Biodegradation Efficiency Research Articles

A novel “reinforcing-foaming-recovering” strategy for achieving thermally insulating green foams with ultrafast degradation

Lightweight porous materials have garnered increasing attention in application domains of intelligent construction and flexible thermal insulation, owing to their customizable 3D porous structures and outstanding performances. Nonetheless, the severe environmental pollution resulting from the accumulation of non-degradable plastic waste in the ecosystem has sparked significant interest in developing bio-degradable thermal insulation foams. The preparation of biodegradable foam, however, typically requires operating specialized equipment for long periods under extreme conditions, which diminishes its environmental friendliness as claimed. Herein, we present a pioneering "Reinforcing-Foaming-Recovering" strategy to achieve ultralight and recyclable green foams with excellent thermal insulation properties. This innovative strategy, involving materials reinforcing and low-pressure foaming complemented by nitrogen-assisted gas recovering enables the preparation of low-density (0.08 g/cm3) biodegradable foams with restricted shrinkage ratio (<5%). Thanks to the easy-to-control foaming method, combined with the improved 3D network cellular structures caused by nitrogen-assisted gas exchange, the achieved green foams exhibit favorable thermal insulation (39.8 mW/m·K) and superior biodegradation efficiency (11.5%/2 months). The approach of energy-efficient nitrogen-assisted low-pressure foaming of degradable polymers offers a promising and practical solution for producing eco-friendly and multifunctional porous materials with economic advantages.

Microbial consortia for multi-plastic waste biodegradation: selection and validation

The accumulation of plastic waste in the environment poses significant ecological and health risks. This study evaluates the effectiveness of microbial consortia in degrading various types of plastics, including low-density polyethylene (LDPE), low linear-density polyethylene (LLDPE), polyethylene terephthalate (PET) and polystyrene (PS). Qualitative enzyme assays for esterases and ligninases, which are related to plastic biodegradation, were conducted in five microbial strains. Four microbial consortia, combining bacterial and fungal strains, were assembled based on the enzyme profile of their components and evaluated for their ability to degrade both virgin and recycled plastics. The results showed that consortia C2 (Bacillus subtilis RBM2, Fusarium oxysporum RHM1, and Alternaria alternata RHM4) and C4 (Bacillus subtilis RBM2 and Pseudomonas alloputida REBP7) exhibited the highest biodegradation efficiency, particularly achieving significant weight loss in recycled LDPE, virgin LLDPE and recycled PET. The biodegradation was further confirmed by FTIR analysis, which revealed changes in the chemical composition and functional groups of the treated plastics, indicating microbial interaction and degradation. This study underscores the potential of microbial consortia in addressing plastic pollution, highlighting the importance of strategic consortia design based on enzymatic profiles and plastic colonization capabilities. These promising results suggest that further optimization of microbial consortia could offer a viable solution for large-scale plastic waste management.

Microalgae-bacterial consortiums for enhanced degradation of nonylphenol: Biodegradability and kinetic analysis

The widespread use of non-ionic surfactant nonylphenol (NP) has led to significant water pollution, posing a threat to both ecological stability and human health. However, the efficient biodegradation method and system of NP-biodegradation remain complex scientific challenges. In this study, we isolated and characterized three Pseudomonas sp. strains SW-1 (Scenedesmus quadricauda-associated), ZL-2 (Ankistrodesmus acicularis-associated), XQ-3 (Chlorella vulgaris-associated), and one NP-degrading Cupriavidus sp. strain EB-4, which exhibited the ability to utilize NP as the sole carbon source. Furthermore, four consortiums of microalgae-bacterial, S. quadricauda and SW-1 (S-SW), A. acicularis and ZL-2 (A-ZL), C. vulgaris and XQ-3 (C-XQ), S. quadricauda and EB-4 (S-EB), were constructed to investigate their biodegradability and kinetic characteristics of NP degradation from water. The consortiums showed higher degradation efficiency compared to individual microalgae or bacteria. The C-XQ consortium exhibited the highest degradation rate, removing over 94% of NP within just seven days. The first-order model with the following order of degradation rate by consortiums was C-XQ (0.3960 d−1) > S-SW (0.3506 d−1) > A-ZL (0.1968 d−1) > S-EB (0.1776 d−1). Compared with the results of our previous study, the interaction between microalgae and bacteria is not a simple additive relationship. Our findings highlight the potential of an algal-bacterial consortium for the remediation of NP-contaminated environments.

Enhancement of the anaerobic biodegradation efficiency of azo dye by anthraquinone-loaded biochar biofilm: factors affecting biofilm formation and the enhancement mechanism

Carbon-based materials that serve as microbial carriers, and the role of surface-formed biofilms in anaerobic digestion, merit further investigation. This study explored the role and mechanism behind the biodegradation enhancement of biofilms formed onto anthraquinone-loaded biochar (AQS-BC) surfaces through the anaerobic decolorization process of azo dye Reactive Red 2, and optimized the conditions for AQS-BC biofilm formation. The results indicated that the AQS-BC biofilm system exhibited high treatment efficiency and stability in RR2 anaerobic decolorization. RR2 led to the accumulation of volatile fatty acids (VFAs) and inhibition of methane production, while the presence of AQS increased methane production. The effects of sludge concentration, contact time, carbon source concentration, and RR2 concentration on biofilm maturity were also analyzed. Combining biochemical characteristics, electrochemical properties, surface structure, and microbial community analysis, a mechanism for the anaerobic decolorization of RR2 via AQS-BC as a microbial carrier was proposed. This study provides insights into the roles of biofilms in the anaerobic wastewater treatment processes.Graphical

Enhancing biogas production from hemp biomass residue through hydrothermal pretreatment and co-digestion with cow manure: Insights into methane yield, microbial communities, and metabolic pathways

This study investigates the enhancement of biogas production from hemp biomass residue (HBR) through hydrothermal pretreatment and co-digestion with cow manure (CM). Hydrothermal pretreatment at 200 °C for 15 min significantly improved the methane yield from 311.5 to 434.3 mL-CH4/g-VSadded (p ≤ 0.05) from HBR at 10% total solids (TS) loading, a 39% increase. Co-digestion with CM at an optimum ratio of 80:20 further increased the methane yield (738.7 mL-CH4/g-VSadded), representing a 70% improvement over pretreated HBR alone and a 137% increase compared to untreated HBR. Microbial community analysis revealed the dominance of Methanosaeta, comprising 83–93% of archaeal genera across samples. Gene expression analysis showed acetoclastic methanogenesis as the dominant pathway, accounting for 80% of methanogenesis sequences. Hydrogenotrophic methanogenesis and CO2 reduction with H2 pathways contributed 10% each. The optimized process achieved a biodegradation efficiency of 94% for hydrothermally pretreated HBR, compared to 68% for untreated HBR. Mass balance analysis demonstrated that combining hydrothermal pretreatment with anaerobic digestion increased biogas yield from 79% for untreated HBR to 86% for pre-treated HBR (PHBR) co-digested with CM. Integrating hydrothermal pretreatment and co-digestion enhances biogas production from lignocellulosic agricultural residues, contributing to sustainable waste management and renewable energy production.

Biodegradation kinetics of petroleum hydrocarbons by composite microbial agents combined with slow release agents in groundwater

Bioremediation of oil-polluted groundwater is often limited by the properties of oil and oligotrophic conditions in the groundwater environment, sometimes causing long biodegradation times and low biodegradation efficiencies. To clarify this issue, dominant oil-degrading bacteria and slow release agents (SRAs) were prepared and mixed to enhance the biodegradation of different oil samples and hydrocarbons in the groundwater environment. The biodegradation efficiencies of diesel oil, Venezuelan crude oil, and Jibei heavy crude oil by the consortia of bacteria increased from 33.66 %–52.21 % to 34.90 %–63.43 % when optimal nitrogen (N) and phosphorus (P) nutrients were added with SRAs. The release kinetics of N and P SRAs (NP-SRAs) followed Fickian diffusion, and the biodegradation processes of the five petroleum hydrocarbons and three oil products were all well approximated by a second-order kinetic model. The half-lives of the five hydrocarbons in the groundwater were shortened from 0.01 to 7.46 d with the NP salt directly added to 0.002–6.67 d when the NP-SRAs and oxygen SRAs were added, and they decreased from 4.85 to 34.00 d to 2.80–28.90 d for the three oil samples. This study provides insights into the biodegradation kinetics of different hydrocarbons, facilitating the development of effective microbial remediation technologies for the oil contaminated groundwater environment.

Pharmaceuticals removal from hospital wastewater by fluidized aerobic bioreactor in combination with tubesettler

Micropollutants, especially pharmaceutical compounds, are of significant concern owing to their ngL− 1 to µgL− 1 concentration, making them difficult for conventional treatment plants to remove from wastewater. Despite municipal wastewater treatment plant being a primary source of these compounds to be released into the wastewater, on comparison little attention has been given to hospital wastewater. The major focus of studies addressing pharmaceutical compounds is based on synthetic wastewater. This study addresses this research gap by treating wastewater to remove micropollutants (Fluvastatin, ketoprofen, paracetamol, ciprofloxacin, carbamazepine, sulfamethoxazole, and lorazepam) by employing a fluidized aerobic bioreactor. Tubesettler was attached to a fluidized-bed bioreactor to see if it could be used as a polishing unit rather than a secondary clarifier. The environmental risk from the effluent discharge into the environment was assessed regarding the hazard quotient. The paracetamol and ketoprofen were removed at an efficiency of 51% and 60%, respectively, followed by carbamazepine at 50%, ciprofloxacin at 40%, fluvastatin at 47%, sulfamethoxazole at 31%, and lorazepam at 20%. The influent posed moderate environmental risk with (Hazard Quotient) HQ > 0.5, while in effluent the risk was reduced with HQ value 0.4. For effluent from fluidized bed bioreactors (HQ 0.13) and tube setters (HQ 0.15). The associated tube settler was found suitable for polishing units with additional removal efficiencies of 15–43% for all the targeted pharmaceutical compounds. Further studies are required to explore disinfectants’ effect on the reactor’s biodegradation efficiency. Also, further modification and a hybrid version of the fluidized bed bioreactor can be used.

Wheat Bran and Saccharomyces Cerevisiae Biomass’ Effect on Aerobic and Anaerobic Degradation Efficiency of Paper Composite

This study is a continuation of research on sustainable food packaging materials made from locally available feedstock and industrial by-products within the Baltic Sea region. Its main focus is the impact of wheat bran filler and Saccharomyces cerevisiae additive, which was used to develop a novel bio-coating for paper composite packaging, on the biodegradation efficiency of paper composites under aerobic and anaerobic conditions. In this study, we analyzed the effect of 15% and 40% concentrations of wheat bran filler and Saccharomyces cerevisiae biomass on the biodegradation efficiency of paper composites. This research was conducted under controlled environmental conditions, with aerobic biodegradation tested at 46 °C in a compost-based mesophilic–thermophilic environment and anaerobic biodegradation tested at 55 °C in an active inoculum thermophilic environment. The results show that the presence of wheat bran filler significantly improves biodegradation efficiency compared to microcrystalline cellulose reference material. Under aerobic conditions, the biodegradation efficiency for the 40% wheat bran and yeast sample was 6.34%, compared to only 0.71% for the cellulose reference material. In anaerobic conditions, the 15% wheat bran and yeast sample showed a biodegradation efficiency of 96.62%, compared to 82.32% for the cellulose reference material.

Isolation and Identification of Four Strains of Bacteria with Potential to Biodegrade Polyethylene and Polypropylene from Mangrove.

With the rapid growth of global plastic production, the degradation of microplastics (MPs) has received widespread attention, and the search for efficient biodegradation pathways has become a hot topic. The aim of this study was to screen mangrove sediment and surface water for bacteria capable of degrading polyethylene (PE) and polypropylene (PP) MPs. In this study, two strains of PE-degrading bacteria and two strains of PP-degrading candidate bacteria were obtained from mangrove, named Pseudomonas sp. strain GIA7, Bacillus cereus strain GIA17, Acinetobacter sp. strain GIB8, and Bacillus cereus strain GIB10. The results showed that the degradation rate of the bacteria increased gradually with the increase in degradation time for 60 days. Most of the MP-degrading bacteria had higher degradation rates in the presence of weak acid. The appropriate addition of Mg2+ and K+ was favorable to improve the degradation rate of MPs. Interestingly, high salt concentration inhibited the biodegradation of MPs. Results of scanning electron microscopy (SEM), atomic force microscopy (AFM), and Fourier-transform infrared spectroscopy (FTIR) indicated the degradation and surface changes of PP and PE MPs caused by candidate bacteria, which may depend on the biodegradation-related enzymes laccase and lipase. Our results indicated that these four bacterial strains may contribute to the biodegradation of MPs in the mangrove environment.

Efficient biodegradation of poly(butylene adipate-co-terephthalate) in mild temperature by cutinases derived from a marine fungus

Poly(butylene adipate-co-terephthalate) (PBAT) waste gradually accumulates in the environment, posing ecological risks. Enzymatic hydrolysis holds great potential in the end-of-life management of PBAT, but reported enzymes require high reaction temperatures, limiting their practical industrial applications. In this study, we discovered that the marine fungus Alternaria alternata FB1 can efficiently degrade PBAT at 28 °C. Two cutinases designated as AaCut4 and AaCut10, were identified and verified as key enzymes responsible for this degradation process. Notably, the recombinant AaCut10 was able to depolymerize 82.14 % PBAT within 24 h and fully decompose it within 48 h at 37 °C. Through protein engineering, the yield of terephthalic acid monomer was increased to 96.01 %, highlighting its potential for facilitating PBAT upcycling. Furthermore, based on the investigation of the distribution patterns of PBAT hydrolases, novel degradative agents have been identified within unique ecological niches, leading to the establishment of a comprehensive screening repository of PBAT hydrolases. Overall, our study provides new candidates for enzymatic PBAT recycling with low energy consumption and offers insights into the PBAT degradation manner in ecosystems.

Innovative RGO-bridged S-scheme CuFe2O4@Ag2S heterojunction for efficient Sun-light-driven photocatalytic disintegration of Ciprofloxacin

Antibiotics contamination in water bodies poses a significant threat to public health and the environment, necessitating advanced methods for their removal from wastewater. In response to this issue, developing a novel magnetic nanocomposite (RGO/CuFe2O4@Ag2S) as an efficient photocatalyst for the degradation of pharmaceuticals like ciprofloxacin (CIP) is of great importance. The synthesized nanocomposite underwent comprehensive characterization to elucidate its crystalline structure, chemical bonding, surface morphology, elemental composition, internal structure, optical properties, surface area, particle size distribution, and magnetic properties. Under optimized conditions (pH=9, nanocomposite dose =0.5 g/L, CIP concentration of 20 mg/L, and duration of 200 minutes), the nanocomposite demonstrated complete degradation of CIP. Moreover, post-treatment analysis revealed significant reductions in total organic carbon (TOC) and chemical oxygen demand (COD) of 70.08% and 85.08%, respectively, indicating extensive mineralization of the antibiotic. Mechanistic investigations revealed a unique S-scheme heterojunction in the RGO/CuFe2O4@Ag2S nanocomposite, where RGO acts as an electronic bridge between CuFe2O4 and Ag2S. This innovative architecture facilitates efficient charge separation and transfer, significantly enhancing the photocatalytic activity. Reusability tests demonstrated the robust nature of the photocatalyst, with only a modest 6% decline in efficiency after six consecutive cycles. To further assess the system's effectiveness in real-world applications, its performance was evaluated in treating pharmaceutical wastewater. The biodegradation efficiency was quantified by measuring the Average Oxidation State (AOS) and Carbon Oxidation State (COS) of the wastewater samples before and after treatment.

Physico-mechanical properties, hydroxyapatite conversion, biodegradability and antibacterial activity studies of melt-derived BGs based on SiO2-CaO-Na2O-P2O5 quaternary system

The slow biodegradation and low hydroxyapatite (HA) conversion of silicate-based bioactive glasses (BGs) have severely limited their compatibility with biological tissues. To address these challenges, four samples in the form of (52-x)SiO2-24Na2O-24CaO-xP2O5, where x is 2, 4, 6, and 8 mol%, were prepared by a unified melt-quenching method, and the feasibility of P2O5 content fine-tuning in improving glass structure, biodegradability, bioactivity, and antibacterial efficiency was evaluated. The results indicated that as the degree of P2O5 substitution increased, the network structure of the glass became looser, which provided favourable conditions for its degradation. The variation in activation energy for Si4+ ion release from 0.39 eV to 0.25 eV also supported this observation. After 7 days of immersion in simulated body fluid (SBF), analyses by energy dispersive spectroscopy (EDS), X-ray diffraction (XRD) and Fourier transform infrared (FTIR) confirmed that the Ca-P compounds deposited on the glass surfaces were essentially hydroxycarbonated apatite (HCA), and scanning electron microscopy (SEM) images revealed that the generation rate of the HCA were positively correlated with the P2O5 content in the glass system. Meanwhile, antibacterial studies showed that after 24 h of incubation, the antibacterial activity of the four glass samples against Escherichia coli (E. coli) successively increased, with the highest percentage reaching 87.13 ± 2.51 %. In conclusion, this study demonstrates that controllable degradation and high-level bioactivity can be achieved by modulating the P2O5 content in silicate-based BGs, which proves to be an effective and practicable strategy.

Engineering dual-functional and thermophilic BMHETase for efficient degradation of polyethylene terephthalate

Polyethylene terephthalate (PET) biodegradation is hindered by the intermediates bis (2-hydroxyethyl) terephthalate (BHET) and mono (2-hydroxyethyl) terephthalate (MHET). BMHETase, a thermophilic hydrolase identified from the UniParc database, exhibits degradation activity towards both BHET and MHET. BMHETase showed higher activity on BHET than LCCICCG and FASTPETase at temperatures ranging from 50 to 70℃. To enhance its activity in degrading MHET, BMHETase was engineered to mimic Ideonella sakaiensis MHETase. The resulting 6-point mutant’s activities on MHET and BHET were 8 and 2 times those of the WT, with both optimal temperatures increased by 5℃. This enhancement may be attributed to the BMHETase6M’s intensified binding ability with MHET and enlarged binding pocket. When combined with LCCICCG, BMHETase6M achieved complete degradation of MHET in PET films to terephthalic acid, indicating broad application potential. These findings suggest that BMHETase6M holds promise as a candidate for enhancing PET biodegradation efficiency and plastic waste management.

Maximizing diclofenac bioremoval efficiency using Chlorella vulgaris strain H1 and Chlorella sorokiniana strain H2: Unveiling the impact of acetic acid on microalgae

BackgroundDiclofenac (DFC) is a commonly detected pharmaceutical pollutant in wastewater, posing environmental risks. Microalgae have emerged as potential candidates for bioremediation due to their ability to degrade pollutants. This study focuses on investigating the biodegradation potential of two newly isolated microalgae strains, Chlorella vulgaris strain H1 and Chlorella sorokiniana strain H2, towards DFC removal. The optimization of pH is crucial for enhancing the efficiency of bioremediation processes. Therefore, in addition to assessing the biodegradation potential of microalgae, this study also investigates the impact of adjusting the pH of the culture medium using acetic acid as an additional carbon source on the biodegradation process. MethodsThrough genetic analysis using 18S rDNA sequencing, the microalgae strains were identified. Various parameters including growth dynamics, chlorophyll content, cell proliferation, photosynthetic activity, and DFC biodegradation efficiency were comprehensively assessed. Additionally, the impact of incorporating acetic acid as an additional carbon source in the culture medium on the biodegradation process was examined. Significant FindingsC. sorokiniana strain H2 demonstrated superior biodegradation rates compared to C. vulgaris strain H1 across varying DFC concentrations. Specifically, C. sorokiniana strain H2 exhibited remarkable biodegradation rates of 84 %, 83.72 %, and 29.57 % for DFC concentrations of 12.5 mg L−1, 25 mg L−1, and 100 mg L−1, respectively. In contrast, C. vulgaris strain H1 showed lower biodegradation rates of 66.64 %, 29.24 %, and 1.83 % for the corresponding DFC concentrations. The study highlights the potential of C. sorokiniana strain H2 as a promising candidate for the removal of pharmaceutical pollutants like DFC from wastewater. Furthermore, the use of acetic acid as a supplementary carbon source enhanced the biodegradation efficiency, suggesting a potential strategy for optimizing bioremediation processes.

The Influence of Activated Sludge Augmentation on Its Ability to Degrade Paracetamol.

Paracetamol is one of the most commonly used painkillers. Its significant production and consumption result in its presence in the environment. For that reason, paracetamol has a negative impact on the organisms living in ecosystems. Therefore, it is necessary to develop effective methods to remove paracetamol from sewage. One of the methods is the bioaugmentation of activated sludge with organisms with increased degradation potential in relation to paracetamol. This study determined the effectiveness of paracetamol degradation by activated sludge augmented with a free or immobilised Pseudomonas moorei KB4. To immobilise the strain, innovative capsules made of cellulose acetate were used, the structure of which provides an optimal environment for the development of bacteria. Augmentation with both a free and immobilised strain significantly improves the efficiency of paracetamol biodegradation by activated sludge. Over a period of 30 days, examined systems allowed ten doses of paracetamol decomposition, while the unaugmented system degraded only four. At the same time, using the immobilised strain does not significantly affect the functioning of the activated sludge, which was reflected in the stability of processes such as nitrification. Due to the high stability of the preparation, it can become a valuable tool in wastewater treatment processes.

The effect of low-temperature plasma pretreatment on the biodegradability of polyethylene films

ABSTRACT With the increasing focus on environmental friendliness and sustainable development, extensive research has been conducted on the biodegradation of plastics. The non-hydrolyzable, highly hydrophobic, and high-molecular-weight properties of polyethylene (PE) pose challenges for cell interaction and biodegradation of PE substrates. To overcome these obstacles, PE films were treated with low-temperature plasma before biodegradation. The morphology, surface chemistry, molecular weight, and weight loss of PE films after plasma treatment and biodegradation were studied. The plasma treatment decreased the surface water contact angle, formed C–O and C = O groups, and decreased the molecular weight of PE films. With the increased pretreatment time, the biodegradation efficiency rose to 2.6% from 0.63% after 20 days of incubation. The mechanism was proposed that the surface oxygen-containing groups formed by plasma treatment can facilitate the bio-accessibility and be further decomposed and utilised by the microbes. This study provided an effective and rapid pretreatment strategy for improving biodegradation of PE.

Lignin-derived compounds assisted with Kocuria marina H-2 and Pseudomonas putida B6-2 co-culture enhanced naphthalene biodegradation

The implementation of environmentally friendly and sustainable remediation strategies positively impacts solid waste management. In this study, the Kocuria marina H-2 and Pseudomonas putida B6-2 co-culture system demonstrated enhanced naphthalene biodegradation efficiency compared to single-strain cultures. Under optimal conditions of 35 °C, 200 rpm/min, and a 1:1 ratio of the co-culture system, the naphthalene biodegradation potential was further increased. Notably, the addition of both ethylenediamine-pretreated lignin and p-hydroxybenzoic acid significantly elevated naphthalene degradation rates to 68.5 %. In addition, the oil-liquid surface tension decreased, while cell surface hydrophobicity and colony-forming units increased with the addition of lignin-derived compounds. The modification of naphthalene bioavailability by ethylenediamine-pretreated lignin would accelerate the uptake and transport of hydrocarbons via ABC transporters and flagellar assembly. Importantly, genes related to bacterial chemotaxis and fatty acid biosynthesis were upregulated during the co-metabolism of naphthalene and p-hydroxybenzoic acid, further enhancing naphthalene bioconversion.

The Ultimate Fate of Reactive Dyes Absorbed onto Polymer Beads: Feasibility and Optimization of Sorbent Bio-Regeneration under Alternated Anaerobic–Aerobic Phases

Dyes employed in many production cycles are characterized by high toxicity and persistence in the environment, and conventional wastewater treatments often fail to reach high removal efficiencies. Consequently, there is an increasing research demand aimed at the development of more efficient and sustainable technologies. A two-step strategy consisting of dye sorption followed by sorbent bio-regeneration is proposed here, with a special focus on the regeneration step. The objective of this study was to establish the best operating conditions to achieve regeneration of dye-loaded polymers and concurrently the ultimate removal of the dyes. To this aim, the bio-regeneration of the Hytrel 8206 polymer, used as a sorbent material to remove Remazol Red dye from textile wastewater, was investigated in a two-phase partitioning bioreactor (TPPB) under alternated anaerobic–aerobic conditions. Comprehensive analysis of operational parameters, including sorbent load and initial contamination levels, was conducted to optimize bio-regeneration efficiency. Experimental data demonstrated high regeneration efficiencies (91–98%) with biodegradation efficiencies up to 89%. This study also examines the biodegradation process to investigate the fate of biodegradation intermediates; results confirmed the successful degradation of the dye without significant by-product accumulation. This research underscores the potential of TPPB-based bio-regeneration of polymeric sorbent material for sustainable wastewater treatment, offering a promising solution to the global challenge of dye pollution in water resources.

MgO anchored N-doping biochar enhances the bensulfuron-methyl biodegradation by Acinetobacter YH0317: Higher reactive oxygen species level and bacterial viability

Bensulfuron-methyl (BSM) is a typical broad-spectrum sulfonylurea herbicide and the runoff of BSM residues from agricultural regions poses a significant threat to the ecosystem. Here we develop a bacteria-material hybrid system constructed by Acinetobacter YH0317 and Mg(NO3)2 modified biochar (MBC) for efficiently degrading BSM under various conditions including pH and temperature. Results showed that BSM biodegradation efficiency by YH0317&MBC (96.7 %) was significantly higher than YH0317&BC (79.5 %) and YH0317 (43.9 %) at 15 °C after 7 d of incubation. The addition of MBC significantly increased the reactive oxygen species (ROS) level, which was significantly higher than group YH0317. Moreover, the bacterial viability, extracellular polymeric substances (EPS) production, and membrane permeability of YH0317 were also enhanced with the addition of MBC. The electron paramagnetic resonance (EPR) and quenching experiments revealed that singlet oxygen (1O2) was the dominant active substance produced by MBC. The YH0317&MBC could effectively remove the BSM, and reduce the oxidative stress to soybean, which was beneficial to the growth of soybean through hydroponic experiment. This study establishes a microorganism-material system that efficiently removes BSM in aquatic environments and emphasizes the importance of ROS in pollution removal by the hybrid system.

Versatile hydrogel drug carrier loading with peptide-carbon dots conjugates for efficient targeting and synergistic suppression of breast cancer cell

Breast cancer become the most prevalent malignancy and is rising up to the first leading cause of cancer-related mortality among the female people globally. Approaches for safe, specific targeting and efficient inhibition of breast cancer cells, are urgently demanded for lifting the survival rate of breast tumor-bearing patients. Herein, a versatile hydrogel drug carrier consisting of doxorubicin (DOX)-loaded hydrogel microsphere and carbon dots (CDs)-loaded peptide nanowires (DOX@PEG/PNFs-CDs) was constructed, presenting specific targeting and synergistic anti-cancer cell potencies. The hydrogel PEG microspheres with a rich porous structure benefited the drug loading efficiency, demonstrating good biodegradability and higher drug release efficiency at acidic environment. Benefiting from the RGD group of the peptide nanowires, the drug-loaded system specific targeted onto the MDA-MB-231 cells, subsequently promoting the synergistic inhibition of the cancer cell growth by DOX and metformin derived CDs. This all-in-one smart drug carrier post a promising strategy for breast cancer treatment.