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Composition and Antioxidant Activity of the Anthocyanins of the Fruit of Berberis heteropoda Schrenk

机译:小ber小Fruit果实中花色苷的组成及抗氧化活性

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摘要

In present study, the anthocyanin composition and content of the fruit of B. heteropoda Schrenk were determined for the first time. The total anthocyanins were extracted from the fruit of B. heteropoda Schrenk using 0.5% HCl in 80% methanol and were then purified using an AB-8 macroporous resin column. The purified anthocyanin extract (PAE) was evaluated by high-performance liquid chromatography with a diode array detector (HPLC-DAD) and HPLC-high resolution-electrospray ionization-mass spectrometry (HPLC-HR-ESI-MS) under the same experimental conditions. The results revealed the presence of seven different anthocyanins. The major anthocyanins purified by preparative HPLC were confirmed to be delphinidin-3-O-glucopyranoside (30.3%), cyanidin-3-O-glucopyranoside (33.5%), petunidin-3-Ο-glucopyranoside (10.5%), peonidin-3-O-glucopyranoside (8.5%) and malvidin-3-O-glucopyranoside (13.8%) using HPLC-HR-ESI-MS and NMR spectroscopy. The total anthocyanin content was 2036.6 ± 2.2 mg/100 g of the fresh weight of B. heteropoda Schrenk fruit. In terms of its total reducing capacity assay, DPPH radical-scavenging activity assay, ferric-reducing antioxidant power (FRAP) assay and ABTS radical cation-scavenging activity assay, the PAE also showed potent antioxidant activity. The results are valuable for illuminating anthocyanins composition of B. heteropoda Schrenk and for further utilising them as a promising anthocyanin pigment source. This research enriched the chemical information of B. heteropoda Schrenk.
机译:在本研究中,首次测定了异双歧杆菌Schrenk果实的花色苷组成和含量。使用在80%甲醇中的0.5%HCl从异交双歧杆菌Schrenk的果实中提取总花色苷,然后使用AB-8大孔树脂柱进行纯化。在相同的实验条件下,使用二极管阵列检测器(HPLC-DAD)和高效液相色谱-高分辨率电喷雾电离质谱(HPLC-HR-ESI-MS),通过高效液相色谱法对纯化的花色苷提取物(PAE)进行了评估。 。结果显示存在七种不同的花色苷。经制备型HPLC纯化的主要花色苷经确认为翠菊素-3-O-吡喃葡萄糖苷(30.3%),花青素3-O-吡喃葡萄糖苷(33.5%),矮牵牛苷-3-O-吡喃葡萄糖苷(10.5%),peonidin-3使用HPLC-HR-ESI-MS和NMR光谱分析得出-O-吡喃葡萄糖苷(8.5%)和Malvidin-3-O-吡喃葡萄糖苷(13.8%)。花青素的总含量为异双歧杆菌Schrenk果实鲜重的2036.6±2.2 mg / 100 g。在其总还原能力测定,DPPH自由基清除活性测定,三价铁还原抗氧化剂能力(ABAP)自由基清除阳离子活性测定方面,PAE还显示出有效的抗氧化剂活性。该结果对于阐明异双歧杆菌Schrenk的花青素组成以及将其进一步用作有希望的花青素色素来源具有重要价值。这项研究丰富了异双歧杆菌Schrenk的化学信息。

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