Concentrations Of Tellurite Research Articles

Effect of tellurite on growth of extensively drug resistant (XDR) Mycobacterium tuberculosis and action on mycobacterial drug efflux pump

In the present study genotypic resistance of bacterial strain to first- and second-line anti-tuberculosis drugs was determined by Line probe assay. Toxic effect of tellurite on the growth of Mycobacterium tuberculosis (MTB) was determined by growing cells in different concentrations of tellurite (1 to 5 mM). Morphological effects of tellurite and uptake of metal in bacterial cells were confirmed by Scanning electron microscope (SEM) and energy dispersive X-ray (EDX) analysis. Change in fold expression of the efflux pump gene was measured by RT-PCR. Mycobacterial strain was characterized as XDR-TB based on the genotypic resistance to rifampicin and isoniazid, along with resistance to fluoroquinolones and second line injectable. XDR-TB showed black colonies in tellurite presence and growth was delayed (2–3 weeks) when compared with the control. The reduced cell size, metal accumulation and the characteristic tellurite peaks appeared in metal-treated cells. MTB showed MIC value of 1 mM and had high susceptibility for higher concentrations (2–5 mM). However, no significant metal inhibitory effect on the mmpL7 efflux system was determined. Tellurite shows significant growth reduction potential against XDR-TB strain. However, the exact mechanism of action needs to be elucidated with further research.

Effect of potassium tellurite concentration in a chromogenic agar medium on isolation of tellurite-resistant “Top Seven” Shiga toxin-producing Escherichia coli from ground beef

The effect of potassium tellurite concentration in a chromogenic agar medium on the detection of tellurite-resistant “top seven” Shiga toxin-producing Escherichia coli (STEC) in beef was evaluated. Samples of ground beef were inoculated with tellurite-resistant STEC O26, O45, O103, O111, O121, O145, or O157 strains at geometric mean (±standard error of the mean) levels of 0, 49 (±1), 490 (±1), or 4900 (±1) CFU/10 g and enriched 1:10 (90 mL) in EC broth (40°C for 6 h). Following enrichment, aliquots of broth culture were treated by immunomagnetic separation with one of three pools of beads against STEC serogroups; pool I: O26, O45, and O121; pool II: O103, O111, and O145; and pool III: O157. After immunomagnetic separation, 50 μL of washed bead suspensions in buffered peptone water was spiral plated onto a modified Possé medium containing 0.5, 1.0, or 1.5 mg/L potassium tellurite, and incubated at 37°C for 18 h. Up to four isolated colonies were picked from each spiral plate based on expected colony phenotypes for STEC, and isolate identity was confirmed with an 11-plex PCR assay targeting the O serogroups and virulence genes. Overall, across all inoculum levels and strains, modified Possé media containing 0.5, 1.0, or 1.5 mg/L potassium tellurite each had a positive predictive value of 100%, and medium containing 0.5 mg/L potassium tellurite had numerically the highest sensitivity (100%) and negative predictive value (100%), which was significantly different from 1.5 mg/L (92.9% and 40.0%, respectively; P < 0.05). Similarly, there was an inverse relationship between potassium tellurite concentration and analytical specificity (number of colonies tested that were STEC-positive): 0.5 (1463 of 1482; 98.7%), 1.0 (1356 of 1411; 96.1%), and 1.5 mg/L (1187 of 1278; 92.9%; P < 0.05). These results suggest that 0.5 mg/L gives better performance than 1.0 or 1.5 mg/L of potassium tellurite in Possé medium for isolation of tellurite-resistant “top seven” STEC from ground beef.

Concurrent tellurite reduction, biogenesis of elemental tellurium nanostructures and biological nutrient removal in aerobic granular sludge sequencing batch reactor

This study investigated the metabolic potential of aerobic granular sludge (AGS) to simultaneously remove tellurium oxyanion (tellurite, TeO32-), COD, ammonium-nitrogen and phosphorus in a sequencing batch reactor (SBR). AGS readily converted soluble and toxic tellurite to biogenic elemental tellurium (Bio-Te0) by following first-order reaction. Bio-Te0 was dark black in colour and largely entrapped in the granules. Although endogenous substrates acted as source of electrons for tellurite reduction, it was sustained by supplying exogenous electron donor. A lab-sale SBR was seeded with AGS and operated at varied initial tellurite concentrations for 185 days to investigate tellurite reduction and biological nutrient removal (BNR). Stable removal efficiencies of > 98% Te was achieved from simulated wastewater containing 0.01–1 mM tellurite. Soluble tellurite was converted to Bio-Te0 and retained in the AGS. SEM-EDS, XRD and Raman spectroscopy confirmed formation of Bio-Te0 and its association with the granules. Enrichment of Bacteroidia, Petrimonas sp. and several other tellurite-reducing bacteria was confirmed by 16S rRNA gene sequencing. Enrichment of ammonium oxidizing bacteria, elimination of nitrite oxidizing bacteria and profiles of reactive-nitrogen compounds suggested occurrence of nitriation-denitriation pathway. Although ammonium removal was inhibited by tellurite, recovery occurred much quickly in the presence of up to 0.1 mM tellurite. Higher P removal under tellurite-reducing condition was linked to hydroxyapatite precipitation as confirmed by EDS and P-fractionation. Efficient BNR under toxic pollutant conditions and excellent metal(loid) immobilization capabilities implicate prospective use of AGS technology in metal-laden waste management and metal(loid) biorecovery applications.

Characterization of the Tellurite-Resistance Properties and Identification of the Core Function Genes for Tellurite Resistance in Pseudomonas citronellolis SJTE-3.

Tellurite is highly toxic to bacteria and commonly used in the clinical screening for pathogens; it is speculated that there is a potential relationship between tellurite resistance and bacterial pathogenicity. Until now, the core function genes of tellurite resistance and their characteristics are still obscure. Pseudomonas citronellolis SJTE-3 was found able to resist high concentrations of tellurite (250 μg/mL) and formed vacuole-like tellurium nanostructures. The terZABCDE gene cluster located in the large plasmid pRBL16 endowed strain SJTE-3 with the tellurite resistance of high levels. Although the terC and terD genes were identified as the core function genes for tellurite reduction and resistance, the inhibition of cell growth was observed when they were used solely. Interestingly, co-expression of the terA gene or terZ gene could relieve the burden caused by the expression of the terCD genes and recover normal cell growth. TerC and TerD proteins commonly shared the conserved sequences and are widely distributed in many pathogenic bacteria, highly associated with the pathogenicity factors.

The putative phosphate transporter PitB (PP1373) is involved in tellurite uptake in Pseudomonas putida KT2440.

Tellurium oxyanions are chemical species of great toxicity and their presence in the environment has increased because of mining industries and photovoltaic and electronic waste. Recovery strategies for this metalloid that are based on micro-organisms are of interest, but further studies of the transport systems and enzymes responsible for implementing tellurium transformations are required because many mechanisms remain unknown. Here, we investigated the involvement in tellurite uptake of the putative phosphate transporter PitB (PP1373) in soil bacterium Pseudomonas putida KT2440. For this purpose, through a method based on the CRISPR/Cas9 system, we generated a strain deficient in the pitB gene and characterized its phenotype on exposing it to varied concentrations of tellurite. Growth curves and transmission electronic microscopy experiments for the wild-type and ΔpitB strains showed that both were able to internalize tellurite into the cytoplasm and reduce the oxyanion to black nano-sized and rod-shaped tellurium particles, although the ΔpitB strain showed an increased resistance to the tellurite toxic effects. At a concentration of 100 μM tellurite, where the biomass formation of the wild-type strain decreased by half, we observed a greater ability of ΔpitB to reduce this oxyanion with respect to the wild-type strain (~38 vs ~16 %), which is related to the greater biomass production of ΔpitB and not to a greater consumption of tellurite per cell. The phenotype of the mutant was restored on over-expressing pitB in trans. In summary, our results indicate that PitB is one of several transporters responsible for tellurite uptake in P. putida KT2440.

Green nanotechnology-based tellurium nanoparticles: Exploration of their antioxidant, antibacterial, antifungal and cytotoxic potentials against cancerous and normal cells compared to potassium tellurite

In this study, the antioxidant, antimicrobial, and cytotoxicity of mycosynthesized tellurium nanoparticles (TeNPs) were evaluated by using DPPH, microbroth dilution, and MTT tests, respectively. Interestingly, nanostructured tellurium (Te) represented strong antioxidant activity with IC50 of 20.66 µg/mL of elemental Te, while the IC50 of potassium tellurite was found to be 20 mM (equivalent to 2500 µg/mL of elemental Te). In addition, TeNPs did not exhibit good antibacterial and antifungal activity up to 250 µg/mL of elemental Te, however, higher concentrations of potassium tellurite exhibited antimicrobial potential. Furthermore, TeNPs represented more cytotoxicity against breast cancer MCF-7 cells with IC50 of 39.83 µg/mL after 48 h of treatment, while no IC50 was found against normal L929 cells up to 50 µg/mL after 48 h of treatment. Moreover, cytotoxic activity of the potassium tellurite against MCF-7 and L929 cells represented more cytotoxicity against L929 cells with IC50 of 76.33 µM (equivalent to 9.739 µg/mL of elemental Te) after 48 h of treatment, while no IC50 was found against MCF-7 cells up to 100 µM (equivalent to 12.76 µg/mL of elemental Te) after 48 h of treatment. Overall, the biogenic nanostructured Te exhibited higher antioxidant and anticancer activity compared to potassium tellurite.

High potential of tellurite bioremediation by moderately halophilic Staphylococcus xylosus

The use of bacteria has been considered as a suitable alternative for metalloids remediation. We isolated 84 tellurite-resistant bacteria, and characterized tellurite-resistant and tellurite-reducing bacterial strains from samples collected in Iran. We report here a halophilic Gram-positive strain can tolerate and accumulate equal to 26.39 mM (6598.66 µg/ml) concentrations of potassium tellurite from media. This strain were identified according to the 16S rRNA gene sequence as Staphylococcus xylosus. Here we show for the first time that S. xylosus can be efficiently remediate K2TeO3. Cell aggregation in the presence of tellurite was visually observed by colony color changes to black in media. Reduction of Te to Te0 determined with the spectrophotometric measurement method and sodium diethyldithiocarbamate trihydrate reagent (DDTC, A340nm). In order to provide high tellurite remediation, the optimum growth conditions of this bacterium were determined. The best terms are included 0.4 mM of oxyanion, 40 °C growth temperature, pH 6–8, 400 mM NaCl, and 50 RPM under aerobic conditions. Resistant to tellurite and a high level of tellurite reduction by S. xylosus might be interesting for further industrial applications.

Oxidative stress mediated cytotoxicity of tellurite in MDA-MB-231 breast cancer cells

Among different metallic compounds, tellurium (Te) was investigated as having anticancer properties. In the current investigation, MDA-MB-231 breast cancer cell line was cultured with or without tellurite to measure live cells by crystal violet staining. TrxR systems can be acted as a leader for anticancer therapy by eliminating cancerous cells through inhibition of TrxR and glutathione reductase (GR). Oxidative stress, generated in higher concentration in tellurite exposed cells, leads to lower the cell reduced environment such as reduced glutathione GSH) and non-protein thiol. Tellurite exposed cells underwent both type of cell death via necrosis and apoptosis. The lateral was slowed as tellurite concentration increased which was measured by caspase-3 activity, thus this finding would be very useful for determination of type and extent of cell death occurred by tellurite via biochemical and morphological ways. By elucidating the role of tellurite in inducing cell death in carcinoma cells by increased production of reactive oxygen species, this method could be employed for the treatment of carcinoma cells.

Morphology-tunable tellurium nanomaterials produced by the tellurite-reducing bacterium Lysinibacillus sp. ZYM-1.

Although tellurite is highly toxic to organisms, elemental tellurium nanomaterials (TeNMs) have many uses. The microbe-mediated reduction of tellurite to Te(0) has been shown to be a green and cost-effective approach for turning waste into wealth. However, it is difficult to tune the morphology of biogenic nanomaterials. In this study, a series of experiments was conducted to investigate the factors influencing tellurite reduction by the tellurite-reducing bacterium Lysinibacillus sp. ZYM-1, including pH, tellurite concentration, temperature, and heavy metal ions. The optimal removal efficiency of tellurite was respectively achieved at pH8, 0.5mM tellurite, and 40°C. All of the tested metal ions retarded the reduction of tellurite, especially Cd2+ and Co2+, which completely inhibited its reduction. Further characterization of the biogenic TeNMs indicated that their morphology could be tuned by the tellurite concentration, pH, temperature, and organic solvents used. Regular Te nanosheets were produced using 5mM tellurite. The TeNMs were primarily synthesized in the cell membrane. Hexagonal Te nanoplates, nanorods, nanoflowers, and nanobranches were synthesized when combining membrane fractions with tellurite and NADH. The diverse morphologies are assumed to be induced by the synergy between the reduction kinetics and the protein structure. Therefore, this study confirmed that the bacterium can tune the morphology of TeNMs, broadening the potential application of biogenic TeNMs.

Tellurite processing by cells of Rhodobacter capsulatus involves a periplasmic step where the oxyanion causes a malfunction of the cytochrome c maturation system

Tellurite (TeO32−) is an oxyanion of increasing concern for soils and water bodies as tellurite is toxic to prokaryotes and eukaryotes. In cells of Rhodobacter capsulatus, a facultative anoxygenic photosynthetic bacterium which tolerates up to 1 mM tellurite, the assembly of c-type cytochromes (cyts) occurs in the periplasm and involves several proteins ensuring the correct redox-state of the cyt cmaturation process (Ccm). Here it is shown that a sub-lethal tellurite concentration (0.2 mM) reduces the amount of cyts c during the early growth-phase of R. capsulatus. This effect is due to a malfunction of the Ccm system and not to an effect on the transcriptional expression of the cyt c genes. Further, growth of mutants MT-G4/S4 and MD21, with mutations at the level of cyt c2 (ΔcycA) and of the Ccm system (ΔdsbA/ΔccdA), respectively, was more affected by tellurite than wild type cells. Both MT-G4/S4 and MD21 mutants, featured by a cyt c2 deficiency, showed a significant decrease in their capacity to reduce TeO32− into Te0, thereby implying the need of a full amount of periplasmic cyt c2 in the microbial-driven speciation of the metalloid. These findings show, for the first time, that tellurite processing by cells starts at the periplasmic level.

Comparison of Agar Media for Detection and Quantification of Shiga Toxin–Producing Escherichia coli in Cattle Feces

The isolation and quantification of non-O157 Shiga toxin-producing Escherichia coli (STEC) from cattle feces are challenging. The primary objective of this study was to evaluate the performance of selected agar media in an attempt to identify an optimal medium for the detection and quantification of non-O157 STEC in cattle feces. Comparison studies were performed using CHROMagar STEC, Possé differential agar (Possé), Possé modified by the reduction or addition of antimicrobials, STEC heart infusion washed blood agar with mitomycin C (SHIBAM), and SHIBAM modified by the addition of antimicrobials. Fourteen STEC strains, two each belonging to serogroups O26, O45, O103, O111, O121, O145, and O157, were used to test detection in inoculated fecal suspensions at concentrations of 10(2) or 10(3) CFU/g. One STEC strain from each of these seven serogroups was used to estimate the concentration of recovered STEC in feces inoculated at 10(3), 10(4), or 10(5) CFU/g. Significantly more suspensions (P < 0.05) were positive for STEC when plated on Possé containing reduced concentrations of novobiocin and potassium tellurite compared with SHIBAM, but not SHIBAM modified by containing these same antimicrobials at the same concentrations. Numerically, more suspensions were positive for STEC by using this same form of modified Possé compared with Possé, but this difference was not statistically significant. More suspensions were positive for STEC cultured on CHROMagar STEC compared with those on Possé (P < 0.05) and on modified Possé (P = 0.05). Most inoculated fecal suspensions below 10(4) CFU/g of feces were underestimated or not quantifiable for the concentration of STEC by using CHROMagar STEC or modified Possé. These results suggest that CHROMagar STEC performs better than Possé or SHIBAM for detection of STEC in bovine feces, but adjustments in the concentrations of novobiocin and potassium tellurite in the latter two media result in significant improvements in their performance.

Variable tellurite resistance profiles of clinically-relevant Shiga toxin-producing Escherichia coli (STEC) influence their recovery from foodstuffs

Tellurite (Tel)-amended selective media and resistance (Tel-R) are widely used for detecting Shiga toxin-producing Escherichia coli (STEC) from foodstuffs. Tel-R of 81 O157 and non-O157 STEC strains isolated from animal, food and human was thus investigated. Variations of STEC tellurite minimal inhibitory concentration (MIC) values have been observed and suggest a multifactorial and variable tellurite resistome between strains. Some clinically-relevant STEC were found highly susceptible and could not be recovered using a tellurite-based detection scheme. The ter operon was highly prevalent among highly Tel-R STEC but was not always detected among intermediately-resistant strains. Many STEC serogroup strains were found to harbor sublines showing a gradient of MIC values. These Tel-R sublines showed statistically significant log negative correlations with increasing tellurite concentration. Whatever the tellurite concentration, the highest number of resistant sublines was observed for STEC belonging to the O26 serogroup. Variations in the number of these Tel-R sublines could explain the poor recovery of some STEC serogroups on tellurite-amended media especially from food products with low levels of contamination. Comparison of tellurite MIC values and distribution of virulence-related genes showed Tel-R and virulence to be related.

Synthesis of CdTe thin films on flexible metal foil by electrodeposition

CdTe thin films have been deposited onto the Mo foil from aqueous acidic bath via electrodeposition method with water-soluble Na2TeO3 instead of the usually used TeO2. X-ray diffraction studies indicate that the CdTe thin films are crystallized in zinc-blende symmetry. The effect of tellurite concentration on the morphology of the deposited thin film is investigated. In such case, the Cd:Te molar ratios in the films are both stoichiometric at different tellurite concentrations. In addition, the reduction in tellurite concentration leads to the porous thin film and weakens the crystallinity of thin film. The island growth model is used to interpret the growth mechanism of CdTe. The bandgap of the CdTe thin films is assigned to be 1.49 eV from the UV–Vis spectroscopy measurement, which is considered to serve as a promising candidate for the heterojunction solar cells.

Tellurite resistance: a putative pitfall in Corynebacterium diphtheriae diagnosis?

Corynebacterium diphtheriae strains continue to circulate worldwide causing diphtheria and invasive diseases, such as endocarditis, osteomyelitis, pneumonia and catheter-related infections. Presumptive C. diphtheriae infections diagnosis in a clinical microbiology laboratory requires a primary isolation consisting of a bacterial culture on blood agar and agar containing tellurite (TeO3(2-)). In this study, nine genome sequenced and four unsequenced strains of C. diphtheriae from different sources, including three samples from a recent outbreak in Brazil, were characterized with respect to their growth properties on tellurite-containing agar. Levels of tellurite-resistance (Te(R)) were evaluated by determining the minimum inhibitory concentrations of potassium tellurite (K2TeO3) and by a viability reduction test in solid culture medium with K2TeO3. Significant differences in Te(R) levels of C. diphtheriae strains were observed independent of origin, biovar or presence of the tox gene. Data indicated that the standard initial screening with TeO3(2-)-selective medium for diphtheria bacilli identification may lead to false-negative results in C. diphtheriae diagnosis laboratories.

The ActP acetate transporter acts prior to the PitA phosphate carrier in tellurite uptake by Escherichia coli

The tellurium oxyanion tellurite is harmful for most microorganisms. Since its toxicity occurs chiefly once the toxicant reaches the intracellular compartment, unveiling the toxicant uptake process is crucial for understanding the whole phenomenon of tellurium toxicity. While the PitA phosphate transporter is thought to be one of the main paths responsible for toxicant entry into Escherichia coli, genetic and physiological evidence have identified the ActP acetate carrier as the main tellurite importer in Rhodobacter capsulatus. In this work, new background on the role of these transporters in tellurite uptake by E. coli is presented. It was found that, similar to what occurs in R. capsulatus, ActP is able to mediate toxicant entry to this bacterium. Lower reactive oxygen species levels were observed in E. coli lacking the actP gene.Antioxidant enzyme catalase and fumarase C activity was almost unchanged after short exposure of E. coli ΔactP to sublethal tellurite concentrations, suggesting a low antioxidant response. In this strain, tellurite uptake decreased significantly during the first 5min of exposure and inductively coupled plasma optical emission spectroscopy assays using an actP-overexpressing strain confirmed that this carrier mediates toxicant uptake. Relative gene expression experiments by qPCR showed that actP expression is enhanced at short times of tellurite exposure, while pitA and pitB genes are induced later. Summarizing, the results show that ActP is involved in tellurite entry to E. coli and that its participation occurs mainly at early stages of toxicant exposure.

Coupled selection of protein solubility in E. coli using uroporphyrinogen III methyltransferase as red fluorescent reporter

Uroporphyrinogen III methyltransferase (UMT) is a novel reporter owing to the catalytic products accumulated in cells emitting red florescence. Overexpression of UMT confers resistance of the Escherichia coli cells to potassium tellurite that inhibits cell growth. In this study, we applied UMT reporter for monitoring protein solubility of MBP or TEV protease variants under different expression conditions, as well as 12 maize proteins with either the designed linker or N-terminal SUMO tag. Effects of five enzymes involved in heme and siroheme biosynthesis on the reporter were also investigated. With increasing concentrations of potassium tellurite, colony numbers of the mixed cells expressing the selected five proteins with different solubility were decreased, but colonies displaying red fluorescence was identified to be produced the protein with relatively high solubility. The developed UMT reporter system is sensitive for monitoring protein solubility based on coupled fluorescence and chemical selection.

Enzyme(s) responsible for tellurite reducing activity in a moderately halophilic bacterium, Salinicoccus iranensis strain QW6.

Oxyanions of tellurium, like tellurate (TeO4 (2-)) and tellurite (TeO3 (2-)), are highly toxic for most microorganisms. There are a few reports on the bacterial tellurite resistance mechanism(s). Salinicoccus iranensis, a Gram-positive halophilic bacterium, shows high tellurite resistance and NADH-dependent tellurite reduction activity in vitro. Since little is known regarding TeO3 (2-) resistance mechanisms in halophilic microorganisms, here one of the enzymatic reduction activities presented in this microorganism is investigated. To enhance the enzymatic activity during purification, the effect of different parameters including time, inoculation, different pHs, different tellurite concentrations and different salts were optimized. We also examined the tellurite removal rates by diethyldithiocarbamate (DDTC) during optimization. In the culture medium the optimum conditions obtained showed that at 30 h, 2 % inoculum, pH 7.5, without tellurite and with 5 % NaCl (w/v) the highest enzyme activity and tellurite removal were observed. Results of the purification procedure done by hydroxyapatite batch-mode, ammonium sulfate precipitation, followed by phenyl-Sepharose and Sephadex G-100 column chromatography, showed that the enzyme consisted of three subunits with molecular masses of 135, 63 and 57 kDa. In addition to tellurite reduction activity, the enzyme was able to reduce nitrate too. Our study extends the knowledge regarding this process in halophilic microorganisms. Besides, this approach may suggest an application for the organism or the enzyme itself to be used for bioremediation of polluted areas with different contaminants due to its nitrate reductase activity.

Isolation, identification and characterization of highly tellurite-resistant, tellurite-reducing bacteria from Antarctica

The tellurium oxyanion, tellurite, is extremely noxious to most living organisms. Its toxicity has been mainly related to the generation of reactive oxygen species (ROS) as well as to an unbalancing of the thiol:redox buffering system. Nevertheless, a few bacteria are capable of thriving at high tellurite concentrations. One mechanism of resistance is the enzymatic and non-enzymatic reduction of tellurite to the less toxic elemental tellurium. This reduction generates nano- to micrometric tellurium crystals that display different shapes and sizes.To date, a very limited number of highly tellurite-resistant and tellurite-reducing bacterial species are available from international culture collections. In this work, we decided to look for tellurite-reducing bacteria from an extreme environment, Antarctica. This environment exhibits a combination of several extreme factors such as high UV-radiation and desiccation and freezing conditions that impact directly on the local biodiversity. Since, as does, all these factors induce ROS formation, we hypothesized that Antarctic bacteria could also exhibit tellurite-resistance. In this context, we isolated 123 tellurite-resistant bacteria, and characterized six new tellurite-resistant and tellurite-reducing bacterial strains from samples collected in Antarctica. These strains were identified according to their 16S rRNA gene sequence as Staphylococcus hameolyticus, Staphylococcus sciuri, Acinetobacter haemolyticus, Pseudomonas lini, and two strains of Psychrobacter immobilis.The isolates display tellurite-resistance about 35- to 500-fold higher than Escherichia coli (Te-sensitive organism), and a high level of tellurite reduction which might be interesting for an application in the field of bioremediation or nanoparticle biosynthesis.

DNA, Cell Wall and General Oxidative Damage Underlie the Tellurite/Cefotaxime Synergistic Effect in Escherichia coli

The constant emergence of antibiotic multi-resistant pathogens is a concern worldwide. An alternative for bacterial treatment using nM concentrations of tellurite was recently proposed to boost antibiotic-toxicity and a synergistic effect of tellurite/cefotaxime (CTX) was described. In this work, the molecular mechanism underlying this phenomenon is proposed. Global changes of the transcriptional profile of Escherichia coli exposed to tellurite/CTX were determined by DNA microarrays. Induction of a number of stress regulators (as SoxS), genes related to oxidative damage and membrane transporters was observed. Accordingly, increased tellurite adsorption/uptake and oxidative injuries to proteins and DNA were determined in cells exposed to the mixture of toxicants, suggesting that the tellurite-mediated CTX-potentiating effect is dependent, at least in part, on oxidative stress. Thus, the synergistic tellurite-mediated CTX-potentiating effect depends on increased tellurite uptake/adsorption which results in damage to proteins, DNA and probably other macromolecules. Our findings represent a contribution to the current knowledge of bacterial physiology under antibiotic stress and can be of great interest in the development of new antibiotic-potentiating strategies.

Isolation and Characterization of Bacteria Capable of Reducing Tellurium Oxyanions to Insoluble Elemental Tellurium for Tellurium Recovery from Wastewater

The recovery of tellurium as an important rare metal from wastes and wastewater must be promoted to satisfy its increasing demand for use in many industries. For development of a biological process for recovering tellurium from wastewater, three bacterial strains capable of reducing soluble tellurite into insoluble elemental tellurium were isolated from the drainage wastewater of a metal refinery plant. The bacterial strains, Stenotrophomonas maltophilia TI-1, Ochrobactrum anthropi TI-2 and O. anthropi TI-3, resisted up to 30 mM tellurite, and removed 86–89 % of 1 mM tellurite from water phase within 21 h in a reductive reaction. They showed a considerably higher tellurite removal rate than the previously reported tellurite-reducing bacteria. Tellurite-reducing activity was observed at 20–40 °C, pH 6.2–8.5 and 0.05–5 % NaCl (0.1 mM/h at maximum). The tellurite-reducing activities of strains TI-2 and TI-3 were not considerably different from each other, however strain TI-1 showed higher tellurite-reducing activity at low temperatures, low pH and high NaCl concentrations than the other strains. Because deposits of elemental tellurium were formed on and free from the bacterial cells, it is possible to recover tellurium from the water phase by centrifugation, ultrafiltration, or coagulation following tellurite reduction. All bacterial strains isolated in this study are inferred to be great candidates to establish bacterial tellurium recovery processes from industrial wastewater containing high concentrations of tellurite.