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Abstract
Marula bark is widely used for bacteria-related diseases by indigenous cultures in
Africa. This study was undertaken to investigate whether the ethnobotanical use can
be validated by laboratory studies. Bark and leaves were extracted with acetone and
MIC values were determined using a microplate serial dilution technique with Staphylococcus
aureus, Pseudomonas aeruginosa, Escherichia coli and Enterococcus faecalis as test
organisms. All extracts were active with MIC values from 0.15 to 3 mg/ml. Based on
minimum inhibitory concentration values, inner bark extracts tended to be the most
potent followed by outer bark and leaf extracts, but the differences were not statistically
significant. There were two major bioactive components visible after bioautography
of leaf extracts: one strongly polar and the other highly non-polar. The bioactive
components could be separated from 92% of the non-active dry matter by solvent-solvent
fractionation into the carbon tetrachloride, chloroform and n-butanol fractions; these
fractions, however, still contained many different compounds. Using bark may be detrimental
to the plant, but leaf material can also be used for antibacterial application.