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Polymer -saccharide interaction

Figure 9.1 Polymer-polymer interactions assisted by boronic acid-diol reaction (a) boronic acid-appended polymer-hydroxylated polymer interaction, (b) boronic acid-appended polymer-saccharide interaction, and (c) boronic acid-functionalized molecule-hydroxylated polymer... Figure 9.1 Polymer-polymer interactions assisted by boronic acid-diol reaction (a) boronic acid-appended polymer-hydroxylated polymer interaction, (b) boronic acid-appended polymer-saccharide interaction, and (c) boronic acid-functionalized molecule-hydroxylated polymer...
One of the clearest pieces of evidence for the reversibility of some covalent interactions came from the work of Gunther Wulff at the University of Dusseldorf, Germany [172], He used imprinted polymers of o-aminomethyl phenylboronic acids as chromatographic stationary phases for the separation of saccharides. Older studies [173] also point to the reversible nature of the boronic acid-saccharide interaction. The pioneering studies of fluorescent transduction of this phenomenon by Czarnik and Yoon [174] (Ohio State University), Aoyama et al. [175] (Kyushu University, Japan), and Shinkai et al. [176] (Kyushu University, Japan) have been reviewed previously [9], Our concern in this review is particularly with the systems that clearly involve PET. Czarnik and Yoon s 93 [177] which interacts with catechol derivatives to produce 94 also belongs here. It... [Pg.134]

Kiessling has pioneered the use of ROMP polymers to explore a variety of protein-saccharide interactions that are critical components of diverse biological processes [59]. [Pg.564]

The ICD of the dyes bound to saccharides through an ionic coupling or hydrophobic interaction may remain a conflicting problem. The side-chain chromophores covalently bound to saccharides permit CD bands in the far or near ultraviolet region. These side-chain chromophores can exhibit CD and thus provide more definitive information on the conformation of saccharide moieties. Thus, acetamide CD has been observed to reflect polymer secondary structure of glycosaminoglycans, which are the connective-tissue proteoglycans. [Pg.90]

The DOC/enzyme/microbe interaction (DEMI) model divides bacterioplankton into two functional guilds, opportunists and decomposers, and DOC into two pools, labile and recalcitrant. In the context of the model, labile DOC is defined as directly assimilable monomers (saccharides, amino acids, and organic acids) and readily hydrolyzed polymers (polysaccharides, proteins, and nucleic acids). Because these substrates turn over rapidly, thus are unlikely to be transported far, most of the carbon in this pool will be autochthonous lysates and exudates, or allochthonous leachates from storms or seasonal litter fall. Recalcitrant DOC is defined as humic substances created by oxidative reactions among proteins, polysaccharides, hydrocarbons, and phenolic molecules. For inland waters, recalcitrant DOC is largely of allochthonous origin. [Pg.441]

To explore interactions of multivalent ligands with ConA, polymers with pendant maimose or glucose residues have been generated by ROMP. The saccharide epitopes were attached to norbornene monomers through C-glycoside linker units... [Pg.237]


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See also in sourсe #XX -- [ Pg.260 , Pg.261 , Pg.262 ]




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Polymer -saccharide

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