LINC01579-204 involved in the development of Hirschsprung's disease maybe by regulating the expression of miR-203a-3p and NEFL.

BACKGROUND: Hirschsprung's disease (HD) is a rare congenital digestive tract malformation in children. Roles of long non-coding RNAs (lncRNAs) are highlighted in various human diseases. However, knowledge on lncRNAs in HD is still limited. METHODS: The profile of lncRNAs in 8 pairs of normal and stenosed intestinal tissue of HD patients were obtained using microarray analysis. Base on bioinformatics analysis, the level of selected LINC01579-204, NEFL and miR-203a-3p was detected by qRT-PCR in 36 pairs of normal and stenosed intestinal tissue of HD patients. Then the predictive accuracy of LINC01579-204, miR-203a-3p and NEFL level to evaluate the progression of HD patients was analyzed with receiver operating characteristic curve (ROC). RESULTS: A total of 90 differentially expressed lncRNAs were detected in normal and stenosed intestinal tissue of HD patients (|fold change| ≥ 1.5, p < 0.05). The level of LINC01579-204 and NEFL decreased and miR-203a-3p increased significantly in 36 pairs of stenosed intestinal tissue of HD patients compared to the control. A notable positive correlation was identified between LINC01579-204 and NEFL (r = 0.9681, p < 0.0001). Areas under the ROC curve of the LINC01579-204, miR-203a-3p and NEFL signature were 0.715, 0.777 and 0.829, respectively. CONCLUSIONS: LINC01579-204, miR-203a-3p, and NEFL are predicted to play important roles in the progression of HD. LINC01579-204, miR-203a-3p and NEFL had a significant overall predictive ability to identify progression of HD patients. The novel experimental and bioinformatic results achieved in this study may provide new insights into the molecular of HD.

Efficient removal of per- and polyfluoroalkyl substances from biochar composites: Cyclic adsorption and spent regenerant degradation.

In order to solve the problem of efficient desorption of per- and polyfluoroalkyl substances (PFAS) and regeneration of adsorbents, a novel biochar composite was prepared based on the quaternary ammonium groups and hydrophobicity of sulfobetaine polymer, which can be used for the efficient removal of various PFASs and has great regeneration ability. Through adsorption, regeneration and degradation experiment, the comprehensive effect of the novel biochar composite on the whole process of removal of PFAS was systematically investigated. The results showed that the maximum adsorption capacity of PFOS, PFOA, PFBS, and PFBA reached 634 mg/g, 536 mg/g, 301 mg/g and 264 mg/g, respectively. The adsorption process involved hydrophobicity, electrostatic, pore diffusion and complexation. The NaI + NaOH solution was used at 50 °C to achieve efficient regeneration of the adsorbent, which can be recycled more than 4 times. When the vacuum-ultraviolet (VUV)/sulfite reduction system was used for deep degradation of the regenerated solution, the effect of hydrated electrons on PFAS was enhanced due to the inclusion of NaI and NaOH in the regeneration reagent, resulting in an increase in the degradation efficiency (89.1%-99.9%) and defluorination efficiency (63.3%-84.1%). Based on the performance of BC-P(SB-co-AM) and the treatment efficiency of PFAS, the design idea of the whole process treatment technology of PFAS proposed in this work is expected to hold great promise in environmental applications. This work provides a novel idea and system for the efficient adsorption removal and desorption of PFAS, and subsequent deep degradation.

Developing self-floating N-defective graphitic carbon nitride photocatalyst for efficient photodegradation of Microcystin-LR under visible light.

The frequent occurrence of algal blooms in water bodies leads to a significant accumulation of microcystin-LR (MC-LR). In this study, we developed a porous foam-like self-floating N-deficient g-C3N4 (SFGN) photocatalyst for efficient photocatalytic degradation of MC-LR. Both the characterization results and DFT calculations indicate that the surface defects and floating state of SFGN synergistically enhance light harvesting and photogenerated carrier migration rate. The photocatalytic process achieved a nearly 100 % removal rate of MC-LR within 90 min, while the self-floating state of SFGN maintained good mechanical strength. ESR and radical capture experiments revealed that the primary active species responsible for the photocatalytic process was OH. This finding confirmed that the fragmentation of MC-LR occurs as a result of OH attacking the MC-LR ring. LC-MS analysis indicated that majority of the MC-LR molecules were mineralized into small molecules, allowing us to infer possible degradation pathways. Furthermore, after four consecutive cycles, SFGN exhibited remarkable reusability and stability, highlighting the potential of floating photocatalysis as a promising technique for MC-LR degradation.

The reconstitution of reed cellulose by the hydrothermal carbonization and acid etching to improve the performance of photocatalytic degradation of antibiotics.

As an economical and environment-friendly material, hydrothermal carbonation carbon (HTCC) has been widely used in the field of adsorption and catalysis. Previous studies mainly used glucose as raw material to prepare HTCC. Cellulose in biomass can be further hydrolyzed into carbohydrate; however, there are few reports on the direct preparation of HTCC from biomass and the relevant synthesis mechanism is unclear. In this study, HTCC with efficient photocatalytic performance was prepared from reed straw using dilute acid etching under hydrothermal conditions and was used for the degradation of tetracycline (TC). The mechanism of photodegradation of TC by HTCC was systematically elucidated through various characterization techniques and density functional theory (DFT) calculations. This study provides a new perspective on the preparation of green photocatalysts and demonstrates their promising application in environmental remediation.

Preparation of reed-based hydrothermal carbonized carbon photocatalyst and effective degradation of methylene blue and tetracycline.

Hydrothermal carbonation carbon (HTCC) is a promising semiconductor material for the photocatalytic degradation of pollutants. However, the poor charge transfer capability of HTCC and the unclear mechanism of photocatalysis limit its practical application. In this study, a novel Z-type heterojunction photocatalyst of silver carbonate (Ag2CO3) and HTCC (Ag2CO3/HTCC) was developed for the degradation of methylene blue (MB) and tetracycline (TC) from wastewater using a hydrothermal- coprecipitation method. Compared to Ag2CO3 and HTCC, 40% Ag2CO3/HTCC had excellent photocatalytic activity and stability. The free radical scavenger experiments showed that •O2- and h+ were the main substances for the degradation of MB and TC. The intermediates formed during the photodegradation were identified by HPLC-MS, and a possible mechanism and pathway for the degradation of MB and TC by Ag2CO3/HTCC was proposed. This study provides a new idea for the synthesis of Z-type HTCC heterojunction with a high-photocatalytic efficiency and its photocatalytic mechanism.

In Situ Coupling Carbon Defective C3N5 Nanosheet with Ag2CO3 for Effective Degradation of Methylene Blue and Tetracycline Hydrochloride.

The development of novel catalysts for degrading organic contaminants in water is a current hot topic in photocatalysis research for environmental protection. In this study, C3N5 nanosheet/Ag2CO3 nanocomposites (CNAC-X) were used as efficient photocatalysts for the visible-light-driven degradation of methylene blue (MB), and tetracycline hydrochloride (TC-HCl) was synthesized for the first time using a simple thermal oxidative exfoliation and in situ deposition method. Due to the synergistic effect of nanosheet structures, carbon defects, and Z-scheme heterojunctions, CNAC-10 exhibited the highest photocatalytic activity, with photodegradation efficiencies of 96.5% and 97.6% for MB (60 mg/L) and TC-HCl (50 mg/L) within 90 and 100 min, respectively. The radical trapping experiments showed that ·O2- and h+ played major roles in the photocatalytic effect of the CNAC-10 system. Furthermore, intermediates in the photodegradation of MB and TC-HCl were investigated to determine possible mineralization pathways. The results indicated that C3N5 nanosheet/Ag2CO3 photocatalysts prepared in this work could provide an effective reference for the treatment of organic wastewater.

Geniposide ameliorated dexamethasone-induced endoplasmic reticulum stress and mitochondrial apoptosis in osteoblasts.

ETHNOPHARMACOLOGICAL RELEVANCE: Eucommia ulmoides Oliver has been traditionally used for treatment of various diseases, including osteoporosis, knee pain, and paralysis. The extract of Eucommia ulmoides has been reported to stimulate the bone formation and suppress the bone resorption, leading to protection against osteoporosis (OP). Geniposide (GEN) has been considered as one of the effective compounds responsible for the therapeutic efficacy of Eucommia ulmoides against OP. AIM OF THE STUDY: To explore whether GEN protected against dexamethasone (DEX)-induced osteoporosis (OP) by activating NRF2 expression and inhibiting endoplasmic reticulum (ER) stress. MATERIALS AND METHODS: The DEX-induced rat OP models were duplicated. The pathological changes were examined by histological/immunohistochemical evaluation and micro-computed tomography (micro-CT) assessment. Apoptosis was detected by a flow cytometer. Mitochondrial Ca2+ concentrations and mitochondrial membrane potential were detected. Western blot assays were used to detect the protein expression. RESULTS: GEN effectively reversed DEX-induced pathological changes of trabecular bone in rats. In addition, the DEX-increased expression of ATF4/CHOP was also ameliorated. In MC3T3-E1 cells, DEX promoted endoplasmic reticulum (ER) stress and mitochondrial apoptosis. Inhibition of ER stress abolished the induction of apoptosis by DEX. Similarly, GEN significantly ameliorated DEX-induced mitochondrial apoptosis. The possible underlying mechanism might be associated with the pharmacological effects of GEN on activating the expression of NRF2 and alleviating ER stress in DEX-treated MC3T3-E1 cells. CONCLUSION: GEN ameliorated DEX-induced ER stress and mitochondrial apoptosis in osteoblasts.

A novel preparation of S-nZVI and its high efficient removal of Cr(VI) in aqueous solution.

The chitosan-stabilized biochar supported S-nZVI (CS@BC/S-nZVI) composite with low aggregation and superior antioxidation were successfully synthesized by liquid-phase reduction method for the outstanding removal of Cr(VI) from wastewater and characterized by SEM, BET, FTIR, XRD, and XPS. The optimized synthesis parameters of CS@BC/S-nZVI were determined as a 0.14 molar ratio of S/Fe and a 0.25 mass ratio of BC/Fe. The CS@BC/S-nZVI possessed a specific surface area of 199.246 m2/g and an average pore size and pore volume of 1.186 nm and 0.272 cc/g. The CS@BC/S-nZVI could remain reductive activity after Cr(VI) removal and present a remarkable tolerance to the coexisting ions during Cr(VI) removal. The adsorption data were fitted well by the pseudo-second order model and the Langmuir model. The removal of Cr(VI) by CS@BC/S-nZVI was an exothermic process with prominent Cr(VI) removal capacities of 244.07 mg/g at 120 min and 221.84 mg/g at 15 min at 25 â„ƒ. Further mechanism analysis proved that the binding of Cr(VI) to CS@BC/S-nZVI was mainly a synergistic effect of reduction and electrostatic attraction. Overall, these findings shed new light on the research of a novel S-nZVI compound and revealed the potential practical application of CS@BC/S-nZVI in the future heavy metal removal from wastewater.

A review: Research progress on microplastic pollutants in aquatic environments.

The ubiquitous problems of microplastics in waters are receiving global attention as microplastics can harm aquatic organisms, and finally can accumulate in the human body through biological chain amplification. In addition, microplastics act as a carrier capable of carrying heavy metals, organics, which form complex pollutants. These new combinations of pollutants, once ingested by aquatic organisms, are amplified through the food chain and can have unpredictable ramifications for aquatic organisms and human beings. Therefore, human beings are not only the source of plastic pollution, but also the sink of microplastic pollution. Therefore, this study reviews the source and distribution of microplastics, and their combined ability with heavy metals, antibiotics, and persistent organic pollutants in aquatic environments. Furthermore, it describes the interaction between aquatic organisms and microplastics. Finally, some suggestions are put forward to promote the sustainable application of microplastics. This work provides theoretical guidance for combining microplastics with other pollutants in water, and the accumulation of microplastics in food chain.

Coupling of kenaf Biochar and Magnetic BiFeO3 onto Cross-linked Chitosan for Enhancing Separation Performance and Cr(VI) Ions Removal Efficiency.

Cr(VI) contamination has posed great threat to both the ecosystem and human health for its carcinogenic and mutagenic nature. A highly effective adsorbent for the removal of Cr(VI) was prepared and its adsorption mechanism was thoroughly discussed in this study. In detail, magnetic BiFeO3 and kenaf biochar were loaded on cross-linked chitosan to obtain chitosan-kenaf biochar@BiFeO3 (CKB) for improving adsorption capacity towards Cr(VI). The adsorption process of Cr(VI) onto CKB was evaluated as a function of the pH, the existence of competing ions, the initial concentration of Cr(VI) and contact time. The results show that CKB exhibits the highest adsorption capacity under the optimal pH 2.0. The presence of competing ions such as Ca2+, NO3-, SO42-, and Cl- decreases the adsorption capacity; among them, Ca2+ and NO3- show the greatest hindrance. By studying the effect of initial Cr(VI) concentration on the adsorption capacity, it was found that CKB in the solution was enough to remove Cr(VI) for all treatments (10-200 mg/L). The adsorption experimental data were well fitted with pseudo-first-order model, suggesting that chemisorption is not the dominant rate-limiting step. Freundlich isotherm model can better explain the adsorption process, indicating a non-ideal adsorption towards Cr(VI) on a heterogeneous surface of CKB. A 25-1 Fractional Factorial Design (FFD) showed that pH and initial concentration of Cr(VI) have significant influence on Cr(VI) adsorption in our reaction system. In general, excellent adsorption efficiency of CKB indicates that it may be a good candidate for the remediation of Cr(VI)-contaminating wastewater.

Effects of peat on plant growth and lead and zinc phytostabilization from lead-zinc mine tailing in southern China: Screening plant species resisting and accumulating metals.

In order to investigate the toxicity-resistance of eighteen Chinese native plants in lead (Pb)-zinc (Zn) mine tailings, we categorized their resistance to Pb and Zn, and tested their potential for phytoremediation effectiveness of Pb and Zn. Fourteen woody plant species belonging to 12 families, and 4 herbaceous species belonging to 4 families, were grown in pots with mixtures of 100% tailing +0% peat (CK), 90% tailing +10% peat (A1), and 80% tailing + 20% peat (A2), respectively. Plant height and biomass, chlorophyll content, and Pb and Zn contents of non-rhizosphere spoil mixtures and plant tissues were measured. Fifteen of the plants grew in all three spoil mixtures. Both A1 and A2 had higher plant height and biomass increment and chlorophyll contents than CK. The content of Pb and Zn in plant shoots and roots was CK > A1 > A2. The value of BCF less than 0.1, compared to 1, was a more precise classification basis for plants excluding metals. Screening for Pb and Zn resistant plants and their bioremediation potential produced the following candidate species: Sapium sebiferum, Salix matsudana, Hibiscus cannabinus, Corchorus capsularis, Ricinus communis, and Populus nigra. These species were highly Pb and Zn tolerant species, with notable growth characteristics and capacities to bioaccumulate Pb and Zn from the mine tailings. Compared to CK, the removal of Pb and Zn from non-rhizosphere spoil increased by an average of 9.64% and 9.6%, respectively in A1, but decreased in A2. The results indicated candidate species and 10% peat addition in the tailing were significant in phytoremediation of Pb and Zn regarding environmental safety.

Exogenous spermidine elevating cadmium tolerance in Salix matsudana involves cadmium detoxification and antioxidant defense.

In this study, exogenous spermidine role on Salix matsudana tolerance to cadmium was evaluated. Spermidine and cadmium presented antagonistic effects on the biomass, copper and zinc concentrations in S. matsudana. cadmium mainly distributed in the cell wall of subcellular fraction; 46.97%-60.43% of cadmium existed in a sodium chloride-extracted form. Cadmium contents in roots, leaves, and twigs ranged from 2002.67 to 3961.00, 111.59 to 229.72, and 102.56 to 221.27 mg/kg, respectively. Spermidine application elevated cadmium concentrations in the roots, cuttings, and cell wall and the ratio of deionized water-extracted cadmium, but decreased cadmium levels in the twigs and leaves and the fractions of cadmium extracted by ethanol and sodium chloride, respectively. Putrescine and malondialdehyde were important indicators of cadmium-induced oxidative damage. Exogenous spermidine alleviated the accumulation of superoxide anion, hydrogen peroxide, malondialdehyde via promoting the levels of spermidine, soluble protein, superoxide dismutase, reductive ascorbate, glutathione reductase, and glutathione peroxidase in S. matsudana leaves under the corresponding cadmium stress. The results indicated that S. matsudana was a candidate for cadmium rhizoremediation and extraction in leaves; the spermidine application enhanced the cadmium tolerance of S. matsudana through promoting cadmium accumulation in roots, cell wall, and less bioactive chemical forms and the antioxidative ability.

Effects of GGCX overexpression on anterior cruciate ligament transection-induced osteoarthritis in rabbits.

Effective therapeutic methods for osteoarthritis (OA) are lacking. γ­glutamyl carboxylase (GGCX) is a key enzyme that regulates carboxylation of cartilage matrix Gla protein (MGP). Whether GGCX overexpression protects against OA remains unknown. The aim of the present study was to explore the effects of GGCX overexpression on anterior cruciate ligament transection (ACLT)­induced OA and its mechanisms in Japanese white rabbits. ACLT surgery was used to establish an OA model in rabbits. A total of 48 rabbits were randomly divided into 4 groups: Sham, OA model + GGCX overexpression plasmid, OA model + saline and OA model + empty vector. The expression of uncarboxylated MGP (ucMGP), carboxylated MGP (cMGP), matrix metalloproteinase (MMP)­13, collagen type X, collagen type II, tumor necrosis factor (TNF)­α and interleukin (IL)­1ß were detected by ELISA, immunohistochemistry, reverse transcription­quantitative polymerase chain reaction and western blotting. Morphological changes to tibial cartilage were assessed by Giemsa and safranin O­fast green staining, respectively. Compared with the Sham control, GGCX expression was significantly decreased in the OA Model group. GGCX expression was increased by injection of a lentivirus­carried overexpression plasmid that encoded GGCX. GGCX overexpression ameliorated ATLC­induced damage in articular cartilage. OA Model rabbits exhibited significantly decreased expression levels of cMGP and collagen type II, and increased expression of ucMGP, collagen type X, MMP­13, IL­1ß and TNF­α. Notably, these expression levels were reversed by GGCX overexpression in OA Model rabbits. Results from the present study indicated that GGCX expression was decreased in OA Model rabbits, whereas overexpression of GGCX was able to promote carboxylation of MGP, reduce inflammation, decrease MMP­13 expression and regulate collagen expression. The results also indicated that GGCX may serve as a therapeutic target for OA.

Single and competitive adsorption of Cd(II) and Pb(II) from aqueous solution by activated carbon prepared with Salix matsudana Kiodz.

In this study, Salix matsudana activated carbon (SAC) was prepared by phosphoric acid activation, and the adsorption characteristics of Cd(II) and Pb(II) on SAC in single- and double-component solutions were investigated. In both systems, the adsorption capacities of both ions on SAC increased with the increasing initial pH value and temperature in the solutions, and the adsorption equilibrium was approached at 10 min. The adsorption process was spontaneous, endothermic, and depicted well by the pseudo-second-order adsorption model, and the equilibrium adsorption fitted reasonably well with the Langmuir isotherm. The maximum adsorption capacity (Qm) of Cd(II) and Pb(II) was 58.48 and 59.01 mg/g, respectively, in the single-element systems. However, it reduced to 25.32 and 31.09 mg/g, respectively, in the double-element system. The physicochemical property analysis showed that the specific surface area, total pore volume, and average pore diameter of SAC was 435.65 m2/g, 35.68 mL/g, and 3.86 nm, respectively. The SAC contained groups of -OH, C = O, and P = O. Results suggest that SAC had a good performance for the adsorption of Cd(II) and Pb(II) from solution, and the adsorption selectivity sequence was Pb(II) > Cd(II).

Adsorption of hexavalent chromium from aqueous solution on raw and modified activated carbon.

Hexavalent chromium [Cr(VI)] is toxic and readily adsorbed by some adsorbents; therefore, its removal from wastewater is extremely important. Batch adsorption of Cr(VI) from aqueous solution using raw and acid-modified activated carbon was investigated in this study. The Cr(VI) sorption was found to be dependent on pH, contact time, initial concentration of solution, adsorbent dose, and temperature. The maximum efficiencies of Cr(VI) removal were 97.67 and 99.87% for activated carbon (AC0) and modified activated carbon (AC1), respectively. The maximum adsorption capacity was found to be 4.75 and 5.95 mg/g for AC0 and AC1, respectively. Thermodynamic parameters indicate that the adsorption process was endothermic and spontaneous in nature. Freundlich adsorption isotherm model was fitted well the equilibrium data for both adsorbents. The Cr(VI) uptake by AC0 and AC1 followed pseudo first-order and second-order kinetics, but was best described by the pseudo second-order rate model. The results also showed that both film diffusion and intraparticle diffusion were concurrently operating, but that intraparticle diffusion controlled the adsorption mechanism.

Electroanalytical determination of acetaminophen using nano-TiO(2)/polymer coated electrode in the presence of dopamine.

We report a new method for selective determination of acetaminophen (AP) in physiological condition. A new hybrid film modified electrode was fabricated using inorganic semiconducting nano-TiO(2) particles and redox active polymer. Redox polymer, poly(acid yellow 9) (PAY) was electrochemically deposited onto nano-TiO(2) coated glassy carbon (GC) electrode. Surface characterizations of modified electrode were investigated by using atomic force microscope and scanning electron microscope. The PAY/nano-TiO(2)/GC hybrid electrode shows stable redox response in the pH range 1-12 and exhibited excellent electrocatalytic activities towards AP in 0.1M phosphate buffer solution (pH 7.0). Consequently, a simple and sensitive electroanalytical method was developed for the determination of AP. The oxidation peak current was proportional to the concentration of acetaminophen from 1.2 x 10(-5) to 1.20 x 10(-4)M and the detection limit was found to be 2.0 x 10(-6)M (S/N=3). Possible interferences were tested and evaluated that it could be possible to selective detection of AP in the presences of dopamine, nicotinamide adenine dinucleotide (NADH), ascorbic acid and uric acid. The proposed method was used to detect acetaminophen in commercial drugs and the obtained results are satisfactory.

Zinc oxide/redox mediator composite films-based sensor for electrochemical detection of important biomolecules.

Electrochemical oxidation of serotonin (SN) onto zinc oxide (ZnO)-coated glassy carbon electrode (GCE) results in the generation of redox mediators (RMs) that are strongly adsorbed on electrode surface. The electrochemical properties of zinc oxide-electrogenerated redox mediator (ZnO/RM) (inorganic/organic) hybrid film-coated electrode has been studied using cyclic voltammetry (CV). The scanning electron microscope (SEM), atomic force microscope (AFM), and electrochemical techniques proved the immobilization of ZnO/RM core/shell microparticles on the electrode surface. The GCE modified with ZnO/RM hybrid film showed two reversible redox peaks in acidic solution, and the redox peaks were found to be pH dependent with slopes of -62 and -60 mV/pH, which are very close to the Nernst behavior. The GCE/ZnO/RM-modified electrode exhibited excellent electrocatalytic activity toward the oxidations of ascorbic acid (AA), dopamine (DA), and uric acid (UA) in 0.1M phosphate buffer solution (PBS, pH 7.0). Indeed, ZnO/RM-coated GCE separated the anodic oxidation waves of DA, AA, and UA with well-defined peak separations in their mixture solution. Consequently, the GCE/ZnO/RMs were used for simultaneous detection of DA, AA, and UA in their mixture solution. Using CV, calibration curves for DA, AA, and UA were obtained over the range of 6.0 x 10(-6) to 9.6 x 10(-4)M, 1.5 x 10(-5) to 2.4 x 10(-4)M, and 5.0 x 10(-5) to 8 x 10(-4)M with correlation coefficients of 0.992, 0.991, and 0.989, respectively. Moreover, ZnO/RM-modified GCE had good stability and antifouling properties.

Poly(4-amino-1-1'-azobenzene-3, 4'-disulfonic acid) coated electrode for selective detection of dopamine from its interferences.

Here, we described a new method for electrochemically selective detection of dopamine (DA). In this report, for the first time, electrochemical polymerization of 4-amino-1-1'-azobenzene-3,4'-disulfonic acid (acid yellow 9 dye (AY)) was carried out onto the surface of glassy carbon (GC) electrode and indium tin oxide coated electrode (ITO) from acidic solution containing AY monomers. A polymerized film of acid yellow on the surface of a glassy carbon electrode was characterized by cyclic voltammetry (CV). The redox response of the poly(AY) film on the GC electrode showed a couple of redox peak in 0.1M sulfuric acid solution and the pH dependent peak potential was -58mV/pH which was close to the Nernst behavior. The poly(AY) film-coated GC electrode (GC/PAY) exhibited excellent electrocatalytic activity towards the oxidations of dopamine (DA) in 0.1M phosphate buffer solution (PBS, pH 7.0) and increased the anodic peak current three time higher than bare GC electrode. GC/PAY did not reduce the considerable overpotential for oxidation of DA when compare to bare GC electrode. However, in contrast to other polymer modified electrode, due to the strong negatively charged back bone of poly(AY) highly repelled the important interference of DA, such as ascorbic acid (AA), uric acid (UA) and reduced form of nicotinamide adenine dinucleotide (NADH) in 0.1M PBS (pH 7.0) and did not showed any response for oxidation of these interferences. This behavior makes the GC/PAY for selective detection of DA in the presence of higher concentrations AA, UA and NADH. Using differential pulse voltammetry the calibration curves for DA were obtained over the range of 1-100muM with good selectivity and sensitivity. The proposed method provides a simple method for selective detection of DA from its interferences.

Enhancing effect of iron on chromate reduction by Cellulomonas flavigena.

Cr(VI) is considerably toxic and the detoxification of Cr(VI) is of great importance. This study investigated the effect of iron on Cr(VI) reduction by Cellulomonas flavigena. The results demonstrated that addition of FeCl3 or lepidocrocite promoted Cr(VI) reduction, with the reduction ratio of above 90 and 80% achieved, respectively, but addition of hematite did not lead to the increase of reduction ratio, which suggests that the effect of iron on chromate reduction appears different with the diversity of iron-oxides. In this study, the effect of initial Cr(VI) and Fe(III) concentration on Cr(VI) reduction and the change of pH value were also investigated. The reduction ratio increased with the increase of the initial concentration ratio of Fe(III)/Cr(VI). The value of pH gradually increased from 7.0 to around 9.0.

Experimental study on Cr (V) reduction by Pseudomonas aeruginosa.

Investigation on Cr(V) reduction was conducted using Pseudomonas aeruginosa. The study demonstrated that the Cr(VI) can be effectively reduced to Cr(III) by Pseudomonas aeruginosa. The effects of the factors affecting Cr(VI) reduction rate including carbon source type, pH, initial Cr(VI) concentration and amount of cells inoculum were thoroughly studied. Malate was found to yield maximum biotransformation, followed by succinate and glucose, with the reduction rate of 60.86%, 43.76% and 28.86% respectively. The optimum pH for Cr(VI) reduction was 7.0, with reduction efficiency of 61.71% being achieved. With the increase of initial Cr(VI) concentration, the rate of Cr(VI) reduction decreased. The reduction was inhibited strongly when the initial Cr(VI) concentration increased to 157 mg/L. As the amount of cells inoculum increased, the rate of Cr(VI) reduction also increased. The mechanism of Cr(VI) reduction and final products were also analysed. The results suggested that the soluble enzymes appear to be responsible for Cr(VI) reduction by Pseudomonas aeruginosa, and the reduced Cr(III) was not precipitated in the form of Cr(OH)3.