ABSTRACT
Pectin, a polysaccharide with potential bioactivity, was inserted in the aqueous subphase of monolayers of the selected lipids DPPC (1,2-dipalmitoyl-sn-glycero-3-phosphocholine) and DPPE (1,2-dipalmitoyl-sn-glycero-3-phosphoethanolamine), representing mammalian and bacterial membranes, respectively. Pectin condensed both monolayers but made the DPPC monolayer more fluid, while for DPPE, it made its monolayer more rigid, as detected with dynamic interfacial rheology. Complementary data using surface potential, infrared spectroscopy, and Brewster angle microscopy also showed distinctive effects of pectin on DPPE and DPPC. We believe these data can be correlated with the action of this polysaccharide with biological lipidic surfaces with different polar heads, which may be relevant, generally speaking, to understanding the molecular mechanism of this bioactive compound for pharmaceutical purposes.