge

One of the major experimental limitations of our design was the reliance on using genetically modified E.coli cells as the method of detection due to the relative difficulty and inefficiency of storing them such that the cells remain viable. As described, a polyacrylamide hydrogel matrix was used to immobilize the E.coli cells which, to maintain cell viability, had to be stored at refrigeration temperature but even then, in our tests, the cells lost viability after a couple of days. This problem led to the necessity of finding a different organism that would be better suited to shuttling our genetic construct for a longer period of time under a wider range of conditions.

Solution

One of our advisors James Provan, suggested using the bacteria Bacillus Subtilis due to its ability to form endospores which are extremely resilient under a vast range of conditions such as high temperatures and lack of nutrients (Tan and Ramamurthi, 2013)^[1]. As the decision to use an alternative organism to E.coli was made approximately half-way through our project, there was not sufficient time to completely redesign our genetic construct such that it could be expressed in Bacillus Subtilis. Because of this, a new experiment had to be thought off to show that the bacteria could be used for our purposes. One of our supervisors, Sean Colloms, got in contact with a researcher from Newcastle University, Richard Daniel, who kindly sent us a sample of Bacillus Subtilis cells that had been genetically modified such that they became blue-green when exposed to the sugar X-Gal. The proposed experiment involved sporulating these cells and then reanimating them on plates containing X-gal to observe if the cells maintained their genetic modification after sporulation and be able to show a colour change, much like we were aiming to do with our genetic construct.

Preliminary Results

Upon receipt of the Bacillus Subtilis containing plate from Newcastle University (shown in figure 1 below), various preliminary tests were performed to find the optimum conditions for the growth of the bacteria.

1. The first test performed involved picking two colonies from the original plate and streaking them on plates, one containing solely LB-agar medium and one containing a LB-agar and X-gal (final concentration of 40μg/ml in agar) medium. The plates were then incubated overnight at 37°C.
   Unfortunately, no photographs of the plates were taken at the time, however, both plates showed growth of white colonies. This was expected in the plate containing no X-gal however, it was expected that the other plate should have showed growth of blue-green colonies indicating that the concentration of X-gal was not sufficient enough to make the colonies change colour. Additionally, the morphology of all of the colonies did not show healthy growth, noted by “spikey” edges of each colony, which suggested that LB-agar was not the correct medium to grow Bacillus Subtilis on. Because of this it was decided that in future tests that nutrient agar would be used in addition to a higher concentration of X-gal.
2. To confirm that the correct conditions for the growth and colour change of Bacillus Subtilis had been met, a second test was performed. Six plates were set up as follows:

1. 25ml nutrient agar, 50μl of X-gal stock solution (100mg/ml) giving a final concentration of X-gal in agar of 200μg/ml and streaked with a colony from the original plate (blue-green) that was sent from Newcastle University.
2. 25ml nutrient agar, 50μl of X-gal stock solution (100mg/ml) giving a final concentration of X-gal in agar of 200μg/ml and streaked with a colony from the first plate of the first test (white).
3. 25ml nutrient agar, 25μl of X-gal stock solution (100mg/ml) giving a final concentration of X-gal in agar of 100μg/ml and streaked with a colony from the original plate (blue-green) that was sent from Newcastle University.
4. 25ml nutrient agar, 25μl of X-gal stock solution (100mg/ml) giving a final concentration of X-gal in agar of 100μg/ml and streaked with a colony from the first plate of the first test (white).
5. 25ml nutrient agar, no X-gal and streaked with a colony from the original plate (blue-green) that was sent from Newcastle University.
6. 25ml nutrient agar, no X-gal and streaked with a colony from the first plate of the first test (white).

These plates were incubated overnight and the growth was observed in the morning as shown in the following image (figure 2).

References