4.4 Article

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

Journal

GLYCOBIOLOGY
Volume 23, Issue 6, Pages 664-676

Publisher

OXFORD UNIV PRESS INC
DOI: 10.1093/glycob/cwt007

Keywords

bovine colostrum; high-performance liquid chromatography; oligosaccharides; tandem mass spectrometry

Funding

  1. University of California Discovery Fund
  2. California Dairy Research Foundation [10GEB-02NH]
  3. National Institutes of Health (Bethesda, MD) from Eunice K. Shriver National Institute of Child Health and Human Development Grant [HD059127]
  4. National Institutes of Health (Bethesda, MD) from National Center for Research Resources, a component of the National Institutes of Health [UL1 RR024146]
  5. National Center for Complementary & Alternative Medicine [1R01AT007079-01]

Ask authors/readers for more resources

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.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.4
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available