Xinwei Xu , Feng Jiang , Kuncheng Lin , Jingjing Fang , Fuquan Chen , Yi Ru , Huifen Weng , Qiong Xiao , Qiuming Yang , Anfeng Xiao
{"title":"在冷冻过程中通过酸酐酯化调节κ-卡拉胶凝胶中水的迁移并减少冰晶的形成","authors":"Xinwei Xu , Feng Jiang , Kuncheng Lin , Jingjing Fang , Fuquan Chen , Yi Ru , Huifen Weng , Qiong Xiao , Qiuming Yang , Anfeng Xiao","doi":"10.1016/j.foodhyd.2023.109726","DOIUrl":null,"url":null,"abstract":"<div><p>In this study, κ-carrageenan was chemically modified by acid anhydride esterification<span> to produce acid anhydride-esterified κ-carrageenan, and its properties were subsequently determined. Acid anhydride-esterified κ-carrageenan can improve the water retention properties of gels and limit the deterioration of gel textural performances during the freezing process. Scanning electron microscopy results before and after freezing showed that the frozen esterified κ-carrageenans had a more regular and less fibrous network structure, which suggests that the esterified κ-carrageenans better maintained the gel network structure. These phenomena were studied in relation to intermolecular forces, water movement, and ice crystal formation. The intermolecular force analysis showed that the esterification of anhydride disrupted the hydrogen bond formed between κ-carrageenan molecules, enhanced hydrophobic interactions among κ-carrageenan molecules, and resulted in stronger electrostatic repulsion. Low-field nuclear magnetic resonance analysis showed that acid anhydride-esterified κ-carrageenan more effectively bound to water molecules during freezing. Differential scanning calorimetry results showed that acid anhydride-esterified κ-carrageenan reduced the amount of freezing water and lowered the eutectic point of the gel. The results showed that hydrogen bonding, electrostatic interactions, and hydrophobic interactions modified the structure of the acid anhydride-esterified κ-carrageenan gel network and its binding to water molecules. This phenomenon allowed acid anhydride-esterified κ-carrageenan to better maintain binding with water molecules during the freezing process, which in turn delayed and reduced the formation of ice crystals and greatly decreased the effect of ice crystals on the structure of the gel network.</span></p></div>","PeriodicalId":320,"journal":{"name":"Food Hydrocolloids","volume":"150 ","pages":"Article 109726"},"PeriodicalIF":11.0000,"publicationDate":"2023-12-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Anhydride esterification to regulate water migration and reduce ice crystal formation in κ-carrageenan gel during freezing\",\"authors\":\"Xinwei Xu , Feng Jiang , Kuncheng Lin , Jingjing Fang , Fuquan Chen , Yi Ru , Huifen Weng , Qiong Xiao , Qiuming Yang , Anfeng Xiao\",\"doi\":\"10.1016/j.foodhyd.2023.109726\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>In this study, κ-carrageenan was chemically modified by acid anhydride esterification<span> to produce acid anhydride-esterified κ-carrageenan, and its properties were subsequently determined. Acid anhydride-esterified κ-carrageenan can improve the water retention properties of gels and limit the deterioration of gel textural performances during the freezing process. Scanning electron microscopy results before and after freezing showed that the frozen esterified κ-carrageenans had a more regular and less fibrous network structure, which suggests that the esterified κ-carrageenans better maintained the gel network structure. These phenomena were studied in relation to intermolecular forces, water movement, and ice crystal formation. The intermolecular force analysis showed that the esterification of anhydride disrupted the hydrogen bond formed between κ-carrageenan molecules, enhanced hydrophobic interactions among κ-carrageenan molecules, and resulted in stronger electrostatic repulsion. Low-field nuclear magnetic resonance analysis showed that acid anhydride-esterified κ-carrageenan more effectively bound to water molecules during freezing. Differential scanning calorimetry results showed that acid anhydride-esterified κ-carrageenan reduced the amount of freezing water and lowered the eutectic point of the gel. The results showed that hydrogen bonding, electrostatic interactions, and hydrophobic interactions modified the structure of the acid anhydride-esterified κ-carrageenan gel network and its binding to water molecules. This phenomenon allowed acid anhydride-esterified κ-carrageenan to better maintain binding with water molecules during the freezing process, which in turn delayed and reduced the formation of ice crystals and greatly decreased the effect of ice crystals on the structure of the gel network.</span></p></div>\",\"PeriodicalId\":320,\"journal\":{\"name\":\"Food Hydrocolloids\",\"volume\":\"150 \",\"pages\":\"Article 109726\"},\"PeriodicalIF\":11.0000,\"publicationDate\":\"2023-12-31\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Food Hydrocolloids\",\"FirstCategoryId\":\"97\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0268005X23012729\",\"RegionNum\":1,\"RegionCategory\":\"农林科学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"CHEMISTRY, APPLIED\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Food Hydrocolloids","FirstCategoryId":"97","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0268005X23012729","RegionNum":1,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, APPLIED","Score":null,"Total":0}
Anhydride esterification to regulate water migration and reduce ice crystal formation in κ-carrageenan gel during freezing
In this study, κ-carrageenan was chemically modified by acid anhydride esterification to produce acid anhydride-esterified κ-carrageenan, and its properties were subsequently determined. Acid anhydride-esterified κ-carrageenan can improve the water retention properties of gels and limit the deterioration of gel textural performances during the freezing process. Scanning electron microscopy results before and after freezing showed that the frozen esterified κ-carrageenans had a more regular and less fibrous network structure, which suggests that the esterified κ-carrageenans better maintained the gel network structure. These phenomena were studied in relation to intermolecular forces, water movement, and ice crystal formation. The intermolecular force analysis showed that the esterification of anhydride disrupted the hydrogen bond formed between κ-carrageenan molecules, enhanced hydrophobic interactions among κ-carrageenan molecules, and resulted in stronger electrostatic repulsion. Low-field nuclear magnetic resonance analysis showed that acid anhydride-esterified κ-carrageenan more effectively bound to water molecules during freezing. Differential scanning calorimetry results showed that acid anhydride-esterified κ-carrageenan reduced the amount of freezing water and lowered the eutectic point of the gel. The results showed that hydrogen bonding, electrostatic interactions, and hydrophobic interactions modified the structure of the acid anhydride-esterified κ-carrageenan gel network and its binding to water molecules. This phenomenon allowed acid anhydride-esterified κ-carrageenan to better maintain binding with water molecules during the freezing process, which in turn delayed and reduced the formation of ice crystals and greatly decreased the effect of ice crystals on the structure of the gel network.
期刊介绍:
Food Hydrocolloids publishes original and innovative research focused on the characterization, functional properties, and applications of hydrocolloid materials used in food products. These hydrocolloids, defined as polysaccharides and proteins of commercial importance, are added to control aspects such as texture, stability, rheology, and sensory properties. The research's primary emphasis should be on the hydrocolloids themselves, with thorough descriptions of their source, nature, and physicochemical characteristics. Manuscripts are expected to clearly outline specific aims and objectives, include a fundamental discussion of research findings at the molecular level, and address the significance of the results. Studies on hydrocolloids in complex formulations should concentrate on their overall properties and mechanisms of action, while simple formulation development studies may not be considered for publication.
The main areas of interest are:
-Chemical and physicochemical characterisation
Thermal properties including glass transitions and conformational changes-
Rheological properties including viscosity, viscoelastic properties and gelation behaviour-
The influence on organoleptic properties-
Interfacial properties including stabilisation of dispersions, emulsions and foams-
Film forming properties with application to edible films and active packaging-
Encapsulation and controlled release of active compounds-
The influence on health including their role as dietary fibre-
Manipulation of hydrocolloid structure and functionality through chemical, biochemical and physical processes-
New hydrocolloids and hydrocolloid sources of commercial potential.
The Journal also publishes Review articles that provide an overview of the latest developments in topics of specific interest to researchers in this field of activity.