Brudzynski Katrina, Sjaarda Calvin P
Department of Drug Discovery, Bee-Bimedical Inc., St. Catharines, Ontario, Canada.
Department of Biological Sciences, Brock University and Department of Drug Discovery, Bee-Biomedicals Inc., St. Catharines, Ontario, Canada.
Compr Rev Food Sci Food Saf. 2021 Mar;20(2):2063-2080. doi: 10.1111/1541-4337.12720. Epub 2021 Feb 10.
Honey colloidal structure emerges as a new trend in research on honey functions since it became recognized as a major factor altering bioactivity of honey compounds. In honey complex matrix, macromolecules self-associate to colloidal particles at the critical concentration, driven by honey viscosity. Sequestration of macromolecules into colloids changes their activities and affects honey antibacterial function. This review fills the 80-year-old gap in research on honey colloidal structure. It summarizes past and current status of the research on honey colloids and describes physicochemical properties and the mechanisms of colloid formation and their dissociation upon honey dilution. The experimental observations are explained in the context of theoretical background of colloidal science. The functional changes and bioactivity of honey macromolecules bound to colloidal particles are illustrated here by the production of H O by glucose oxidase and the effect they have on antibacterial activity of honey. The changes in the production of H O and antibacterial activity of honey were coordinated with the changes in the aggregation-dissociation states of honey colloidal particles upon dilution. In all cases, these changes were nonlinear, assuming an inverted U-shaped dose-response curve. At the curve maximum, the production of H O and antibacterial activity reached the peak. The curve maximum signaled the minimum honey concentration required for the phase separation. With phase transition from two-phase colloidal condense state to dilute state dispersion, the change to opposite effects of dilution on these honey's activities occurred. Thus, the colloidal structure strongly influences bioactivity of honey compounds and affects its antibacterial activity.
自从蜂蜜的胶体结构被认为是改变蜂蜜化合物生物活性的主要因素以来,它已成为蜂蜜功能研究中的一个新趋势。在蜂蜜复杂的基质中,大分子在临界浓度下通过蜂蜜的粘度驱动自组装成胶体颗粒。大分子被隔离到胶体中会改变它们的活性,并影响蜂蜜的抗菌功能。这篇综述填补了蜂蜜胶体结构研究中80年的空白。它总结了蜂蜜胶体研究的过去和现状,描述了其物理化学性质、胶体形成和解离机制以及蜂蜜稀释时的情况。实验观察结果在胶体科学理论背景的框架下进行了解释。这里通过葡萄糖氧化酶产生H₂O₂以及它们对蜂蜜抗菌活性的影响,来说明与胶体颗粒结合的蜂蜜大分子的功能变化和生物活性。蜂蜜中H₂O₂产生量和抗菌活性的变化与稀释后蜂蜜胶体颗粒的聚集 - 解离状态的变化相协调。在所有情况下,这些变化都是非线性的,呈现倒U形剂量反应曲线。在曲线最大值处,H₂O₂的产生量和抗菌活性达到峰值。曲线最大值标志着相分离所需的最低蜂蜜浓度。随着从两相胶体凝聚态到稀态分散的相变,稀释对这些蜂蜜活性的影响发生了相反的变化。因此,胶体结构强烈影响蜂蜜化合物的生物活性并影响其抗菌活性。