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A new bioactive curvularin macrolide from an endolichenic fungus, Curvularia trifolii, isolated from Usnea sp., in Sri Lanka

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dc.contributor.author Samanthi, K.A.U. en_US
dc.contributor.author Wickramaarachchi, S. en_US
dc.contributor.author Wijeratne, E.M. en_US
dc.contributor.author Paranagama, P.A. en_US
dc.date.accessioned 2014-12-23T08:31:00Z
dc.date.available 2014-12-23T08:31:00Z
dc.date.issued 2014
dc.identifier.citation Annual Research Symposium,Faculty of Graduate Studies, University of Kelaniya, Sri Lanka; 2014 :84p en_US
dc.identifier.uri http://repository.kln.ac.lk/handle/123456789/4903
dc.description.abstract The search for new bioactive natural products is still the main way of discovering new drug leads. Although fungi are well-known producers of secondary metabolites with new structurally diverse bioactive compounds, isolation of bioactive compounds from endolichenic fungi still remain underexplored as potential source of natural products. Endolichenic fungi are microorganisms living in the thalli of lichens that are analogous to the plant endophytic fungi inhabiting the intercellular spaces of the host. Curvularia trifolii was isolated from the lichen, Usnea sp., available in Hakgala botanical garden, Sri Lanka. Identification of the fungus was confirmed using morphological characters followed by the molecular identification (DNA sequencing). Invitro large scale cultures of C.trifolii were prepared in 60 large Petri dishes containing potato dextrose agar medium and after 10 days secondary metabolites were extracted into ethyl acetate. The crude extract was tested using two types of bio assays, for the investigation of antioxidant and anti-inflammatory activities. Antioxidant activity of the crude ethyl acetate extract was explored by carrying out DPPH free radical scavenging assay and Anti-inflammatory activity was evaluated using Human Red Blood Cell Membrane Stability (HRBC) assay. Since the crude extract showed high activity in both the assays, it was partitioned into hexane, chloroform (CHCl3) and 60% aq.MeOH and identified the bioactive fractions. The activity of CHCl3 fraction was confirmed and it was further fractionated using bioassay guided column chromatography (silica, sephadex) and preparative TLC to isolate pure compounds. One florescent active pure bioactive compound (C23H30O6) was isolated from the CHCl3 fraction and identified as using 1D, 2D NMR, MS, IR and UV spectral data. The structure of new compound was thus established as 5-methoxy-4,8,15-trimethyl-3,7-dioxo-1,3,7,8,9,10,11,12,13,14,15,15?-dodecahydrocyclododeca[de]isochromene-15-carboxylic acid and the bioassay results revealed that it is a new curvularin macrolide with IC50 values, 68.6�4.3 ?g/mL and 310�48.2 ?g/mL for DPPH antioxidant assay and anti-inflammatory assay respectively. Hence it is revealed that derivative isolated from C. trifolii can be developed as an important antioxidant and anti-inflammatory drug. en_US
dc.publisher Book of Abstracts, Annual Research Symposium 2014 en_US
dc.title A new bioactive curvularin macrolide from an endolichenic fungus, Curvularia trifolii, isolated from Usnea sp., in Sri Lanka
dc.type Article en_US
dc.identifier.department Chemistry en_US


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