Leif Lundin

Impact of gastric structuring on the lipolysis of emulsified lipids

Understanding and manipulating how emulsion structure impacts on fat digestion is an important step towards understanding the role of fat in our diet. This article reports on the nature of emulsion structuring within the digestive tract and how it affects the dynamics of fat digestion. Emulsions were designed a priori to have specific structuring behaviours (stable, coalesced, partially coalesced and fully broken) under gastrointestinal conditions, through careful emulsifier selection and control of solid fat composition. The impact these structures had on lipolysis was then assessed in vitro using a digestion model and in vivo by measuring the postprandial change in blood triglyceride concentration as a marker of fat absorption. The major factor controlling the rate of fat digestion in vitro was the droplet surface area available for lipase adsorption, which was governed by emulsion instability. The rate of fat absorption in vivo was only affected by large changes in the droplet surface area, and only if these changes remained until the droplets reached the small intestine. This was most evident in emulsions that had undergone extensive partial coalescence under gastric conditions. Partial coalescence resulted in a dramatic reduction in triglyceride absorption, in part because the network of fat crystals provided the agglomerates with an internal scaffold to resist re-dispersion as they passed through the pylorus. The differences in fat absorption profile achieved by controlling emulsion structural stability during digestion provide a basis for examining the physiological effects of food structure on lipid metabolism, which will be the subject of a follow-up clinical paper.

Chemical Cross-Linking Gelatin with Natural Phenolic Compounds as Studied by High-Resolution NMR Spectroscopy

Cross-linking gelatin with natural phenolic compound caffeic acid (CA) or tannic acid (TA) above pH 9 resulted in formation of insoluble hydrogels. The cross-linking reactivity was controlled by variation of pH, the concentration of the gelatin solution, or the amount of CA or TA used in the reaction. The cross-linking chemistry was studied by high-resolution NMR technique in both solution and solid state via investigation on small molecular model systems or using (13)C enriched caffeic acid (LCA) in the reaction with gelatin. Direct evidence was obtained to confirm the chemical reactions occurring between the phenolic reactive sites of the phenolic compounds and the amino groups in gelatin to form C-N covalent bonds as cross-linking linkages in gelatin matrix. The cross-linked network was homogeneous on a scale of 2-3 nm. The cross-linking resulted in a significant decrease in the molecular mobility of the hydrogels, while the modulus of the films remained at high values at high temperatures.

Chemical modification of gelatin by a natural phenolic cross-linker, tannic acid.

Chemical modification of gelatin by a natural phenolic compound tannic acid (TA) at pH 8 was studied, and the properties of the modified gelatin materials were examined. The cross-linking effect was predominant when the TA content was lower, resulting in the formation of a partially insoluble cross-link network. The cross-linking structure was stable even under boiling, and the protein matrix became rigid, whereas the mechanical properties were enhanced. An effective cross-linking effect on gelatin matrix was achieved when the amount of TA was around 3 wt %. Further increase in the TA content enhanced the grafting and branching reactions between gelatin and TA in conjunction with the hydrogen bonding between gelatin and TA molecules. These effects produced an increase in molecular mobility of gelatin matrix, and the materials displayed a behavior similar to that of plasticized protein materials.

Molecular interactions in, and rheological properties of, a mixed biopolymer system undergoing order/disorder transitions

Abstract Gelatin from cold water fish species and κ-carrageenan are both thermo-setting biopolymers of a poly-electrolytic character. By adjusting parameters such as pH and ionic strength, these polymers can, in the disordered state, associatively interact through electrostatic interactions. In the present study, the changes taking place at the molecular level are sought and linked to the rheological properties in a mixed system of these two biopolymers under conditions initially favouring associative phase separation (pH below IEP of the gelatin and low ionic strength). More specifically, these changes were followed as function of temperature with special emphasis on changes taking place close to the order/disorder temperature regimes of the two polymers. The present study concludes that a variety of complex structural arrangements can be obtained, and that dynamic processes in the form of structural re-arrangements are present when the single components are forced to undergo order/disorder transitions.

Using SAXS to reveal the degree of bundling in the polysaccharide junction zones of microrheologically distinct pectin gels.

The results of microrheological studies carried out on ionotropic pectin gels, particularly the manifest power law behavior observed at high frequencies, indicate that by using different assembly conditions gels can be formed in which the elementary network strands have different stiffnesses. It has been hypothesized that these differences reflect different network architectures, the extreme cases of which might be described as (i) dimeric calcium-chelating junction-zones of limited extent, linked by considerably longer, flexible, single-chain sections, or (ii) semiflexible bundles consisting of extensively aggregated dimeric junction zones that latterly become entangled and cross-linked. To test this hypothesis directly, microrheologically distinct pectin gels have been generated using different assembly modalities, in particular by using different concentrations of polymer and cross-linking ions and by contrasting the controlled-release of ions or ion-binding groups, and the resulting systems have been studied by small-angle X-ray scattering. The results straightforwardly reveal that gels that are clearly more semiflexible from a microrheological point-of-view contain larger scattering entities than those with a more flexible character. Furthermore, a more detailed interpretation of the scattering data with the aid of molecular modeling suggests that for the gels formed here those with a semiflexible microrheological signature consist predominantly of network filaments consisting of four or more chains, whereas those with a more flexible signature are predominantly single-chain sections linked by dimeric associations with no more that a few percent of the chains bundled to any higher extent. The ability to generate differing network architectures from the same polymer that fulfill different functional requirements, either in vivo in the plant cell wall, where pectin plays a crucial structural and mechanical role, or in vitro in a myriad of applications, makes these biomimetic biopolymer networks of considerable interest.

Effects of Agar Gel Strength and Fat on Oral Breakdown, Volatile Release, and Sensory Perception Using in Vivo and in Vitro Systems.

The density and composition of a food matrix affect the rates of oral breakdown and in-mouth flavor release as well as the overall sensory experience. Agar gels of increasing concentration (1.0, 1.7, 2.9, and 5% agarose) with and without added fat (0, 2, 5, and 10%) were spiked with seven aroma volatiles. Differences in oral processing and sensory perception were systematically measured by a trained panel using a discrete interval time intensity method. Volatile release was measured in vivo and in vitro by proton transfer reaction mass spectrometry. Greater oral processing was required as agar gel strength increased, and the intensity of flavor-related sensory attributes decreased. Volatile release was inversely related to gel strength, showing that physicochemical phenomena were the main mechanisms underlying the perceived sensory changes. Fat addition reduced the amount of oral processing and had differential effects on release, depending on the fat solubility or lipophilicity of the volatiles.

Zooming in : Structural Investigations of Rheologically Characterized Hydrogen-Bonded Low-Methoxyl Pectin Networks

Self-assembled hydrogen-bonded networks of the polysaccharide pectin, a mechanically functional component of plant cell walls, have been of recent interest as biomimetic exemplars of physical gels, and the microrheological and strain-stiffening behaviors have been previously investigated. Despite this detailed rheological characterization of preformed gels, little is known about the fundamental arrangement of the polymers into cross-linking junction zones, the size of these bonded regions, and the resultant network architecture in these hydrogen-bonded materials, especially in contrast to the plethora of such information available for their well-known calcium-assembled counterparts. In this work, in concert with pertinent rheological measurements, an in-depth structural study of the hydrogen-bond-mediated gelation of pectins is provided. Gels were realized by using glucona-delta-lactone to decrease the pH of solutions of pectic polymers that had a (blockwise) low degree of methylesterification. Small-angle X-ray scattering and transmission electron microscopy were utilized to access structural information on length scales on the order of nanometers to hundreds of nanometers, while complementary mechanical properties were measured predominantly using small amplitude oscillatory shear rheology.

Fundamental studies on the structural functionality of whey protein isolate in the presence of small polyhydroxyl compounds as co-solute

The present work deals with the changing network morphology of whey protein isolate (15%, w/w) in the presence of glucose syrup (co-solute) with concentrations ranging from 0% to 65% (w/w) in 10 mM CaCl2 solution, thus producing formulations with a total level of solids of up to 80% (w/w). Denaturation behaviour and aggregation of whey protein systems were investigated using small deformation dynamic oscillation on shear, micro and modulated differential scanning calorimetry, and confocal laser scanning microscopy. A progression in the mechanical strength of protein aggregates was observed resulting from enhanced protein-protein interactions in the presence of glucose syrup. Addition of the co-solute resulted in better thermal stability of protein molecules by shifting the process of denaturation to higher temperature, as observed by calorimetry. Observations are supported by micrographs showing coherent networks with reduced size of whey protein aggregates in the presence of high levels of glucose syrup, as opposed to thick and random clusters for systems of whey protein by itself. Glass transition phenomenon was observed for condensed protein/co-solute systems, which were treated with theoretical concepts adapted from synthetic polymer research to pinpoint the mechanical glass transition temperature.

Influence of boron on carrot cell wall structure and its resistance to fracture.

Plant cell wall structure integrity and associated tissue mechanical properties is one of key determinants for the perceived texture of plant-based foods. Carrots (Daucus carota) were used to investigate the effect of mineral supply of boron (B) and/or calcium (Ca), during plant growth, on the plant cell wall structure and mechanical properties of matured root tissues. Five commercial cultivars of carrots, Kuroda (orange), Dragon Purple, Kuttiger White, Yellow, and Nutri-Red, were cultivated under controlled glasshouse conditions over two seasons. Significant increases in the accumulation of B and Ca were found for all cultivars of carrots when additional B and Ca were included in the nutrient feeding solutions throughout the plant growth period. Elevated levels of B in carrot root tissue reduced the uptake of Ca and other mineral nutrients and enhanced plant cell wall structural integrity, its resistance to fracture, and the weight and size (both diameter and length) of carrots. Although higher amounts of Ca were accumulated in the plant materials, the additional supply of Ca did not have a significant effect on the mechanical properties of mature plant tissues or on the uptake of B by the plant. The results suggest that B cross-linking of pectin (rhamnogalacturonan II) has a greater influence on mature tissue mechanical properties than Ca cross-linking of pectin (homogalacturonan) when supplied during plant growth.

Why is Abalone So Chewy? Structural Characterization and Relationship to Textural Attributes

ABSTRACT Abalone is a highly regarded food in many cultures. It is consumed as a luxury food, valued for its unique sensory properties, which include both flavor and texture. The aim of this research was to understand the texture of abalone and to link textural attributes to the microstructure of the muscle tissue. Two different sources, and species, of abalone—wild (Haliotis rubra) and farmed (Haliotis laevigata)—were characterized structurally using light microscopy and confocal laser scanning microscopy. The structure at different length scales of the abalone foot muscle tissues was related to perceived texture by a trained sensory panel. The results of the microscopy work showed isotropic assemblies of interwoven muscle bundles with a diameter of approximately 20–40 µm. The muscle fibers consisted of bundles of aligned muscle fibrils, 2–4 µm in diameter, that were interconnected with anisotropic collagen. During steaming, the muscle fibers were observed to separate as a result of configurational changes of the protein. The sample from wild abalone was found by the sensory panel to be the most chewy, firm and springy. The size of the collagen-rich areas was linked to the texture perception, with the toughest pieces of meat displaying the largest collagen-rich areas. The size of the muscle fiber bundles also contributed to the perceived texture, in which samples containing larger bundles were perceived as more chewy than samples with fewer fibers per bundle.