The Rehydration Ability of Whey Ingredients

The purpose of this research was to studythe ability of whey protein concentrates (WPC) and whey permeate produced with ultrafiltration of cheese whey to rehydrate. The products studied were cheese whey concentrate witha PDM percentage of 80% (WPC-80), and cheese whey permeate, both produced under the conditions of the PJSC Dairy “Voronezhsky”.WPC-80 and the whey permeate dissolution processes were studied using microscopy. Water-impermeable hydrophobic layers were formed at the boundary, preventing water penetration into dry particles. The result was a higher dissolution timeforWPC-80 compared with whey permeate. When WPC-80 came into contact with water,it initially formed an obtuse wetting angle with a slow change over time. Whey permeate reached the equilibrium wetting angle more quickly. Quickreconditioning of WPC moisture content required avoiding capillary penetration of water, which created a turbulent liquid flow. The application of these ingredients in different food industry areas can reduce the costs for finished products, contribute to cost-effectiveness, increase the total production, and reduce environmental risks. Keywords: whey protein concentrate, whey permeate powder, water-wetting, dissolutio

Učinak dodatka proteina iz otpada kože na hematološke i biokemijske pokazatelje metabolizma i mliječnost visokoproduktivnih krava

This study was aimed to establish the effect of a fodder protein supplement from minced subcutaneous epithelium of farm animals on hematological, biochemical parameters of metabolism and milk productivity of high-yielding cows during the early lactation. For this, three groups of cows, six animals each, were formed according to the principle of analogous pairs. The control group received the main diet, the second and third experimental groups were daily fed with 300 g and 500 g of protein supplement for 60 days in addition to the main diet, respectively. The effect of prolongation of the supplement was studied over the next 30 days. Hematological and biochemical blood parameters, qualitative and quantitative composition of milk were studied in all animals. The animals of the experimental groups showed an increase in metabolic and redox processes during the experiment. An increase in the metabolism of nutrients in the liver has been found. Due to the sufficient intake of protein in the organism of animals, there was an increase in milk productivity and milk quality indicators.Cilj je ovog istraživanja utvrditi učinak dodatka proteina iz mljevenog potkožnog epitela domaćih životinja, na hematološke i biokemijske parametre metabolizma te proizvodnost visokoproduktivnih krava tijekom rane laktacije. Za to su prema principu analognih parova formirane tri skupine krava, svaka po šest životinja. Kontrolna skupina hranjena je osnovnim obrokom, a druga i treća eksperimentalna skupina svakodnevno su uz osnovnu hranidbu hranjene s 300 g i 500 g proteinskog dodatka tijekom 60 dana. Učinak dodatka proučavan je tijekom sljedećih 30 dana. U svih životinja proučavani su hematološki i biokemijski parametri krvi, te kvalitativni i kvantitativni sastav mlijeka. Životinje pokusnih skupina pokazale su porast metaboličkih i redoks procesa tijekom pokusa. Utvrđen je porast metabolizma hranjivih sastojaka u jetri. Zbog dovoljnog unosa proteina u organizam životinja eksperimentalnih skupina došlo je do povećanja pokazatelja mliječne proizvodnosti i pokazatelja kvalitete mlijeka

“PETERSBURG TEXT” BY TATYANA TOLSTAYA (motifs in the story “The Okkervil River”)

In the article devoted to the analysis of “The Okkervil River”, a short story by Tatyana Tolstaya, a variety of motifs are distinguished and interpreted. Those refer the reader to the main motifs of Russian classical literature, however, their semantics is reconsidered by the contemporary writer and presented with different connotations. Saint Petersburg chronotope is analyzed, its simplification and shifts of spatial frameworks are considered. The ironic depreciation of the image of Saint Petersburg – Leningrad sets a playful (derisive) tone of the narration about the “little hero”, Simeonov, a descendant of poor Eugene from “The Bronze Horseman” by Pushkin, as well as Gogol’s and Dostoevsky’s “little heroes”. One of the leading motifs of the narration is that of a circle, closely interacting with the image-motif of the luring “silver voice”. It allows for revealing musical allusions, encouraging the development of the “romancing” intertextuality of the story

The Differential Effect of Senolytics on SASP Cytokine Secretion and Regulation of EMT by CAFs

The tumor microenvironment (TME) plays an essential role in tumor progression and in modulating tumor response to anticancer therapy. Cellular senescence leads to a switch in the cell secretome, characterized by the senescence-associated secretory phenotype (SASP), which may regulate tumorigenesis. Senolytic therapy is considered a novel anticancer strategy that eliminates the deleterious effects of senescent cells in the TME. Here, we show that two different types of senolytic drugs, despite efficiently depleting senescent cells, have opposite effects on cancer-associated fibroblasts (CAFs) and their ability to regulate epithelial–mesenchymal transition (EMT). We found that senolytic drugs, navitoclax and the combination of dasatinib/quercetin, reduced the number of spontaneously senescent and TNF-induced senescent CAFs. Despite the depletion of senescent cells, the combination of dasatinib/quercetin versus navitoclax increased the secretion of the SASP pro-inflammatory cytokine IL-6. This differential effect correlated with the promotion of enhanced migration and EMT in MC38 colorectal cancer cells. Our results demonstrate that some senolytics may have side effects unrelated to their senolytic activity and may promote tumorigenesis. We argue for more careful and extensive studies of the effects of senolytics on various aspects of tumor progression and tumor resistance to therapy before the senolytic strategy is implemented in the clinic

The Rehydration Ability of Whey Ingredients

The purpose of this research was to studythe ability of whey protein concentrates (WPC) and whey permeate produced with ultrafiltration of cheese whey to rehydrate. The products studied were cheese whey concentrate witha PDM percentage of 80% (WPC-80), and cheese whey permeate, both produced under the conditions of the PJSC Dairy “Voronezhsky”.WPC-80 and the whey permeate dissolution processes were studied using microscopy. Water-impermeable hydrophobic layers were formed at the boundary, preventing water penetration into dry particles. The result was a higher dissolution timeforWPC-80 compared with whey permeate. When WPC-80 came into contact with water,it initially formed an obtuse wetting angle with a slow change over time. Whey permeate reached the equilibrium wetting angle more quickly. Quickreconditioning of WPC moisture content required avoiding capillary penetration of water, which created a turbulent liquid flow. The application of these ingredients in different food industry areas can reduce the costs for finished products, contribute to cost-effectiveness, increase the total production, and reduce environmental risks. Keywords: whey protein concentrate, whey permeate powder, water-wetting, dissolutio

Highly Purified Conjugates of Natural Chlorin with Cobalt Bis(dicarbollide) Nanoclusters for PDT and BNCT Therapy of Cancer

To combine the neutron-capturing and photodynamic properties of boron nanoclusters and derivatives of natural chlorins, respectively, in one molecule, conjugate of chlorin e6 methyl ester with cyclen and dioxane and nitrile derivatives of cobalt bis(dicarbollide) were synthesized. The conditions for the purification of compounds by HPLC were selected since the work with natural compounds is complicated by the production of closely related impurities

A Novel Method for SNP Detection Using a New Duplex-Specific Nuclease From Crab Hepatopancreas

We have characterized a novel nuclease from the Kamchatka crab, designated duplex-specific nuclease (DSN). DSN displays a strong preference for cleaving double-stranded DNA and DNA in DNA-RNA hybrid duplexes, compared to single-stranded DNA. Moreover, the cleavage rate of short, perfectly matched DNA duplexes by this enzyme is essentially higher than that for nonperfectly matched duplexes of the same length. Thus, DSN differentiates between one-nucleotide variations in DNA. We developed a novel assay for single nucleotide polymorphism (SNP) detection based on this unique property, termed “duplex-specific nuclease preference” (DSNP). In this innovative assay, the DNA region containing the SNP site is amplified and the PCR product mixed with signal probes (FRET-labeled short sequence-specific oligonucleotides) and DSN. During incubation, only perfectly matched duplexes between the DNA template and signal probe are cleaved by DSN to generate sequence-specific fluorescence. The use of FRET-labeled signal probes coupled with the specificity of DSN presents a simple and efficient method for detecting SNPs. We have employed the DSNP assay for the typing of SNPs in methyltetrahydrofolate reductase, prothrombin and p53 genes on homozygous and heterozygous genomic DNA. [Supplemental material is available online at www.genome.org. The sequence data from this study have been submitted to GenBank/EMBL/Date Bank under accession nos. AF520591. The following individuals kindly provided reagents, samples, or unpublished information as indicated in the paper: N.K. Yankovsky, A.V. Polyakov, and G.N. Rudenskaya.

Live-Cell STED Microscopy with Genetically Encoded Biosensor

Of the various super-resolution techniques, stimulated emission depletion (STED) microscopy achieves the best temporal resolution at high spatial resolution, enabling live-cell imaging beyond the diffraction limit. However, STED and most other super-resolution imaging methods utilize a particular type of information extractable from the raw data, namely the positions of fluorophores. To expand on the use of super-resolution techniques, we report here the live-cell STED microscopy of a dynamic biosensor. Using the fluorescent H₂O₂ sensor HyPer2 for subdiffraction imaging, we were able not only to image filaments with superior resolution by localizing emission but also to trace H₂O₂ produced within living cell by monitoring brightness of the probe. STED microscopy of HyPer2 demonstrates potential utility of FP-based biosensors for super-resolution experiments in situ and in vivo