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中國精品科技期刊2020
王崑侖,管立軍,高揚,等. 裂褶菌發酵西洋參工藝優化及體外抗氧化能力研究[J]. 食品工業科技,2024,45(7):142?151. doi: 10.13386/j.issn1002-0306.2023040063.
引用本文: 王崑侖,管立軍,高揚,等. 裂褶菌發酵西洋參工藝優化及體外抗氧化能力研究[J]. 食品工業科技,2024,45(7):142?151. doi: 10.13386/j.issn1002-0306.2023040063.
WANG Kunlun, GUAN Lijun, GAO Yang, et al. Optimization of Fermentation Process of Panax quinquefolius L. by Schizophyllum commune and Its Antioxidant Capacity in Vitro[J]. Science and Technology of Food Industry, 2024, 45(7): 142?151. (in Chinese with English abstract). doi: 10.13386/j.issn1002-0306.2023040063.
Citation: WANG Kunlun, GUAN Lijun, GAO Yang, et al. Optimization of Fermentation Process of Panax quinquefolius L. by Schizophyllum commune and Its Antioxidant Capacity in Vitro[J]. Science and Technology of Food Industry, 2024, 45(7): 142?151. (in Chinese with English abstract). doi: 10.13386/j.issn1002-0306.2023040063.

裂褶菌發酵西洋參工藝優化及體外抗氧化能力研究

Optimization of Fermentation Process of Panax quinquefolius L. by Schizophyllum commune and Its Antioxidant Capacity in Vitro

  • 摘要: 為提高西洋參的經濟價值,本研究以西洋參為原料,利用裂褶菌固態發酵西洋參,提高西洋參中活性成分的含量,并對發酵工藝進行優化。本研究以西洋參中總人參皂苷含量為指標,先從3種裂褶菌菌株中篩選出2號菌株作為固態發酵西洋參用菌。再對影響裂褶菌西洋參發酵物的總人參皂苷含量的4個因素(發酵溫度、裂褶菌接種量、pH和發酵時間)進行單因素實驗。在此結果基礎上,利用響應面Box-Behnken試驗設計進一步優化裂褶菌固態發酵西洋參工藝,確定優化后的工藝條件為:裂褶菌接種量10.90%,發酵溫度31 ℃、發酵時間10 d,發酵pH5.9。在上述條件下,裂褶菌西洋參發酵物的總人參皂苷含量為10.28%,粗多糖含量為12.85%,總黃酮含量為0.67%,均比未發酵西洋參的高。并且大分子人參皂苷Rb1、Rg2和Re含量降低,小分子人參皂苷Rg1、Rc、Rb2、>、Rd、Rg3、s-Rh2、r-Rh2和擬人參皂苷CK含量升高。其中,稀有人參皂苷Rg3、s-Rh2、r-Rh2和擬人參皂苷CK為新出現皂苷。體外抗氧化實驗表明裂褶菌西洋參發酵物的DPPH和ABTS+自由基清除能力的IC50值分別為31365和10910 μg/mL,均強于未發酵西洋參。本研究證明了裂褶菌固態發酵西洋參提高了總人參皂苷、粗多糖、總黃酮和稀有人參皂苷的含量,增強了抗氧化能力,為西洋參的開發利用提供數據支持。

     

    Abstract: In order to improve the economic value of Panax quinquefolius L., this study used Panax quinquefolius L. as raw material to solid state ferment Panax quinquefolius L. by Schizophyllum commune, increased the content of active components in Panax quinquefolius L., and optimized the fermentation technology. In this study, the total ginsenoside content of Panax quinquefolius L. was used as the indicator. First, strain 2 was selected from three strains of Streptomyces as the solid state fermentation strain for Panax quinquefolius L.. Then single factor experiment was conducted on four factors affecting total ginsenoside content. The four factors included: fermentation temperature, inoculation amount of Schizophyllum commune, pH value and fermentation time. On the basis of these results, the technology of solid state fermentation of Panax quinquefolius L. by Schizophyllum commune was further optimized by response surface Box Behnken experimental design. The optimized process conditions were determined as follows: inoculation amount of Schizophyllum commune 10.90%, fermentation temperature 31 ℃, fermentation time 10 d, pH value 5.9. Under the above conditions, the total ginsenoside content of Panax quinquefolius L. fermented by Schizophyllum commune was 10.28%, the content of crude polysaccharide was 12.85%, and the content of total flavonoids was 0.67%, which were higher than that of unfermented Panax quinquefolius L., and the contents of macromolecules ginsenoside Rb1, Rg2 and Re decreased, while the contents of micromolecules ginsenoside Rg1, Rc, Rb2, Rd, Rg3, s-Rh2, r-Rh2 and pseudo-ginsenoside CK increased. Among them, rare ginsenoside Rg3, s-Rh2, r-Rh2, and pseudo-ginsenoside CK were new saponins. In vitro antioxidant tests showed that the IC50 values of DPPH and ABTS+ free radicals scavenging ability of the fermented products of Panax quinquefolius L. by Schizophyllum commune were 3165 and 10910 μg/mL, respectively, which were stronger than those of unfermented Panax quinquefolius L.. This study proved that the solid state fermentation of Panax quinquefolius L. by Schizophyllum commune increased the contents of total ginsenoside, crude polysaccharide, total flavone and rare ginsenoside, and enhanced the antioxidant capacity, which provided data support for the development and utilization of Panax quinquefolius L..

     

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