Browsing by Author "Gunasekara, D.S."

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    Isolation of bioactive secondary metabolites from the endolichenic fungi, Neosartorya sp. inhabiting the lichen Parmotrema sp. in Sri Lanka
    (Faculty of Graduate Studies, University of Kelaniya, 2015) Manthrirathna, M.A.T.P.; Kandiah, R.; Gunasekara, D.S.; Paranagama, P.A.
    Natural products are a potential source of novel pharmaceutical agents. Therefore, isolation and identification of bioactive compounds from organisms adapted to various biotopes and unraveling their bioactivities in search for new pharmacophores has a mounting interest. Fungi are known to be prominent producers of useful metabolites. Endolichenic fungi (ELF) that occur asymptomatically within the lichen thalli are one of the ecological groups of fungi. ELF in Sri Lanka remain almost unexplored as a source of useful bioactive compounds. The objective of this study is to isolate bioactive secondary metabolites from ELF Neosartorya sp. isolated from Parmotrema sp. that occur in Hakgala Botanical Garden. ELF Neosartorya sp. was cultivated on 48 PDA plates and incubated at room temperature. Secondary metabolites were extracted into ethyl acetate from 9 days old cultures. Antibacterial activity of the crude extract was evaluated against Bacillus subtilis (BS) and Staphylococcus aureus (SA) using agar well diffusion method. Standard antibiotic Azithromycin was used as the positive control and Dimethyl sulfoxide as the negative control. Since the crude extract showed antibacterial activity against both BS and SA, it was partitioned with hexane, chloroform (CHCl3) and aqueous methanol. All three fractions showed activity against SA, with the CHCl3 fraction having higher activity compared to the other two fractions. Chloroform and methanol fractions showed significant activity against BS, while CHCl3 fraction showed activity comparable with Azithromycin. Chloroform fraction of Neosartorya sp. was further fractionated using bio-assay guided fractionation (silica gel column chromatography). Pure compounds were isolated using preparative TLC. One major pure compound was isolated from CHCl3 fraction and the characterization still in progress.
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    Secondary Metabolites with Radical Scavenging Activity from Daldinia Eschcholzii, Isolated from The Lichen Parmotrema Sp. In Sri Lanka-Isolation and Structure Determination
    (Faculty of Graduate Studies, University of Kelaniya, Sri Lanka, 2016) Manthrirathna, M.A.T.P.; Kandiah, R.; Gunasekara, D.S.; Paranagama, P.A.
    Natural products are promising leads for novel therapeutic agents. Isolation and characterization of bioactive compounds in search for potential pharmocophores has acquired a developing interest in on-going research. Although Endolichenic fungi (EF) are a rich source of bioactive secondary metabolites, they still remain almost unexploited. The present study is focused on isolation and structure elucidation of compounds with radical scavenging activity from the EF, Daldinia eschscholzii that occur in the lichen Parmotrema sp. in Hakgala Botanical Garden, Sri Lanka. Daldinia eschscholzii cultivated on 48 large petri dishes with PDA were incubated at room temperature for one week. Mycelia were cut in to small pieces along with the medium and extracted with ethyl acetate twice. The radical scavenging activity of the crude extract was evaluated using DPPH assay. Standard antioxidant, Butylated Hydroxy Toluene (BHT) and MeOH were used as the positive control (IC50= 38.2 ± 4.0 μg/ mL) and negative control respectively. The crude extract with high radical scavenging activity (IC50 = 77.9 ± 5.1 μg/ mL), was partitioned with hexane, chloroform and aqueous methanol. All three organic extracts were then subjected to DPPH assay. Chloroform fraction with the highest activity (IC50= 63.8 ± 4.8 μg/ mL) was further fractionated using silica gel, sephadex column chromatography and preparative TLC to isolate two pure compounds. The structures of the compounds were elucidated using 1H, 13C, 2D NMR and MS data. The compounds were identified as 7-hydroxy- 2-methylchroman-4-one (1) and 5-methoxynaphthalen-1-ol (2). Compound 1 showed no activity in the assay. Compound 2 showed higher activity than the standard BHT, with IC50 value of 10.2 ± 5.8 μg/ mL.