A simple and defined method to study calcification by isolated matrix vesicles effect of ATP and vesicle phosphatase

A simplified and defined system was developed to study in vitro calcium phosphate deposition by isolated matrix vesicles from rabbit growth plate cartilage, and to examine the relationship between vesicle phosphatase and calcium deposition. Samples of suspended vesicles containing 25 μg of protein, were incubated for 2 h in a ⁴⁵Ca-labelled solution with 2.2 mM Ca²⁺, 1.6 mM PO₄^3? and 1 mM ATP at pH 7.6. Calcium deposition was related to the amount of PO₄ hydrolysed by matrix vesicle phosphatases from ATP and other phosphate esters. Ca²⁺ or Mg²⁺ was found to stimulate matrix vesicle. ATPase, but the hydrolysis of phosphoenolpyruvate, glucose 1-phosphate, β-glycerol phosphate and AMP was independent of either cation. All of the above substrates supported calcium deposition. 1 mM ATP was more effective than 5 mM in supporting calcium deposition, indicating inhibition of mineralization at higher ATP concentrations. Our results suggest that, in addition to concentrating calcium, veiscles provide phosphate from ATP for mineral formation and at the same time remove the inhibitory effect of ATP upon mineral deposition.     

Uptake and accumulation of lead by roots,hypocotyls and shoots of Indian mustard [Brassica juncea (L.)]

The effects of different concentrations of lead nitrate on root, hypocotyl and shoot growth of Indian mustard (Brassica juncea var. Megarrhiza), and the uptake and accumulation of Pb²⁺ by its roots, hypocotyls and shoots were investigated in the present study. The concentrations of lead nitrate (Pb(NO₃)₂) used were in the range of 10⁻⁵–10⁻³ M. Root growth decreased progressively with increasing concentration of Pb²⁺ in solutions. The seedlings exposed to 10⁻³ M Pb exhibited substantial growth reduction and produced chlorosis. Brassica juncea has considerable ability to remove Pb from solutions and accumulate it. The Pb content in roots of B. juncea increased with increasing solution concentration of Pb²⁺. The amount of Pb in roots of plants treated with 10⁻⁴, 10⁻³ and 10⁻⁵ M Pb²⁺ were 184-, 37- and 6-fold, respectively, greater than that of roots of the control plant. However, the plants transported and concentrated only a small amount of Pb in their hypocotyls and shoots, except for the group treated with 10⁻³ M Pb²⁺.     

Resonance Scattering Spectral Detection of Trace Pb<Superscript>2+</Superscript> Using Aptamer-Modified AuPd Nanoalloy as Probe

The resonance scattering spectral probe for Pb²⁺ was obtained using aptamer-modified AuPd Nanoalloy. In the pH 7.0 Na₂HPO₄–NaH₂PO₄ buffer solution, the aptamer interacted with AuPd nanoalloy particles to form stable aptamer-AuPd nanoalloy probe for Pb²⁺ that is stable in high concentration of salt. The probe combined with Pb²⁺ ions to form a G-quadruplex and to release AuPd nanoalloy particles that aggregate to form big particles which led the resonance scattering (RS) intensity enhancing. The reaction solution was filtered by 0.15 μm membrane to obtain the filtration containing aptamer-AuPd nanoalloy probe that has strong catalytic effect on the electrodeless nickel particle plating reaction between Ni(II) and PO₂³⁻ that exhibited a strong RS peak at 508 nm. The RS intensity at 508 nm decreased when the Pb²⁺ concentration increased. The decreased intensity (ΔI _508nm) is linear to the concentration of 0.08–42 nM Pb²⁺, with regress equation of DI_508nm = 16.3 c + 1.5 \Delta {I_{{5}0{\rm{8nm}}}} = {16}.{3}\,c + {1}.{5} , correlation coefficient of 0.9965, and detection limit of 0.04 nM Pb²⁺. The RS assay was applied to the analysis of Pb²⁺ in wastewater, with satisfactory results.     

A label‐free DNAzyme‐cleaving fluorescence method for the determination of trace Pb2+ based on catalysis of AuPd nanoalloy on the reduction of rhodamine 6G

The substrate chain of double‐stranded DNA (dsDNA) could be specifically cleaved by Pb²⁺ to release single‐stranded DNA (ssDNA) that adsorbs onto the AuPd nanoalloy (AuPdNP) to form a stable AuPdNP–ssDNA complex, but the dsDNA can not protect AuPdNPs in large AuPdNP aggregates (AuPdNPA) under the action of NaCl. AuPdNP–ssDNA and large AuPdNPA could be separated by centrifugation. On increasing the concentration of Pb²⁺, the amount of released ssDNA increased; AuPdNP–ssDNA increased in the centrifugation solution exhibiting a catalytic effect on the slow reaction of rhodamine 6G (Rh6G) and NaH₂PO₂, which led to fluorescence quenching at 552 nm. The decrease in fluorescence intensity (ΔF) was linear to the concentration of Pb²⁺ within the range 0.33–8.00 nmol/L, with a detection limit of 0.21 nmol/L. The proposed method was applied to detect Pb²⁺ in water samples, with satisfactory results. Copyright © 2014 John Wiley & Sons, Ltd.     

Inhibition of chlorophyll biosynthesis by lead in greeningPisum sativum leaf segments

Supply of 0.01 to 1.0 mM lead acetate to greening pea(Pisum sativum L.) leaf segments either in the absence or in the presence of inorganic nitrogen lowered total chlorophyll (Chl) content. During a time course study, there was not any appreciable effect of Pb²⁺ upto 4 h but thereafter Pb inhibited Chl synthesis. While supply of succinate, cysteine dithiothreitol, 5,5-dithio-bis-2-nitrobenzoic acid and NH₄C1 had no protective action against Pb²⁺ toxicity, and glycine, glutamate 2-oxoglutarate, MgCl₂, KH₂PO₄, CaCl₂, KC1 protected only partially, reduced glutathione (GSH) could completely overcome the inhibition of Chl biosynthesis by the metal. It is suggested that Pb²⁺ interferes with Chl biosynthesis through GSH availability     

Effects of low pH and Pb2+ stress on living cyanobacterium, Phormidium angustissimum West & G.S.West : A test of its feasibility as a living biosorbent

Pb²⁺ adsorption by the living cyanobacterium, Phormidium angustissimum followed the Langmuir adsorption model, with the maximum adsorption capacity (q _max ) of 295.4?±?13.8 mg g^?1. This result suggests that P. angustissimum is a promising living biosorbent to remove Pb²⁺ from wastewaters. Living biosorbents are better able to remove Pb²⁺ from wastewater than dead biosorbents, however there are practical limitations for their use are encountered in extreme conditions such as low pH and high Pb²⁺ concentration. The feasibility of using cyanobacterium, P. angustissimum, as a living biosorbent for the extraction of Pb²⁺ from wastewater was studied by investigating its photosynthestic performance and tolerance under Pb²⁺ (0–5 mg ?L^?1) contamination and low pH (pH?3–7). Decreased photosynthetic performance caused by Pb²⁺ contamination and low pH stress was detected in this study by means of a reduction of the maximum photochemical efficiency of PSII (F_v/F_m). Detoxification mechanisms of P. angustissimum on Pb²⁺ appeared to increase its intracellular polysaccharides (IPS), exocellular polysaccharides (EPS), and protein. Living P. angustissimum could increase the pH of the solution which resulted in Pb²⁺ precipitation. The unique ability of P. angustissimum to remove Pb²⁺ and to grow under toxic conditions, demonstrated herein, indicates that it is a promising living biosorbent for mildly acidic water contaminated with Pb²⁺ in bioremoval systems in the which pH is not lower than 5 and Pb²⁺ is not higher than 5 mg L^?1.     

重金属铅与两种淡水藻的相互作用

为了研究重金属铅与淡水藻类之间的相互作用,采用不同Pb2+浓度处理铜绿微囊藻(Microcysis aeruginosa Kutz.)和斜生栅藻[Scenedesmus obliquus(Turp.)Kutz.],分别对两种藻的生物量、藻液电导率、O-·2含量、过氧化物酶(POD)、过氧化氢酶(CAT)活性以及藻对Pb2+的吸收作用等进行了测定,并通过扫描电镜观察了不同Pb2+浓度处理下两种藻细胞的表面结构。结果显示:(1)Pb2+浓度低于3 mg/L促进铜绿微囊藻生长,高于9 mg/L抑制其生长;但在3—12 mg/L范围内,Pb2+均明显抑制了斜生栅藻的生长,说明斜生栅藻对Pb2+毒性的敏感程度要高于铜绿微囊藻。(2)受到铅离子的胁迫,两种藻细胞膜通透性均有一定改变,扫描电子显微镜的照片观察,两种藻细胞表面的絮状物随着Pb2+的升高而增多,尤其是斜生栅藻细胞结构改变明显,多数细胞变形破裂;同时,O-·2含量升高,POD、CAT活性早期均可随Pb2+的增加而上升,表明氧自由基的产生增多以及由其引起的细胞生理生化改变可能是铅离子作用于藻细胞的主要机制。(3)两种淡水藻对Pb2+均有吸收作用,单位量藻细胞内,斜生栅藻对Pb2+的吸收能力好于铜绿微囊藻。所有结果提示:斜生栅藻不仅可以作为对重金属敏感的指示生物来监测水体Pb2+污染程度;同时由于斜生栅藻比铜绿微囊藻具有更好的Pb2+吸收能力,因此还可以利用斜生栅藻作为处理水体Pb2+的生物材料。     

The effect of Pb2+ on the structure and hydroxyapatite binding properties of osteocalcin

Lead toxicity is a major environmental health problem in the United States. Bone is the major reservoir for body lead. Although lead has been shown to impair bone metabolism in animals and at the cellular level, the effect of Pb²⁺ at the molecular level is largely unknown. We have used circular dichroism (CD), and a hydroxyapatite binding assay to investigate the effect of Pb²⁺ on the structure and mineral binding properties of osteocalcin, a noncollagenous bone protein. The CD data indicate Pb²⁺ induces a similar structure in osteocalcin as Ca²⁺ but at 2 orders of magnitude lower concentration. These results were explained by the more than 4 orders of magnitude tighter binding of Pb²⁺ to osteocalcin (K_d=0.085 μM) than Ca²⁺ (K_d=1.25 mM). The hydroxyapatite binding assays show that Pb²⁺ causes an increased adsorption to hydroxyapatite, similar to Ca²⁺, but at 2–3 orders of magnitude lower concentration. Low Pb²⁺ levels (1 μM) in addition to physiological Ca²⁺ levels (1 mM) caused a significant (40%) increase in the amount of mineral bound osteocalcin as compared to 1 mM Ca²⁺ alone. These results suggest a molecular mechanism of Pb²⁺ toxicity where low Pb²⁺ levels can inappropriately perturb Ca²⁺ regulated processes. In-vivo, the increased mineral bound osteocalcin could play a role in the observed low bone formation rates and decreased bone density observed in Pb²⁺-intoxicated animals.     

Stimulation of root acid phosphatase by phosphorus deficiency is regulated by ethylene in Medicago falcata

Plants have developed numerous strategies to cope with phosphorus (P) deficiency resulting from low availability in soils. Evolution of ethylene and up-regulation of root secreted acid phosphatase activity are common for plants in response to P deficiency. To determine the role of ethylene in response of plants to P deficiency, we investigated the effects of ethylene precursor (1-amino cyclopropane-1-carboxylic acid, ACC) and ethylene synthesis antagonists (aminoethoxyvinylglycine AVG, cobalt, Co²⁺) on P concentrations in roots and shoots of Medicago falcata seedlings grown in P-sufficient (500 μM H₂PO₄⁻) and P-deficient (5 μM H₂PO₄⁻) solution. After transferring M. falcata seedlings from P-sufficient to P-deficient solution for 2 days, root P concentration was significantly reduced. The reduction in root P concentration was reversed by AVG and Co²⁺, and a similar reduction in root P concentration of seedlings exposed to P-sufficient solution was observed by ACC. Expression of high-affinity phosphate transporters (MfPT1, MfPT5) was enhanced by P-deficiency and this process was reversed by AVG and Co²⁺. There was a marked increase in activity of root acid phosphatase (APase) and expression of gene encoding APase (MfPAP1) under P-deficient conditions, and the increase in APAse activity and expression of MfPAP1 was inhibited by AVG and Co²⁺. APase activity and expression of MfPAP1 expression in seedlings grown in P-sufficient solution were enhanced by ACC. Root and shoot P concentrations were increased when organic phosphorus was added to the P-deficient solution, and the increase in P concentration was significantly inhibited by AVG and Co²⁺. These results indicate that ethylene plays an important role in modulation of P acquisition by possibly mobilizing organic P via up-regulating root APase activity and high-affinity phosphate transporters.     

Shoot specific fungal endophytes alter soil phosphorus (P) fractions and potential acid phosphatase activity but do not increase P uptake in tall fescue

Aims

An experiment was performed to test how different fungal endophyte strains influenced tall fescue’s ability to access P from four P sources varying in solubility.

Methods

Novel endophyte infected (AR542E+ or AR584E+), common toxic endophyte infected (CTE+), or endophyte-free (E-) tall fescues were grown for 90 days in acidic soils amended with 30 mg kg^?1 P of potassium dihydrogen phosphate (KH₂PO₄), iron phosphate (FePO₄), aluminum phosphate (AlPO₄), or tricalcium phosphate ((Ca₃(PO₄)₂), respectively.

Results

Phosphorus form strongly influenced plant biomass, P acquisition, agronomic P use efficiency, microbial communities, P fractions. P uptake and vegetative biomass were similar for plants grown with AlPO₄, Ca₃(PO₄)₂, and KH₂PO₄ but greater than in control and FePO₄ soils. Infection with AR542E+ resulted in significantly less shoot biomass than CTE+ and E- varieties; there was no influence of endophyte on root biomass. The biomarker for arbuscular mycorrhizal fungi (AM fungi, 16:1ω5c) was selected as an effective predictor of variations in P uptake and tall fescue biomass. Potential acid phosphatase activity was strongly influenced by endophyte x P form interaction.

Conclusions

Endophyte infection in tall fescue significantly affected the NaOH-extractable inorganic P fraction, but had little detectable influence on soil microbial community structure, root biomass, or P uptake.

     

Isolation,Growth, Ultrastructure,and Metal Tolerance of the Green Alga,Chlamydomonas acidophila (Chlorophyta)

An acidophilic volvocine flagellate, Chlamydomonas acidophila (Volvocales) that was isolated from an acid lake, Katanuma, in Miyagi prefecture, Japan was studied for growth, ultrastructural characterization, and metal tolerance.

Chlamydomonas acidophila is obligately photoautotrophic, and did not grow in the cultures containing acetate or citrate even in the light. The optimum pH for growth was 3.5-4.5. To characterize metal tolerance, the toxic effects of Cd, Co, Cu, and Zn on this alga were also studied. Effective metal concentrations, which limited the growth by 50%, EC₅₀ were measured, after 72h of static exposure. EC₅₀s were 14.4 μM Cd²⁺, 81.3 μM Co²⁺, 141μM Cu²⁺, and 1.16 mM Zn²⁺ for 72 h of exposure. Thus, this alga had stronger tolerance to these metals than other species in the genus Chlamydomonas.     

Uptake of Metal Ions by Rhizopus arrhizus Biomass

Rhizopus arrhizus biomass was found to absorb a variety of different metal cations and anions but did not absorb alkali metal ions. The amount of uptake of the cations was directly related to ionic radii of La³⁺, Mn²⁺, Cu²⁺, Zn²⁺, Cd²⁺, Ba²⁺, Hg²⁺, Pb²⁺, UO₂²⁺, and Ag⁺. The uptake of all the cations is consistent with absorption of the metals by sites in the biomass containing phosphate, carboxylate, and other functional groups. The uptake of the molybdate and vanadate anions was strongly pH dependent, and it is proposed that the uptake mechanism involves electrostatic attraction to positively charged functional groups.     

Adsorption kinetics of Pb and Cd by two plant growth promoting rhizobacteria

A bench study was carried out to characterize the kinetics of two plant growth promoting rhizobacteria (PGPR) Azotobacter chroococcum and Bacillus megaterium to adsorb heavy metals from solution. Adsorption of Pb²⁺ and Cd²⁺ by bacterial cells was processed quickly with an equilibration achieved within 5 min. The adsorptions were fitted well with Freundlich and Langmuir isotherm models. The comparison of isotherm parameters indicated that A. chroococcum had a stronger capacity to bind metal ions than B. megaterium, with an average increase of 59.8% for Pb²⁺ and 75.6% for Cd²⁺, respectively. Both bacteria had a stronger affinity to Pb²⁺ than Cd²⁺ since Pb²⁺ was more easily bound with the phosphoryl groups on the cell surface than Cd²⁺. This demonstrated that the presence of bacteria in the rhizosphere may result in the reduction of mobile ions in soil solution.     

Pb tolerance and bioaccumulation by the mycelia of Flammulina velutipes in artificial enrichment medium

Mushrooms have the ability to accumulate high concentrations of heavy metals, which gives them potential for use as bioremediators of environmental contamination. The Pb²⁺ tolerance and accumulation ability of living mycelia of Flammulina velutipes were studied in this work. Mycelial growth was inhibited when exposed to 1 mM Pb²⁺. The colony diameter on solid medium decreased almost 10% compared with the control. Growth decreased almost 50% when the Pb²⁺ concentration increased to 4 mM in the medium, with the colony diameter decreasing from 80 mm to 43.4 mm, and dry biomass production in liquid cultures decreasing from 9.23±0.55 to 4.27±0.28 g/L. Lead ions were efficiently accumulated in the mycelia. The amount of Pb²⁺ in the mycelia increased with increasing Pb²⁺ concentration in the medium, with the maximum concentration up to 707±91.4 mg/kg dry weight. We also show evidence that a large amount of the Pb²⁺ was adsorbed to the mycelial surface, which may indicate that an exclusion mechanism is involved in Pb tolerance. These results demonstrate that F. velutipes could be useful as a remediator of heavy metal contamination because of the characteristics of high tolerance to Pb²⁺ and efficient accumulation of Pb²⁺ ions by the mycelia.     

Site-specific inactivation of phosphatases by ferrate lon.

Ferrate ion, FeO₄^2?, an analog of orthophosphate ion, PO₄^3?, has been found to be a potent inactivator of phosphatase. All phosphatases tested, including acid and alkaline nonspecific monoesterases as well as some specific monoesterases and a diesterase, were inactivated by treatment with ferrate. Inactivation, which occurs rapidly and irreversibly, can be demonstrated with concentrations of ferrate ion of 1 to 10 μm. Protection against ferrate inactivation was afforded by phosphate and by specific competitive inhibitors. It is therefore postulated that ferrate ion interacts on a phosphate binding site in the inactivation of phosphatases. Phosphoglucomutase and alcohol dehydrogenase were inactivated by ferrate ion while several enzymes which do not utilize phosphate-containing substrates were unaffected.     

Bioremoval of heavy metals and nutrients from sewage plant by Anabaena oryzae and Cyanosarcina fontana

The present study demonstrated the growth of two species of cyanobacteria on wastewater isolated from sewage plant in Aswan, Egypt. We evaluated their efficiency for eliminating nitrogen, phosphorus, chemical oxygen demand (COD) and heavy metals (Fe²⁺, Pb²⁺, Cu²⁺, and Mn²⁺). The growth of Cyanosarcina fontana has supported wastewater as a growth medium than Anabaena oryzae compared to standard medium. The nutrients concentration such as COD, NO₃–N and PO₄–P were decreased by the growth of A. oryzae and C. fontana in the wastewater after primary settling and centrate. However, the reduction of COD was less efficient than the other nutrients. The reduction percentage of COD, NO₃–N and PO₄–P reached 39.3, 84.1 and 90.7% as well as 54.6, 83.1, and 89.8%, in cultures of A. oryzae and C. fontana grown in the wastewater after primary settling, respectively. The reduction amounted to 10.1, 76.8, and 63.0% by A. oryzae and 43.2, 62.1, and 74.8% by C. fontana, grown in the centrate, respectively. Cyanobacteria species have the ability to accumulate the heavy metals from the wastewater to level far than the exceeding metal level in the water. Whereas, the heavy metals biosorption performance of C. fontana was higher in accumulating Fe²⁺ (93.95%), Pb²⁺ (81.21%), Cu²⁺ (63.9%), and Mn²⁺ (48.49%) compared to A. oryzae. The biosorption ability is dependent on the nature of the adsorbent studied and the type of wastewater treated. Therefore, removal of heavy metals and nutrients by the tested algae is strongly recommended as a powerful technique for the removal of pollutants from wastewater.     

Photosynthetic Properties of Chloroplasts from Chlamydomonas reinhardii

Chloroplasts isolated from synchronous cultures of the unicellular green alga Chlamydomonas reinhardii, SAG 11-32/b (−), fix CO₂ at rates between 25 and 50 micromoles per milligram chlorophyll per hour. The upper value is approximately half of the rate of the intact cell.

During storage in the dark on ice, the chloroplast preparation loses 30 to 50% of its CO₂ fixing capability per hour. Under reducing conditions (+ 1 millimolar dithiothreitol), this loss of activity is about twice as fast. The same reducing conditions stimulate CO₂ fixation in the light.

High concentrations of inorganic phosphate (>2 millimolar) inhibit CO₂ fixation. This inhibition is overcome by the addition of glycerate 3-phosphate. It is concluded that chloroplasts from C. reinhardii possess a higher plant type phosphate translocator. With respect to dependency upon light intensity, pH and Mg²⁺ concentration, the results were similar to that reported for chloroplasts from higher plants. However, in contrast to higher plant chloroplasts, maximum CO₂ fixation is observed at the relatively low osmotic concentration of 0.12 molar mannitol in the reaction buffer.

     

Stabilities of complexes formed between lead(II) and simple phosphonate or phosphate monoester ligands including some pyrimidine-nucleoside 5′-monophosphates (CMP2–, UMP2–, dTMP2–)

 The stability constants of the 1 : 1 complexes formed between Pb²⁺ and several simple phosphate monoesters (4-nitrophenyl phosphate, phenyl phosphate, d-ribose 5-monophosphate, n-butyl phosphate) or phosphonate ligands (methylphosphonate, ethylphosphonate) (R-PO^2– ₃) were determined by potentiometric pH titrations in aqueous solution (25  °C;I=0.1 M, NaNO₃). The construction of a log K ^P _P ^b _b(R-PO3) versus pK ^H _H(R-PO3) plot for the mentioned ligand systems results in a straight line on which the data pairs (the corresponding equilibrium constants were also measured) for uridine 5′-monophosphate (UMP^2–) and thymidine 5′-monophosphate (dTMP^2–) also fall; this result shows that in the Pb²⁺ complexes of UMP^2– and dTMP^2– the nucleobase residues do not interfere, in neither a positive nor a negative way, with the binding of Pb²⁺ and that the stability of all these complexes is determined by the basicity of the phosph(on)ate group. The mentioned straight-line correlation (as defined by the least-squares procedure) allowed us to demonstrate (via constants determined now) that the stability of the Pb²⁺ complex of cytidine 5′-monophosphate (CMP^2–) is also solely determined by the basicity of its phosphate group. A similar evaluation, based on literature data, for the Pb(HPO₄) complex reveals that its stability corresponds closely to the expectations based on the Pb(R-PO₃) data, though there is a slight hint that Pb(HPO₄) may be somewhat more stable [which would be in agreement with previous observations of other M(HPO₄) complexes]; clearly, more such comparisons are possible with the reference line given now. Based on the stability constants of the monoprotonated Pb(H;CMP)⁺ complex and the Pb(cytidine)²⁺ species (which was also measured now), it is concluded that in Pb(H;CMP)⁺ the proton is located at the phosphate group and Pb²⁺ mainly at the N3/(C2)O site of the cytosine residue. Regarding nucleic acids in solution, it is further concluded that the affinity of Pb²⁺ towards the negatively mono-charged phosphate unit, —O—P(O)₂ ^–—O—, of a nucleic acid backbone is comparable to that of the cytosine moiety, the affinity towards other nucleobase residues being smaller. This information may prove helpful regarding the properties of lead ribozymes. Received: 16 April 1999 / Accepted: 2 June 1999     

Highly selective and sensitive coumarin–triazole‐based fluorometric ‘turn‐off’ sensor for detection of Pb2+ ions

Exposure to even very low concentrations of Pb²⁺ is known to cause cardiovascular, neurological, developmental, and reproductive disorders, and affects children in particular more severely. Consequently, much effort has been dedicated to the development of colorimetric and fluorescent sensors that can selectively detect Pb²⁺ ions. Here, we describe the development of a triazole‐based fluorescent sensor L5 for Pb²⁺ ion detection. The fluorescence intensity of chemosensor L5 was selectively quenched by Pb²⁺ ions and a clear color change from colorless to yellow could be observed by the naked eye. Chemosensor L5 exhibited high sensitivity and selectivity towards Pb²⁺ ions in phosphate‐buffered solution [20 mM, 1:9 DMSO/H₂O (v/v), pH 8.0] with a 1:1 binding stoichiometry, a detection limit of 1.9 nM and a 6.76 × 10⁶ M^?1 binding constant. Additionally, low‐cost and easy‐to‐prepare test strips impregnated with chemosensor L5 were also produced for efficient of Pb²⁺ detection and proved the practical use of this test.     

The Degradation of Dimethoate and the Mineral Immobilizing Function for Cd2+ by Pseudomonas putida

Organophosphorus pollution and heavy metal pollution are prominent in China and have caused increasingly severe environmental pollution. This research used Pseudomonas putida to degrade dimethoate so as to induce the formation of calcium carbonate (CaCO₃) and calcium phosphate (Ca₃(PO₄)₂) in beef extract peptone medium. In addition, the mineral immobilizing function of the generated Ca₃(PO₄)₂ and CaCO₃ for Cd²⁺ was studied by adding different concentrations of Cd²⁺ to the culture solution. Meanwhile, transmission electron microscopy (TEM), scanning electronic microscopy (SEM), X-ray diffraction, gas chromatography and atomic absorption spectrophotometry were used to investigate the biodegradation of dimethoate, the concentration variation of Ca²⁺ and Cd²⁺, the mineral and chemical compositions of the precipitates. The results showed that the growth of P. Putida could increase the pH value of the culture solution and effectively degrade the organophosphorus pesticide dimethoate. Besides, the concentration of Ca²⁺ in the culture solution decreased significantly in the first four days and then tended to be stable. Moreover, the TEM and SEM results presented that there were large amounts of biogenic sedimentary CaCO₃ and a little Ca₃(PO₄)₂ in the precipitates. Furthermore, in the employed culture system, the removal rates of Cd²⁺, when added at two different concentrations (6 ppm and 15 ppm), reached 100%. Therefore, this study provided a new idea for treating wastewater polluted with organophosphorus pesticide and heavy metals by using microorganisms.