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Establishing relationships between physical and sensorial properties of semi-solid foods is essential to develop tailored products. Whey protein/polysaccharide mixed gels were used to model both natural and fabricated semi-solid foods. The presence of various polysaccharides modulated the microstructure and large deformation properties of the mixed gels. The gels exhibited a large spectrum of sensorial properties as evaluated by panellists in a quantitative descriptive analysis. Mouthfeel attributes that discriminated best between the gels were wateriness, crumbliness, and spreadability. Wateriness strongly correlated with the amount of exuded phase (serum) measured during uniaxial compression. Serum release may have a positive effect on, for instance, the juiciness of a product. Large deformation measurements showed that highly crumbly gels fracture readily via a free-running crack. Low serum release is a requirement for that. Low crumbly gels fracture slowly, often releasing a high amount of serum. Spreadability related to the occurrence of multiple microcracks during deformation as observed by confocal laser scanning microscopy, which resulted in a large number of pieces after oral processing

Background Betaine (trimethylglycine) lowers plasma homocysteine, a possible risk factor for cardiovascular disease. However, studies in renal patients and in obese individuals who are on a weight-loss diet suggest that betaine supplementation raises blood cholesterol; data in healthy individuals are lacking. Such an effect on cholesterol would counteract any favourable effect on homocysteine. We therefore investigated the effect of betaine, of its precursor choline in the form of phosphatidylcholine, and of the classical homocysteine-lowering vitamin folic acid on blood lipid concentrations in healthy humans. Methods and Findings We measured blood lipids in four placebo-controlled, randomised intervention studies that examined the effect of betaine (three studies, n = 151), folic acid (two studies, n = 75), and phosphatidylcholine (one study, n = 26) on plasma homocysteine concentrations. We combined blood lipid data from the individual studies and calculated a weighted mean change in blood lipid concentrations relative to placebo. Betaine supplementation (6 g/d) for 6 wk increased blood LDL cholesterol concentrations by 0.36 mmol/l (95% confidence interval: 0.25¿0.46), and triacylglycerol concentrations by 0.14 mmol/l (0.04¿0.23) relative to placebo. The ratio of total to HDL cholesterol increased by 0.23 (0.14¿0.32). Concentrations of HDL cholesterol were not affected. Doses of betaine lower than 6 g/d also raised LDL cholesterol, but these changes were not statistically significant. Further, the effect of betaine on LDL cholesterol was already evident after 2 wk of intervention. Phosphatidylcholine supplementation (providing approximately 2.6 g/d of choline) for 2 wk increased triacylglycerol concentrations by 0.14 mmol/l (0.06¿0.21), but did not affect cholesterol concentrations. Folic acid supplementation (0.8 mg/d) had no effect on lipid concentrations. Conclusions Betaine supplementation increased blood LDL cholesterol and triacylglycerol concentrations in h

Background: A high plasma concentration of total homocysteine (tHcy) is associated with increased risk of cardiovascular disease. A high protein intake and hence a high intake of methionine¿the sole dietary precursor of homocysteine¿may raise plasma tHcy concentrations. Objectives: We studied whether high intake of protein increases plasma concentrations of tHcy in the fasting state and throughout the day. Design: We conducted a randomized, dietary controlled, crossover trial in 20 healthy men aged 18¿44 y. For 8 d, men consumed a controlled low-protein diet enriched with either a protein supplement [high-protein diet (21% of energy as protein)] or an isocaloric amount of short-chain glucose polymers [low-protein diet (9% of energy as protein)]. After a 13-d washout period, treatments were reversed. On days 1 and 8 of each treatment period, blood was sampled before breakfast (fasting) and throughout the day. Results: Fasting tHcy concentrations did not differ significantly after the 1-wk high-protein and the 1-wk low-protein diets. The high-protein diet resulted in a significantly higher area under the 24-h homocysteine-by-time curves compared with the low-protein diet, both on day 1 (difference: 45.1 h · µmol/L; 95% CI: 35.3, 54.8 h · µmol/L; P <0.0001) and on day 8 (difference: 24.7 h · µmol/L; 95% CI: 15.0, 34.5 h · µmol/L; P <0.0001). Conclusions: A high-protein diet increases tHcy concentrations throughout the day but does not increase fasting tHcy concentrations. As previously shown, the extent of the tHcy increase is modified by the amino acid composition of the protein diet. The clinical relevance of this finding depends on whether high concentrations of tHcy¿particularly postprandially¿cause cardiovascular disease

Background: A high plasma total homocysteine (tHcy) concentration is a risk factor for cardiovascular disease. The increase in tHcy induced by methionine, the sole dietary precursor of homocysteine, might be modulated by other amino acids present in dietary proteins. Objectives: Our objectives were to compare the postprandial effect of free and dietary methionine on plasma tHcy concentrations and to investigate whether serine and cystine modify the effect of free methionine on tHcy. Design: We conducted a randomized crossover trial in 24 healthy men. Each subject ingested 4 meals on separate days, which were separated by 1 wk. tHcy concentrations were measured in the fasting state and at 2, 4, 6, 8, 10, and 24 h after meal ingestion. The meals were 1) a low-protein meal fortified with 30 mg methionine/kg body wt (reference, denoted by "Met"), 2) meal I additionally fortified with 60.6 mg serine/kg body wt (MetSer), 3) meal I additionally fortified with 12.3 mg cystine/kg body wt (MetCys), and 4) a protein-rich meal containing 30 mg methionine, 60.6 mg serine, and 12.3 mg cystine per kg body wt (Protein). Results: The mean (SD) fasting tHcy concentration was 9.1 +/- 2.7 mumol/L. Mean peak tHcy concentrations were 17.9 +/- 4.5, 14.3 +/- 3.3, 14.8 +/- 3.9, and 11.2 +/- 3.1 mumol/L after Met, MetSer, MetCys, and Protein, respectively. Compared with the mean 24-h area under the tHcy-by-time curve after Met, the mean curves after MetSer, MetCys, and Protein were 37%, 32%, and 77% smaller, respectively (all P <0.0005). Conclusions: Dietary methionine increases tHcy much less than does free methionine. Serine and cystine attenuate the tHcy-raising effect of free methionine. Thus, dietary proteins with a high content of serine or cystine relative to methionine may lead to lower postprandial tHcy responses.

Brownian Dynamics (BD) simulations have been performed to study structure and rheology of particle gels under large shear deformation. The model incorporates soft spherical particles, and reversible flexible bond formation. Two different methods of shear deformation are discussed, namely affine and non-affine deformation, the second being novel in simulation studies of gels. Also two dynamic descriptions of the model are presented, with and without inertia effects. Non-affine deformation resulted in a slower increase of the stress at small deformation than affine deformation. At large deformation both models gave similar stress responses, although the inertia model resulted in lower stresses. The particle gels, regardless of the model used, were observed to fracture into lumps that compactified due to local reorganization. A reversible yielding transition, as observed in polymer gels, was not found. Fractal properties of the gels were irreversibly lost at large deformation

Load-extension tests on flour dough are widely used by plant breeders, millers and bakers. The 'Kieffer dough and gluten extensibility rig' is a small-scale version of the Brabender extensograph, in which test pieces of about 0.4 g are extended. With the Kieffer rig, lower strain rates can be applied than in the Brabender extensograph and the experimental data can be expressed in terms of stress and strain. In this paper the performance of the Kieffer rig is illustrated by measurements on a weak and a strong dough. Formulas are given for the calculation of fundamental rheological parameters from the results of measurements with the Kieffer rig. Sagging and bending of the test pieces before measurements could be started, caused difficulties in the determination of the exact starting point of extension. The deformation was not purely uniaxial extension, because a shear component was also observed. The amount of dough that is extended did not increase throughout the test. This is probably due to the occurrence of a shear component fracture which occurred mainly near the hook. A relatively large variation in stress and strain at fracture was observed. The maximum in stress represents the strain at which the sample fractures macroscopically better than the maximum in force. Variation in deformation history and volume of the test pieces have a negative effect on the reproducibility.

Interfacial rheological properties and their suitability for foam production and stability of two vegetable proteins were studied and compared to ß-casein. Proteins used ranged from flexible to rigid/globular in the order of ß-casein, gliadin and soy glycinin. Experiments were performed at pH 6.7. Network forming properties were characterised by the surface dilational modulus (determined with the ring trough) and the critical falling film length (Lstill) at which a stagnant protein film will break. Gliadin had the highest dilational modulus, followed by glycinin and ß-casein, whereas glycinin formed the strongest film against fracture in the overflowing cylinder. The rate of decrease in the surface tension was studied at the air–water (Wilhelmy plate method) and the oil–water interface (bursting membrane) and the dynamic surface tension during compression and expansion in the caterpillar. Gliadin had the lowest equilibrium interfacial tensions and ß-casein the lowest dynamic surface tension during expansion. Hardly any foam could be formed at a concentration of 0.1 g/l by shaking. At a concentration of 1.4 g/l most foam was formed by ß-casein, followed by gliadin and glycinin. It seems that in the first place the rate of adsorption is important for foam formation. For the vegetable proteins, adsorption was slow. This resulted in lower foamability, especially for glycinin.

The use of enzymes such as peroxidases or glucose oxidase instead of chemical oxidants is a very interesting option for improving breadmaking performance of doughs. In this study the effect of such enzymes on bulk rheological properties of dough was quantified and their influence on the polymer network in dough deduced. Small deformation oscillation and relaxation tests (strain 0·001) are not suitable for discriminating between doughs prepared in the presence of the different enzymes. Flow relaxation tests at high deformation and long relaxation times showed a clear distinction between the effect of peroxidase and glucose oxidase. Peroxidase increases only the number or lifetime of transient bonds, whereas glucose oxidase additionally produced cross-links that were permanent on time scales up to 3 h. Peroxidase probably introduced a second, more transient structure (arabinoxylan network) through the gluten network, whereas glucose oxidase may also have strengthened the gluten network. A higher water addition could not compensate for the effect of peroxidase; on longer time scales the stress remained at a higher level. Similar results were obtained in large deformation biaxial and uniaxial extension tests. Peroxidases only increased stress levels. The addition of glucose oxidase resulted in a higher stress and more intense strain hardening. Only in biaxial extension was an influence of pH observed. An increase in stress level was accompanied by a decrease in fracture strain, making predictions of the effects on bread structure complicated. Author Keywords: dough rheology, relaxation, peroxidase, glucose oxidase

Background: A high plasma total homocysteine concentration is associated with increased risk of cardiovascular disease. Consumption of unfiltered or filtered coffee raises total homocysteine concentrations in healthy volunteers. The responsible compound, however, is unknown. Objective: The objective was to determine whether caffeine explains the homocysteine-raising effect of coffee. Design: Forty-eight subjects aged 19–65 y completed this randomized crossover study with 3 treatments, each lasting 2 wk. Subjects consumed 6 capsules providing 870 mg caffeine/d (test treatment), 0.9 L paper-filtered coffee providing 870 mg caffeine/d, or 6 placebo capsules. Blood samples were drawn fasting and 4 h after consumption of 0.45 L coffee or 3 capsules. Results: The mean fasting plasma homocysteine concentration after the placebo treatment was 9.6 ± 3.1 ?mol/L. The caffeine and coffee treatments increased fasting homocysteine by 0.4 ?mol/L (95% CI: 0.1, 0.7; P = 0.04), or 5%, and by 0.9 ?mol/L (95% CI: 0.6, 1.2; P = 0.0001), or 11%, respectively, compared with placebo. The increase in homocysteine concentrations 4 h after consumption of 0.45 L coffee relative to consumption of 3 placebo capsules was 19% (P = 0.0001). Caffeine treatment had a much weaker acute effect on homocysteine (4%; P = 0.09). Effects of caffeine were stronger in women than in men, but the effects of coffee did not differ significantly between men and women. Conclusions: Caffeine is partly responsible for the homocysteine-raising effect of coffee. Coffee, but not caffeine, affects homocysteine metabolism within hours after intake, although the effect is still substantial after an overnight fast. Key Words: Caffeine … paper-filtered coffee … homocysteine … B vitamins … crossover experiment