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首页> 外文期刊>Carbohydrate research >Investigation of the galacturonic acid distribution of pectin with enzymes part 2 - Characterization of non-esterified galacturonic acid sequences in pectin with endopolygalacturonase
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Investigation of the galacturonic acid distribution of pectin with enzymes part 2 - Characterization of non-esterified galacturonic acid sequences in pectin with endopolygalacturonase

机译:用酶研究果胶中半乳糖醛酸的分布第2部分-用内聚半乳糖醛酸酶表征果胶中未酯化的半乳糖醛酸序列的特性

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A method was developed that enabled the study of non-esterified galacturonic acid sequences (so-called blocks) in pectin. Endopolygalacturonase of Kluyveromyces fragilis was used to extensively degrade pectin, and the composition of the galacturonic acid molecules produced was determined with high-performance anion-exchange chromatography at pH 5. With this technique, the amount of non-esterified mono-, di-, and trigalacturonic acid released was determined. In addition, the relative amounts of methyl-esterified oligomers - up to 10 galacturonic acid residues - could be observed. By comparing the percentages of non-esterified mono-, di-, and trigalacturonic acids released, pectins with large enzyme-degradable blocks could be distinguished from pectins with small enzyme-degradable blocks. High percentages of mono- and digalacturonic acid were found for pectins containing small non-esterified blocks. The total area of all peaks corresponding to methyl-esterified oligomers was found to be indicative for the distribution of these blocks. The higher the ratio of the methyl- to non-esterified peak areas, the more closely associated blocks are present. Randomly esterified pectins, with degrees of methyl esterification of 50 and higher, contained smaller, more clustered blocks than commercial extracted pectins of comparable degrees of esterification. The approach developed enables a very detailed study of the methyl-ester distribution of pectin to be carried out and is a very important addition in the study of the functional behavior of this complex polymer. (C) 2000 Elsevier Science Ltd. All rights reserved. [References: 29]
机译:已开发出一种方法,可以研究果胶中的非酯化半乳糖醛酸序列(所谓的嵌段)。使用脆弱克鲁维酵母的内聚半乳糖醛酸酶广泛降解果胶,并通过高效阴离子交换色谱法在pH 5下测定所产生的半乳糖醛酸分子的组成。测定释放的三半乳糖醛酸。此外,可以观察到甲基酯化的低聚物的相对数量(最多10个半乳糖醛酸残基)。通过比较释放的非酯化单,二和三半乳糖醛酸的百分比,可以将具有较大酶可降解嵌段的果胶与具有较小酶可降解嵌段的果胶区分开。对于含有小的未酯化嵌段的果胶,发现了较高百分比的单和半乳糖醛酸。发现对应于甲基酯化的低聚物的所有峰的总面积指示这些嵌段的分布。甲基与非酯化峰面积之比越高,存在的嵌段越紧密。甲基酯化度为50或更高的无规酯化果胶,与可比酯化度相当的市售提取果胶相比,含有更小,更簇状的嵌段。开发的方法可以对果胶的甲酯分布进行非常详细的研究,并且在研究这种复杂聚合物的功能行为方面是非常重要的补充。 (C)2000 Elsevier ScienceLtd。保留所有权利。 [参考:29]

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