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51.
Contamination of the biosphere by heavy metals has been rising, due to accelerated anthropogenic activities, and is nowadays, a matter of serious global concern. Removal of such inorganic pollutants from aquatic environments via biological processes has earned great popularity, for its cost-effectiveness and high efficiency, compared to conventional physicochemical methods. Among candidate organisms, microalgae offer several competitive advantages; phycoremediation has even been claimed as the next generation of wastewater treatment technologies. Furthermore, integration of microalgae-mediated wastewater treatment and bioenergy production adds favorably to the economic feasibility of the former process—with energy security coming along with environmental sustainability. However, poor biomass productivity under abiotic stress conditions has hindered the large-scale deployment of microalgae. Recent advances encompassing molecular tools for genome editing, together with the advent of multiomics technologies and computational approaches, have permitted the design of tailor-made microalgal cell factories, which encompass multiple beneficial traits, while circumventing those associated with the bioaccumulation of unfavorable chemicals. Previous studies unfolded several routes through which genetic engineering-mediated improvements appear feasible (encompassing sequestration/uptake capacity and specificity for heavy metals); they can be categorized as metal transportation, chelation, or biotransformation, with regulation of metal- and oxidative stress response, as well as cell surface engineering playing a crucial role therein. This review covers the state-of-the-art metal stress mitigation mechanisms prevalent in microalgae, and discusses putative and tested metabolic engineering approaches, aimed at further improvement of those biological processes. Finally, current research gaps and future prospects arising from use of transgenic microalgae for heavy metal phycoremediation are reviewed. 相似文献
52.
Halim M Kennedy RD Suzuki M Khan SI Diaconescu PL Rubin Y 《Journal of the American Chemical Society》2011,133(17):6841-6851
Gold(I), silver(I), and copper(I) phosphine complexes of 6,9,12,15,18-pentaaryl[60]fullerides 1a and 1b, namely, [(4-MeC(6)H(4))(5)C(60)]Au(PPh(3)) (2a), [(4-t-BuC(6)H(4))(5)C(60)]Au(PPh(3)) (2b), [(4-MeC(6)H(4))(5)C(60)]Ag(PCy(3)) (3a), [(4-t-BuC(6)H(4))(5)C(60)]Ag(PPh(3)) (3b), [(4-t-BuC(6)H(4))(5)C(60)]Ag(PCy(3)) (3c), [(4-MeC(6)H(4))(5)C(60)]Cu(PPh(3)) (4a), and [(4-t-BuC(6)H(4))(5)C(60)]Cu(PPh(3)) (4b), have been synthesized and characterized spectroscopically. All complexes except for 3c were also characterized by single-crystal X-ray diffraction. Several coordination modes between the cyclopentadienyl ring embedded in the fullerene and the metal centers are observed, ranging from η(1) with a slight distortion toward η(3) in the case of gold(I), to η(2)/η(3) for silver(I), and η(5) for copper(I). Silver complexes 3a and 3b are rare examples of crystallographically characterized Ag(I) cyclopentadienyls whose preparation was possible thanks to the steric shielding provided by fullerides 1a and 1b, which stabilizes these complexes. Silver complexes 3a and 3b both display unexpected coordination of the cyclopentadienyl portion of the fulleride anion with Ag(I). DFT calculations on the model systems (H(5)C(60))M(PH(3)) and CpMPH(3) (M = Au, Ag, or Cu) were carried out to probe the geometries and electronic structures of these metal complexes. 相似文献
53.
Humayun Ajaz Sajjad Hussain Muhammad Altaf Helen Stoeckli‐Evans Anvarhusein A. Isab Rashid Mahmood Shahnila Altaf Saeed Ahmad 《中国化学》2011,29(2):254-258
Antimony(III) complexes of thioamides [thioamides=thiourea (Tu), N,N′‐dimethylthiourea (Dmtu), tetramethylthiourea (Tmtu), imidazolidine‐2‐thione (Imt) and diazinane‐2‐thione (Diaz)] with the general formulae, Sb(thione)nCl3 (n=1, 2, 2.5, 3) were prepared and characterized by elemental analysis, IR and NMR (1H, 13C) spectroscopic methods. The spectral data of the complexes are consistent with the coordination of the thiones to antimony(III). The crystal structure of one of them, {[Sb(Imt)2Cl2]2(μ2‐Imt)}Cl2 ( 1 ), was determined by X‐ray crystallography, which shows that the complex is dinuclear consisting of two [Sb(Imt)2Cl2] units bridged by an Imt molecule. In 1 , the antimony atom is bonded to two chlorine atoms, two sulfur atoms of coordinated Imt molecules and one sulfur atom of a bridging Imt molecule. The antimony environment can be considered to be distorted octahedral with one Cl? ion weakly bound to antimony. 相似文献
54.
Sara Darvishi Mohammad Reza Ardakani Saeed Vazan Hossein Ghafourian Farzad Paknejad Amir Hossein Faregh 《Journal of Radioanalytical and Nuclear Chemistry》2012,293(1):167-173
Activated carbons (AC) have been long recognized as prominent absorbents in industries and feature numerous applications in preventing or absorbing the harmful gases and liquids and could be employed for filtration and remediation or even reutilization of chemicals. In order to investigate the capacity of AC in reducing the absorption of heavy metals (HM) including lead (Pb) and cadmium (Cd) and dual complex (Pb?×?Cd) by spinach, a factorial experiment in a completely randomized design with three replications on a pot trial was conducted. Three factors including five levels of AC 0, 5000, 10000, 15000, 20000?mg/kg soil, one concentration level of Pb 4,000?mg/kg soil and one concentration level of cadmium Cd 8?mg/kg soil were tested. The index of heavy metal concentration was calculated in leaf, stem and root and their corresponding dry weights. Results illustrated that in contaminated soils, plants with AC exhibited a superior reduction of absorption of HM vis-à-vis the plants without AC. The foremost result regarding the impact of AC on reducing the concentration of Pb and Cd was observed in 20,000 level of AC. This reveals that AC declined the soil contamination and lessened the accumulation of HM into the shoots and roots. Results suggest that the application of AC may be an eligible solution for decreasing the translocation of HM into the plants. 相似文献
55.
56.
Efficient Solvent‐Free Synthesis of Benzothiazine‐Fused Pyrrolo[3,4‐c]coumarins: Cycloaddition Reactions between Coumarin‐Based Dihydrobenzothiazoles and Isocyanides 下载免费PDF全文
Mehdi Khoobi Ali Ramazani Mohammad Mahdavi Alireza Foroumadi Saeed Emami Sang Woo Joo Katarzyna Ślepokura Tadeusz Lis Abbas Shafiee 《Helvetica chimica acta》2014,97(6):847-853
A new and unusual synthesis of benzothiazine‐fused pyrrolo[3,4‐c]coumarins, involving the ring‐opening of coumarin‐based dihydrobenzothiazoles and subsequent [4+1] cycloaddition reaction with isocyanides, was described. Thus, simple heating of various 3‐(2,3‐dihydro‐2‐methylbenzo[d]thiazol‐2‐yl)coumarins with isocyanides produced the title compounds in good yields under solvent‐free conditions. 相似文献
57.
The electrosynthesis of polypyrrole (PPy) film has been achieved on glassy carbon electrode (GCE) in aqueous medium of Congo red (CR) by means of cyclic voltammetry (CV). The modified electrode exhibits high electrocatalytic activity toward dopamine (DA) oxidation, with drastic enhancement of the reversibility and peak currents. This modified electrode, due to electrostatic interactions, is capable to mask the response of ascorbic acid (AA) completely and provide an effective method for the detection of minor amounts of dopamine in the presence of high concentrations of AA. The electrochemical response of the film modified electrode is strongly dependent to the switching potential applied in the CV procedure of the electro‐polymerization. The results show that by increasing the switching potential more than 0.75 V, the peak of AA is gradually disappeared. This peak in potential of 0.85 V is reached to capacitive background current. With respect to the destruction of the conjugated structure of ppy and lowering the conductivity of the film at the surface of modified electrode, higher switching potentials cannot be suitable for electropolymerization procedure. The effects of various experimental parameters such as, number of polymerization cycles, switching potential, pH and potential sweep rate on the voltammetric response of dopamine were also investigated. The modified electrode shows a linear response to DA in the range of 0.5 to 100 μM with a detection limit of 0.1 μM. The prepared modified electrode does not show any considerable response toward sulfhydryl compounds, such as, cysteine, penicillamine and glutathione, revealing a good selectivity for voltammetric response to DA. The effective electrocatalytic property, ability for masking the voltammetric responses of the other biological reducing agents together with high reproducibility and stability make the modified electrode suitable for selective and sensitive voltammetric detection of sub‐micromolar amounts of DA in clinical and pharmaceutical preparations. 相似文献
58.
Maryam Ataeefard Siamak Moradian Mojtaba Mirabedini Morteza Ebrahimi Saeed Asiaban 《Plasma Chemistry and Plasma Processing》2008,28(3):377-390
The surface of a LDPE was modified by Ar, O2, N2, CO2 gaseous plasma. The changes in surface morphology and surface wettability were investigated using AFM and SEM. The surface
chemical changes of LDPE were also characterized by FTIR-ATR. The SEM and AFM results demonstrated variable changes in surface
roughness for different types of plasma gas used, the changes being more for the Ar and N2 plasma treatments. Considering the nature of the LDPE film, XRD studies were carried out to determine changes in the percentage
crystalinity. The results showed that all low pressure O2, Ar, N2, CO2 gas plasmas improved the wettability of LDPE films. Contact angles decreased significantly depending on the discharge powers
and exposure times. Surface morphology was also found to vary with plasma discharge powers, exposure times, and the type of
gas being used. Ar and N2 gas plasmas in general produced more superior results. 相似文献
59.
A facile one-pot three-component condensation of terephthalic aldehyde with urea and fluorinated 1,3-dicarbonyl derivatives is developed using catalytic quantities of chlorotrimethylsilane at ambient temperature. As a consequence, efficient synthesis of novel trifluoromethyl derivatives of bis(tetrahydropyrimidinone)benzenes is observed within short time periods. The procedure is shown to be equally efficient when urea is replaced with thiourea or guanidine. 相似文献
60.
Soap-free emulsion polymerization (SFEP) of methyl methacrylate, butyl acrylate was conducted in water/methanol media with sodium salts of four different acidic comonomers, namely styrene sulfonic acid (NaSS), 2-acrylamide-2-methyl-1-propane sulfonic acid (NaAmps), acrylic acid (NaAA), and itaconic acid (Na2ita). It was found that the introduction of methanol as co-solvent (35 wt%) to the medium greatly decreases the amount of water-soluble polyelectrolyte in the cases NaAA and Na2ita while it does not make difference for NaSS and NaAmps. Having employed the concept of conductance dependency to the ion mobility, the onset concentration in which soluble chains were formed was detected. The addition of sulfonic-based comonomers (NaSS and NaAmps), first decreased particle size and then led to predomination of solution polymerization over SFEP. On the contrary, the incorporation of carboxylic-based comonomers (NaAA and Na2ita) led to increase in particle size. Moreover, the particle size results were in good qualitative agreement with the classical Smith–Ewart theory. 相似文献