Towards an Understanding of the Fine Structure of Starch Molecules

S. Hizukuri
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引用次数: 18

Abstract

Molecular structures of amylose and amylopectin from several sources have been analyzed in detail by newly developed methods. Amylose content has been suggested to be determined based on the iodine affinities (or blue value) of amylose, amylopectin and starch of each specimen. The value was slightly lower than the value by assuming the iodine affinities of amylose and amylopectin as 18-20 and 0, respectively. The latter value was defined as apparent amylose content. Reducing and non-reducing residues were determined by the modified Park-Johnson's colorimetric assay and the rapid Smith degradation coupled with determination of glycerol by enzymic assay. Number-average molecular weight (or d. p. n) and number-average chain length (c.1. n) were calculated from these values and total carbohydrate measured by phenol-sulfuric acid method. Molar fractions of linear and branched amylose were determined by 1) (number of branch linkage of amylose)/(number of branch linkages of β-limit dextrin) or 2) radioactivities of H3-amylose and H3-limit dextrin. Molecular weight distribution and weight-average molecular weight (or i p, w) of amylose and debranched amylopectin (chain-length distribution) were analyzed by high-performance-gel-exclusion chromatography monitoring with a low-angle laser-light-scattering photometer and a differential refractometer. The mode of chain-linking of amylopectin was analyzed by β, i, p-degradation, which supported the irregular Meyer structure. It was found that the B chains of wheat and rice amylopectins linked increased number of A chains with increased chain length. Some B chains of wheat amylopectin were (37%) found to link no A chains but only B chains. A key factor for the cause of crystalline polymorphism of starch granules was found to be the chain length of amylopectin. The temperature and various materials appear to be secondary modulators. This suggests that molecular structure is the most basic factor on the functional properties of starch, but still we know only a part. We need more effort toward the full understanding of starch.
对淀粉分子精细结构的认识
用新方法对几种来源的直链淀粉和支链淀粉的分子结构进行了详细的分析。直链淀粉含量建议根据每个样品的直链淀粉、支链淀粉和淀粉的碘亲和力(或蓝值)来测定。该值略低于假设直链淀粉和支链淀粉的碘亲和度分别为18-20和0时的值。后者的值定义为表观直链淀粉含量。还原性和非还原性残留物采用改良的帕克-约翰逊比色法和快速史密斯降解结合酶法测定甘油。数平均分子量和数平均链长。N)和苯酚-硫酸法测定的总碳水化合物。直链直链淀粉和支链直链淀粉的摩尔分数分别由1)直链淀粉支链数/(β-极限糊精支链数)或2)h3 -直链淀粉和h3 -极限糊精的放射性测定。采用低角度激光散射光度计和差示折射仪进行高效凝胶排除色谱监测,分析直链淀粉和脱支链淀粉的分子量分布和分子量-平均分子量(或i p, w)(链长分布)。通过β、i、p降解分析支链淀粉的链联模式,证实支链淀粉具有不规则的Meyer结构。研究发现,随着链长增加,小麦和水稻支链淀粉的B链连接的A链数量增加。小麦支链淀粉的部分B链(37%)不连接A链而只连接B链。支链淀粉的链长是导致淀粉颗粒结晶多态性的关键因素。温度和各种材料似乎是二次调制器。这表明分子结构是影响淀粉功能特性的最基本因素,但我们对其了解的还只是一部分。我们需要更多的努力来全面了解淀粉。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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