Tryptophan Protein-like Substances Research Articles

Spectra metrology for interaction of heavy metals with extracellular polymeric substances (EPS) of Pseudomonas aeruginosa OMCS-1 reveals static quenching and complexation dynamics of EPS with heavy metals

The adsorption behavior and interaction mechanisms of extracellular polymeric substances (EPS) of Pseudomonas aeruginosa OMCS-1 towards chromium (Cr), lead (Pb), and cadmium (Cd) were investigated. EPS-covered (EPS-C) cells exhibited significantly higher (p < 0.0001; two-way ANOVA) removal of Cr (85.58 ± 0.39%), Pb (81.98 ± 1.02%), and Cd (73.88 ± 1%) than EPS-removed (EPS-R) cells. Interactions between EPS-heavy metals were spontaneous (ΔG<0). EPS-Cr(VI) and EPS-Pb(II) binding were exothermic (ΔH<0), while EPS-Cd(II) binding was endothermic (ΔH>0) process. EPS bonded to Pb(II) via inner-sphere complexation by displacement of surrounding water molecules, while EPS-Cr(VI) and EPS-Cd(II) binding occurred through outer-sphere complexation via electrostatic interactions. Increased zeta potential of Cr (29.75%), Pb (41.46%), and Cd (46.83%) treated EPS and unchanged crystallinity (CIXRD=0.13), inferred EPS-metal binding via both electrostatic interactions and complexation mechanism. EPS-metal interaction was predominantly promoted through hydroxyl, amide, carboxyl, and phosphate groups. Metal adsorption deviated EPS protein secondary structures. Strong static quenching mechanism between tryptophan protein-like substances in EPS and heavy metals was evidenced. EPS sequestered heavy metals via complexation with C-O, C-OH, CO/O-C-O, and NH/NH2 groups and ion exchange with –COOH group. This study unveils the fate of Cr, Pb, and Cd on EPS surface and provides insight into the interactions among EPS and metal ions for metal sequestration.

Relation between hydrophilic/hydrophobic characteristics of sludge extracellular polymeric substances and sludge moisture-holding capacity in hot-pressing drying

Sludge poses a serious threat to the environmental health. Hot-pressing drying has been proven efficient in sludge treatment because of the reduced thermal contact resistance, rapid increase in sludge temperature, and high drying rate. Sludge extracellular polymeric substances (EPS) significantly influence moisture transfer. However, whether in hot-pressing or traditional thermal drying, the effect of EPS on sludge moisture-holding capacity is rarely reported. Thereby, this study investigated the relationship between hydrophilic/hydrophobic characteristics of EPS and sludge moisture-holding capacity at various drying time and mechanical compression using XAD resin fractionation. Thermodynamic analysis indicated that sludge moisture desorption isotherms, net isosteric heat of desorption, and differential entropy presented a downward trend with the increase in drying time and mechanical compression, suggesting reduced sludge moisture-holding capacity. EPS analysis showed that at the same drying time, applying 25 kPa mechanical compression increased sludge temperature by 16 % and protein content by 13.8 %. At the same sludge temperature, protein content rose by 7.3 % compared to the drying without mechanical compression. It was concluded that the fast rise in sludge temperature and the mechanical extrusion facilitated the destruction of sludge microbial flocs, accelerating the release of intracellular and EPS-bound moisture and contributing to the decrease in moisture-holding capacity. Besides, tryptophan protein-like substances were the major source of hydrophilic/hydrophobic organic matter, compared to polysaccharide and humic acid-like substances. The gradually reduced sludge moisture-holding capacity was divided into three stages. Below 67 °C, the moisture desorption was dominated by the release of intracellular moisture. Below 85 °C, the increase in protein and the enhanced exposure of hydrophobic functional groups in protein improved the hydrophobicity of EPS. Above 85 °C, protein consumption due to thermal decomposition and browning reaction facilitated the desorption of EPS-bound moisture. Hence, this study provided novel insights into the mechanism of sludge drying.

Molecular complexation properties of Cd2+ by algal organic matter from Scenedesmus obliquus

A detailed understanding the metals binding with algal organic matter (AOM) is essential to gain a deeper insight into the toxicity and migration of metals in algae cell. However, the molecular complexation mechanism of the metals binding with AOM remains unclear. In this study, cadmium ion (Cd2+) binding properties of AOMs from Scenedesmus obliquus, which included extracellular organic matter (EOM) and intracellular organic matter (IOM), were screened. When Cd2+ < 0.5 mg/L, the accumulation of Cd2+ could reach 40%, while Cd2+ > 0.5 mg/L, the accumulation of Cd2+ was only about 10%. EOM decreased gradually (from 8.51 to 3.98 mg/L), while IOM increased gradually (from 9.62 to 21.00 mg/L). The spectral characteristics revealed that IOM was richer in peptides/proteins and had more hydrophilic than EOM. Both EOM and IOM contained three protein-like components (containing tryptophan and tyrosine) and one humic-like component, and their contents in IOM were higher than that in EOM. The tryptophan protein-like substances changed greatly during Cd2+ binding, and that the tryptophan protein-like substances complexed to Cd2+ before tyrosine protein-like substances in IOM was identified. Moreover, the functional groups of N-H, O-H, and CO in AOM played an important role, and the N-H group was priority to interacts with Cd2+ in the complexing process. More functional groups (such as C-O and C-N) were involved in the metals complexing in EOM than in IOM. It could be concluded that Cd2+ stress promoted the secretion of AOM in Scenedesmus obliquus, and proteins in AOM could complex Cd2+ and alleviate its toxicity to algal cell. These findings provided deep insights into the interaction mechanism of AOM with Cd2+ in aquatic environments.

The contradictory roles of tightly bound and loosely bound extracellular polymeric substances of activated sludge in trimethoprim adsorption process

Extracellular polymeric substances (EPS) of activated sludge are a mixture of high molecular weight polymers secreted by microorganisms, which have the double structure of tightly-bound EPS (TB-EPS) in inner layer and loosely-bound EPS (LB-EPS) in outer layer. The characteristic of LB- and TB-EPS were different, which would affect their adsorption of antibiotics. However, the adsorption process of antibiotics on LB- and TB-EPS was still unclear yet. Therefore, in this work, the roles of LB-EPS and TB-EPS in adsorption of a typical antibiotic-trimethoprim (TMP) at environmentally relevant concentration (25.0 μg/L) were investigated. The results showed the content of TB-EPS was higher than that of LB-EPS, which was 17.08 and 10.36 mg/g VSS, respectively. The adsorption capacity of raw, LB-EPS extracted and both LB- and TB-EPS extracted activated sludges for TMP were 5.31, 4.65 and 9.51 μg/g VSS, respectively, which indicated LB-EPS had positive effect on TMP removal, while TB-EPS had negative effect. The adsorption process can be well described by a pseudo-second-order kinetic model (R2 > 0.980). The ratio of different functional groups was calculated and the CO and C–O bond might be responsible for the adsorption capacity difference between LB- and TB-EPS. The fluorescence quenching results indicated that tryptophan protein-like substances in LB-EPS provided more binding sites (n = 0.36) than that of tryptophan amino acid in TB-EPS (n = 0.1). Furthermore, the extend DLVO results also demonstrated that LB-EPS promoted the adsorption of TMP, while TB-EPS inhibited the process. We hope the results of this study were helpful for understanding the fate of antibiotics in wastewater treatment systems.

Biosynthesis of bionanomaterials using Bacillus cereus for the recovery of rare earth elements from mine wastewater

The growing demand for rare earth elements (REEs) increasingly requires secondary resources such as mine wastewater containing high concentrations of REEs, to be used as a source of REEs. The current challenge is how to efficiently recover REEs from this feed source. In this paper, a functional bionanomaterial (FeNPs-EPS) was biosynthesized using Bacillus cereus as a possible means of recovering REEs. This composite was composed of both synthesized iron nanoparticles (FeNPs) and extracellular polymeric substances (EPS). Synthesis of the FeNPs-EPS composite via a one-step biosynthesis was confirmed by materials characterization. The peak in the material's UV–Vis spectra at 511 nm demonstrates the formation of FeNPs-EPS, where 3D-EEM showed that FeNPs-EPS was wrapped predominantly with tryptophan protein-like and humic acid-like substances. In addition, while FTIR indicated that the functional groups present in EPS where virtually identical to those observed in FeNPs-EPS, XPS demonstrated that Fe and O were the major elemental present as both FeO and Fe2O3. Zeta potential measurements indicated that FeNPs-EPS had good stability under different pH conditions, where BET analysis supported multilayer adsorption. Finally, on exposure to high concentrations of Eu(III) and Tb(III) in mine wastewater, the synthesized FeNPs-EPS demonstrated strong potential to remove two cations from the wastewater and hence a potentially practical way to efficiently recover REEs from such waste streams.

Exposure to Cr(VI) affects partial denitrification process-nitrite accumulation, EPS characteristic and microbial community assembly

This study was aimed at assessing the effects of elevated Cr(VI) stresses on partial denitrification (PD) process. The results showed that 0.5–5 mg/L Cr(VI) exposure significantly decreased nitrite accumulation rate, while COD removal efficiencies increased due to the further conversion of NO2--N to N2. This suggested that Cr(VI) exposure shifted the biological process from partial denitrification to complete denitrification. The Cr(VI) removal efficiency decreased from 37.75 ± 15.97% to 10.48 ± 3.78% with increasing Cr(VI) concentration. Excitation-emission matrix fluorescence spectroscopy showed that Cr(VI) exposure significantly stimulated the synthesis of tryptophan protein-like, aromatic protein-like and humic acid-like substances in extracellular polymeric substances (EPS). In addition, significant changes in functional groups of EPS were found as revealed by Fourier transform infrared spectroscopy. Particularly, there was a considerable decrease in the α-Helix from 31.36% to 0% and a major increase in the antiparallel β-Sheet from 4.81% to 9.03% with increasing Cr(VI) stresses. The biodiversity decreased significantly under Cr(VI) stresses, and the microbial community structures gradually shifted with increasing Cr(VI) dosage. Sloan model revealed that the relative importance of deterministic processes on the community assembly increased after Cr(VI) exposure, indicating that Cr(VI)-induced selective processes have a profound influence on microbial community of PD process. Network analysis revealed that Cr(VI) exposure significantly altered species-species associations, topological features of individual OTU, and keystone species, implying that substantial changes occurred in bacterial ecology after exposure to Cr(VI).

Harsh temperature induces Microcystis aeruginosa growth enhancement and water deterioration during vernalization

Cyanobacterial blooms are seasonal phenomena in eutrophic water. Cyanobacteria grow fast in the warm spring/summer while disappearing in cold autumn/winter. The temperature change induces algal vernalization. However, whether vernalization affects cyanobacterial blooms, and the regulatory signaling mechanisms are unclear. This study used Microcystis aeruginosa as the model cyanobacteria, and 4 °C and 10 °C as the low-temperature stimulation to explore the cell growth, metabolites, and signaling pathways in cyanobacteria vernalization. Low temperatures induced M. aeruginosa vernalization; the growth rate and cell density increased by 35±4% and 33±2%. Vernalization influenced peptidoglycan synthesis and cell permeability. Soluble microbial products (SMPs) in water increased by 109±5%, resulting in water deterioration. Polysaccharides were the predominant SMPs during the initial term of vernalization. Tryptophan protein-like & humic acid-like substances became the main increased SMPs in the middle-later period of vernalization. Harsh temperatures triggered quorum sensing and two-component system. Signaling sensing systems upregulated photosynthesis, glycolysis, TCA cycle, oxidative phosphorylation, and DNA replication, enhancing M. aeruginosa growth and metabolism during vernalization. This study verified that low temperature stimulates cyanobacteria growth and metabolism, and vernalization possibly aggravates cyanobacterial blooms and water deterioration. It provides new insights into the mechanism of seasonal cyanobacterial blooms and the pivotal role of signaling regulation.

Enhanced performance of thallium(I) removal by in situ-generated manganese oxides during biogenic Mn(II) oxidation

Little is known about the reciprocal effect of manganese-oxidizing bacteria (MOB), in situ-generated biogenic manganese oxide (BMO) and thallium (Tl) removal. In this study, the Tl(I) removal characteristics during extracellular BMO formation by Pseudomonas putida strain MnB1 were investigated. BMO with a final maturity of 91.25 % achieved 95.20 % Tl(I) removal during biogenic Mn(II) oxidation. The improvement mechanisms of Tl(I) removal in biological systems were mainly due to the involvement of Mn(III) intermediates and tyrosine and tryptophan protein-like substances from MOB. The addition of exogenous MOB reoxidized the residual Mn2+ to BMO, thus promoting Tl(I) removal. BMO showed a higher adsorption ability for Tl(I) at inner depths owing to its layer stacking structure, and 64.02 % Tl(I) was further oxidized to Tl(III) by highly matured BMO. Surface complexation also played an important role during Tl(I) removal. Moreover, BMO showed good adsorption selectivity for Tl(I) with coexisting Fe(III), Cr(III) and Cd(II). These findings expand existing knowledge on the characteristics of in situ-generated BMO and indicate that BMO has practical application value in Tl(I) decontamination from water.

Insight into the interaction between trimethoprim and soluble microbial products produced from biological wastewater treatment processes

Soluble microbial products (SMPs), dissolved organic matter excreted by activated sludge, can interact with antibiotics in wastewater and natural water bodies. Interactions between SMPs and antibiotics can influence antibiotic migration, transformation, and toxicity but the mechanisms involved in such interactions are not fully understood. In this study, integrated spectroscopy approaches were used to investigate the mechanisms involved in interactions between SMPs and a representative antibiotic, trimethoprim (TMP), which has a low biodegradation rate and has been detected in wastewater. The results of liquid chromatography-organic carbon detection-organic nitrogen detection indicated that the SMPs used in the study contained 15% biopolymers and 28% humic-like substances (based on the total dissolved organic carbon concentration) so would have contained sites that could interact with TMP. A linear relationship of fluorescent intensities of tryptophan protein-like substances in SMP was observed (R2>0.99), indicating that the fluorescence enhancement between SMP and TMP occurred. Fourier-transform infrared spectroscopy and X-ray photoelectron spectroscopy indicated that carboxyl, carbonyl, and hydroxyl groups were the main functional groups involved in the interactions. The electrostatic and π-π interactions were discovered by the UV-vis spectra and 1H nuclear magnetic resonance spectra. Structural representations of the interactions between representative SMP subcomponents and TMP were calculated using density functional theory, and the results confirmed the conclusions drawn from the 1H nuclear magnetic resonance spectra. The results help characterize SMP–TMP complexes and will help understand antibiotic transformations in wastewater treatment plants and aquatic environments.

Enhanced photodegradation of antibiotics based on anoxygenic photosynthetic bacteria and bacterial metabolites: A sustainably green strategy for the removal of high-risk organics from secondary effluent

Antibiotic residues in effluents discharged from wastewater treatment plants (WWTPs) have been considered high-risk organics due to biorefractory property and potential toxicity. Secondary pollution and unsustainability existed in advanced treatment of secondary effluent are currently in urgent need of improvement. In this study, a sustainably green strategy based on Rhodopseudomonas palustris (R.palustris) by regulating the structure of extracellular polymeric substances (EPS) was proposed for the first time to achieve efficiently removal of sulfadiazine (SDZ). Results showed that 0.2 V was the optimal external potential for R.palustris to efficiently remove SDZ, where the biodegradation rate constant obtained at this potential was 4.87-folds higher than that in open-circuit mode and a complete removal was achieved within 58 h in the presence of EPS extracted at this potential. Three-dimensional excitation-emission matrix (3D-EEM) spectra analysis suggested that tryptophan protein-like, tyrosine protein-like, humic acid-like and fulvic acid-like substances present in EPS were the main effective components which was responsible for the indirect photodegradation of SDZ. The quenching experiments showed that 3EPS* was the dominant reactive species which accounted for 90% of SDZ removal. This study provides new implications for the advanced treatment of secondary effluent organic matters by developing eco-friendly bioaugmentation technology and biomaterials.

Combined effects of Penicillium oxalicum and tricalcium phosphate on lead immobilization: Performance, mechanisms and stabilities

Phosphorus (P) containing minerals are identified as effective Pb stabilizers in soil, while their low solubility limit the Pb immobilization efficiency. In this work, the combination of phosphate solubilizing fungi (PSF) Penicillium oxalicum and tricalcium phosphate (TCP) was constructed and applied to improve Pb immobilization stabilities in medium and soils. P. oxalicum+ TCP could significantly improve Pb2+ removal to above 99% under different TCP/Pb2+ and pH values. TCP and P. oxalicum could remarkably immobilize Pb by ion exchange, and PbC2O4 precipitation or surface adsorption, respectively. While the enhanced Pb immobilization in P. oxalicum+ TCP was explained by stronger Pb2+ interaction with tryptophan protein-like substances in extracellular polymeric substance, and the formation of the most stable Pb-phosphate compound hydroxypyromorphite (Pb5(PO4)3OH). Toxicity characteristic leaching procedure test showed that only 0.91% of Pb2+ was leachable in P. oxalicum+ TCP treatment, significantly lower than that in P. oxalicum (2.90%) and TCP (7.52%) treatments. In addition, the lowest soil exchangeable Pb fraction (37.1%) and the highest available soil P (88.0 mg/kg) were both found in P. oxalicum+ TCP treatment. By synergistically forming stable Pb-containing products, thus the combination of PSF and P minerals could significantly improve Pb2+ immobilization and stability in soils.

The responses of activated sludge to membrane cleaning reagent H2O2 and protection of extracellular polymeric substances

Hydrogen peroxide (H2O2) is evaluated as a potential replacement for chlorine to control biofouling in membrane bioreactors (MBRs). However, H2O2 might diffuse into the mixed liquor and damage microorganisms during membrane cleaning. This study comprehensively analyzed the impacts of H2O2 on microbes. Key enzymes involved in phenol biodegradation were inhibited with H2O2 concentration increased, and thus phenol degradation efficiency was decreased. Increase of lactic dehydrogenase (LDH) and intracellular reactive oxygen species (ROS) indicated more severe cell rupture with H2O2 concentration increased. At the same H2O2 concentration, Extracellular polymeric substances (EPS) extraction further led to inhibiting the activity of key enzymes, decreasing phenol degradation efficiency, and enhancing LDH release and ROS production, demonstrating that the existence of EPS moderated the adverse impacts on microbes. Spectroscopic characterization revealed the increase of H2O2 decreased tryptophan protein-like substances, protein-associated bonds and polysaccharide-associated bonds. Hydroxyl and amide groups in EPS were attacked, which might lead to the consumption of H2O2, indicated EPS protect the microorganism through sacrificial reaction with H2O2.

Insight investigation of the on-site activated sludge reduction induced by metabolic uncoupler: Effects of 2,6-dichlorophenol on soluble microbial products, microbial activity, and environmental impact

Metabolic uncoupling technology was one of the methods widely used to on-site control the production of excess sludge in wastewater treatment processes. However, the uncoupler effects on soluble microbial products (SMP), microbial activity, and environment impact have few been reported. This study showed that sludge yield was reduced by 33.3% at 2,6-dichlorophenol (2,6-DCP) concentrations of 10 mg/L. The addition of 2,6-DCP also reduced the content of polysaccharide and protein in SMP, and the three-dimension excitation emission matrix (3D-EEM) suggested that the fluorescence intensities of humic acid-like, fulvic acid-like, and tryptophan protein-like substances decreased, proving that 2,6-DCP addition will weaken the interaction between microorganisms and the environmental matrix. Moreover, 2,6-DCP addition will change the microbial morphology and community of activated sludge. The active or respiring bacteria portion was lessened, and sludge flocs become dispersed, but it will not affect its settling performance. Surprisingly, 2,6-DCP has certain biodegradability and could be used as an environmentally friendly metabolic uncoupler under low-concentration dosing conditions. This study systematically evaluated the effect of 2,6-DCP on sludge production, SMP contents, microbial morphology, microbial community, demonstrating the environmental impact and application feasibility in the wastewater treatment systems.

Denitrification performance, biofilm formation and microbial diversity during startup of slow sand filter using powdery polycaprolactone as solid carbon source

To solve the problem of unsatisfactory nitrogen removal effect and long start-up in slow sand filter (SSF), the powdery polycaprolactone (PCL) with different particle sizes (40 and 200 mesh) were added to the lab-scale SSFs. This study compared the two solid carbon sources release capacity and enhanced denitrification performance in each SSF, and revealed the inner mechanism by analyzing the physical and chemical characteristics of the biofilm. The results represented that PCL200 could release organic carbon up to 273.9 mg/L, which was much higher than PCL40 (121.2 mg/L). Since the higher organic carbon release and specific surface area, the PCL200 was conducive to the rapid start-up of the SSF and achieving a desired removal efficiency of NO3--N (> 95%) and TN (> 80%) at the early stage of operation. In addition, large amounts of biomass and extracellular polymeric substances (EPS) were detected in the PCL200 system. Spectroscopic characterization further revealed EPS from two SSFs expressed similar fluorescence peak locations but different intensities. Specifically, the aromatic and tryptophan protein-like substances were the main fractions in EPS, and more functional bonds (C-(C, H), C˭O, O-C-O) conducive to microbial flocculation were observed when adding PCL200. Furthermore, the high-throughput sequencing analysis showed the denitrifying bacteria almost accounted for 62.12% in the reactor with PCL200, and microorganisms in two SSFs were significant difference in amino acid and carbohydrate transportation and metabolism. Findings from this study would be valuable for enhancement of the denitrification and stability of SSF treating nitrogen-contaminated water bodies.

Insight the roles of loosely-bound and tightly-bound extracellular polymeric substances on Cu2+, Zn2+ and Pb2+ biosorption process with Desulfovibrio vulgaris

The aim of this study is to explore the fate and mechanism of metal cations of biosorption in the Desulfovibrio vulgaris system (including bacterial cells and secreted loosely-bound extracellular polymeric substances (LB-EPS) and tightly-bound extracellular polymeric substances (TB-EPS)). The relative contribution of EPS (TB-EPS and LB-EPS) to the adsorption of three metal cations is much greater than that of bacterial cells, and the adsorption capacity of Pb2+ on EPS (TB-EPS and LB-EPS) is much greater than that of Cu2+ and Zn2+ (Pb2+ > Cu2+ > Zn2+). The order of absorption capacity was as follows: LB-EPS > TB-EPS > bacterial cells, the adsorption contribution of EPS (including TB-EPS and LB-EPS) to Cu2+, Zn2+ and Pb2+ accounted for total adsorption capacity was 82%, 83% and 86%, respectively. It was suggested that LB-EPS was the first reaction barrier of immobilization metal cations before metal cations was able to pass through EPS and react with cells. The adsorption process was dominated by complexation and electrostatic interaction. The three-dimensional excitation-emission matrix (3D-EEM) identified two main fluorescence peaks of the aromatic and tryptophan protein-like substances in EPS. According to the synchronous fluorescence spectra, the tryptophan protein-like substances were gradually quenched with increased metal cations concentrations, which the quencher mechanism is dynamic quenching. The findings of this work are significant to reveal the fate of Cu2+, Zn2+ and Pb2+ during its sorption process onto Desulfovibrio vulgaris, and provide useful information of the interaction between Desulfovibrio vulgaris and its secreted EPS with metal cations.

Improving dewaterability of waste activated sludge by thermally-activated persulfate oxidation at mild temperature

The mass production of waste activated sludge in wastewater treatment plants may lead to environmental pollution and sludge dewatering is an essential process during its treatment. The oxidation of extracellular polymeric substances (EPS) was the core step to achieve deep sludge dewatering. In this study, thermally-activated sodium persulfate (SPS) process was managed to improve the dewaterability of waste activated sludge (WAS) and its internal mechanism was systematically elaborated. Experimental results showed that with 2.0 mmol/g VSS SPS at 80 °C, capillary suction time (CST) was roughly 59.74% of that in raw sludge. Under this condition, 14.66 ± 0.10 × 1011 kg/m of specific resistance to filtration (SRF) and 61.8% ± 0.1% of water content (WC) was determined, respectively. A solubilization/oxidation process was proposed to unravel the mechanism of the enhanced dewaterability of WAS in thermally-activated SPS process. Mild temperature efficiently disrupted the sludge flocs and broke cell walls, releasing large amounts of EPS into bulk phase. Meanwhile, mild temperature accelerated the decomposition of SPS to generate sulfate radicals (SO4−) and hydroxyl radicals (OH) for oxidizing EPS, facilitating the conversion of bound hydrated water into free water and achieving solid-water separation. The higher reaction temperature favored sludge dewatering, whereas overdosing SPS posed no significant impact. Further analysis illustrated that tyrosine protein-like, tryptophan protein-like, fulvic acid-like and humic acid-like substances in various EPS fractions together exerted the influence on sludge dewatering. Furthermore, the synergy process could alter the secondary structure of protein, which caused a loose structure of EPS and the exposure of hydrophobic sites, facilitating the dehydration of sludge flocs. The details of how thermally-activated SPS process enhanced sludge dewaterability provided the theoretical and technical basis for the application of the process under a real-world situation.

Effects of pure oxygen aeration on organic pollutants removal performance and soluble microbial products characteristics of salt-tolerant activated sludge

ABSTRACT The effects of pure oxygen aeration on organic pollutants removal performance and effluent soluble microbial products (SMP) characteristics of salt-tolerant sludge for the treatment of wastewater with the salinity from 1.0% to 3.5% were investigated. The results showed that the oxygen transfer efficiency of the pure oxygen aeration was higher than that of the air aeration. At the low salinities (0.5%, 1.0%, 1.5%), the total organic carbon (TOC) removal rates were 71.42%, 72.88% and 76.30%, respectively, much higher than those with air aeration. However, there were no significant differences of TOC removal efficiency between the air aeration and the pure oxygen aeration at high salinities (2.5% and 3.5%). The SMP contents showed a trend of first decline and then increase generally. The content of SMP with pure oxygen aeration was lower than that with air aeration at low salinity, whereas an opposite result was obtained for salinity above 2.5%. Five excitation–emission matrix (EEM) fluorescence peaks detected in the SMP with pure oxygen aeration and air aeration were assigned to tryptophan protein-like, tyrosine protein-like and humic acid-like substances. Humic acid-like fluorescence mainly appeared in the SMP with air aeration, which may be due to respiratory failure under air aeration conditions.

Simultaneous nitrate and dissolved organic matter removal from wastewater treatment plant effluent in a solid-phase denitrification biofilm reactor

In the present study, an up-flow solid-phase denitrification biofilm reactor (US-DBR) was established for simultaneous nitrate and dissolved organic matter (DOM) removal from wastewater treatment plant effluent. After 100 days operation, the nitrate and COD removal efficiencies were high of 97% and 80%, respectively. According to EEM-FRI analysis, aromatic and tryptophan protein-like, humic-like and fulvic acid-like substances were identified in DOM. Additionally, protein-like substances in DOM components were much easier transformed as carbon source for denitrification. Moreover, protein secondary structure of DOM changed significantly due to the biodegradation and microorganisms metabolic process. High-throughput sequencing analysis implied that Simplicispira, Diaphorobacter, Hydrogenophaga, Pseudoxanthmonas and Stenotrophomonas were the dominate genera in the whole of US-DBR, that were responsible for the removal of nitrate, organics and degradation of solid carbon source, respectively. This study provided a further biological basis about practical application of solid-phase denitrification for simultaneously remove nitrate and organic matter.

Preparation of antibiofouling nanocomposite PVDF/Ag-SiO2 membrane and long-term performance evaluation in the MBR system fed by real pharmaceutical wastewater

In this work, the Ag-SiO2 nanoparticles were successfully synthesized and their antibacterial property was confirmed using the plate colony counting method. The SiO2 and Ag-SiO2 nanoparticles were used to prepare the PVDF/SiO2 and PVDF/Ag-SiO2 nanocomposite membranes, respectively. Pure water flux, contact angle and mechanical strength measurement analyses were conducted to characterize and compare the performance of the neat and nanocomposite membranes. Moreover, in order to investigate the structure of the prepared membranes scanning electron microscope (SEM) was used to obtain surface and cross-section images. A long-term filtration test was carried out in a bench scale submerged membrane bioreactor (MBR) system, fed by real pharmaceutical wastewater, to evaluate the antibiofouling performance of the prepared neat and nanocomposite membranes. In comparison to the neat PVDF, the pure water flux of the nanocomposite PVDF membrane (PVDF/Ag-SiO2; 0.6 wt%) increased about 60% and the water contact angle decreased from about 99° to 89°. The obtained results showed that the nanocomposite PVDF/Ag-SiO2 membrane exhibits considerable antibiofouling properties such that the accumulated dried biofilm as well as the extra cellular polymeric substances (EPSs) collected from the cake layer decreased considerably for the nanocomposite membrane. Moreover, the flux recovery ratio increased from 58% for the neat PVDF membrane to 76% for the nanocomposite PVDF/Ag-SiO2 membrane. The excitation and emission matrix (EEM) fluorescence spectroscopy analysis revealed that the accumulated protein on the surface of nanocomposite membranes decreased considerably in a way that the peak corresponding to tryptophan protein-like substances diminished completely, indicating the high antibiofouling potential of nanocomposite membranes. The chemical oxygen demand (COD) and ammonium removal efficiencies of the neat and nanocomposite membranes were higher than 90% and 95%, respectively, indicating negligible impact of the membrane modification on the effluents’ quality.

Exposure to polyamide 66 microplastic leads to effects performance and microbial community structure of aerobic granular sludge.

Microplastic polyamide 66 (PA66) was used to explore its mechanism of influence on the contaminants removal from aerobic granular sludge (AGS) and the corresponding change to the microbial community. Results showed that the removal pollution efficiency of the experimental groups with PA66 were inhibited during the early treatment stage. However, as the experiment progressed, the removal efficiencies of chemical oxygen demand (COD) (92.66%, 93.10%, 93.11%, 93.79%) and ammonia nitrogen (94.25%, 94.58%, 95.61%, 94.73%) were similar in the addition 0g/L (A), 0.1g/L (B), 0.2g/L (C) and 0.5g/L (D) PA66 beakers at the last 10 days. On the first day, the intensity of fluorescence peaks representing tryptophan protein-like and aromatic protein-like substances of loosely-bound extracellular polymeric substances (LB-EPS) indicated that the PA66 microplastic caused damage to the sludge structure, and the intensity of fluorescence peaks representing fulvic acid-like and humic acid-like substances were stronger than those in the control beaker (A). Microbial community analysis showed that the main phyla were Firmicutes (49.11%, 59.77%, 44.33%, 41.21%), Proteobacteria (26.44%, 11.96%, 31.44%, 19.4%) and Bacteroidetes (9.24%, 13.05%, 11.89%, 14.71%) in the four beakers. According to Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway analysis, genes representing [T] Signal transduction mechanisms illustrated that adding PA66 microplastic resulted in more signaling molecules in the AGS.