Binding of phenolic compounds and their derivatives to bovine and reindeer beta-lactoglobulin.

Autor: Riihimäki LH; Drug Discovery and Development Technology Center, Faculty of Pharmacy, University of Helsinki, P.O. Box 56 (Viikinkaari 5 E), Finland., Vainio MJ, Heikura JM, Valkonen KH, Virtanen VT, Vuorela PM
Jazyk: angličtina
Zdroj: Journal of agricultural and food chemistry [J Agric Food Chem] 2008 Sep 10; Vol. 56 (17), pp. 7721-9. Date of Electronic Publication: 2008 Aug 14.
DOI: 10.1021/jf801120a
Abstrakt: In plant-based food, phenolic compounds usually do not exist in their native form, but as esters, glycosides, or polymers. The native forms, however, require deglycosylation for their intestinal absorption, and aglycone has been considered to be the potential health-protecting/promoting form. The binding of the aglycones of phenolic compounds to bovine and reindeer beta-lactoglobulins (betaLG) using fluorescence quenching was studied. The effects of pH and storage were also studied. Of the compounds investigated, the majority of flavones, flavonols, flavanones, and isoflavones were bound to betaLG. In the pH studies, no significant effects were found. The fact that the phenolic compounds were not released at pH 2 might indicate that they bind to an external part rather than to the central cavity. Studies implicated that betaLG could act as a binder or carrier for phenolic compounds in acidic, basic, or neutral conditions and that the ligand/betaLG complex can remain stable during storage.
Databáze: MEDLINE