Search Results (20)

The relationship between the structure and function of bacterial laccases has garnered significant research attention thanks to their straightforward molecular structure. Nevertheless, studies examining the impact of an altered molecular structure on the heterologous expression of bacterial laccases in Escherichia coli remain scarce. Our research focuses on elucidating the impact of incorporating copper ions into the molecular structure of modified CotA on its exogenous expression in E. coli as well as its impact on the significance of the amino acid residues surrounding the internal electron channels and water molecule channels of the enzyme molecule. The results show that single-site mutation may affect the expression of CotA by affecting its soluble expression with different binding capacities for copper ions. In addition, the mutants exhibited different laccase activity levels. The catalytic efficiency of T466A was found to be significantly enhanced, reaching 2.29 times that of the wild type. We used structural models to illustrate the correlation between molecular structure and function after the replacement of three mutation sites with alanine. The reduction of hydrogen bonds may be an important factor influencing Cu²⁺’s binding ability and the water molecule production rate. The T466A mutant exhibited strong decolorization ability for Reactive Blue 19 and Eriochrome Black T with 42.2% and 58.2% decolorization rates after one hour of reaction, respectively. This study demonstrates that the molecular mutation studied influences the CotA expression level, enzyme activity, and dye decolorization. Full article

This study investigates Fenton-based processes for textile dye degradation, focusing on Direct Red 28 (DR28), Reactive Blue 19 (RB19), and Reactive Black 5 (RBk5). Results reveal varying effectiveness of catalyst–radical combinations, with copper and peroxydisulfate consistently performing well, especially on RBk5 with 100% and 98.5% decolorization and total organic carbon (TOC) reduction, respectively. Iron faces limitations with DR28 due to sediment formation, resulting in 3.5% and 52.7% TOC removal when paired with hydroxyl and peroxydisulfate radicals, correspondingly. Unexpectedly, cobalt shows notable capabilities with RBk5, reaching 87.2% TOC removal, but performs poorly on the other two dyes, with less than 20% TOC removal when paired with hydroxyl radicals. Cost analysis highlights the cost-effectiveness of the standard photo-Fenton process for easy-to-degrade dyes with a cost of $0.174/g TOC removed, while copper emerges as a viable option for recalcitrant dyes, costing $0.371/g TOC removed. Overall, this research enhances understanding of catalyst–radical interactions on various dyes, a topic that is scarcely discussed in other research, and expands upon it by using techno-economic analysis for Fenton-based technologies for textile wastewater treatment, as a consideration for technology selection in actual application. Full article

An outstanding adsorbent, such as the metal–organic framework (MOF) MIL-101 (Cr), was employed to study the adsorption of two dyes, namely reactive red 2 (RR2) and reactive blue 19 (RB19). Experimental adsorption data were retrieved at T = 25, 35 and 45 °C and analyzed to define the adsorption mechanism of these dyes. A modeling approach based on a double-layer model derived from statistical physics was used. The maximum adsorption capacity (MAC) was found to be 875, 954 and 1002 mg/g for RR2 and 971, 1093 and 1148 mg/g for RB19, at T = 25, 35 and 45 °C, respectively. These values indicate that MIL-101 (Cr) exhibits outstanding performance in removing potential water pollutants such as the RR2 and RB19 dyes. The possible orientations of the RR2 and RB19 dyes upon adsorption were determined by analyzing the number of dye molecules bound per MIL-101 (Cr) active sites during the adsorption process. It was found that the RR2 dye was removed via a mixed parallel and non-parallel orientation on MIL-101 (Cr), while RB19 was removed via an inclined orientation at higher temperatures. The adsorption mechanism suggested that MIL-101 (Cr) site density was reduced due to an exothermic effect, which decreases the number of active sites participating in dye adsorption, even though the reduction in water adsorption may be attributed to the overall endothermic behavior. From the adsorption energy (AE) and the chemical structure of MIL-101 (Cr) and both dyes, it was concluded that hydrogen bonds, Van der Waals forces and π-π stacking are involved in the dye removal process. This research provides new physical insights into the adsorption mechanism of two relevant dyes on an outstanding adsorbent such as the MIL-101 (Cr) MOF. Full article

Bismuth basic nitrates (BBNs) were synthesized via an electrochemical method, i.e., by electrodeposition from an acidic solution of bismuth nitrate, followed by thermal treatment in an air environment. For the first time, the influence of various electrochemical parameters on the morphology, crystal structure, and chemical structure of BBNs was examined. The following synthesis parameters were investigated: electrodeposition current density, thermal treatment temperature of the obtained deposit, and working electrode material (cathode). The obtained materials were characterized by SEM-EDX, XRD, FTIR, TG, and N₂ adsorption/desorption methods and were applied for the sorption of the textile dye RB19. The results showed that the electrodeposition current density and thermal treatment temperature affect the surface morphology, chemical composition, and crystal structure of the obtained materials, as well as the RB19 sorption efficiency. On the other hand, the working electrode material does not affect the properties of the synthesized materials mentioned. Kinetic, isotherm, and thermodynamic analysis of the sorption process were also examined. Full article

Researchers have focused on deriving environmentally benign materials from biomass waste and converting them into value-added materials. In this study, cellulosic crystals derived from sugarcane bagasse (SCB) are augmented with magnetite (M) nanoparticles. Following the co-precipitation route, the composite was prepared, and then the mixture was subjected to a green microwave solvent-less technique. Various mass ratios of SCB:M (1:1, 2:1, 3:1, 5:1, and 1:2) were prepared and efficiently utilized as photocatalysts. To look at the structural and morphological properties of the prepared samples, X-ray diffraction pattern (XRD), scanning electron microscopy (SEM), and elemental analysis were used to describe the composite fibers. SCB:M augmented with H₂O₂ as a Fenton reaction was used to eliminate Reactive blue 19 (RB19) from polluted water and was compared with pristine SCB and M. Additionally, the response surface methodology (RSM) statistically located and assessed the optimized parameters. The optimal operating conditions were recorded at pH 2.0 and 3:1 SCB: M with 40 mg/L and 100 mg/L of hydrogen peroxide. However, the temperature increase inhibits the oxidation reaction. The kinetic modeling fit showed the reaction following the second-order kinetic model with an energy barrier of 98.66 kJ/mol. The results show that such photocatalyst behavior is a promising candidate for treating textile effluent in practical applications. Full article

Coronavirus disease 19 (COVID-19) has occurred for more than four years, and the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) causing COVID-19 is a strain of coronavirus, which presents high rates of morbidity around the world. Up to the present date, there are no therapeutics that can avert this form of illness, and photodynamic therapy (PDT) may be an alternative approach against SARS-CoV-2. Curcumin and methylene blue have been approved and used in clinical practices as a photosensitizer in PDT for a long time with their anti-viral properties and for disinfection through photo-inactivated SARS-CoV-2. Previously, curcumin and methylene blue with antibacterial properties have been used against Gram-positive bacteria, Staphylococcus aureus (S. aureus), and Gram-negative bacteria, Escherichia coli (E. coli), Enterococcus faecalis (E. faecalis), and Pseudomonas aeruginosa (P. aeruginosa). Methods: To conduct a literature review, nine electronic databases were researched, such as WanFang Data, PubMed, Science Direct, Scopus, Web of Science, Springer Link, SciFinder, and China National Knowledge Infrastructure (CNKI), without any regard to language constraints. In vitro and in vivo studies were included that evaluated the effect of PDT mediated via curcumin or methylene blue to combat bacteria and SARS-CoV-2. All eligible studies were analyzed and summarized in this review. Results: Curcumin and methylene blue inhibited the replication of SARS-CoV-2. The reactive oxygen species (ROS) are generated during the treatment of PDT with curcumin and methylene blue to prevent the attachment of SARS-CoV-2 on the ACE2 receptor and damage to the nucleic acids either DNA or RNA. It also modulates pro-inflammatory cytokines and attenuates the clotting effects of the host response. Conclusion: The photodynamic action of curcumin and methylene blue provides a possible approach against bacteria and SARS-CoV-2 infection because they act as non-toxic photosensitizers in PDT with an antibacterial effect, anti-viral properties, and disinfection functions. Full article

UV-based advanced oxidation processes (AOPs) (UV/H₂O₂ and UV/S₂O₈²⁻) with a titanium(IV)-doped carbon dot, TiP-CD, as a catalyst were developed for the decomposition of Remazol Brilliant Blue R (Reactive Blue 19), an anthraquinone textile dye (at T = 25 °C and pH = 7). The Ti-CD, with marked catalytic UV properties, was successfully synthesized by the one-pot hydrothermal procedure, using L-cysteine as carbon precursor, ethylenediamine as nitrogen source, PEG (polyethylene glycol) as a capping agent, and titanium(IV) isopropoxide (precursor of TiO₂ doping). Contrary to azo dyes (methyl orange, orange II sodium salt, and reactive black 5), which achieved complete degradation in a time interval less than 30 min in the developed AOP systems (UV/H₂O₂, UV/S₂O₈²⁻, and UV/TiO₂), the RBB-R showed relatively low degradation rates and low discoloration rate constants. In the presence of the catalyzer, the reaction rate significantly increased, and the pseudo-first-order rate constants for the RBB-R discoloration were UV/3.0 mM H₂O₂/TIP-CD-0.0330 min⁻¹ and UV/1.02 mM S₂O₈²⁻/TIP-CD-0.0345 min⁻¹. Full article

In this work, an innovative nano-carbon material (N-CM) adsorbent was reported for exploring its adsorption behaviors toward cationic methylene blue (MB) and anionic reactive blue 19 (RB19) pollutants. The proposed N-CM was synthesized by a one-step solvothermal treatment of citric acid and zinc gluconate small precursors. N-CM consists of nanosheets that have an advantageous specific surface area, large sp²/sp³ hybridized domains, and abundant nitrogen/oxygen-containing surface functional groups. The synergistic effects of these features are conducive to the MB and RB19 adsorption. Different from anionic RB19 adsorption (79.54 mg/g) by the cooperative π-π stacking and hydrogen bonding, cationic MB adsorbed onto N-CM mainly by the electrostatic attraction at the natural pH solution (> pH_pzc), with an adsorption capacity up to 118.98 mg/g. Interestingly, both MB and RB19 adsorption conformed to the pseudo-second order kinetic (R² ≥ 0.995) and Langmuir isothermal (R² ≥ 0.990) models, accompanied by similar maximum monolayer adsorption capacities of 120.77 and 116.01 mg/g, respectively. Their adsorption processes exhibited spontaneously endothermic characteristics. Moreover, N-CM showed superior selective capability toward MB in different mixed dye systems, with high removal efficiencies of 73–89%. These results demonstrate that the high-performance carbon adsorbent prepared from small precursors via low-temperature carbonization shows great potentials in wastewater treatment. Full article

Eu-doped Y₂O₃ coated diatomite nanostructures with variable Eu³⁺ contents were synthesized by a facile hydrothermal technique. The products were characterized by means of energy dispersive X-ray photoelectron spectroscopy (EDX), scanning electron microscopy (SEM), powder X-ray diffraction (PXRD), Brunauer–Emmett–Teller (BET), UV-vis diffuse reflectance spectroscopy, and photoluminescence spectroscopy techniques. As claimed by PXRD, the particles were crystallized excellently and attributed to the cubic phase of Y₂O₃. The influence of substitution of Eu³⁺ ions into Y₂O₃ lattice caused a redshift in the absorbance and a decrease in the bandgap of as-prepared coated compounds. The pore volume and BET specific surface area of Eu-doped Y₂O₃-coated diatomite is greater than uncoated biosilica. The sonophotocata-lytic activities of as-synthesized specimens were evaluated for the degradation of Reactive Blue 19. The effect of various specifications such as ultrasonic power, catalyst amount, and primary dye concentration was explored. Full article

With an increased consumption of seafood products, food fraud with fish resources has been continuously reported. In particular, codfish has been exploited worldwide as a processed product in fresh, frozen, smoked, canned, or ready-to-eat dish forms. However, it is challenging to identify processed fish products after processing because of their similar morphological characteristics. Substitution and mislabeling of codfish among different species are also happening deliberately or unintentionally. Thus, it is necessary to distinguish cod species to prevent fish adulteration and food fraud. In this study, we developed a multiplex PCR for simultaneously identifying five cod species within Gadidae using capillary electrophoresis. Then, their species-specific primer sets were designed by targeting the mitochondrial cytochrome b gene. Subsequently, the amplicon sizes obtained were 237 bp, 204 bp, 164 bp, 138 bp, and 98 bp for Atlantic cod, Pacific cod, blue whiting, haddock, and Alaska pollock, respectively. The specificity of each primer was further tested using 19 fish species, and no cross-reactivity was observed. The limit of detection of this multiplex PCR assay was 1 pg. The developed multiplex PCR assay can be applied to 40 commercial food products successfully. This detection method will be efficient for managing seafood authentication by simultaneously analyzing multiple cod species. Full article

Ligninolytic enzymes, including laccase, manganese peroxidase, and dye-decolorizing peroxidase (DyP), have attracted much attention in the degradation of mycotoxins. Among these enzymes, the possible degradation pathway of mycotoxins catalyzed by DyP is not yet clear. Herein, a DyP-encoding gene, StDyP, from Streptomyces thermocarboxydus 41291 was identified, cloned, and expressed in Escherichia coli BL21/pG-Tf2. The recombinant StDyP was capable of catalyzing the oxidation of the peroxidase substrate 2,2′-azino-bis(3-ethylbenzothiazoline-6-sulfonic acid), phenolic lignin compounds 2,6-dimethylphenol, and guaiacol, non-phenolic lignin compound veratryl alcohol, Mn²⁺, as well as anthraquinone dye reactive blue 19. Moreover, StDyP was able to slightly degrade zearalenone (ZEN). Most importantly, we found that StDyP combined the catalytic properties of manganese peroxidase and laccase, and could significantly accelerate the enzymatic degradation of ZEN in the presence of their corresponding substrates Mn²⁺ and 1-hydroxybenzotriazole. Furthermore, the biological toxicities of the main degradation products 15-OH-ZEN and 13-OH-ZEN-quinone might be remarkably removed. These findings suggested that DyP might be a promising candidate for the efficient degradation of mycotoxins in food and feed. Full article

The co-occurrence of multiple mycotoxins, including aflatoxin B₁ (AFB₁), zearalenone (ZEN) and deoxynivalenol (DON), widely exists in cereal-based animal feed and food. At present, most reported mycotoxins degrading enzymes target only a certain type of mycotoxins. Therefore, it is of great significance for mining enzymes involved in the simultaneous degradation of different types of mycotoxins. In this study, a dye-decolorizing peroxidase-encoding gene BsDyP from Bacillus subtilis SCK6 was cloned and expressed in Escherichia coli BL21/pG-Tf2. The purified recombinant BsDyP was capable of oxidizing various substrates, including lignin phenolic model compounds 2,6-dimethylphenol and guaiacol, the substrate 2,2′-azino-bis (3-ethylbenzothiazoline-6-sulfonic acid), anthraquinone dye reactive blue 19 and azo dye reactive black 5, as well as Mn²⁺. In addition, BsDyP could efficiently degrade different types of mycotoxins, including AFB₁, ZEN and DON, in presence of Mn²⁺. More important, the toxicities of their corresponding enzymatic degradation products AFB₁-diol, 15-OH-ZEN and C₁₅H₁₈O₈ were significantly lower than AFB₁, ZEN and DON. In summary, these results proved that BsDyP was a promising candidate for the simultaneous degradation of multiple mycotoxins in animal feed and food. Full article

Mixed matrix membranes have received ever-growing attention due to their high separation performance, taking the advantages of both porous fillers and polymer backbones. However, limitations still exist due to the instability of polymers in harsh environments. Here, Kevlar aramid nanofibers, a nanoscale version of poly(paraphenylene terephthalamide), were applied to fabricate a nanofiltration membrane by a thermo-assisted phase inversion method due to their high mechanical strength, physical stability and resistance to solvents. Biochar was incorporated in the Kevlar nanofibers to evaluate its performance in dye/salt separation performance. The fillers’ distribution in the polymeric matrix, structural characteristics, and the interaction of fillers with the polymer in the membrane were characterized via SEM, FTIR, AFM and contact angle analysis. Under the optimal fabrication conditions, the obtained membrane exhibited a pure water flux of 3.83 L m⁻² h⁻¹ bar⁻¹ with a dye rejection of 90.55%, 93.54% and 95.41% for Congo red, methyl blue and Reactive blue 19, respectively. Meanwhile, the mixed matrix membrane maintained a salt rejection of 59.92% and 85.37% for NaCl and Na₂SO₄, respectively. The obtained membrane with high separation performance suggested that Kevlar nanofiber and biochar are good candidates for membrane synthesis. Full article

The functional diversity of the New Caledonian mangrove sediments was examined, observing the distribution of fungal dye-decolorizing peroxidases (DyPs), together with the complete biochemical characterization of the main DyP. Using a functional metabarcoding approach, the diversity of expressed genes encoding fungal DyPs was investigated in surface and deeper sediments, collected beneath either Avicennia marina or Rhizophora stylosa trees, during either the wet or the dry seasons. The highest DyP diversity was observed in surface sediments beneath the R. stylosa area during the wet season, and one particular operational functional unit (OFU1) was detected as the most abundant DyP isoform. This OFU was found in all sediment samples, representing 51–100% of the total DyP-encoding sequences in 70% of the samples. The complete cDNA sequence corresponding to this abundant DyP (OFU 1) was retrieved by gene capture, cloned, and heterologously expressed in Pichia pastoris. The recombinant enzyme, called DyP1, was purified and characterized, leading to the description of its physical–chemical properties, its ability to oxidize diverse phenolic substrates, and its potential to decolorize textile dyes; DyP1 was more active at low pH, though moderately stable over a wide pH range. The enzyme was very stable at temperatures up to 50 °C, retaining 60% activity after 180 min incubation. Its ability to decolorize industrial dyes was also tested on Reactive Blue 19, Acid Black, Disperse Blue 79, and Reactive Black 5. The effect of hydrogen peroxide and sea salt on DyP1 activity was studied and compared to what is reported for previously characterized enzymes from terrestrial and marine-derived fungi. Full article

Wastewater released from textile and dye-based industries is one of the major concerns for human and aquatic beings. Biological decolorization using ligninolytic bacteria has been considered as an effective and alternative approach for the treatment of dyeing wastewater. This study aimed to assess the isolation, characterization and application of soil bacteria isolated from mangrove wetlands in Thailand. Four active bacteria were genetically identified and designated as Klebsiella pneumoniae strain RY10302, Enterobacter sp. strain RY10402, Enterobacter sp. strain RY11902 and Enterobacter sp. strain RY11903. They were observed for ligninolytic activity and decolorization of nine reactive dyes under experimental conditions. All bacteria exhibited strong decolorization efficiency within 72 h of incubation at 0.01% (w/v) of reactive dyes. The decolorization percentage varied from 20% (C.I. Reactive Red 195 decolorized by K. pneumoniae strain RY10302) to 92% (C.I. Reactive Blue 194 decolorized by Enterobacter sp. strain RY11902) in the case of bacterial monoculture, whereas the decolorization percentage for a mixed culture of four bacteria varied from 58% (C.I. Reactive Blue 19) to 94% (C.I. Reactive Black 1). These findings confer the possibility of using these bacteria for the biological decolorization of dyeing wastewater. Full article