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不同直链淀粉含量玉米淀粉体外消化试验方法的作用机制及酶学贡献。

Mechanism and enzymatic contribution to in vitro test method of digestion for maize starches differing in amylose content.

机构信息

College of Agriculture, Department of Grain Science and Industry, Kansas State University, Manhattan, Kansas 66506, USA.

出版信息

J Agric Food Chem. 2012 May 2;60(17):4379-87. doi: 10.1021/jf300393m. Epub 2012 Apr 17.

Abstract

To determine the rapidly digestible starch (RDS), slowly digestible starch (SDS), and resistant starch (RS) contents in a starch sample, the addition of amyloglucosidase is often used to convert hydrolyzates from α-amylase digestion to glucose. The objectives of this study were to investigate the exact role of amyloglucosidase in determining the digestibility of starch and to understand the mechanism of enzymatic actions on starch granules. Four maize starches differing in amylose content were examined: waxy maize (0.5% amylose), normal maize (≈27% amylose), and two high-amylose starches (≈57 and ≈71% amylose). Notably, without amyloglucosidase addition, the RS content increased from 4.3 to 74.3% for waxy maize starch, 29.7 to 76.5% for normal maize starch, 65.8 to 88.0% for starch with 57% amylose, and 68.2 to 90.4% for the starch with 71% amylose. In the method without α-amylase addition, less RS was produced than without added amyloglucosidase, except in maize at 71% amylose content. Scanning electron microscopy (SEM) revealed the digestive patterns of pinholes with α-amylase and burrowing with amyloglucosidase as well as the degree of digestion between samples. To understand the roles of amyloglucosidase and α-amylase in the in vitro test, multiple analytical techniques including gel permeation chromatography, SEM, synchrotron wide-angle X-ray diffraction, and small-angle X-ray scattering were used to determine the molecular and crystalline structure before and after digestion. Amyloglucosidase has a significant impact on the SDS and RS contents of granular maize starches.

摘要

为了测定淀粉样品中快速消化淀粉(RDS)、缓慢消化淀粉(SDS)和抗性淀粉(RS)的含量,通常会添加糖化酶将α-淀粉酶消化的水解产物转化为葡萄糖。本研究的目的是探究糖化酶在确定淀粉消化率方面的确切作用,并了解酶对淀粉颗粒作用的机制。研究考察了 4 种直链淀粉含量不同的玉米淀粉:蜡质玉米(0.5%直链淀粉)、普通玉米(≈27%直链淀粉)和两种高直链淀粉玉米(≈57%和≈71%直链淀粉)。值得注意的是,在不添加糖化酶的情况下,蜡质玉米淀粉的 RS 含量从 4.3%增加到 74.3%,普通玉米淀粉的 RS 含量从 29.7%增加到 76.5%,直链淀粉含量为 57%的淀粉的 RS 含量从 65.8%增加到 88.0%,直链淀粉含量为 71%的淀粉的 RS 含量从 68.2%增加到 90.4%。在不添加α-淀粉酶的方法中,除了直链淀粉含量为 71%的玉米外,产生的 RS 少于不添加糖化酶的方法。扫描电子显微镜(SEM)揭示了有α-淀粉酶时的针孔消化模式和有糖化酶时的钻孔消化模式,以及不同样品之间的消化程度。为了理解糖化酶和α-淀粉酶在体外试验中的作用,使用凝胶渗透色谱、SEM、同步辐射广角 X 射线衍射和小角 X 射线散射等多种分析技术,在消化前后测定了分子和结晶结构。糖化酶对颗粒状玉米淀粉的 SDS 和 RS 含量有显著影响。

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