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利用各种糖原分支酶生产具有增强的缓慢消化性的高度支化的α-极限糊精。

Production of highly branched α-limit dextrins with enhanced slow digestibility by various glycogen-branching enzymes.

机构信息

Department of Food Science and Biotechnology, Gachon University, Seongnam 13120, Republic of Korea; Core-Facility for Bionano Materials, Gachon University, Seongnam 13120, Republic of Korea.

Department of Food Science and Biotechnology, Gachon University, Seongnam 13120, Republic of Korea.

出版信息

Carbohydr Polym. 2023 Jun 15;310:120730. doi: 10.1016/j.carbpol.2023.120730. Epub 2023 Feb 21.

DOI:10.1016/j.carbpol.2023.120730
PMID:36925263
Abstract

α-Limit dextrins (α-LDx) are slowly digestible carbohydrates that attenuate postprandial glycemic response and trigger the secretion of satiety-related hormones. In this study, more highly branched α-LDx were enzymatically synthesized to enhance the slowly digestible property by various origins of glycogen branching enzyme (GBE), which catalyzes the transglycosylation to form α-1,6 branching points after cleaving α-1,4 linkages. Results showed that the proportion of branched α-LDx in starch molecules increased around 2.2-8.1 % compared to α-LDx from starch without GBE treatment as the ratio of α-1,6 linkages increased after different types of GBE treatments. Furthermore, the enzymatic increment of branching points enhanced the slowly digestible properties of α-LDx at the mammalian α-glucosidase level by 17.3-28.5 %, although the rates of glucose generation were different depending on the source of GBE treatment. Thus, the highly branched α-LDx with a higher amount of α-1,6 linkages and a higher molecular weight can be applied as a functional ingredient to deliver glucose throughout the entire small intestine without a glycemic spike which has the potential to control metabolic diseases such as obesity and type 2 diabetes.

摘要

α-极限糊精(α-LDx)是一种缓慢消化的碳水化合物,可减轻餐后血糖反应并触发饱腹感相关激素的分泌。在这项研究中,通过使用不同来源的糖原分支酶(GBE)来酶促合成具有更高支化度的α-LDx,从而增强其缓慢消化特性,GBE 可在切断α-1,4 键后催化形成α-1,6 分支点的转糖苷反应。结果表明,与未经 GBE 处理的淀粉相比,淀粉分子中支化α-LDx 的比例增加了约 2.2-8.1%,因为不同类型的 GBE 处理后α-1,6 键的比例增加了。此外,分支点的酶促增加增强了哺乳动物α-葡萄糖苷酶水平上α-LDx 的缓慢消化特性,增加了 17.3-28.5%,尽管葡萄糖生成的速率因 GBE 处理的来源而异。因此,具有更高α-1,6 键比例和更高分子量的高度支化的α-LDx 可以作为一种功能性成分应用于整个小肠,而不会出现血糖飙升,这有可能控制肥胖和 2 型糖尿病等代谢疾病。

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