Laccase-immobilized on superparamagnetic iron oxide nanoparticles incorporated polymeric ultrafiltration membrane for the removal of toxic pentachlorophenol.

A biocatalytic membrane offers an ideal alternative to the conventional treatment process for the removal of toxic pentachlorophenol (PCP). The limelight of the study is to utilize superparamagnetic iron oxide nanoparticles (SPIONs) incorporated (poly (methyl vinyl ether-alt-maleic acid) (PMVEAMA) and poly (ether - ether) sulfone (PEES)) membrane for immobilization of laccase and its application towards the removal of PCP. In regard to immobilization of Tramates versicolor laccase onto membranes, 5 mM glutaraldehyde with 10 h cross-linking time was employed, yielding 76.92% and 77.96% activity recovery for PEES/PMVEAMA/La and PEES/PMVEAMA/SPIONs/Lac, respectively. In the context of kinetics and stability studies, the immobilized laccase on PEES/PMVEAMA/Lac membrane outperforms the free and PEES/PMVEAMA laccases. At pH 7.0, the free enzyme loses half of its activity, while the immobilized laccases maintained more than 87% of their initial activity even after 480 min. With regard to PCP removal, the removal efficiency of immobilized laccase on the membrane was more than free enzyme. With 100 ppm of PCP, immobilized laccase on PEES/PMVEAMA/SPIONs membrane at pH 4.0 and 50 °C had a removal efficacy of 61.65% in 24 h. Furthermore, to perk up the removal of PCP, the laccase-aided system with mediators was investigated. Amongst, veratryl alcohol displayed 71.04% of PCP removal using immobilized laccase. The reusability of the laccase heightened after immobilization on PEES/PMVEAMA/SPIONs portraying 62.44% of the residual activity with 39.4% of PCP removal even after five cycles. The current investigation reveals the efficacy of the mediator-aided PEES/PMVEAMA/lac membrane system towards removing PCP from the aqueous solution, which can also be proposed for a membrane bioreactor.

Designing a novel poly (methyl vinyl ether maleic anhydride) based polymeric membrane with enhanced antifouling performance for removal of pentachlorophenol from aqueous solution.

In this current study, poly (methyl vinyl ether maleic anhydride) (PMVEAMA), a sustainable additive, was incorporated into poly (ether-ether sulfone) (PEES) polymer to design a novel polymeric hybrid membrane for the efficient filtration of toxic pentachlorophenol (PCP) from an aqueous medium. Hydrophilic additives significantly altered the membrane's morphology, structure, porosity, water content, and flux performance compared to the bare PEES membrane. The influence of PMVEAMA on the structural modification of the synthesized polymer membrane was confirmed by SEM, ATR-FTIR, XRD, AFM, zeta potential and contact angle. Findings revealed that the addition of PMVEAMA to the PEES polymer enhances the porosity (17.7%-28.9%), water content (29.8%-39.8%), and pure water flux (186 Lm-2h-1 to 349 Lm-2h-1). The effect of PMVEAMA concentration on the PEES membrane exhibited more finger like pores, better porosity and hydrophilicity, reduced surface roughness, fouling and increased permeability. The fouling studies exhibit an improved 57% PCP rejection and permeation flux of 22.3 Lm-2h-1 due to the addition of the hydrophilic additive. Surprisingly, the incorporation of PMVEAMA into the bare PEES membrane resulted in a high flux recovery ratio of 73.7%. The antifouling properties and enhanced permeability of the PEES/PMVEAMA membrane indicates its potential application in water purification sectors for the efficient separation of contaminants.

Enhancement of antifouling properties, metal ions and protein separation of poly(ether-ether-sulfone) ultrafiltration membranes by incorporation of poly ethylene glycol and n-ZnO.

Composite polymeric membranes with enhanced anti-fouling properties, antimicrobial activities and flux were produced via the phase inversion technique using poly (ether-ether-sulfone) (PEES)/polyethylene glycol (PEG) and n-ZnO. SEM and ATR-FTIR spectroscopy were used to study the morphological and chemical properties of the resulting ultrafiltration membranes. PEG and n-ZnO concentration has an effect on membrane morphologies, ultrafiltration performance, thermal characteristics, metal ion separation studies, surface hydrophilicity and anti-fouling capabilities. The permeate flux increased when the PEG concentration was raised. This results revealed that adding PEG and n-ZnO to membranes increased their surface hydrophilicity and anti-fouling properties. The inclusion of 1.5 wt % n-ZnO and 5 wt % PEG to the pristine PEES membrane resulted in a higher flux of 233.76 L m-2 h-1, 70.09 % of water content, 47.46° of contact angle, the porosity of 30.20 %, and hydraulic resistance of 0.22 kPa/Lm-2h-1. Anti-fouling properties of the fabricated membrane were assessed using a model foulant BSA, which revealed a high flux recovery ratio value. As a result, the PEG and n-ZnO incorporated membrane is more hydrophilic than the virgin membrane. In addition, the prepared PEES/PEG/n-ZnO membrane showed a significant increase in metal ions and protein rejection. Furthermore, an antibacterial test of the membrane revealed that the PEG and n-ZnO composite membrane outperformed the bare PEES membrane in terms of antibacterial capabilities. Overall, the findings reveal that combining n-ZnO and PEG resulted in a membrane with improved anti-fouling capabilities and hydrophilicity, making it suitable for water purification.

Efficient decolorization and detoxification of triarylmethane and azo dyes by porous-cross-linked enzyme aggregates of Pleurotus ostreatus laccase.

In this preset study, porous-cross-linked enzyme aggregates (CLEAs) of Pleurotus ostreatus laccase were utilized for the spontaneous decolorization and detoxification of triarylmethane and azo dyes, reactive blue 2 (RB) and malachite green (MG). The specific surface area and pore radius of the porous-CLEAs are 136.3 m2/g and 19.47 Ao, and the higher specific surface indicated greater biocatalytic efficiency, as increased mass transfer and dye interaction with the CLEAs laccase. CLEAs laccase decolorized 500 ppm of MG and RB with 98.12-58.33% efficiency after 120 min, at pH 5.0 and 50°C, without a mediator. Furthermore, the biotransformation of the MG and RB with immobilized laccase was confirmed with the help of UV-visible spectroscopy, high-performance liquid chromatography, and Fourier transform infrared spectroscopy. The reusability potential of CLEAs was assessed in batch mode for 10 cycles of dye decolorization. The decolorization activities for the immobilized laccase were 89% and 12% at the 6th cycle for MG and RB, respectively. This immobilized enzyme could effectively remove dyes from aqueous solution, and demonstrated significant detoxification in experimental plants (Triticum aestivum and Phaseolus mungo) and plant growth-promoting rhizobacteria (Azospirillum brasilense, Bacillus megaterium, Rhizobium leguminosarum, Bacillus subtilis, and Pseudomonas fluorescens). In conclusion, porous CLEAs laccase could be useful as a potential bioremediation tool for the detoxification and decolorization of dyeing wastewater in future.

Laccase production by Pleurotus ostreatus using cassava waste and its application in remediation of phenolic and polycyclic aromatic hydrocarbon-contaminated lignocellulosic biorefinery wastewater.

The treatment of contaminants from lignocellulosic biorefinery effluent has recently been identified as a unique challenge. This study focuses on removing phenolic contaminants and polycyclic aromatic hydrocarbons (PAHs) from lignocellulosic biorefinery wastewater (BRW) applying a laccase-assisted approach. Cassava waste was used as a substrate to produce the maximum yield of laccase enzyme (3.9 U/g) from Pleurotus ostreatus. Among the different inducers supplemented, CuSO4 (0.5 mM) showed an eight-fold increase in enzyme production (30.8 U/g) after 240 h of incubation. The catalytic efficiency of laccase was observed as 128.7 ± 8.47 S-1mM-1 for syringaldazine oxidation at optimum pH 4.0 and 40 °C. Laccase activity was completely inhibited by lead (II) ion, mercury (II) ion, sodium dodecyl sulphate, sodium azide and 1,4 dithiothretiol and induced significantly by manganese (II) ion and rhamnolipid. After treating BRW with laccase, the concentrations of PAHs and phenolic contaminants of 1144 µg/L and 46160 µg/L were reduced to 96 µg/L and 16100 µg/L, respectively. The ability of laccase to effectively degrade PAHs in the presence of different phenolic compounds implies that phenolic contaminants may play a role in PAHs degradation. After 240 h, organic contaminants were removed from BRW in the following order: phenol >2,4-dinitrophenol > 2-methyl-4,6-dinitrophenol > 2,3,4,6-tetrachlorophenol > acenaphthene > fluorine > phenanthrene > fluoranthene > pyrene > anthracene > chrysene > naphthalene > benzo(a)anthracene > benzo(a)pyrene > benzo(b)fluoranthene > pentachlorophenol > indeno(1,2,3-cd)pyrene > benzo(j) fluoranthene > benzo[k]fluoranthène. The multiple contaminant remediation from the BRW by enzymatic method, clearly suggests that the laccase can be used as a bioremediation tool for the treatment of wastewater from various industries.

Insolubilization of Tramates versicolor laccase as cross-linked enzyme aggregates for the remediation of trace organic contaminants from municipal wastewater.

The novelty of this study deals with the biocatalytic treatment of trace organic contaminants (TrOCs) from municipal wastewater by insolubilized laccase. Laccase from Trametes versicolor was aggregated by three-phase partitioning technique followed by cross-linking with glutaraldehyde to produce insolubilized laccase as cross-linked enzyme aggregates (CLEAs). The optimal conditions for CLEAs preparation include ammonium sulphate concentration of 83% (w/v), crude to t-butanol ratio of 1.00: 1.05 (v/v), pH 5.3, and glutaraldehyde concentration of 20 mM obtained via statistical design. The efficiency of insolubilization of the CLEAs laccase based on the kcat/km ratio was approximately 4.8-fold greater than that of free laccase. The developed CLEAs showed greater resistance to product inhibition mediated by ABTS than the free enzyme and exhibited excellent catalytic activity even after the tenth successive cycle. Further, free laccase and the synthesized CLEAs laccase were utilized to treat five analgesics, two NSAIDS, three antibiotics, two antilipemics, and three pesticides in the municipal wastewater. Under the batch process with operating conditions of pH 7.0 and 20 °C, 1000 U/L of CLEAs, laccase removed 11 TrOCs in the range of about 20-99%. However, the inactivated CLEAs only adsorbed 2-25% of TrOCs. It was observed that acetaminophen, mefenamic acid, trimethoprim, and metolachlor depicted almost complete removal with CLEAs laccase. The performance of CLEAs laccase in a perfusion basket reactor was tested for the removal of TrOCs from municipal wastewater.

Performance study of fouling resistant novel ultrafiltration membranes based on the blends of poly (ether ether sulfone)/poly (vinyl pyrrolidone)/nano-titania for the separation of humic acid, dyes and biological macromolecular proteins from aqueous solutions.

This study explains the use of a ultrafiltration membrane made of polyvinyl pyrrolidone (PVP) and poly(ether ether sulfone) (PEES)/Nano-titania (n-TiO2) for the separation of organic compounds. The results of the tests for porosity, water content, surface chemistry, membrane morphology, and contact angle demonstrated that the developed membranes have more hydrophilicity than PEES membranes due to the redundant hydrophilic nature of PVP and n-TiO2. The membrane pure water flux, which contains 5 wt% PVP and 1.5 wt% n-TiO2, was 312.76 Lm-2h-1, about three-fold higher than that of pristine membrane (95.71 Lm-2h-1). Employing bovine serum albumin as a model foulant, the fouling resistance of the PEES/PVP/n-TiO2 membrane was examined. According to the analysis of flux recovery ratio and irreversible resistance, modified membranes were less likely to foul, and the PEES/n-TiO2 membrane with 5% PVP addition was recommended as optimal. The fabricated membranes effectively removed more than 95% of various organic compounds such as humic acid, safranin O, egg albumin, pepsin, and trypsin from aqueous solution. Permeability of safranin O and humic acid of PEES/PVP/n-TiO2 membranes was about 118 Lm-2h-1 and 138 Lm-2h-1, respectively.

Development of a sustainable route for the production of high-fructose syrup from the polyfructan inulin.

The authors used mesoporous silica microspheres as a support for the immobilization of inulinase from Aspergillus brasiliensis MTCC 1344 by the process of cross-linking. Under optimized operating conditions of pH 6.0, particle/enzyme ratio of 2.0:1.0 and glutaraldehyde concentration of 7 mM, a maximum immobilization yield of 90.7% was obtained after a cross-linking time of 12.25 h. Subsequently, the cross-linked inulinase was utilized for the hydrolysis of 5% inulin, and a maximum fructose concentration of 31.7 g/L was achieved under the optimum conditions of pH 6.0 and temperature 60°C in 3 h. Furthermore, on performing reusability studies during inulin hydrolysis, it was observed that the immobilized inulinase could be reused up to 10 subsequent cycles of hydrolysis, thus providing a facile and commercially attractive process of high-fructose syrup production.