Advances in Enzymatic Measurement of β-Glucan in Mushrooms, Yeast, Algae, and Dietary Supplements.

IF 1.7
Lucie C Sweeney, Caoilfhionn Walsh, Amaya O'Cochlain, Ruth Ivory, David Mangan
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Abstract

Background: The rapid expansion of the functional mushroom, yeast, and algae market has increased the need for enzymatic quantification of 1,3-/1,6-β-glucans. The longstanding indirect approach, which calculates β-glucans by subtracting enzymatically measured α-glucans from total glucans obtained through acid hydrolysis, is increasingly challenged by modern supplement formulations containing resistant starches, trehalose, and sweeteners such as maltitol.

Objective: To evaluate the current indirect enzymatic method for β-glucan measurement and to refine the analytical workflow to support reliable β-glucan quantification across the expanding functional mushroom, yeast, and algae market and associated dietary supplement formats.

Methods: Key steps of the established indirect β-glucan method were systematically evaluated to identify matrix-dependent limitations related to acid solubilization, glucose stability during hydrolysis, α-glucan specificity, and formulation-derived interferences. Based on these findings, a refined analytical workflow was defined and applied for benchmarking and performance evaluation across mushrooms, yeast, algae, and multiple supplement delivery formats.

Results: Targeted refinements increased measured total glucan values, improved α-glucan determination in matrices containing resistant starches, trehalose, and maltitol, and reduced systematic glucose loss associated with acid hydrolysis. Comparative evaluation demonstrated matrix-dependent differences relative to the conventional method, while maintaining consistent analytical performance across complex formulations and reducing total assay time.

Conclusion: These advances in enzymatic β-glucan measurement address recognized limitations of the indirect approach and support more consistent β-glucan quantification across diverse natural product matrices and modern supplement formats.

Highlights: Advances in enzymatic β-glucan measurement were achieved through targeted refinements to total and α-glucan determination, improving measurement consistency across mushrooms, yeast, algae, and complex supplement formulations and supporting further collaborative evaluation.

蘑菇、酵母、藻类和膳食补充剂中β-葡聚糖酶法测定的研究进展
背景:功能性蘑菇、酵母和藻类市场的快速扩张增加了对1,3-/1,6-β-葡聚糖酶定量的需求。长期存在的间接方法是通过从酸水解获得的总葡聚糖中减去酶测α-葡聚糖来计算β-葡聚糖,这种方法越来越受到含有抗性淀粉、海藻糖和麦芽糖醇等甜味剂的现代补充剂配方的挑战。目的:评价目前用于β-葡聚糖测定的间接酶法,并改进分析流程,以支持在不断扩大的功能性蘑菇、酵母和藻类市场以及相关膳食补充剂形式中可靠的β-葡聚糖定量。方法:对建立的间接β-葡聚糖法的关键步骤进行系统评价,以确定酸增溶、水解过程中的葡萄糖稳定性、α-葡聚糖特异性和配方衍生干扰等基质依赖性限制。基于这些发现,我们定义了一个精细的分析工作流程,并将其应用于蘑菇、酵母、藻类和多种补充剂递送格式的基准测试和性能评估。结果:有针对性的改进提高了总葡聚糖的测量值,改善了含有抗性淀粉、海藻糖和麦芽糖醇的基质中α-葡聚糖的测定,减少了与酸水解相关的系统性葡萄糖损失。对比评价显示了相对于传统方法的基质依赖性差异,同时在复杂配方中保持一致的分析性能并减少总分析时间。结论:酶促β-葡聚糖测量的这些进展解决了间接方法的公认局限性,并支持在不同天然产物基质和现代补充剂格式中更一致的β-葡聚糖定量。重点:通过有针对性地改进总葡聚糖和α-葡聚糖的测定,提高了蘑菇、酵母、藻类和复杂补充剂配方的测量一致性,并支持进一步的协同评估,取得了酶促β-葡聚糖测定的进展。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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