14 research outputs found

    Induced current in the presence of magnetic flux tube of small radius

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    The induced current density, corresponding to the massless Dirac equation in (2+1) dimensions in a magnetic flux tube of small radius is considered. This problem is important for graphene. In the case, when an electron can not penetrate the region of nonzero magnetic field, this current is the odd periodical function of the magnetic flux. If the region inside the magnetic tube is not forbidden for penetration of electron, the induced current is not a periodical function of the magnetic flux. However in the limit R0R\to 0, where RR is the radius of magnetic flux tube, this function has the universal form which is independent of the magnetic field distribution inside the magnetic tube at fixed value of the magnetic flux.Comment: 5 pages, 1 figur

    The Induced Charge Generated By The Potential Well In Graphene

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    The induced charge density, ρind(r)\rho_{ind}(\bm r), generated in graphene by the potential well of the finite radius RR is considered. The result for ρind(r)\rho_{ind}(\bm r) is derived for large distances rRr\gg R. We also obtained the induced charges outside of the radius rRr\gg R and inside of this radius for subcritical and supercritical regimes. The consideration is based on the convenient representation of the induced charge density via the Green's function of electron in the field.Comment: 12 pages, 2 figures, version published in Phys.Rev.

    Screening of Coulomb Impurities in Graphene

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    We calculate exactly the vacuum polarization charge density in the field of a subcritical Coulomb impurity, Ze/rZ|e|/r, in graphene. Our analysis is based on the exact electron Green's function, obtained by using the operator method, and leads to results that are exact in the parameter ZαZ\alpha, where α\alpha is the "fine structure constant" of graphene. Taking into account also electron-electron interactions in the Hartree approximation, we solve the problem self-consistently in the subcritical regime, where the impurity has an effective charge ZeffZ_{eff}, determined by the localized induced charge. We find that an impurity with bare charge Z=1 remains subcritical, Zeffα<1/2Z_{eff} \alpha < 1/2, for any α\alpha, while impurities with Z=2,3Z=2,3 and higher can become supercritical at certain values of α\alpha.Comment: 4 pages, 2 figure

    Bremsstrahlung in α decay reexamined

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    A high-statistics measurement of bremsstrahlung emitted in the α decay of 210Po has been performed, which allows us to follow the photon spectra up to energies of ~500keV. The measured differential emission probability is in good agreement with our theoretical results obtained within the quasiclassical approximation as well as with the exact quantum mechanical calculation. It is shown that, due to the small effective electric dipole charge of the radiating system, a significant interference between the electric dipole and quadrupole contributions occurs, which is altering substantially the angular correlation between the α particle and the emitted photon

    Deep Functional Profiling Facilitates the Evaluation of the Antibacterial Potential of the Antibiotic Amicoumacin

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    The global spread of antibiotic resistance is forcing the scientific community to find new molecular strategies to counteract it. Deep functional profiling of microbiomes provides an alternative source for the discovery of novel antibiotic producers and probiotics. Recently, we implemented this ultrahigh-throughput screening approach for the isolation of Bacillus pumilus strains efficiently producing the ribosome-targeting antibiotic amicoumacin A (Ami). Proteomics and metabolomics revealed essential insight into the activation of Ami biosynthesis. Here, we applied omics to boost Ami biosynthesis, providing the optimized cultivation conditions for high-scale production of Ami. Ami displayed a pronounced activity against Lactobacillales and Staphylococcaceae, including methicillin-resistant Staphylococcus aureus (MRSA) strains, which was determined using both classical and massive single-cell microfluidic assays. However, the practical application of Ami is limited by its high cytotoxicity and particularly low stability. The former is associated with its self-lactonization, serving as an improvised intermediate state of Ami hydrolysis. This intramolecular reaction decreases Ami half-life at physiological conditions to less than 2 h, which is unprecedented for a terminal amide. While we speculate that the instability of Ami is essential for Bacillus ecology, we believe that its stable analogs represent attractive lead compounds both for antibiotic discovery and for anticancer drug development

    First Multy-Proxy Studies Of High-Mountain Lakes In Armenia: Preliminary Results

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    Within the framework of the Russian-Armenian project “The Paleolimnological Aspect of Studying the Evolution of Ecosystems of High-Mountain Lakes of Russia and Armenia” in July-August 2018, we investigated four high-mountain lakes of Armenia. The research focuses on the lakes Kari, Umroi, Akna and Sev. All investigated lakes are located at the altitudes about 3000 m above sea level. We first time these lakes were investigated using a multi-proxy method that includes paleolimnological, geomorphological, hydrological, geochemical and biogeographic studies. The research offers the first statistical characteristics of lake depth distribution, water volume and other morphometrics. Lake sediments sequences and radiocarbon dates were received and analyzed for Armenian small lakes for the first time. We determined that all the studied lakes were formed during the Holocene. Sediments of Lake Kari were deposited in the last 4000 years, sediments of Lake Umroi – within the last 8000 years, while maximum thickness of sediments is around 1 m in both lakes. Hence, we assume low deposition rate in Armenian high-mountain lakes, however, it varied significantly in different periods of lake history

    A kinase bioscavenger provides antibiotic resistance by extremely tight substrate binding

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    Microbial communities are self-controlled by repertoires of lethal agents, the antibiotics. In their turn, these antibiotics are regulated by bioscavengers that are selected in the course of evolution. Kinase-mediated phosphorylation represents one of the general strategies for the emergence of antibiotic resistance. A new subfamily of AmiN-like kinases, isolated from the Siberian bear microbiome, inactivates antibiotic amicoumacin by phosphorylation. The nanomolar substrate affinity defines AmiN as a phosphotransferase with a unique catalytic efficiency proximal to the diffusion limit. Crystallographic analysis and multiscale simulations revealed a catalytically perfect mechanism providing phosphorylation exclusively in the case of a closed active site that counteracts substrate promiscuity. AmiN kinase is a member of the previously unknown subfamily representing the first evidence of a specialized phosphotransferase bioscavenger

    Deep Functional Profiling of Wild Animal Microbiomes Reveals Probiotic <i>Bacillus pumilus</i> Strains with a Common Biosynthetic Fingerprint

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    The biodiversity of microorganisms is maintained by intricate nets of interactions between competing species. Impaired functionality of human microbiomes correlates with their reduced biodiversity originating from aseptic environmental conditions and antibiotic use. Microbiomes of wild animals are free of these selective pressures. Microbiota provides a protecting shield from invasion by pathogens in the wild, outcompeting their growth in specific ecological niches. We applied ultrahigh-throughput microfluidic technologies for functional profiling of microbiomes of wild animals, including the skin beetle, Siberian lynx, common raccoon dog, and East Siberian brown bear. Single-cell screening of the most efficient killers of the common human pathogen Staphylococcus aureus resulted in repeated isolation of Bacillus pumilus strains. While isolated strains had different phenotypes, all of them displayed a similar set of biosynthetic gene clusters (BGCs) encoding antibiotic amicoumacin, siderophore bacillibactin, and putative analogs of antimicrobials including bacilysin, surfactin, desferrioxamine, and class IId cyclical bacteriocin. Amicoumacin A (Ami) was identified as a major antibacterial metabolite of these strains mediating their antagonistic activity. Genome mining indicates that Ami BGCs with this architecture subdivide into three distinct families, characteristic of the B. pumilus, B. subtilis, and Paenibacillus species. While Ami itself displays mediocre activity against the majority of Gram-negative bacteria, isolated B. pumilus strains efficiently inhibit the growth of both Gram-positive S. aureus and Gram-negative E. coli in coculture. We believe that the expanded antagonistic activity spectrum of Ami-producing B. pumilus can be attributed to the metabolomic profile predetermined by their biosynthetic fingerprint. Ultrahigh-throughput isolation of natural probiotic strains from wild animal microbiomes, as well as their metabolic reprogramming, opens up a new avenue for pathogen control and microbiome remodeling in the food industry, agriculture, and healthcare
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