In our most recent lab meeting Sammy and I tested our
mystery microbe for catalase activity. To accomplish this we first tested some
controls that we could compare our microbe to. We used a positive (S.
epideidermis) control and a negative (E. faecalis) control. We observed bubble formation with our
positive control when a drop of 3% H2O2 was added and no reaction with our
negative control.
We then added the drop to our microbe and observed bubble
formation indicating a positive result for our catalase test. A potential explanation for the evolvement of catalase activity in certain microbe is the
aerobic microbes adapting to fight against elements that anaerobic microbes do not encounter such
as oxygen.
The other experiment we did regarding our microbe was the
triple sugar iron test to determine carbohydrate metabolism. The TSI slant
provides the culture with an aerobic and anaerobic environment in which to
grow. This allows us to observe how different bacterium ferment and metabolize.
All five of our control tubes grew as expected. I compared the information
provided to us about the predicted reactions for each bacterium and confirmed
the results by observing the color of the TSI agar of each control after
incubation.
E. coli |
P. vulgaris |
P. aeruginosa |
B. Megaterium |
For our unknown microbe, the media at the top of the tube
was pink/red indicating an alkaline reaction. The bottom, or butt ,of the tube
was yellow indicating an acidic reaction. There was no evidence of hydrogen
sulfide formation. These results mean that our microbe metabolized glucose
but
not sucrose or lactose.
In the last blog post, Sammy followed the dichotomous key up
until the question regarding catalase activity…
Dichotomous
Key
Below,
I have used a dichotomous key in order to begin identifying our microbe…Below
is the steps that I followed in the dichotomous key:
1.
Gram Positive
2.
Morphology, Rod Shaped (Bacilli)
3.
Non-acid fast organism
Now we know that our microbe is catalase (+) so we can
continue!
4. Catalase positive
We know that our microbe metabolized glucose in both the
aerobic and anaerobic areas of the slant so I’m unsure of the answer to the
next step in the key. We might have to have further discussions to determine the
answer.
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