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Identification and Accurate Quantitation of Biological Oligosaccharide Mixtures

机译:生物低聚糖混合物的鉴定和准确定量

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Structure-specific characterization and quantitation is often required for effective functional studies of oligosaccharides. Inside the gut, HMOs are preferentially bound and catabolized by the beneficial bacteria. HMO utility by these bacteria employs structure-specific catabolism based on a number of glycosidases. Determining the activity of these enzymes requires accurate quantitation of a large number of structures. In this study, we describe a method for the quantitation of human milk oligosaccharide (HMO) structures employing LC/MS and isotopically labeled internal standards. Data analysis was accomplished with a newly developed software tool, LC/MS Searcher, that employs a reference structure library to process LC/MS data yielding structural identification with accurate quantitation. The method was used to obtain a meta-enzyme analysis of bacteria, the simultaneous characterization of all glycosidases employed by bacteria for the catabolism of milk oligosaccharides. Analysis of consumed HMO structures confirmed the utility of a β-1,3-galactosidase in Bifidobacterium longum subsp. infantis ATCC 15697 (B. infantis). In comparison, Bifidobacterium breve ATCC 15700 showed significantly less HMO catabolic activity compared to B. infantis.
机译:有效的寡糖功能研究通常需要特定结构的表征和定量。在肠道内部,HMOs被有益细菌优先结合并分解代谢。这些细菌对HMO的利用利用了基于多种糖苷酶的结构特异性分解代谢。确定这些酶的活性需要准确定量大量结构。在这项研究中,我们描述了一种使用LC / MS和同位素标记的内部标准品定量人乳寡糖(HMO)结构的方法。数据分析是使用新开发的软件工具LC / MS Searcher完成的,该工具使用参考结构库来处理LC / MS数据,从而以准确的定量结果进行结构鉴定。该方法用于获得细菌的元酶分析,同时表征细菌用于牛奶寡糖分解代谢的所有糖苷酶。消耗的HMO结构的分析证实了β-1,3-半乳糖苷酶在长双歧杆菌亚种中的效用。婴儿ATCC 15697(婴儿B.)相比之下,与婴儿双歧杆菌相比,短双歧杆菌ATCC 15700的HMO分解代谢活性显着降低。

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