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Core region of Citrobacter lipopolysaccharide from strain PCM 1487 Structure elucidation by two‐dimensional 1H‐NMR spectroscopy at 500 MHz and methylation analysis/mass spectrometry

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Dabrowski,  Janusz
Department of Organic Chemistry, Max Planck Institute for Medical Research, Max Planck Society;

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Citation

Romanowska, E., Gamian, A., & Dabrowski, J. (1986). Core region of Citrobacter lipopolysaccharide from strain PCM 1487 Structure elucidation by two‐dimensional 1H‐NMR spectroscopy at 500 MHz and methylation analysis/mass spectrometry. European Journal of Biochemistry, 161(3), 557-564. doi:10.1111/j.1432-1033.1986.tb10478.x.


Cite as: https://hdl.handle.net/21.11116/0000-0006-9422-C
Abstract
The core structure of Citrobacter PCM 1487 lipopolysaccharide has been established using methylation analysis/mass spectrometry, chemical degradations and one- and two-dimensional 1H-NMR spectroscopy at 500 MHz. 1H-NMR assignments are given for all sugar components of the core oligosaccharide. In the formula shown below, the alternative locations of branch terminal heptose (LDHep) and diphosphorylethanolamine (PPEtN) residues are marked by dashed lines; dOclA stands for 3-deoxy-D-manno-octulosonic acid. (Formula: see text). The sample of the core oligosaccharide showed some microheterogeneity due to a slightly incomplete substitution by terminal N-acetylgalactosamine and a partial splitting of diphosphorylethanolamine residues.