Effects of iron on growth, antioxidant enzyme activity, bound extracellular polymeric substances and microcystin production of Microcystis aeruginosa FACHB-905.

Toxic cyanobacterial blooms have occurred in various water bodies during recent decades and made serious health hazards to plants, animals and humans. Iron is an important micronutrient for algal growth and recently, the concentration of which has increased remarkably in freshwaters. In this paper, the cyanobacterium Microcystis aeruginosa FACHB-905 was cultivated under non-iron (0µM), iron-limited (10µM) and iron-replete (100µM) conditions to investigate the effects of iron on growth, antioxidant enzyme activity, EPS and microcystin production. The results showed that algal cell density and chlorophyll-a content were maximal at the highest iron concentration. Antioxidant enzymes activity increased notably under all three conditions in the early stage of experiment, of which the SOD activity recovered soon from oxidative stress in 10µM group. The productions of some protein-like substances and humic acid-like substances of bound EPS were inhibited in iron-containing groups in the early stage of experiment while promoted after the adaptation period of Microcystis aeruginosa. Iron addition is a factor affecting the formation of cyanobacterial blooms through its impact on the content of LB-EPS and the composition of TB-EPS. The intracellular MC-LR concentration and the productivity potential of MC-LR were the lowest in 0µM group and highest in 10µM group. No obvious extracellular release of MC-LR was observed during the cultivation time. Therefore, iron addition can promote the physiological activities of M. aeruginosa, but a greater harm could be brought into environment under iron-limited (10µM) condition than under iron-replete (100µM) condition.

Dynamic assembly/disassembly processes of photoresponsive DNA origami nanostructures directly visualized on a lipid membrane surface.

Here, we report the direct visualization of the assembly/disassembly processes of photoresponsive DNA origami nanostructures which can be placed on a lipid bilayer surface. The observation relies on controlled interactions between the bilayer components and cholesterol moieties introduced to the hexagonal origami structures, one of whose outer edges carries Azo-ODNs. The bilayer-placed hexagonal dimer was disassembled into monomer units by UV irradiation, and reversibly assembled again during visible light irradiation. These dynamic processes were directly monitored with high-speed atomic force microscopy. The successful application of our approach should facilitate studies of interactive and functional behaviors of various DNA nanostructures.

Investigation of the adsorption-desorption behavior of antibiotics by polybutylene succinate and polypropylene aged in different water conditions.

Microplastics (MPs) are widely present in aqueous environments and aged by natural components of complex water environments, such as salinity (SI) and dissolved organic matter (DOM). However, the effects of multicondition aging on the physicochemical properties and environmental behavior of MPs have not been completely investigated. In this study, the degradable MP polybutylene succinate (PBS) was used to investigate the environmental behavior of sulfamethoxazole (SMZ) and was compared with polypropylene (PP). The results showed that the single-factor conditions of DOM and SI, particularly DOM, promoted the aging process of MPs more significantly, especially for PBS. The degrees of MP aging under multiple conditions were lower than those under single-factor conditions. Compared with PP, PBS had greater specific surface area, crystallinity, and hydrophilicity and thus a stronger SMZ adsorption capacity. The adsorption behavior of MPs fitted well with the pseudo-second-order kinetic and Freundlich isotherm models, indicating multilayer adsorption. Compared with PP, PBS showed relatively a higher adsorption capacity, for example, for MPs aged under DOM conditions, the adsorption of SMZ by PBS was up to 5.74 mg/g, whereas that for PP was only 3.41 mg/g. The desorption experiments showed that the desorption amount of SMZ on MPs in the simulated intestinal fluid was greater than that in Milli-Q water. In addition, both the original PBS and the aged PBS had stronger desorption capacities than that of PP. The desorption quantity of PBS was 1.23-1.84 times greater than PP, whereas the desorption rates were not significantly different. This experiment provides a theoretical basis for assessing the ecological risks of degradable MPs in complex water conditions.

Insights into the characteristics, adsorption and desorption behaviors of microplastics aged with or without fulvic acid.

Many aging experiments on microplastics (MPs) have been carried out using UV radiation or strong oxidants. Little attention has been paid to the role of water environmental factors such as dissolved organic matter (DOM). In this study, the role of fulvic acid (FA), the main component of DOM, in the UV-aging process of MPs was explored. MPs aged under UV, and UV along with 0.5 mg/L and 2 mg/L FA, were selected as subjects. The results showed that (1) FA accelerated the aging process of polyethylene (PE). PE aged with FA had a larger specific area (SBET), with more holes and cracks on the surface. (2) FA enhanced the adsorption capacity of PE. The TC adsorption quantities of 0, 0.5, and 2 mg/L FA-aged PE were 1.100, 1.447, and 1.812 mg/L, respectively. (3) The quantity of TC desorbed by PE increased, whereas the desorption rate decreased as the FA concentration increased. The desorption rates of TC at 0, 0.5, and 2 mg/L FA-aged PE were 25.16%, 22.05%, and 19.52% in water, and 72.10%, 70.36%, and 59.51% in simulated intestinal fluid. This study explored the role of FA in the aging process of MPs. Moreover, research on the aging mechanism of MPs is enriched.

Chitooligosaccharide accelerated wound healing in potato tubers by promoting the deposition of suberin polyphenols and lignin at wounds.

Chitooligosaccharide (COS) is a low molecular weight product of chitosan degradation. Although COS induces plant resistance by activating phenylpropanoid metabolism, there are few reports on whether COS accelerates wound healing in potato tubers by promoting the deposition of phenolic acids and lignin monomers at wounds. The results showed that COS activated phenylalanine ammonialyase and cinnamate 4-hydroxylase and promoted the synthesis of cinnamic, caffeic, p-coumaric, ferulic acids, total phenolics and flavonoids. COS activated 4-coumaric acid coenzyme A ligase and cinnamyl alcohol dehydrogenase and promoted the synthesis of sinapyl, coniferyl and cinnamyl alcohols. COS also increased H2O2 levels and peroxidase activity and accelerated the deposition of suberin polyphenols and lignin on wounds. In addition, COS reduced weight loss and inhibited lesion expansion in tubers inoculated with Fusarium sulfureum. Taken together, COS accelerated wound healing in potato tubers by inducing phenylpropanoid metabolism and accelerating the deposition of suberin polyphenols and lignin at wounds.

Emerging microplastics in the environment: Properties, distributions, and impacts.

Microplastics (MPs) are emerging and recalcitrant micropollutants in the environment, which have attracted soaring interests from a wide range of research disciplines. To this end, numerous technologies have been devised to understand the properties, environmental behaviors, and potential impacts/hazards of MPs. Herein, we present a review on the properties, environmental distribution and possible impacts. In this review, a comprehensive introduction of the most universal types of MPs, their shapes and characters will be first presented. Then the distributions of MPs in the environment and the impacts on microbe, plants, and human will be reported. Finally, major challenges and directions will be discussed to provide some clues to the better understanding, control and migration of MPs pollution in future studies.

DNA-Based Daisy Chain Rotaxane Nanocomposite Hydrogels as Dual-Programmable Dynamic Scaffolds for Stem Cell Adhesion.

Interlocked DNA nanostructures perform programmable movements in nanoscales such as sliding, contraction, and expansion. However, utilizing nanoscaled interlocked movements to regulate the functions of larger length scaled matrix and developing their applications has not yet been reported. Herein we describe the assembly of DNA-based daisy chain rotaxane nanostructure (DNA-DCR) composed of two hollow DNA nanostructures as macrocycles, two interlocked axles and two triangular prism-shaped DNA structures as stoppers, in which three mechanical states─fixed extended state (FES), sliding state (SS), and fixed contracted state (FCS)─are characterized by using toehold-mediated strand displacement reaction (SDR). The DNA-DCRs are further used as nanocomposites and introduced into hydrogel matrix to produce interlocked hydrogels, which shows modulable stiffness by elongating the interlocked axles to regulate the hydrogel swelling with hybridization chain reaction (HCR) treatment. Then the DCR-hydrogels are employed as dynamic biointerfaces for human mesenchymal stem cells (hMSCs) adhesion studies. First, hMSCs showed lower cell density on bare DCR-hydrogel treated with HCR-initiated swelling for stiffness decreasing. Second, the cell adhesion ligand (RGD) modified DNA-DCRs are constructed for hydrogel functionalization. DCR(RGD) hydrogel endows the mobility of RGDs by switching the mechanical states of DNA-DCR. HMSCs showed increased cell density on DCRSS(RGD) hydrogel than on DCRFCS(RGD) hydrogel. Therefore, our DNA-DCR nanocomposite hydrogel exhibit dual-programmable performances including swelling adjustment and offering sliding for incorporated ligands, which can be both utilized as dynamic scaffolds for regulating the stem cell adhesion. The dual-programmable cross-scale regulation from interlocked DNA nanostructures to hydrogel matrix was achieved, demonstrating a new pathway of DNA-based materials.

Microplastics remediation in aqueous systems: Strategies and technologies.

In recent years, the ubiquitous detection and accumulation of microplastics (MPs) in the aquatic environment have raised significant concerns on water security and long-term ecological impacts all around the world. Nevertheless, critical reviews on strategic control and effective remediation of MPs in the aqueous phase are still lacking. In this work, we summarise the origins and types of MPs, and then introduce the methodologies for extraction, identification and quantification. More importantly, we for the first time provide a comprehensive overview of the recent advances in the emerging MPs removal and transformation technologies. Except for biodegradation, this review presents new applications of advanced oxidation processes (AOPs) for MPs degradation and utilisation, including photocatalysis, photoreforming and Fenton-like reactions. Physical or catalytic thermal treatment can transform plastics into value-added nanocarbons or hydrocarbons. These transformation technologies demonstrate great potentials in dealing with MPs. The review will guide researchers to further explore the feasible approaches and develop new strategies for advanced control and remediation of MPs in the future.

Influence of extracellular polymeric substances on cell-NPs heteroaggregation process and toxicity of cerium dioxide NPs to Microcystis aeruginosa.

The presence of abundant extracellular polymeric substances (EPS) play a vital role in affecting heteroaggregation process and toxicity of nanoparticles (NPs) to Microcystis aeruginosa. Interactions between n-CeO2 and cyanobacteria with/without EPS and the toxicity of n-CeO2 to M. aeruginosa were investigated in this study. Aggregation kinetics of n-CeO2 under both soluble EPS (SEPS) and bound EPS (BEPS) indicated the presence of EPS could induced the formation of EPS-NPs aggregates. Heteroaggregation between cells and n-CeO2 was confirmed through co-settling experiment and SEM-EDS observation. SEPS contributed to the observable heteroaggregation using spectral measurement. Heteroaggregation between cells and n-CeO2 under no BEPS was hardly obtained through spectral measurement, but SEM-EDS observation convinced this process. And the DLVO theory explained this heteroaggregation process under various EPS conditions, where the energy barrier decreased with gradual EPS extraction. In addition, the order for 96 h half growth inhibition concentration (IC50) was Raw M9 > M9-SEPS > M9+BEPS > M9-BEPS. These results revealed that not all heteroaggregation between cell-NPs can lead to the NPs toxicity to cells. BEPS act more important role in buffering against the toxicity of NPs from ambient adverse factors, but SEPS increase the stability of NPs which could aggravate the adverse effects of NPs in the environment.

Effects of CeO2, CuO, and ZnO nanoparticles on physiological features of Microcystis aeruginosa and the production and composition of extracellular polymeric substances.

Extracellular polymeric substances (EPS) are key components of the cyanobacterium Microcystis aeruginosa and play an important role in cyanobacteria blooms formation. Here, we analyzed the effects of 48-h exposure to nanosized CeO2 (n-CeO2), CuO (n-CuO), and ZnO (n-ZnO) on the production and composition of EPS of M. aeruginosa. Toxicity experiments revealed that soluble nanoparticles (NPs) (n-ZnO, n-CuO) demonstrated higher toxicity to cells and caused membrane damage. The production of LB-EPS increased by 34.48, 20.09, and 46.33 %, and TB-EPS increased by -5.78, 22.3, and -2.67 % in the presence of n-CeO2, n-CuO, and n-ZnO NPs, respectively, and polysaccharides are the main incremental portion compared with protein and humic acids. Three-dimensional excitation-emission fluorescence spectra revealed the enhancement of fulvic-humic-like and disappearance of tyrosine aromatic substances in TB-EPS compared with the slight changes observed in LB-EPS. Fourier-transform infrared spectroscopy illustrated the susceptibility of -NH2 and double-bonded carbon and oxygen in amides to three types of NPs. These results improve our understanding of the potential influence of NPs on the aggregation behaviors of cyanobacteria and formation process of cyanobacteria blooms. Graphical abstract ᅟ.

Effects of cerium oxide nanoparticles on the species and distribution of phosphorus in enhanced phosphorus removal sequencing batch biofilm reactor.

The short term (8h) influences of cerium oxide nanoparticles (CeO2NPs) on the process of phosphorus removal in biofilm were investigated. At concentration of 0.1mg/L, CeO2 NPs posed no impacts on total phosphorus (TP) removal. While at 20mg/L, TP removal efficiency reduced from 85.16% to 59.62%. Results of P distribution analysis and 31P nuclear magnetic resonance spectroscopy implied that the anaerobic degradation of polyphosphate (polyP) and the release of orthophosphate in extracellular polymeric substances (EPS) were inhibited. After aerobic exposure, the average chain length of polyP in microbial cells and EPS was shorter than control, and monoester and diester phosphates in cells were observed to release into EPS. Moreover, the EPS production and its contribution to P removal increased, while the capacity of EPS in P storage declined. X-ray diffraction analysis and saturation index calculation revealed that the formation of inorganic P precipitation in biofilm was inhibited.

Transport, retention, and long-term release behavior of polymer-coated silver nanoparticles in saturated quartz sand: The impact of natural organic matters and electrolyte.

This study investigated the transport and long-term release of stabilized silver nanoparticles (AgNPs), including polyvinylpyrrolidone-coated AgNPs (PVP-AgNPs) and bare AgNPs (Bare-AgNPs), in the presence of natural organic matters (NOMs; both humic acids (HA) and alginate (Alg)) and an electrolyte (Ca2+) in a sand-packed column. Very low breakthrough rate (C/C0) of AgNPs (below 0.04) occurred in the absence of NOM and the electrolyte. Increasing the concentration of NOM and decreasing the influent NOM solution's ionic strength (IS) reduced the retention of AgNPs. The reduced NP retention at high NOM and low IS was mainly attributed to the increased energy barrier between the AgNPs and the sand grain surface. Notably, the retention of PVP-AgNPs was enhanced at high Alg concentration and low IS, which mainly resulted from the improved hydrophobicity that could increase the interaction between the PVP-AgNPs and the collector. The total release amount of PVP-AgNPs (10.03%, 9.50%, 28.42%, 6.37%) and Bare-AgNPs (3.28%, 2.58%, 10.36%, 1.54%) were gained when exposed to four kinds of NOM solutions, including deionized water, an electrolyte solution (1 mM Ca2+), HA with an electrolyte (1 mM Ca2+), and a Alg (40 mg/L) solution with an electrolyte (1 mM Ca2+). The long-term release of retained silver nanoparticles in the quartz sand was mostly through the form of released Ag NPs. The factors that increased the mobility of AgNPs in quartz sand could improve the release of the AgNPs. The release of AgNPs had no significant change in the presence Ca2+ but were increased in the presence of HA. The Alg slightly decreased the release of AgNPs by increasing the hydrophobicity of AgNPs. The results of the study indicated that all the tested NOM and Ca2+ have prominent influence on the transport and long-term release behavior of silver nanoparticles in saturated quartz sand.

Transport and long-term release behavior of polymer-coated silver nanoparticles in saturated quartz sand: The impacts of input concentration, grain size and flow rate.

This study investigated the transport and long-term release of stabilized poly vinylpyrrolidone-coated silver nanoparticles (PVP-AgNPs) in a quartz sand column with various sand grain sizes (0.3-0.5 µm, 0.5-1.0 µm, 1.0-2.0 µm), input concentrations of PVP-AgNP solution (1, 5, 15, 25 mg/L), and flow rates corresponding to a filter velocities (1.0, 1.5, 2.0, 2.5 mL/min-0.14, 0.21, 0.28, 0.35 cm/min) by determining breakthrough curves, retention profiles, and long-term release curves. Breakthrough curves and retention profiles were simulated by a mathematical model based on the advection dispersion equation coupled with second-order kinetics. The increased transport of PVP-AgNPs in quartz sand occurred with increased grain sizes and reduced input concentrations, and the transport can be predicted by the colloid filtration theory and DLVO theory. The long-term (one week) release amounts of retained PVP-AgNPs were 42.78%, 31.45%, and 10.95% in the fine, medium, and coarse sand columns, respectively, and were 34.70%, 40.79%, 47.24%, and 57.32% at flow rates of 0.0363, 0.0436, 0.0545, and 0.0726 mL/min, respectively. The released quantity of retained PVP-AgNPs decreased as the sand grain size increased. This phenomenon is opposite with the trend of increased transport of PVP-AgNPs with increased grain size in the transport test, which most likely because colloidal filtration regulates the transport process and adsorption (and desorption) dominates the release process. Increasing the flow rate increased the shear force on the particles, which improved the release of PVP-AgNPs. The results of the release tests further verified our previous published studies showing that the long-term release of retained PVP-AgNPs in the quartz sand was mostly in the form of released nanoparticles rather than ions. The results of this study indicated that sand grain size, input concentration, and flow rate have a prominent influence on the transport and long-term release behavior of PVP-AgNPs in saturated quartz sand.