Department of Chemistry, University of California, Davis, 95616, United States.
Anal Chem. 2012 Sep 18;84(18):7793-801. doi: 10.1021/ac301128s. Epub 2012 Aug 29.
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.
通常需要对寡糖进行结构特异性的表征和定量,以进行有效的功能研究。在肠道内,HMO 优先被有益细菌结合和代谢。这些细菌利用 HMO 的功能依赖于许多糖苷酶的结构特异性代谢。要确定这些酶的活性,需要对大量结构进行准确的定量。在这项研究中,我们描述了一种使用 LC/MS 和同位素标记内标定量人乳寡糖 (HMO) 结构的方法。数据分析采用了一种新开发的软件工具 LC/MS Searcher,该工具使用参考结构库处理 LC/MS 数据,可进行结构鉴定并进行准确的定量。该方法用于对细菌进行元酶分析,同时对细菌用于代谢乳寡糖的所有糖苷酶进行特征分析。对消耗的 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作用。婴儿 ATCC 15697(婴儿双歧杆菌)。相比之下,与婴儿双歧杆菌相比,短双歧杆菌 ATCC 15700 显示出的 HMO 代谢活性明显较低。