Physicochemical and macromolecule properties of RG-I enriched pectin from citrus wastes by manosonication extraction

被引:56
作者
Hu, Weiwei [1 ]
Chen, Shiguo [1 ]
Wu, Dongmei [1 ]
Zhu, Kai [1 ]
Ye, Xingqian [1 ]
机构
[1] Zhejiang Univ, Zhejiang Engn Lab Food Technol & Equipment, Zhejiang Key Lab Agrofood Proc, Coll Biosyst Engn & Food Sci, Hangzhou 310058, Peoples R China
基金
中国国家自然科学基金;
关键词
RG-I enriched pectin; Manosonication extraction; Property characterisation; ULTRASONIC-ASSISTED EXTRACTION; RICH RHAMNOGALACTURONAN I; RHEOLOGICAL PROPERTIES; POLYSACCHARIDES; PEEL; HOMOGALACTURONAN; OPTIMIZATION;
D O I
10.1016/j.ijbiomac.2021.01.216
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The properties of pectin extracted from mandarin citrus peels by manosonication extraction (MSp) were systematically studied and compared with pectin obtained by the conventional maceration method (CMp). The yield of MSp (25.5%) was significantly higher than that of CMp (18.3%), while MSp exhibited two Mw fraction distributions. Monosaccharide analysis demonstrated that MSp had more branched RG-I regions (78.3 mol%) than CMp (36.6 mol%) with a high content of arabinose and galactose. The branched-chain morphological characteristics of samples were directly imaged by atomic force microscopy. MSp exhibited a significantly lower degree of methoxylation than CMp by FT-IR and NMR analysis, but X-ray diffraction analysis showed little difference in the level of crystallinity. Moreover, MSp and CMp showed non-Newtonian behaviour, and the increasing order of apparent viscosities was 1.0 w/v% MSp < 1.0 w/v% CMp < 2.0 w/v% CMp < 2.0 w/v% MSp. Thermal analysis and weight loss measurements indicated MSp exhibited greater thermal stability. The results also indicated that both MSp and CMp significantly enhanced the emulsion activity at high concentrations; the emulsions containing 1.5 w/v% pectin showed no phase separation over 21 days, suggesting that MSp could be a potential effective stabiliser in the food and beverage industry. (c) 2021 Elsevier B.V. All rights reserved.
引用
收藏
页码:332 / 341
页数:10
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