Abstract:
Medicinal plants represent a rich source of antimicrobial agents.In this study L.camara was selected due to lack
of information in our region about the antifungal activity of its stem bark and the selected fungi were plant
pathogens. Objective of the study was to carry out fractionation of crude extract and to investigate their antifungal
activity. The air dried stem bark (100g) of L.camara was powdered and extracted with ethyl acetate (2× 200mL)
at room temperature and the resulting extract was concentrated under reduced pressure to give 4.2g of crude extract.
By usingVacuumLiquid Chromatography (VLC), the ethyl acetate crude was divided into two fractions (A and B)
by the Thin Layer Chromatography (TLC)analysis. The antifungal bioassay was done to the above two fractions
against Aspergillus sp.,Alternaria sp.,Fusarium sp.,Trichoderma sp. and Penicillium sp. The diameter of the
inhibition zone was measured after 24, 48, 72 and 96 hour incubation periods. Zone of inhibition of extracts were
compared with synthetic antifungal agent Mancozeb(positive control) and the solvent ethyl acetate
(negativecontrol).Fraction B showed higher antifungal activity than fraction A. Therefore fraction B was subjected
to further chromatographic fractionation. By using column chromatography, the fraction B was divided into two
fractions X and Y and gave single spot based on TLC analysis. The antifungal bioassay was also done to fractions
X and Y against same fungi. Both fractions X and Y showed highest inhibition on Fusarium sp. were 25mm and
32mm and on Penicillium sp. were 26mm and 34mm respectively after 48 hours of incubation. Further studies
should be carried out to find out pure antifungal compounds,since this work contributed as a primary platform.
