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Characterization of dextrins obtained by enzymatic treatment of cationic potato starch

机译:通过酶处理阳离子马铃薯淀粉获得的糊精的表征

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The substitution pattern of cationic potato starches was studied using starch hydrolyzing enzymes and a characterization of the hydrolysis products. Native and cationic starch samples were hydrolyzed with pullulanase, isoamylase, and alpha-amylase and the molecular-weight distributions of the resulting dextrins were studied using gel permeation chromatography. Isoamylase hydrolyzed the native potato starch sample readily, whereas hydrolysis with pullulanase was incomplete. Pullulanase hydrolyzed, however, cationic starch with higher DS (degree of substitution) more efficiently than isoamylase. The hydrolysis products obtained with pullulanase were separated according to charge using cation-exchange chromatography into one unbound and two bound fractions. The unbound fraction possessed an increasing number of short chains from amylopectin with increasing DS of the starch sample. The bound material contained amylose and dextrins with sizes corresponding to the long B-chains. The high portion of uncharged dextrins after alpha-amylolysis suggested that the substitution pattern, on the molecular level, was non-random. The composition of the unbound and bound material, obtained by ion-exchange chromatography of alpha-amylase treated starches, suggested a more intense fragmentation with increasing DS of the sample. Possibly, the substituents influence substrate conformation and thereby alter the hydrolysis patterns. It is concluded that a thorough understanding of the enzymatic hydrolysis patterns is of ultimate importance in structural studies of modified starch.
机译:用淀粉水解酶研究了阳离子马铃薯淀粉的取代方式,并对水解产物进行了表征。用支链淀粉酶,异淀粉酶和α-淀粉酶水解天然和阳离子淀粉样品,并使用凝胶渗透色谱法研究所得糊精的分子量分布。异淀粉酶容易水解天然马铃薯淀粉样品,而支链淀粉酶水解不完全。但是,支链淀粉酶比异淀粉酶更有效地水解具有较高DS(取代度)的阳离子淀粉。使用阳离子交换色谱根据电荷将用支链淀粉酶获得的水解产物分离为一个未结合的部分和两个结合的部分。随着淀粉样品的DS增加,未结合的部分具有来自支链淀粉的越来越多的短链。结合的物质包含直链淀粉和糊精,其大小对应于长B链。 α-淀粉分解后大部分不带电的糊精表明分子水平上的取代模式是非随机的。通过α-淀粉酶处理的淀粉的离子交换色谱获得的未结合和结合的物质的组成表明,随着样品DS的增加,碎片会更强烈。取代基可能会影响底物构象,从而改变水解方式。结论是,在改性淀粉的结构研究中,对酶促水解模式的透彻理解至关重要。

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