Oil
Eaters:
Microbial
Bioremediation
Student
Guide
Background:
Biodegradation is a natural
process by which microorganisms such as bacteria, fungi, and yeast break
down complex compounds into simpler products to obtain energy and nutrients.
Due to the biodiversity of the microorganisms that exist in soil and in
water, this process may occur anywhere. Many types of toxic soil or water
contamination exist. The diversity of microbes allows for specific responses
to these contaminants. Common types of microbial "cleanups" are old oil
dumps, oil-contaminated land, old landfills, diesel and jet fuels from
estuaries, and shoreline contaminations.
In an aquatic
environment, biodegradation of oil is a painstakingly slow process, sometimes
lasting years. However, rapid removal of spilled oil from shorelines and
wetlands is necessary in order to minimize potential environmental damage
to the sensitive marine habitats. Bioremediation is the use of microorganisms
to help the biodegradation processes occur faster.
In bioremediation,
scientists add materials to the environment, such as nitrogen and phosphates
to stimulate growth and increase the population size of the microorganisms.
This is called nutrient enrichment. Seeding is another method of bioremediation.
This is the addition of more of the microorganisms also increasing the
population size, thus increasing the rate of natural biodegradation.
Optional
Materials:
Step
1(For agar experiment model)
-
Five covered deep tubes of sterile prepared
nutrient agar.
-
One-600 ml beaker.
-
Hot plate.
-
Five sterile Petri dishes.
(For
nutrient broth experiment model)
-
Five 125 ml Erlenmeyer flasks and stoppers.
-
10 ml of dilute nutrient solution.
-
80 ml of distilled water.
(For
either experiment model)
-
One sterile stirring rod.
-
Five milliliters of automobile oil.
-
One gram of the following bacterial
sources:
-
Soil.
-
Benthic soil.
-
Parking lot oil shavings.
-
Used automobile oil.
-
Optional sources
-
One squeeze bottle of the following:
-
Distilled water.
-
Soap.
-
Lysol.
-
Pipette
Step
2:
-
Tap water.
-
600 ml beaker.
-
Hot Plate.
-
Five deep tubes.
-
Dilute nutient solution.
-
Five Petri dishes.
-
Filter disks.
-
Five ml motor oil.
Procedure:
Step
1:/Step 2:
-
Acquaint yourself with the location
and procedure for proper bacterial disposal.
-
Disinfect lab area with lysol.
-
Formulate a hypothesis to be tested
using the background information and materials provided.
-
Outline an experiment, paying close
attention to variable and controls. Include a model for a data table, or
other method for recording your results.
-
Discuss your outline with your instructor.
-
Obtain the necessary materials for your
experiment.
-
Set up the experiment
-
Place experiment in the area designated
by your instructor.
-
Clean up the lab materials properly.
-
Clean up the lab station.
Results/Data:
SAMPLE
DATA TABLE
|
Petri Dish
|
Data
|
|
Soil
|
|
|
Benthic Soil
|
|
|
Parking lot oil shavings
|
|
|
Used automobile oil
|
|
|
Optional Source
|
|
|
Control
|
|
Conclusions:
-
Do your results support your hypothesis? Support and explain your
answer completely.
-
What worked well in this activity? Explain.
-
What difficulties did you encounter in this experiment?
-
What would you suggest to improve this experiment?
| b |
The
Woodrow Wilson National Fellowship Foundation
CN 5281, Princeton NJ 08543-5281 - Tel:(609)452-7007
- Fax:(609)452-0066
Technical contact: lpt@woodrow.org |