In vitro Antimicrobial and Antioxidant Properties of Ganoderma lucidum Extracts Grown in Turkey
Gokcen Yuvalı Celık
Department of Pharmaceutical Technology, Faculty of Pharmacy, Erciyes University, Kayseri 38039, Turkey
Dilsad Onbaslı
Department of Pharmaceutical Technology, Faculty of Pharmacy, Erciyes University, Kayseri 38039, Turkey
Berrak Altınsoy *
Department of Pharmaceutical Technology, Faculty of Pharmacy, Erciyes University, Kayseri 38039, Turkey
Hakan Allı
Deparment of Biology, Faculty of Science, Muğla Sıtkı Koçman University, Muğla, 48000, Turkey
*Author to whom correspondence should be addressed.
Abstract
Aim: To determine antimicrobial and antioxidative effects of Ganoderma lucidum.
Place and Duration of Study: Erciyes University, Faculty of Pharmacy, Pharmaceutical Biotechnology research laboratory,Kayseri, Turkey, between January to March, 2013.
Methodology: Antimicrobial inhibitory effects were carried out on the extracts using disc diffusion method. Antioxidant activities of the ethanolic and methanolic extracts from G.lucidum were evaluated by using 2,2-diphenyl-1-picrylhydrazyl [DPPH] radical scavenging, metal chelating, total flavonoid and total antioxidant activity assays. In addition, the amounts of phenolic compound, β-carotene and lycopene components in the extracts were determined.
Results: The antimicrobial effects of ethanolic and methanolic extracts of G. lucidum were tested against one species of Gram positive bacteria, two species of Gram-negative bacteria and two yeast. The highest inhibitory activity was determined against Candida glabrata RSKK 04019 [25±1 mm, inhibition zone diameter]. On the other hand, the lowest inhibitory activity was determined against Candida albicans ATCC 90028 and Bacillus subtilis RSKK 244 [10±1 and 10±0 mm, inhibition zone diameter]. DPPH radical scavenging effect was detected in the methanol extract [IC50 = 3.82±0.04 µg/mL] was higher than the ethanol extracts [IC50 = 7.03±0.07 µg/mL]. Compared to reference antioxidant, the methanol and ethanol extracts of G.lucidum provided a lower IC50 than butylated hydoxyanisole [BHA] [IC50 = 0.30±0.01 µg/mL]. Phenolic compounds were the major antioxidant component found in the mushroom extracts.
Conclusion: These results showed that G. lucidum may be used in pharmaceutical applications because of its effective antioxidant properties.
Keywords: Antimicrobial activity, Antioxidant capacity, G. lucidum