Kristina Wolf

Interaction of phloretin with membranes: on the mode of action of phloretin at the water-lipid interface

Abstract The interaction of phloretin with single lipid bilayers on a spherical support and with multilamellar vesicles was studied by differential scanning calorimetry (DSC) and nuclear magnetic resonance (NMR). The results indicated that phloretin interacts with the lipid layer and changes its structural parameters. In DSC experiments, phloretin in its neutral form strongly decreased the lipid phase transition temperature and slightly reduced the cooperativity of the phase transition within the lipid layer. In NMR measurements, phloretin led to an increase of the transverse relaxation time constant but had no effect on the spin-lattice relaxation time constant. The overall dipole moment of phloretin was experimentally determined and was found to be roughly 40% lower than has been published previously. This result suggested that the size of the dipole moment of phloretin does not provide such a high contribution to the effect of phloretin on the dipole potential of monolayers and bilayers as has been published previously. To understand the discrepancy between phloretin adsorption and dipole potential change, we performed computational conformational analysis of phloretin in the gas phase. The results showed that a wide distribution of the dipole moments of phloretin conformers exists, which mainly depends on the orientation of the OH moieties. The adsorption of phloretin as determined from its binding to solid supported bilayers differed from the one determined from dipole potential measurements on black lipid membranes. The difference between the phloretin dissociation constants of both types of experiments suggested a change of its dipole moment normal to the membrane surface in a concentration-dependent manner, which was in agreement with the results of the computational conformational analysis.

4-Oxonicotinamide-1-(1′-β-d-ribofuranoside) from Rothmannia longiflora Salisb. (Rubiaceae)

Abstract The first isolation of 4-oxonicotinamide-1-(1′-β- d -ribofuranoside) from a nonmammalian source, the West African plant Rothmannia longiflora Salisb. (Rubiaceae), is described. Its stereostructure was established by spectroscopic methods and an X-ray structure analysis of its tri-O-acetyl derivative. This N-glycoside had previously been isolated only from human urine. In addition, the plant was found to contain monomethyl fumarate and d -mannitol.