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中国精品科技期刊2020
崔瑞彤,赵元寿,魏文利,等. 鲜黄芪采后低温贮藏中的品质变化规律J. 食品工业科技,2026,47(7):1−9. doi: 10.13386/j.issn1002-0306.2025040129.
引用本文: 崔瑞彤,赵元寿,魏文利,等. 鲜黄芪采后低温贮藏中的品质变化规律J. 食品工业科技,2026,47(7):1−9. doi: 10.13386/j.issn1002-0306.2025040129.
CUI Ruitong, ZHAO Yuanshou, WEI Wenli, et al. Quality Change Rule of Fresh Radix Astragali during Postharvest Storage at Low Temperature ConditionJ. Science and Technology of Food Industry, 2026, 47(7): 1−9. (in Chinese with English abstract). doi: 10.13386/j.issn1002-0306.2025040129.
Citation: CUI Ruitong, ZHAO Yuanshou, WEI Wenli, et al. Quality Change Rule of Fresh Radix Astragali during Postharvest Storage at Low Temperature ConditionJ. Science and Technology of Food Industry, 2026, 47(7): 1−9. (in Chinese with English abstract). doi: 10.13386/j.issn1002-0306.2025040129.

鲜黄芪采后低温贮藏中的品质变化规律

Quality Change Rule of Fresh Radix Astragali during Postharvest Storage at Low Temperature Condition

  • 摘要: 目的:探讨鲜黄芪在4 ℃低温避光条件下的贮藏特性及其品质变规律。方法:测定鲜黄芪在4 ℃低温贮藏期间的生理、品质、抗氧化和酸败指标,并结合感官评价及腐烂指标解析鲜黄芪的低温贮藏特性与品质变化规律。结果:鲜黄芪在0~60 d的低温贮藏过程中,水分含量逐渐降低,由57.92%下降至48.19%;呼吸强度在15 d时达到峰值15.17 mg·kg−1·h−1;,后续逐渐降低,呈现先升后降趋势;质量损失率逐渐增加,至贮后60 d约为9.76%。低温贮藏0~30 d鲜黄芪品质维持稳定,贮藏30~60 d感官品质和b*显著下降(P<0.05),表现为色泽褐变及质地软化,贮后60 d鲜黄芪切面的b*较初始降低33.07%。总黄酮含量在贮藏前15 d略有上升,达到峰值(0.56 mg/g),随后显著下降(P<0.05),至60 d降至0.34 mg/g。毛蕊异黄酮含量持续下降,60 d降至0.0175 mg/g。DPPH、ABTS+及羟自由基清除能力在15 d达到峰值,贮后60 d时分别降低了54.81%、17.5%和23.40%。超氧阴离子含量显著上升(P<0.05),至60 d时升至3.92 μmol/g,酸价和过氧化值随时间升高,至60 d分别达39.36 mg/g和4.86%,后期氧化严重,品质显著劣变。随着低温贮藏时间的延长,鲜黄芪的腐烂率和病情指数呈显著上升趋势(P<0.05),30 d后出现霉变,在贮后45 d及60 d时腐烂率分别达到8.83%和12.57%,病情指数为7.34%和10.59%。结论:鲜黄芪在4 ℃低温避光条件下贮藏30 d内可较好地保持感官品质与生物活性,黄酮类成分、抗氧化能力及代谢状态相对稳定;贮藏超过30 d后,腐烂逐渐加重,品质快速劣变,产品的抗氧化能力降低。该研究结果为鲜黄芪采后贮藏保鲜和品质控制提供理论参考。

     

    Abstract: Objective: To investigate the storage characteristics and quality evolution of fresh Radix Astragali under low-temperature of 4  ℃ and dark storage conditions. Methods: The storage characteristics and quality changes of fresh Radix Astragali at 4  ℃ were analyzed by monitoring its physiological parameters and storage quality during storage. Results: The moisture content of fresh Radix Astragali decreased from 57.92% to 48.19%, accompanied by a steady increase in weight loss, which reached 9.76% at 60 days. Respiration intensity showed a rise-then-fall trend, peaking at 15 days (15.17 mg·kg−1·h−1), indicating active metabolism in the early storage stage. In the initial 30 days, overall quality remained stable; however, in the later period, sensory quality and b* value declined significantly (P<0.05), with surface browning and texture softening. The b* value of the cross-section decreased by 33.07% at 60 days compared to day 0. Total flavonoid content slightly increased initially, peaking at 0.56 mg/g at 15 days, then declined markedly to 0.34 mg/g by 60 days (P<0.05). Calycosin content continuously decreased, reaching 0.0175 mg/g at 60 days. Antioxidant capacities (DPPH, ABTS+, and hydroxyl radical scavenging) also peaked at 15 days, but dropped by 54.81%, 17.5%, and 23.40%, respectively, at 60 days. Superoxide anion content increased significantly (P<0.05), reaching 3.92 μmol/g by day 60. Both acid value and peroxide value increased over time, reaching 39.36 mg/g and 4.86% at 60 days, reflecting severe oxidative deterioration. With prolonged storage, decay rate and disease index increased notably. Mold appeared after 30 days, with decay rates of 8.83% and 12.57%, and disease indices of 7.34% and 10.59% at 45 and 60 days, respectively. Conclusion: A storage duration of up to 30 days at 4  ℃ under dark conditions was found to effectively preserve the sensory quality and biological activity of fresh Radix Astragali, with flavonoid levels, antioxidant capacity, and metabolic status remaining relatively stable. Beyond this period, decay became progressively severe, accompanied by a rapid decline in overall quality and antioxidant function. This study provides a theoretical foundation for optimizing postharvest storage strategies and quality control of fresh Radix Astragali.

     

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