2,4,6-Tribromophenol (TBP), an intermediate of brominated flame retardants, can easily release to environment and recalcitrant to degradation. Previously, Bacillus sp. GZT, a pure aerobic strain capable of simultaneously debrominating and mineralizing TBP, was successfully isolated by us. To further obtain a practical application and dig up its TBP degradation mechanism, a total of 46.7-fold purification of a novel dehalogenase with a final specific activity of 18.9 U mg−1 and a molecular mass of 63.4 kDa was achieved. Under optimal conditions (35 °C and 200 rpm), up to 80% degradation efficiencies were achieved within 120 min. Adding H2O2, NADPH, Mn2+ and Mg2+ promoted enzyme reaction effectively; while EDTA, methyl viologen, Ni2+, Cu2+, Ca2+ and Fe2+ strongly inhibited reaction activities. The debromination of TBP was catalyzed by the enzyme at a Km of 78 μM and a Vmax of 0.65 min−1 mg protein−1, which indicated that this dehalogenase could specifically eliminate TBP with a high efficiency and stability. Based on MALDI-TOF/TOF analysis, the dehalogenase shared 98% identity with peptide ABC transporter substrate-binding protein. One open reading frame (ORF) encoding this peptide was found in Strain GZT genome, subjected to clone and expressed in Escherichia coli (E. coli) to characterize the encoding gene. Result showed that this recombinant strain could also remove as similar amount of TBP as Bacillus sp. GZT under the identical condition. Based on these results, we suggest that this newly-isolated TBP dehalogenase highlights a new approach for remediating TBP pollution.

Solid digestate, a by-product of anaerobic digestion systems, has led to a range of environmental issues. In the present study, a novel composite based on a solid digestate-biochar-Cu NP composite was synthesized for tetracycline removal from an aqueous medium. The removal efficiency values for tetracycline (200 mg L⁻¹) were 31.5% and 97.8%, respectively, by the biochar-Cu NP composite (0.5 g L⁻¹) in the absence and presence of hydrogen peroxide (H2O2, 20 mM) within 6 h of reaction time. The possible degradation pathway of tetracycline was investigated using liquid chromatography-mass spectrometry. The desorption experiment results suggested that no significant concentration of tetracycline was detected on the composite after the reaction, but a small amount of intermediates in terms of total organic carbon (TOC) accounting for 3.1%, and 23.3% of the end-product NH4⁺ was adsorbed onto the biochar sheets. The dispersive Cu NPs on the biochar resulted in an increase in the surface area and pore volume of the biochar-Cu NP composite, which enhanced tetracycline adsorption as well as the degradation efficiency. Relative tetracycline removal mechanisms were dominantly ascribed to ·OH generation from the Cu(II)/Cu(I) redox reaction with H2O2 and the electron-transfer process of free radicals (FRs) in biochar. The proposed approach serves dual purposes of waste digestate reuse and treatment of antibiotic pollutants.This study highlights the activation of H2O2 by the dispersive Cu NPs coupling with biochar derived from a waste solid digestate for tetracycline treatment.

Environmental pollution by organic pollutants (OPs) has become a global concern due to its detrimental effects on the environment and human health. As plants are used to remediate contaminated sites, understanding the responses of plants to various OPs and fortification of plant tolerance are of great significance. In this work, we studied the biochemical and molecular responses of cucumber plants to three well-known OPs, 2,4,6-trichlorophenol, chlorpyrifos and oxytetracycline in the absence or presence of 24-epibrassinolide (EBR), a potent regulator of plant growth and stress tolerance. The results showed that the selected three OPs retarded root elongation; however, the phytotoxic effects of OPs were attenuated by exogenous EBR. OPs induced accumulations of both hydrogen peroxide (H2O2) and nitric oxide (NO) in root tips and resulted in an increased malondialdehyde (MDA) content, an indicator of membrane lipid peroxidation. Exogenous EBR reduced accumulations of H2O2, NO and MDA in the roots by increasing the expression of antioxidant and detoxification genes and the activities of the corresponding enzymes. Intriguingly, EBR not only promoted the activities of glutathione S-transferase and glutathione reductase, but also increased the content of reduced glutathione without altering the content of oxidized glutathione, which resulted in a reduced redox state under OPs stress. Furthermore, EBR increased the free radical scavenging capacity, flavonoid content and the activity and transcription of secondary metabolism related enzymes. Our results suggest that EBR treatment may fortify secondary metabolism to enhance antioxidant capacity in response to OPs treatment, which might have potential implication in phytoremediation of OPs.

White rot fungi have been proved to be a promising option for the removal of heavy metals, understanding their toxic response to heavy metals is conducive to developing and popularizing fungi-based remediation technologies so as to lessen the hazard of heavy metals. In this study, Cr(VI)-induced oxidative stress and apoptosis in Pycnoporus sanguineus, a species of white rot fungi were investigated. The results suggested that high level of Cr(VI) promoted the formation of ROS, including H2O2, O2•− and ·OH. With the increment of Cr(VI) concentration, the SOD and CAT activity along with GSH content increased within the first 24 h, but decreased afterwards, companied with a significant enhancement of MDA content. Cr(VI)-induced oxidative damage further caused and aggravated apoptosis in Pycnoporus sanguineus, especially at Cr(VI) concentrations above 20 mg/L. Cr(VI)-induced apoptosis was involved with mitochondrial dysfunction including mitochondrial depolarization, the enhancement of mitochondrial permeability and release of cytochrome c. The early and late apoptosis hallmarks, such as metacaspase activation, phosphatidylserine (PS) externalization, DNA fragmentation and the nuclear condensation and fragmentation were observed. Moreover, we also found disturbances of ion homeostasis, which was featured by K+ effluxes and overload of cytoplasmic and mitochondrial Ca2+.Based on these results, we suggest that Cr(VI) induced oxidative stress and apoptosis in white rot fungi, Pycnoporus sanguineus.

Acetylacetone (AcAc) has proven to be a potent photo-activator in the degradation of color compounds. The effects of AcAc on the photochemical conversion of five colorless pharmaceuticals were for the first time investigated in both pure and natural waters with the UV/H2O2 process as a reference. In most cases, AcAc played a similar role to H2O2. For example, AcAc accelerated the photodecomposition of carbamazepine, oxytetracycline, and tetracycline in pure water. Meanwhile, the toxicity of tetracyclines and carbamazepine were reduced to a similar extent to that in the UV/H2O2 process. However, AcAc worked in a way different from that of H2O2. Based on the degradation kinetics, solvent kinetic isotope effect, and the inhibiting effect of O2, the underlying mechanisms for the degradation of pharmaceuticals in the UV/AcAc process were believed mainly to be direct energy transfer from excited AcAc to pharmaceuticals rather than reactive oxygen species-mediated reactions. In natural waters, dissolved organic matter (DOM) played a crucial role in the photoconversion of pharmaceuticals. The role of H2O2 became negligible due to the scavenging effects of DOM and inorganic ions. Interestingly, in natural waters, AcAc first accelerated the photodecomposition of pharmaceuticals and then led to a dramatic reduction with the depletion of dissolved oxygen. Considering the natural occurrence of diketones, the results here point out a possible pathway in the fate and transport of pharmaceuticals in aquatic ecosystems.

Light-sticks are used as bait in surface long-line fishing, to capture swordfish and other large pelagic predators. When discharged in the ocean, it may reach the beaches. The traditional Brazilian community of Costa dos Coqueiros, Bahia, use light-sticks as a medicine for rheumatism, vitiligo and mycoses. It may affect the marine life when its content leak in the open ocean. This work evaluated and identified the acute and chronic toxicity of the light-stick. A high acute toxicity was observed in the mobility/mortality of Artemia sp.; in the fertilization of sea urchin eggs, and a high chronic toxicity in the development of the pluteus larvae of the same sea urchin. The main compounds that probably caused toxicity were the volatiles such as the fluorescent PAH and oxidants such as the hydrogen peroxide. Its disposal in the open ocean is a potential threat for marine life.

The ultraviolet (UV)-based advanced oxidation process (AOP) is a powerful technology commonly utilised in recent potable water reuse (PR) schemes. The AOP involves the generation of highly reactive free radicals (e.g. hydroxyl, HO•) and is primarily applied for the removal of two target trace organic chemicals—N-nitrosodimethylamine (NDMA) and 1,4-dioxane — in the PR schemes. Both of these organics are not well removed by the reverse osmosis (RO) process. NDMA is a probable carcinogen and is often present in reclaimed water at concentrations higher than the guidelines established for PR. This review aimed to provide an understanding of the current UV-based advanced oxidation technologies for NDMA removal in PR, their limitations and the future of advanced technologies for their removal. NDMA is readily photolysed by direct UV irradiation, while an AOP such as UV/H₂O₂ process is necessary for the destruction of 1,4-dioxane. Unfortunately, the generation of hydroxyl radicals through UV photolysis of H₂O₂ is largely inefficient with conversion on the order of 20% under normal plant operations and the addition of H₂O₂ (e.g. 3 mg/L) provides only a negligible improvement in NDMA destruction. However, AOP can also be achieved without continuous chemical addition through the application of UV irradiation to heterogeneous photocatalysts (e.g. TiO₂). The UV/TiO₂ process generates hydroxyl radicals and singlet oxygen molecules, both of which degrade NDMA into by-products (e.g. methylamine or dimethylamine). Recent studies revealed that modification of the surface morphology of TiO₂ can not only enhance NDMA destruction but also alter the composition of the degradation by-products.

We collected plastic debris in the Stockholm Archipelago using a manta trawl, and additionally along a transect in the Baltic Sea from the island of Gotland to Stockholm in a citizen science study. The samples were concentrated by filtration and organic material was digested using hydrogen peroxide. Suspected plastic material was isolated by visual sorting and 59 of these were selected to be characterized with Fourier transform infrared spectroscopy. Polypropylene and polyethylene were the most abundant plastics identified among the samples (53% and 24% respectively). We found nearly ten times higher abundance of plastics near central Stockholm than in offshore areas (4.2×105plastics km−2 compared to 4.7×104plastics km−2). The abundance of plastic debris near Stockholm was similar to urban areas in California, USA, and the overall abundance in the Stockholm Archipelago was similar to plastic abundance reported in the northwestern Mediterranean Sea.

The purpose of this review is to investigate the use of advanced oxidation processes (AOPs) including ozonation, UV photolysis, Fenton-type processes, UV/H₂O₂, and other photocatalytic processes to degrade persistent pharmaceutically active contaminants in water. The review focuses on four common pharmaceuticals carbamazepine (CBZ), diclofenac (DCF), sulfamethoxazole (SMX), and trimethoprim (TMP) which are used as exemplars. Insights into the removal efficiency of each compound by AOPs under various applied conditions are systematically elucidated. This review also investigates the fate of these pharmaceuticals during treatment by advanced oxidation treatment. The effectiveness of AOP processes for the degradation of pharmaceuticals varies significantly, depending on factors such as the nature of the process itself, operating conditions, and the target compound. Ozone can completely remove all four pharmaceuticals. By contrast, direct UV photolysis was effective for the removal of DCF and SMX, whereas the combination with H₂O₂ was essential to improve CBZ and TMP removal. In addition, a large number of transformation products were frequently detected during the degradation of the selected pharmaceuticals by AOPs. In addition, it has been confirmed that several transformation products were more resistant toward the applied AOPs than their original parent compounds. A major challenge with the use of AOPs for the degradation of the selected pharmaceutically active contaminants is the formation of by-products that are often more persistent than the original contaminants. Therefore, the existence of transformation products must be essentially investigated after the treatment of target pharmaceutical contaminants by AOPs in order to evaluate the effectiveness of the applied technique.

Polybrominated diphenyl ethers (PBDEs), a persistent organic pollutant are ubiquitous in aquatic ecosystems, which are causing serious environmental concerns. In this study, we chose BDE-47 as a representative PBDEs, to investigate its toxic effects on two microalgal species and the response of their antioxidant system. The results indicated Alexandrium minutum (a dinoflagellate) was more sensitive to BDE-47 than Dunaliella salina (a chlorophyte), as determined by growth rates, cellular structure and photosynthetic parameters. Cellular reactive oxygen species (ROS) levels were significantly elevated under the exposure of BDE-47 in both species, corresponding to an increase of superoxide dismutase (SOD), catalase (CAT) and glutathione reductase (GR) activities, while glutathione peroxidase (GPX) activities decreased in D. salina and increased in A. minutum. The different enzymes responses between the two species indicated different mechanisms in their antioxidant system, and we deduced that A. minutum might have a higher efficiency for scavenging H2O2 than D. salina.