直链淀粉
淀粉
化学
酶水解
聚合度
微晶
水解
食品科学
聚合
生物化学
结晶学
有机化学
聚合物
作者
Hongxin Jiang,Mark Campbell,Mike Blanco,Jay‐lin Jane
标识
DOI:10.1016/j.carbpol.2009.10.060
摘要
Abstract GEMS-0067 maize ae -line starches developed by the Germplasm Enhancement of Maize (GEM) project consist of 39.4–43.2% resistant starch (RS), which is larger than the existing ae -line starches of H99 ae , OH43 ae , B89 ae , and B84 ae (11.5–19.1%) as reported in part I of the study. The objective of this study was to understand the mechanism of the RS formation in the GEMS-0067 ae -line starch. In the current study, we analyzed the structures and properties of the RS residues that remained after enzymatic hydrolysis of the ae -line starches at 95–100 °C. The RS residues consisted of two major components: large starch molecules of average degrees of polymerization (DP) 840–951 with a few branches and small starch molecules (average DP 59–74) with mostly linear chains. All the RS residues had a semi-crystalline structure with the B-type polymorph and displayed high onset (100.7–107.7 °C), peak (118.6–121.4 °C), and conclusion (139.7–158.8 °C) gelatinization temperatures. After the maize ae -mutant starches were defatted with methanol, the RS contents decreased to 27.8–28.9% for the GEMS-0067 ae -line starches and 9.0–11.0% for the existing ae -line starches. The RS residues were attributed to the presence of long-chain double-helical crystallites derived from amylose and the intermediate component (IC). These crystallites present in native ae -line starches had gelatinization temperatures above 100 °C and maintained the semi-crystalline structures after enzymatic hydrolysis at 95–100 °C.
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