Annotation and structural elucidation of bovine milk oligosaccharides and determination of novel fucosylated structures

被引:150
作者
Aldredge, Danielle L. [1 ]
Geronimo, Maria R. [1 ]
Hua, Serenus [1 ]
Nwosu, Charles C. [1 ]
Lebrilla, Carlito B. [1 ,3 ,4 ]
Barile, Daniela [2 ,4 ]
机构
[1] Univ Calif Davis, Dept Chem, Davis, CA 95616 USA
[2] Univ Calif Davis, Dept Food Sci & Technol, Davis, CA 95616 USA
[3] Univ Calif Davis, Dept Biochem & Mol Med, Davis, CA 95616 USA
[4] Univ Calif Davis, Foods Hlth Inst, Davis, CA 95616 USA
基金
美国国家卫生研究院;
关键词
bovine colostrum; high-performance liquid chromatography; oligosaccharides; tandem mass spectrometry; PERFORMANCE LIQUID-CHROMATOGRAPHY; HOLSTEIN-FRIESIAN COLOSTRUM; TANDEM MASS-SPECTROMETRY; CHEMICAL-STRUCTURE; MICROFLUIDIC CHIP; ESCHERICHIA-COLI; INHIBIT; LIBRARY; GLYCANS;
D O I
10.1093/glycob/cwt007
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Bovine milk oligosaccharides (BMOs) are recognized by the dairy and food industries, as well as by infant formula manufacturers, as novel, high-potential bioactive food ingredients. Recent studies revealed that bovine milk contains complex oligosaccharides structurally related to those previously thought to be present in only human milk. These BMOs are microbiotic modulators involved in important biological activities, including preventing pathogen binding to the intestinal epithelium and serving as nutrients for a selected class of beneficial bacteria. Only a small number of BMO structures are fully elucidated. To better understand the potential of BMOs as a class of biotherapeutics, their detailed structure analysis is needed. This study initiated the development of a structure library of BMOs and a comprehensive evaluation of structure-related specificity. The bovine milk glycome was profiled by high-performance mass spectrometry and advanced separation techniques to obtain a comprehensive catalog of BMOs, including several novel, lower abundant neutral and fucosylated oligosaccharides that are often overlooked during analysis. Structures were identified using isomer-specific tandem mass spectroscopy and targeted exoglycosidase digestions to produce a BMO library detailing retention time, accurate mass and structure to allow their rapid identification in future studies.
引用
收藏
页码:664 / 676
页数:13
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