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논문 기본 정보

자료유형
학술저널
저자정보
Tong Woei Yenn (Universiti Sains Malaysia) Darah Ibrahim (Universiti Sains Malaysia) Lee Kok Chang (Universiti Sains Malaysia) Syarifah Ab Rashid (Universiti Sains Malaysia) Leong Chean Ring (Universiti Kuala Lumpur) Tan Wen Nee (Universiti Sains Malaysia) Muhamad Izham bin Muhamad Noor (Universiti Sains Malaysia)
저널정보
한국미생물학회 미생물학회지 미생물학회지 제53권 제3호
발행연도
2017.9
수록면
193 - 199 (7page)

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초록· 키워드

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This study was aimed to evaluate the antimicrobial activity of Penicillium purpurogenum ED76 on several clinically important microorganisms. The endophytic fungus P. purpurogenum ED76 was previously isolated from Swietenia macrophylla leaf. The antimicrobial efficacy of P. purpurogenum ED76 dichloromethane extract was determined via disc diffusion and broth microdilution assay. A kill curve study was conducted and the morphology of extract treated bacterial cells were viewed under scanning electron microscope. The dichloromethane extract showed significant inhibitory activity on 4 test bacteria and 2 test yeasts. The minimal inhibitory concentration of the extract ranged from 125 to 1,000 μg/ml, which indicates the different susceptibility levels of the test microorganisms to the fungal extract. The kill curve study has revealed a concentration-dependent inhibition for all test microorganisms. With the increase of the extract concentration, the microbial growth was significantly reduced. The scanning electron micrograph of dichloromethane extracttreated Staphylococcus aureus cells showed the total damage of the cells. The cell wall invagination of the bacterial cells also indicates the loss of cellular materials and metabolic activity. The gas chromatography mass spectrometry analysis of the extract also showed that the major compound was stigmasterol, which constitutes 45.30% of the total area. The dichloromethane extract of P. purpurogenum ED76 exhibited significant inhibitory activity on several clinically important bacteria and yeasts. The study proposed a possible mode of action that the extract cause significant damage to the morphology of S. aureus cells.

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Materials and Methods
Results and Discussion
Conclusion
References

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UCI(KEPA) : I410-ECN-0101-2018-475-001327775