aJiangsu Key Laboratory of Crop Genetics and Physiology/Co-Innovation Center for Modern Production Technology of Grain Crops, Yangzhou University, Yangzhou 225009, China
bKey Laboratory of Biology and Genetic Improvement of Maize in Arid Area of Northwest Region, Ministry of Agriculture, Northwest A & F University, Yangling 712100, China
Received 14 November 2015. Revised 23 February 2016. Accepted 1 March 2016. Available online 3 March 2016.
Highlights
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Starches were isolated from high-amylose maize inbred lines and their hybrids.
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Molecular structure of starch was investigated by Sepharose CL-2B GPC and HPAEC.
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Enzymatic hydrolysis of starch was determined with α-amylase and amyloglucosidase.
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In vitro digestion was measured in native, gelatinized, and retrograded starches.
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The correlation of molecular structure and enzyme hydrolysis was analyzed.
Abstract
High-amylose maize starch has health benefits and special industrial uses. In this study, starches were isolated from normal maize and high-amylose inbred and hybrid maizes. Their molecular structure and enzymatic hydrolysis properties were investigated and analyzed. The high-amylose hybrid maize starch contained lower amylose, intermediate component, amylopectin long branch-chains, and amylopectin average chain length, and higher amylopectin short branch-chains than did high-amylose inbred maize starch. High-amylose maize starch was more resistant to α-amylase and amyloglucocidase hydrolysis and had a significantly lower hydrolysis rate coefficient than normal maize starch did. The native, gelatinized and retrograded starches of the high-amylose hybrid maize had significantly higher rapidly digestible starch and lower resistant starch than those of the high-amylose inbred maize. The retrogradation of gelatinized starch markedly increased the resistance of high-amylose starch to in vitro digestion. The high contents of amylose and intermediate component and the long branch-chains of amylopectin increased the resistance of maize starch to enzymatic hydrolysis and in vitro digestion.
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