Endophytic fungus Serendipita indica reduces arsenic mobilization from root to fruit in colonized tomato plant.

The accumulation of arsenic in crop plants has become a worldwide concern that affects millions of people. The major source of arsenic in crop plants is irrigation water and soil. In this study, Serendipita indica, an endophytic fungus, was used to investigate the protection against arsenic and its accumulation in the tomato plant. We found that inoculation of S. indica recovers seed germination, plant growth and improves overall plant health under arsenic stress. A hyper-colonization of fungus in the plant root was observed under arsenic stress, which results in reduced oxidative stress via modulation of antioxidative enzymes, glutathione, and proline levels. Furthermore, fungal colonization restricts arsenic mobilization from root to shoot and fruit by accumulating it exclusively in the root. We observed that fungal colonization enhances the arsenic bioaccumulation factor 1.48 times in root and reduces the arsenic translocation factor by 2.96 times from root to shoot and 13.6 times from root to fruit compared to non colonized plants. Further, investigation suggests that S. indica can tolerate arsenic by immobilizing it on the cell wall and accumulating it in the vacuole. This study shows that S. indica may be helpful for the reduction of arsenic accumulation in crops grown in arsenic-contaminated agriculture fields.

Preparation, characterization and agri applications of biochar produced by pyrolysis of sewage sludge at different temperatures.

Sewage sludge (SS) is an abundantly available feedstock, which is generally considered as potential threat to human health and environment. Its utilization in any process would be of great help for environmental sustainability. Accordingly, this work aimed to prepare and characterize the sewage sludge biochar (SSB) at temperatures, i.e. (500, 450, 400, and 350 °C), and further analyze the available nutrients and contaminants as well as agri application potential. The results indicated that the total nitrogen (TN), electrical conductivity (EC), and total organic carbon (TOC) content in SSBs decreased with increasing pyrolysis temperature. The overall concentration of polycyclic aromatic hydrocarbons (PAHs) in SSBs was substantially lower (1.8-9.7-fold depending on pyrolysis temperature) than in SS. Pyrolysis of SS enriched the heavy metals content in SSBs and the relative enrichment factor (RE) factor varied between 1.1 and 2.1 depending on the pyrolysis temperature. Furthermore, compared to SS, the leaching rate of heavy metals was significantly decreased in SSBs (1.1-100-fold depending on the pyrolysis temperature) and the pyrolysis temperature of 400-450 °C prevented the Ni, Pb, Cr, and Zn leaching in SSB. The total PAH and heavy metals content in biochars were below the control standard for land application. Finally, testing of the growth-promoting effect of biochar extracts on fenugreek plants revealed that SSB prepared at 350 °C significantly stimulated the root and shoot length of 5-days old seedlings. This study provides important data for potential environmental risks of SSB applications.

Orthosilicic acid (OSA) reduced grain arsenic accumulation and enhanced yield by modulating the level of trace element, antioxidants, and thiols in rice.

Arsenic (As), a toxic metalloid, is finding its route to human through intake of As-contaminated water and consumption of food grown on contaminated soil. Rice is the most As-affected crop. Present study is aimed to assess the impact of stabilized orthosilicic acid (a proprietary formulation for plant-available silicon (Si) and earlier used as fertilizer for rice to enhance growth and yield) in reducing the accumulation of As in rice grains. Application of arsenic in the form of arsenate (AsV) and arsenite (AsIII) significantly affected plant growth in a dose-dependent manner. Higher doses of AsV and AsIII (50 and 25 mg L-1 respectively) significantly decreased the yield attributes leading to lower yield. A significant accumulation of As in grain was observed in both AsV- and AsIII-exposed plants in a dose-dependent manner. Arsenic exposure also increased the level of Si in rice grains. Application of Si, either in soil or on leaves (foliar), greatly reduced grain As accumulation (up to 67% in AsV and 78% in AsIII) and enhanced the growth and yield of plants under As stress. The level of thiols and activities of antioxidant enzymes were also enhanced under Si application. Foliar Si application was more effective in increasing grain Si level and reducing grain As than soil Si. The level of other trace elements was also significantly enhanced by Si application irrespective of the presence or absence of As in comparison with control. Arsenic exposure constrained some of the trace elements, such as Zn and Co, which were restored by Si application. Results of the present study showed that the application of currently used Si formulation may effectively reduce grain As level even in highly As-contaminated soil and improve grain quality of rice.

Simultaneous quantitative determination of bioactive terpene indole alkaloids in ethanolic extracts of Catharanthus roseus (L.) G. Don by ultra high performance liquid chromatography-tandem mass spectrometry.

A rapid, sensitive and reproducible method using ultra-high-performance liquid chromatography coupled with electrospray ionization hybrid triple quadrupole-linear ion trap mass spectrometry (UHPLC-ESI-QqQLIT-MS/MS) in multiple reaction monitoring (MRM) mode was developed and validated for simultaneous quantitation of anticancer (vincristine, vinblastine, vindesine), antihypertensive (ajmaline, ajmalicine, reserpine), aphrodisiac (yohimbine), sedative (serpentine) agents, dietary supplement (vinpocetine, yohimbine) and precursor of vinblastine (vindoline) from crude extracts of Catharanthus roseus. The precursor to product ion transitions for these compounds were observed at m/z 327 → 144, 355 → 144, 754 → 355, 353 → 144, 349 → 317, 825 → 225, 811 → 224, 458 → 188, 351 → 280 and 609 → 195, respectively in positive ionization mode. Chromatographic separation of all targeted TIAs was performed on ACQUITY UPLC BEH™ C18 column (1.7 µm, 2.1 mm × 50 mm). The calibration curves were linear within the concentration range 0.5-1000 ng/mL and correlation coefficients (R2) were closer to 1. Limit of detection (LOD) and limit of quantitation (LOQ) ranged from 0.039-0.583 ng/mL and 0.118-1.767 ng/mL, respectively. The intra-day (0.23-2.71% RSD) and inter-day (0.40-2.90% RSD) precision, stability (0.69-3.45% RSD) and recovery (99.63-104.30% ±â€¯%RSD ≤ 3.03%) were acceptable indicating good accuracy of the developed method. The method was successfully applied in ethanolic extracts of 39 samples of C. roseus parts (leaf, stem and root) collected from five different locations in India. Serpentine was detected as one of the most abundant TIA. Principal component analysis (PCA) was able to successfully discriminate among C. roseus samples on the basis of content of targeted TIAs.

Quantitative determination of multi markers in five varieties of Withania somnifera using ultra-high performance liquid chromatography with hybrid triple quadrupole linear ion trap mass spectrometer combined with multivariate analysis: Application to pharmaceutical dosage forms.

An ultra-high performance liquid chromatography electrospray ionization tandem mass spectrometry method has been developed and validated for simultaneous quantification of six major bioactive compounds in five varieties of Withania somnifera in various plant parts (leaf, stem and root). The analysis was accomplished on Waters ACQUITY UPLC BEH C18 column with linear gradient elution of water/formic acid (0.1%) and acetonitrile at a flow rate of 0.3mLmin(-1). The proposed method was validated with acceptable linearity (r(2), 0.9989-0.9998), precision (RSD, 0.16-2.01%), stability (RSD, 1.04-1.62%) and recovery (RSD ≤2.45%), under optimum conditions. The method was also successfully applied for the simultaneous determination of six marker compounds in twenty-six marketed formulations. Hierarchical cluster analysis and principal component analysis were applied to discriminate these twenty-six batches based on characteristics of the bioactive compounds. The results indicated that this method is advance, rapid, sensitive and suitable to reveal the quality of Withania somnifera and also capable of performing quality evaluation of polyherbal formulations having similar markers/raw herbs.

Photosensitizing activity of ferrocenyl bearing Ni(II) and Cu(II) dithiocarbamates in dye sensitized TiO2 solar cells.

Biferrocene bearing planar metal dithiocarbamates, namely, [M(FcCH2dtc)2] (dtc = furan-2-ylmethyldithiocarbamate, M = Cu(II) 1, Ni(II) 4; dtc = benzo[d][1,3]dioxol-5-ylmethyl dithiocarbamate, M = Cu(II) 2, Ni(II) 5; dtc = pyridin-2-ylmethyldithiocarbamate, M = Cu(II) 3, Ni(II) 6; Fc = ferrocenyl; Fe(η(5)-C5H5)(η(5)-C5H4-)), have been synthesized and characterized by microanalysis, magnetic susceptibility and cyclic voltammetry. Structures of 1, 2 and 4 have been obtained by single crystal X-ray diffraction. These complexes with pyridyl, piperonyl and furfuryl as heteroaromatic groups in the dithiocarbamate ligands have been exploited as sensitizers in dye sensitized TiO2 solar cells for converting sunlight into electrical energy. Light-to-electrical energy conversion efficiencies achieved using these sensitizers are considerably greater than those obtained with analogous compounds previously reported by us. The overall conversion efficiency (η) is found to be dependent upon the nature of the heteroaromatic conjugated linkers and increases in the order η (ferrocenylfurfuryl) > η (ferrocenylpiperonyl) > η (ferrocenylpyridyl) all values being lower than that obtained in the reference Ru dye N719 under similar experimental conditions. The conversion efficiencies also vary with the metal being higher for Ni (4, 5 and 6) than for Cu complexes (1, 2 and 3). The X-ray structural analyses reveal the existence of rare M···H-C intermolecular anagostic interactions involving the metal atom in chain motifs in 1 and 4, which are retained in solution as evidenced by (1)H NMR spectroscopy.

Enhanced light harvesting efficiencies of bis(ferrocenylmethyl)-based sulfur rich sensitizers used in dye sensitized TiO2 solar cells.

In this work, the photosensitizing properties of ferrocene (Fc)-based compounds FcCH(2)CS(3)CH(2)Fc (1) and FcCH(2)SSCH(2)Fc (2) were investigated and significant enhancement in the light harvesting efficiency was observed compared to those achieved with previously reported compounds from our lab. The compounds were fully characterized by spectroscopy and X-ray crystallography, and their electrochemical properties studied. DSSCs based on these dyes display efficiencies comparable to those of a standard cell based on N719 under similar experimental conditions. These studies demonstrate that ferrocenyl-based sulfur rich compounds with proper orientation of the Fc groups assisted via suitable linkers, together with desired redox properties and visible region electronic absorption features could constitute a new class of photosensitizers targeting light driven reactions.

Application of π-extended ferrocene with varied anchoring groups as photosensitizers in TiO2-based dye-sensitized solar cells (DSSCs).

Two new compounds, FcCH=NC(6)H(4)COOH (1) and FcCH=NCH(2)CH(2)OH (2) (Fc=C(5)H(4)FeC(5)H(5)), have been synthesized and characterized by elemental analyses, IR and (1)H NMR spectroscopy, and ESI-MS. Attempt has been made to explain their quasi-reversible redox behavior evidenced by cyclic voltammetry using density functional theory (DFT) calculations. Light-harvesting properties of both the compounds and also the starting material, FcCHO (3), have been studied using these compounds as photosensitizers in TiO(2)-based dye-sensitized solar cells having either a propylene carbonate-based electrolyte or ionic liquid electrolyte, namely, 1-propyl-3-methyl imidazolium iodide (PMII). Long-term stability of the photocurrent output of the cell using compound 1 as photosensitizer has been monitored periodically over 1400 h.

Efficient phenylmercury(II) methylferrocenyldithiocarbamate functionalized dye-sensitized solar cells.

Two new heterobimetallic phenylmercury(ii) dithiocarbamate complexes incorporating the ferrocenyl moiety (C(5)H(5))Fe(C(5)H(4)) (Fc), namely PhHgS(2)CN(CH(2)Fc)CH(2)C(5)H(4)N, (1) and PhHgS(2)CN(CH(2)Fc)CH(2)C(4)H(3)O, (2) have been prepared and characterized by elemental analysis, UV-Vis, IR, (1)H and (13)C NMR spectroscopies. The crystal structures of 1 and 2 showed a linear core at the Hg(ii) centre of the molecule, bound by the sulfur atom of the dithiocarbamate ligand and carbon atom of the aromatic ring. Weak intermolecular HgS interactions form "head-to-tail" dimers in the cases of 1 and 2. The observed quasi-reversible cyclic voltammograms of the complexes have been corroborated by calculating gross natural electron population and gross natural electron spin population at each atom for the neutral as well its oxidized species obtained at density functional level (DFT) of theory, which suggests that the delocalization of electron spin population can affect the magnitude of ΔE(p). The electronic absorption bands of both the complexes were assigned with the help of time dependent density functional theory (TD-DFT) calculations. The light harvesting properties of both 1 and 2 in conjunction with our previously reported compound PhHgS(2)CN(CH(2)Fc)CH(2)C(6)H(5) (3) have been reported.

Synthesis, structure and light-harvesting properties of some new transition-metal dithiocarbamates involving ferrocene.

Nine new transition-metal dithiocarbamates involving ferrocene (Fc), namely, [M(FcCH(2)Bzdtc)(2)] (M=Ni(II) (1), Cu(II) (2), Cd(II) (3), Hg(II) (4), Pd(II) (5), Pt(II) (6) and Pb(II) (7); Bzdtc=N-benzyl dithiocarbamate) and [M(FcCH(2)Bzdtc)(3)] (M=Co(II) (8) and UO(2) (VI) (9)), have been synthesised and characterised by micro analyses, IR spectroscopy, (1)H and (13)C NMR spectroscopy, and in three cases by single-crystal X-ray analysis. The peak broadening in the (1)H spectrum of the copper complex indicates the paramagnetic behaviour of this compound. A square-planar geometry around the nickel and copper complexes and distorted linear geometry around the mercury complex have been found. The latter geometry is attributed to the bulkiness of the methylferrocenyl and benzyl groups. The observed single quasi-reversible cyclic voltammograms for complexes 2, 8 and 9 indicate the stabilisation of a metal centre other than Fe in their characteristic oxidation state. These complexes have been used as a photosensitiser in dye-sensitised solar cells.