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通过短链葡聚糖的酶促水解和自组装制备的淀粉纳米颗粒。

Starch nanoparticles prepared by enzymatic hydrolysis and self-assembly of short-chain glucans.

作者信息

Oh Seon-Min, Lee Byung-Hoo, Seo Dong-Ho, Choi Hyun-Wook, Kim Byung-Yong, Baik Moo-Yeol

机构信息

1Department of Food Science and Biotechnology, Institute of Life Science and Resources, Graduate School of Biotechnology, Kyung Hee University, Yongin, 17104 Republic of Korea.

2Department of Food Science and Biotechnology, Gachon University, Seongnam, Republic of Korea.

出版信息

Food Sci Biotechnol. 2020 May 7;29(5):585-598. doi: 10.1007/s10068-020-00768-w. eCollection 2020 May.

Abstract

Enzymatic hydrolysis and self-assembly are considered promising methods for preparation of starch nanoparticles (SNPs) because they are environmentally friendly, and time- and cost-effective. These methods are based on the self-assembly of short-chain glucans released from the α-1,6 bonds in amylopectin. Since their discovery, many studies have described the structural and physicochemical properties of self-assembled SNPs. Self-assembled SNPs can be prepared by two methods: using only the soluble portion containing the short-chain glucans, or using the whole hydrolyzate including both insoluble and soluble fractions. Although the structural and physical properties of self-assembled SNPs can be attributed to the composition of the hydrolyzates that participate in self-assembly, this aspect has not yet been discussed. This review focuses on SNPs self-assembled with only soluble short-chain glucans and addresses their characteristics, including formation mechanisms as well as structural and physicochemical properties, compared with SNPs prepared with total hydrolyzates.

摘要

酶促水解和自组装被认为是制备淀粉纳米颗粒(SNP)的有前景的方法,因为它们环保、省时且经济高效。这些方法基于从支链淀粉中的α-1,6键释放的短链葡聚糖的自组装。自发现以来,许多研究描述了自组装SNP的结构和物理化学性质。自组装SNP可通过两种方法制备:仅使用含有短链葡聚糖的可溶部分,或使用包括不溶和可溶部分的全水解产物。尽管自组装SNP的结构和物理性质可归因于参与自组装的水解产物的组成,但这方面尚未得到讨论。本综述聚焦于仅由可溶短链葡聚糖自组装的SNP,并与用全水解产物制备的SNP相比,阐述其特性,包括形成机制以及结构和物理化学性质。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b210/7221041/54dc6b8e232a/10068_2020_768_Fig1_HTML.jpg

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