A novel aerobic moderately thermophilic bacterium, strain 3753O^T, was isolated from a Chukotka hot spring (Arctic, Russia) using the newly developed technology of laser engineering of microbial systems. Сells were regular short rods, 0.4×0.8–2.0 µm in size, with a monoderm-type envelope and a single flagellum. The temperature and pH ranges for growth were 42–60 °C and pH 6.5–8.5, the optima being 50–54 °C and pH 7.3. Strain 3753O^T grew chemoorganoheterotrophically on a number of carbohydrates or peptidic substrates and volatile fatty acids, and chemolithoautotrophically with siderite (FeCO₃) as the electron donor. The major cellular fatty acid was branched C_19 : 0. Phosphatidylethanolamine, phosphatidylglycerol and two unidentified phospholipids as well as two yellow carotenoid-type pigments were detected in the polar lipid extract. Strain 3753O^T was inhibited by chloramphenicol, polymyxin B, vancomycin, streptomycin, neomycin and kanamycin, but resistant to the action of novobiocin and ampicillin. The DNA G+C content was 69.9 mol%. The 16S rRNA gene as well as 51 conservative protein sequence-based phylogenetic analyses placed strain 3753O^T within the previously uncultivated lineage OLB14 in the phylum Chloroflexi . Taking into account the phylogenetic position as well as phenotypic properties of the novel isolate, the novel genus and species Tepidiforma bonchosmolovskayae gen. nov., sp. nov., within the Tepidiformaceae fam. nov., the Tepidiformales ord. nov. and the Tepidiformia classis nov. are proposed. The type strain of Tepidiforma bonchosmolovskayae is 3753O^T (=VKM B-3389^T=KTCT 72284^T).

Quantum dots (QD) are widely used for cellular labeling due to enhanced brightness, resistance to photobleaching, and multicolor light emissions. CdS and Cd_xZn_1−xS nanoparticles with sizes of 6–8 nm were synthesized via a ligand assisted technique inside and outside of 50 nm diameter halloysite clay nanotubes (QD were immobilized on the tube’s surface). The halloysite–QD composites were tested by labeling human skin fibroblasts and prostate cancer cells. In human cell cultures, halloysite–QD systems were internalized by living cells, and demonstrated intense and stable fluorescence combined with pronounced nanotube light scattering. The best signal stability was observed for QD that were synthesized externally on the amino-grafted halloysite. The best cell viability was observed for Cd_xZn_1−xS QD immobilized onto the azine-grafted halloysite. The possibility to use QD clay nanotube core-shell nanoarchitectures for the intracellular labeling was demonstrated. A pronounced scattering and fluorescence by halloysite–QD systems allows for their promising usage as markers for biomedical applications.

Aqueous dispersions of gold and silver nanoparticles (NPs) stabilized with sodium citrate, as well as polymeric NPs based on poly(lactide- co -glycolide) (70 : 30 mol %) stabilized with poly(vinyl alcohol) have been obtained. The sizes of NPs have been determined by transmission electron microscopy (TEM), dynamic light scattering (DLS), and analytical ultracentrifugation (AUC). It has been shown that the diameter of both metallic and polymeric particles measured by TEM is significantly lower than their hydrodynamic diameter D _h determined by DLS. Moreover, it has been found that the D _h value obtained for the studied particles from DLS distributions is overestimated compared to that determined by AUC, because the AUC method is less sensitive to the particle size polydispersity and the presence of large objects in a dispersion.

Surface-enhanced Raman spectroscopy is a powerful analytical method, and is especially useful for the detection of nitrogen- and sulfur-containing organic substances in trace amounts. SERS substrates with high enhancement factors can be produced via the aggregation of gold nanoparticles, leading to the formation of ‘hot spots’ – regions of highest electric field intensity and Raman scattering enhancement. Thus, the availability of gold surfaces in ‘hot spots’ for the adsorption of analyte molecules strongly influences the enhancement factor of a substrate. We studied the kinetics of oxidation of dyes with hydrogen peroxide in the presence of citrate-capped gold nanoparticles and discovered the amplification of surface-enhanced Raman scattering, probably due to the oxidation of citrate ligands and the additional adsorption of dye molecules onto vacant spots on the gold surface. Maximum amplification was observed with 3% (v/v) hydrogen peroxide in the reaction medium. Under optimized conditions, model analytes can be detected at concentrations as low as 1 × 10⁻⁹ M, which is ten times lower than the detection limit without hydrogen peroxide addition.