Structural, topographical, and rheological characteristics of beta-casein-dioleoyl phosphatidylcholine (DOPC) mixed monolayers.

The surface pressure (pi)-area (A) isotherms and Brewster angle microscopy (BAM) images of beta-casein-dioleoyl phosphatidylcholine (DOPC) mixed films spread on buffered water at pH 7 and 9 and at 20 degrees C were determined as a function of the mass fraction of DOPC in the mixture (X(DOPC)). The structural characteristics, miscibility, and topography (morphology and reflectivity) of DOPC-beta-casein mixed films were very dependent on surface pressure and monolayer composition. The structure in DOPC-beta-casein mixed monolayers was liquid-expanded-like, as for pure components.

Monoglycerides and beta-lactoglobulin adsorbed films at the air-water interface. structure, microscopic imaging, and shear characteristics.

In this work we have analyzed the structural, topographical, and shear characteristics of mixed monolayers formed by adsorbed beta-lactoglobulin (beta-lg) and spread monoglyceride (monopalmitin or monoolein) on a previously adsorbed protein film. Measurements of the surface pressure (pi)-area (A) isotherm, Brewster angle microscopy (BAM), and surface shear characteristics were obtained at 20 degrees C and at pH 7 in a modified Wilhelmy-type film balance. The pi-A isotherm and BAM images deduced for adsorbed beta-lactoglobulin-monoglyceride mixed films at pi lower than the equilibrium surface pressure of beta-lactoglobulin (pi(e)(beta-lg)) indicate that beta-lactoglobulin and monoglyceride coexist at the interface.

Dynamic properties of soy globulin adsorbed films at the air-water interface.

In this paper we present surface dilatational properties of soy globulins (beta-conglycinin, glycinin, and reduced glycinin with 10 mM of dithiothreitol (DTT)) adsorbed onto the air-water interface, as a function of adsorption time. The experiments were performed at constant temperature (20 degrees C), pH (8.0), and ionic strength (0.