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木葡聚糖片段的分级分离及其与纤维素的相互作用。

Fractionation of xyloglucan fragments and their interaction with cellulose.

作者信息

Vincken J P, de Keizer A, Beldman G, Voragen A G

机构信息

Department of Food Science, Wageningen Agricultural University, The Netherlands.

出版信息

Plant Physiol. 1995 Aug;108(4):1579-85. doi: 10.1104/pp.108.4.1579.

Abstract

Tamarind seed xyloglucan was partially degraded with a purified endoglucanase (endoV) from Trichoderma viride. Analysis by high-performance anion-exchange chromatography showed that this digest was composed of fragments consisting of 1 to 10 repeating oligosaccharide units ([xg]1-[xg]10). To study the adsorption of xyloglucan fragments to cellulose in detail, this digest was fractionated on BioGel P-6. Fragments were separated satisfactorily up to 5 repeating oligosaccharide units ([xg]5). The galactose substitution of the fragments increased with increasing molecular weight. The BioGel P-6 pools, as well as polymeric xyloglucan ([xg] infinity), were tested for their ability to interact with Avicel crystalline cellulose. Quantitative binding to cellulose occurred for sequences consisting of (at least) 4 repeating units. The adsorption of [xg]4 to Avicel was very high relative to that of [xg] infinity. The dimensions of these fragments were such that they could also penetrate the smaller pores of cellulose. Apparently, the effective surface area for the polymers is much smaller. Adsorption isotherms of [xg] infinity and [xg]4 showed a pattern that is typical for polydisperse systems. However, the mechanisms underlying these patterns were different. At high xyloglucan concentrations, this polydispersity resulted in preferential adsorption of the larger molecules in the case of [xg] infinity and a more extensive colonization of the smaller pores of cellulose in the case of [xg]4. The pH influenced the interaction between xyloglucan (fragments) and cellulose to only a small extent.

摘要

罗望子种子木葡聚糖用来自绿色木霉的纯化内切葡聚糖酶(内切酶V)进行部分降解。通过高效阴离子交换色谱分析表明,该消化产物由由1至10个重复寡糖单元([xg]1-[xg]10)组成的片段组成。为了详细研究木葡聚糖片段对纤维素的吸附,该消化产物在BioGel P-6上进行分级分离。片段在多达5个重复寡糖单元([xg]5)时得到了令人满意的分离。片段的半乳糖取代度随分子量增加而增加。测试了BioGel P-6级分以及聚合木葡聚糖([xg]无穷大)与微晶纤维素Avicel相互作用的能力。对于由(至少)4个重复单元组成的序列,发生了与纤维素的定量结合。相对于[xg]无穷大,[xg]4对Avicel的吸附非常高。这些片段的尺寸使得它们也能够穿透纤维素的较小孔隙。显然,聚合物的有效表面积要小得多。[xg]无穷大和[xg]4的吸附等温线显示出多分散体系典型的模式。然而,这些模式背后的机制是不同的。在高木葡聚糖浓度下,这种多分散性导致在[xg]无穷大的情况下较大分子的优先吸附,而在[xg]4的情况下纤维素较小孔隙的更广泛占据。pH对木葡聚糖(片段)与纤维素之间的相互作用影响很小。

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