PRODUCTION AND ISOLATION OF POLYSACCHARIDES FROM MYCELIA OF NATURAL ISOLATES OF HIGHER FUNGI

PRODUCTION AND ISOLATION OF POLYSACCHARIDES FROM MYCELIA OF NATURAL ISOLATES OF HIGHER FUNGI

  • Miona Miljkovic Tehnolosko-metalurski fakultet, Univerzitet u Beogradu
  • Slađana Davidović University of Belgrade, Faculty of Technology and Metallurgy
  • Nevena Ilić Innovation Centre of the Faculty of Technology and Metallurgy, University of Belgrade
Keywords: higher fungi, intracellular polysaccharides, extracellular polysaccharides

Abstract


The traditional use of higher fungi in medicine and nutrition is largely attributed to their rich content of bioactive polysaccharides. This study evaluated the ability of four fungal isolates: Ganoderma resinaceum NMKSS, Bjerkander aadusta TMF1, Fomes fomentarius TMF2and Ganoderma sp.to produce intracellular (IPS) and extracellular polysaccharides (EPS) during submerged fermentation using glucose as the carbon source. Polysaccharides were extracted from dried mycelial biomass and culture supernatants, respectively, and quantified via the phenol-sulfuric acid assay. Initial screening revealed that EPS yields ranging from 0.1 to 0.759 mg/ml and IPS yields between 0.5 and 113.3 mg/g dry biomass. Notably, B. adusta TMF1 and F. fomentarius TMF2 exhibited significantly higher polysaccharide production and were selected for further work. The influence of organic nitrogen sources on polysaccharide yield was assessed, demonstrating that peptone supplementation maximized both EPS and IPS production. F. fomentarius TMF2 achieved the highest EPS yield of 0.84 mg/mL, conversely, B. adusta TMF1 produced a maximum IPS yield of 134.12 mg/g dry biomass. Yeast extract favored biomass accumulation but was less effective in stimulating polysaccharide synthesis. These findings suggest that nitrogen source composition critically influences the balance between fungal growth and polysaccharide production. Further research is needed to optimize culture conditions and fully exploit the biotechnological potential of these isolates for food and pharmaceutical applications.

 

References

Berger, R. G., Bordewick, S., Krahe, N. K., & Ersoy, F. (2022). Mycelium vs. Fruiting Bodies of Edible Fungi—A Comparison of Metabolites. Microorganisms, 10(7). https://doi.org/10.3390/microorganisms10071379
Chang, M. Y., Tsai, G. J., & Houng, J. Y. (2006). Optimization of the medium composition for the sub-merged culture of Ganoderma lucidum by Taguchi array design and steepest ascent method. En-zyme and Microbial Technology, 38(3–4), 407–414. https://doi.org/10.1016/j.enzmictec.2005.06.011
Dong, Q., Wang, Y., Shi, L., Yao, J., Li, J., Ma, F., & Ding, K. (2012). A novel water-soluble β-D-glucan isolated from the spores of Ganoderma lucidum. Carbohydrate Research, 353, 100–105. https://doi.org/10.1016/j.carres.2012.02.029
Dubois, M., Gilles, K. A., Hamilton, J. K., Rebers, P. A., & Smith, F. (1956). Colorimetric Method for Determination of Sugars and Related Substances. Analytical Chemistry, 28(3), 350–356. https://doi.org/10.1021/ac60111a017
Hawksworth, D. L., & Lücking, R. (2017). Fungal diversity revisited: 2.2 to 3.8 million species. The Fungal Kingdom, 79–95. https://doi.org/10.1128/9781555819583.ch4
Ilić, N., Davidović, S., Milić, M., Rajilić-Stojanović, M., Pecarski, D., Ivančić-Šantek, M., Mihajlovski, K., & Dimitrijević-Branković, S. (2023). Valorization of lignocellulosic wastes for extracellular enzyme production by novel Basidiomycetes: screening, hydrolysis, and bioethanol production. Bi-omass Conversion and Biorefinery, 13(18), 17175–17186. https://doi.org/10.1007/s13399-021-02145-x
Krsmanović, N., Mišković, J., Novaković, A., & Karaman, M. (2024). An evaluation of the fundamental factors influencing the characteristics of mycelium-based materials: A review. Journal on Pro-cessing and Energy in Agriculture, 28(1), 17–22. https://doi.org/10.5937/jpea28-49739
Li, F., Fan, H., Sun, Q., Di, Y., & Xia, H. (2024). Effects of Medium Additives on the Mycelial Growth and Polysaccharide Biosynthesis in Submerged Culture of Bjerkandera fumosa. Molecules, 29(2). https://doi.org/10.3390/molecules29020422
Prajapati, D., Bhatt, A., & Gupte, A. (2022). Production, optimization, partial-purification and pyrolysis kinetic studies of exopolysaccharide from a native brown-rot fungi Fomitopsis meliae AGDP-2. Bioresource Technology Reports, 17(January), 100948. https://doi.org/10.1016/j.biteb.2022.100948
Serody, J., Matthew, B., & Hewlett, J. (2024). Submerged Fermentation of Ganoderma tsugae for the Optimized Production of Exopolysaccharides. Journal of Advanced Technological Education, 3(3), 69–80. https://doi.org/10.5281/zenodo.13377111
Sun, Y., He, H., Wang, Q., Yang, X., Jiang, S., & Wang, D. (2022). A Review of Development and Utili-zation for Edible Fungal Polysaccharides: Extraction, Chemical Characteristics, and Bioactivities. Polymers, 14(20). https://doi.org/10.3390/polym14204454
Vetvicka, V., & Vetvickova, J. (2014). Immune-enhancing effects of Maitake (Grifola frondosa) and Shiitake (Lentinula edodes) extracts. Annals of Translational Medicine, 2(2). https://doi.org/10.3978/j.issn.2305-5839.2014.01.05
Wang, W., Tan, J., Nima, L., Sang, Y., Cai, X., & Xue, H. (2022). Polysaccharides from fungi: A review on their extraction, purification, structural features, and biological activities. Food Chemistry: X, 15(July), 100414. https://doi.org/10.1016/j.fochx.2022.100414
Yang, M., Qin, X., & Liu, X. (2025). A review of polysaccharides from Ganoderma lucidum: Prepara-tion methods, structural characteristics, bioactivities, structure-activity relationships and potential applications. International Journal of Biological Macromolecules, 303(92), 140645. https://doi.org/10.1016/j.ijbiomac.2025.140645
Zhong, X., Wang, G., Li, F., Fang, S., Zhou, S., Ishiwata, A., Tonevitsky, A. G., Shkurnikov, M., Cai, H., & Ding, F. (2023). Immunomodulatory Effect and Biological Significance of β-Glucans. Pharma-ceutics, 15(6), 1–16. https://doi.org/10.3390/pharmaceutics15061615
Published
2026/04/03
Section
Papers