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Water released by industries that generate coloured pollutants must be treated to safeguard the environment and ensure that the treated water is non-toxic. In this study, we demonstrate the utility of glycine-derived designer micelles, N-lauroyl-N-(pyridin-2-ylmethyl)glycine (PyN12G), as a capping agent to prepare black bismuth oxide nanoparticles (Bi2O3 NPs). The obtained Bi2O3 NPs were confirmed by X-ray photoelectron spectroscopy and energy-dispersive X-ray spectroscopy. Transmission electron microscopy demonstrated that the Bi2O3 NPs are crystalline, with a quasi-spherical morphology and an average size of 42.3 nm, which are further corroborated by powder X-ray diffraction studies to be monoclinic. Fourier transform infrared spectra revealed that the surface of Bi2O3 NPs was stabilized by PyN12G and that the –COOH group of the micelles was involved in surface functionalization. The application of Bi2O3 NPs in environmental remediation was demonstrated by degrading a toxic dye, Congo red (CR). Bi2O3 NPs catalyze sodium borohydride-mediated CR degradation with an efficiency of 88.8% in 15 minutes and a rate constant of 1.92 × 10−3 s−1. Besides CR, Bi2O3 NPs catalyzed the degradation of methylene blue, bromophenol blue, Coomassie blue, crystal violet, and rhodamine B with efficiencies of 95%, 92%, 95%, 90%, and 86%, respectively. Gas chromatography-mass spectrometry analysis reveals that CR is degraded into smaller molecules. The disclosed dye degradation process eliminates the hazardous feature of the dye, which was proven by the seed germination assay. Furthermore, toxicology experiments revealed that Bi2O3 NPs do not affect bacterial growth or seed germination, proving that the NPs are non-toxic and safe to use as a chemocatalyst to eliminate toxic dyes without affecting the environment. [ABSTRACT FROM AUTHOR]

The pathogenicity of foodborne Vibrio parahaemolyticus is a major concern for global public health. This study aimed to optimize the liquid–solid extraction of Wu Wei Zi extracts (WWZE) against Vibrio parahaemolyticus, identify its main components, and investigate the anti-biofilm action. The extraction conditions optimized by the single-factor test and response surface methodology were ethanol concentration of 69%, temperature at 91 °C, time of 143 min, and liquid–solid ratio of 20:1 mL/g. After high performance liquid chromatography (HPLC) analysis, it was found that the main active ingredients of WWZE were schisandrol A, schisandrol B, schisantherin A, schisanhenol, and schisandrin A–C. The minimum inhibitory concentration (MIC) of WWZE, schisantherin A, and schisandrol B measured by broth microdilution assay was 1.25, 0.625, and 1.25 mg/mL, respectively, while the MIC of the other five compounds was higher than 2.5 mg/mL, indicating that schisantherin A and schizandrol B were the main antibacterial components of WWZE. Crystal violet, Coomassie brilliant blue, Congo red plate, spectrophotometry, and Cell Counting Kit-8 (CCK-8) assays were used to evaluate the effect of WWZE on the biofilm of V. parahaemolyticus. The results showed that WWZE could exert its dose-dependent potential to effectively inhibit the formation of V. parahaemolyticus biofilm and clear mature biofilm by significantly destroying the cell membrane integrity of V. parahaemolyticus, inhibiting the synthesis of intercellular polysaccharide adhesin (PIA), extracellular DNA secretion, and reducing the metabolic activity of biofilm. This study reported for the first time the favorable anti-biofilm effect of WWZE against V. parahaemolyticus, which provides a basis for deepening the application of WWZE in the preservation of aquatic products. [ABSTRACT FROM AUTHOR]

Cell-imprinted polydimethylsiloxane substrates, in terms of their ability to mimic the physiological niche, low microfabrication cost, and excellent biocompatibility were widely used in tissue engineering. Cells inside the mature cells' cell-imprinted PDMS pattern have been shown in previous research to be capable of being differentiated into a specific mature cell line. On the other hand, the hydrophobicity of PDMS substrate leads to weak cell adhesion. Moreover, there was no guarantee that the cells would be exactly located in the cavities of the cells' pattern. In many studies, PDMS surface was modified by plasma treatment, chemical modification, and ECM coating. Hence, to increase the efficiency of cell-imprinting method, the concavity region created by the cell-imprinted pattern is conjugated with collagen. A simple and economical method of epoxy silane resin was applied for the selective protein immobilization on the desired regions of the PDMS substrate. This method could be paved to enhance the cell trapping into the cell-imprinted pattern, and it could be helpful for stem cell differentiation studies. The applied method for selective protein attachment, and as a consequence, selective cell integration was assessed on the aligned cell-imprinted PDMS. A microfluidic chip created the aligned cell pattern. After Ar+ plasma and APTES treatment of the PDMS substrate, collagen immobilization was performed. The immobilized collagen was removed by epoxy silane resin stamp from the ridge area where the substrate lacked cell pattern and leaving the collagen only within the patterned areas. Coomassie brilliant blue staining was evaluated for selective collagen immobilization, and the collagen-binding stability was assessed by BCA analysis. MTT assay for the evaluation of cell viability on the modified surface was further analyzed. Subsequently, the crystal violet staining has confirmed the selective cell integration to the collagen-immobilized site on the PDMS substrate. The results proved the successfully selective collagen immobilization on the cell-imprinted PDMS and showed that this method increased the affinity of cells to attach inside the cell pattern cavity. [ABSTRACT FROM AUTHOR]

A biocatalytic system comprising fungal laccase and mediators can generate phenol radicals and efficiently eliminate various triarylmethane dyes. This study systematically explores the kinetic impact of dissolved organic matter (DOM), represented by humic substance (HS consisting of 90% fulvic acid, from lignite), on the decolorization of seven typical triarylmethane dyes by Trametes versicolor laccase and twenty natural mediators. Among these, 4-hydroxybenzyl alcohol (4-HA) and methyl violet (MV) undergo in-depth investigation regarding degradation products, pathways, and reaction mechanisms. In instances where HS hampers laccase-alone decolorization, such as malachite green, Coomassie brilliant blue, bromophenol blue, and acid magenta, this inhibition may persist despite mediator introduction. Conversely, in cases where HS facilitates decolorization, such as crystalline violet and ethyl violet, most laccase-mediator systems (LMSs) can still benefit. For MV decolorization by laccase and 4-HA, HS's kinetic effect is controlled by concentration and reaction time. A 5 mg/L HS increased the decolorization rate from 50% to 67% within the first hour, whereas 10 mg/L HS only achieved 45%. After 16 h of reaction, HS's impact on decolorization rate diminishes. Furthermore, the addition of HS enhances precipitation production, probably due to its involvement in polymerization with MV and mediator. Computational simulations and spectral monitoring reveal that low HS concentrations accelerate laccase-mediated demethylation by disrupting the chromophores bound to MV, thus promoting the decolorization of MV. Conversely, inhibition by high HS concentrations stems from the competitive binding of the enzyme pocket to the mediator, and the reduction of phenol free radicals in the system. Molecular docking and kinetic simulations revealed that laccase forms complexes with both the mediator and MV. Interestingly, the decolorization of MV occurred through a non-radical mechanism in the presence of HS. This work provided a reference for screening of high catalytic performance mediators to remove triarylmethane dyes in the actual water environment. [Display omitted] • Dissolved HS had a trade-off effect on laccase-mediator (LMS) biocatalysis system. • The impact on dye removal by HS depends on its concentration and reaction time. • Competitive inhibition and radical quenching by HS lead to reduced removal rate. • Dye decolorization occurred through non-radical mechanism with HS around. [ABSTRACT FROM AUTHOR]

Laccases are enzymes able to catalyze the oxidation of a wide array of phenolic and non-phenolic compounds using oxygen as co-substrate and releasing water as by-product. They are well known to have wide substrate specificity and in recent years, have gained great biotechnological importance. To date, most well studied laccases are from fungal and mesophilic origin, however, enzymes from extremophiles possess an even greater potential to withstand the extreme conditions present in many industrial processes. This research work presents the heterologous production and characterization of a novel laccase from a thermoalkaliphilic bacterium isolated from a hot spring in a geothermal site. This recombinant enzyme exhibits remarkably high specific activity (>450,000 U/mg) at 70 °C, pH 6.0, using syringaldazine substrate, it is active in a wide range of temperature (20–90 °C) and maintains over 60% of its activity after 2 h at 60 °C. Furthermore, this novel spore-coat laccase is able to biodecolorize eight structurally different recalcitrant synthetic dyes (Congo red, methyl orange, methyl red, Coomassie brilliant blue R250, bromophenol blue, malachite green, crystal violet and Remazol brilliant blue R), in just 30 min at 40 °C in the presence of the natural redox mediator acetosyringone. • Novel spore-coat bacterial laccase from thermoalkaliphile overexpressed in E. coli • With high activity towards structurally diverse substrates without need of mediator • Exhibits remarkable activity, >450,000 U/mg, with syringaldazine at 70 °C, pH 6.0 • The recombinant enzyme is active over a wide range of temperature (20–90 °C). • Biodecolorizes 8 different synthetic dyes in 30 min at 40 °C with acetosyringone [ABSTRACT FROM AUTHOR]

Pure graphene oxide (GO) membranes have a tendency to swell in water and have a relatively low flux, making them impractical for water treatment applications. Herein, a novel two-dimensional (2D) composite membrane based on reduced-holey GO (r-HGO) and MXene materials was developed. As a consequence of synergistic effects arising from its unique heterogeneous structure, the r-HGO/MXene composite membrane exhibited an exemplary performance for water treatment, in terms of its permeability and pollutant rejection, and high physical stability. The preparation conditions, especially the reduction degree of GO and the proportions of r-HGO and MXene, determine the properties and performance of the composite membrane. The water flux of the r-HGO/MXene composite membrane with a r-HGO/MXene mass ratio of 1/1 achieved 121.0 L m−2 h−1·bar−1, which was 23 times higher than that of pure GO membrane (∼5.2 L m−2 h−1·bar−1). The removal rates of Coomassie brilliant blue, Methyl blue, Crystal violet, Rhodamine B, Methylene blue, were all above 90 %. Furthermore, the r-HGO/MXene composite membrane was found to be physically stable for more than a week in an aqueous environment. The results of this work show that the r-HGO/MXene composite membrane has great potential as a separation method in water treatment by overcoming some of the important limitations of other current 2D materials. [Display omitted] • The r-HGO/MXene membrane had a high water permeability of ∼ 120.96 L m−2 h−1 bar−1. • Five common dyes were rejected up to 90 %. • Long-term stability of r-HGO/MXene membrane was demonstrated in water environment. • There was a remarkable synergistic effect between r-HGO and MXene. [ABSTRACT FROM AUTHOR]

Green fabrication of copper nanoparticles (CuNPs) is an environmentally friendly and cost-effective method of synthesis for biomedical and bioremediation applications. In recent times, bacterial pathogens contaminating or affecting food and food crops pose the greatest threat to the food industry. In addition to this issue, synthetic dyes released from the textile and dyeing industries are polluting aquatic ecosystems and agricultural lands. The combined impact of these two factors is considered a major threat to life. Therefore, the use of CuNPs will provide an effective and long-term solution as an antibacterial and dye removing agent. The current study focuses on the synthesis of CuNPs using the leaf extract of Chloroxylon swietenia (C-CuNPs). The formation of a peak at 390 nm and a change in color from yellow to dark brown confirmed the synthesis of C-CuNPs. Subsequent synthesis at pH 9 was suitable for preparing C-CuNPs. Structural and chemical characterization of C-CuNPs was performed using Fourier Transfer Infra-Red (FTIR), X-ray diffraction (XRD), Dynamic Light scattering (DLS), and Scanning Electron Microscopy (SEM) analysis. The synthesized C-CuNPs possess a crystalline nature, a functional group that resembles C. swietenia , and are negatively charged and spherical in shape. C-CuNPs were tested against Congo red, Coomassie blue, and crystal violet and they showed complete degradation within 24 h under optimum conditions. Disk diffusion and broth dilution assay were used to test the antibacterial activity of C-CuNPs against Staphylococcus nepalensis , Staphylococcus gallinarum , Pseudomonas stutzeri, Bacillus subtilis , and Enterococcus faecalis. Therefore, the present study represents the first report on C-CuNPs' ability to degrade synthetic dyes and kill foodborne bacterial pathogens. Thus, the study has shed light on the potential of green synthesized CuNPs as bioremediation and packaging material in the future. [ABSTRACT FROM AUTHOR]

Green synthesized silver nanoparticles (AgNPs) are becoming an important candidate for bioremediation and biomedical applications. But in recent trends, more focus is given towards degradation of dyes and application against food pathogens. The synthesis of efficient AgNPs depends on the selection of potential biological material for synthesis. Therefore, in the present study, AgNPs were synthesized using Chloroxylon swietenia. The synthesis AgNPs was confirmed by the formation of dark brown precipitate. Further physicochemical characterization performed using XRD, FTIR, SEM and DLS showed the formation of crystalline structure, presence of functional group from the C. swietenia , dispersed spherical and rod-shaped nanoparticles (6.9 nm) and possess good stability due to the negative partial charges. The dye degrading efficacy of Chloroxylon swietenia mediated synthesized AgNPs (C-AgNPs) was >95%, 90% and >90% tested against Congo red (CR), Coomassie blue (CB) and crystal violet (CV) dye, respectively withing 24 h of treatment under optimum conditions. The antibacterial activity of C-AgNPs (10 mg/mL) was analysed against Staphylococcus nepalensis (3.03 ± 0.35 cm), Staphylococcus gallinarum (2.96 ± 0.15 cm), Bacillus subtilis (2.86 ± 0.23 cm), Enterococcous faecalis (2.8 ± 0.30 cm) and Pseudomonas stuteria (2.06 ± 0.25 cm) using Disc diffusion method, Minimum inhibitory concentration (MIC) and Minimum bactericidal activity (MBC). Therefore, the present study is the first and foremost report on C-AgNPs application as dye degrading and antibacterial agents against food dyes and pathogens. This will provide a major strategy to unveil the complications in food and packaging industries worldwide. [ABSTRACT FROM AUTHOR]

In the last few decades, nanotechnology-based approaches are emerging in biomedical and environmental applications, which include antimicrobial, anticancer, and photocatalytic applications. Green synthesis is advantageous than the conventional methods since it is environmentally friendly, economically viable and convenient to scale up for commercial production. The present study is aimed to synthesize silver nanoparticles (AgNPs) using Ruellia tuberosa leaf extract. AgNPs was analyzed using UV–visible spectroscopy, FT-IR, FESEM, EDAX, TEM, SAED and DLS analyses.SPR absorbance spectrum of the AgNPs was witnessed at 455 nm. Morphological characterization using AgNPs using FE-SEM with EDX, TEM with SAED and DLS analysis showed that the nanoparticles are in spherical shape with an average size of 55.65 nm. Further, antimicrobial activity of the green fabricated AgNPs was tested against Gram negative and Gram positive bacterial pathogens, which exhibited potential bactericidal activity. Also, the cytotoxic activity of AgNPs in A549 lung cancer cell line showed activity at the IC 50 of 68 μg/mL as revealed by MTT assay. Further, apoptosis of A549 cells treated with AgNPs were analyzed by fluorescence microscopy. The photocatalytic degradation of AgNPs was assessed against crystal violet (CV) and Coomassie brilliant blue (CBB). Above-mentioned findings clearly demonstrate that AgNPs exhibited photocatalytic degradation and biomedical application. ga1 • Ruellia tuberosa leaf extract for the first-time attempt by green phyto-synthesis. • AgNPs assed by UV–vis, FT-IR, FESEM-EDX, TEM-SAED and DLS were tested. • AgNPs were exhibited excellent antibacterial, anticancer and photocatalytic activities. • Synthesized AgNPs showed effective anticancer activity against A549 lung cancer cells. • Photocatalytic degradation properties against CV and CBB under sunlight irradiation. [ABSTRACT FROM AUTHOR]