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Production, structural characterization, and antiproliferative activity of exopolysaccharide produced by Scleroderma areolatum Ehrenb with different carbon source

  • Biotechnology and Industrial Microbiology - Research Paper
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Abstract

The effects of different three carbon sources, that is, glucose, fructose, and sucrose, on production, molecular properties and antiproliferative activity of exopolysaccharide (EPS), were evaluated in the submerged culture of Scleroderma areolatum Ehrenb. Among carbon sources examined, the addition of sucrose maximizes the mycelia production, while fructose could maximize the EPS yield. Although the predominant carbohydrate compositions identified were gluconic acid and mannose, the monosaccharide composition of EPSs was also different significantly. FT-IR spectral analysis revealed there was no significant difference among the prominent characteristic groups in three EPSs. The molecular weight of EPSs was also affected by carbon source, being generally lower compared with that with glucose. However, all EPSs molecule existed as nearly globular shape form in aqueous solution. The variation of carbon sources also affected antiproliferative activity examined in vitro using cell proliferation assay. Fructose was optimal carbon source giving higher antiproliferative activity probably due to the relatively high contents of xylose in the EPS with low molecular weight.

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References

  1. Dai YC (2010) Hymenochaetaceae (Basidiomycota) in China. Fungal Divers 45:131–343

    Article  Google Scholar 

  2. Sa VDS, Blunt JW, Cole AL, Din LB, Munro MH (2005) Dichlorinated pulvinic acid derivative from a Malaysian scleroderma sp. J Nat Prod 68:1799–1801

    Article  CAS  Google Scholar 

  3. Soytong K, Sibounnavong P, Kanokmedhakul K, Kanokmedhakul S (2014) Biological active compounds of scleroderma citrinum that inhibit plant pathogenic fungi. Int J Agr Tech 10(1):79–86

    CAS  Google Scholar 

  4. Kanokmedhakul S, Kanokmedhakul K, Prajuabsuk T, Soytong K, Kongsaeree P, Suksamrarn A (2003) A bioactive triterpenoid and vulpinic acid derivatives from the mushroom scleroderma citrinum. Planta Med 69:568–571

    Article  CAS  PubMed  Google Scholar 

  5. Mahapatra S, Banerjee D (2013) Fungal exopolysaccharide: production, composition and applications. Microbiol Insights 6:1–16

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  6. Wasser SP (2002) Medicinal mushrooms as a source of antitumor and immunomodulating polysaccharides. Appl Microbiol Biotechnol 60:258–274

    Article  CAS  PubMed  Google Scholar 

  7. Tang YJ, Zhu LL, Li DS, Mi ZY, Li HM (2008) Significance of inoculation density and carbon source on the mycelial growth and tuber polysaccharides production by submerged fermentation of Chinese truffle tuber sinense. Process Biochem 43:576–586

    Article  CAS  Google Scholar 

  8. Xiang Y, Xu X, Li J (2012) Chemical properties and antioxidant activity of exopolysaccharides fractions from mycelial culture of Inonotus obliquus in a ground corn Stover medium. Food Chem 134:1899–1905

    Article  CAS  PubMed  Google Scholar 

  9. Mozzi F, Rollán G, de Giori GS (2001) Font dVG. Effect of galactose and glucose on the exopolysaccharide production and the activities of biosynthetic enzymes in lactobacillus casei CRL 87. J Appl Microbiol 91:160–167

    Article  CAS  PubMed  Google Scholar 

  10. Mozzi F, Giori GSD, Valdez GFD (2003) UDP-galactose 4-epimerase: a key enzyme in exopolysaccharide formation by lactobacillus casei CRL 87 in controlled pH batch cultures. J Appl Microbiol 94:175–183

    Article  CAS  PubMed  Google Scholar 

  11. Fan Y, He XJ, Zhou S, Luo A, He T, Chun Z (2009) Composition analysis and antioxidant activity of polysaccharide from Dendrobium denneanum. Int J Biol Macromol 45:169–173

    Article  CAS  PubMed  Google Scholar 

  12. Hwang HJ, Kim SW, Xu CP, Choi JW, Yun JW (2003) Production and molecular characteristics of four groups of exopolysaccharides from submerged culture of Phellinus gilvus. J Appl Microbiol 94:708–719

    Article  CAS  PubMed  Google Scholar 

  13. Dubois M, Gilles KA, Hamilton JK, Rebers PA, Smith F (1956) Colorimetric method for determination of sugars and related substances. Anal Chem 28:350–356

    Article  CAS  Google Scholar 

  14. Jumel K, Fiebrig I, Harding SE (1996) Rapid size distribution and purity analysis of gastric mucus glycoproteins by size exclusion chromatography/multi angle laser light scattering. Int J Biol Macromol 18:133–139

    Article  CAS  PubMed  Google Scholar 

  15. He P, Geng L, Wang J, Wang Z, Mao D, Xu C (2012) Purification, characterization and bioactivity of an extracellular polysaccharide produced from Phellinus igniarius. Ann Microbiol 62:1697–1707

    Article  CAS  Google Scholar 

  16. Cong C, Wu W, Xu X, Zhang L, Ying L, Wang K (2014) Chain conformation and anti-tumor activity of derivatives of polysaccharide from Rhizoma Panacis Japonici. Carbohydr Polym 105:308–316

    Article  CAS  Google Scholar 

  17. Xu H, Zou S, Xu X, Zhang L (2016) Anti-tumor effect of beta-glucan from Lentinus edodes and the underlying mechanism. Sci Rep 6:28802

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  18. Kai A, Kikawa M, Hatanaka K, Matsuzaki K, Mimura T, Kaneko Y (2003) Biosynthesis of hetero-polysaccharides by Pestalotiopsis microspora from various monosaccharides as carbon source. Carbohydr Polym 54:381–383

    Article  CAS  Google Scholar 

  19. Khondkar P, Aidoo KE, Tester RF (2002) Sugar profile of extracellular polysaccharides from different Tremella species. Int J Food Microbiol 79:121–129

    Article  CAS  PubMed  Google Scholar 

  20. Chen X, Wu JY, Gui X (2016) Production and characterization of exopolysaccharides in mycelial culture of Cordyceps sinensis fungus Cs-HK1 with different carbon sources. Chin J Chem Eng 24:158–162

    Article  CAS  Google Scholar 

  21. Degeest B, Janssens B, Vuyst LD (2001) Exopolysaccharide (EPS) biosynthesis by lactobacillus sakei 0–1: production kinetics, enzyme activities and EPS yields. J Appl Microbiol 91:470–477

    Article  CAS  PubMed  Google Scholar 

  22. Wang J, Ma Z, Zhang L, Fang Y, Jiang F, Phillips GO (2011) Structure and chain conformation of water-soluble heteropolysaccharides from Ganoderma lucidum. Carbohydr Polym 86:844–851

    Article  CAS  Google Scholar 

  23. Vaningelgem F, Zamfir M, Adriany T, Vuyst LD (2004) Fermentation conditions affecting the bacterial growth and exopolysaccharide production by Streptococcus thermophilus ST 111 in milk-based medium. J Appl Microbiol 97:1257–1273

    Article  CAS  PubMed  Google Scholar 

  24. Zhang M, Zhang L, Cheung PCK, Ooi VEC (2004) Molecular weight and anti-tumor activity of the water-soluble polysaccharides isolated by hot water and ultrasonic treatment from the sclerotia and mycelia of Pleurotus tuber-regium. Carbohydr Polym 56:123–128

    Article  CAS  Google Scholar 

  25. Zhang Y, Li S, Wang X, Zhang L, Cheung PCK (2011) Advances in lentinan: isolation, structure, chain conformation and bioactivities. Food Hydrocoll 25:196–206

    Article  CAS  Google Scholar 

  26. Zhu F, Du B, Xu B (2016) A critical review on production and industrial applications of beta-glucans. Food Hydrocoll 52:275–288

    Article  CAS  Google Scholar 

  27. Chen NY, Hsu TH, Lin FY, Lai HH, Wu JY (2006) Effects on cytokine-stimulating activities of EPS from Tremella mesenterica with various carbon sources. Food Chem 99:92–97

    Article  CAS  Google Scholar 

  28. Deng X, Li X, Luo S, Zheng Y, Luo X, Zhou L (2017) Antitumor activity of Lycium barbarum polysaccharides with different molecular weights: an in vitro and in vivo study. Food Nutr Res 61:1399770

    Article  CAS  PubMed  PubMed Central  Google Scholar 

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Funding

This work was supported by the National Science Foundation of China (Grant No U1604176 and 31571778).

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Correspondence to Chunping Xu.

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Responsible Editor: Solange I. Mussatto.

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Wu, Y., Jia, X., Huang, D. et al. Production, structural characterization, and antiproliferative activity of exopolysaccharide produced by Scleroderma areolatum Ehrenb with different carbon source. Braz J Microbiol 50, 625–632 (2019). https://doi.org/10.1007/s42770-019-00071-9

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