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The timeline of tellurite prokaryotic biology and biochemistry is now over 50 years long. Its start was in the clinical microbiology arena up to the 1970s. The 1980s saw the cloning of tellurite resistance determinants while from the 1990s through to the present, new strains were isolated and research into resistance mechanisms and biochemistry took place. The past 10 years have seen rising interest in more technological developments and considerable advancement in the understanding of the biochemical mechanisms of tellurite metabolism and biochemistry in several different prokaryotes. This research work has provided a list of genes and proteins and ideas about the fundamental metabolism of Te oxyanions. Yet the biomolecular mechanisms of the tellurite resistance determinants are far from established. Regardless, we have begun to see a new direction of Te biology beyond the clinical pathogen screening approaches, evolving into the biotechnology fields of bioremediation, bioconversion and bionanotechnologies and subsequent technovations. Knowledge on Te biology may still be lagging behind that of other chemical elements, but has moved beyond its dark ages and is now well into its renaissance.

This work investigated the structural, thermal, mechanical, and shielding characteristics of a tellurite-based glass series with the composition 60TeO 2 –12.5Nb 2 O 5 –12.5ZnO–(15– x )LiF– x Pr 2 O 3 , where x ranged from 0.5 to 5.0 mol%. The novelty of this study lay in a comprehensive analysis that combined multiple techniques. The research involved using the radial distribution function (RDF) with Gaussian fitting to determine structural parameters and the fraction of trigonal bipyramidal (TeO 4 ), N 4 (X-ray) representation for each glass sample. The study also utilized deconvoluted FTIR spectra to further characterize the glass structure. Results showed the transformation of trigonal pyramidal (TeO 3 ) tp units to trigonal bipyramidal (TeO 4 ) tbp units and consequently enhanced the rigidity of the glass structure with addition of Pr 2 O 3 . Additionally, it established a logarithmic correlation across the entire glass series, linking the molar volume (V m ) with the experimental bulk modulus (K exp ​), , and explored the correlations between these properties and the power (α). The ring deformation model was applied to calculate the average atomic ring diameter. Increased Pr 2 ​O 3 ​ content enhanced the glass’s thermal stability. This was evidenced by a significant rise in its glass transition temperature and onset crystallization temperature, indicating a more rigid and stable structure. In addition, various shielding parameters were determined. The results of this investigation highlight the excellent gamma photon shielding capabilities of these glasses.

Phosphor-glass composites (PGC) are excellent candidates for highly efficient and stable photonic converters; however, their synthesis generally requires harsh procedures and long time, resulting in additional performance loss and energy consumption. Here we develop a rapid synthetic route to PGC within about 10 seconds, which enables uniform dispersion of Y 3 Al 5 O 12 :Ce 3+ (YAG:Ce) phosphor particles through a particle self-stabilization model in molten tellurite glass. Thanks for good wettability between YAG:Ce micro-particles and tellurite glass melt, it creates an energy barrier of 6.94 × 10 5 zJ to prevent atomic-scale contact and sintering of particles in the melt. This in turn allows the generation of YAG:Ce-based PGC as attractive emitters with high quantum efficiency (98.4%) and absorption coefficient (86.8%) that can produce bright white light with luminous flux of 1227 lm and luminous efficiency of 276 lm W −1 under blue laser driving. This work shows a generalizable synthetic strategy for the development of functional glass composites. Phosphor-glass composites can serve as efficient and stable photonic converters, but their synthesis generally requires harsh and time-consuming procedures. Here, the authors report an alternative synthesis route that requires only a few seconds and is based on particle self-stabilization.

The current work seeks to fabricate a series of four bulk glasses using the melt-quenching method according to the chemical formula of (35-x) B 2 O 3  + 10GeO 2  + 20TeO 2  + 35MgO + x Dy 2 O 3 , where x = 1.25, 2.5, 3.75, and 5 mol%. XRD detected the amorphous nature of the fabricated glasses with a 2θ range from 10 to 80°, whereas the glasses’ absorption spectra were explored in the 350–1000 nm wavelength region. The band gap (E g ) values were calculated using Mott and Davis’s concept while calculating several optical parameters, including the optical basicity (Λ), reflection loss (R), optical electronegativity (χ), electron polarizability (αₒ), metallization, and transmission (T). The impact of substitution of B 2 O 3 by Dy 2 O 3 on the mechanical properties was examined utilizing the Makishima and Mackenzie method. Moreover, the prepared glasses’ γ-ray shielding was found via a Monte Carlo simulation. The simulated data showed that the increase in B 2 O 3 ’s partial substitution by Dy 2 O 3 content enhances the prepared glasses’ shielding properties. The highest linear attenuation coefficient in the current study was achieved for the 5 mol% Dy 2 O 3 -doped glass sample, where its LACs decreased over the range of 152.849–0.124 cm −1 , with the gamma-ray energy raised throughout 0.015–15 MeV, respectively.

The bacterium Stenotrophomonas rhizophila is known to be beneficial for plants and has been frequently isolated from the rhizosphere of crops. In the present work, we isolated from the phyllosphere of an ornamental plant an epiphytic strain of S. rhizophila that we named Ep2.2 and investigated its possible application in crop protection. Compared to S. maltophilia LMG 958, a well-known plant beneficial species which behaves as opportunistic human pathogen, S. rhizophila Ep2.2 showed distinctive features, such as different motility, a generally reduced capacity to use carbon sources, a greater sensitivity to fusidic acid and potassium tellurite, and the inability to grow at the human body temperature. S. rhizophila Ep2.2 was able to inhibit in vitro growth of the plant pathogenic fungi Alternaria alternata and Botrytis cinerea through the emission of volatile compounds. Simultaneous PTR-MS and GC-MS analyses revealed the emission, by S. rhizophila Ep2.2, of volatile organic compounds (VOCs) with well-documented antifungal activity, such as furans, sulphur-containing compounds and terpenes. When sprayed on tomato leaves and plants, S. rhizophila Ep2.2 was able to restrict B. cinerea infection and to prime the expression of Pti5 , GluA and PR1 plant defense genes.

Metalloid tellurium is characterized as a chemical element belonging to the chalcogen group without known biological function. However, its compounds, especially the oxyanions, exert numerous negative effects on both prokaryotic and eukaryotic organisms. Recent evidence suggests that increasing environmental pollution with tellurium has a causal link to autoimmune, neurodegenerative and oncological diseases. In this review, we provide an overview about the current knowledge on the mechanisms of tellurium compounds’ toxicity in bacteria and humans and we summarise the various ways organisms cope and detoxify these compounds. Over the last decades, several gene clusters conferring resistance to tellurium compounds have been identified in a variety of bacterial species and strains. These genetic determinants exhibit great genetic and functional diversity. Besides the existence of specific resistance mechanisms, tellurium and its toxic compounds interact with molecular systems, mediating general detoxification and mitigation of oxidative stress. We also discuss the similarity of tellurium and selenium biochemistry and the impact of their compounds on humans.

Despite their prevalence in Europe, the source of contamination of humans by Attaching-Effacing Shigatoxigenic Escherichia coli (AE-STEC) O80:H2 remains unidentified. This study aimed to assess a procedure based on non-melibiose fermentation and resistance to tellurite to isolate AE-STEC and enteropathogenic (EPEC) O80:H2 from healthy cattle. The genome sequences of 40 calf and human AE-STEC and EPEC O80:H2 were analyzed: (i) none harbored the mel operon, but the 70mel DNA sequence instead; (ii) the ter-type 1 operon was detected in 16 EPEC and stx1a or stx2a AE-STEC, while no ter-type 1 operon was detected in the remaining 24 EPEC and stx2d AE-STEC. The 21 calf AE-STEC and EPEC O80:H2 were tested phenotypically: (i) none fermented melibiose on melibiose-MacConkey agar plates; (ii) ten of the 11 ter-type 1-positive strains had Minimal Inhibitory Concentrations (MIC) ≥ 128 µg/mL to potassium tellurite; (iii) conversely, the ten ter-negative strains had MIC of two µg/mL. Accordingly, enrichment broths containing two µg/mL of potassium tellurite and inoculated with one high MIC (≥256 µg/mL) stx1a AE-STEC O80:H2 tested positive with the O80 PCR after overnight growth, but not the enrichment broths inoculated with one low MIC (two µg/mL) EPEC. Nevertheless, neither AE-STEC nor EPEC O80:H2 were recovered from 96 rectal fecal samples collected from healthy cattle at one slaughterhouse after overnight growth under the same conditions. In conclusion, this procedure may help to isolate stx1a and stx2a AE-STEC and EPEC O80:H2, but not stx2d AE-STEC that are tellurite sensitive, and new surveys using different procedures are necessary to identify their animal source, if any.

Pyrroloquinoline quinone (PQQ) is a natural antioxidant with diverse applications in food and pharmaceutical industries. A lot of effort has been devoted toward the discovery of PQQ high-producing microbial species and characterization of biosynthesis, but it is still challenging to achieve a high PQQ yield. In this study, a combined strategy of random mutagenesis and adaptive laboratory evolution (ALE) with fermentation optimization was applied to improve PQQ production in Hyphomicrobium denitrificans H4-45. A mutant strain AE-9 was obtained after nearly 400 generations of UV-LiCl mutagenesis, followed by an ALE process, which was conducted with a consecutive increase of oxidative stress generated by kanamycin, sodium sulfide, and potassium tellurite. In the flask culture condition, the PQQ production in mutant strain AE-9 had an 80.4% increase, and the cell density increased by 14.9% when compared with that of the initial strain H4-45. Moreover, batch and fed-batch fermentation processes were optimized to further improve PQQ production by pH control strategy, methanol and H 2 O 2 feed flow, and segmented fermentation process. Finally, the highest PQQ production and productivity of the mutant strain AE-9 reached 307 mg/L and 4.26 mg/L/h in a 3.7-L bioreactor, respectively. Whole genome sequencing analysis showed that genetic mutations in the ftfL gene and thiC gene might contribute to improving PQQ production by enhancing methanol consumption and cell growth in the AE-9 strain. Our study provided a systematic strategy to obtain a PQQ high-producing mutant strain and achieve high production of PQQ in fermentation. These practical methods could be applicable to improve the production of other antioxidant compounds with uncleared regulation mechanisms. Key points • Improvement of PQQ production by UV-LiCl mutagenesis combined with adaptive laboratory evolution (ALE) and fermentation optimization. • A consecutive increase of oxidative stress could be used as the antagonistic factor for ALE to enhance PQQ production. • Mutations in the ftfL gene and thiC gene indicated that PQQ production might be increased by enhancing methanol consumption and cell growth.

The discovery of ultraconfined polaritons with extreme anisotropy in a number of van der Waals (vdW) materials has unlocked new prospects for nanophotonic and optoelectronic applications. However, the range of suitable materials for specific applications remains limited. Here we introduce tellurite molybdenum quaternary oxides—which possess non-centrosymmetric crystal structures and extraordinary nonlinear optical properties—as a highly promising vdW family of materials for tunable low-loss anisotropic polaritonics. By employing chemical flux growth and exfoliation techniques, we successfully fabricate high-quality vdW layers of various compounds, including MgTeMoO 6 , ZnTeMoO 6 , MnTeMoO 6 and CdTeMoO 6 . We show that these quaternary vdW oxides possess two distinct types of in-plane anisotropic polaritons: slab-confined and edge-confined modes. By leveraging metal cation substitutions, we establish a systematic strategy to finely tune the in-plane polariton propagation, resulting in the selective emergence of circular, elliptical or hyperbolic polariton dispersion, accompanied by ultraslow group velocities (0.0003 c ) and long lifetimes (5 ps). Moreover, Reststrahlen bands of these quaternary oxides naturally overlap that of α-MoO 3 , providing opportunities for integration. As an example, we demonstrate that combining α-MoO 3 (an in-plane hyperbolic material) with CdTeMoO 6 (an in-plane isotropic material) in a heterostructure facilitates collimated, diffractionless polariton propagation. Quaternary oxides expand the family of anisotropic vdW polaritons considerably, and with it, the range of nanophotonics applications that can be envisioned. Tellurite molybdenum quaternary oxides, a family of van der Waals materials, show slow group velocity and long lifetimes with promising implications for tunable low-loss anisotropic polaritonics.

Background Bacteria have developed different mechanisms for the transformation of metalloid oxyanions to non-toxic chemical forms. A number of bacterial isolates so far obtained in axenic culture has shown the ability to bioreduce selenite and tellurite to the elemental state in different conditions along with the formation of nanoparticles—both inside and outside the cells—characterized by a variety of morphological features. This reductive process can be considered of major importance for two reasons: firstly, toxic and soluble (i.e. bioavailable) compounds such as selenite and tellurite are converted to a less toxic chemical forms (i.e. zero valent state); secondly, chalcogen nanoparticles have attracted great interest due to their photoelectric and semiconducting properties. In addition, their exploitation as antimicrobial agents is currently becoming an area of intensive research in medical sciences. Results In the present study, the bacterial strain Ochrobactrum sp. MPV1, isolated from a dump of roasted arsenopyrites as residues of a formerly sulfuric acid production near Scarlino (Tuscany, Italy) was analyzed for its capability of efficaciously bioreducing the chalcogen oxyanions selenite (SeO 3 2− ) and tellurite (TeO 3 2− ) to their respective elemental forms (Se 0 and Te 0 ) in aerobic conditions, with generation of Se- and Te-nanoparticles (Se- and TeNPs). The isolate could bioconvert 2 mM SeO 3 2− and 0.5 mM TeO 3 2− to the corresponding Se 0 and Te 0 in 48 and 120 h, respectively. The intracellular accumulation of nanomaterials was demonstrated through electron microscopy. Moreover, several analyses were performed to shed light on the mechanisms involved in SeO 3 2− and TeO 3 2− bioreduction to their elemental states. Results obtained suggested that these oxyanions are bioconverted through two different mechanisms in Ochrobactrum sp. MPV1. Glutathione (GSH) seemed to play a key role in SeO 3 2− bioreduction, while TeO 3 2− bioconversion could be ascribed to the catalytic activity of intracellular NADH-dependent oxidoreductases. The organic coating surrounding biogenic Se- and TeNPs was also characterized through Fourier-transform infrared spectroscopy. This analysis revealed interesting differences among the NPs produced by Ochrobactrum sp. MPV1 and suggested a possible different role of phospholipids and proteins in both biosynthesis and stabilization of such chalcogen-NPs. Conclusions In conclusion, Ochrobactrum sp. MPV1 has demonstrated to be an ideal candidate for the bioconversion of toxic oxyanions such as selenite and tellurite to their respective elemental forms, producing intracellular Se- and TeNPs possibly exploitable in biomedical and industrial applications.