Antibacterial activity of Pandacaqui Puti (Tabernaemontana Pandacaqui Poir) plant parts extract against staphylococcus and Escherichia coli / by Ermie Jay B. Arca and Clarize Z. Candalo.

By: Contributor(s): Material type: TextTextLanguage: English Publication details: Indang, Cavite : Cavite State University- Main Campus, 2018.Description: xii, 76 pages : illustrations ; 28 cmContent type:
  • text
Media type:
  • unmediated
Carrier type:
  • volume
Subject(s): DDC classification:
  • 615  Ar2 2018
Online resources: Production credits:
  • College of Nursing (CON), Department of Medical Technology
Abstract: ARCA, ERMIE JAY B., CANDADO, CLARICE Z. Antibacterial Activity Of Pandakaki Puti (Tabernaemontana Pandacaqui Poir) Plant Parts Extract Against Staphylococcus Aureus and Escherichia Coll. Undergraduate Research Study. Bachelor of Science in Medical Technology. Cavite State University, Indang, Cavite. May 2018. This study on the antibacterial activity of T. pandacaquiPoirplant parts extract aimed to determine the concentration of the plant parts extract that inhibit bacterial growth of the S. aureus and E. coli in terms of inhibition zones; to determine the significant differences among the inhibition zones caused by the positive control and the leaf and stem extracts; and to determine the minimum inhibitory concentration of the plant part extract that caused the highest inhibition zone. The antibacterial activity of T. pandacaqui Poir was laid out in a Completely Randomized Design (CRD) with four replications of the different treatments of the leaf and stem extracts of T. pandacaqui Poir. The antibacterial activity was done using Kirby-Bauer Test (Disk Diffusion Method). Five treatments were prepared for leaf and stem extracts separately; 0.1 g/ m1 ,0.2 g/ml, 0.3g/ml, 0.4 glml and 0.5 g/ml, respectively. On the other hand, the test organisms, namely, Staphylococcus aureus and Escherichia coli, were purchased from Philippine National Collection of Microorganism, University of the Philippines Los Banos. The test organisms were sub cultured and standardized. The filter paper impregnated with the different concentration of leaf and stem extracts were placed onto the inoculated surface of the Mueller Hinton Agar (MHA) and pressed firmly and were incubated. After 24 hours of incubation, the zones of inhibition were measured and interpreted using the Clinical Laboratory Standard Institute (CLSI) standard. On the plates with S. aureus, the concentrations of leaf extracts that yielded a Resistant interpretation were the 0.1 g/ml, 0.4 g/m1 and 0.5 g/ml with inhibition zones of 12,25 mm, 12 mm and 10 mm, respectively. The leaf extracts that yielded an Intermediate interpretation were the 0.2 g/m1 and 0.3 g/ml with inhibition zones of 14.5 mm and 14.25 mm. The stem extracts that exhibited a resistant interpretation were 0.1 g/ml, 0.2 g/ml and 0.4 g/ml with inhibition zones of 10.75 mm, 11.25 mm and 13.5 mm, respectively. Concentrations with Intermediate interpretation were 0.3 g/ml and 0.5 g/ml with inhibition zones of 14.15 mm and 15 mm. The 0.3 g/ml and 0.5 g/m1 leaf extract were interpreted as Resistant with inhibition zones of 13.75 mm and 6.75 mm. The Intermediate inhibition zones were 0.1 g/ml and 0.2 g/ml with inhibition zones of 14.5 mm and 15.75 mm. The 0.4 g/ml leaf extract was interpreted as Susceptible with an inhibition zone of 22.75 mm. On the other hand, the stem extracts with concentrations of 0.1 g/ml, 0.2 g/ml, 0.3 g/ml, 0.4 g/ml and 0.5 g/ml were interpreted as Resistant with inhibition zones of 10.5 mm, 9.75 mm, 9.75 mm, 9.5 mm and 9.25 mm, respectively. The plant part extracts that exhibited the highest zone of inhibition were subjected to Minimum Inhibitory Concentration (MIC). The 0.2 g/ml leaf extract and 0.5 g/ml stem extract were evaluated for its minimum inhibitory concentration against S. aureus. On the other hand, 0.4 g/ml leaf extract and 0.1 g/ml stem extract were applied to E. coil in varying concentrations. The varying concentrations of 0.2 g/ml leaf extract, 0.5 g/ml leaf extract and 0.1 g/ml stem extract did not caused inhibition of bacterial growth while the 0.4 g/ml leaf extract inhibited bacterial growth.
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Theses / Manuscripts Theses / Manuscripts Ladislao N. Diwa Memorial Library Theses Section Non-fiction 615 Ar2 2018 (Browse shelf(Opens below)) Link to resource Room use only RS-823 00079793

Research Study (Bachelor of Science in Medical Technology) Cavite State University.

Includes bibliographical references.

College of Nursing (CON), Department of Medical Technology

ARCA, ERMIE JAY B., CANDADO, CLARICE Z. Antibacterial Activity Of Pandakaki Puti (Tabernaemontana Pandacaqui Poir) Plant Parts Extract Against Staphylococcus Aureus and Escherichia Coll. Undergraduate Research Study. Bachelor of Science in Medical Technology. Cavite State University, Indang, Cavite. May 2018.
This study on the antibacterial activity of T. pandacaquiPoirplant parts extract aimed to determine the concentration of the plant parts extract that inhibit bacterial growth of the S. aureus and E. coli in terms of inhibition zones; to determine the significant differences among the inhibition zones caused by the positive control and the leaf and stem extracts; and to determine the minimum inhibitory concentration of the plant part extract that caused the highest inhibition zone. The antibacterial activity of T. pandacaqui Poir was laid out in a Completely Randomized Design (CRD) with four replications of the different treatments of the leaf and stem extracts of T. pandacaqui Poir. The antibacterial activity was done using Kirby-Bauer Test (Disk Diffusion Method). Five treatments were prepared for leaf and stem extracts separately; 0.1 g/ m1 ,0.2 g/ml, 0.3g/ml, 0.4 glml and 0.5 g/ml, respectively. On the other hand, the test organisms, namely, Staphylococcus aureus and Escherichia coli, were purchased from Philippine National Collection of Microorganism, University of the Philippines Los Banos. The test organisms were sub cultured and standardized. The filter paper impregnated with the different concentration of leaf and stem extracts were placed onto the inoculated surface of the Mueller Hinton Agar (MHA) and pressed firmly and were incubated. After 24 hours of incubation, the zones of inhibition were measured and interpreted using the Clinical Laboratory Standard Institute (CLSI) standard. On the plates with S. aureus, the concentrations of leaf extracts that yielded a Resistant interpretation were the 0.1 g/ml, 0.4 g/m1 and 0.5 g/ml with inhibition zones of 12,25 mm, 12 mm and 10 mm, respectively. The leaf extracts that yielded an Intermediate interpretation were the 0.2 g/m1 and 0.3 g/ml with inhibition zones of 14.5 mm and 14.25 mm. The stem extracts that exhibited a resistant interpretation were 0.1 g/ml, 0.2 g/ml and 0.4 g/ml with inhibition zones of 10.75 mm, 11.25 mm and 13.5 mm, respectively. Concentrations with Intermediate interpretation were 0.3 g/ml and 0.5 g/ml with inhibition zones of 14.15 mm and 15 mm. The 0.3 g/ml and 0.5 g/m1 leaf extract were interpreted as Resistant with inhibition zones of 13.75 mm and 6.75 mm. The Intermediate inhibition zones were 0.1 g/ml and 0.2 g/ml with inhibition zones of 14.5 mm and 15.75 mm. The 0.4 g/ml leaf extract was interpreted as Susceptible with an inhibition zone of 22.75 mm. On the other hand, the stem extracts with concentrations of 0.1 g/ml, 0.2 g/ml, 0.3 g/ml, 0.4 g/ml and 0.5 g/ml were interpreted as Resistant with inhibition zones of 10.5 mm, 9.75 mm, 9.75 mm, 9.5 mm and 9.25 mm, respectively. The plant part extracts that exhibited the highest zone of inhibition were subjected to Minimum Inhibitory Concentration (MIC). The 0.2 g/ml leaf extract and 0.5 g/ml stem extract were evaluated for its minimum inhibitory concentration against S. aureus. On the other hand, 0.4 g/ml leaf extract and 0.1 g/ml stem extract were applied to E. coil in varying concentrations. The varying concentrations of 0.2 g/ml leaf extract, 0.5 g/ml leaf extract and 0.1 g/ml stem extract did not caused inhibition of bacterial growth while the 0.4 g/ml leaf extract inhibited bacterial growth.

Submitted to the University Library July 16,2018 RS-823

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