Although phosphine is ubiquitously present in anaerobic environments, little is known regarding the microbial community dynamics and metabolic pathways associated with phosphine formation in an anaerobic digestion system. This study investigated the production of phosphine in anaerobic digestion, with results indicating that phosphine production mainly occurred during logarithmic microbial growth. Dehydrogenase and hydrogen promoted the production of phosphine, with a maximum phosphine concentration of 300 mg/m3. The abundance of Ruminococcaceae and Escherichia was observed to promote phosphine generation. The analysis of metabolic pathways based on the Kyoto Encyclopedia of Genes and Genomes (KEGG) and the MetaCyc pathway database revealed the highest relative abundance of replication and repair in genetic information processing; further, the cofactor, prosthetic group, electron carrier, and vitamin biosynthesis were observed to be closely related to phosphine formation. A phylogenetic tree was reconstructed based on the neighbor-joining method. The results indicated the clear evolutionary position of the isolated Pseudescherichia sp. SFM4 strain, adjacent to Escherichia, with a stable phosphate-reducing ability for a maximum phosphine concentration of 26 mg/m3. The response surface experiment indicated that the initial optimal conditions for phosphine production by SFM4 could be achieved with nitrogen, carbon, and phosphorus loads of 6.17, 300, and 10 mg/L, respectively, at pH 7.47. These results provide comprehensive insights into the dynamic changes in the microbial structure, isolated single bacterial strain, and metabolic pathways associated with phosphine formation. They also provide information on the molecular biology associated with phosphorus recycling.
- MeSH
- anaerobióza MeSH
- bioreaktory mikrobiologie MeSH
- Clostridiales genetika metabolismus MeSH
- dusík metabolismus MeSH
- Escherichia genetika metabolismus MeSH
- fosfáty metabolismus MeSH
- fosfiny analýza metabolismus MeSH
- fosfor metabolismus MeSH
- fylogeneze MeSH
- metabolické sítě a dráhy * genetika MeSH
- mikrobiota * MeSH
- odpadní vody mikrobiologie MeSH
- vodík metabolismus MeSH
- Publikační typ
- časopisecké články MeSH
Layered double hydroxide (LDH) is one of the key host phases of Cr(VI) in the natural environment and chromite ore processing residue (COPR), causing serious pollution by Cr(VI). Therefore, efficient extraction or immobilization of the incorporated Cr(VI) in LDH is urgently needed. In this work, simultaneous separation and immobilization of Cr(VI) in LDH by using MgCl2·6H2O under thermal treatment is innovatively proposed. Cr was volatilized as CrCl3 and was immobilized as MgCr2O4 accounted for 62.2% and 37.8%, respectively, under the optimal condition (the mole ratio of Cl/Cr is 9, 700 °C and 120 min). The underlying reaction mechanisms are as follows: (i) HCl produced by MgCl2·6H2O accelerates the destruction of Cr(VI)-LDH layer structure, completely exposing the incorporated Cr(VI), (ii) Cr(VI) is reduced to Cr(III) by Cl-, part of which is directly immobilized as MgCr2O4, and the other part generates CrCl3, which is volatilized or further combined with Mg2+ to form MgCr2O4. The total Cr leaching concentration of the practical COPR sample treated by this method dramatically decreases from 421 to 0.7 mg/L, well below the landfill standard limit (4.5 mg/L). This work provides an attainable strategy for thorough remediation of COPR and inspires the treatment of heavy metal-containing LDH.
In this work, magnesium ferrite (MgFe2O4) nano-platelets with rich defects and abundant surface hydroxyl groups were synthesized, and used for the removal of low concentration As(V) in aqueous solution. Results from scanning electron microscopy (SEM) showed that the as-synthesized MgFe2O4 nano-platelets were consisted of many individual nanospheres. Rietveld refinement of X-ray diffraction (XRD) data indicated that the Mg2+ ions substituted the Fe3+ ions at both the octahedral and the tetrahedral sites of the crystal structure. Batch adsorption experiment showed that the equilibrium concentration of As(V) could be reduced down to 4.9 μg·L-1 when the initial concentration of As(V) is 1 mg·L-1, which complied with the drinking water standard of WHO (10 μg·L-1). The adsorption capacity of synthesized MgFe2O4 towards As(V) was higher than commonly used iron oxide adsorbents (Fe3O4, γ-Fe2O3 and α-Fe2O3). Mechanistic studies proved that the superior adsorption capacity was attributed to: (1) increased amount of surface hydroxyl groups that resulted from the surface defects. (2) formation of tridentate hexanuclear surface complexes instead of bidentate binuclear complexes, and (3) formation of excess Mg-OH surface hydroxyl groups and As-Mg monodentate mononuclear surface complexes. This work disclosed the correlation of the superior As(V) adsorption ability with the surface hydroxyl groups in defective MgFe2O4, and propose MgFe2O4 as a potential candidate for the remediation of As-contaminated water.
- MeSH
- adsorpce MeSH
- arsen analýza chemie MeSH
- biodegradace MeSH
- chemické látky znečišťující vodu analýza MeSH
- čištění vody metody MeSH
- difrakce rentgenového záření MeSH
- hydroxylový radikál chemie MeSH
- kovové nanočástice chemie MeSH
- sloučeniny hořčíku chemie MeSH
- železité sloučeniny chemie MeSH
- Publikační typ
- časopisecké články MeSH
Increasing attention has been dedicated to trace phthalates in bottled water due to the serious concerns on public health, while there is still a lack of systematic analysis and assessment of current global situation. Through analyzing five representative phthalates in bottled water over 20 countries, this work clearly revealed the phthalates-associated potential risks in both human daily intake and estrogenic effect. In the risk assessment, the kinetic models were also developed to describe and predict phthalates migration. In more than three hundred brands of bottled waters from twenty one countries, the detection frequency of the five targeted phthalates was found to be in the order of dibutyl phthalate (DBP, 67.6%), di-2-(ethyl hexyl) phthalate (DEHP, 61.7%), diethyl phthalate (DEP, 47.1%), benzyl butyl phthalate (BBP, 36.9%), and dimethyl phthalate (DMP, 30.1%). Among the countries studied relating concentrations of DEHP in bottled waters, the top five countries ranked in the order of high to low were Thailand, Croatia, Czech Republic, Saudi Arabia and China with an average level of 61.1, 8.8, 6.3, 6.2 and 6.1 μg/L, respectively. The average levels of BBP, DBP, DMP and DEP in bottled water from Pakistan were high, in which DEP and DMP were ranked 1st among all countries with the average levels of 22.4 and 50.2 μg/L, while BBP and DBP were ranked 2nd and 3rd with the average levels of 7.5 and 17.8 μg/L, respectively. The human daily intake-based risk assessment revealed that phthalates in bottled waters studied would not pose a serious concern on public health. However, the adverse estrogenic effects of phthalates in bottled water from some countries appeared to be significant. This study just shed light on global situation of phthalates in bottled water, and more efforts should be needed to systematically examine the phthalates-related safety of bottled water.
- MeSH
- kyseliny ftalové * MeSH
- lidé MeSH
- pitná voda * MeSH
- Check Tag
- lidé MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- přehledy MeSH
- Geografické názvy
- Česká republika MeSH
- Chorvatsko MeSH
- Čína MeSH
- Pákistán MeSH
- Saudská Arábie MeSH
- Thajsko MeSH
Current studies reveal that the biomineralization of U(VI) by anaerobes normally produces nano-sized U(IV) minerals that can easily re-migrate/re-oxidize, while the biomineralization of U(VI) by aerobes has been constrained because the general mechanism has not yet been fully characterized. The biomineralization of U(VI) by Bacillus cereus 12-2 was investigated in this work. The maximum biosorption capability of intact cells was 448.68 mg U/g biomass (dry weight) at pH 5, while a decrease over 60% was induced when phosphate, amino, and especially carboxyl groups were shielded. X-ray diffraction, electron microscopy, and tracing the concentration of soluble intracellular U(VI) demonstrated that extracellular amorphous uranium particles can directly enter cells as solid, and about 10 nm-sized (NH4)(UO2)PO4·3H2O was formed subsequently. It was also revealed that the biosorption capability was not affected by a high uranium concentration, while biomineralization was inhibited, suggesting that a high concentration of heavy metals may inhibit the enzyme activity involved in biomineralization. Besides, U(VI) could trigger the overexpression of proteins with a molecular weight of 22 kD, including various phosphatases, kinases, and other enzymes that are related to metabolism and stimulus response, which may contribute to the intracellular transformation of U(VI) compounds from amorphous to crystalline phase. Taken together, the immobilization of U(VI) by B. cereus 12-2 contains two major steps: (1) fast immobilization of U(VI) on the cell surface as amorphous compounds, in which the carboxyl groups served as the predominant coordination functional groups and (2) transport of amorphous particles to cells directly and enzyme-related formation of uramphite.
- MeSH
- Bacillus cereus chemie MeSH
- difrakce rentgenového záření metody MeSH
- minerály chemie MeSH
- uran chemie MeSH
- Publikační typ
- časopisecké články MeSH
Mg-Al-Cl layered double hydroxide (Cl-LDH) was prepared to simultaneously remove Cu(II) and Cr(VI) from aqueous solution. The coexisting Cu(II) (20mg/L) and Cr(VI) (40mg/L) were completely removed within 30min by Cl-LDH in a dosage of 2.0g/L; the removal rate of Cu(II) was accelerated in the presence of Cr(VI). Moreover, compared with the adsorption of single Cu(II) or Cr(VI), the adsorption capacities of Cl-LDH for Cu(II) and Cr(VI) can be improved by 81.05% and 49.56%, respectively, in the case of coexisting Cu(II) (200mg/L) and Cr(VI) (400mg/L). The affecting factors (such as solution initial pH, adsorbent dosage, and contact time) have been systematically investigated. Besides, the changes of pH values and the concentrations of Mg(2+) and Al(3+) in relevant solutions were monitored. To get the underlying mechanism, the Cl-LDH samples before and after adsorption were thoroughly characterized by X-ray powder diffraction, transmission electron microscopy, Fourier transform infrared spectroscopy, and X-ray photoelectron spectroscopy. On the basis of these analyses, a possible mechanism was proposed. The coadsorption process involves anion exchange of Cr(VI) with Cl(-) in Cl-LDH interlayer, isomorphic substitution of Mg(2+) with Cu(2+), formation of Cu2Cl(OH)3 precipitation, and the adsorption of Cr(VI) by Cu2Cl(OH)3. This work provides a new insight into simultaneous removal of heavy metal cations and anions from wastewater by Cl-LDH.
The remediation of Pb(II) through biomineralization is rergarded as a promising technique as well as an interesting phenomenon for transforming heavy metals from mobile species into very stable minerals in the environment. Studies are well needed for in-depth understanding the mechanism of Pb(II) immobilized by bacteria. In the present study, we investigated the uptake and biomineralization of Pb(II) using Bacillus cereus 12-2 isolated from lead-zinc mine tailings. The maximum Pb(II) uptake capacity of B. cereus 12-2 was 340 mg/g at pH 3.0. Zeta potential analyses and selective passivation experiments demonstrated that electrostatic attraction was the main force driving the uptake of Pb(II), while the carboxyl, amide and phosphate functional groups of the bacteria provided the binding sites for immobilizing Pb(II). XRD and TEM investigation revealed that the Pb(II) loaded on bacteria could be stepwise transformed into rod-shaped Ca2.5Pb7.5(OH)2(PO4)6 nanocrystal. Combined with protein denaturalization experiments, we proposed that the biomineralization of Pb(II) possibly consisted of two steps: (1) Rapid biosorption of Pb(II) on B. cereus 12-2 through the synergy of electrostatic attraction, ionic exchange and chelating activity of functional groups; (2) enzyme-mediated mineral transformation from amorphous precipitate to rod-shaped crystalline minerals happening gradually inside the bacteria.
The mechanism of uranium transformation from U(VI) into nano-uramphite by two indigenous Bacillus thuringiensis strains was investigated in the present work. Our data showed that the bacteria isolated from uranium mine possessed highly accumulation ability to U(VI), and the maximum accumulation capacity was around 400 mg U/g biomass (dry weight). X-ray powder diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM) and Fourier transform infrared spectroscopy (FT-IR) analyzes indicated that the U(VI) was adsorbed on the bacterial surface firstly through coordinating with phosphate, CH2 and amide groups, and then needle-like amorphous uranium compounds were formed. With the extension of time, the extracellular crystalline substances were disappeared, but some particles were appeared in the intracellular region, and these particles were characterized as tetragonal-uramphite. Moreover, the disrupted experiment indicated that the cell-free extracts had better uranium-immobilization ability than cell debris. Our findings provided the understanding of the uranium transformation process from amorphous uranium to crystalline uramphite, which would be useful in the regulation of uranium immobilization process.
- MeSH
- adsorpce MeSH
- amidy chemie MeSH
- Bacillus thuringiensis metabolismus MeSH
- biodegradace MeSH
- biomasa MeSH
- chemické látky znečišťující vodu analýza MeSH
- difrakce rentgenového záření MeSH
- fosfáty chemie MeSH
- hornictví MeSH
- koncentrace vodíkových iontů MeSH
- mikroskopie elektronová rastrovací MeSH
- odpadní voda MeSH
- spektroskopie infračervená s Fourierovou transformací MeSH
- transmisní elektronová mikroskopie MeSH
- uran chemie MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
In this study, we investigated the Cr(VI) uptake mechanism of planktonic cells and biofilms of Bacillus subtilis (B. subtilis) ATCC-6633. Data showed that the effect of planktonic cells on the Cr(VI) uptake was quite different from that of biofilms. Planktonic cells had strong ability of Cr(VI) reduction, while biofilms possessed a great potential of Cr(III) immobilization. For planktonic cells, 100 mg/L Cr(VI) could be completely reduced. Both exopolymeric substances and cytoplasmic extracts contributed to high capacity of Cr(VI) reduction. After the reduction, noticeable Cr(III) precipitates were accumulated on bacterial surfaces, but 37.5% Cr(III) still remained in the supernatant. For biofilms, the biofilm debris became the main active ingredient of the Cr(VI) reduction. However, only 20 mg/L Cr(VI) could be reduced probably because of unavailability of reducing active sites during the biofilm formation. Further studies showed that biofilms had a better Cr(III) immobilization capacity than planktonic cells with 100% Cr(III) immobilized. Moreover, for the first time, we proposed a strategy combining the advantages of both planktonic cells and biofilms, and a successful Cr(VI) removal from typical Cr(VI)-containing plating wastewater was achieved through a 10-L pilot-scale experiment.
Lead contamination is now widespread, and exposure to lead may cause adverse effects on human beings. In this study, a photoelectrochemical sensor based on flower-like ZnO nanostructures was developed for Pb(2+) detection, using a Pb(2+)-dependent DNAzyme as the recognition unit and a double-strand DNA intercalator, Ru(bpy)2(dppz)(2+) (bpy=2,2'-bipyridine, dppz=dipyrido[3,2-a:2',3'-c] phenazine) as the photoelectrochemical signal reporter. The ZnO nanoflower was fabricated on an indium tin oxide (ITO) electrode by the convenient hydrothermal decomposition method. The morphology and photoelectrochemical property of the ZnO nanoflowers were characterized by SEM, XRD and photocurrent measurements. DNAzyme-substrate duplex was assembled on an ITO/ZnO electrode through electrostatic adsorption. In the presence of Pb(2+), RNA-cleavage activity of the DNAzyme was activated and its substrate strand was cleaved, resulting in the release of Ru(bpy)2(dppz)(2+) from the DNA film and the concomitant photocurrent decrease. The detection principle was verified by fluorescence measurements. Under the optimized conditions, a linear relationship between photocurrent and Pb(2+) concentration was obtained over the range of 0.5-20 nM, with a detection limit of 0.1 nM. Interference from other common metal ions was found negligible. Applicability of the sensor was demonstrated by analyzing lead level in human serum and Pb(2+) spiked water samples. This facile and economical sensor system showed high sensitivity and selectivity, thus can be potentially applied for on-site monitoring of lead contaminant.
- MeSH
- biosenzitivní techniky přístrojové vybavení MeSH
- chemické látky znečišťující vodu analýza MeSH
- design vybavení MeSH
- DNA katalytická chemie MeSH
- elektrochemické techniky přístrojové vybavení MeSH
- interkalátory chemie MeSH
- jezera analýza MeSH
- limita detekce MeSH
- nanostruktury chemie ultrastruktura MeSH
- olovo analýza MeSH
- oxid zinečnatý chemie MeSH
- pitná voda analýza MeSH
- Publikační typ
- časopisecké články MeSH
- hodnotící studie MeSH
- práce podpořená grantem MeSH
