Where's
the Bacteria?
Problem:
Hypothesis:
Materials:
Procedure:
- Streak Plate
Instructions
- 1. Lay petri
dish on a level surface with the lid side up.
- 2. Remove the
cap of an Easygel bottle. Do not touch the rim or inside of the
bottle, or petri dish.
- 3. Pour all
the liquid Easygel into the dish bottom. Replace the lid.
- Gently swirl
to cover the bottom.
- 4. Wait at
least 45 minutes until the Easy gel is solid.
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- Bacteria
Collection
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- Bacteria
Growth
- 1. Place the
petri dish in the incubator set at 38-40 degrees Celcius for
48 hours.
- 2. Remove the
dish from the incubator and observe the bacterial growth. If
possible, count the colonies in each section of the plate and
record.
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Questions:
- 1. Why was
it important to set aside one petri dish that was never opened
after being prepared?
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- 2. Why was
it important to have one petri dish that was opened at the same
times that another one was, but nothing was spread on it?
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- 3. How did
the appearance of each section compare to the others?
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- 4. Where in
this lab could error have occurred? Could the bacteria on the
petri dishes have come from somewhere other than where you collected
it?
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