Speciation of Pb(II) sorbed by Burkholderia cepacia/goethite composites

Bacterial-mineral composites are important in the retention of heavy metals such as Pb due to their large sorption capacity under a wide range of environmental conditions. However, the partitioning of heavy metals between components in such composites is not probed directly. Using Burkholderia cepacia biofilms coated with goethite (alpha-FeOOH) particles, the partitioning of Pb(II) between the biological and iron-(oxyhydr)oxide surfaces has been measured using an X-ray spectroscopic approach. EXAFS spectra were fit to quantitatively determine the fraction of Pb(II) associated with each component as a function of pH and [Pb]. At pH < 5.5, at least 50% of the total sorbed Pb(II) is associated with the biofilm component, whereas the total uptake within the composite is dominated by goethite (> 70% Pb/goethite) above pH 6. Direct comparison can be made between the amount of Pb(II) bound to each component in the composite vs separate binary systems (i.e., Pb/biofilm or Pb/goethite). At high pH, Pb(II) uptake on the biofilm is dramatically decreased due to competition with the goethite surface. In contrast, Pb uptake on goethite is significantly enhanced at low pH (2-fold increase at pH 5) compared to systems with no complexing ligands. The mode of Pb(II)-binding to the goethite component changes from low to high [Pb]. Structural fitting of the EXAFS spectra collected from 10(-5.6) to 10(-3.6) M [Pb]eq at pH 6 shows that the Pb-goethite surface complexes at low [Pb] are dominated by inner-sphere bidentate, binuclear complexes bridging two adjacent singly coordinated surface oxygens, giving rise to Pb-Fe distances of approximately 3.9 A. At high [Pb], the dominant Pb(II) inner-sphere complexes on the goethite surface shift to bidentate edge-sharing complexes with Pb-Fe distances of approximately 3.3 A.     

Sorption of copper (II) ions by pine sawdust

The sawdust of Calabrian pine was used as sorbent for the removal of Cu(II) ions from aqueous solution of copper sulfate pentahydrate (CuSO₄.5H₂O) at different concentrations, pHs and temperatures. The results showed that about 65–81% of Cu(II) ions in the solution could be adsorbed on the sawdust. The percentage of adsorped Cu(II) ions onto the sawdust increased with increasing initial concentration. Kinetic studies indicated that the sorption process followed the first order reversible kinetic model. It was also determined that the sorption process obeyed the Freundlich isotherm. Furthermore, the sorption thermodynamic was investigated in detail.     

Burkholderia cepacia中具有解脂作用的胆固醇酯酶的酶学特性

为了更好地应用于工业领域,系统研究Burkholderia cepacia ZWS15胆固醇酯酶(EC 3. 1. 1. 13 cholesterol esterase,CHE)的酶学特性。通过DEAE离子交换从该菌发酵液中获得一种CHE,并探讨其有机溶剂与表面活性剂耐受性,以及底物水解特性。CHE在p H 5. 5～9. 0保持稳定,最适反应温度为40℃,在70℃温育2 h仍能保留70%以上的酶活,具有显著耐热性;在50%(体积分数)有机溶剂或5%(体积分数)表面活性剂存在下也具有较高酶活。飞行时间质谱鉴定该酶分子质量为37 k Da,其与胆固醇酯酶(源于洋葱伯尔霍尔德菌,Burkholderia cepacia)及脂肪酶(源于假单胞菌属,Pseudomonas sp.)具有较高匹配度。与商品化酶相比,CHE不仅具有胆固醇酯酶活性(对长链胆固醇酯类底物有明显偏好性),还具有解脂功能(可作用于三酰基甘油酯及对硝基苯酯)。该酶的优良性能可为其在食品、诊断、制浆造纸等领域的工业应用提供参考与借鉴。     

Development of a time-temperature integrator system using Burkholderia cepacia lipase

A time-temperature integrator (TTI) is a device used to show a time-temperature dependent change that reflects the temperature history and quality status of the food to which it is attached. An enzymatic TTI system based on the reaction between Burkholderia cepacia lipase and tricaprylin, which causes a pH change, was developed. The temperature dependence of the response rate of this new lipase-type TTI was modeled using the Arrhenius equation, and the estimated activation energy was calculated as 70.61±11.10 kJ/mol (±95% confidence interval). The TTI response was validated under dynamic storage conditions with independent variable temperature experiments, and a good agreement was obtained between the predicted and measured values.     

Recovery of Burkholderia pseudomallei and B. cepacia from drinking water

Samples of drinking water were examined in order to evaluate the occurrence of two gram-negative bacteria: Burkholderia pseudomallei and B. cepacia. A total of 85 samples were collected from public and private buildings in the province of Bologna (Italy). Other bacteriological indicators (heterotrophic plate count at 22 and 36 degrees C) were also examined, together with physical and chemical parameters (temperature, pH, residual chlorine, total hardness and chemical oxygen demand (COD)). High levels of B. pseudomallei were recovered (mean value = 578 cfu/100 ml) in about 7% of samples, while B. cepacia was recovered in 3.5% (mean value = < 1) of the samples. The two microorganisms were found to correlate positively with heterotrophic plate counts at 22 and 36 degrees C, but not with the physical and chemical parameters taken into consideration.     

Factors affecting the biodegradation of cyanide by Burkholderia cepacia strain C-3

The utilization of cyanide as a nitrogen source for growth in a liquid minimal medium by Burkholderia cepacia strain C-3 isolated from soil was demonstrated. The effects of various parameters on the biodegradation of cyanide by the strain were investigated. Growth at the expense of cyanide occurred over a pH range from 8 to 10, and was optimal at pH 10. Growth and cyanide biodegradation were optimal at 30 degrees C. The presence of Cu2+ or Fe2+ in the liquid medium at a concentration of 1 mM inhibited both the growth of the bacterium and its cyanide degradation. The effects of Ni2+ and Co2+, and to a lesser extent Mn2+ and Mo2+, on cyanide degradation rate were concentration dependent. Addition of the cyanide-containing waste contaminants ethanol and methanol reduced the cyanide utilization of the isolate, but phenol was completely inhibitory. Microbial depletion of cyanide occurred even in the presence of other organic and inorganic nitrogen sources. Fructose, glucose, and mannose were the preferred carbon sources for cyanide biodegradation. The highest rate of cyanide degradation by B. cepacia C-3, 1.85 mg CN h(-1), was observed with 0.25% (w/v) fructose; the degradation rate decreased progressively thereafter with increasing fructose concentration.     

玉米芯生物炭对水中Pb(Ⅱ)的吸附

以玉米芯为原料制备生物炭,采用扫描电镜及N_2吸附等温线对其表面形貌及孔结构进行了表征,通过批次吸附试验,研究了其对水中Pb(II)的吸附行为。结果表明:玉米芯生物炭对Pb(II)的吸附在120 min达到平衡,吸附过程符合准二级动力学方程。Langmuir吸附模型能够很好地模拟吸附等温线,最大饱和吸附量为79.36 mg/g。热力学结果显示:玉米芯生物炭对Pb(II)的吸附主要以化学吸附为主,升高温度有利于吸附。在Cd(II)共存的条件下,玉米芯生物炭对Pb(II)的吸附受到一定的抑制。     

Mechanisms of Pb(II) sorption on a biogenic manganese oxide

Macroscopic Pb(II) uptake experiments and Pb L3-edge extended X-ray absorption fine structure (EXAFS) spectroscopy were combined to examine the mechanisms of Pb(II) sequestration by a biogenic manganese oxide and its synthetic analogues, all of which are layer-type manganese oxides (phyllomanganates). Relatively fast Pb(II) sorption was observed, as well as extremely high sorption capacities, suggesting Pb incorporation into the structure of the oxides. EXAFS analysis revealed similar uptake mechanisms regardless of the specific nature of the phyllomanganate, electrolyte background, total Pb(II) loading, or equilibration time. One Pb-O and two Pb-Mn shells at distances of 2.30, 3.53, and 3.74 A, respectively, were found, as well as a linear relationship between Brunauer-Emmett-Teller (BET; i.e., external) specific surface area and maximum Pb(II) sorption that also encompassed data from previous work. Both observations support the existence of two bonding mechanisms in Pb(II) sorption: a triple-corner-sharing complex in the interlayers above/ below cationic sheet vacancies (N theoretical = 6), and a double-corner-sharing complex on particle edges at exposed singly coordinated -O(H) bonds (N theoretical = 2). General prevalence of external over internal sorption is predicted, but the two simultaneous sorption mechanisms can account for the widely noted high affinity of manganese oxides for Pb(ll) in natural environments.     

Role of transition metals,Fe(II), Cr(II), Pb(II), and Cd(II) in lipid peroxidation

Cod liver oil was oxidized with Fenton-like systems containing transition metals Fe(II), Cr(II), Pb(II), and Cd(II). Malonaldehyde (MA) formed from 10 μl cod liver oil oxidized by a Fenton-like system containing each metal at levels of 0.25, 0.5, 1 and 4 μmol was analyzed by a gas chromatograph equipped with a nitrogen phosphorus detector. The MA production exhibited dose response and the greatest amount (837.0 ± 19.1 nmol) was obtained by the Fe(II) system at the level of l μmol. Generally, higher MA formation is observed in the lower the third ionization potential of the metal. The decreasing order of MA formed in the metal systems at the level of 1 μmol is Fe(II) > Cr(II)(274.1 ± 20.1 nmol) > Pb(II)(150.7 ± 13.0 nmol) > Cd(II)(95.4 ± 6.7 nmol). The amounts of MA formed in Cr(II), Pb(II), and Cd(II) systems were considerably lower than those in the Fe(II) system. The relative formations of MA in the Cr(II) and Pb(II) systems were similar to those in the Fe(II) system. The results suggest that trace amounts of metals contribute oxidative effects to lipid peroxidation followed by various diseases.     

Sorption studies of Zn(II)- and Cd(II)ions from aqueous solution on treated sawdust of sissoo wood

Sawdust, an inexpensive material, has been utilized as an adsorbent for the removal of Zn(II)- and Cd(II)ions from aqueous solution. The effects of time of equilibrium, pH, temperatures and dosage of the adsorbent on the removal of Zn(II)- and Cd(II)ions have been studied. The equilibrium nature of Zn(II)- and Cd(II)ions adsorption at different temperatures (25–60 °C) has been studied. The percent adsorption of Zn(II)- and Cd(II)ions increased with an increase in pH, temperature and dosage of treated sawdust. The applicability of the Langmuir isotherm suggests the formation of monolayer coverage of Zn(II)- and Cd(II)ions at the surface of the adsorbent. The thermodynamic parameters like free energy, enthalpy and entropy changes for the adsorption of Zn(II)- and Cd(II)ions has also been computed and discussed. The heat of adsorption [ΔH=17.706 kJmole^-1 for Zn(II) and ΔH=16.949 kJmole^-1 for Cd(II)] implied that the adsorption was an endothermic adsorption. The sawdust was found to be a metal adsorbent as effective as activated carbon.     

Reactivity of Pb(II) at the Mn(III,IV) (oxyhydr)oxide--water interface

In this study, the reactivity of lead (Pb(II)) on naturally occurring Mn(III,IV) (oxyhydr)oxide minerals was evaluated using kinetic, thermodynamic, and spectroscopic investigations. Aqueous Pb(II) was more strongly adsorbed to birnessite (delta-MnO1.7) than to manganite (gamma-MnOOH) under all experimental conditions. The isoteric heat of Pb adsorption (delta HT) or birnessite was 94 kJ mol-1 at a surface loading of 1.1 mmol g-1, and decreased with increasing adsorption density. This indicated that adsorption was an endothermic process and that birnessite possessed heterogeneous sites of reactivity for Pb. X-ray absorption fine structure (XAFS) spectra revealed that Pb was adsorbed as inner-sphere complexes on both birnessite and manganite with no evidence to suggest oxidation as an operative sorption mechanism. Lead appeared to coordinate to vacancy sites in the birnessite layer structure with concurrent release of Mn to solution, which resulted in a greater number of second shell Mn scatterers in Pb-birnessite when compared to Pb-manganite samples. The difference in Pb coordination apparently explained the contrasting desorption behavior between the two Mn minerals. These results have significant implications for Pb partitioning in soil environments containing solid-phase Mn(III,IV) (oxyhydr)oxides.     

Enhancing activity and stability of Burkholderia cepacia lipase by immobilization on surface-functionalized mesoporous silicates

Burkholderia cepacia lipase was immobilized on various types of phenyl-functionalized mesoporous silicates (MPS). MPS, anchored with a phenyl group on the silica wall and with three dimensional (3D) mesoporosity, showed highest lipase adsorption capacity and best activities both in aqueous and organic reagents.     

Monitoring of Zn(II), Cd(II), Pb(II) and Cu(II) During Refining of Some Vegetable Oils Using Differential Pulse Anodic Stripping Voltammetry

In this study, a novel approach has been developed using differential pulse anodic stripping voltammetry (DPASV) for the simultaneous determination of Zn(II), Cd(II), Pb(II) and Cu(II) in edible oils at hanging mercury drop electrode. The microwave digestion of oil samples was carried out with concentrated HNO₃ and H₂O₂. KNO₃ was used as a supporting electrolyte. The experimental conditions optimized such as deposition time, stirring rate and size of mercury drop were 300 s, 600 rpm and 10 mm², respectively. The method was applied to quantify Zn(II), Cd(II), Pb(II) and Cu(II) in crude and refined hazelnut, corn, sunflower and olive oils. During refining of different vegetable oils, the removal efficiencies of Zn(II), Cd(II), Pb(II) and Cu(II) were calculated as 98.20–99.91, 98.50–99.90, 95.26–99.76 and 95.93–99.92 %, respectively. The limits of detection for Zn(II), Cd(II), Pb(II) and Cu(II) were 2.1?×?10^?8, 8.7?×?10^?10, 7.1?×?10^?9 and 3.4?×?10^?9 and the limits of quantification were 6.8?×?10^?8, 2.9?×?10^?9, 2.3?×?10^?8 and 1.1?×?10^?8 M with linear regression coefficients (R ²) of 0.9930, 0.9928, 0.9893 and 0.9931, respectively. It was observed that the above metals in crude and refined vegetable oils could be determined simultaneously by the DPASV method.     

Comparison of Cd(II), Cu(II), and Pb(II) biouptake by green algae in the presence of humic acid

The present study examines the role of humic acid, as a representative of dissolved organic matter, in Cd(II), Cu(II), and Pb(II) speciation and biouptake by green microalgae. Cellular and intracellular metal fractions were compared in the presence of citric and humic acids. The results demonstrated that Cd and Cu uptake in the presence of 10 mg L(-1) humic acid was consistent with that predicted from measured free metal concentrations, while Pb biouptake was higher. By comparing Cd, Cu, and Pb cellular concentrations in the absence and presence of humic acid, it was found that the influence of the increased negative algal surface charge, resulting from humic acid adsorption, on cellular metal was negligible. Moreover, the experimental results for all three metals were in good agreement with the ternary complex hypothesis. Given that metal has much higher affinity with algal sites than humic acid adsorbed to algae, the contribution of the ternary complex to metal bioavailability was negligible in the case of Cd (II) and Cu (II). In contrast, the ternary complex contributed to over 90% of total cellular metal for Pb(II), due to the comparable affinity of Pb to algal sites in comparison with humic acid adsorbed to algae. Therefore, the extension of the biotic ligand model by including the formation of the ternary complex between the metal, humic acid, and algal surface would help to avoid underestimation of Pb biouptake in the presence of humic substances by green algae Chlorella kesslerii.     

Removal of Pb(II) from aqueous solutions by carbons prepared from Sal wood (Shorea robusta)

In the present work, physically and chemically activated carbons are prepared using Sal wood (Shorea robusta) sawdust by thermal process and using sulfuric acid as the activation agent to remove Pb(II) from aqueous solutions. Adsorption equilibrium studies have been done at a pH of 4 and a room temperature of 30 °C. It was found that the adsorption isotherms are favorable and chemically activated carbons are better than physically activated carbon in terms of adsorption capacity. Various two-parameter adsorption isotherm models, viz. Freundlich, Langmuir, Temkin and Dubinin-Radushkevich, were used to fit the equilibrium data and it was found that the Freundlich adsorption model provided best-fit. The first-order irreversible unimolecular reaction model and the pseudo-second-order kinetic models were used to fit the kinetic data and it was found that both the models provided good fit. Kinetic and film diffusion studies show that the adsorption of lead(II) on the activated carbons tested in this work are both intra-particle and film diffusion controlled.     

Oxidation of aromatic aldehyde to aromatic carboxylic acid by Burkholderia cepacia TM1 isolated from humus

Burkholderia cepacia TM1 isolated from humus was able to oxidize aromatic aldehydes to the corresponding aromatic carboxylic acids with an extreme by high yield in distilled water containing only the aromatic aldehyde as the substrate. The molar yields of vanillic acid from vanillin, p-hydroxybenzoic acid from p-hydroxybenzaldehyde, and syringic acid from syringaldehyde were approximately 94%, 92% and 72%, respectively. Until the added aromatic aldehyde was significantly consumed, consumption of the produced acid hardly occurred. The findings of this study indicate that an appropriate reactor residence time for continuous production can be set, and that aromatic carboxylic acid can be produced efficiently and continuously from the corresponding aldehyde.     

Application of an in situ bismuth-coated glassy carbon electrode for electroanalytical determination of Cd (II) and Pb (II) in Korean polished rices

Rapid on-site monitoring of heavy metals in plants is necessary to minimize the exposure of humans to the contaminated food. The potential of using anodic stripping voltammetry (ASV) for simultaneous determination of cadimium (Cd) and lead (Pb) in rice was evaluated. Eight different Korean polished rices were digested using concentrated HNO₃ solution in a microwave oven. The peak currents measured with an in situ bismuth-coated electrode were linearly proportional to Cd and Pb concentrations (1.5 to 200 ppb) in 0.1 M HNO₃ (R² ⩾0.98). The electrode was feasible for measuring Pb in acid digests of the tested polished rices with measurement errors of <16.3 ppb. However, even though there was acceptable agreement in 4 of the 8 samples tested for Cd between the ASV and inductively coupled argon plasma (ICP) methods, further studies would be needed to improve the predictive capability of the electrode while reducing the variability in measurement and lowering the detection limit.     

Occurrence of Burkholderia cepacia in foods and waters: clinical implications for patients with cystic fibrosis.

Two hundred forty-eight retail "ready-to-eat" foodstuffs in eight food categories and 134 waters categorized into nine types were analyzed for the presence of the Burkholderia cepacia complex of organisms. Of these, 14 of 26 (53.8%) samples of raw unpasteurized bovine milk were positive for this organism. Consumption of raw unpasteurized milk may therefore act as a potential source of infection with this organism, which is of particular concern for patients with cystic fibrosis, where colonization and infection with this organism can lead to a fatal necrotizing pneumonia and premature death. In addition to the associated risk of infection from fecal pathogens, patients with cystic fibrosis should therefore avoid the consumption of raw unpasteurized milk to minimize the risk of becoming infected with this organism.     

A novel 4-(2-pyridylazo) resorcinol functionalised magnetic nanosorbent for selective extraction of Cu(II) and Pb(II) ions from food and water samples

This paper describes a novel sorbent based on 4-(2-pyridylazo) resorcinol functionalised magnetic nanoparticles and its application for the extraction and pre-concentration of trace amounts of Cu(II) and Pb(II) ions. The nanosorbent was characterised by Fourier transform infrared spectroscopy, X-ray powder diffraction, thermal analysis, elemental analysis and scanning electron microscopy. The effects of various parameters such as pH, sorption time, sorbent dosage, elution time, volume and concentration of eluent were investigated. Following the sorption and elution of analytes, Cu(II) and Pb(II) ions were quantified by flame atomic absorption spectrometry. The limits of detection were 0.07 and 0.7 μg l^?1 for Cu(II) and Pb(II), respectively. The relative standard deviations of the method were less than 7%. The sorption capacity of this new sorbent were 92 and 78 mg g^?1 for Cu(II) and Pb(II), respectively. Finally this nanosorbent was applied to the rapid extraction of trace quantities of Cu(II) and Pb(II) ions in different real samples and satisfactory results were obtained.