| Literature DB >> 28650649 |
Antonio Laezza1, Angela Casillo1, Sandro Cosconati2, Caroline I Biggs3, Antonio Fabozzi1, Luigi Paduano1, Alfonso Iadonisi1, Ettore Novellino4, Matthew I Gibson3,5, Antonio Randazzo4, Maria M Corsaro1, Emiliano Bedini1.
Abstract
Several threonine (Thr)- and alanine (Ala)-rich antifreeze glycoproteins (AFGPs) and polysaccharides act in nature as ice recrystallization inhibitors. Among them, the Thr-decorated capsular polysaccharide (CPS) from the cold-adapted Colwellia psychrerythraea 34H bacterium was recently investigated for its cryoprotectant activity. A semisynthetic mimic thereof was here prepared from microbial sourced chondroitin through a four-step strategy, involving a partial protection of the chondroitin polysaccharide as a key step for gaining an unprecedented quantitative amidation of its glucuronic acid units. In-depth NMR and computational analysis suggested a fairly linear conformation for the semisynthetic polysaccharide, for which the antifreeze activity by a quantitative ice recrystallization inhibition assay was measured. We compared the structure-activity relationships for the Thr-derivatized chondroitin and the natural Thr-decorated CPS from C. psychrerythraea.Entities:
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Year: 2017 PMID: 28650649 PMCID: PMC5718299 DOI: 10.1021/acs.biomac.7b00326
Source DB: PubMed Journal: Biomacromolecules ISSN: 1525-7797 Impact factor: 6.988