Behavioral Responses of Bemisia Tabaci Cryptic Species Med to Three Host Plants and Their Volatiles

Bemisia tabaci Gennadius (Hemiptera: Aleyrodidae) is a worldwide pest that damages more than 900 host plant species. The infestation behavior of this pest is affected by the volatile organic compounds (volatiles) of different plants and their growth stage. We investigated the chemical constituents of the volatiles extracted from three plants (Gossypium hirsutum, Abutilon theophrasti and Ricinus communis) at different growth stages (pre-flowering, florescence and fruiting) and their effects on the behavior of adult B. tabaci. The selectivity studies on three plants showed that the B. tabaci preferred piemarker. The olfactometer studies showed that growth periods of the three plants also affected the preference of B. tabaci. Volatiles of piemarker and cotton plant had different levels of attraction to adults during all stages. Volatile substances released by castor at stage of flowering have a repellent effect on B. tabaci. In the plant VS plant combination ,the adults showed the strongest preference to volatiles from before and during anthesis of piemarker, followed by cotton, and then castor. A total of 23, 22 and 18 compounds were detected from volatiles of piemarker, cotton and castor, respectively, and proportions among the compounds changed during different stages of plant development. The olfactory responses of B. tabaci to volatile compounds showed that linalool and high concentration of leaf acetate had strong trapping effect on this pest, while 1-nonanal had significant repellent effect at high concentration. This study indicates that different plants and their growth stage affects their attractiveness or repellency to B. tabaci adults which is mediated by plant constitutive and dynamic changes. The compounds obtained by analysis screening can be used as potential attractants or repellents to control Mediterranean (MED) B. tabaci.

A multi-responsive coumarin–benzothiazole fluorescent probe for selective detection of biological thiols and hydrazine

Biothiols play important roles in various physiological and biological processes, which closely related to many diseases. Hydrazine is widely used in the chemical industry, but it is harmful to humans and animals. Therefore, it is very important to develop a fluorescent probe that can simultaneously detect biological thiols and hydrazine. In this work, a new fluorescent probe (2E,4Z)-2-(benzo[d]thiazol-2-yl)-5-chloro-5-(7-(diethylamino)-2-oxo-2H-chromen-3-yl)penta-2,4-dienenitrile (BCD) was synthesized by integrating coumarin and benzothiazole acetonitrile. Featured with four binding sites and different bonding mechanism between probe with biothiols and hydrazine, this probe exhibited fluorescent turn-on for distinguishing Cys, Hcy, GSH and hydrazine with 760-, 8-, 6- and 637-fold fluorescent intensity increase at 502, 479, 476 and 458 nm, respectively, through different excitation wavelengths. Research on the effect of pH on the fluorescent performance of BCD shows that the probe exhibits superior stability in a weakly alkaline to weakly acidic environment, which will facilitate the detection of biological thiols or hydrazine hydrate by BCD. Selectivity studies have shown that the probe has high specificity to biological thiols and hydrazine, which is of great significance to the application of BCD.

Isotherm and selectivity studies of Ni(II) removal using natural and acid-activated nanobentonites

In this research, natural bentonite and its acid-activated forms were employed as adsorbents for the adsorption of Ni2+ ions from wastewater. Natural bentonite was activated with 2M sulfuric acid, 4.5 h and 95 °C (the beast acid-activated sample with the highest adsorption capacity) and the other 6M sulfuric acid, 7.5 h and 95 °C (the worst acid-activated sample with the lowest adsorption capacity). The adsorption of Ni2+ was studied through experiments including equilibrium contact time and selectivity. The equilibrium time of contact for bentonite was obtained at 180 min. The Ni2+ separation process along with Zn2+ selectivity studies was considered through adsorption experiments. The results showed that there was a maximum amount of Ni2+ adsorption in the absence of Zn2+ for all samples. The results showed the best fit is obtained with the pseudo-second-order kinetic model. Working out different bentonite types to determine the best kinetic models, we explored the Langmuir and Florry–Huggins models provided a good fit with experimental data for acid-activated bentonites and the best results from linear forms of the adsorption isotherm models for fitting the experimental data of natural bentonite are obtained Langmuir, Temkin and Freundlich models.

Antiplasmodial and Cytotoxic Flavonoids from Pappea capensis (Eckl. & Zeyh.) Leaves

Ethnobotanical surveys indicate that the Masai and Kikuyu in Kenya, the Venda in South Africa, and the Gumuz people of Ethiopia use Pappea capensis for the treatment of malaria. The present study aimed to investigate the phytochemical and antiplasmodial properties of the plant leaves. The bioactive compounds were isolated using chromatographic techniques. The structures were established using NMR, HRMS, and UV spectroscopy. Antiplasmodial activity of P. capensis leaf extract and isolated compounds against chloroquine-sensitive 3D7 P. falciparum was evaluated using the parasite lactate dehydrogenase assay. Cytotoxicity against HeLa (human cervix adenocarcinoma) cells was determined using the resazurin assay. The extract inhibited the viability of Plasmodium falciparum by more than 80% at 50 µg/mL, but it was also cytotoxic against HeLa cells at the same concentration. Chromatographic purification of the extract led to the isolation of four flavonoid glycosides and epicatechin. The compounds displayed a similar activity pattern with the extract against P. falciparum and HeLa cells. The results from this study suggest that the widespread use of P. capensis in traditional medicine for the treatment of malaria might have some merits. However, more selectivity studies are needed to determine whether the leaf extract is cytotoxic against noncancerous cells.

Pyridine based cross-linked chitosan: a biopolymer adsorbent for the green removal of toxic metals from water

Herein we report the green recovery of toxic metals [namely: Cd2+, Cr3+, Mn2+, Pb2+, and Ni2+] from water utilizing a biopolymer: 2,6-pyridine dicarboxylic acid cross-linked chitosan (PDC-CCS) as the adsorbent. Adsorption studies were performed at a previously determined optimum adsorption conditions for Cu(II) [i.e temperature = 30 ℃, pH of about 7.5, contact time = 60 mins and initial metal ion concentration of 2.5 mM]. At the RI-PB/def2-SVP level of theory, the Density Functional Theory (DFT) approach has been used to evaluate adsorption energy for metal ions. Selectivity studies were performed at pH 4.20, 5.56, 6.65 and 7.61. While Mn(II), Cd(II) and Ni(II) were strongly adsorbed at higher pH (7.5), Cr(III) and Pb(II) were seen to be strongly adsorbed at lower pH (around 4.0). Selectivity studies revealed that PDC-CCS can be utilized for simultaneous removal of the metals at pH 4.2; selective adsorption of Mn(II) at pH 5.56 as well as simultaneous-selective removal of Ni(II) and Mn(II) near neutral pH. The maximum adsorption limit of PDC-CCS for Mn(II), Cd(II) and Ni(II), were found to be 1258.79, 1118.70 and 829.62 mmol/g respectively. When compared with some relevant previously used adsorbent, PDC-CCS shows an exceptional adsorption capacity. Consequently, a successful biopolymer adsorbent for the treatment of water contaminated by hazardous metals.

Equilibrium, Thermodynamic, Reuse, and Selectivity Studies for the Bioadsorption of Lanthanum onto Sericin/Alginate/Poly(vinyl alcohol) Particles

In a scenario of high demand, low availability, and high economic value, the recovery of rare-earth metals from wastewater is economically and environmentally attractive. Bioadsorption is a promising method as it offers simple design and operation. The aim of this study was to investigate lanthanum bioadsorption using a polymeric bioadsorbent of sericin/alginate/poly(vinyl alcohol)-based biocomposite. Batch system assays were performed to evaluate the equilibrium, thermodynamics, regeneration, and selectivity of bioadsorption. The maximum capture amount of lanthanum at equilibrium was 0.644 mmol/g at 328 K. The experimental equilibrium data were better fitted by Langmuir and Dubinin–Radushkevich isotherms. Ion exchange mechanism between calcium and lanthanum (2:3 ratio) was confirmed by bioadsorption isotherms. Thermodynamic quantities showed that the process of lanthanum bioadsorption was spontaneous (−17.586, −19.244, and −20.902 kJ/mol), endothermic (+15.372 kJ/mol), and governed by entropic changes (+110.543 J/mol·K). The reusability of particles was achieved using 0.1 mol/L HNO3/Ca(NO3)2 solution for up to five regeneration cycles. The bioadsorbent selectivity followed the order of lanthanum > cadmium > zinc > nickel. Additionally, characterization of the biocomposite prior to and post lanthanum bioadsorption showed low porosity (9.95 and 12.35%), low specific surface area (0.054 and 0.019 m2/g), amorphous character, and thermal stability at temperatures up to 473 K. This study shows that sericin/ alginate/poly(vinyl alcohol)-based biocomposites are effective in the removal and recovery of lanthanum from water.

Silver-assisted gold-catalyzed formal synthesis of the anticoagulant Fondaparinux pentasaccharide

Clinically approved anti-coagulant Fondaparinux is safe since it has zero contamination problems often associated with animal based heparins. Fondaparinux is a synthetic pentasaccharide based on the antithrombin-binding domain of Heparin sulfate and contains glucosamine, glucuronic acid and iduronic acid in its sequence. Here, we show the formal synthesis of Fondaparinux pentasaccharide by performing all glycosidations in a catalytic fashion for the first time to the best of our knowledge. Designer monosaccharides were synthesized avoiding harsh reaction conditions or reagents. Further, those were subjected to reciprocal donor-acceptor selectivity studies to guide [Au]/[Ag]-catalytic glycosidations for assembling the pentasaccharide in a highly convergent [3 + 2] or [3 + 1 + 1] manner. Catalytic and mild activation during glycosidations that produce desired glycosides exclusively, scalable route to the synthesis of unnatural and expensive iduronic acid, minimal number of steps and facile purifications, shared use of functionalized building blocks and excellent process efficiency are the salient features.

Adsorption and selectivity studies of direct and magnetite-cored molecularly imprinted polymers (MIPs and magMIPs) towards chosen chalcones investigated with various analytical methods

The following article presents a method for obtaining molecularly imprinted polymers (MIPs) and their magnetic equivalents (magMIPs) using chalcones as imprinting molecules, and their application for direct and competitive chalcones' adsorption.