Insight into the distribution of amino groups along the chain of chemically deacetylated hyaluronan

•Methodology to describe distribution of deacetylation along HA chain was developed.•Deacetylation pattern was independent on Mw of HA and reaction conditions.•Deacetylation pattern did not agree with random distribution model.•Probability of deacetylation at the closest neighboring disaccharide was...

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Bibliographic Details
Published in:Carbohydrate polymers 2019-12, Vol.225, p.115156-115156, Article 115156
Main Authors: Sedláček, Jakub, Hermannová, Martina, Mrázek, Jiří, Buffa, Radovan, Lišková, Petra, Šatínský, Dalibor, Velebný, Vladimír
Format: Article
Language:English
Subjects:
Acetylation
Acetylglucosamine - chemistry
Deacetylation
Distribution of modification
Hyaluronan
Hyaluronic Acid - chemistry
Nitrous Acid - chemistry
Polysaccharide-Lyases - chemistry
Streptococcus pneumoniae - enzymology
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Summary:•Methodology to describe distribution of deacetylation along HA chain was developed.•Deacetylation pattern was independent on Mw of HA and reaction conditions.•Deacetylation pattern did not agree with random distribution model.•Probability of deacetylation at the closest neighboring disaccharide was reduced. Deacetylated hyaluronan (daHA) containing reactive free amino groups is an important intermediate for further modification. Comparing direct and indirect NMR and HPLC to characterize the degree of HA deacetylation (DD), direct NMR approach using area ratio of anomeric CH and CH–NH2 groups was the most precise one. To describe the substitution pattern, daHA was selectively cleaved by nitrous acid generated in situ or hyaluronan lyase from Streptococcus pneumoniae. The resulting oligomers were identified by LC-ESI-MS. The experimental distribution of these oligomers was compared with theoretically expected random oligomer distribution. Independently on the starting HA molecular weight and deacetylation conditions, the experimental data differed from the random distribution model and suggested that deacetylation of certain N-acetyl-d-glucosamine had reduced the probability of deacetylation at the neighbouring disaccharide. This phenomenon was explained by conformational changes of HA caused by intra- and intermolecular interactions between positively charged amino and negatively charged carboxylic groups.
ISSN:0144-8617
1879-1344
DOI:10.1016/j.carbpol.2019.115156