b-(D)-glucopyranoside, neohesperidin dihydrochalcone and their non-covalent association with b-cyclodextrin. Two examples of interaction of a carbohydrate host with glycoconjugate guests



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Eur. J. Mass Spectrom. 3, 347 - 354 (1997)

Fast-atom bombardment mass spectrometric and tandem mass spectrometric study of ()-menthol-b-(D)-glucopyranoside, neohesperidin dihydrochalcone and their non-covalent association with b-cyclodextrin. Two examples of interaction of a carbohydrate host with glycoconjugate guests

Andrea Mele,# Walter Panzeri and Antonio Selva
Dipartimento di Chimica del Politecnico di Milano and C.N.R.Centro di Studio sulle Sostanze Organiche Naturali, Via Mancinelli 7, I-20131 Milano, Italy.

ABSTRACT:
()-Menthol-b-(D)-glucopyranoside 1 and neohesperidin dihydrochalcone 2 are lycoconjugates of practical interest. Compound 1 releases ()-menthol in foods by slow hydrolysis and 2 is a sweetener used as an alternative to sucrose for diet food and beverages. Their molecular encapsulation in b-cyclodextrin (bCD) is Currently under investigation with the purpose of obtaining long lasting properties in the final product. From a mass spectrometric point of view, the study of the protonated gaseous 1 : 1 hostguest complexes of 1 and 2 withaCD is of particular interest, since the guest molecules possess an apolar aglycon, likely to interact with the lipophilic cavity of bCD, and a saccharidic part, whose capability of interaction with the polar external surface of bCD has not been investigated so far. We carried out a fast-atom bombardment (FAB) mass spectrometric and tandem mass spectrometric (MS/MS) study in thioglycerol on 1 and 2 and their gaseous protonated 1 : 1 association complexes with bCD. The FAB and tandem mass spectrometry results are later presented and discussed. Collisionally-activated decomposition data from native 1 and 2 are compared with those of the complexes of 1 and 2 with bCD. The experimental data indicate that the presence of bCD may dramatically alter the fragmentation pattern of the two glycoconjugates. The observed fragmentation patterns are consistent with an attractive interaction between the polar external surface of bCD and the sugar residues of the guest Molecules 1 and 2. The mass spectrometric data not only provide information on the nature of non-covalent interaction in controlling binding phenomena, but also point out a role for carbohydratecarbohydrate interactions, possibly mediated via hydrogen bonding.

Keywords: Fast-atom bombardment, FAB, tandem mass spectrometry, .beta.-cyclodextrin, ()-menthol-b(D)-glucopyranoside, neohesperidin dihydrochalcone, non-covalent associations.


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