ISOLATION AND ANTIFUNGAL ACTIVITY TEST OF SECONDARY METABOLITES MARINE FUNGUS ASPERGILLUS FLAVUS
As a tropical country, Indonesia is a fertile region for fungi to grow, so that fungal infections often infect Indonesian citizen. The use of inappropriate antifungal drugs can increase the risk of antifungal resistance. Several attempts have been made to overcome antifungal resistance problem...
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Format: | Final Project |
Language: | Indonesia |
Online Access: | https://digilib.itb.ac.id/gdl/view/78446 |
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Institution: | Institut Teknologi Bandung |
Language: | Indonesia |
Summary: | As a tropical country, Indonesia is a fertile region for fungi to grow, so that fungal infections often
infect Indonesian citizen. The use of inappropriate antifungal drugs can increase the risk of
antifungal resistance. Several attempts have been made to overcome antifungal resistance
problem, one of them is to isolate antifungal compounds with better antifungal activity so that they
can be used as active ingredients candidate in the future. A fraction isolated from marine fungi
Aspergillus flavus has been shown to have activity against Candida albicans. This research aimed to
determine the antifungal activity of fractions, subfractions, and isolate candidate from marine fungi
Aspergillus flavus, determine their characteristics, and isolates the target compound. The
preliminary screening test for the antifungal activity of fractions against Candida albicans was
carried out using disc diffusion method. The inhibition diameter of fraction was 18,97 ? 1,41 mm.
The sample fraction was sub fractionated by flash preparative chromatography with a mix of
methanol-water as a mobile phase and C-18 column as a stationary phase. Each subfractions was
tested for its antifungal activity against Candida albicans by microdilution method. Subfraction A,
subfraction B, subfraction C, and subfraction-waste had antifungal activity with MIC values of 128
?g/mL. Densitometry TLC analysis of selected subfractions showed that the dominant compound
had Rf 0,66 (candidate isolate 4) with %area value of 81,54% and maximum wavelength of 325 nm.
TLC profile analysis of the compounds was carried out with specific dyeing reagents citroboric,
Liebermann-Burchard, and Dragendorff. The selected subfraction, subfraction B, was purified by
preparative thin layer chromatography (TLC) with chloroform-methanol = 9,5:0,5 as mobile phase.
The purifications result obtained several candidates, isolate 1, isolate 2, isolate 3, isolate 4, and
isolate 5. Monitoring of the isolate candidates was carried out using TLC silica gel GF254 with
chloroform-methanol = 9,5:0,5 as mobile phase which showed that isolate candidate 2 and isolate
5 already showed a single spot. It was found that subfraction B allegedly contained
steroids/triterpenoids. Isolation of targeted compound from active fraction of marine fungi
Aspergillus flavus has been successfully carried out, but its activity against Candida albicans has not
been confirmed.
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