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中国精品科技期刊2020
高若涵,马楠,杨明哲,等. 燕麦非淀粉多糖发酵富集法工艺优化及其免疫刺激活性分析[J]. 食品工业科技,2025,46(10):21−32. doi: 10.13386/j.issn1002-0306.2024090061.
引用本文: 高若涵,马楠,杨明哲,等. 燕麦非淀粉多糖发酵富集法工艺优化及其免疫刺激活性分析[J]. 食品工业科技,2025,46(10):21−32. doi: 10.13386/j.issn1002-0306.2024090061.
GAO Ruohan, MA Nan, YANG Mingzhe, et al. Optimization of the Fermentation Enrichment Method for Oat Non-starch Polysaccharides and Study of Their Immunostimulatory Activity[J]. Science and Technology of Food Industry, 2025, 46(10): 21−32. (in Chinese with English abstract). doi: 10.13386/j.issn1002-0306.2024090061.
Citation: GAO Ruohan, MA Nan, YANG Mingzhe, et al. Optimization of the Fermentation Enrichment Method for Oat Non-starch Polysaccharides and Study of Their Immunostimulatory Activity[J]. Science and Technology of Food Industry, 2025, 46(10): 21−32. (in Chinese with English abstract). doi: 10.13386/j.issn1002-0306.2024090061.

燕麦非淀粉多糖发酵富集法工艺优化及其免疫刺激活性分析

Optimization of the Fermentation Enrichment Method for Oat Non-starch Polysaccharides and Study of Their Immunostimulatory Activity

  • 摘要: 为提高燕麦非淀粉多糖(ONSP)的产率,优化ONSP的提取工艺并探究其免疫活性。本研究采用微生物发酵辅助提取,并利用单因素实验、响应面试验优化了微生物发酵辅助提取燕麦非淀粉多糖(ONSP1)的提取工艺。利用傅里叶变换红外光谱(FTIR)、气相色谱-质谱联用(GC-MS)测定ONSP的结构,同时对ONSP的免疫活性进行探究,并与传统热水浸提法提取出的燕麦非淀粉多糖(ONSP2)进行比较。结果表明:ONSP1的最佳提取工艺为接菌量5%,发酵温度34 ℃,发酵时间26 h,此时ONSP1的产率为8.60%±0.04%。ONSP1和ONSP2均由葡萄糖、阿拉伯糖和木糖组成,而ONSP1的阿拉伯糖和木糖含量显著高于ONSP2(P<0.05)。检测发现,虽然ONSP1的分子量(47.2 kDa)显著低于ONSP2的分子量(53.2 kDa),但是ONSP1的β-葡聚糖含量显著高于ONSP2(P<0.05)。并且ONSP1和ONSP2均能促进RAW264.7细胞增殖,ONSP1表现出更强的免疫刺激活性。综上所述,微生物发酵富集法得到的燕麦非淀粉多糖中β-葡聚糖含量更高,免疫刺激活性更强。本研究为进一步探究燕麦非淀粉多糖的结构特征、免疫刺激活性及其构效关系提供新的见解。

     

    Abstract: In order to enhance the yield of oat non-starch polysaccharide (ONSP), the extraction process was optimized and its immunological activity was investigated. This study employed microbial fermentation-assisted extraction, optimizing the process for oat non-starch polysaccharide (ONSP1) using a one-way response surface methodology. Fourier transform infrared spectroscopy (FTIR) and gas chromatography-mass spectrometry (GC-MS) were employed to determine the structural characteristics of ONSP. Additionally, the immunological activity of ONSP was investigated and compared with that of oat non-starch polysaccharide (ONSP2) extracted through the conventional hot water method. The results demonstrated that the optimal extraction process for ONSP1 was achieved with a 5% of the inoculum and fermentation at 34 ℃ for 26 h, resulting in a yield of ONSP1 at 8.60%±0.04%. Both ONSP1 and ONSP2 were composed of glucose, arabinose, and xylose, with the contents of arabinose and xylose of ONSP1 were significantly higher than those of ONSP2 (P<0.05). Despite the lower molecular weight of ONSP1 (47.2 kDa) compared to ONSP2 (53.2 kDa), ONSP1 had a significantly higher β-glucan content (P<0.05). Furthermore, both ONSP1 and ONSP2 demonstrated the capacity to promote the proliferation of RAW264.7 cells, with ONSP1 exhibiting a more pronounced immune-stimulating activity. In conclusion, microbial fermentation enrichment resulted in oat non-starch polysaccharides with a higher β-glucan content and stronger immunostimulatory activity. This study provides new insights for further investigation into the bioimmunological activities and structural relationships of oat non-starch polysaccharides.

     

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