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BACKGROUND: Quinoline is an ubiquitous pollutant widely spread in the environment, which can be eliminated efficiently by microbial degradation In this study, two quinoline-degrading Comamonas sp strains Z1 and Z3 were isolated from activated sludge, and the degradation characteristics and genome annotation were investigated in detail RESULTS: Strain Z1 exhibited a superior capacity for quinoline degradation, which could completely degrade 50–300 mg L−1 quinoline within 8–24 h, whereas strain Z3 required 14–36 h to remove 50–200 mg L−1 quinoline The suitable pHs for strains Z1 and Z3 were 8 0 and 7 0, respectively, and metal ions such as Mn2+, Ni2+, Cu2+, Co2+ and Hg2+ could greatly inhibit bacterial growth and quinoline degradation Intermediates of 2-hydroxyquinoline, 2,8-dihydroxyquinoline, 8-hydroxycoumarin, 2,3-dihydroxyphenylpropionic acids and 2-hydroxy-6-oxonona-2,4-diene-1,9-dioate were detected by liquid chromatography coupled to Q-Exactive high-resolution mass spectrometry Thus, the biodegradation of quinoline by Comamonas sp strains possibly proceeded via the 8-hydroxycoumarin pathway Genomic sequencing of strains Z1 and Z3 revealed a similar pattern, and a large number of functional genes were predicted to participate in degradation of aromatics The key genes responsible for quinoline degradation also were identified, such as qor, mhp and bph Furthermore, quinoline 2-oxidoreductase (Qor) from strains Z1 and Z3 displayed 47 74%–61 17% similarities with previously reported Qor, which catalyzed the first step of quinoline degradation, and the maximal specific activity in cell-free extracts of strains Z1 and Z3 was 0 264 and 0 062 U mg protein−1, respectively CONCLUSION: This study should provide efficient microbial resources and useful genomic information for quinoline bioremediation © 2020 Society of Chemical Industry

Periodate (PI)-based advanced oxidation processes are a newly discovered approach for effective pollutant elimination. In this study, we demonstrated that biochar obtained from pyrolysis of anaerobic sewage sludge without any pretreatment can be used for PI activation. The biochar obtained at 800 °C (SBC-800) exhibited the best PI activation capacity using acid organic II (AO7) as substrate. The PI activation was strongly dependent on pH and exhibited the highest AO7 removal rate at pH 3.0. Meanwhile, the anti-interference capacity with common wastewater components and reusability of the SBC-800/PI system were confirmed. Combined with the results of chemical quenching, reactive oxygen species (ROS) trapping, X-ray photoelectric spectroscopy (XPS), electrochemical and density function theory (DFT)-based calculations, singlet oxygen production and electron transfer mediated by the SBC-800-PI complex were the dominant AO7 oxidation mechanisms. This study provides easily prepared catalysts for PI activation and paves the way for solid waste recycling and reuse.

The combined effect of polystyrene (PS) particles and triphenyltin chloride (TPTCl) to the green algae Chlorella pyrenoidosa was studied. The 96 h IC50 of TPTCl to the green algae C. pyrenoidosa was 30.64 μg/L. The toxicity of PS particles to C. pyrenoidosa was size-dependent, with the 96 h IC50 at 9.10 mg/L for 0.55 μm PS but no toxicity observed for 5.0 μm PS. The exposure to 0.55 μm PS led to damage on structure of algal cells, which could in turn cause inhibition on photosynthesis and population growth of the green algae. TPTCl concentrations in test medium were lowered by 15–19% at presence of 0.55 μm PS particles, indicating a reduced bioavailability of TPTCl. In spite of this reduced bioavailability, the presence of PS increased the toxicity of TPTCl, which might be attributed to facilitated uptake of TPTCl by the green algae after the damage of cell structure. The overall results of the present study provided important information on the effect of PS on the bioavailability and toxicity of TPTCl to phytoplankton species.

In this study, an aerosol-assisted Fe

The toxicity of polystyrene (PS) particles of different sizes was investigated using Gram-negative Escherichia coli and Gram-positive Bacillus cereus. PS particles could inhibit the cell growth of E. coli but promote the cell growth of B. cereus, and this difference might be attributed to different composition in their cell walls and the different interactions between the two bacteria and PS particles. Direct adhesion of E. coli cells on the surface of 5 μm PS microbeads by flagella was observed, indicating the putative role of E. coli on biofilm formation of plastisphere. The regulations of malondialdehyde, lactate dehydrogenase and glutathione were similar between the two bacteria, so the difference in the toxicity effect of PS between the two bacteria was not caused by the antioxidant activity. The overall results of the present study could help to understand the responses of different bacteria to microplastic exposure.

Polycyclic aromatic hydrocarbons (PAHs) have been known for decades to threaten human health. Various physical, chemical and biological methods have been developed to remove PAHs from different matrices. Microbial biodegradation processes are thought to be effective and environmentally friendly, but the low bioavailability of PAHs and their slow removal rate often limit the application of biodegradation. In this study, novel self-assembled PAH-degrading fungal mycelium (Penicillium oxalicum SYJ-1)-carbon nanotube (CNT) composites were applied for pyrene removal. The addition of CNTs did not affect the growth of strain SYJ-1 and promoted the total PAH removal efficiency. The composite could completely remove pyrene at 20 mg L−1 within 48 h, while the sole fungus and CNTs alone could only remove 72% and 80% of pyrene at 72 h, respectively. A cytochrome P450 inhibition experiment, together with degradation product identification and transcriptomic analysis, suggested that an intracellular PAH transformation pathway was employed by strain SYJ-1. The versatility of this assembly approach was also confirmed by adding different nanomaterials and using them to remove different pollutants. This study provides a strategy of coupling the chemical adsorption and biodegradation capacity of inorganic nanomaterials and microorganisms as composites to treat hydrophobic substrates in restricted bioreactor.

Phenylalanine (Phe) is widely present in natural water and serves as a precursor of disinfection by-products (DBPs). We reported the identification of chloramination DBPs from Phe in drinking water using ultra-high performance liquid chromatography (UHPLC) coupled with complementary high-resolution quadrupole time-of-flight (QTOF) and triple quadrupole (tQ) tandem mass spectrometry (MS/MS). In the chloraminated Phe water solution, sixteen new DBPs in a total of seventeen were identified based on their accurate mass, MS/MS spectra and 35Cl/37Cl isotopic patterns. Three of these DBPs were verified as benzamide, phenylacetamide, and p-hydroxyphenylacetamide with their standards, while the others were chlorinated derivatives of Phe, hydrazone, amidine, amide and peroxide, in which the unique structures of these DBPs were rarely reported. Their stability and formation process were investigated as well. Furthermore, a method consisting of solid phase extraction (SPE) and UHPLC-MS/MS using dynamic multiple reaction monitoring (dMRM) was developed to investigate these DBPs in authentic waters. Phe, benzamide, phenylacetamide, and N-Cl-2-phenylacetimidamide were detected in chlorinated tap water. Compared with the other identified DBPs, these three DBPs were exceptionally stable and could be formed in wide formation conditions. Our work not only provided ideas for the identification of new chloramination DBPs, but also demonstrated that some DBPs usually generated in the chloramination disinfection process could also be found in the chlorinated drinking water.

Marine organisms are naturally exposed to different environmental pollutants including organic pollutants and nanoparticles. The interactive effects between nanoparticles and other chemicals on aquatic organisms have raised concerns regarding the potential of nanomaterials as the vector for other chemicals. In the present study, the effect of nano zinc oxide (nZnO) on the bioavailability of triphenyltin chloride (TPTCl) was studied, and their combined acute and reproductive toxicity to the marine copepod Tigriopus japonicus were evaluated. At experimental concentration ranges of nZnO in this study, the percentage of dissolution of Zn2+ was relative stable (from 62% to 66%), and nZnO did not affect the bioavailability of TPTCl to the copepods. The acute toxicity of binary mixtures of nZnO/TPT was equivalent to that of the mixture of Zn2+/TPT. In agreement with the decrease in TPTCl's LC50 values at the presence of nZnO, their interacting effect was synergistic based on response addition response surface model, and the interacting parameter was modelled to be −1.43. In addition to acute toxicity test, reproductive toxicity tests revealed that exposure to nZnO and TPTCl didn't affect the successful mating rate and the number of nauplii in the 1st brood, but they extended the time for the eggs to hatch from 2.53 days to 3.94 and 3.64 days, respectively. The exposure to nZnO/TPTCl mixture delayed the time to hatch to 5.78 days.

Phenolic wastewater containing phenol and 4-chlorophenol pose a risk to the environment and to human health. Treating them using chemical-biological coupling method is challenging. In this study, manganese oxidizing bacteria (MnOB) were enriched in moving bed biofilm reactor (MBBR) using synthetic phenol wastewater (800 mg L−1) to facilitate in situ production of biogenic manganese oxides (BioMnOx) after 90 days of operation. Then, 4-chlorophenol (4-CP) was added to the MBBR to simulate mixed phenolic wastewater. Comparing the MBBR (R1) without feeding Mn(II) and the MBBR with BioMnOx (R2) production, R2 exhibited robust phenol and 4-CP removal performance. 16S rRNA gene sequencing was employed to determine the microbial community. Subsequently, a batch experiment demonstrated that partly purified BioMnOx does not exhibits a capacity for phenol removal, but can efficiently remove 4-CP. Interestingly, 5-chloro-2-hydroxymuconic semialdehyde was found in the products of 4-CP degradation, which was the unique product of 4-CP degradation by catechol 2,3-dioxygenase (C23O). In both reactors, only catechol 1,2-dioxygenase (C12O) activity from microbes can be detected, indicating that the existence of BioMnOx provide an alternative pathway in addition to microbe driven 4-CP degradation. Overall, MBBR based MnOB enrichment under high phenol concentration was achieved, and 4-CP/phenol removal can be accelerated by in situ-formed BioMnOx. Considering the C23O-like activity of BioMnOx, our results suggest a new coupling strategy that involves nanomaterials and a microbial consortium.

Marine organisms are often exposed to a mixture of various pollutants in marine environment (i.e., nanoparticles, organic pollutants). The present study investigated the potential effects of multi-walled carbon nanotubes (MWCNTs) on the toxicity of triphenyltin chloride (TPTCl). The results revealed an antagonistic interaction between MWCNTs and TPTCl on the copepod through 96 h acute exposure, which was attributed to the adsorption of TPTCl to MWCNTs and aggregation of MWCNTs in the test solutions. Results of 21 days’ chronic exposure showed that the effect concentration of MWCNTs could be 100 times lower than that of acute exposure. The exposure to binary mixture of MWCNT (1.0 mg/L) and TPTCl (0.3 µg/L) caused a reduction by 94% for the 3rd time spawning and 83% for the total number of hatched nauplii. The ingestion and exterior attachment of MWCNTs to the copepod might be the main reasons causing the adverse effect in reproduction.

Prorocentrum lima is a dinoflagellate that forms hazardous blooms and produces okadaic acid (OA), leading to adverse environmental consequences associated with the declines of zooplankton populations. However, little is known about the toxic effects and molecular mechanisms of P. lima or OA on zooplankton. Here, their toxic effects were investigated using the brine shrimp Artemia salina. Acute exposure of A. salina to P. lima resulted in lethality at concentrations 100-fold lower than densities observed during blooms. The first comprehensive results from global transcriptomic and metabolomic analyses in A. salina showed up-regulated mRNA expression of antioxidant enzymes and reduced non-enzyme antioxidants, indicating general detoxification responses to oxidative stress after exposure to P. lima. The significantly up-regulated mRNA expression of proteasome, spliceosome, and ribosome, as well as the increased fatty acid oxidation and oxidative phosphorylation suggested the proteolysis of damaged proteins and induction of energy expenditure. Exposure to OA increased catabolism of chitin, which may further disrupt the molting and reproduction activities of A. salina. Our data shed new insights on the molecular responses and toxicity mechanisms of A. salina to P. lima or OA. The simple zooplankton model integrated with omic methods provides a sensitive assessment approach for studying hazardous algae.

Endocrine-disrupting chemicals (EDCs) cause serious threats to human health. Five types of MnO2 were synthesized and characterized. They exhibited different removal performances for three EDCs, i.e., estrone (E1), ethynylestradiol (EE2) and bisphenol A (BPA). Only δ-MnO2 can completely remove E1 within 120 min at pH 3.0. Free Mn (III) was determined at the beginning of the reaction and participated in the EDCs removal process. Electron spin resonance (ESR) indicated that δ-MnO2 could produce superoxide anions (·O2−) and singlet oxygen (1O2) in the existence of methanol. The reactive oxygen species (ROS) quenching experiments showed 1O2 have certain contribution to the E1 removal by δ-MnO2. The source of ROS is mainly the lattice oxygen from δ-MnO2, and can be replenished through the layer structure destruction caused by the reaction between Mn(III) and E1. The ROS dependent EDCs removal by δ-MnO2 leads to a deep understanding on this well-known oxidant.

Paralytic shellfish toxins (PSTs) cause risks to human health through food chains. Understanding the change of PSTs in seawater is critical for predicting the safety of seafood. Most reported methods for the detection of PSTs in microalgae or shellfish are not applicable in seawater because of extremely low concentration and matrix interferences. High resolution mass spectrometry (HRMS), quadrupole exactive orbitrap detects molecular ions accurately, and molecularly imprinted solid-phase extraction (MISPE) is recognized effective to reduce the matrix interference. GTXs 2&3 are two of common marine toxins in PSTs. In this study, a sensitive method consisting MISPE and liquid chromatography LC-HRMS was developed for the detection of GTXs 2&3 with a limit of detection (LOD) of 47.4 ng/L in seawater. With this method, samples obtained from the estuaries of the Shuangtaizi and Daliao Rivers were analyzed, and the results indicated the concentrations were lower than LOD in the area under investigation.

A moving bed biofilm reactor (MBBR) effectively removes pollutants and even runs under extreme conditions. However, the pH shock resistance of a biofilm in MBBRs has been rarely reported. In this study, simulated phenol wastewater with acidic shock (pH 7.5–3.0) was used. In the pH shock phase, the phenol and COD removal efficiencies initially decreased and gradually increased to more than 90%. Microscopic studies showed that the superficial biofilm was mainly composed of fungi (yeasts) in the acidic pH shock phase. The microbial community composition in the acidic pH shock phase was significantly different from those in other phases. Firmicutes and Ascomycota were the dominant bacterial and fungal phyla in this stage, respectively. 16S rRNA gene-based functional annotation indicated that functional profiles related to aromatic compound degradation existed in all of the stages. Therefore, MBBRs show potential for the treatment of phenolic wastewater exposed to pH shock.