Oriented Design of Transition-Metal-Oxide Hollow Multishelled Micropolyhedron Derived from Bimetal–Organic Frameworks for the Electrochemical Detection of Multipesticide Residues

Transition-metal oxides (TMOs) with a hollow multishelled structure have emerged as highly potential materials for high-performance electrochemical sensing, benefiting from their superior electronic conductivity, exceptionally large specific surface area, excellent stability, and electrochemistry properties. In particular, binary TMOs are expected to outperform unitary TMOs due to the synergistic effect of the different metals. Herein, MnCo2O4.5 hollow quadruple-shelled porous micropolyhedrons (MnCo2O4.5 HoQS-MPs) were prepared and employed to construct an ultrasensitive sensing platform for a multipesticide assay. Profiting from complex hollow interior structures and abundant active sites, the MnCo2O4.5 HoQS-MPs manifest outstanding electrochemical properties as electrode materials for the pesticide assay. The MnCo2O4.5 HoQS-MP-based biosensor demonstrated remarkable performance for monocrotophos, methamidophos, and carbaryl detection, with wide linear ranges, as well as low detection limits. This work unveils a new pathway for the ultrasensitive detection of pesticides and demonstrates tremendous potential for detecting other environmentally deleterious chemicals

Highly Transparent and Efficient Counter Electrode Using SiO₂/PEDOT–PSS Composite for Bifacial Dye-Sensitized Solar Cells

A highly transparent and efficient counter electrode was facilely fabricated using SiO₂/poly­(3,4-ethylenedioxythiophene)-poly­(styrenesulfonate) (PEDOT–PSS) inorganic/organic composite and used in bifacial dye-sensitized solar cells (DSCs). The optical properties of SiO₂/PEDOT–PSS electrode can be tailored by the blending amount of SiO₂ and film thickness, and the incorporation of SiO₂ in PEDOT–PSS provides better transmission in the long wavelength range. Meanwhile, the SiO₂/PEDOT–PSS counter electrode shows a better electrochemical catalytic activity than PEDOT–PSS electrode for triiodide reduction, and the role of SiO₂ in the catalytic process is investigated. The bifacial DSC with SiO₂/PEDOT–PSS counter electrode achieves a high power conversion efficiency (PCE) of 4.61% under rear-side irradiation, which is about 83% of that obtained under front-side irradiation. Furthermore, the PCE of bifacial DSC can be significantly increased by adding a reflector to achieve bifacial irradiation, which is 39% higher than that under conventional front-side irradiation

Background Nutrients Affect the Biotransformation of Tetracycline by <i>Stenotrophomonas maltophilia</i> as Revealed by Genomics and Proteomics

Certain bacteria are resistant to antibiotics and can even transform antibiotics in the environment. It is unclear how the molecular mechanisms underlying the resistance and biotransformation processes vary under different environmental conditions. The objective of this study is to investigate the molecular mechanisms of tetracycline resistance and biotransformation by <i>Stenotrophomonas maltophilia</i> strain DT1 under various background nutrient conditions. Strain DT1 was exposed to tetracycline for 7 days with four background nutrient conditions: no background (NB), peptone (P), peptone plus citrate (PC), and peptone plus glucose (PG). The biotransformation rate follows the order of PC > P > PG > NB ≈ 0. Genomic analysis showed that strain DT1 contained <i>tet</i>(X1), a gene encoding an FAD-binding monooxygenase, and eight peroxidase genes that could be relevant to tetracycline biotransformation. Quantitative proteomic analyses revealed that nodulation protein transported tetracycline outside of cells; hypoxanthine–guanine phosphoribosyltransferase facilitated the activation of the ribosomal protection proteins to prevent the binding of tetracycline to the ribosome and superoxide dismutase and peroxiredoxin-modified tetracycline molecules. Comparing different nutrient conditions showed that the biotransformation rates of tetracycline were positively correlated with the expression levels of superoxide dismutase

DataSheet1_Minoxidil delivered via a stem cell membrane delivery controlled release system promotes hair growth in C57BL/6J mice.docx

Objective: Umbilical cord-derived mesenchymal stem cell membrane-loaded minoxidil (MXD) nanoparticles (STCM-MXD-NPs) were prepared to investigate their effects on hair growth in C57BL/6J mice.Methods: STCM-MXD-NPs were obtained by freeze-thawing and differential centrifugation, and their effects on hair growth were evaluated using C57BL/6J mice. The mRNA and protein expression levels of vascular endothelial growth factor (VEGF) and insulin-like growth factor-1 (IGF-1) were detected by real-time polymerase chain reaction and enzyme-linked immunosorbent assays, respectively. Protein expression levels of marker of proliferation Ki-67 (MKI67) and β-catenin (CTNNB) in skin tissue were detected by immunohistochemistry.Results: STCM-MXD-NPs improved MXD solubility. They released the drug slowly, increasing its transdermal properties, accumulation in the skin, and content in the hair bulb tissues with a better efficacy than that of ordinary MXD. Moreover, STCM-MXD-NPs significantly upregulated the mRNA and protein levels of VEGF and IGF-1 and promoted the protein expression of MKI67 and CTNNB in mouse skin tissues, promoting mouse hair growth.Conclusion: Stem cell membrane-loaded MXD nanoparticles with slow-release properties increased MXD accumulation in the skin by improving its transdermal properties, increasing VEGF, IGF-1, MKI67, and CTNNB expression levels and promoting hair growth in C57BL/6J mice.</p

Highly Efficient and Operational Stability Polymer Solar Cells Employing Nonhalogenated Solvents and Additives

The power conversion efficiencies (PCEs) of potential polymer solar cells have been shown to rapidly exceed 15%. However, these high-performance devices are based on halogenated solvents that pose a significant hazard to the atmospheric environment and human beings. The use of nonhalogenated solvents makes the device less efficient because of its solubility issues. In this work, we report high-efficiency devices utilizing PffBT4T-2OD and [6,6]-phenyl C₇₁ butyric acid methyl ester system from nonhalogenated solvents such as <i>o</i>-xylene (<i>o</i>-XY) and 1-methylnaphthalene (Me) hydrocarbon solvent. When Me was used as the additive, the PCE of prepared devices improved from 1.83 to 10.13%, which is rather higher than that of the devices processed with traditional solvents combined with chlorobenzene and 1,8-diiodooctane (8.18%). Both atomic force microscopy and transmission electron microscopy confirmed that after nonhalogen solvents are treated, a more finely phase-separated dense morphology of active layers than after halogen solvents. At the same time, grazing incident wide-angle X-ray scattering patterns show that the combination of nonhalogenated solvents <i>o</i>-XY and Me ingeniously formed an ordered crystal and π–π stacking. Also, the stability of devices prepared from nonhalogenated solvents was significantly better than that of halogenated solvents under continuous illumination in the air without encapsulation

Additional file 2: Figure S2 of Homology modeling and docking studies of ENPP4: a BCG activated tumoricidal macrophage protein

a: The binding pocked of ENPP4 (calculated by CASTp, 2237.4 Å3); b: The binding pocket of ENPP1 (PDB Id 4GTX) (calculated by CASTp,. 1177.7 Å3). (JPG 223 kb

Additional file 1: Table S3. of A novel multi-epitope recombined protein for diagnosis of human brucellosis

The Accession Numbers of OMPs of Brucella spp. in NCBI Protein database. (DOC 32 kb

Additional file 3: Table S2. of A novel multi-epitope recombined protein for diagnosis of human brucellosis

Isotype specific reactivity positive results from the sera of brucellosis patients(146 samples) and controls(102 samples) in ELISA. (DOC 30 kb

Image_2.TIF

<p>Chilling stress affects plant growth and productivity. However, the multi-underlying mechanisms of chilling tolerance are not well understood. Arabidopsis PCaP2 is involved in regulating the dynamic of microtubules (MTs) and F-actin and Ca²⁺-binding ability. Here, the results showed that the PCaP2 expression was highly induced in roots, cotyledons, true leaves, lateral roots and flowers under cold stress. Compared with the wild type, PCaP2-overexpressing plants displayed the enhanced tolerance, whereas its RNAi and mutant were more sensitive in seed germination, seedling and reproductive growth under chilling stress in Arabidopsis. In addition, PCaP2 was also a positive regulator of ABA signaling pathway by analyzing the expression of PCaP2 and the phenotypes of PCaP2-overexpressing, mutant and RNAi plants under ABA treatment. Interestingly, disruption of PCaP2 inhibited the expression of CBF1, -3 and CBF-target COR genes, while increased the CBF2 expression in response to cold or ABA. Moreover, we found that SnRK2s were involved in cold stress and PCaP2 mutants down-regulated the transcription level of SnRK2.2, -2.3 and SnRK2-mediated downstream genes including ABF2, RD29A, KIN1, KIN2, but up-regulated SnRK2.6, ABF1, -3, -4 in ABA and cold treatments. It is well-accepted that PCaP2 as a Ca²⁺-binding protein triggers the gene expression to enhance plant chilling tolerance. Our further studies showed that MT destabilizing activity of PCaP2, but not F-actin-severing function, may be involved in chilling stress. Taken together, our results highlight that PCaP2 plays an important role in chilling tolerance and ABA response by triggering the CBF- and SnRK2-meditated transcriptional regulatory pathways, providing novel evidences of underlying mechanisms of multi-pathways in chilling stress.</p

Image_1.TIF

<p>Chilling stress affects plant growth and productivity. However, the multi-underlying mechanisms of chilling tolerance are not well understood. Arabidopsis PCaP2 is involved in regulating the dynamic of microtubules (MTs) and F-actin and Ca²⁺-binding ability. Here, the results showed that the PCaP2 expression was highly induced in roots, cotyledons, true leaves, lateral roots and flowers under cold stress. Compared with the wild type, PCaP2-overexpressing plants displayed the enhanced tolerance, whereas its RNAi and mutant were more sensitive in seed germination, seedling and reproductive growth under chilling stress in Arabidopsis. In addition, PCaP2 was also a positive regulator of ABA signaling pathway by analyzing the expression of PCaP2 and the phenotypes of PCaP2-overexpressing, mutant and RNAi plants under ABA treatment. Interestingly, disruption of PCaP2 inhibited the expression of CBF1, -3 and CBF-target COR genes, while increased the CBF2 expression in response to cold or ABA. Moreover, we found that SnRK2s were involved in cold stress and PCaP2 mutants down-regulated the transcription level of SnRK2.2, -2.3 and SnRK2-mediated downstream genes including ABF2, RD29A, KIN1, KIN2, but up-regulated SnRK2.6, ABF1, -3, -4 in ABA and cold treatments. It is well-accepted that PCaP2 as a Ca²⁺-binding protein triggers the gene expression to enhance plant chilling tolerance. Our further studies showed that MT destabilizing activity of PCaP2, but not F-actin-severing function, may be involved in chilling stress. Taken together, our results highlight that PCaP2 plays an important role in chilling tolerance and ABA response by triggering the CBF- and SnRK2-meditated transcriptional regulatory pathways, providing novel evidences of underlying mechanisms of multi-pathways in chilling stress.</p