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中国精品科技期刊2020
苏雪娇, 张秀娟, 常维娜, 黎晓莹, 孙丽平. 凉薯(Pachyrrhizus erosus L.)块茎的营养品质分析[J]. 食品工业科技, 2013, (19): 349-351. DOI: 10.13386/j.issn1002-0306.2013.19.055
引用本文: 苏雪娇, 张秀娟, 常维娜, 黎晓莹, 孙丽平. 凉薯(Pachyrrhizus erosus L.)块茎的营养品质分析[J]. 食品工业科技, 2013, (19): 349-351. DOI: 10.13386/j.issn1002-0306.2013.19.055
SU Xue-jiao, ZHANG Xiu-juan, CHANG Wei-na, LI Xiao-ying, SUN Li-ping. Study on nutritional quality of Pachyrrhizus erosus L.Tuber[J]. Science and Technology of Food Industry, 2013, (19): 349-351. DOI: 10.13386/j.issn1002-0306.2013.19.055
Citation: SU Xue-jiao, ZHANG Xiu-juan, CHANG Wei-na, LI Xiao-ying, SUN Li-ping. Study on nutritional quality of Pachyrrhizus erosus L.Tuber[J]. Science and Technology of Food Industry, 2013, (19): 349-351. DOI: 10.13386/j.issn1002-0306.2013.19.055

凉薯(Pachyrrhizus erosus L.)块茎的营养品质分析

Study on nutritional quality of Pachyrrhizus erosus L.Tuber

  • 摘要: 对云南产凉薯块茎中基本营养成分及其含量、多酚含量及其组成、多酚提取物的抗氧化活性进行了研究。结果表明:云南产凉薯块茎富含水溶性糖和淀粉,VC的含量为11.55mg·100g-1鲜重(FW);B族维生素中B3和B6含量较高,分别为0.166和0.207mg·100g-1FW;多酚含量为2.06mg·g-1干重(DW),其中没食子酸、香草酸、咖啡酸和芦丁为主要成分,含量分别为0.55、0.27、0.12和0.15mg·g-1DW;多酚提取物表现出与其浓度线性正相关的强抗氧化活性,其在还原能力的EC50值为1.33μg·mL-1,DPPH自由基清除能力、羟自由基清除能力和抑制脂质体过氧化能力的IC50分别为4.15、7.70和17.00μg·mL-1。表明凉薯是一种营养品质较好的食源材料。 

     

    Abstract: The nutritional components, the content and composition of the polyphenolics in the tuber of Pachyrrhizus erosus L.from Yunnan province was investigated, and the antioxidant activities of the polyphenolics were determined.The results showed that the tuber of Pachyrrhizus erosus L.had a high-level of soluble carbohydrate and starch, a significant amount of ascorbic acid, niacin and pyridoxine, being 11.55, 0.166 and 0.207mg·100g-1 fresh weight (FW) , respectively.The polyphenolic content in tuber was 2.06mg·g-1dry weight (DW) .Gallic acid, vanillic acid, caffeic acid and rutin were the dominate components, being 0.55, 0.27, 0.12 and 0.15mg /g DW, respectively.The polyphenolic extracts showed significant reducing power, DPPH-scavenging activity, OH-scavenging activity and lipid peroxidation inhibition ability, with EC 50 and IC 50 being 1.33μg·mL-1, 4.15, 7.70 and 17.00μg·mL-1respectively.

     

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