淀粉
静水压力
没食子酸
Boosting(机器学习)
复合材料
包裹体(矿物)
化学
材料科学
食品科学
化学工程
矿物学
生物化学
计算机科学
物理
抗氧化剂
热力学
工程类
机器学习
作者
Pedro Rivero-Ramos,James Railton,Dolores Rodrigo,Maria Benlloch‐Tinoco
标识
DOI:10.1016/j.ijbiomac.2024.139257
摘要
Influencing the starch postprandial glycemia via interventions that are sourced from natural plant materials has gained attention recently. Amylose present in starch is reported to form complexes with small ligands such as gallic acid (GA) through a conformational change that are digested slowly and contribute to the formation of resistant starch. In this study, the molecular interactions, multi-scale structure and in vitro digestion properties of normal neat rice starch and rice starch-GA composites (2, 5 % w / v ) obtained either by high hydrostatic pressure (HHP) or thermal (T) treatment were compared. The multi-scale structure changes experienced by the rice starch gels (neat and composite) during simulated oro-gastrointestinal (OGIT) digestion were also characterised. Overall, formation of the V 7 type inclusion complex was demonstrated in the composite gels processed by HHP and T, although the main molecular interactions found in the composites were non-inclusion complexes. Sample A-GA-5-HHP formed gels with a unique microstructure, whilst also displaying a significant increase of the resistant starch fraction (∼13 %) and a large decrease of the rapidly digestible starch fraction than A-GA-5-T ( p < 0.05). The lower digestibility in A-GA-5-HHP was attributed to increased molecular interactions between amylose and GA, as suggested by the greater intensity peak at 3520 cm −1 in the FTIR, and the downfield chemical shifts (0.12 ppm) in the 13 C NMR spectra. Our findings indicate that HHP gelatinisation of starch-GA composites represents a promising approach for the design of novel starch-based systems with distinct microstructure and digestion characteristics.
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