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首页> 外文期刊>Carbohydrate Polymers: Scientific and Technological Aspects of Industrially Important Polysaccharides >Structural features of water soluble (1,3)(1,4)-beta-D-glucans from high-beta-glucan and traditional oat lines
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Structural features of water soluble (1,3)(1,4)-beta-D-glucans from high-beta-glucan and traditional oat lines

机译:来自高β-葡聚糖和传统燕麦品系的水溶性(1,3)(1,4)-β-D-葡聚糖的结构特征

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摘要

Information on structural features of beta-glucans purified from a traditional (4.4% beta-glucan) and two high beta-glucan oat lines (6.0 and 7.3%) was obtained by partial and complete hydrolysis with lichenase.The depolymerization process was monitored with disodium 2,2'-bicinchoninate reductometry (BCA),fluorophore-assisted capillary-electrophoresis (FACE)and nuclear-magnetic-resonance spectroscopy (NMR).The average degree of polymerization (DP)of the completely hydrolyzed beta-glucans was the same for beta-glucans from te three oat lines,as determined from NMR spectra (3.7),by FACE (3.4),and by BCA (3.9).By FACE,the beta-glucans from all three lines had the same molar ratio of cellobiosyl-(1,3)-D-glucose/cellotriosyl-(1,3)-D-glucose units of 1.6.By NMR the ratio of beta (1,4)/beta(1,3) before hydrolysis was 2.4 and after complete hydrolysis 1.7,with no significant differences among oat lines.Identical molar ratios of penultimate oligosaccharides (DP6,DP7 and DP8)released during partial depolymerization suggested the same arrangement of cellotriosyl/cellotetraosyl residues in the beta-glucan polymers from normal and high beta-glucan oat lines.Differences in lichenase specificity toward the beta-glucans from the three sources,however,were observed during partial depolymerization,which were attributed to differences in chain lengths of the three polymers.The preferred substrate was the polymer with the highest initial DP.A more limited specificity was observed for the beta-glucans with the lowest initial DP.
机译:通过用地衣酶部分和完全水解获得了从传统(4.4%β-葡聚糖)和两个高β-葡聚糖燕麦品系(6.0和7.3%)纯化得到的β-葡聚糖的结构特征的信息。 2,2'-二辛可尼酸酯还原法(BCA),荧光团辅助毛细管电泳(FACE)和核磁共振波谱(NMR)。完全水解的β-葡聚糖的平均聚合度(DP)相同根据NMR光谱(3.7),FACE(3.4)和BCA(3.9)测得的这三个燕麦品系的β-葡聚糖。通过FACE,所有三个品系的β-葡聚糖具有相同的纤维二糖基-摩尔比(1,3)-D-葡萄糖/纤维三糖基-(1,3)-D-葡萄糖单元为1.6。通过NMR,水解前和完成后β(1,4)/β(1,3)的比率为2.4水解1.7,燕麦品系之间没有显着差异。部分发酵过程中释放的倒数第二个低聚糖(DP6,DP7和DP8)的摩尔比相同部分解聚表明正常和高β-葡聚糖燕麦品系的β-葡聚糖聚合物中的纤维二糖基/纤维四糖基残基的排列相同。然而,在部分解聚过程中,观察到了三种来源对β-葡聚糖的地衣酶特异性的差异。这归因于这三种聚合物链长的差异。首选的底物是具有最高初始DP的聚合物。对于具有最低初始DP的β-葡聚糖,观察到的特异性更有限。

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