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Biology Project On Effect of Antibiotics On Microorganisms
Biology Project On Effect of Antibiotics On Microorganisms
PROJECT
2023-2024
St. Paul School. CBSE.
Dhamna
Prepared By:
Anushree Solanki
Assigned By:
Sonu Rathod sir
CERTIFICATE
This is to certify that Anushree Solanki of
class XII have successfully completed the project
work on study on “Effects of antibiotics on
microorganisms” of Biology practical
examination of central board of secondary
education[CBSE] in year 2023-2024.
signature
signature signature
ACKNOWLEDGEMENT
I would like to express my special thanks to
my Biology teacher Mr. Sonu Rathod sir
and management for their able guidance
and support in completing my project
Step 2: Get a sample of polluted water for test. Mix 2 ml of polluted water
with 10 ml chicken broth in a test tube and incubate it for 24 hours so
the bacteria will reproduce and increase. Usually this is done on a
device that constantly moves, so the bacteria can freely move in the
liquid. Most likely you will not have a vibrator, so it is good if you
shake the test tube a few times during this incubation period.
Step 3: While the bacteria are being incubated, prepare some antibiotic disks
asdescribed here. (Antibiotic disks can also be purchased from
biologysuppliers).Break an antibiotic capsule (I used Ampicilin)and
empty the contents in a clean petri-dish.One capsule will be enough
for hundreds ofdisks.Dispose of the plastic shell and add a few
dropsof water to the remaining powder. Cut somefilter papers in
small pieces and soak them inthe antibiotic solution. Let the disks dry
in aclean space. You may cover them with anotherfilter paper to
protect them from dust.
Although they are known as antibiotic disks,you can cut them in small
squares.The reason that we use filter paper, is thatother papers often
have starch and otherpolymers that may affect the results of
ourexperiments. Filter paper is pure cellulosefiber.
Step 4 :Use the bacteria that you grown in step 2 and prepare dilution
ofbacteria.
1.Prepare 1:10 dilution of the sample. To do this, take 2 mL of the
sample andblend it with 18 mL of distilled water.
2.Pipette 0.1ml of each dilution onto a Plates Count Agar (PCA) plate
3.Take a glass hockey stick submersed in ethanol and run it through a
flame tosterilize it.(Glass hockey stick is a glass rod bent on one end
like a hockeystick. It is used to spread bacteria on the surface of agar
plate. You may usea steel spoon instead.)
4.Let it cool and use it to spread dilution around the plate
5.Do this on two plates for each of the five different dilutions.
6.Place an antibiotic disk on the plate of dilution.
7.incubate the plate at 35 degrees Celsius for 24 hours and then count
thebacterial colonies.
8.take 3 nutrient agar plate and added 0.5 ml of the solution on each
ofplates. I left one plate without any antibiotics, placed one antibiotic
disk onthe second plate and two antibiotic disk on the third plate. All
plates wereincubated for 48 hours.
OBSERVATION
CONCLUSION
The growth of bacteria around the
antibiotic disks is less. Inhibition
zones are more in the plates with
more antibiotic disks. Hence,
antibiotics stop proliferation of
bacteria.
Bibliography
Biology Practical Manual
www.wikipedia.com
Ncert biology Book