International journal of medicinal mushrooms · 2014 · 32 citations · 11 references
Life SciencesBiologyMicrobiologyMycologyOrganic ChemistryStructure-activity RelationshipsAntifungal AgentsMedicinal PlantsActivitiesFungal Bioactive CompoundsMinimum Inhibitory Concentration DeterminationMinimum Inhibitory Concentration TestingNatural Antifungal Compounds
Mushrooms are considered one of the richest sources of natural antibiotics, and various species of them inhibit the growth of a wide diversity of microorganisms. Ganoderma lucidum, a well-known medicinal mushroom. has many pharmacological and biological activities including an antimicrobial effect, although few studies have investigated the antibacterial and antifungal effects of its purified compounds. The chemical structure of the purified compounds from the hexane fraction was elucidated as ergosta-7,22-dien-3β-yl acetate, ergosta-5,7,22-trien-3β-yl acetate (isopyrocalciferol acetate), ergosta-7,22-dien-3-one, ergosta-7,22-dien-3β-ol, and ergosta-5,7,22-trien-3β-ol (ergostrol). In addition, the structure of ganodermadiol was demonstrated after purification from the chloroform fraction. The fractions inhibited Gram-positive bacteria and yeast, with minimum inhibitory concentration values of 6.25 mg/mL, but were ineffective against Gram-negative bacteria in the tested concentrations. The results were comparable for isolated compounds, whereas the mixture of ergosta-7,22-dien-3β-yl acetate and isopyrocalciferol acetate was weakly effective against Escherichia coli (minimum inhibitory concentration, 10 mg/mL). It could be assumed that the antimicrobial effect of crude fractions is the consequence of mixing triterpenoid and steroid compounds.
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Inmaculada Suay · Antonie van Leeuwenhoek · 2000 · 222 citations
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Huey-Jiun Ko, Chi‐Feng Hung, Jih-Pyang Wang et al. · Phytochemistry · 2007 · 140 citations
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Life Sciences, Biology, Microbiology +14