Skip to main content
Log in

Efficiency of β-glucan production by Sparassis crispa depends on mycelium shape

  • Original Article
  • Published:
Biomass Conversion and Biorefinery Aims and scope Submit manuscript

Abstract

Sparassis crispa contains various bioactive substances, such as β-glucan, which exhibits antitumor activity. In this study, we investigated the effect of the mycelial shape of S. crispa and the combination of flask type and agitation method on β-glucan production. With the combination of the Erlenmeyer flask and shaken culture, the mycelia grew in the shape of pellets, whereas with the combination of the baffled Erlenmeyer flask and stirred culture, the mycelia grew in the shape of filaments. The dried cell weight (DCW) and β-glucan production of the filamentous mycelia were 5.91 g/L and 1.71 g/L, respectively, 1.34-fold and 1.73-fold higher, respectively, than that of the pelleted mycelia (4.42 g/L and 0.99 g/L, respectively). The production was further increased using the homogenization process; the DCW was 1.03-fold (7.23 g/L) higher and β-glucan production 1.34-fold (3.50 g/L) higher, respectively, than that without the treatment (7.01 g/L and 2.61 g/L, respectively). In the filamentous mycelia, β-glucan production increased with suppressed ethanol production, and a negative correlation was observed between β-glucan production and ethanol production. In the cultivation of S. crispa mycelia, filamentous mycelia have been suggested to be more suitable for β-glucan production than pelleted mycelia.

Graphical abstract

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Fig. 1
Fig. 2
Fig. 3
Fig. 4
Fig. 5
Fig. 6

Similar content being viewed by others

Data availability

Not applicable.

Code availability

Not applicable.

References

  1. Yadav D, Negi PS (2021) Bioactive components of mushrooms: processing effects and health benefits. Food Res Int 148:110599. https://doi.org/10.1016/j.foodres.2021.110599

    Article  Google Scholar 

  2. Nowakowski P, Markiewicz-Żukowska R, Bielecka J, Mielcarek K, Grabia M, Socha K (2021) Treasures from the forest: evaluation of mushroom extracts as anti-cancer agents. Biomed Pharmacother 143:112106. https://doi.org/10.1016/j.biopha.2021.112106

    Article  Google Scholar 

  3. Ba DM, Gao X, Al-Shaar L, Muscat JE, Chinchilli VM, Beelman RB, Richie JP (2021) Mushroom intake and depression: a population-based study using data from the US National Health and Nutrition Examination Survey (NHANES), 2005–2016. J Affect Disord 294:686–692. https://doi.org/10.1016/j.jad.2021.07.080

    Article  Google Scholar 

  4. Kimura T (2013) Natural products and biological activity of the pharmacologically active cauliflower mushroom Sparassis crispa. Biomed Res Int 2013:982317. https://doi.org/10.1155/2013/982317

    Article  Google Scholar 

  5. Ohno N, Miura NN, Nakajima M, Yadomae T (2000) Antitumor 1,3-beta-glucan from cultured fruit body of Sparassis crispa. Biol Pharm Bull 23:866–872. https://doi.org/10.1248/bpb.23.866

    Article  Google Scholar 

  6. Ohno N, Nameda S, Harada T, Miura NN, Adachi Y, Nakajima M, Yoshida K, Yoshida H, Yadomae T (2003) Immunomodulating activity of a β-glucan preparation, SCG, extracted from a culinary–medicinal mushroom, Sparassis crispa Wulf.:Fr. (Aphyllophoromycetideae), and application to cancer patients. Int J Med Mushrooms 5:359–368. https://doi.org/10.1615/InterJMedicMush.v5.i4.30

    Article  Google Scholar 

  7. Yamamoto K, Kimura T, Sugitachi A, Matsuura N (2009) Anti-angiogenic and anti-metastatic effects of β-1,3-D-glucan purified from Hanabiratake, Sparassis crispa. Biol Pharm Bull 32:259–263. https://doi.org/10.1248/bpb.32.259

    Article  Google Scholar 

  8. Lee SY, Lee YG, Byeon SE, Han S, Choi SS, Kim AR, Lee J, Lee SJ, Hong S, Cho JY (2010) Mitogen activated protein kinases are prime signalling enzymes in nitric oxide production induced by soluble β-glucan from Sparassis crispa. Arch Pharm Res 33:1753–1760. https://doi.org/10.1007/s12272-010-1107-3

    Article  Google Scholar 

  9. Yoshitomi H, Iwaoka E, Kubo M, Shibata M, Gao M (2011) Beneficial effect of Sparassis crispa on stroke through activation of Akt/eNOS pathway in brain of SHRSP. J Nat Med 65:135–141. https://doi.org/10.1007/s11418-010-0475-9

    Article  Google Scholar 

  10. Kwon AH, Qiu Z, Hashimoto M, Yamamoto K, Kimura T (2009) Effects of medicinal mushroom (Sparassis crispa) on wound healing in streptozotocin-induced diabetic rats. Am J Surg 197:503–509. https://doi.org/10.1016/j.amjsurg.2007.11.021

    Article  Google Scholar 

  11. Yoshikawa K, Kokudo N, Hashimoto T, Yamamoto K, Inose T, Kimura T (2010) Novel phthalide compounds from Sparassis crispa (Hanabiratake), Hanabiratakelide A-C, exhibiting anti-cancer related activity. Biol Pharm Bull 33:1355–1359. https://doi.org/10.1248/bpb.33.1355

    Article  Google Scholar 

  12. Yang H, Min W, Bi P, Zhou H, Huang F (2013) Stimulatory effects of Coix lacryma-jobi oil on the mycelial growth and metabolites biosynthesis by the submerged culture of Ganoderma lucidum. Biochem Eng J 76:77–82. https://doi.org/10.1016/j.bej.2013.04.012

    Article  Google Scholar 

  13. Ryu SR, Ka KH, Park H, Bak WC, Lee BH (2009) Cultivation characteristics of Sparassis crispa strains using sawdust medium of Larix kaempferi. Kor J Mycol 37:49–54. https://doi.org/10.4489/KJM.2009.37.1.049

    Article  Google Scholar 

  14. Singh U, Gautam A, Singha TK, Tiwari A, Tiwari P, Sahai V, Sharma S (2020) Mass production of Pleurotus eryngii mycelia under submerged culture conditions with improved minerals and vitamin D2. LWT 131:109665. https://doi.org/10.1016/j.lwt.2020.109665

    Article  Google Scholar 

  15. Wasser SP (2011) Current findings, future trends, and unsolved problems in studies of medicinal mushrooms. Appl Microbiol Biotechnol 89:1323–1332. https://doi.org/10.1007/s00253-010-3067-4

    Article  Google Scholar 

  16. Bakratsas G, Polydera A, Katapodis P, Stamatis H (2021) Recent trends in submerged cultivation of mushrooms and their application as a source of nutraceuticals and food additives. Future Foods 4:100086. https://doi.org/10.1016/j.fufo.2021.100086

    Article  Google Scholar 

  17. Petre M, Petre P (2016) Chapter 1 - Biotechnology of mushroom growth through submerged cultivation. In: Petre M (ed) Mushroom Biotechnology. Academic Press, Cambridge, pp 1–18

    Google Scholar 

  18. Yang FC, Yang MJ, Cheng SH (2009) A novel method to enhance the mycelia production of Ganoderma lucidum in submerged cultures by polymer additives and agitation strategies. J Taiwan Inst Chem Eng 40:148–154. https://doi.org/10.1016/j.jtice.2008.09.003

    Article  Google Scholar 

  19. Wen Y, Erika AH, Aiqi F, Arnold LD (2003) Effects of carboxymethylcellulose and carboxypolymethylene on morphology of Aspergillus fumigatus NRRL 2346 and fumagillin production. Curr Microbiol 46:24–27. https://doi.org/10.1007/s00284-002-3711-z

    Article  Google Scholar 

  20. Perez-Leblic MI, Reyes F, Martinez MJ, Lahoz R (1982) Cell wall degradation in the autolysis of filamentous fungi. Mycopathologia 80:147–155. https://doi.org/10.1007/BF00437577

    Article  Google Scholar 

  21. Xu N, Liu Y, Hu Y, Zhou M, Wang C, Dongsheng L (2016) Autolysis of Aspergillus oryzae mycelium and effect on volatile flavor compounds of soy sauce. J Food Sci 81:1883–1890. https://doi.org/10.1111/1750-3841.13396

    Article  Google Scholar 

  22. Asada C, Okumura R, Sasaki C, Nakamura Y (2012) Acceleration of Hericium erinaceum mycelial growth in submerged culture using yogurt whey as an alternative N source. Adv Biosci Biotechnol 3:828–832. https://doi.org/10.4236/abb.2012.37103

    Article  Google Scholar 

  23. Okumura R, Nakamura Y, Sasaki C, Asada C (2021) Effects of Tween series and agar additives on mycelia biomass and β-glucan production by Hericium erinaceus in submerged culture. Biomass Convers Biorefin. https://doi.org/10.1007/s13399-021-01342-y

    Article  Google Scholar 

  24. Gibbs PA, Seviour RJ, Schmid F (2000) Growth of filamentous fungi in submerged culture: Problems and possible solutions. Crit Rev Biotechnol 20:17–48. https://doi.org/10.1080/07388550091144177

    Article  Google Scholar 

  25. Papagianni M (2004) Fungal morphology and metabolite production in submerged mycelial processes. Biotechnol Adv 22:189–259. https://doi.org/10.1016/j.biotechadv.2003.09.005

    Article  Google Scholar 

  26. Lee BC, Bae JT, Pyo HB, Choe TB, Kim ST, Hwang HJ, Yun JW (2004) Submerged culture conditions for the production of mycelial biomass and exopolysaccharides by the edible basidiomycete Grifola frondose. Enzyme Microb Technol 35:369–376. https://doi.org/10.1016/j.enzmictec.2003.12.015

    Article  Google Scholar 

  27. Tan YH, David M (1992) Convenient and effective methods for in vitro cultivation of mycelium and fruiting bodies of Lentinus edodes. Mycol Res 96:1077–1084. https://doi.org/10.1016/S0953-7562(09)80119-6

    Article  Google Scholar 

  28. Li C, Xia JY, Chu J, Wang YH, Zhuang YP, Zhang SL (2013) CFD analysis of the turbulent flow in baffled shake flasks. Biochem Eng J 70:140–150. https://doi.org/10.1016/j.bej.2012.10.012

    Article  Google Scholar 

  29. Rossi MJ, Nascimento FX, Giachini AJ, Oliveira VL, Furigo A Jr (2017) Transfer and consumption of oxygen during the cultivation of the ectomycorrhizal fungus Rhizopogon nigrescens in an airlift bioreactor. Appl Microbiol Biotechnol 101:1013–1024. https://doi.org/10.1007/s00253-016-7854-4

    Article  Google Scholar 

  30. Tang YJ, Zhong JJ (2003) Role of oxygen supply in submerged fermentation of Ganoderma lucidum for production of Ganoderma polysaccharide and ganoderic acid. Enzyme Microb 32:478–484. https://doi.org/10.1016/S0141-0229(02)00338-1

    Article  Google Scholar 

  31. Kurosumi A, Kobayasi F, Mtui G, Nakamura Y (2006) Development of optimal culture method of Sparassis crispa mycelia and a new extraction method of antineoplastic constituent. Biochem Eng J 30:109–113. https://doi.org/10.1016/j.bej.2006.02.004

    Article  Google Scholar 

  32. Okabe M, Lies D, Kanamasa S, Park EY (2009) Biotechnological production of itaconic acid and its biosynthesis in Aspergillus terreus. Appl Microbiol Biotechnol 84:606–697. https://doi.org/10.1007/s00253-009-2132-3

    Article  Google Scholar 

  33. Amanullah A, Christensen LH, Hansen K, Nienow AW, Thomas CR (2002) Dependence of morphology on agitation intensity in fed-batch cultures of Aspergillus oryzae and its implications for recombinant protein production. Biotechnol Bioeng 30:815–826. https://doi.org/10.1002/bit.10181

    Article  Google Scholar 

  34. Kawagoe M, Hyakumura K, Suye S, Miki K, Naoe K (1997) Application of bubble column fermentors to submerged culture of Schizophyllum commune for production of L-malic acid. J Ferment Bioeng 84:333–336. https://doi.org/10.1016/S0922-338X(97)89254-9

    Article  Google Scholar 

  35. Galindo E, Flores C, Larralde-Corona P, Corkidi-Blanco G, Rocha-Valadez JA, Serrano-Carreón L (2004) Production of 6-pentyl-α-pyrone by Trichoderma harzianum cultured in unbaffled and baffled shake flasks. Biochem Eng J 18:1–8. https://doi.org/10.1016/S1369-703X(03)00115-3

    Article  Google Scholar 

  36. McDaniel LE, Bailey EG, Zimmerli A (1965) Effect of oxygen supply rates on growth of Escherichia coli: I. Studies in unbaffled and baffled shake flasks. Appl Microbiol 13:109–114. https://doi.org/10.1128/am.13.1.109-114.1965

    Article  Google Scholar 

  37. Pittet V, Morrow K, Ziola B (2011) Ethanol tolerance of lactic acid bacteria, including relevance of the exopolysaccharide gene Gtf. J Am Soc Brew Chem 69:57–61. https://doi.org/10.1094/ASBCJ-2011-0124-01

    Article  Google Scholar 

  38. Suzuki S, Kimoto-Nira H, Suganuma H, Suzuki C, Saito T, Yajima N (2014) Cellular fatty acid composition and exopolysaccharide contribute to bile tolerance in Lactobacillus brevis strains isolated from fermented Japanese pickles. Can J Microbiol 60:183–191. https://doi.org/10.1139/cjm-2014-0043

    Article  Google Scholar 

  39. Sabir F, Beyatli Y, Cokmus C, Onal-Darilmaz D (2010) Assessment of potential probiotic properties of Lactobacillus spp., Lactococcus spp., and Pediococcus spp. strains isolated from kefir. J Food Sci 75:568–573. https://doi.org/10.1111/j.1750-3841.2010.01855.x

    Article  Google Scholar 

Download references

Funding

This study was financed in part by the by the Grant-in-Aid for Young Scientists (A) (Grant No. 17H04717) and the Grant-in-Aid for Scientific Research (A) (Grant No. 20H00664) from the Ministry of Education, Culture, Sports, Science, and Technology of Japan.

Author information

Authors and Affiliations

Authors

Contributions

Ryosuke Okumura: conceptualization, methodology, writing-original. Yoshitoshi Nakamura: investigation, data curation and analysis, writing-review and editing. Chikako Asada: methodology, validation, funding acquisition, supervision.

Corresponding author

Correspondence to Chikako Asada.

Ethics declarations

Ethics approval

Not applicable.

Consent to participate

Not applicable.

Consent for publication

Not applicable.

Conflict of interest

The authors declare no competing interests.

Additional information

Publisher's note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Rights and permissions

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Okumura, R., Nakamura, Y. & Asada, C. Efficiency of β-glucan production by Sparassis crispa depends on mycelium shape. Biomass Conv. Bioref. 14, 1939–1947 (2024). https://doi.org/10.1007/s13399-022-02555-5

Download citation

  • Received:

  • Revised:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s13399-022-02555-5

Keywords

Navigation