Optimization of sporulation of Trametes sanguinea ZHSJ and untargeted metabolomics of spores, mycelium and fruiting body

Posted on
optimization-of-sporulation-of-trametes-sanguinea-zhsj-and-untargeted-metabolomics-of-spores,-mycelium-and-fruiting-body
Optimization of sporulation of Trametes sanguinea ZHSJ and untargeted metabolomics of spores, mycelium and fruiting body

References

  1. Lesage-Meessen, L. et al. Phylogeographic relationships in the polypore fungus Pycnoporus inferred from molecular data. FEMS Microbiol. Lett. 325, 37–48 (2011).

    Google Scholar 

  2. Cui, B. et al. Species diversity, taxonomy and phylogeny of Polyporaceae (Basidiomycota) in China. Fungal Diversity 97, 137–392 (2019).

    Google Scholar 

  3. Yan, M. et al. Structural Characterization and Tumor Microvascular Inhibition Activity of Total Polysaccharide from Trametes sanguinea Lloyd. Chem. Biodivers. 19, e202100765 (2022).

    Google Scholar 

  4. Zovckovx, Z. et al. Mannosidase and Mannanase of Some Wood-rotting Fungi. (1977).

  5. Hoshida’, H. Isolation of Five Lactase Gene Sequences from the White-Rot Fungus Trametes sanguinea by PCR, and Cloning. Characterization and Expression of the Lactase cDNA in Yeasts. (2001).

  6. Sánchez-Corzo, L. et al. Lignocellulolytic enzyme production from wood rot fungi collected in chiapas, mexico, and their growth on lignocellulosic material. J. Fungi 7, (2021).

  7. Sigoillot, C. et al. Natural and recombinant fungal laccases for paper pulp bleaching. Appl. Microbiol. Biotechnol. 64, 346–352 (2004).

    Google Scholar 

  8. Brijwani, K., Rigdon, A. & Vadlani, P. V. Fungal laccases: Production, function, and applications in food processing. (2010).

  9. Sakamoto, M. et al. Purification and characterization of a rhamnogalacturonase with protopectinase activity from Trametes sanguinea. Eur. J. Biochem. 226, 285–291 (1994).

    Google Scholar 

  10. Shen, C. et al. Cardioprotective effect of crude polysaccharide fermented by Trametes sanguinea Lyoyd on doxorubicin-induced myocardial injury mice. BMC Pharmacol. Toxicol, 24, (2023).

  11. Lomascolo, A., Uzan-Boukhris, E., Herpoël-Gimbert, I., Sigoillot, J. C., and Lesage-Meessen, L. Peculiarities of Pycnoporus species for applications in biotechnology. (2011).

  12. Zhang, M. et al. Structural characterization of a polysaccharide from Trametes sanguinea Lloyd with immune-enhancing activity via activation of TLR4. Int. J. Biol. Macromol. 206, 1026–1038 (2022).

    Google Scholar 

  13. Zhou, L. et al. Astragalus polysaccharides exerts immunomodulatory effects via TLR4-mediated MyD88-dependent signaling pathway in vitro and in vivo. Sci. Rep. https://doi.org/10.1038/srep44822 (2017).

    Google Scholar 

  14. Li, J. et al. Purification, structural characterization, and immunomodulatory activity of the polysaccharides from Ganoderma lucidum. Int. J. Biol. Macromol. 143, 806–813 (2020).

    Google Scholar 

  15. Zheng, T. et al. Purification, characterization and immunomodulatory activity of polysaccharides from Leccinum crocipodium (Letellier.) Watliag. Int. J. Biol. Macromol. 148, 647–656 (2020).

    Google Scholar 

  16. He, R., Zhao, Y., Zhao, R. & Sun, P. Antioxidant and antitumor activities in vitro of polysaccharides from E. sipunculoides. Int. J. Biol. Macromol. 78, 56–61 (2015).

    Google Scholar 

  17. Xie, L. et al. Chemical modifications of polysaccharides and their anti-tumor activities. (2020).

  18. Sun, Y. et al. Biological characteristics, bioactive components and antineoplastic properties of sporoderm-broken spores from wild Cordyceps cicadae. Phytomedicine 36, 217–228 (2017).

    Google Scholar 

  19. Thuy, N. H. L. et al. Pharmacological activities and safety of Ganoderma lucidum spores: A systematic review. Cureus https://doi.org/10.7759/cureus.44574 (2023).

    Google Scholar 

  20. Liu, D., Sun, X., Qi, X. & Liang, C. Sexual spores in mushrooms: bioactive compounds, factors and molecular mechanisms of spore formation. Springer Sci. Bus. Media Deutschland GmbH 207, 38 (2025).

    Google Scholar 

  21. Jhan, M. H. et al. Enhancing the antioxidant ability of trametes versicolor polysaccharopeptides by an enzymatic hydrolysis process. Molecules 21, 1215 (2016).

    Google Scholar 

  22. Bains, A. & Chawla, P. In vitro bioactivity, antimicrobial and anti-inflammatory efficacy of modified solvent evaporation assisted Trametes versicolor extract. 3 Biotech. 10, (2020).

  23. Guo, N. Y. et al. New synthetic approaches for the construction of 2-aminophenoxazinone architectures. Royal Soc. Chemistry 28, (2025).

  24. Cajka, T. et al. Rapid LC-MS-based metabolomics method to study the Fusarium infection of barley. J. Sep. Sci. 37, 912–919 (2014).

    Google Scholar 

  25. Zhao, Q., Yang, Z., Zhou, Z., Yang, Y. & Wang, W. Toxicity mechanism of organosilicon adjuvant in combination with S-metolachlor on Vigna angularis. J Hazard. Mater 480, (2024).

  26. Kanehisa, M., Furumichi, M., Sato, Y., Matsuura, Y. & Ishiguro-Watanabe, M. KEGG: Biological systems database as a model of the real world. Nucleic Acids Res. 53, D672–D677 (2025).

    Google Scholar 

  27. Kanehisa, M. Toward understanding the origin and evolution of cellular organisms. Protein Sci. 28, 1947–1951 (2019).

    Google Scholar 

  28. Kanehisa, M. & Goto, S. K. E. G. G. Kyoto Encyclopedia of Genes and Genomes. Nucleic Acids Res. 28, 27–30 (2000).

    Google Scholar 

  29. Sokovi, M., Glamo Lija, J., Iri, A., Petrovi, J. & Stojkovi, D. Chapter 5 – mushrooms as sources of therapeutic foods. In Therapeutic Foods 141–178 (2018).

    Google Scholar 

  30. Ezike, T. C. et al. Substrate specificity of a new laccase from Trametes polyzona WRF03. Heliyon 7, e06080 (2021).

    Google Scholar 

  31. Mehna, A., Bajpai, P. & Bajpa, P. K. Studies on decolorization of effluent from a small pulp mill utilizing agriresidues with Trametes versicolor. Enzyme Microbial Technol. 17, 18–22 (1995).

    Google Scholar 

  32. Wu, J. et al. Novel salt-tolerant xylanase from a mangrove-isolated fungus phoma sp. MF13 and its application in Chinese steamed bread. ACS Omega 3, 3708–3716 (2018).

    Google Scholar 

  33. Kishimoto, T., Hiyama, A., Toda, H. & Urabe, D. Effect of pH on the dehydrogenative polymerization of monolignols by laccases from Trametes versicolor and Rhus vernicifera. ACS Omega 7, 9846–9852 (2022).

    Google Scholar 

  34. Hai, T. T. Incubation temperature affects growth and efficacy of white-rot fungi to improve the nutritive value of rice straw. Anim. Prod. Sci. https://doi.org/10.1071/AN23403 (2024).

    Google Scholar 

  35. Boddy, L. Effect of temperature and water potential on growth rate of wood-rotting basidiomycetes. Trans. Br. Mycol. Soc. 80, 141–149 (1983).

    Google Scholar 

  36. Magan, N. Chapter 4 Ecophysiology: Impact of environment on growth, synthesis of compatible solutes and enzyme production. British Mycological Soc. Symposia Series 63–78 (2008).

  37. Ningsih, F., Yanto, D. H. Y., Mangunwardoyo, W., Anita, S. H. & Watanabe, T. Optimization of lacease production from a newly isolated Trametes sp. EDN134. IOP Conference Series. Earth and Environmental Science. 572, 012024 (2020).

  38. Saltarelli, R. et al. A high concentration of glucose inhibits Tuber borchii mycelium growth: A biochemical investigation. Mycol. Res. 107, 72–76 (2003).

    Google Scholar 

  39. Zhang, H., Li, Q., He, P. & Xu, C. Effect of carbon source on properties and antioxidant potential of exopolysaccharides produced by Trametes robiniophila (Higher Basidiomycetes). Int. J. Med. Mushrooms https://doi.org/10.1615/IntJMedMushrooms.v17.i2.90 (2015).

    Google Scholar 

  40. Jin, X. & Wei, S. Efficient short time pretreatment on lignocellulosic waste using an isolated fungus Trametes sp. W-4 for the enhancement of biogas production. Heliyon https://doi.org/10.1016/j.heliyon.2023.e14573 (2023).

    Google Scholar 

  41. Ottoni, C., Simões, M. F., Fernandes, S., Santos, C. R. & Lima, N. High laccase expression by Trametes versicolor in a simulated textile effluent with different carbon sources and PHs. Int. J. Environ. Res. Public Health https://doi.org/10.3390/ijerph13080778 (2016).

    Google Scholar 

  42. Wang, F., Hu, J. H., Guo, C. & Liu, C. Z. Enhanced laccase production by Trametes versicolor using corn steep liquor as both nitrogen source and inducer. Bioresour. Technol. 166, 602–605 (2014).

    Google Scholar 

  43. Velásquez-Quintero, C., Merino-Restrepo, A. & Hormaza-Anaguano, A. Production, extraction, and quantification of laccase obtained from an optimized solid-state fermentation of corncob with white-rot fungi. J. Clean. Prod. https://doi.org/10.1016/j.jclepro.2022.133598 (2022).

    Google Scholar 

  44. Lodi, R. S. et al. Current research on the medical importance of Trametes species. (2025).

  45. Lodi, R. S. et al. Whole genome sequencing and annotations of Trametes sanguinea ZHSJ. Scientific Data 12, (2025).

  46. Yao, L. et al. Discovery of novel xylosides in co-culture of basidiomycetes Trametes versicolor and Ganoderma applanatum by integrated metabolomics and bioinformatics. Sci. Rep. https://doi.org/10.1038/srep33237 (2016).

    Google Scholar 

  47. Luo, F. et al. Metabolomic differential analysis of interspecific interactions among white rot fungi Trametes versicolor, Dichomitus squalens and Pleurotus ostreatus. Sci. Rep. https://doi.org/10.1038/s41598-017-05669-3 (2017).

    Google Scholar 

  48. Shen, X. T. et al. Unusual and highly bioactive sesterterpenes synthesized by Pleurotus ostreatus during coculture with Trametes robiniophila Murr. Appl. Environ. Microbiol. 85, e00293-19 (2019).

    Google Scholar 

  49. Castaño, J. D. et al. Metabolomics highlights different life history strategies of white and brown rot wood-degrading fungi. mSphere https://doi.org/10.1128/msphere.00545-22 (2022).

    Google Scholar 

Download references

Related Posts