HAN Chunran, LIU Tong, NA Zhiguo, LIU Siqi. Extraction optimization and structural characterization of ergosterol from Phlebopus portentosus[J]. Journal of Henan University of Technology(Natural Science Edition), 2025, 46(3): 90-97,117. DOI: 10.16433/j.1673-2383.202411260001
    Citation: HAN Chunran, LIU Tong, NA Zhiguo, LIU Siqi. Extraction optimization and structural characterization of ergosterol from Phlebopus portentosus[J]. Journal of Henan University of Technology(Natural Science Edition), 2025, 46(3): 90-97,117. DOI: 10.16433/j.1673-2383.202411260001

    Extraction optimization and structural characterization of ergosterol from Phlebopus portentosus

    • Phlebopus portentosus, as an edible fungus with significant health-care value, contains a variety of bioactive substances. Ergosterol, as an important component of bolete mushrooms, has functions such as anti-tumor, anti-viral, antibacterial, immune regulation, anti-inflammatory, and inhibition of lipid accumulation. This study aims to extract and purify ergosterol from Phlebopus portentosus and characterize its structure. On the basis of single-factor experiments, response surface optimization experiments were carried out to determine the optimal extraction process of ergosterol. Fourier transform infrared spectroscopy(FT-IR), ultraviolet spectroscopy(UV), nuclear magnetic resonance(NMR), and high-resolution liquid chromatography-mass spectrometry(LC-MR) were used to analyze and characterize its structure. The results showed that the optimal extraction process of ergosterol from Phlebopus portentosus was as follows: the extraction solvent was methanol, the particle size was 80 mesh, the solid-to-liquid ratio was 1∶ 30(g/mL), the ultrasonic temperature was 40 ℃, the ultrasonic time was 30 min, and the centrifugation speed was 6 000 r/min. Under these conditions, the yield of ergosterol was 0.528 3%. The analysis of the separated and purified ergosterol by high-performance liquid chromatography showed that there was only one chromatographic peak, and the purity of ergosterol was >95%. Through the analysis of FT-IR, UV, 1H nuclear magnetic resonance, 13C nuclear magnetic resonance spectrum and LC-MR of the product, itsmolecular formula was determined to be C28H44O, which was consistent with the structural formula of ergosterol. Its structural formula was further identified by NMR. This study obtained the optimal process for the ultrasonic-assisted extraction of ergosterol from Phlebopus portentosus and determined its structure, providing a reference for the subsequent utilization of ergosterol from Phlebopus portentosus.
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