食品科学 ›› 2025, Vol. 46 ›› Issue (18): 36-41.doi: 10.7506/spkx1002-6630-20250317-131

• 基础研究 • 上一篇    下一篇

酯化度、分子质量对果胶乳化性能的调控机制

赵少杰,缪立平,康源,张大伟,马昕,张丽珍   

  1. (1.山西大学生命科学学院,山西?太原 030006;2.山西神农渔业科技有限公司,山西?太原 030400)
  • 出版日期:2025-09-25 发布日期:2025-08-19
  • 基金资助:
    国家自然科学基金青年科学基金项目(32101880);山西省基础研究计划资助项目(202403021221005); 山西大学“文瀛青年学者”人才计划项目

Regulatory Mechanism of Degree of Esterification and Molecular Mass on the Emulsifying Performance of Pectin

ZHAO Shaojie, MIAO Liping, KANG Yuan, ZHANG Dawei, MA Xin, ZHANG Lizhen   

  1. (1. School of Life Science, Shanxi University, Taiyuan 030006, China; 2. Shanxi Shennong Fishery Science and Technology Co., Ltd., Taiyuan 030400, China)
  • Online:2025-09-25 Published:2025-08-19

摘要: 为探究酯化度、分子质量对果胶乳化性能的调控机制,本实验对不同结构果胶的聚集行为、聚集体结构、界面性质、乳化性质及其在界面的吸附层结构进行分析。结果表明:果胶酯化度从35%增至73%过程中,果胶聚集体直径由1 950 nm规律地降至1 443 nm,聚集体内疏水微区的极性不断降低,向油-水界面的扩散速率显著提升,其界面吸附量从54.4 ng/cm2增加至95.9 ng/cm2,界面吸附层厚度从76.9 nm降低至43.6 nm,平衡界面张力从24 mN/m降低至18 mN/m,其乳化性能显著改善。果胶分子质量从0.55×105 Da增至1.30×105 Da过程中,聚集体直径由1 195 nm增至1 443 nm,向油-水界面的扩散速率降低,界面吸附量由127.3 ng/cm2降至95.9 ng/cm2,其界面性质与乳化性能均变差;但由于聚集体内部疏水性增加,抑制了果胶从界面脱附,提升了乳液在贮藏过程中的稳定性。本研究结果从聚集体的角度阐明了分子结构对果胶乳化性能的潜在调控机制,可为果胶乳化剂的开发与利用提供理论依据。

关键词: 果胶;酯化度;分子质量;聚集体;界面性质;乳化性能

Abstract: To investigate the regulatory mechanisms of the degree of esterification and molecular mass on the emulsifying properties of pectin, this study analyzed the aggregation behavior, aggregate structure, interfacial properties, emulsifying properties, and the structure of the adsorption layer at the interface of pectins with different structures. The results showed that: 1) as the degree of esterification increased from 35% to 73%, the size of pectin aggregates decreased regularly from 1 950 to 1 443 nm, the polarity of hydrophobic microdomains in the aggregates decreased, the diffusion rate to the oil-water interface increased significantly, the amount of pectin adsorbed onto the interface increased from 54.4 to 95.9 ng/cm2, the interfacial adsorption layer thickness decreased from 76.9 to 43.6 nm, the equilibrium interfacial tension decreased from 24 to 18 mN/m, and the emulsifying performance was significantly improved; 2) as the molecular mass increased from 0.55 × 105 to 1.30 × 105 Da, the size of pectin aggregates increased from 1 195 to 1 443 nm, the diffusion rate to the oil-water interface decreased, the interfacial adsorption amount decreased from 127.3 to 95.9 ng/cm2, and both the interfacial and emulsifying properties deteriorated. However, since the internal hydrophobicity of the aggregates increased, the desorption of pectin from the interface was inhibited, thereby improving the emulsion stability during storage. The findings of this study provide a theoretical basis for the development and utilization of pectin emulsifiers.

Key words: pectin; degree of esterification; molecular mass; aggregate; interfacial properties; emulsifying performance

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