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固态 C 核磁共振研究从. 中提取的可溶性和不可溶性β-葡聚糖。

Solid-State C Nuclear Magnetic Resonance Study of Soluble and Insoluble β-Glucans Extracted from .

机构信息

Department of Microbiology and Biotechnology, Institute of Biosciences, Life Sciences Center, Vilnius University, Saulėtekio Ave. 7, LT-10257 Vilnius, Lithuania.

Department of Medical Technology and Dietetics, Faculty of Health Care, Vilniaus Kolegija/Higher Education Institution, Didlaukio Str. 45, LT-08303 Vilnius, Lithuania.

出版信息

Molecules. 2023 Dec 13;28(24):8066. doi: 10.3390/molecules28248066.

Abstract

β-glucans are widely known for their biological activities. However, the choice of extraction method can significantly influence their structural characteristics, thereby potentially impacting their biological functions. In this paper, three fractions of β-glucans were obtained from yeast via alkali and hot-water extraction methods and were analyzed using solid-state C nuclear magnetic resonance (NMR) spectroscopy. Solid-state NMR spectroscopy was used as a nondestructive technique that preserves the structure of the analyzed molecules. The results suggest that differences in the β-glucan structure are affected by the choice of extraction method. The main difference occurred in the 82-92 ppm region with signal presence suggesting that β-glucans have a linear structure when hot-water-extracted, which is absent in alkali-extracted fractions resulting in the acquisition of β-glucans with an ordered, possibly helical structure. A hot-water extracted water-insoluble (HWN) fraction consists of linear β-1,3-glucans with other signals indicating the presence of β-1,6-linked side chains, chitin and small amounts of α-glucan impurities. For those that are alkali-extracted, alkali-insoluble (AN) and water-soluble (AWS) fractions are structurally similar and consist of an ordered β-1,3-glucan structure with β-1,6-linked side chains and a significant amount of α-glucan and chitin in both fractions.

摘要

β-葡聚糖以其生物活性而广为人知。然而,提取方法的选择会显著影响其结构特征,从而可能影响其生物功能。在本文中,通过碱法和热水提取法从酵母中得到了 3 种β-葡聚糖级分,并采用固态 C 核磁共振(NMR)光谱进行了分析。固态 NMR 光谱是一种无损技术,可保持被分析分子的结构。结果表明,β-葡聚糖结构的差异受提取方法的选择影响。主要差异发生在 82-92 ppm 区域,存在信号表明热水提取的β-葡聚糖具有线性结构,而碱提取级分中不存在这种结构,从而获得具有有序、可能为螺旋结构的β-葡聚糖。热水提取的不溶性水(HWN)级分由线性β-1,3-葡聚糖组成,其他信号表明存在β-1,6 键合的侧链、几丁质和少量α-葡聚糖杂质。对于那些经过碱提取的,碱不溶性(AN)和水溶性(AWS)级分在结构上相似,由有序的β-1,3-葡聚糖结构组成,具有β-1,6 键合的侧链,并且在两个级分中都有大量的α-葡聚糖和几丁质。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7749/10745363/6f27ec40ba82/molecules-28-08066-g001.jpg

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