Many biological surfaces have hairs, known as trichomes in plants. Here, the wettability and macro- and micro-scale features of olive leaves are analyzed. The upper leaf side has few trichomes, while the lower side has a high trichome density. By combining different techniques including electron and atomic force microscopy, trichome surfaces are found to be chemically (hydrophilic-hydrophobic) heterogeneous at the nano-scale. Both olive leaf surfaces are wettable by water, having a high water contact angle hysteresis and great drop adhesion. The ultra-structural pattern observed for epidermal pavement cells differs from the reticulate cuticle structure of trichomes which shows that leaf surface areas may be substantially different despite being located nearby. Our study provides evidence for the nano-scale chemical heterogeneity of a trichome which may influence the functional properties of biological surfaces, such as water and solute permeability or water capture as discussed here for plants.
Extracellular vesicles (EVs) are small lipid vesicles released by both prokaryotic and eukaryotic cells, involved in intercellular communication, immunomodulation and pathogenesis. In this study, we performed a characterization of the EVs produced by trophozoites of a clinical isolate of the free-living amoeba Naegleria fowleri (N. fowleri). Size distribution, zeta potential, protein profile and protease activity were analyzed. Under our incubation conditions, EVs of different sizes were observed, with a predominant population ranging from 206 to 227 nm. SDS-PAGE revealed protein bands of 25 to 260 KDa. The presence of antigenic proteins was confirmed by Western blot, which evidenced strongest recognition by rat polyclonal antibodies raised against N. fowleri in the region close to 80 KDa and included peptidases, as revealed by zymography. Proteins in selected immunorecognized bands were further identified using nano-ESI-MS/MS. A preliminary proteomic profile of the EVs identified at least 184 proteins as part of the vesicles’ cargo. Protease activity assays, in combination with the use of inhibitors, revealed the predominance of serine proteases. The present characterization uncovers the complexity of EVs produced by N. fowleri, suggesting their potential relevance in the release of virulence factors involved in pathogenicity. Owing to their cargo’s diversity, further research on EVs could reveal new therapeutic targets or biomarkers for developing rapid and accurate diagnostic tools for lethal infections such as the one caused by this amoeba.
Mancozeb is a worldwide fungicide used on a large scale in agriculture. The active component and its main metabolite, ethylene thiourea, has been related to health issues. Robust, fast, and reliable methodologies to quantify its presence in water are of great importance for environmental and health reasons. The electrochemical evaluation of mancozeb using a low-cost electrochemical electrode modified with poly (3,4-ethylene dioxythiophene), multi-walled carbon nanotubes, and gold nanoparticles is a novel strategy to provide an in-situ response for water pollution from agriculture. Additionally, the thermal-, electrochemical-, and photo-degradation of mancozeb and the production of ethylene thiourea under controlled conditions were evaluated in this research. The mancozeb solutions were characterized by electrochemical oxidation and ultraviolet-visible spectrophotometry, and the ethylene thiourea concentration was measured using ultra-high-performance liquid chromatography high-resolution mass spectrometry. The degradation study of mancozeb may provide routes for treatment in wastewater treatment plants. Therefore, a low-cost electrochemical electrode was fabricated to detect mancozeb in water with a robust electrochemical response in the linear range as well as a quick response at a reduced volume. Hence, our novel modified electrode provides a potential technique to be used in environmental monitoring for pesticide detection.
24 February 2017 in Physical Chemistry Chemical Physics
Graphite surfaces can be manipulated by several methods to create graphene structures of different shapes and sizes. Scanning tunneling microscopy (STM) can be used to create these structures either through mechanical contact between the tip and the surface or through electro-exfoliation. In the latter, the mechanisms involved in the process of exfoliation at an applied voltage are not fully understood. Here, we show how a graphite surface can be locally exfoliated in a systematic manner by applying an electrostatic force with a STM tip at the edge of a terrace, forming triangular flakes several nanometers in length. We demonstrate, through experiments and simulations, how these flakes are created by a two-step process: first a voltage ramp must be applied at the edge of the terrace, and then the tip must be scanned perpendicular to the edge. Ab initio electrostatic calculations reveal that the presence of charges on the graphite surface weakens the interaction between layers allowing for exfoliation at voltages in the same range as those used experimentally. Molecular dynamics simulations show that a force applied locally on the edge of a step produces triangular flakes such as those observed under STM. Our results provide new insights into surface modification that can be extended to other layered materials.
Organic conductive polymers have been widely used as active layers in bioelectronic devices. In this work, a novel approach to entrap enzymes directly into the conductive active layer is described, using a polysaccharide as a surfactant. The surfactant allowed the electropolymerization from a micellar media and it acted as a doping agent in the conductive polymer. Gold nanotriangles were added to the matrix in order to enhance the enzymatic product quantification. The composition and oxidation state of the biocompatible conductive layer were confirmed by infrared spectrophotometric and Raman studies. Meanwhile, the gold nanotriangles presence, distribution and electrochemical activity were studied by transmission electron microscopy, atomic force microscopy, dynamic light scattering and cyclic voltammetry techniques. The inhibition of the enzyme, due to the presence of pesticides, was used to electrochemically quantify their concentration in real water samples. The concentration was confirmed by gas and liquid chromatography. Therefore, this novel composite active layer allows building a biosensor with suitable performance for an early warning in environmental control, especially in countries highly impacted by agricultural activities.
Pineapple leaf fibers (PALFs), obtained from abundant yet underutilized pineapple leaf residues, represent a promising feedstock for producing fibrillated cellulose. In this work, cellulosic fibers were isolated and characterized by Fiber Quality Analysis (FQA), showing lengths between 0.33 and 0.47 mm and widths of 12.2 µm after organosolv pulping using ethanol and acetic acid as a catalyst, followed by hydrogen peroxide bleaching with diethylenetriaminepentaacetic acid as a chelating agent. The cellulosic fibers were then subjected to TEMPO-mediated oxidation and subsequently disintegrated by microfluidization to produce micro-/nanofibrillated cellulose (MNFC) with a carboxylate content of 0.85 and 1.00 mmol COO−/g, zeta potential of −41 and −53 mV, and average widths of 15 and 12 nm for unbleached and bleached nanofibrils, respectively. The nanofibrillation yields were 73% and 68% for the bleached and unbleached MNFC samples, indicating the presence of some non-fibrillated or partially fibrillated fractions. X-ray diffraction analysis confirmed preservation of cellulose type I crystalline structure, with increased crystallinity, reaching 85% in the bleached MNFC. These findings demonstrate the feasibility of a sequential process, combining organosolv pulping, hydrogen peroxide bleaching, TEMPO-mediated oxidation, and microfluidization, for preparing MNFC from pineapple leaf fibers. Overall, this study highlights pineapple leaf residues as a sustainable source of MNFC, supporting strategies to transform agricultural waste into valuable bio-based materials.