Biosorption of thorium (IV) by a Pseudomonas biomass

Lyophilized biomass of a Pseudomonas soilisolate adsorbed thorium (IV) (430 mg g^–1 dry wt) optimally at pH 4, with 91% of equilibrium loading being reached in 1 min. Equilibrium metal sorption showing conformity to Langmuir isotherm model suggested a monolayered thorium binding. Thorium binding remained unaffected or slightly affected (< 20% inhibition) in presence of equimolar (430 M) concentration of several interfering ions except Fe³⁺ (40% inhibition). More than 90% of loaded thorium could be recovered using 1 M CaCO₃, though mineral acids and Na₂CO₃ were also effective.     

Nanodiamond-promoted white light emission in Eu,Dy, and Cu-containing phosphate glass: quantitative analysis and colorimetric study

A thorough analysis of glass containing Eu₂O₃ and Dy₂O₃, or Eu₂O₃, Dy₂O₃, and CuO melted together with nanodiamond powder was pursued based on measurements of optical absorption, photoluminescence (PL) emission and excitation spectra, and colorimetry. Nanodiamond facilitated the stabilization of Cu⁺ and Eu²⁺ ions with blue-emitting characteristics that, along with yellow-emitting Dy³⁺ and red-emitting Eu³⁺ led to the white light-emitting glass. Novel intensity notations implemented in intensity-based spectral ratios, and difference intensity correlation analysis were proposed for the assessment of PL properties. The chromaticity and correlated colour temperature of the emission were ultimately investigated as a two-parametric problem based on: (1) the different ionic components; and (2) the various excitation wavelengths employed. The optical analysis approach adds to the characterization methods to further fundamental understanding and provide helpful analytical tools for designing materials for tunable white light-emitting devices.     

Continuous Biosorption of Pb,Cu, and Cd by Phanerochaete chrysosporium in a Packed Column Reactor

The dynamic removal of lead, copper and cadmium in a single component system by Phanerochaete chrysosporium was studied in packed columns. The packed columns consisted of biomass of P. chrysosporium immobilized on polyurethane foam cubes. The performances of packed columns were described through the concept of breakthrough and the values of column parameters predicted as a function of bed depth. The column biosorption data were evaluated in terms of maximum (equilibrium) capacity of the column, the amount of metal loading and the yield of the process. The maximum capacities for lead, copper and cadmium were 70.7, 43.7 and 70.8 mg, respectively, and their yields were 39.2, 40.6 and 41%, respectively. The kinetic and mass transfer aspects of the dynamic removal of the three metals were studied using three mathematical models commonly used to describe the column performance in adsorption processes. Column studies showed good agreement between the experimental data and the simulated breakthrough curves obtained with Adams-Bohart or the Wolborska model and the Clark model. While the initial segment of the breakthrough curve was defined by the Adams-Bohart and Wolborska models, the whole breakthrough curve was well predicted by the Clark model for all the three metals studied.     

Biosorption and Desorption of Lead(II) by Hydrilla verticillata

The potential of nonliving biomass of Hydrilla verticillata to adsorb Pb(II) from an aqueous solution containing very low concentrations of Pb(II) was determined in this study. Effects of shaking time, contact time, biosorbent dosage, pH of the medium, and initial Pb(II) concentration on metal-biosorbent interactions were studied through batch adsorption experiments. Maximum Pb(II) removal was obtained after 2 h of shaking. Adsorption capacity at the equilibrium increased with increasing initial Pb(II) concentration, whereas it decreased with increasing biosorbent dosage. The optimum pH of the biosorption was 4.0. Surface titrations showed that the surface of the biosorbent was positively charged at low pH and negatively charged at pH higher than 3.6. Fourier transform infrared (FT-IR) spectra of the biosorbent confirmed the involvement of hydroxyl and C?O of acylamide functional groups on the biosorbent surface in the Pb(II) binding process. Kinetic and equilibrium data showed that the adsorption process followed the pseudo-second-order kinetic model and both Langmuir and Freundlich isothermal models. The mean adsorption energy showed that the adsorption of Pb(II) was physical in nature. The monolayer adsorption capacity of Pb(II) was 125 mg g^?1. The desorption of Pb(II) from the biosorbent by selected desorbing solutions were HNO₃ > Na₂CO₃ > NaOH > NaNO₃.     

Biosorption and desorption studies of chromium (III) by free and immobilized Rhizobium (BJVr 12) cell biomass

Experiments with free cell biomass (cells + exopolysaccharides) ofRhizobium BJVr 12 (mungbean isolate) showed that amount ofCr³⁺ ion sorbed is influenced by the amount of biomass toCr³⁺ concentration ratio and time of contact. A ratio of 0.5 gfresh biomass to 10.0 ml 5.03 ppm Cr³⁺ sorbed 0.0275 mg Crequivalent to an uptake of 2.86 mg Cr g-¹ dry biomass and 1.0g: 10.0 ml sorbed 0.0366 mg Cr equivalent to an uptake of 1.9 mg Crg-¹ biomass. Immobilized cell biomass in ceramic beads and inaquacel (a porous cellulose carrier with a charged surface) were moreefficient than free cell biomass in adsorbing Cr(III). A reduction of49.7percnt; of Cr(III) for free cells, 95.6% for cells immobilized inceramic beads and 94.6% for cells in aquacel was achieved after 48hours under shaken conditions. Sorption capacities of immobilized cellbiomass in ceramic beads and aquacel ranged from 5.01 to 5.06 mg Crg^-1 dry cell biomass. The biosorption of Cr³⁺follows generally the Langmuir and Freundlich models of adsorption at lowCr³⁺ concentrations. The Langmuir constant for immobilizedcells in ceramic beads are: Q₀, 0.065 mmol Crg^-1 biomass; b (affinity constant), - 694 lmmol^-1 Cr and for cells in aquacel Q, 0.07 mmol Crg^-1 biomass; b, - 694 l mmol Cr g^-1 Cr. TheFreundlich constants are: K, 0.071 mmol Cr g^-1 biomass; n,0.13 g^-1 biomass l^-1 and for aquacel: K, 0.074mmol g^-1 biomass; n, 0.13 g^-1 biomass. Biotrapsmade up of immobilized cells in ceramic beads and aquacel were tested foradsorbing Cr(III) using two different flow rates: 0.5 ml/min and 1.5 ml/min.A significantly higher amount of Cr(III) was adsorbed at the lower flow rateof 0.5 ml/min. Biosorption of Cr³⁺ is competitive. Thetreatment of a waste water sample containing 6.03 ppm Cr³⁺ andother cations with the biomass reduced the Cr³⁺ concentrationto that much lower than for the test solution containing only Cr. Recoveryof biosorbed Cr(III) was by treatment at a different pH using dilute HClsolution. Recovery was higher for cells imbibed in ceramic beads thanaquacel. Percentage recoveries for cells in aquacel are 46.4% at pH1.0, 33.0% at pH 3.0 and 6.6% at pH 6.0–7.0. For cellsin ceramic beads, percentage recoveries are: 93.1% at pH 1.0,75.6% at pH 3.0 and 16.4% at pH 6.0–7.0. Biosorption ofCr³⁺ by cells immobilized in ceramic beads is reversible butonly partially for cells in aquacel.     

Biosorption and desorption of lanthanum(III) and neodymium(III) in fixed-bed columns with Sargassum sp.: perspectives for separation of rare earth metals

Rare earth (RE) metals are essentials for the manufacturing of high-technology products. The separation of RE is complex and expensive; biosorption is an alternative to conventional processes. This work focuses on the biosorption of monocomponent and bicomponent solutions of lanthanum(III) and neodymium(III) in fixed-bed columns using Sargassum sp. biomass. The desorption of metals with HCl 0.10 mol L(-1) from loaded biomass is also carried out with the objective of increasing the efficiency of metal separation. Simple models have been successfully used to model breakthrough curves (i.e., Thomas, Bohart-Adams, and Yoon-Nelson equations) for the biosorption of monocomponent solutions. From biosorption and desorption experiments in both monocomponent and bicomponent solutions, a slight selectivity of the biomass for Nd(III) over La(III) is observed. The experiments did not find an effective separation of the RE studied, but their results indicate a possible partition between the metals, which is the fundamental condition for separation perspectives.     

Biosorption of Arsenic from Contaminated Water onto Solid Psidium guajava Leaf Surface: Equilibrium,Kinetics, Thermodynamics,and Desorption Study

A batch study on the removal of As(III) and As(V) ions from contaminated water by biosorption using powdered Psidium guajava (Guava) leaf as biosorbent was carried out in the present work. FT-IR (Fourier transform infrared) and SEM (scanning electron microscopy) were used to characterize the surface of the biosorbent. The effect of sorption parameters such as pH, temperature (T _c), adsorbent dose (D _c), and contact time (t _c) were studied. At optimum treatment conditions, the maximum uptake of 1.06 mg of As(III) per gram and 2.39 mg of As(V) per gram onto the surface of biosorbent were obtained. Langmuir and Freundlich isotherm models were examined for sorption equilibrium at various temperatures. The sorption isotherm was favorable with the Freundlich model with the experimental data. Furthermore, higher uptake kinetics was tested for the pseudo-first-order and pseudo-second-order models. The pseudo-second-order model appeared to be the more suitable model to describe arsenic biosorption. ΔG ₀ values were negative at all temperatures, confirming the feasible and spontaneous nature of the biosorption process. Solvent desorption studies help in understanding the mechanism of the adsorption process and also to check the stability of the loaded/spent adsorbents. HCl was found to show maximum effectiveness in the desorption of both As(III) and As(V) with the comparison of other solvents.     

Photoluminescence properties of LiBaPO4:M3+ phosphor for near‐UV light‐emitting diode (M = Eu and Dy)

A novel phosphor LiBaPO₄ doped with rare earths Eu and Dy prepared by high temperature solid‐state reaction method is reported. The phosphors were characterized by X‐ray powder diffraction (XRD), scanning electron microscopy (SEM) and photoluminescence (PL). The emission and excitation spectra of these materials were measured at room temperature with a spectrofluorophotometer. The excitation spectra of LiBaPO₄:Eu³⁺ phosphor can be efficiently excited by 394 nm, which is matched well with the emission wavelength of near‐UV light‐emitting diode (LED) chip. PL properties of Eu³⁺‐doped LiBaPO₄ exhibited the characteristic red emission coming from ⁵D₀ → ⁷ F₁ (593 nm) and ⁵D₀ → ⁷ F₂ (617 nm) electronic transitions with color co‐ordinations of (0.680, 0.315). The results demonstrated that LiBaPO₄:Eu³⁺ is a potential red‐emitting phosphor for near‐UV LEDs. Emission spectra of LiBaPO₄:Dy³⁺ phosphors showed efficient blue (481 nm) and yellow (574 nm) bands, which originated from ⁴ F_9/2 → ⁶H_15/2 and ⁴ F_9/2 → ⁶H_13/2 transitions of the Dy³⁺ ion, respectively. The 574 nm line is more intense than the 481 nm lines, which indicates that the site Dy³⁺ is located with low symmetry. This article summarizes fundamentals and possible applications of optically useful inorganic phosphates with visible photoluminescence of Eu³⁺ and Dy³⁺ ions. Copyright © 2015 John Wiley & Sons, Ltd.     

Biosorption of Chromium,Copper, and Nickel Ions by Tamarindus Indica Fruit Nut Testa

Biosorption of chromium, copper, and nickel from aqueous solution by Tamarindus indica fruit nut testa (TFNT) in its pristine and acid-treated forms was studied under equilibrium and column-flow conditions. TFNT, a tannin-containing material, was characterized by energy dispersion x-ray fluorescence (EDXRF) and Fourier transform infrared (FTIR) spectral techniques and surface analysis. The effect of experimental variable parameters such as pH, concentration of metal ions, amount of adsorbent, and contact time on adsorption was investigated. Batch isothermal equilibrium data were analyzed on the basis of Langmuir and Freundlich adsorption isotherms. The kinetics of the adsorption process were studied in terms of Lagergren first-order kinetic model. The monolayer adsorption capacities of pristine and acid-treated forms of tamarind seed coat were found to be 44.8 and 77.5 mg/g for Cr(VI), 55.8 and 99.0 mg/g for Ni(II), and 84.7 and 85.4 mg/g for Cu(II) ions, respectively. The column-flow adsorption data were used to obtain breakthrough curves. The biosorbent loaded with the metal ions was regenerated using 1.0 M HCl and the regenerated bed was used for subsequent adsorption-desorption cycle.     

Optical properties of CaAl(SO4)2Br:RE (RE = Dy,Eu, Ce) novel phosphors

A new phosphor CaAl(SO₄)₂Br doped with Dy, Ce and Eu is reported. Rare earth (Dy, Eu and Ce)‐doped polycrystalline CaAl(SO₄)₂Br phosphors were prepared using a wet chemical reaction method and studied for X‐ray diffraction and photoluminescence (PL) characteristics. Dy³⁺ emission in the CaAl(SO₄)₂Br lattice was observed at 484 and 574 nm in the blue and yellow regions of the spectrum, which are assigned to ⁴ F_9/2 → ⁶H_15/2 and ⁴ F_9/2 → ⁶H_13/2 transitions of the Dy³⁺ ion, respectively. While the PL emission spectra of CaAl(SO₄)₂Br:Ce phosphor showed Ce³⁺ emission at 347 nm due to 5d → 4f transition of the Ce³⁺ ion. In a CaAl(SO₄)₂Br:Eu lattice, Eu³⁺ emissions were observed at 593 and 617 nm, coming from the ⁵D₀ → ⁷ F₁ and ⁵D₀ → ⁷ F₂ electron transitions, respectively. The PL study showed that the intensity of electric dipole transition at 617 nm dominates over that of magnetic dipole transition at 590 nm. The maximum PL intensity was obtained for a 1 mol% concentration of Eu³⁺ in CaAl(SO₄)₂Br host lattice. The results showed that the material may be a promising candidate as a blue‐, yellow‐ and red‐emitting phosphor. Copyright © 2013 John Wiley & Sons, Ltd.     

Syntheses, structures and photophysical properties of a series of Zn-Ln coordination polymers (Ln = Nd, Pr, Sm, Eu, Tb, Dy)

Six novel heterometallic Zn-Ln coordination polymers {[ZnLnCl(pydc)₂(H₂O)₆]·3H₂O}_n (Ln = Nd 1, Pr 2, Sm 3, Eu 4, Tb 5, Dy 6; pydc = pyridine-2,5-dicarboxylate) were synthesized by the hydrothermal method, and their structures were measured by the single-crystal X-ray diffraction. The IR and UV-Vis-NIR absorption spectra, and the luminescence spectra in the visible and near-infrared (NIR) regions of the six complexes were determined at room temperature. They possess the same crystal structure, and the Zn(II) and Ln(III) ions in each complex are bridged into 1D infinite chain by pyridine-2,5-dicarboxylates. Meanwhile, there are numerous hydrogen bonds which result in the 3D hydrogen bonding network in the crystal. In the visible and NIR regions, the emission spectra of the complexes show the characteristic bands of the corresponding Ln(III) ions, which are mainly attributed to the sensitization from the d-L-moiety to f-L-moiety after forming the Zn-Ln complexes. In this paper, we first report the Zn-Sm complex which can exhibit the emission bands of Sm(III) in the NIR region, and discuss the sensitization from the d-L-moiety to f-L-moiety on the basis of the different characteristics of levels for different Ln(III) ions.     

Biosorption of chromium, copper, manganese and zinc by Pseudomonas aeruginosa AT18 isolated from a site contaminated with petroleum

The study describes the sorption of Cr, Cu, Mn and Zn by Pseudomonas aeruginosa AT18 isolated from a site contaminated with petroleum and heavy metals. The concentrations studied were 50, 49, 60 and 70 (mg L(-1)) for Cr, Cu, Mn and Zn, respectively. The solution pH and ionic strength were very important factors in the metal biosorption performance and the biosorption capacity of P. aeruginosa AT18 for Cr3+,Cu2+, Mn2+ and Zn2+. In aqueous solution, the biosorption increased with increasing pH in the range 5.46-7.72. The results obtained in the experimental assays show that P. aeruginosa AT18 has the capacity for biosorption of the metallic ions Cr3+, Cu2+ and Zn2+ in solutions, although its capacity for the sorption of manganese is low (22.39 mg Mn2+/g of biomass) in comparison to the Cr3+, Cu2+ and Zn2+ ions, as shown by the individual analyses. However, 20% of the manganese was removed from an initial concentration of 49.0 mg L(-1), with a Qm value similar to that obtained in solutions containing mixtures of Cr3+, Cu2+, Mn2+and Zn2+. The chromium level sorbed by P. aeruginosa AT18 biomass was higher than that for Cu, Mn and Zn, with 100% removal in the pH range 7.00-7.72 and a Qm of 121.90-200.00 mg of Cr3+/g of biomass. The removal of Cr, Cu and Zn is also a result of precipitation processes.     

Mechanoluminescence of SrAl2O4:Eu,Dy nanophosphors induced by low impact velocity

The present paper reports the impulsive excitation of mechanoluminescence (ML) in Sr_0.97Al₂O₄:Eu_0.01,Dy_0.02 nanophosphors prepared using a combustion technique. The phosphors are characterized using X‐ray powder diffraction (XRD), high‐resolution transmission electron microscopy (HRTEM) and photoluminescence (PL). The XRD results show that the samples exhibit a monoclinic α‐phase in the crystal structure. The space group of SrAl₂O₄:Eu,Dy nanophosphors is monoclinic P2₁. The PL and ML spectra of SrAl₂O₄:Eu,Dy nanophosphors are excited using light with a wavelength of 365 nm and emission is found at 516 nm. The prepared nanophosphors exhibits an intense ML that can be seen in daylight with the naked eye. When a sample powder is deformed impulsively by the impact of a moving piston, the ML intensity initially increases linearly with time, attains a peak value, I_m, at time t_m, and then decreases with time. The peak ML intensity, I_m, and total ML intensity, I_T, increase linearly with applied pressure and impact velocity. The ML intensity decreases with successive impacts of load onto the phosphors, and the diminished ML intensity can be approximately recovered by UV irradiation. The activation energy using thermoluminescence is found to be 0.57 eV for SrAl₂O₄:Eu,Dy nanophosphors. Copyright © 2016 John Wiley & Sons, Ltd.     

Biosorption of cadmium,cobalt, nickel,and strontium by aBacillus simplex strain isolated from the vadose zone

A subsurface Gram-positive, endospore-forming, filamentous bacterium, designated ZAN-044, was isolated from a depth of 96.2 m in the vadose zone of the Hanford Site in Washington State. A phylogenetic analysis of the 16S rRNA gene sequence of strain ZAN-044 revealed it to be 99.5% similar toBacillus simplex strain DSM 1321, indicating that they may be members of the same species.B. simplex ZAN-044 was studied along withBacillus subtilis 168, andEscherichia coli K-12 (AB264), two well-characterized metal-sorbing bacteria, for the binding of Cd²⁺, Co²⁺, Ni²⁺, and Sr²⁺. There was rapid (less than 1 h) uptake of 1 M metal by the three bacteria in the order Cd>NiCo>Sr. Binding followed a saturation isotherm at cation concentrations from 0.1 M to 1 mM. Cation binding was pH-dependent, with less binding at low pH.B. simplex ZAN-044 bound more metal thanB. subtilis orE. coli, demonstrating that subsurface microorganisms can remove significant quantities of metals from solution and may be able to influence radionuclide and metal transport in the subsurface.     

Effect of pH on the biosorption of nickel and other heavy metals by Pseudomonas fluorescens 4F39

Accumulation of heavy metals by Pseudomonas fluorescens 4F39 was rapid and pH-dependent. The affinity series for bacterial accumulation of metal cations decreased in the order Ni>>Hg>U>>As>Cu>Cd>Co>Cr>Pb. Metal cations were grouped into those whose accumulation increased as the pH increased, with a maximum accumulation at the pH before precipitation (Ni, Cu, Pb, Cd, Co), and those whose maximum accumulation was not associated with precipitation (Cr, As, U, Hg). High Ni²⁺ accumulation was studied. Electron microscopy indicated that at pH 9, Ni²⁺ accumulated on the cell surface as needle and hexagon-like precipitates, whose crystalline structure was confirmed by electron diffraction analysis and corresponded to two different orientations of the nickel hydroxide crystals. Crystals on cells showed marked anisotropy by X-ray powder diffraction, which differentiated them from crystals observed in nickel solution at pH 10 and 11 and from commercial nickel hydroxide. Nickel biosorption by Pseudomonas fluorescens 4F39 was a microprecipitation consequence of an ion exchange. Journal of Industrial Microbiology & Biotechnology (2000) 24, 146–151. Received 22 June 1999/ Accepted in revised form 04 December 1999     

Synthesis, crystalline structure and photoluminescence investigations of the new trivalent rare earth complexes (Sm, Eu and Tb) containing 2-thiophenecarboxylate as sensitizer

New complexes with the general formula [RE(TPC)₃ · (H₂O)₂], where RE=Eu³⁺, Sm³⁺, Gd³⁺, Tb³⁺ and TPC=2-thiophenecarboxylate, have been prepared and investigated by photoluminescence spectroscopy. These compounds were characterized by complexometric titration, elemental analyses and infrared spectroscopy. The X-ray crystal structure has been determined for the [Eu(TPC)₃ · (H₂O)₂] compound, indicating that this complex is in dimeric form bridged by two carboxylate ions with monoclinic crystal system and space group P2₁/n. The coordination polyhedron can be described as a distorted square antiprism, where six oxygen atoms belong to the TPC ligand and two oxygen atoms belong to the water molecules, with site symmetry close to C_2v. The theoretical value of the intensity parameter , which is in agreement with the experimental one, indicates that the Eu³⁺ ion is in a highly polarizable chemical environment. Based on the luminescence spectra, the energy transfer from the ligand triplet state (T) of TPC to the excited levels of the Eu³⁺ ion is discussed. The emission quantum efficiency of the ⁵D₀ emitting level of the Eu³⁺ ion was also determined. In the case of the Tb³⁺ ion, the photoluminescence data show the high emission intensity of the characteristic transitions ⁵D₄ → ⁷F_J (J=0-6), indicating that the TPC ligand is a good sensitizer. It is also noticed that the complexes with the Eu³⁺ and Tb³⁺ ions are more luminescent than the complex with the Sm³⁺ ion.     

Adsorption of several actinide (Th,U) and lanthanide (La,Eu, Yb) ions by Mycobacterium smegmatis

Adsorption measurements of several actinide [thorium (Th), uranium (U)] and lanthanide [lanthanum (La), europium (Eu), ytterbium (Yb)] cations by Mycobacterium smegmatis showed that sorption kinetics followed a three-phase pattern. For 5% (w/w) bacterial suspensions at pH 1, maximum cation biosorption per gram dry biomass corresponded to 170 mol Th⁴⁺ and 187 mol UO _inf2 ^sup2+ . Adsorption of all cations studied obeyed the Brunauer-Emmett-Teller isotherm, which assumes multilayer binding at constant energy. Plots for the Scatchard model showed the existence of at least two types of cation complexation site, with strong and weak affinity and negative cooperation. Th⁴⁺ was preferentially adsorbed with respect to the other cations, although all species appeared to compete for the same sites independently of bacterial viability. Adsorption of these cations was accompanied by partial release of magnesium from the cell wall, indicating that exchange reactions occurred at magnesium (Mg)-bonding sites.     

Molecular cloning, characterisation and ligand-bound structure of an azoreductase from Pseudomonas aeruginosa

The gene PA0785 from Pseudomonas aeruginosa strain PAO1, which is annotated as a probable acyl carrier protein phosphodiesterase (acpD), has been cloned and heterologously overexpressed in Escherichia coli. The purified recombinant enzyme exhibits activity corresponding to that of azoreductase but not acpD. Each recombinant protein molecule has an estimated molecular mass of 23,050 Da and one non-covalently bound FMN as co-factor. This enzyme, now identified as azoreductase 1 from Pseudomonas aeruginosa (paAzoR1), is a flavodoxin-like protein with an apparent molecular mass of 110 kDa as determined by gel-filtration chromatography, indicating that the protein is likely to be tetrameric in solution. The three-dimensional structure of paAzoR1, in complex with the substrate methyl red, was solved at a resolution of 2.18 A by X-ray crystallography. The protein exists as a dimer of dimers in the crystal lattice, with two spatially separated active sites per dimer, and the active site of paAzoR1 was shown to be a well-conserved hydrophobic pocket formed between two monomers. The paAzoR1 enzyme is able to reduce different classes of azo dyes and activate several azo pro-drugs used in the treatment of inflammatory bowel disease (IBD). During azo reduction, FMN serves as a redox centre in the electron-transferring system by mediating the electron transfer from NAD(P)H to the azo substrate. The spectral properties of paAzoR1 demonstrate the hydrophobic interaction between FMN and the active site in the protein. The structure of the ligand-bound protein also highlights the pi-stacking interactions between FMN and the azo substrate.     

Crystal structure and magnetic properties of lanthanide-trans-2-butenoate polymers (Ln = La, Pr, Dy, Ho)

Four lanthanide coordination polymers formulated as {[La₃L₉(H₂O)₃]EtOH · H₂O}_n1, {[Pr₂L₆(H₂O)₂]HL · H₂O}_n2, {[Dy₂L₆(H₂O)]0.5HL · H₂O}_n3 and {[Ho₂L₆(H₂O)]0.5HL · H₂O}_n4 and HL = trans-2-butenoic acid have been synthesized from the corresponding pure lanthanide oxide and HL acid in water at pH 3. The compounds were characterized by chemical analysis, IR spectroscopy, thermogravimetry, variable-temperature magnetic susceptibility and single crystal X-ray diffraction studies. A common feature in these materials is the presence of two differentiated lanthanide nodes linked by carboxylates into extended chains. These are further connected by inter- and intra-molecular hydrogen-bonds involving ligand and solvate molecules. Weak ferromagnetic interactions appear to be operative in the Dy material.     

铜绿假单胞菌中III型分泌系统受Rhl和PQS群体感应系统调节

摘要：【目的】研究铜绿假单胞菌中群体感应系统（Quorum sensing, QS）与III型分泌系统（Type III secretion system, T3SS）的关系。【方法】通过基因敲除的方法破坏铜绿假单胞菌QS系统相关基因,将T3SS相关基因exoS、exoY、exoT、exsD-pscA-L启动子-报道子luxCDABE融合体整合到野生型菌株及QS系统突变菌株的染色体组上,通过检测启动子活性,比较这些基因在不同菌株中的表达情况。【结果】研究结果表明,T3SS中的exoS与exoT在pqsR基因突变体中的表达有明显的增强,Rhl系统对这四种基因的表达具有抑制作用,而Las系统存在与否对T3SS基本没有影响。【结论】铜绿假单胞菌中的Rhl系统和奎诺酮信号（Pseudomonas Quinolone Signal, PQS）系统对T3SS相关基因的表达具有重要的调节作用。