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The enzymatic degradation of plastic offers a green, sustainable strategy and scalable circular carbon route for solving polyester waste. Among the earlies discovered plastic-degrading enzymes are PET hydrolase (PETase) and MHET hydrolase (MHETase), which act synergistically. To promote the adsorption of enzymes on PET surfaces, increase their robustness, and enable directly depolymerization, we designed hydrophobin HFBI fused-PETase and MHETase. A customized self-assembled synergistic biocatalyst (MC@CaZn-MOF) was further developed to promote the two-step depolymerization process. The tailored catalysts showed better adhesion to the PET surface and desirable durability, retaining over 70% relative activity after incubation at pH 8.0 and 60 °C for 120 h. Importantly, MC@CaZn-MOF could directly decompose untreated AGf-PET to generate 9.5 mM TPA with weight loss over 90%. The successful implementation of a bifunctional customized catalyst makes the large-scale biocatalytic degradation of PET feasible, contributing to polymer upcycling and environmental sustainability. [Display omitted] • Coprecipitation fabricated biocatalysts with a specific spatial distribution. • MC@CaZn-MOF rapidly degrade PET via synergy's enzymatic adsorption and degradation. • Immobilized improved the enzymatic durability in an inhospitable environment. • The MC@CaZn-MOF composite catalyzes the complete degradation of PET to TPA. [ABSTRACT FROM AUTHOR]

The widespread use of polyethylene terephthalate (PET) in various industries has led to a surge in microplastics (MPs) pollution, posing a significant threat to ecosystems and human health. To address this, we have developed a bacterial enzyme cascade reaction system (BECRS) that focuses on the efficient degradation of PET. This system harnesses the Escherichia coli (E. coli) surface to display CsgA protein, which forms curli fibers, along with the carbohydrate-binding module 3 (CBM3) and PETases, to enhance the adsorption and degradation of PET. The study demonstrated that the BECRS achieved a notable PET film degradation rate of 3437 ± 148 μg/(d*cm²), with a degradation efficiency of 21.40% for crystalline PET MPs, and the degradation products were all converted to TPA. The stability of the system was evidenced by retaining over 80% of its original activity after multiple uses and during one month of storage. Molecular dynamics simulations confirmed that the presence of CsgA did not interfere with the enzymatic activity of PETases. This BECRS represents a significant step forward in the biodegradation of PET, particularly microplastics, offering a practical and sustainable solution for environmental pollution control. [Display omitted] • Surface display of PETase on E. coli using the CsgA module-mediated display system. • Co-displaying CBM3 and PET hydrolase on the ECN surface with MHETase intracellularly. • Structural modeling analysis of the effect of CsgA on the catalytic mechanism. • The system exhibits robust repeatability and long-term storage stability. • BECRS effectively converts PET MPs to TPA without byproducts. [ABSTRACT FROM AUTHOR]

Continuous exposure to plastic pollutants may have serious consequences on human health. However, most toxicity assessments focus on non-environmentally relevant particles and rarely investigate long-term effects such as cancer induction. The present study assessed the carcinogenic potential of two secondary nanoplastics: polyethylene terephthalate (PET) particles generated from plastic bottles, and a biodegradable polylactic acid material, as respective examples of environmentally existing particles and new bioplastics. Pristine polystyrene nanoplastics were also included for comparison. A broad concentration range (6.25–200 μg/mL) of each nanoplastic was tested in both the initiation and promotion conditions of the regulatory assessment-accepted in vitro Bhas 42 cell transformation assay. Parallel cultures allowed confirmation of the efficient cellular internalisation of the three nanoplastics. Cell growth was enhanced by polystyrene in the initiation assay, and by PET in both conditions. Moreover, the number of transformed foci was significantly increased only by the highest PET concentration in the promotion assay, which also showed dose-dependency, indicating that nano PET can act as a non-genotoxic tumour promotor. Together, these findings support the carcinogenic risk assessment of nanoplastics and raise concerns regarding whether real-life co-exposure of PET nanoplastics and other environmental pollutants may result in synergistic transformation capacities. [Display omitted] • Polyethylene terephthalate, polylactic acid, and polystyrene nanoplastics were used. • Carcinogenicity was assessed using the in vitro Bhas 42 cell transformation assay. • Only polyethylene terephthalate (PET) nanoplastics induced cell transformation. • PET nanoplastics acted through a tumour promotion mode of action. • The three types of nanoplastics were efficiently internalised into cells. [ABSTRACT FROM AUTHOR]

Pyrolysis-gas chromatography coupled to Orbitrap-mass spectrometry is a novel technique that allows the low level and precise determination of microplastics in environmental samples. In this paper, we develop and assess the target and untargeted performance of Pyr-GC-Orbitrap-MS. The method was optimized for 10 plastic polymers: polymethyl methacrylate, nylon-6,6, polypropylene, nitrile butadiene rubber, polyvinyl chloride, polyethylene terephthalate, acrylonitrile butadiene styrene, polyethylene, polycarbonate, and polystyrene. Standards were home-made using a diamond driller to attain mean sizes within the range of 45–382 µm. A step-by-step optimization of the analytical procedure was carried out. First, accurate mass measurement of each polymer at 60,000 resolution was studied to select the 3 most intense and selective quantification and confirmation ions. Second, internal standard quantification was optimized, and good linearity, repeatability, and reproducibility were obtained. Blank contribution and instrumental detection limit were evaluated for each polymer. Finally, the combined and expanded uncertainty of the Pyr-GC-Orbitrap-MS method was calculated to determine the sources of variation, considering that home-made standards were used. To evaluate method performance, targeted and non-targeted analysis of indoor air samples collected from gyms and department stores were carried out. The Pyr-GC-Orbitrap-MS methodology herein described can be applied for the quantitative assessment of MPs and other substances in different matrices. [Display omitted] • Pyrolysis with orbitrap mass spectrometry allows detection of microplastics in air. • Microplastic standards allow calibration and calculation of quality parameters. • Exact mass measurements allows target and non-target analysis of microplastics. • The uncertainty of the method allows validating the method for trace concentrations. • Microplastics and other contaminants have been detected in air from stores and gyms. [ABSTRACT FROM AUTHOR]

Discarding PET plastic (dPET) causes serious environmental pollution and enormous fossil resources waste. Processing techniques have mainly focused on the conversion of dPET into monomers, with minimal reports highlighting their transformation into high–value materials. This work intends to transform dPET into a high–performance material with potential alternative value in harsh production environments. The soft and hard segments of the thermoplastic polyester elastomeric (TPEE) molecular structure are reacted and cross–linked with dPET using a facile one–pot process, and two main polymers, (C 8 H 4 O 4) n and ((C 16 H 18 O 4) 0.76 ·(C 4 H 8 O) 0.24) n are generated after the reaction. Through chemical reactions between TPEE and dPET, new characteristic products and chemical bond–crossing structures are formed, while the resulting product particles or multiple TPEE particles are anchored by the high viscosity of dPET, which endows the material with superior tensile strength (34.21 MPa) and impact resistance. The glass transition temperature (T g) of the material implies that neither the molecular chain nor the chain segments can move, while only the atoms or groups composing the molecule vibrate at their equilibrium positions. The development of this new treatment method may contribute to the reduction of environmental pollution and the improvement of the high–value conversion and utilization of dPET. [Display omitted] • An innovative strategy to convert dPET into functional materials was developed. • The fabricated material showed excellent tensile strength and impact resistance. • (C 8 H 4 O 4) n and (C 16 H 18 O 4) 0.76 ·(C 4 H 8 O) 0.24) n were generated after polymerization. • Newly formed long–chain polymer is responsible for superior tensile strength. • This study gives a new alternative approach to high-value utilization of dPET. [ABSTRACT FROM AUTHOR]

Nanoplastics are emerging environmental contaminants, but their presence in environmental and potable water remains largely understudied due to the absence of quantitative analytical methods. In this study, we developed and validated a pretreatment method that combines hydrogen peroxide digestion and Amicon® Stirred Cell ultrafiltration (at 100 kDa, approximately 10 nm) with subsequent detection by pyrolysis gas chromatography–mass spectrometry (Pyr-GC/MS). This method allows for the simultaneous identification and quantification of nine selected nanoplastic types, including poly(ethylene terephthalate) (PET), polyethylene (PE), polycarbonate (PC), polypropylene (PP), poly(methyl methacrylate) (PMMA), polystyrene (PS), polyvinylchloride (PVC), nylon 6, and nylon 66, in environmental and potable water samples based on polymer-specific mass concentration. Limits of quantification ranged from 0.01 to 0.44 µg/L, demonstrating the method's ability to quantitatively detect nanoplastics in environmental and potable water samples. Most of the selected nanoplastics were detected at concentrations of between 0.04 and 1.17 µg/L, except for PC, which was consistently below the limit of detection (<0.44 µg/L). The prevalent polymer components in the samples were PE (0.10 – 1.17 µg/L), PET (0.06 – 0.91 µg/L), PP (0.04 – 0.79 µg/L), and PS (0.06 – 0.53 µg/L) nanoplastics. The presented analytical method offers an accurate means to identify, quantify, and monitor nanoplastics in complex environmental and potable water samples. It fills gaps in our understanding of nanoplastic pollution levels, providing a valuable methodology and crucial reference data for future studies. [Display omitted] • Presentation of a methodology for the quantification of nanoplastics in water. • Mass concentrations of nanoplastics across water samples were assessed by Pyr-GC/MS. • Eight nanoplastics (PMMA, Nylon 6, Nylon 66, PC, PS, PET, PP, PE) quantified. • PE, PET, PP and PS were the predominant nanoplastics. • Total nanoplastics concentrations of between 0.04 and 1.17 µg/L in water samples. [ABSTRACT FROM AUTHOR]

The release of additives from microplastics is known to harm organisms. In the environment, microplastics are exposed to weathering processes which are suspected to influence additive leaching kinetics, the extent and mechanism of which remain poorly understood. We examined the impact of weathering on stabiliser additive leaching kinetics using environmentally relevant accelerated weathering and leaching procedures. Nine binary polymer-additive formulations were specifically prepared, weathered, analysed, and evaluated for their leaching characteristics. Cumulative additive release (Ce) varied widely between formulations, ranging from 0.009 to 1162 µg/g. Values of Ce generally increased by polymer type in the order polyethylene terephthalate < polyamide 6 < polyethylene. The change in leaching kinetics after accelerated weathering was incongruous across the nine formulations, with a significant change in Ce only observed for three out of nine formulations. Physicochemical characterisation of the microplastics demonstrated that additive blooming was the primary mechanism influencing the leaching response to weathering. These findings highlight the dependency of additive fate on the polymer type, additive chemistry, and the extent of weathering exposure. This has significant implications for risk assessment and mitigation, where the general assumption that polymer weathering increases additive leaching may be too simplistic. [Display omitted] • Additive leaching kinetics from weathered microplastics were assessed. • The leaching response to weathering was specific to the plastic formulation. • Additive blooming and water solubility were key processes influencing leaching. • Best practise and implications for risk assessment are highlighted. [ABSTRACT FROM AUTHOR]

An in-depth understanding of urban road-deposited MPs is important for the accurate prediction of the risk posed by MPs in different exposure scenarios. This study provides new insights into the intrinsic/extrinsic factors in terms of the variability of concentration and species in urban road-deposited MPs. The study results confirmed that a considerable abundance of road-deposited MPs can be identified with the average concentration ranging from 0.33 to 3.64 g m-2. Land use types and sediment particle size are the important factors that contribute to MPs abundance. The majority of detected MPs including polyethylene (PE), polypropylene (PP), polystyrene (PS) and polyethylene terephthalate (PET) are mainly derived from anthropogenic activities in commercial and residential land uses while rubber MP particles in urban road surfaces are mainly derived from tyre wear. The significant correlation (p < 0.05) between MPs and fine dust particles (< 150 µm) indicated the high affinity of small dust particles for MPs. The risk scores from MPs varied greatly from 10 to 11,000 among the study sites, which indicated the significant spatial variation of potential environmental risks posed by road-deposited MPs. The hotspots of risks posed by MPs were in areas with a high fraction of industrial, commercial and residential land uses. Specifically, the highest risk from MPs was found in mixed industrial and residential areas. [Display omitted] • Land use and particle size are the crucial factors for road-deposited MPs abundance. • Particles < 75 µm show stronger correlation with MPs concentration than MPs species. • Mixed industrial and residential land use has the highest risk posed by MPs. [ABSTRACT FROM AUTHOR]

Plastic aging occurs in all environmental media and affects their environmental behavior and toxicity. In this study, non-thermal plasma was applied to simulate the aging process of plastics, with polyethylene terephthalate (PET-film) being used as a model. The surface morphology, mass defects, toxicity of aged PET-film and the generation of airborne fine particles were comprehensively characterized. The surface of PET films began to become rough and then gradually became uneven, generating pores, protrusions and cracks. The toxicity of aged PET films was assessed in Caenorhabditis elegans which significantly reduced head thrashing, body bending and brood size. A single particle aerosol mass spectrometry instrument was used to characterize the size distribution and chemical composition of airborne fine particles in real-time. Few particles were observed during the first 90 min, while the generation of particles accelerated significantly after aging time beyond 90 min. For two pieces of PET film with surface area of 5 cm2, during the 180 min, at least 15113 ± 153 fine particles were generated, having a unimodal size distribution with a peak of 0.4 µm. The main components of these particles included metals, inorganic non-metals, and organic components. The results provide useful information on plastic aging and are beneficial in assessing the potential environmental risks. [Display omitted] • Non-thermal plasma was applied to simulate the aging process of plastics. • Acute exposure to aged PET-film caused more severe neurotoxicity than that to virgin PET-film. • The toxicity of aged PET films was assessed in Caenorhabditis elegans. • The airborne fine particles from PET-film aging carry metals and organic components. [ABSTRACT FROM AUTHOR]

Recently, biodegradable plastics (BPs) are emerging as a sustainable alternative to traditional plastics. When released into an aquatic environment, the biodegradable performance of BPs is influenced by biochemical processes, especially the developed plastisphere. However, studies addressing the biodegrading capacity of BPs and traditional plastics within the plastisphere are still limited. Here, we investigated plastisphere community variations and their capacity to biodegrade polyethylene terephthalate (PET) and starch-based plastics (SBP) for four time periods (15, 30, 45, and 80 days) in three freshwaters. Unexpectedly, there is no significant difference in the microbial communities and network structure of the plastisphere between SBP and PET. Moreover, SBP tended to age rapidly at the early stage (0–15 days), while the aging degree of SBP and PET did not display an obvious difference at 80 days. Partial least squares path modeling suggested that plastic aging was mainly dominated by keystone taxa of network and aquatic environmental factors. These results suggest that the aging rate of commercial BPs may not be as fast as we imagine in freshwaters (SBP ≈ PET), and the environmental behaviors of BPs in the aquatic environment should be paid more attention to. [Display omitted] • Studied effects of microbial succession on aging of BPs and PET in freshwaters. • Similar microbial community and structure of plastisphere observed on SBP and PET. • Similar aging degree of SBP and PET was observed at 80 days in freshwaters. • Microbial keystone taxa and environmental factors co-dominated the plastic aging. [ABSTRACT FROM AUTHOR]

The uncontrolled release of plastics in the environment has rendered them ubiquitous around the planet, threatening the wildlife and human health. Biodegradation and valorization of plastics has emerged as an eco-friendly alternative to conventional management techniques. Discovery of novel polymer-degrading enzymes with diversified properties is hence an important task in order to explore different operational conditions for plastic-waste upcycling. In the present study, a barely studied psychrophilic enzyme (MoPE) from the Antractic bacterium Moraxella sp. was heterologously expressed, characterized and its potential in polymer degradation was further investigated. Based on its amino acid composition and structure, MoPE resembled PET-degrading enzymes, sharing features from both mesophilic and thermophilic homologues. MoPE hydrolyzes non-biodegradable plastics, such as polyethylene terephthalate and polyurethane, as well as biodegradable synthetic polyesters, such as polycaprolactone, polyhydroxy butyrate, polybutylene succinate and polylactic acid. The mass fraction crystallinity of the aliphatic polymers tested ranged from 11% to 64% highlighting the potential of the enzyme to hydrolyze highly crystalline plastics. MoPE was able to degrade different types of amorphous and semi-crystalline PET, releasing water-soluble monomers and showed synergy with a feruloyl esterase of the tannase family for the release of terephthalic acid. Based on the above, MoPE was characterized as a versatile psychrophilic polyesterase demonstrating a broad-range plastics degradation potential. [Display omitted] • Moraxella sp. esterase (MoPE) was found capable of degrading a broad range of synthetic polymers. • Plastics were ranked based on glass transition temperature, crystallinity and molecular weight. • MoPE was capable of hydrolyzing high crystallinity PBS while PCL suffered the highest mass loss. • MoPE mode of action was elucidated by using PET model substrates. • Terephthalic acid was released from PET by the synergistic action of MoPE with a feruloyl esterase. [ABSTRACT FROM AUTHOR]

Different plastic types considered as compostable are found on the market such as petro-based (e.g., polybutylene adipate terephthalate (PBAT)) or bio-based plastics (e.g., polylactic acid, (PLA)). Even if their degradation has been confirmed in industrial compost conditions, investigation of their degradation in natural marine environment has been limited. To better understand biodegradation into natural marine environment, commercial compostable (PBAT, semi-crystalline and amorphous PLA) and non-compostable polymers (low density polyethylene, polystyrene, polyethylene terephthalate, polyvinyl chloride) were submerged in situ on the sediment and in the water column in the Mediterranean Sea. These samples were studied by chemical and microbiological approaches. After 82 days of immersion, no significant bacterial degradation of the different polymers was observed, except some abiotic alterations of PBAT and LDPE probably due to a photooxidation process. However, after 80 days in an enrichment culture containing plastic films as a main carbon source, Marinomonas genus was specifically selected on the PBAT and a weight loss of 12% was highlighted. A better understanding of the bacterial community colonizing these plastics is essential for an eco-design of new biodegradable polymers to allow a rapid degradation in aquatic environment. [Display omitted] • The sample position in the water column influences the abiotic degradation and the bacterial community. • The composition of plastic-associated microbial communities is not plastic nature dependent. • Plastics are mainly used as a support for the bacterial community. • Marinomonas genus was selected on polybutylene adipate terephthalate after enrichment culture. • The eco-design of new polymers with optimized properties is essential to improve the plastic biodegradation in environments. [ABSTRACT FROM AUTHOR]

Growing evidence have demonstrated that microplastics in the marine ecosystem can provide novel substrates for biofilm formation, potentially facilitating the spread of antibiotic resistance. However, the occurrence of antibiotic resistance genes (ARGs) in the biofilm on microplastics has not been fully explored. This study used the metagenomic data of biodegradable and non-biodegradable microplastics staged at a coastal lagoon in the northern Gulf of Mexico to profile the ARGs and their bacterial hosts. The abundance and Shannon diversity of ARGs on biodegradable poly hydroxy alkanoate (PHA) and non-biodegradable polyethylene terephthalate (PET) have no significant differences. Nevertheless, the abundance of multidrug resistance genes on PET (3.05 copies per 16S rRNA) was statistically higher than that on PHA (2.05). Beta diversity showed that the overall pattern of resistome on PHA was significantly distinct with that on PET. Procrustes analysis suggested a good-fit correlation between ARG profiles and bacterial community composition. The host-tracking analysis identified that Pseudomonas was always the major host for glycopeptide and multidrug resistance genes in PET and PHA biofilms, whereas the primary host for macrolide-lincosamide-streptogramin (MLS) changed to Desulfovibrio on PET. This study provided the first metagenomic insights into the ARGs and their hosts on biodegradable and non-biodegradable microplastics, suggesting that both two types of plastics harbor ARGs with preferences. ga1 • The resistance genes on biodegradable and non-biodegradable plastics were profiled. • Plastic type significantly influenced the ARG composition in the biofilms. • The abundance of multidrug resistance genes on PET was relatively higher. • A good-fit correlation between ARG profile and bacterial composition was obtained. • The ARG-harboring bacterial hosts were distinct on different substrates. [ABSTRACT FROM AUTHOR]

Biodegradable plastics are becoming increasingly popular due to global concerns about plastic pollution. In this study, the impacts of glitter manufactured of conventional, non-biodegradable polyethylene terephthalate (PET) versus glitter of alternative materials (modified regenerated cellulose (MRC), mica or synthetic mica) on the biodiversity and ecosystem functioning of freshwater, lotic habitats were compared using a semi-natural mesocosm experiment. After 36 days, there was no effect of glitter on overall assemblage structure or diversity indices, however there was a two-fold increase in the abundance of New Zealand mud snails (Potamopyrgus antipodarum) in response to MRC glitter. In addition, the root length of common duckweed (Lemna minor) and phytoplankton biomass (based on chlorophyll content) were significantly reduced by exposure to any type of glitter. On the contrary, the chlorophyll content in the sediment (indicating microphytobenthos biomass) was significantly greater in those exposed to synthetic mica glitter. Organic matter content of sediment did not differ amongst any of the treatments. However initially, on days 8 and 15, NO 3 2− concentration in the control treatment were significantly greater than in all glitter treatments, but this observation disappeared over time. Overall, results indicate that both conventional and alternative glitters can cause ecological impacts in aquatic ecosystems. ga1 • This is the first study to test the effects of glitter on the environment. • PET, modified regenerated cellulose & mica glitter reduced root length of duckweed. • All glitter reduced chlorophyll content in the water column. • Modified regenerated cellulose glitter led to an increase of invasive mud snails. [ABSTRACT FROM AUTHOR]

• N-doped microporous carbon was newly prepared using waste PET plastic bottles. • A simple and efficient one-pot synthesis method was successfully applied. • PET-derived N-doped microporous carbon is promising for CO 2 capture. • Disposal of waste PET plastics and mitigation of CO 2 emission can be achieved simultaneously. Valorization of waste polyethylene terephthalate (PET) plastic into microporous carbon with N-doping treatment was successfully performed in a one-pot synthesis and the N-doped microporous carbon was used for CO 2 capture, which can mitigate plastic pollution and climate change simultaneously. The PET-derived microporous carbon developed by KOH activation and urea treatment in a one-pot synthesis at 700 °C exhibited the highest CO 2 adsorption uptake of 6.23 mmol g−1 at 0 °C and 4.58 mmol g−1 at 25 °C (1 atm). The Langmuir and pseudo second-order models displayed well-fitting relationships with equilibrium and kinetic experimental data obtained in this study. The N-doped microporous carbon showed high CO 2 selectivity over N 2 , implying that it is feasible for treating flue gases (10% CO 2 and 90% N 2) at 50 °C. In addition, the CO 2 uptake was not only affected by micropores but also related with nitrogen and oxygen functional groups. Compared to the porous carbon prepared by two-pot synthesis where KOH activation and urea treatment were conducted separately, the porous carbon prepared by one-pot synthesis had higher oxygen contents and higher CO 2 adsorption uptake. All of findings implied that the N-doped microporous carbon was successfully developed from waste PET plastic for capturing CO 2 and can play a promising role in both sustainable waste management and environmental protection. [ABSTRACT FROM AUTHOR]