Hohenheim University, Institute of Food Science and Biotechnology, Chair Plant Foodstuff Technology, Garbenstrasse 25, D-70599 Stuttgart, Germany.
Food Chem. 2013 Aug 15;139(1-4):1168-78. doi: 10.1016/j.foodchem.2013.02.005. Epub 2013 Feb 16.
The effects of different pectins on the stabilisation of black currant anthocyanins in viscous model solutions at pH 3.0 were investigated. For this purpose, low esterified amidated (AM), low (LM) and high (HM) methoxylated citrus and apple pectins and a sugar beet pectin were added to a purified anthocyanin extract (ACN-E) and to an extract containing anthocyanins and non-anthocyanin phenolics (PP-E). Model systems were stored at 20±0.5°C in the dark. Anthocyanin contents were monitored by HPLC analysis over a period of 18 weeks, and half-life and destruction values were calculated. In all pectic model solutions anthocyanin stability was significantly improved compared to stability of the extracts without added pectins (blank). Best stabilisation was obtained with AM pectin, followed by LM and HM pectins. In model systems containing citrus pectins, anthocyanin stabilisation was better compared to that of apple pectins having similar degrees of esterification and amidation, respectively. This was primarily due to the strong interaction of delphinidin glycosides with the citrus pectins, whereas stabilisation of cyanidin derivatives was less important. Sugar beet pectin improved anthocyanin stability only to a limited extent. In the presence of non-anthocyanin phenolics (PP-E) the impact of the pectin source was even more pronounced than the effect of the pectin type. Addition of citrate to pectic systems accelerated anthocyanin decay. Stabilising effects of pectins were hardly noticeable when evaluating total phenolic content (TPC, Folin-Ciocalteu) and antioxidant capacity during storage. Highest TPC, TEAC- and FRAP values were observed in systems containing citrus pectin, which was in contrast to sugar beet pectin, where values fell below those of the blank after storage.
研究了不同果胶在 pH 3.0 的粘性模型溶液中对黑加仑花色苷稳定化的影响。为此,将低酯化酰胺化(AM)、低(LM)和高(HM)甲氧基化柑橘和苹果果胶以及糖甜菜果胶添加到纯化的花色苷提取物(ACN-E)和含有花色苷和非花色苷酚类物质的提取物(PP-E)中。模型系统在 20±0.5°C黑暗中储存。通过 HPLC 分析在 18 周的时间内监测花色苷含量,并计算半衰期和破坏值。与未添加果胶的提取物(空白)相比,所有果胶模型溶液中的花色苷稳定性均显著提高。AM 果胶的稳定效果最好,其次是 LM 和 HM 果胶。在含有柑橘果胶的模型系统中,花色苷的稳定性优于具有相似酯化和酰胺化程度的苹果果胶。这主要是由于飞燕草苷糖苷与柑橘果胶的强烈相互作用,而氰定衍生物的稳定化作用则不那么重要。糖甜菜果胶仅在一定程度上提高了花色苷的稳定性。在存在非花色苷酚类物质(PP-E)的情况下,果胶来源的影响甚至比果胶类型的影响更为明显。向果胶系统中添加柠檬酸盐会加速花色苷的降解。在评估储存过程中的总酚含量(Folin-Ciocalteu)和抗氧化能力时,果胶的稳定作用几乎不明显。在含有柑橘果胶的系统中观察到最高的 TPC、TEAC 和 FRAP 值,这与糖甜菜果胶形成对比,后者在储存后 TPC 值低于空白值。