The determination of soya and meat protein in raw and processed meat products by specific peptide analysis. An evaluation

The detection and measurement of characteristic peptides formed on enzymatic hydrolysis of soya protein products, meats and offals is described. Samples were heated at 120°C for 3h prior to digestion with trypsin overnight, and the resultant peptide mixtures passed through an Amicon ultrafiltration membrane. After concentration the ultrafiltrates were analysed by ion exchange chromatography on Aminex A5 resin. Peptides were detected by post-column reaction with ninhydrin. Characteristic peaks designated SP 2 and MP 1 were seen in chromatograms of digests of soya protein isolate and beef respectively, and these peaks were well resolved in beef and soya protein isolate mixtures. The SP 2 peak was shown to contain peptides derived from soya 11 S globulin. The soya protein and beef contents of a series of mixtures of freeze-dried, defatted beef and soya protein isolate were determined by measurement of the SP 2 and MP 1 peaks respectively. Soya protein content could be determined within 2% of the true value over the range 30–70% soya protein isolate and beef content could be determined within 5% of the true value in the range 20–100% beef. Analysis of five soya protein isolates, four soya protein concentrates, six soya flours and 13 textured soya products indicated considerable interproduct variation in the yield of SP 2. The MP 1 peak was seen in a range of meats, both cooked and raw. It was also present in digests of offals which contained smooth or striated muscle but not in ‘non-muscle’ offals. The protein origin of the MP 1 peak was not established but the yield appeared lower in meat products which had been heated during manufacture than in those which had received no such treatment. Analysis of a series of laboratory prepared canned and heated pork and soya protein isolate mixtures enabled the pork content to be determined to within 8% of the true value, 2% soya protein isolate could be detected but not quantified accurately.     

MR spectroscopy as a tool for in vivo determination of steatosis in liver transplant recipients

Object  

Among several non-invasive methods of liver fat analysis, the most important role is played by MR imaging and spectroscopy (MRS). This study describes the 1H MRS at 3T measurement of liver fat volume fraction f_fat{\phi_{{\rm fat}}} in a group of liver transplant patients, an at-risk group for the development of de novo steatosis.     

Raman and infrared spectroscopy of Na<Subscript>0.5</Subscript>Bi<Subscript>0.5</Subscript>TiO<Subscript>3</Subscript> - BaTiO<Subscript>3</Subscript> ceramics

Lead-free Na_0.5Bi_0.5TiO₃ -BaTiO₃ ceramics have been prepared in the whole range of concentrations and studied at room-temperature by means of X-ray, Raman scattering and infrared techniques. X-ray measurements revealed rhombohedral, rhombohedral-tetragonal boundaries and tetragonal modifacations depending on the contents of BaTiO₃. The distinct changes of the Raman and infrared spectra with increasing of BaTiO₃ content, which were correlated with X-ray results, were observed. The broad phonon spectra indicated the disorder in the A site of Na_0.5Bi_0.5TiO₃ -BaTiO₃ system.     

Supplier ranking by multi-alternative proposal analysis for agile projects

Changing requirements and on-going decision making along the entire project life cycle are well handled by Agile methods. However Agile projects still use evaluation methods during the RFP stage that do not fulfill the flexibility mandated by the Agile manifesto.     

Proteome analysis of tissues by mass spectrometry

Tissues and biofluids are important sources of information used for the detection of diseases and decisions on patient therapies. There are several accepted methods for preservation of tissues, among which the most popular are fresh‐frozen and formalin‐fixed paraffin embedded methods. Depending on the preservation method and the amount of sample available, various specific protocols are available for tissue processing for subsequent proteomic analysis. Protocols are tailored to answer various biological questions, and as such vary in lysis and digestion conditions, as well as duration. The existence of diverse tissue‐sample protocols has led to confusion in how to choose the best protocol for a given tissue and made it difficult to compare results across sample types. Here, we summarize procedures used for tissue processing for subsequent bottom‐up proteomic analysis. Furthermore, we compare protocols for their variations in the composition of lysis buffers, digestion procedures, and purification steps. For example, reports have shown that lysis buffer composition plays an important role in the profile of extracted proteins: the most common are tris(hydroxymethyl)aminomethane, radioimmunoprecipitation assay, and ammonium bicarbonate buffers. Although, trypsin is the most commonly used enzyme for proteolysis, in some protocols it is supplemented with Lys‐C and/or chymotrypsin, which will often lead to an increase in proteome coverage. Data show that the selection of the lysis procedure might need to be tissue‐specific to produce distinct protocols for individual tissue types. Finally, selection of the procedures is also influenced by the amount of sample available, which range from biopsies or the size of a few dozen of mm² obtained with laser capture microdissection to much larger amounts that weight several milligrams.     

Novel glucose-derived gemini surfactants with a 1,1′-ethylenebisurea spacer: Preparation, thermotropic behavior, and biological properties

In the search for environmentally safe surfactants made from inexpensive and renewable sources, the interest has mainly been focused on new saccharide derivatives. This report describes the synthesis of newly designed nonionic gemini compounds comprising two reduced sugar headgroups, two alkyl tails, and a 1,1′-ethylenebisurea entity as the spacer linking two amphiphilic glucose-derived moieties. Thus, the series of N,N′-bis[(3-alkyl-3-deoxy-d-glucitol)ureido]ethylenediamines (bis(C_nGT), with C_n=n-C₉H₉, n-C₆-H₁₃, n-C₈H₁₇, n-C₁₀H₂₁, or n-C₁₂H₂₅), were prepared using a convenient procedure starting from easily accessible reagents such as d-glucose, n-alkylamines, urea, and ethylenediamine. Their structure and purity were confirmed by means of elemental analysis, electrospray ionization mass spectrometry, and ¹H and ¹³C nuclear magnetic resonance spectroscopy. Additionally, the present contribution introduces selected properties of these surfactants, including their thermotropic behavior and biological properties. The presence of two phase transition points, determined using the differential scanning calorimetry method, indicates liquid-crystalline mesophase formation upon heating. Furthermore, using the closed-bottle test (OECD Guideline 301D) as well as the biological oxygen demand test for insoluble substances for biodegradability measurements, it has been concluded that the tested glucose-derived gemini structures achieve more than 60% biodegradation after 64–75 test days. All tested surfactants were practically nontoxic to bacteria, yeast, and molds. Owing to their fitting aggregation ability as well as their nontoxicity, they constitute an interesting group of surfactants for various applications.     

Towards a deeper understanding of plastic deformation in mono-crystalline silicon

This paper investigates the plastic deformation in mono-crystalline silicon under complex loading conditions. With the aid of various characterization techniques, it was found that the mechanism of plasticity in silicon is complex and depends on loading conditions, involving dislocations, phase transformations and chemical reactions. In general, plastic deformation in silicon is the coupled result of mechanical deformation controlled by the stress field applied, chemical reaction determined by the external loading environment, and mechanical–chemical interaction governed by both the loading type and environment. Temperature rise accelerates the penetration of oxygen into silicon and reduces the critical stress of plastic yielding. When the chemical effect is avoided, the initiation of plasticity is enabled by octahedral shear stress but the further development of plastic deformation is influenced by hydrostatic stress. Plasticity of silicon in the form of phase transformations, e.g., from the diamond to amorphous or from the amorphous to bcc structures, is determined by loading history.     

Excitation and spectral dependence of the rise and decay time responses of Eu2+- and Dy3+-doped strontium aluminates

Journal of Materials Science: Materials in Electronics - In this paper, we study the phosphorescence rise and decay time responses of Eu2+- and Dy3+-doped strontium aluminates prepared by different...     

Bonelike apatite formation on niobium metal treated in aqueous NaOH

The essential condition for a biomaterial to bond to the living bone is the formation of a biologically active bonelike apatite on its surface. In the present work, it has been demonstrated that chemical treatment can be used to create a calcium phosphate (CaP) surface layer, which might provide the alkali treated Nb metal with bone-bonding capability. Soaking Nb samples in 0.5 M NaOH, at 25 degrees C for 24 h produced a nano-porous approximately 40 nm thick amorphous sodium niobate hydrogel layer on their surface. Immersion in a simulated body fluid (SBF) lead to the deposition of an amorphous calcium phosphate layer on the alkali treated Nb. The formation of calcium phosphate is assumed to be a result of the local pH increase caused by the cathodic reaction of oxygen reduction on the finely porous surface of the alkali-treated metal. The local rise in pH increased the ionic activity product of hydroxyapatite and lead to the precipitation of CaP from SBF that was already supersaturated with respect to the apatite. The formation of a similar CaP layer upon implantation of alkali treated Nb into the human body should promote the bonding of the implant to the surrounding bone. This bone bonding capability could make Nb metal an attractive material for hard tissue replacements.     

Investigation of the applicability of dielectric relaxation properties of amino acid solutions within the resonant recognition model

The resonant recognition model (RRM) is a physicomathematical approach used to analyze the interactions of a protein and its target, using digital signal processing methods. The RRM is based on the finding that there is a significant correlation between the spectra of numerical presentation of protein sequences and their biological activities. Initially, the electron-ion interaction potential was used to represent each amino acid in the protein sequences. In this paper, the dielectric constant (/spl epsiv/') and dielectric loss tangent (tan /spl delta/) parameters have been determined for their possible use in the RRM. These parameters are based on the values of capacitance and conductance obtained experimentally for 20 amino acid solutions using dielectric spectroscopy for the case of the real component of dielectric permittivity; the parameter used is the dielectric increment (/spl Delta//spl epsiv/'), the difference between dielectric constant of the amino acid solution and that of the solvent alone. The results of multiple cross-spectral analyses have shown that parameters analyzed generate in the consensus spectrum one dominant peak corresponding to the common biological activity of proteins studied, allowing the conclusion that these new parameters are suitable for use in the RRM approach.