4.4 Article

Antimelanogenesis Effects of Fungal Exopolysaccharides Prepared from Submerged Culture of Fomitopsis castanea Mycelia

Journal

JOURNAL OF MICROBIOLOGY AND BIOTECHNOLOGY
Volume 29, Issue 8, Pages 1204-1211

Publisher

KOREAN SOC MICROBIOLOGY & BIOTECHNOLOGY
DOI: 10.4014/jmb.1905.05037

Keywords

Fomitopsis castanea; exopolysaccharides; SK-MEL-5 human melanoma cells; zebrafish; tyrosinase

Funding

  1. OTTOGI Corporation through the Research and Publication Project
  2. Korean Institute of Planning and Evaluation for Technology in Food, Agriculture, Forestry, and Fisheries (IPET) through the Agriculture, Food and Rural Affairs Research Center Support Program - Ministry of Agriculture, Food, and Rural Affairs (MAFRA), Repu [710012-03-1-HD220]
  3. NRF, Republic of Korea [2018R1D1A1A09083366]
  4. National Research Foundation of Korea [2018R1D1A1A09083366] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

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Fungal exopolysaccharides are important natural products having diverse biological functions. In this study, exopolysaccharides from Fomitopsis castanea mycelia (FEPS) were prepared, and the highest mushroom tyrosinase inhibitory activity was found. FEPS were prepared from cultivation broth by ethanol precipitation method. The extraction yield and protein concentration of FEPS were 213.1 mg/l and 0.03%, respectively. FEPS inhibited mushroom tyrosinase with the half maximal inhibitory concentration (IC50) of 16.5 mg/ml and dose-dependently inhibited cellular tyrosinase activity (63.9% at 50 mu g/ml, and 83.3% at 100 mu g/ml) in the cell-free extract of SK-MEL-5 human melanoma cell and alpha-melanocyte-stimulating hormone (alpha-MSH)-stimulated melanin formation in intact SK-MEL-5 human melanoma cell. The IC50 of FEPS against NO production from RAW264.7 macrophage cells was 42.8 +/- 0.64 mu g/ml. By in vivo study using a zebrafish model, exposure of FEPS at 400 mu g/ml to dechorionated zebrafish embryos for 18 h decreased the pigment density, compared to that without FEPS-treated control.

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