Formation and microstructural characterization of scallop (Patinopecten yessoensis) male gonad hydrolysates/sodium alginate coacervations as a function of pH

化学 离子强度 水解物 氢键 动态力学分析 流变仪 虾夷盘扇贝 多糖 酰胺 化学工程 有机化学 扇贝 水溶液 水解 聚合物 分子 工程类 生物 生态学
作者
Yuqiao Wang,Jia‐Nan Yan,Yi‐Nan Du,Shiqi Xu,Zhujun Zhang,Bin Lai,Ce Wang,Hai-Tao Wu
出处
期刊:International Journal of Biological Macromolecules [Elsevier]
卷期号:253 (Pt 2): 126508-126508 被引量:5
标识
DOI:10.1016/j.ijbiomac.2023.126508
摘要

Studying the noncovalent interactions between proteins and polysaccharides is quite important mainly due to the wide number of applications such as developing pH-responsive complexes. Scallop Patinopecten yessoensis male gonad hydrolysates‑sodium alginate (SMGHs-SA) was investigated as noncovalent complexes at pH from 1 to 10. The critical pH values pHC (around 6) and pHφ (around 4) were independent of the SMGHs-SA ratio, indicating the formation of soluble and insoluble complexes. The pH response of SMGHs-SA complexes was evaluated by investigating the rheological behavior, moisture distribution, functional group change and microstructure. Compared to the co-soluble and soluble complexes phases, the SMGHs-SA complexes had a higher storage modulus and viscosity as well as a lower relaxation time (T23) in the insoluble complexes phase (pHφ>3). Additionally, the amide I band and COO- stretching vibration peaks were redshifted and the amide A band vibration peaks were blueshifted by acidification. Electrostatic interactions and intermolecular/intramolecular hydrogen bonding led to SMGHs-SA agglomeration at pH 3, forming a uniform and dense gel network structure with strong gel strength and water-retention capacity. This study provides a theoretical and methodological basis for the design of novel pH-responsive complexes by studying SMGHs-SA complex coacervation.
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