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Definitive Structural Assessment of Enterococcal Diheteroglycan
Authors:Dr. Vadim B. Krylov  Dr. Alexey G. Gerbst  Dmitry A. Argunov  Dr. Andrey S. Dmitrenok  Prof. Dr. Alexander S. Shashkov  Prof. Dr. Zbigniew Kaczynski  Prof. Dr. Johannes Huebner  Prof. Dr. Otto Holst  Prof. Dr. Nikolay E. Nifantiev
Affiliation:1. N.D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, Leninsky prospect 47, 119991 Moscow (Russian Federation);2. Faculty of Chemistry, University of Gdansk, Wita Stwosza 63, 80‐308, Gdansk (Poland);3. Division of Pediatric Infectious Diseases, Hauner Children's Hospital, Ludwigs‐Maximilian University, Munich (Germany);4. Research Center Borstel, Leibniz‐Center for Medicine and Biosciences, Borstel (Germany)
Abstract:
Enterococcus faecalis is one of most important nosocomial and often multi‐antibiotic resistant pathogens responsible for infections that are difficult to treat. Previously, a cell‐wall polysaccharide termed diheteroglycan (DHG) was isolated and characterized as a promising vaccine candidate. However, the configuration of its lactic acid (LA) residue attached to the galactofuranoside unit was not assessed, although it influences conformation of DHG chain in terms of biological recognition and immune evasion. This study proves the R configuration of the LA residue by means of chemical analysis, investigation of intramolecular NMR nuclear Overhauser effects and molecular dynamics simulations of native DHG and corresponding R and S models, which were obtained by using pyranoside‐into‐furanoside rearrangement. As alternative treatment and prevention strategies for E. faecalis are desperately needed, this discovery may offer the prospect of a synthetic vaccine to actively immunize patients at risk.
Keywords:carbohydrates  conformation analysis  furanoside  lactic acid  rearrangement
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