Polysaccharides In Extracellular Polymeric Substances Research Articles

Response of aerobic granular sludge under acute inhibition by polystyrene microplastics: Activity, aggregation performance, and microbial analysis

In this study, the activity, aggregation performance, microbial community and functional proteins of aerobic granular sludge (AGS) in response to acute inhibition by different concentrations of polystyrene microplastics (PS-MPs) were investigated. As the PS-MPs concentration increased from 0 mg/L to 200 mg/L, the specific nitrogen removal rate and the activity of enzymes were inhibited. The inhibition of specific nitrite reduction rate (SNIRR) and specific nitrate reduction rate (SNRR) was most obvious at the PS-MPs concentration of 100 mg/L, and that of nitrite reductase (NIR) and nitrate reductase (NR) was most obvious at the concentration of 50 mg/L. But the inhibitory effects were mitigated at the concentration of 200 mg/L. The increase of reactive oxygen species (ROS) and lactate dehydrogenase (LDH) indicated that the cells were damaged with the increase of PS-MPs concentration. The content of proteins and polysaccharides in extracellular polymeric substances (EPS) decreased, especially the polysaccharides were more affected. Analysis of zeta potential, hydrophobicity and surface thermodynamics of AGS revealed that addition of PS-MPs was unfavorable for AGS aggregation. It was also found that bacteria genera associated with EPS secretion and nitrogen removal functions were inhibited, while functions associated with cell metabolism, protein synthesis and cell repair were enhanced. This also confirmed that acute inhibition of PS-MPs had a detrimental effect on the nitrogen removal and aggregation performance of AGS. This study can provide theoretical support for the operation of AGS reactors under microplastics impact load.

Biotransformation characteristics of tetracycline by strain Serratia marcescens MSM2304 and its mechanism evaluation based on products analysis and genomics

Microbial biotransformation is a recommended and reliable method in face of formidable tetracycline (TC) with broad-spectrum antibacterial activity. Herein, comprehensive characteristics of a newfound strain and its molecular mechanism in process of TC bioremediation were involved in this study. Specifically, Serratia marcescens MSM2304 isolated from pig manure sludge grew well in presence of TC and achieved optimal removal efficiency of 61% under conditions of initial TC concentration of 10 mg/L, pH of 7.0, cell inoculation amount of 5%, and tryptone of 10 g/L as additional carbon. The pathways of biotransformation include EPS biosorption, cell surface biosorption and biodegradation, which enzymatic processes of biodegradation were occurred through TC adsorbed by biofilms was firstly broken down by extracellular enzymes and part of TC migrated towards biofilm interior and degraded by intracellular enzymes. Wherein extracellular polysaccharides in extracellular polymeric substances (EPS) from biofilm of strain MSM2304 mainly performed extracellular adsorption, and changes in position and intensity of CO, =CH and C–O–C/C–O of EPS possible further implied TC adsorption by it. Biodegradation accounting for 79.07% played a key role in TC biotransformation and could be fitted well by first-order model that manifesting rapid and thorough removal. Potential biodegradation pathway including demethylation, dihydroxylation, oxygenation, and ring opening possibly involved in TC disposal process of MSM2304, TC-degrading metabolites exhibited lower toxicity to indicator bacteria relative to parent TC. Whole genome sequencing as underlying molecular evidence revealed that TC resistance genes, dehydrogenases-encoding genes, monooxygenase-encoding genes, and methyltransferase-encoding genes of strain MSM2304 were positively related to TC biodegradation. Collectively, these results favored a theoretical evaluation for Serratia marcescens MSM2304 as a promising TC-control agent in environmental bioremediation processes.

Research on enhancing sewage sludge lysis and bioreactor initiation through composite thermophilic strains

Returning lysed sludge to biochemical tanks to achieve in-situ sludge reduction is promising. A novel approach for regulating and initiating the sludge lysis process utilizing thermophilic strains is proposed. In this study, three strains were isolated from sludge, and sequencing of the 16 S rDNA amplicon revealed that the three thermophilic strains were the closest relatives to the genus Geobacillus, and they were designated as Geobacillus sp. DX5, Geobacillus sp. DX8 and Geobacillus sp. DX11. Sludge lysis experiments demonstrated that composite thermophilic strains (CTS) were dosed at 65°C, and the sludge VSS removal efficiency after 24 h was 37.8%, significantly surpassing individual strains. Moreover, 65.8% of proteins and 52.0% of polysaccharides in Extracellular polymeric substances (EPS) of sludge were degraded. Furthermore, Three-dimensional excitation-emission matrix (3D-EEM) fluorescence spectroscopy results revealed a substantial release of dissolved organic matter during sludge lysis. Inoculation of CTS under optimal conditions (65°C, pH 7, 4 × 1010cfu/L) resulted in VSS removal efficiency and protease activity of 42.7% and 2584 U/L, respectively. After 20 days of inoculation with CTS to initiate sludge lysis reactor, VSS removal efficiency reached 46%. Additionally, it stimulated the growth of the thermophilic bacterial community, engaging indigenous thermophilic strains in the sludge lysis process.

Selenium bio-nanocomposite based on extracellular polymeric substances (EPS): Synthesis, characterization and application in alleviating cadmium toxicity in rice (Oryza sativa L.)

Selenium nanoparticles (SeNPs) have gained significant attention owing to their favorable bioavailability and low toxicity, making them widely applications in the fields of medicine, food and agriculture. In this study, bacterial extracellular polymeric substances (EPS) were used as a novel stabilizer and capping agent to prepare dispersed SeNPs. Results show that EPS-SeNPs presented negative potential (−38 mV), spherical morphologies with average particle size about 100–200 nm and kept stable at room temperature for a long time. X-ray diffraction (XRD) analysis demonstrated that the synthesized nanoparticles were pure amorphous nanoparticles, and X-ray photoelectron spectroscopy (XPS) spectrum showed a spike at 55.6 eV, indicating the presence of zero-valent nano‑selenium. Fourier-transform infrared spectroscopy (FTIR) and three-dimensional excitation-emission matrix (3D-EEM) fluorescence spectroscopy analysis confirmed proteins and polysaccharides in EPS played a crucial role in the synthesis of EPS-SeNPs. Compared to EPS or sodium selenite (Na2SeO3), EPS-SeNPs showed a relatively moderate result in terms of scavenging free radicals in vitro. In contrast, EPS-SeNPs demonstrated lower toxicity to rice seeds than Na2SeO3. Notably, the exogenous application of EPS-SeNPs effectively alleviated the growth inhibition and oxidative damaged caused by cadmium (Cd), and significantly reduced Cd accumulation in rice plants.

Unveiling the Occurrence and Non-Negligible Role of Amino Sugars in Waste Activated Sludge Fermentation by an Enriched Chitin-Degradation Consortium.

Polysaccharides in extracellular polymeric substances (EPS) can form a hybrid matrix network with proteins, impeding waste-activated sludge (WAS) fermentation. Amino sugars, such as N-acetyl-d-glucosamine (GlcNAc) polymers and sialic acid, are the non-negligible components in the EPS of aerobic granules or biofilm. However, the occurrence of amino sugars in WAS and their degradation remains unclear. Thus, amino sugars (∼6.0%) in WAS were revealed, and the genera of Lactococcus and Zoogloea were identified for the first time. Chitin was used as the substrate to enrich a chitin-degrading consortium (CDC). The COD balances for methane production ranged from 83.3 and 95.1%. Chitin was gradually converted to oligosaccharides and GlcNAc after dosing with the extracellular enzyme. After doing enriched CDC in WAS, the final methane production markedly increased to 60.4 ± 0.6 mL, reflecting an increase of ∼62%. Four model substrates of amino sugars (GlcNAc and sialic acid) and polysaccharides (cellulose and dextran) could be used by CDC. Treponema (34.3%) was identified as the core bacterium via excreting chitinases (EC 3.2.1.14) and N-acetyl-glucosaminidases (EC 3.2.1.52), especially the genetic abundance of chitinases in CDC was 2.5 times higher than that of WAS. Thus, this study provides an elegant method for the utilization of amino sugar-enriched organics.

Construction of synthetic anti-fouling consortia: fouling control effects and polysaccharide degradation mechanisms

The physical states and chemical components of bulk sludge determine the occurrence and development of membrane fouling in membrane bioreactors. Thus, regulation of sludge suspensions can provide new strategies for fouling control. In this study, we used “top-down” enrichment to construct a synthetic anti-fouling consortium (SAC) from bio-cake and evaluate its roles in preventing membrane fouling. The SAC was identified as Massilia-dominated and could almost wholly degrade the alginate solution (1,000 mg/L) within 72 h. Two-dimensional Fourier transformation infrared correlation spectroscopy (2D-FTIR-CoS) analysis demonstrated that the SAC induced the breakage of glycosidic bond in alginates. The co-cultivation of sludge with a low dosage of SAC (ranging from 0 to 1%) led to significant fouling mitigation, increased sludge floc size, and decreased unified membrane fouling index value (0.55 ± 0.06 and 0.11 ± 0.05). FTIR spectra and X-ray spectroscopy analyses demonstrated that the addition of SAC decreased the abundance of the O-acetylation of polysaccharides in extracellular polymeric substances. Secondary derivatives analysis of amide I spectra suggested a strong reduction in the α-helix/(β-sheet + random coil) ratio in the presence of SAC, which was expected to enhance cell aggregation. Additionally, the extracellular secretions of SAC could both inhibit biofilm formation and strongly disperse the existing biofilm strongly during the biofilm incubation tests. In summary, this study illustrates the feasibility and benefits of using SAC for fouling control and provides a new strategy for fouling control.

Examining the role of glycoside hydrolases in local rheology of Pseudomonas aeruginosa biofilms

Current research strategies in the treatment of biofilm infections have focused on dispersal, in which bacteria are made to vacate the extracellular polymeric substance (EPS) surrounding them and return to a planktonic state where antimicrobial treatments are more effective. Glycoside hydrolases (GHs), which cleave bonds in EPS polysaccharides, have been shown to promote dispersal in Pseudomonas aeruginosa biofilms. The dispersal mechanism is possibly due to GHs’ ability to directly release bacteria from the EPS, disrupt EPS’ ability to regulate the environment, or reduce overall mechanical stability. In this work, passive microrheology is used to examine the relevance of the last mechanism by exploring the effects of three GHs (α-amylase, cellulase, and xylanase) known to disperse P. aeruginosa on local biofilm viscoelasticity. Compared to control studies in wild-type strains, it is found that treatment with all three GHs results in statistically relatively less elastic and stiffer biofilms, indicating that changes to mechanical stability may be a factor in effective dispersal. Both cellulase and xylanase were observed to have the greatest impact in creating a less stiff and elastic biofilm; these GHs have been observed to be effective at dispersal in the published results. Each GH was further tested on biofilms grown with strains that produced EPS missing specific polysaccharide components. Cellulase specifically targeted Psl, which forms the major structural and mechanical backbone of the EPS, explaining its efficacy in dispersal. However, xylanase did not appear to exhibit any affinity to any polysaccharide within the EPS based on the microrheology results. Overall, these results suggest that the local microrheology of the biofilms is impacted by GHs and that may be one of the factors that is causing the ability of these therapeutics to enhance dispersal.

Strengthen high-loading operation of wastewater treatment plants by composite micron powder carrier: Microscale control of carbon, nitrogen, and sulfur metabolic pathways

The concentration of activated sludge is a crucial factor influencing the capacity and efficiency of sewage wastewater treatment plants (WWTPs). However, high sludge concentrations can lead to sludge loss in the secondary sedimentation tank, resulting in reduced processing capacity, particularly during low-temperature stages and sludge bulking. This study investigated the impact of adding composite micron powder carriers (CMPC) in high-concentration powder carrier biofluidized bed (HPB) technology to the biochemical units of WWTPs on sludge concentration and settling performance. For the traditional activated sludge method (ASM), its hydraulic retention time (HRT) was 8 h, with an average effluent total nitrogen (TN) of 15.14 mg/L. Sludge bulking was prone to occur in low-temperature environments, resulting in a high average sludge volume index (SVI) of 560 mL/g. Conversely, with a CMPC dosage of 4 g/L, the HRT of HPB technology was 4.8 h, and the average effluent TN was 11.40 mg/L, with a removal efficiency of 67.43 %. During operation of HPB technology under high sludge concentration conditions (8 g/L), the average SVI remained at 85 mL/g, indicating excellent settling characteristics. Moreover, in the sequencing batch reactor (SBR), the SVI value of bulking sludge decreased from the original 695 to 111 mL/g by the 9th day of operation with the CMPC dosage of 2 g/L. At the same time, the filamentous bacteria almost disappeared, suggesting that CMPC inhibit the growth of filamentous bacteria. Metagenomic analysis demonstrated that CPMC enhance the utilization of small molecular fatty acids in activated sludge and promote electron transfer between nitrate and nitrite, thereby improving wastewater treatment capacity. Additionally, CMPC enhanced the relative abundance of Saprospiraceae in sludge, which accelerate the degradation of polysaccharides in extracellular polymeric substances, weaken sludge's hydrophilic properties, and improve sludge's settling performance. Overall, these findings suggested that CMPC effectively strengthen the high-loading operation of WWTPs by improving sludge concentration and sedimentation performance.

Positive effects of lignocellulose on the formation and stability of aerobic granular sludge.

Lignocellulose is one of the major components of particulate organic matter in sewage, which has a significant influence on biological wastewater treatment process. However, the effect of lignocellulose on aerobic granular sludge (AGS) system is still unknown. In this study, two reactors were operated over 5 months to investigate the effect of lignocellulose on granulation process, structure stability and pollutants removal of AGS. The results indicated that lignocellulose not only promoted the secretion of tightly bound polysaccharide in extracellular polymeric substances, but also acted as skeletons within granules, thereby facilitating AGS formation, and enhancing structural strength. Lignocellulose imposed little effect on the removal efficiency of pollutants, with more than 95, 99, and 92% of COD, NH4+-N, and PO43--P were removed in both reactors. However, it did exhibit a noticeable influence on pollutants conversion processes. This might be due to that the presence of lignocellulose promoted the enrichment of functional microorganisms, including Candidatus_Accumulibacter, Candidatus_Competibacter, Nitrosomonas, and Nitrospira, etc. These findings might provide valuable insights into the control strategy of lignocellulose in practical AGS systems.

Unravelling the complex adsorption behavior of extracellular polymeric substances onto pristine and UV-aged microplastics using two-dimensional correlation spectroscopy

In this study, we examined the preferential adsorption behavior of extracellular polymeric substances (EPS) on two commonly used microplastics (MPs), including polyethylene (PE) and polypropylene (PP), through adsorption kinetics and isotherm experiments. The effects of UV aging on EPS adsorption were also explored. The results showed that EPS adsorption was greater on UV-aged MPs than on pristine MPs, with an adsorption capacity of approximately 27.0 mg-C/m2 for aged PP-MPs and 23.5 mg-C/m2 for pristine PP-MPs, and 16.4 mg-C/m2 for aged PE-MPs and 12.5 mg-C/m2 for pristine PE-MPs. Fourier transform infrared (FTIR) spectra revealed that EPS adsorption was governed by hydrogen bonds between EPS molecules and methylene groups in pristine MPs and CO, C–O groups in UV-aged MPs, as evidenced by the addition and the reduction of the related peaks shown in MP surfaces and residual EPS after adsorption, respectively. Fluorescence spectroscopy revealed that protein-like components exhibited higher Freundlich adsorption affinity (i.e., Kf), ranging from 0.34 to 1.29 (RU⋅L m−2) (RU⋅L−1)n than humic-like components (0.01 to 0.12 (RU⋅L m−2) (RU⋅L−1)n). The EPS molecular distribution was consistent with the FTIR results, showing preferable adsorption of biopolymer versus humic substances fraction. Two-dimensional correlation spectroscopy combined with FTIR (2D-COS-IR) revealed that polysaccharides in EPS were more preferentially adsorbed onto MPs and the order of the sequence was polysaccharides > proteins > humic-like substances for all MPs tested. This study provides new insight into the complex adsorption behavior of heterogeneous EPS on MPs and the associated alterations in the potential environmental fate of MPs.

Protection of electroactive biofilms against hypersaline shock by quorum sensing

Quorum sensing (QS) is an ideal strategy for boosting the operating performance of electroactive biofilms (EABs), but its potential effects on the protection of electroactive biofilms against environmental shocks (e.g., hypersaline shock) have been rarely revealed. In this study, a QS signaling molecule, the N-(3-oxo-dodecanoyl)-L-homoserine lactone, was employed to promote the anti-shock property of the EABs against extreme saline shock. The maximum current density of the QS-regulated biofilm recovered to 0.17 mA/cm2 after 10% salinity exposure, which was much higher than those of its counterparts. The laser scanning confocal microscope confirmed a thicker and more compact biofilm with the presence of the QS signaling molecule. The extracellular polymeric substances (EPS) might play a crucial role in the anti-shocking behaviors, as the polysaccharides in EPS of QS-biofilm had doubled compared to the groups with acylase (the QS quencher). The microbial community analysis indicated that the QS molecule enriched the relative abundance of key species including Pseudomonas sp. and Geobacter sp., which were both beneficial to the stability and electroactivity of the biofilms. The functional genes related to the bacterial community were also up-regulated with the presence of the QS molecule. These results highlight the importance of QS effects in protecting electroactive biofilm under extreme environmental shock, which provides effective and feasible strategies for the future development of microbial electrochemical technologies.

Mitigating the inhibition of antibacterial agent chloroxylenol on nitrification system-The role of Rhodococcus ruber in a bioaugmentation system

The chloroxylenol (PCMX) degrading strain was successfully isolated from sludge and identified as Rhodococcus ruber (R. ruber). Afterwards, a bioaugmentation system was constructed by seeding R. ruber into nitrifying sludge to fasten degradation efficiency of highly toxic PCMX from wastewater. Results showed that R. ruber presented high PCMX-degrading performance under aerobic conditions, 25 °C, pH 7.0 and inoculum sizes of 4% (v/v). These optimized conditions were used in subsequent bioaugmentation experiment. In bioaugmentation system, R. ruber could detoxify nitrifiers by degrading PCMX, and the content of polysaccharide in extracellular polymeric substances increased. The quantitative polymerase chain reaction results exhibited that the absolute abundance of 16S rRNA gene and ammonia oxidizing bacteria (AOB) slightly elevated in bioaugmentation system. After analyzing the results of high-throughput sequencing, it was found that the loaded R. ruber can colonize successfully and turn into dominant strains in sludge system. Molecular docking simulation showed that PCMX had a weaker suppressed effect on AOB than nitrite oxidizing bacteria, and R. ruber can alleviate the adverse effect. This study could provide a novel strategy for potential application in reinforcement of PCMX removal in wastewater treatment.

Microbial interaction energy and EPS composition influenced ultrafiltration membrane biofouling and the role of UV pretreatment

Biofouling is still an important factor limiting ultrafiltration further application, and previous mechanism analyses were mainly focused on extracellular polymeric substances (EPS) composition and concentration. In this study, both biofouling and alleviation mechanisms were further investigated in detail with three typical microorganisms, particularly toward the microbial interaction energy. The results showed that a stronger fouling degree was induced by Pseudomonas putida (rod-shaped) than that induced by Staphylococcus aureus and Enterococcus faecalis (sphere). The computational fluid dynamics results suggested that the larger membrane filtration resistance caused by P. putida was due to more EPS secretion. EPS composition and confocal laser scanning microscopy analysis indicated that polysaccharide in EPS played greater roles on the biofouling than protein. According to the extended Derjaguin-Landau-Verwey-Overbeek (XDLVO) theory, higher interaction energy was induced because of higher content of polysaccharide (e.g., hydroxyl groups) and protein (e.g., aggregated strands of amide I band) in EPS from P. putida, resulting in a thicker biofilm and stronger biofouling degree than that caused by S. aureus and E. faecalis. In addition, both EPS secretion and microbial interaction energy were inhibited by UV pretreatment, resulting in fouling alleviated. This work will be beneficial for further biofouling control in actual water treatment plants.

Establishment of anammox coupled with sulfide-depending autotrophic denitrification process and its efficient pollutants removal performance

Nitrogen and sulfur pollutants coexist in many industrial wastewaters, which may cause serious water pollution issues. In this study, Anammox coupled with sulfide-depending autotrophic denitrification process (coupling process) was established by adding sulfide to an Anammox system in a membrane bioreactor. Variations in nitrogen and sulfur removal performance, extracellular polymeric substances (EPS), key enzyme activities, and microbial components were analyzed. The sulfide in 25.0 mg L−1 successfully induced denitrification, and then helped establish the coupling process. This process achieved 96.1% TN removal and complete sulfide removal when the sulfide was increased to 100.0 mg L−1. The protein and polysaccharide in EPS gradually increased to 2.0 and 4.9 mg g−1 SS, respectively. The hydroxylamine oxidoreductase activity, Heme-c content, nitrite reductase activity, and nitrate reductase activity slightly decreased to 19.1 EU g−1 SS, 0.001 mmol g−1 SS, 0.002 μg min−1 mg−1 protein, and 0.005 μg min−1 mg−1 protein, respectively, indicating the slight suppression of sulfide in high concentration on the coupling process. However, after acclimatization, the Anammox and denitrifying bacteria interacted and cooperatively contributed to the simultaneous nitrogen and sulfur removal, with relative abundances of Thiobacillus-denitrifying bacteria and Candidatus Kuenenia-Anammox bacteria of 31.7% and 9.0%, respectively. The establishing strategy was proposed and then verified in another Anammox system, in which the coupling process was also established, with TN removal increasing from 73.4% to 82.5%.

Geographic imprint and ecological functions of the abiotic component of periphytic biofilms.

We revealed abiotic components (extracellular polymeric substances, EPSs) in the periphytic biofilms. Further, the effect of the microbial community on the EPS, and the geodistribution patterns and ecological functions of the EPS were studied.

The fate of extracellular proteins and polysaccharides of waste activated sludge oxidative in aqueous and granular sludge phase upon degradation using Fe(II)-persulfate conditioning

Dissolved organic matter, particularly proteins (PN) and polysaccharides (PS) in extracellular polymeric substances (EPS), are regarded as the key factors influencing the dewaterability of waste activated sludge (WAS). An investigation was conducted on the treatment of WAS by Fe(II) activated sodium persulfate (SPS) to evaluate the kinetics of oxidative degradation of EPS in the aqueous and granular sludge phase, and to quantify the oxidation of SPS in aqueous and granular sludge phase in Fe(II)-SPS system. The WAS was divided into granular sludge (GS) and raw sludge filtrate (RSF) by filtration and elutriation. The PN and PS components underwent rapid degradation on treatment with Fe(II)-SPS, which followed pseudo-first-order kinetics for both GS and RSF. EPS protein was preferentially oxidatively degraded over EPS polysaccharide in the same phase system. However, the degradation rates of PN and PS in GS were 1/6 and 16 times higher than those in RSF, respectively. 23% of the sodium persulfate was consumed by all the substances in the bulk solution where the GS was located, reducing the amount of “effective free radicals” that degrade EPS in the system. The mass balance of PN and PS indicated that the use of Fe(II)-SPS conditioning has an obvious degradative effect on EPS, and PN and PS in WAS were oxidized by 76.2% and 58.3%, respectively. These findings provide mechanistic insight into the oxidation and competitive reactions of PN and PS between sludge aqueous and granular sludge phases, which is beneficial to the selection and optimization of sludge conditioning.

Marine Colloids Promote the Adaptation of Diatoms to Nitrate Contamination by Directional Electron Transfer.

Nitrate contamination from human activities (e.g., domestic pollution, livestock breeding, and fertilizer application) threatens marine ecosystems and net primary productivity. As the main component of primary productivity, diatoms can adapt to high nitrate environments, but the mechanism is unclear. We found that electron transfer from marine colloids to diatoms enhances nitrogen uptake and assimilation under visible-light irradiation, providing a new pathway for nitrogen adaptation. Under irradiation, marine colloids exhibit semiconductor properties (e.g., the separation of electron-hole pairs) and can trigger the generation of free electrons and singlet oxygen. They also exhibit electron acceptor and donor properties, with the former being stronger than the latter, reacting with polysaccharides in extracellular polymeric substances (EPSs) under high nitrogen stress, enhancing the elasticity and permeability of cells, and promoting nitrogen assimilation and electron transfer to marine diatom EPSs. Electron transfer promotes extracellular-to-intracellular nitrate transport by upregulating membrane nitrate transporters and nitrate reductase. The upregulation of anion transport genes and unsaturated fatty acids contributes to nitrogen assimilation. We estimate that colloids may increase the nitrate uptake efficiency of marine diatoms by 10.5-82.2%. These findings reveal a mechanism by which diatoms adapt to nitrate contamination and indicate a low-cost strategy to control marine pollution.

Unrevealing the role of in-situ Fe(II)/S2O82- oxidation in sludge solid–liquid separation and membrane fouling behaviors of membrane bioreactor (MBR)

Membrane bioreactor (MBR) has received continuous attention in waste activated sludge treatment, however, membrane fouling still remains a big and inevitable challenge to its wide applications. Ferrous-persulfate (Fe(II)/S2O82–) oxidation possesses the outstanding oxidizing capability and high-efficiency in degrading refractory organics and enhancing sludge solubilization. In this study, in-situ Fe(II)/S2O82- oxidation was coupled for pretreating sludge, and the effect on the subsequent filtration performance and membrane fouling behaviors in MBR was investigated. Fe(II)/S2O82- oxidation had an outstanding effect on enhancing filterability of mixed sludge liquor and alleviating membrane fouling. Under the optimal pretreatment condition of 1.5/1.2 mmol-Fe(II)-S2O82-/g-VS, the membrane flux of reactor reached 20.6 mL/s/m2, and a 46.6% decrease in trans-membrane pressure (TMP) was obtained compared to the raw sludge without pretreatment. Correlation analysis reveal that polysaccharides in extracellular polymeric substances was the decisive factor affecting the membrane fouling behavior. The strong oxidizing ability of in-situ Fe(II)/S2O82- pretreatment could effectively break the glutinous and pilotaxitic biopolymer matrix deposited on the membrane surface, and rupture the hydrophilic bonds of proteins and polysaccharides. The high molecular weight biopolymers were brought down, with the water bounded inside the flocs released into liquid phase. Iron-mediated coagulation was also conductive to the re-aggregation of the fine particles and subsequent membrane fouling control. For raw sludge, the predominated fouling mechanisms were intermediate pore blocking and cake layer formation, while complete pore blocking and standard pore blocking occurred more frequently for pretreated sludge. This work provides a promising approach based on Fe(II)/S2O82- oxidation processes for efficient abatement of membrane fouling and sludge treatment.

Environmental free radicals efficiently inhibit the conjugative transfer of antibiotic resistance by altering cellular metabolism and plasmid transfer

Spread of antibiotic-resistant genes (ARGs) is a global public safety issue and inhibition their transfer is imperative. In this study, a novel strategy using environmental free radical exposure was developed to inhibit conjugative transfer of ARGs (RP4 plasmid) in aqueous solutions. Long-time free radical (·OH, 1O2, and O2·−) exposure significantly suppressed the conjugative transfer frequency of ARGs between Escherichia coli (E. coli) strains, and ·OH was more likely to attack ARG, thereby inhibiting the conjugate transfer frequency, compared to 1O2 and O2·−. Compared with the control, the conjugative transfer frequency significantly decreased from 4.08 × 10−5 to 1.2 × 10−8 after 10 min free radical exposure, confirming that the transfer and proliferation of ARGs were well inhibited. Correspondingly, the number of transconjugant significantly decreased by 61.7% after 10 min free radical exposure. Significant reductions in reactive oxygen species levels (ROS content and enzyme levels) and DNA damage-induced responses in the donor strains were observed after 10 min free radical exposure. Concurrently, intercellular contact was also weakened via inhibiting the synthesis of polysaccharides in extracellular polymeric substances. Moreover, the expressions of plasmid transfer genes were down-regulated after 10 min exposure due to the shortage of adenosine-triphosphate supply. This study firstly disclosed the underneath mechanisms for depressing ARGs transfer and dissemination via environmental free radical exposure.

Dibutyl phthalate weakens the role of electroactive biofilm as an efficient wastewater handler and related mechanism

Plasticizer plays an imperceptible role in interfering with the structure and function of wastewater biofilms, but the inherent influence mechanism still remains unknown. Here, the responses in electrochemical, structural, microbial properties of electroactive biofilm (EAB) to plasticizer (dibutyl phthalate, DBP) were comprehensively elucidated, especially for the property variation of extracellular polymeric substances (EPS). The biofilm-0 in DBP-absent environment contributed to 22.9% and 63.9% higher current, compared to those in 1 mg/L and 10 mg/L DBP environment (biofilm-1 and biofilm-10). Chronic exposure to high-concentration DBP significantly boosted the content and distribution width of polysaccharide in EPS, but the electron exchange capacity of EPS decreased 76.6% to 0.146 μmol e−/mg EPS for biofilm-10. The bacteria were subjected to metabolic function loss, in terms of esterase activity and membrane integrity, by using flow cytometry. The DBP exposure also imposed selective pressure on enrich EPS-secretion-related bacteria, while the Geobacter species decreased from 71.2% (biofilm-0) to 55.8% (biofilm-10). Consequently, the DBP exposure suppressed the pollutant degradation rate, which provided new insights into the EAB role as a promising core for wastewater treatment in plasticizer-existing environments.