Determination of stability of food emulsions Part 1. The influence of the type and concentration of protein on creaming stability determined by analytical ultracentrifugation

A centrifugal method is presented for the determination of emulsion stability against creaming (separation of continuous phase). It is based on the centrifugation to final values (equilibrium) for the separated continuous phase and cream. On this methodical basis two indices for the characterization of this kind of stability are obtained, the cream- or continuous phase-quotient. The influence of the type and concentration of protein on the emulsion stability has been investigated with O/W emulsions containing acetylated (AFBPI) and non-acetylated (FBPI) faba bean protein isolate in a concentration range of 0.1–4 %. The emulsions containing the two types of protein show a clear raise in stability with increasing AFBPI- and FBPI-concentration with the exception of that with 2 % AFBPI at a short storage period of the emulsion. The method is sensitive and indicates small changes in stability during storage, for example. It can be applied to emulsions which show different final values with stepwise increasing centrifugal fields. The method proposed is particularly interesting for preparation and characterization of high concentrated emulsions.     

Schwertmannite formation adjacent to bacterial cells in a mine water treatment plant and in pure cultures of Ferrovum myxofaciens

Schwertmannite has previously been found in iron- and sulfate-rich mine waters at pH 2.8-4.5. In the present study, schwertmannite (Fe(8)O(8)(OH)(6)SO(4)) was shown to be the major mineral in a mine water treatment plant at pH 3, in which ferrous iron is mainly oxidized by bacteria belonging to the species Ferrovum myxofaciens. Strain EHS6, which is closely related to the type strain of Fv. myxofaciens, was isolated from the pilot plant and characterized as an acidophilic, iron-oxidizing bacterium. In contrast to the pilot plant, the mineral phase formed by a pure culture of Fv. myxofaciens EHS6 was a mixture of schwertmannite and jarosite (KFe(3)(SO(4))(2)(OH)(6)). In contrast to other reports of neutrophilic, iron-oxidizing bacteria, acidophilic microorganisms in the pilot plant and cultures of strain EHS6 did not show encrustation of the cell surface or deposition of minerals inside the cell, though a few cells appeared to be in contact with jarosite crystals. It was concluded that no direct biomineralization occurred in the pilot plant or in laboratory cultures. The lack of encrustation of bacterial cells in the pilot plant is considered advantageous since the cells are still able to get in contact with ferrous iron and the iron oxidation process in the mine water treatment plant can proceed.     

Nonenzymatic Transformation of Amorphous CaCO3 into Calcium Phosphate Mineral after Exposure to Sodium Phosphate in Vitro: Implications for in Vivo Hydroxyapatite Bone Formation

Studies indicate that mammalian bone formation is initiated at calcium carbonate bioseeds, a process that is driven enzymatically by carbonic anhydrase (CA). We show that amorphous calcium carbonate (ACC) and bicarbonate (HCO₃^?) cause induction of expression of the CA in human osteogenic SaOS‐2 cells. The mineral deposits formed on the surface of the cells are rich in C, Ca and P. FTIR analysis revealed that ACC, vaterite, and aragonite, after exposure to phosphate, undergo transformation into calcium phosphate. This exchange was not seen for calcite. The changes to ACC, vaterite, and aragonite depended on the concentration of phosphate. The rate of incorporation of phosphate into ACC, vaterite, and aragonite, is significantly accelerated in the presence of a peptide rich in aspartic acid and glutamic acid. We propose that the initial CaCO₃ bioseed formation is driven by CA, and that the subsequent conversion to calcium phosphate/calcium hydroxyapatite (exchange of carbonate by phosphate) is a non‐enzymatic exchange process.     

Structure-Based Design,Docking and Binding Free Energy Calculations of A366 Derivatives as Spindlin1 Inhibitors

The chromatin reader protein Spindlin1 plays an important role in epigenetic regulation, through which it has been linked to several types of malignant tumors. In the current work, we report on the development of novel analogs of the previously published lead inhibitor A366. In an effort to improve the activity and explore the structure–activity relationship (SAR), a series of 21 derivatives was synthesized, tested in vitro, and investigated by means of molecular modeling tools. Docking studies and molecular dynamics (MD) simulations were performed to analyze and rationalize the structural differences responsible for the Spindlin1 activity. The analysis of MD simulations shed light on the important interactions. Our study highlighted the main structural features that are required for Spindlin1 inhibitory activity, which include a positively charged pyrrolidine moiety embedded into the aromatic cage connected via a propyloxy linker to the 2-aminoindole core. Of the latter, the amidine group anchor the compounds into the pocket through salt bridge interactions with Asp184. Different protocols were tested to identify a fast in silico method that could help to discriminate between active and inactive compounds within the A366 series. Rescoring the docking poses with MM-GBSA calculations was successful in this regard. Because A366 is known to be a G9a inhibitor, the most active developed Spindlin1 inhibitors were also tested over G9a and GLP to verify the selectivity profile of the A366 analogs. This resulted in the discovery of diverse selective compounds, among which 1s and 1t showed Spindlin1 activity in the nanomolar range and selectivity over G9a and GLP. Finally, future design hypotheses were suggested based on our findings.     

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Fluidic flow control applied for improved performance of Darrieus wind turbines

The focus of the present research is performance enhancement of a vertical axis Darrieus‐type wind turbine using flow control techniques. The academic and industrial interest in vertical‐axis wind turbines (VAWTs) is increasing because of its suitability to urban areas, characterized by high turbulence and low wind speeds. The paper describes experimental work performed on a GOE222 asymmetrical airfoil intended to be used in a straight‐bladed Darrieus VAWT. Airfoil characteristics were measured in a wide range of incidence angles and Reynolds numbers, relevant for the operation of a small to medium size wind turbine. A variety of passive flow control (passive porosity and surface roughness) and active flow control techniques (boundary layer suction, pulsed suction) were tested in order to evaluate their effects on the airfoil performance. The measured effects of flow control on the 2D airfoil are integrated into a modified version of a double‐multiple streamtube model in order to predict the effects on the performance and efficiency of the turbine. It was found that the improvement of 2D airfoil characteristics can be translated into improvement of total turbine performance. By the use of active flow control, it was possible to increase the VAWT maximum mechanical output. When active flow control is properly activated taking into account the azimuth and Reynolds number conditioning, the effects could be greatly increased while consuming less energy, increasing the net efficiency of the entire system. Copyright © 2015 John Wiley & Sons, Ltd.     

Microstructure and ferroelectric properties of soft-doped sol–gel derived PZT/SKN fibers

Sol–gel derived PZT/SKN fibers with a final composition of 0.98(PbO)_1+z (Zr_0.53Ti_0.47)O₂-0.02Sr(K_0.25Nb_0.75)O₃ and a PbO content of z = +0.04 and +0.14 in the spinning sol were sintered at different temperatures. Fiber stoichiometry, phase content and microstructure as well as the physical properties of the fibers were investigated. A fully densified microstructure independent from the initial PbO content was obtained for fibers sintered at 950 °C or higher. Enhanced porosity was found only for fibers sintered at 900 °C. The densification of the fiber batches at the lower temperatures is dominated by solid state sintering, while liquid phase sintering is promoted by sintering at temperatures above 900 °C. TEM investigations confirmed the homogeneous nature of the PZT/SKN fibers devoid of compositional gradients. Typical dielectric permittivity is in the range of 650–1000. The ferroelectric hysteresis loops are well pronounced showing typical soft-doped behavior with remanent polarization values in the range of 15 and 34 μC/cm² and coercivities of about 1.9 V/μm.     

Examination of ligand-induced conformational changes in the beta2 adrenergic receptor

The environmentally sensitive and cysteine reactive fluorescent probe, IANBD, was used to monitor ligand-induced structural changes in the beta2 adrenergic receptor (beta2AR) by fluorescent spectroscopy. We found that agonists caused a dose-dependent and reversible decrease in fluorescence from the purified IANBD-labeled beta2AR. This suggested that agonists promote a conformational change in the receptor that leads to an increase in the polarity of the environment around one or more IANBD labeled cysteines. The wildtype receptor contains eight free cysteines and mutagenesis and peptide mapping experiments have indicated that several of these sites are accessible for chemical derivatization. Thus, to identify the cysteine(s) involved in the agonist-induced change in fluorescence and thereby map agonist-induced conformational changes in the beta2AR, we generated a series of mutant receptors having limited numbers of cysteines available for fluorescent labeling. Fluorescence spectroscopy analysis of the purified and site-selectively IANBD-labeled mutants showed that IANBD labeled 125Cys and 285Cys are responsible for the observed changes in fluorescence consistent with movements of TM III and VI in response to agonist binding.     

Durability and performance of polystyrene‐b‐poly(vinylbenzyl trimethylammonium) diblock copolymer and equivalent blend anion exchange membranes

Anion exchange membranes (AEM) are solid polymer electrolytes that facilitate ion transport in fuel cells. In this study, a polystyrene‐b‐poly(vinylbenzyl trimethylammonium) diblock copolymer was evaluated as potential AEM and compared with the equivalent homopolymer blend. The diblock had a 92% conversion of reactive sites with an IEC of 1.72 ± 0.05 mmol g^?1, while the blend had a 43% conversion for an IEC of 0.80 ± 0.03 mmol g^?1. At 50°C and 95% relative humidity, the chloride conductivity of the diblock was higher, 24–33 mS cm^?1, compared with the blend, 1–6 mS cm^?1. The diblock displayed phase separation on the length scale of 100 nm, while the blend displayed microphase separation (～10 μm). Mechanical characterization of films from 40 to 90 microns thick found that elasticity and elongation decreased with the addition of cations to the films. At humidified conditions, water acted as a plasticizer to increase film elasticity and elongation. While the polystyrene‐based diblock displayed sufficient ionic conductivity, the films' mechanical properties require improvement, i.e., greater elasticity and strength, before use in fuel cells. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2015 , 132, 41596.