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Script For TD
Script For TD
with three replicates each were employed for antibacterial activity. The treatments
were 50% of C. woodsonii maas rhizome extract (T1), 100% of C. woodsonii maas
rhizome extract (T2), and Amoxicillin as the positive control.
The mean zones of inhibition of the S. aureus using the treatments were measured
using a vernier caliper after 24 hours for the antibacterial activity. The study was
conducted at General Santos City, specifically at the Pharmacy Laboratory and Biology
Laboratory of Notre Dame of Dadiangas University.
RELATED LITERATURE
Amoxicillin
E. Antibacterial activity
There are three treatments that were used for antibacterial activity. These are the
T1 is 50% rhizome extract, T2 is 100% rhizome extract and T3 the positive control,
Amoxicillin.
In preparing filter discs, the filter paper is punched with a two holed puncher to
form the filter discs. The filter discs are sterilized by autoclaving it for 15 minutes. Nine
filter discs were soaked in each treatment for 24 hours.
Nutrient agar powder is dissolved using the ratio of 200g/100mL according to the
manufacturing guide. 4.14g of nutritional agar powder were suspended in 180 mL of
distilled water. It is heated while stirring until completely dissolved. The dissolved
mixture is autoclaved for 1 hour at 121 degrees Celsius. The plate is filled with
nutritional agar and set aside on a sterile surface until the agar has hardened.
Pure culture of Staphylococcus aureus was obtained from the Biology Laboratory
in Notre Dame of the Dadiangas University, General Santos City. Streak plate method is
followed for the inoculation of bacterium where a loopful of S. aureus is transferred to
hardened agar by zigzag motion until the entire surface was the covered.
After the disks are prepared and soaked on our positive and negative controls.
The disks are transferred to our agar plates that are swabbed with each test culture.
Sterile forceps were use to ensure complete contact between disk and surface. The
plates are incubated at inverted position for 18 to 24 hours at 37 degrees Celsius.
After the incubation period, the zone of inhibition is determined by a point at
which no growth is visible to the unaided eye. The inhibition zone around each disk was
measured using a caliper, and the results were recorded (Das, J., et. al, 2018). To
analyze the data gathered, one-way anova is used in order to determine if there is a
significant difference in the mean zone of inhibition.
Justification of Results
Conclusion