Rheological properties and stability of low-in-fat dressings prepared with high-pressure homogenized yeast

The aim of present study was to investigate the feasibility of application high-pressure homogenized (HPH) yeast aqueous dispersions with low nucleic acid content for the formulation of low-in-fat dressings. The HPH treatment (1500 bar, 3 passes) in alkaline medium improved the protein dispersibility (>50%). Emulsions were prepared using sunflower oil (12.0% or 25% w/w oil), xhantan/guar gums (0.5% w/w), modified starch (0–4.0% w/w), salt, sucrose, acidulants, EDTA, and antimicrobial agents. All emulsions (pH 3.97 ± 0.27; a_w = 0.97 ± 0.01), whatever the starch content, behaved clearly as pseudoplastic fluids in steady flow measurements. Moreover, as the frequency sweep measurements were made they also exhibited a weak gel behavior. Although the presence of starch produced an increase of mean particle size (D_3,2 values), the rheological parameters (consistency index, proportionality coefficient and coordination number) also increased, so that the starch contributes to reinforce the three-dimensional network formed by oil droplets, protein aggregates and other polysaccharides. Yeast dressings were stable to coalescence after 28 days of quiescent storage (7.0 ± 0.5 °C) and only the highest starch concentration at 25% w/w oil was sufficient to maintain the stability of network.     

Drying of ultrasound pretreated apple and its selected physical properties

The aim of this work was to investigate the utilization of ultrasound as a mass transfer enhancing method prior to drying of apples tissue. Ultrasound power was provided at a frequency of 35 kHz for 10, 20 and 30 min in the ultrasound bath. Apple cubes were dried using convection method in 70 °C and at air velocity of 1.5 m/s. The effects of ultrasound pre-treatment upon drying were investigated.     

Characterization of the major whey proteins from milk of Mediterranean water buffalo (Bubalus bubalis)

In this work, the whey protein fractions from 120 Mediterranean water buffalo individual milks were analysed by microchip electrophoresis (MCE), reverse-phase high-performance liquid chromatography (RP-HPLC) and mass spectrometry (ESI-MS). Validation procedures were carried out for both MCE and HPLC. The chromatographic analysis allowed the complete separation of the whey protein fractions, resulting in a well-defined peak structure; the adopted RP-HPLC and ESI-MS protocols provided identification of β-lactoglobulin (18,266 Da), α-lactoalbumin (14,236 Da) and serum albumin (66,397 Da). The calculated mean concentrations were 4.04 g/l, 2.45 g/l and 0.35 g/l, respectively.     

Changes in solution color during phenol oxidation by Fenton reagent

Fenton reaction is a highly effective treatment for degrading phenolic compounds in an aqueous solution. However, during phenol oxidation, the oxidized water takes on a dark brown color associated with increased toxicity. Then, although phenol can be completely removed, if the oxidation process is not carried out properly, the final wastewater will be brown in color and have higher toxicity, two parameters in which legislation imposes restrictions. This paper analyzes the development of the dark color observed in the solution under oxidation treatment and formulates a reaction mechanism to explain the color generation. The experiments were carried out following the batch-wise procedure, but with the solution pH being kept constant throughout the reaction at its optimum value for phenol removal, i.e., pH 3.0. It is checked experimentally that color is formed at the beginning of the reaction in less than five minutes, and follows the kinetic-path of a reaction intermediate. During the first steps of the reaction phenol is degraded to dihydroxylated rings (catechol, resorcinol, and hydroquinone). These aromatic intermediates generate higher colored compounds such as ortho- and parabenzoquinone. On the other hand the dihydroxylated rings can react with their own quinones to generate charge-transfer complexes (quinhydrone), compounds which take on a dark color at low concentrations. Moreover, when iron reacts with hydrogen peroxide, ferric ions are generated that can be coordinated to benzene rings to produce colored metal complexes. The observed color of the solution is not a fortuitous result depending on trace components of low significance, but depends directly on the main reaction intermediates, so it is concluded that observed color depends on the level of oxidation reached. The maximum color observable during oxidation treatment (A(o)) depends only on initial phenol concentration and not on oxidant or catalyst doses.     

Steam gasification of selected energy crops in a fixed bed reactor

The increasing world's energy demand and environmental concerns related to GHG emissions as well as depleting fossil fuel resources and unstable prices of crude oil and natural gas have caused a renewed interest in renewable energy sources, and in particularly in biomass, as an alternative to fossil fuels. In the paper the results of steam gasification of Salix Viminalis, Miscanthus X Giganteus (MXG), and Andropogon Gerardi in a laboratory-scale fixed bed reactor in the temperature range of 650–900 °C are presented as well as the procedure and results of biomass chars reactivity testing in the process of steam gasification. The highest reactivity R₅₀ in the whole temperature range was observed for MXG. Hydrogen content in the synthesis gas was comparable for MXG and Andropogon Gerardi and lower for Salix Viminalis, while the volumes of the synthesis gas and hydrogen were highest for MXG at all temperatures.     

Laccase and Mn-peroxidase production by Coriolus hirsutus strain 075 in a jar fermentor

The white-rot fungus Coriolus hirsutus strain 075 excretes considerable amounts of laccase and Mn-peroxidase into culture broth over a brief production time. The effects of agitation speed, temperature, aeration and inoculum amount on laccase production using a 10-l fermentor were studied. The optimum fermentation conditions were a 15% inoculum, an aeration rate of 0.88 vvm, an agitation speed of 160 rpm, and a temperature of 28 degrees C. By optimizing the fermentation conditions, the laccase activity reached 80+/-3 U/ml in 3 d and the purified enzyme output was 30 mg/l. The laccase and Mn-peroxidase were purified by means of isoelectrofocusing and ion-exchange chromatography. The pIs of the laccase isoenzymes were 4.2 and 4.5. Mn-peroxidase had only one isoenzyme with a pI of 3.2. The optimum pH was 4.5 for laccase with syringaldazine as the substrate and 5.0-5.3 for Mn-peroxidase with Mn(+2) and H2O2 as the substrates. The laccase and Mn-peroxidase retained 50% of their activities at 50 degrees C after 55 h and 12 h of incubation time, respectively.     

Inhibition of Clostridium tyrobutyricum in Vidiago cheese by Lactococcus lactis ssp. lactis IPLA 729, a nisin Z producer

Lactococcus lactis ssp. lactis IPLA 729 is a nisin Z producer isolated from raw milk cheese able to grow and produce nisin Z in milk. The ability of this strain to inhibit the growth of Clostridium tyrobutyricum CECT 4011, a late blowing agent, in Vidiago cheese, a semi-hard farmhouse variety, manufactured in Asturias, Northern Spain, was investigated. For control purposes, cheeses were manufactured with the mesophilic mixed starter IPLA-001. In experimental cheeses, the nisin-producing strain L. lactis IPLA 729 was combined with this starter. Nisin Z activity reached a concentration of 1600 AU/ml in 1-day cheeses and this level was maintained until 15 days of ripening. Furthermore, to compare the inhibitory activity of the nisin-producing strain to nitrate, cheeses were also manufactured with a commercial starter culture and potassium nitrate as anti-blowing agent was added in accordance with Vidiago's cheesemakers. The control, experimental and commercial cheeses were contaminated with C. tyrobutyricum CECT 4011. The composition of the three different cheeses showed only slight differences with respect to total solids, protein and fat, although control and experimental cheeses showed a richer flavour-compound profile than commercial cheeses. The level of the spoilage strain C. tyrobutyricum CECT 4011 decreased from 1.2x10(6) to 1.3x10(3) cfu/g during ripening in presence of the nisin Z producer, while it increased to 1.99x10(9) cfu/g in control cheeses and to 3.5x10(7) cfu/g in commercial cheeses.     

Minimising food waste: a call for multidisciplinary research

Food losses and waste have always been a significant global problem for mankind, and one which has become increasingly recognised as such by policy makers, food producers, processors, retailers, and consumers. It is, however, an emotive subject whereby the extent, accuracy and resolution of available data on postharvest loss and waste are questionable, such that key performance indicators on waste can be misinformed. The nature and extent of food waste differ among developed economies, economies in transition and developing countries. While most emphasis has been put on increasing future crop production, far less resource has been and is still channelled towards enabling both established and innovative food preservation technologies to reduce food waste while maintaining safety and quality. Reducing food loss and waste is a more tractable problem than increasing production in the short to medium term, as its solution is not directly limited, for instance, by available land and water resources. Here we argue the need for a paradigm shift of current funding strategies and research programmes that will encourage the development, implementation and translation of collective biological, engineering and management solutions to better preserve and utilise food. Such multidisciplinary thinking across global supply chains is an essential element in the pursuit of achieving sustainable food and nutritional security. The implementation of allied technological and management solutions is reliant on there being sufficient skilled human capital and resources. There is currently a lack of robust postharvest research networks outside of the developed world, and insufficient global funding mechanisms that can support such interdisciplinary collaborations. There is, thus, a collective need for schemes that encourage inter‐supply chain research, knowledge exchange and capacity building to reduce food losses and waste. © 2017 Society of Chemical Industry     

Differential Effects of Betacyanin and Betaxanthin Pigments on Oxidative Stress and Inflammatory Response in Murine Macrophages

Scope: Betalain pigments are increasingly highlighted for their bioactive and anti-inflammatory properties, although research is lacking to demonstrate contributions of individual betalains. The work herein aimed to compare effects of four main betalains on inflammatory and cell-protective markers and to highlight potential structure-related relationships of the two main subgroups: betacyanins vs betaxanthins. Methods and results: Murine RAW 264.7 macrophages were stimulated with bacterial lipopolysaccharide following incubation with betacyanins (betanin, neobetanin) and betaxanthins (indicaxanthin, vulgaxanthin I) in concentrations from 1 to 100 µM. All betalains suppressed expression of pro-inflammatory markers IL-6, IL-1β, iNOS, and COX-2 with tendency for stronger effects of betacyanins compared to betaxanthins. In contrast, HO-1 and gGCS showed mixed and only moderate induction, while more emphasized effects were observed for betacyanins. While all betalains suppressed mRNA levels of NADPH oxidase 2 (NOX-2), a superoxide generating enzyme, only betacyanins were able to counteract hydrogen peroxide induced reactive oxygen species (ROS) generation, in alignment with their radical scavenging potential. Furthermore, betaxanthins exerted pro-oxidant properties, elevating ROS production beyond hydrogen peroxide stimulation. Conclusion: In summary, all betalains display anti-inflammatory properties, although only betacyanins demonstrate radical scavenging capacities, indicating potential differing responses under oxidative stress conditions, which requires further research.