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首页> 外文期刊>Journal of the Institute of Brewing >Analysis of polysaccharide and proteinaceous macromolecules in beer using asymmetrical flow field-flow fractionation
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Analysis of polysaccharide and proteinaceous macromolecules in beer using asymmetrical flow field-flow fractionation

机译:非对称流场-流分离技术分析啤酒中的多糖和蛋白质大分子

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This paper demonstrates the potential of asymmetrical flow field flow fractionation coupled with online multi-angle light scattering, differential refractive index and UV detection for the fractionation and analysis of macromolecules in beer regarding their composition, molar mass (M) and relative concentration. The macromolecules in the liquid and foam of two types of beer, light lager and porter, were analysed in their native state with minimal sample preparation. The results showed the presence of three major populations of macromolecules. In lager beer liquid, the early eluting population has an average M of 2 × 10~4 g/mol and an intense UV absorbance at 280 nm suggesting the presence of proteinaceous macromolecules. The second and the third populations, which elute at consecutively longer retention times, have M ranging from 10~5 to 10~7 g/mol. They are not UV-active at 280 nm, suggesting the elution of polysaccharides. The second population was identified as β-glucans as a result of β-glucanase treatment. The third population was not identified in the present study. The results show that similar populations are present in lager beer foam and that the macromolecules appear to be present in a more aggregated state. The M range of macromolecules in porter beer liquid ranged from 10~5 to 10~8 g/mol. A fraction of macromolecules eluting at longer retention times is highly UV-active, which shows that there are great variations in the macromolecular profile of lager and porter beer.
机译:本文证明了不对称流场流动分馏与在线多角度光散射,微分折光率和紫外线检测相结合的潜力,可用于分馏和分析啤酒中大分子的组成,摩尔质量(M)和相对浓度。两种啤酒(轻型啤酒和波特酒)的液体和泡沫中的大分子都以其原始状态进行了分析,只需最少的样品制备。结果表明存在三个主要的大分子种群。在较大的啤酒液中,早期洗脱的群体的平均M为2×10〜4 g / mol,并且在280 nm处具有很强的UV吸光度,表明存在蛋白质大分子。第二个和第三个种群以连续更长的保留时间洗脱,其M范围为10〜5至10〜7 g / mol。它们在280 nm处不具有紫外线活性,这表明可以洗脱多糖。由于β-葡聚糖酶处理,第二群体被鉴定为β-葡聚糖。在本研究中未鉴定出第三人群。结果表明,在较大的啤酒泡沫中存在相似的种群,并且大分子似乎以更聚集的状态存在。波特啤酒液体中大分子的M范围为10〜5至10〜8 g / mol。在较长的保留时间洗脱下来的一部分大分子具有很高的紫外线活性,这表明储藏啤酒和波特啤酒的大分子特征存在很大差异。

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