Effect of thiochrome capronate on lipid metabolism in rats

Thiochrome caproate modified by the oxyethyl radical of the thiochrome derivative was studied for its effect on different indices of lipid metabolism in the liver and blood of albino rats. It was shown that when animals were fed on a standard laboratory diet, thiochrome caproate changed the amount of total and free fatty acids in the studied tissues and the fatty acid composition in the liver to a greater extent than thiochrome and hydroxythiamine.     

A hypothetic scheme for evolution of probionts

The origin of life cannot be assumed as a single, indissoluble chain of events. The objects we observe on this developmental pathway appeared many times in different biogenetic provinces of the Earth's surface. However, these systems might undergo decomposition and later appeared again. Such process especially might occur with the multimolecular, phase separated systems (probionts), interacting with the surrounding solution in the manner of the open systems. The modelling experiments demonstrate, that basing upon such interaction the systems could well maintain growth and passed through natural selection in the original Darwinian interpretation of this term, i.e. survival of the forms better adapted to the exterior environment. On this basis there proceeded the development of probionts organization, in particular, there arose the ‘fitness’ of molecular structure of proteins and other polymers. However, the maintenance of steady organization and selfreproduction of probionts were still far from perfection. Their evolution was still connected with the regular and strong decomposition processes. The decomposition products, which had already acquired somewhat better fittness than the original polymers, might either be assimilated by more developed probionts or enter a selfassembly process to form the new systems, like that had occured at the early stage of the development. The appearance of nucleic acids and their coding relations with proteins have provided significantly more high stability of developing probionts and primitive organisms. But on this stage, too, the decomposition andde novo formation of the developing systems had to occur. This fact makes us to approach in a new angle the problems of the origin of viruses, symbiosys and parasitism.     

Scientific Bases for Enuring Productive Longevity of Agrolandscapes in Russia

Biology Bulletin - V.V. Dokuchaev’s ideas are the foundation of modern ideas about rational nature-usage methods in our steppes in order to ensure productive longevity of agro-ecosystems and...     

Buckwheat trypsin inhibitor with helical hairpin structure belongs to a new family of plant defence peptides

A new peptide trypsin inhibitor named BWI-2c was obtained from buckwheat (Fagopyrum esculentum) seeds by sequential affinity, ion exchange and reversed-phase chromatography. The peptide was sequenced and found to contain 41 amino acid residues, with four cysteine residues involved in two intramolecular disulfide bonds. Recombinant BWI-2c identical to the natural peptide was produced in Escherichia coli in a form of a cleavable fusion with thioredoxin. The 3D (three-dimensional) structure of the peptide in solution was determined by NMR spectroscopy, revealing two antiparallel α-helices stapled by disulfide bonds. Together with VhTI, a trypsin inhibitor from veronica (Veronica hederifolia), BWI-2c represents a new family of protease inhibitors with an unusual α-helical hairpin fold. The linker sequence between the helices represents the so-called trypsin inhibitory loop responsible for direct binding to the active site of the enzyme that cleaves BWI-2c at the functionally important residue Arg(19). The inhibition constant was determined for BWI-2c against trypsin (1.7×10(-1)0 M), and the peptide was tested on other enzymes, including those from various insect digestive systems, revealing high selectivity to trypsin-like proteases. Structural similarity shared by BWI-2c, VhTI and several other plant defence peptides leads to the acknowledgement of a new widespread family of plant peptides termed α-hairpinins.     

Statistical Analysis of the Influence of a Disturbance Factor on Formation of the Spatial Structure of the Great Bustard (<Emphasis Type="Italic">Otis tarda</Emphasis> L.) (Otididae,Aves) Population in the Trans-Volga Region

This paper examines the influence of the location of settlements, railroads, and highways on the spatial structure of the Otis tarda population in the Trans-Volga region that was studied in the years 1998–2016 in a model area of 12000 km² that is located in the southern part of the Saratov Trans-Volga region. The zone of the impact made by our estimated disturbance factor due to the movement of people and a variety of ground vehicles along various-purpose roads on the territorial distribution of bustards in autumn can be denoted as a 300–500 m width band on both sides of the transport communications. Shelterbelts that were created along transport communications render a beneficial effect on the distribution of O. tarda and reduce the influence of the disturbance factor. Furthermore, crop rotation fields with side sizes of more than 1 km can be considered a factor that compensates for the anxiety of birds. We have found that in the Saratov Trans-Volga region, because of the large size of crop rotation fields and significant development of roadside and shelter belts, no special measures are required to protect O. tarda such as restrictions on the movement of people and vehicles over the territory where this species lives.     

Optimization of hydroxythiamine administration regimen in vitaminological research

A correlation between the different doses and inhibitory effect of hydroxythiamine relative to the activity of main thiamine pyrophosphate-dependent enzymes is studied in experiments on animals. It is established that the maximal inhibitory effect on the transketolase and oxoglutarate dehydrogenase activities is at a dose of antivitamin of 0.35 mmol/kg and that of pyruvate dehydrogenase of 0.55 mmol/kg. At lower doses of hydroxythiamine the inhibition of enzyme activities occurred in a dose-dependent manner.     

African Wild Cat (<Emphasis Type="Italic">Felis lybica</Emphasis> Forster, 1780) in the Saratov Transvolga Region

Analysis of the area limits where African wild cat was found as well as of published data on its distribution in the Saratov Transvolga Region demonstrated that the local range of this species extended and its northwestern limit advanced almost 1000 km to the Volga zoogeographical boundary.     

A new variant of Charcot-Marie-Tooth disease type 2 is probably the result of a mutation in the neurofilament-light gene

Charcot-Marie-Tooth (CMT) disease is the most common inherited motor and sensory neuropathy. The axonal form of the disease is designated as "CMT type 2" (CMT2). Although four loci known to be implicated in autosomal dominant CMT2 have been mapped thus far (on 1p35-p36, 3q13. 1, 3q13-q22, and 7p14), no one causative gene is yet known. A large Russian family with CMT2 was found in the Mordovian Republic (Russia). Affected members had the typical CMT2 phenotype. Additionally, several patients suffered from hyperkeratosis, although the association, if any, between the two disorders is not clear. Linkage with the CMT loci already known (CMT1A, CMT1B, CMT2A, CMT2B, CMT2D, and a number of other CMT-related loci) was excluded. Genomewide screening pinpointed the disease locus in this family to chromosome 8p21, within a 16-cM interval between markers D8S136 and D8S1769. A maximum two-point LOD score of 5.93 was yielded by a microsatellite from the 5' region of the neurofilament-light gene (NF-L). Neurofilament proteins play an important role in axonal structure and are implicated in several neuronal disorders. Screening of affected family members for mutations in the NF-L gene and in the tightly linked neurofilament-medium gene (NF-M) revealed the only DNA alteration linked with the disease: a A998C transversion in the first exon of NF-L, which converts a conserved Gln333 amino acid to proline. This alteration was not found in 180 normal chromosomes. Twenty unrelated CMT2 patients, as well as 26 others with an undetermined form of CMT, also were screened for mutations in NF-L, but no additional mutations were found. It is suggested that Gln333Pro represents a rare disease-causing mutation, which results in the CMT2 phenotype.