Tryptophan-like Proteins Research Articles

Research on the Properties of DOM from the Microalgal Treatment Process for Leachate from Incineration Fly Ash Based on EEM-PARAFAC Analysis

Fly ash derived from the incineration of garbage is known to contain hazardous materials that can affect the growth of plants and animals and pose a threat to human health. In this study, we explored how treatment of fly ash leachate with microalgae could alter the properties of dissolved organic matter (DOM). Fly ash leachate samples obtained from a landfill site in Wenzhou were treated with the microalgae Chlorella vulgaris or Scenedesmus obliquus without and with the addition of ammonium ferric citrate (C6H8FeNO7) for 24 days, and changes in DOM levels and types were measured using excitation emission matrix fluorescence technology. The following results were obtained: Analysis of three-dimensional fluorescence spectral indices indicated that the algal treatment process consistently generated new autogenous DOM, with most of the organic matter being newly formed. Additional nutrients had a minor effect on the production and composition of DOM in the system. Using a parallel factor model to analyze the three-dimensional fluorescence spectral matrices of water samples from various systems revealed common components in each group, including arginine, tryptophan-like proteins and fulvic acid-like substances. This study aimed to explore the changes in DOM properties during microalgae treatment of fly ash leachate from the perspective of three-dimensional fluorescence.

Optimization of microalgal-bacterial consortium flocculation through chitosan-diatomite composite materials: A sustainable approach to biomass harvesting

Chitosan-based flocculants are emerging as a promising technology for microalgae harvesting. However, the implementation of cost-effective and sustainable chitosan-inorganic composites within algal-bacterial symbiosis (ABS) systems for harvesting microalgal-bacterial consortiums (MBC) is still underdeveloped. This study addresses this gap by synthesizing and evaluating chitosan-diatomite composite materials (CTS/DTE), with a focus on their concentration impact on MBC flocculation. Optimal biomass production and flocculation performance were achieved at a CTS/DTE concentration of 60 mg/L during MBC co-culture. Comprehensive characterizations revealed that the largest particle size significantly contributed to superior flocculation efficiency. This efficacy was primarily attributed to the synergistic effects of net trapping and adsorption cross-linking, facilitated by the unique interaction between CTS and DTE. These interactions not only enhanced the bond between the flocculant and microalgal cells but also promoted the structural stabilization of the MBC flocs. Additionally, tryptophan-like proteins in the extracellular polymeric substances (EPS), as identified through three-dimensional fluorescence (EEM) analysis, were found to be the primary contributor to the hydrophobic properties of MBC flocs, significantly enhancing their adhesion and aggregation thermodynamics. Collectively, this research elucidates innovative strategies and provides both theoretical and practical insights for the efficient and cost-effective harvesting of MBC, underscoring the potential of CTS/DTE composites in enhancing the sustainability of ABS systems.

Uncovering the toxic effects and adaptive mechanisms of aminated polystyrene nanoplastics on microbes in sludge anaerobic digestion system: Insight from extracellular to intracellular

The impacts of polystyrene nanoplastics (PS NPs) with amino functional groups on sludge anaerobic digestion process and the underlying microbial feedbacks remains unclear. Herein, PS NPs coated with and without amino functional groups were employed to explore their impacts on the sludge digestion performance. Experimental results showed that aminated PS NPs (PS-NH2) deteriorated the methane yield and hydrolysis rate. The Derjaguin-Landau-Verwey-Overbeek theory analysis suggested that the PS-NH2 decreased the interaction energy barrier, making it easier to contact with sludge and disrupting the structure of extracellular polymeric substances. Metagenomic analysis showed that the abundance of functional microbes (e.g., Longilinea, Leptolinea, and Methanosarcina) decreased, accompanied with lower network complexity and fewer keystone taxa. Molecular docking revealed that PS-NH2 occupy the antioxidant enzyme active binding sites through hydrogen bonding and hydrophobic interactions, impairing degradation of reactive oxygen species. The severe intracellular oxidative stress up-regulated genes associated with quorum sensing (e.g., luxI and luxR) and protein biosynthesis (e.g., algA, trpG and trpE), and further inducing compact tryptophan-like proteins as a defense against NPs. These findings provide new understanding of the toxic effects from PS-NH2 in biological systems and offer valuable insights into the regulation strategies aimed at alleviating NPs inhibition.

Unveiling the effects of dissolved organic matter (DOM) extracted from coastal algae and river on the photooxidation of arsenite

The coastal environment is an important ecosystem connecting land and sea, and arsenite (As(III)) in coastal seawater can seriously affect human health through the food chain. However, the effects of dissolved organic matter (DOM) extracted from coastal algae and rivers on As(III) photooxidation remain unclear. Results show that coastal algal DOM (CA-DOM) is significantly more effective than Suwannee River natural organic matter (SRNOM) in photooxidation of As(III), with a rate 8.3 times higher after correcting for light screening effects. CA-DOM accelerates As(III) photooxidation mainly through the 3DOM⁎ pathway, contributing 78.7 % to the process, whereas 3NOM⁎ contributes only 37.2 % for SRNOM. CA-DOM consists primarily of low-excited tyrosine and tryptophan-like protein substances, whereas SRNOM consists of humic and fulvic acid-like substances. Thus, CA-DOM exhibits a higher steady-state concentration of 3DOM⁎, and the 3DOM⁎ reacts much faster with As(III) than the 3NOM⁎. The increase in CA-DOM concentration can significantly accelerate the photooxidation of As(III), whereas the effect of SRNOM concentration is negligible. Increased salinity can accelerate As(III) photooxidation for all types of DOM. Our results provide new insights into the role of DOM from different sources in the photooxidation of As(III) in the natural environment or engineering applications.

An insight into PANI-TiO2 photocatalysis of refractory organic matter through molecular size fractionation.

Refractory organic matter (RfOM) is ubiquitous in aquatic environment and plays various roles in regulating the fate, transport, toxicity, and bioavailability of chemical species, such as metals, emerging organic contaminants, and nanomaterials. RfOM is mainly represented by humic acids (HA) as the acid insoluble fraction of organic matrix. Considering the complex and multicomponent characteristic of HA, a detailed study was designed to elucidate the fate of molecular size fractions (MSFrs) of humic under solar irradiation in the presence of polyaniline (PANI)-modified TiO2 composites. Humic acid as a consortium of diverse molecular size fractions with different tendencies towards oxidation requires further assessment by UV-vis and fluorescence spectroscopic parameters complementary to previous studies on the photocatalytic degradation of RfOM by using TiO2 and PANI-TiO2 composites. Absorbance-based removal efficiencies under initial and post-photocatalytic conditions showed a re-formation trend during photocatalysis in the presence of PANI and TiO2 where higher MSFrs were transformed to lower MSFrs that was apparent for < 3kDa fraction. Completely different profiles were observed for PT-41 and PT-81 indicating similar degradation pathways independent of PANI ratio in the composite. As confirmed by the investigated parameters, formation of both 450kDa and 220kDa MSFrs were evident under all conditions indicating in situ generation of higher MSFrs. The eligibility of coupled absorbance-fluorescence measurements to discern molecular size distribution of humic acid via oxidative degradation was also investigated. Excitation-emission matrix (EEM) contour plots emphasized the ratio dependency of PANI modification of TiO2 and revealed sample specific variations that were more pronounced in terms of the emergence of tyrosine- and tryptophan-like aromatic proteins.

Mechanism of membrane fouling mitigation by microalgae biofilm formation for low C/N mariculture wastewater treatment: EPS characteristics, composition and interfacial interaction energy

Membrane fouling is considered one of the main limitations of membrane bioreactor (MBR) in wastewater treatment applications, including low C/N aquaculture wastewater. Although much research has focused on the integration of MBR with bacterial biofilm, there has been limited exploration into the mitigation mechanism of membrane fouling by microalgae biofilm. In this study, extracellular polymeric substances (EPS) before and after the formation of microalgae biofilm were compared, leading to the conclusion that the microalgae biofilm formation could reduce membrane fouling potential of EPS, thereby mitigating membrane fouling. EPS content and fluorescence components analysis indicated that microalgae biofilm formation could effectively reduce protein to polysaccharide ratios (PN/PS) of three types of EPS (soluble EPS (S-EPS), loosely bound EPS (LB-EPS), and tightly bound EPS (TB-EPS)), lowering the membrane fouling potential associated with protein substances, especially tryptophan-like protein. Moreover, the analysis of molecular weight (MW) suggested that microalgae biofilm could considerably decrease the MW of both S-EPS and LB-EPS, thus mitigating the influence of high MW substances on membrane fouling. Meanwhile, the precise composition of EPS revealed a reduction in hydrophobic alkanes and recalcitrant aromatics, which often lead to membrane fouling. Furthermore, the extended Derjaguin-Landau-Verwey-Overbeek (XDLVO) theory further highlighted that microalgae biofilm weakened the interfacial interaction energy between the three EPS and membrane to mitigate membrane fouling. Therefore, this study provides a comprehensive elucidation of how microalgae biofilm formation mitigates membrane fouling, offering theoretical support for utilizing microalgae biofilm MBR in treating low C/N mariculture wastewater.

Crucial role of extracellular polymeric substances from anammox sludge in wastewater phosphorus recovery via magnesium phosphate crystallization

The magnesium phosphate (Mg-P) crystallization based on anaerobic ammonia oxidation is of interest for simultaneous nitrogen and phosphorus removal in wastewater treatment due to cost-effectiveness. Understanding the role of extracellular polymeric substances (EPS) in crystal growth is pivotal for bio-induced Mg-P crystallization. In this work, the effects of EPS in Mg-P crystallization were thoroughly investigated. Results indicated that EPS decreased the initial crystallization rate but slightly improved the final crystallization yield. The maximum removal efficiencies of Mg and P ions increased by 2.8 % and 3.1 %, respectively, when EPS concentration was 80 mg/L. Additionally, the presence of EPS enhanced Mg3(PO4)2·10 H2O production and facilitated the formation of larger rhombic plate-like structures crystals (maximum particle size increased by 215 %). Analysis of EPS composition changes during the crystallization process and characterization of the final crystals suggested that tryptophan-like proteins preferentially involved in the Mg-P crystallization process, while β-sheet proteins potentially influencing crystal morphology. Furthermore, the formation of phosphate ester groups, hydrogen bonding, and COOH-Mg2+ complexes were considered triggering factors for the interaction between EPS and Mg-P crystals. This study elucidated the underlying mechanism of EPS on Mg-P crystallization, further enhancing the understanding of the interaction between inorganic mineralization processes and microorganisms.

Spectral characteristics of dissolved organic matter in Plateau Lakes: Identifying eutrophication indicators in Southwest China

Dissolved organic matter (DOM) acts as a chemical intermediary between terrestrial and lacustrine ecosystems and significantly affects the structure and function of lakes. The trophic state of lakes, driven by terrestrial input and phytoplankton biomass, alters the optical properties of DOM. From November 2018 to July 2019, we collected 119 water samples from the Erhai watershed and analyzed them using UV–Vis and EEM-PARAFAC to study the optical properties of DOM in relation to the trophic conditions. Our result indicated that the tyrosine-like protein (C1), tryptophan-like protein (C2), and humic-like compounds (C3) were among the mostly autochthonous components of the DOM. The percentage of the C3 was higher in eutrophic lakes than in mesotrophic and light-eutrophic lakes. The ultraviolet absorption coefficients at 254 nm (aCDOM(254)) and fluorescence intensity at 355 nm (Fn(355)) increased significantly (p < 0.01) with an increased trophic state. Our findings indicate that the influence of nutrients and environmental factors (such as pH and water temperature) on DOM varies with the trophic state. The development of novel predictive models for trophic state assessment was largely based on the significant correlations between TSI and aCDOM(254) (R2 = 0.762, p < 0.01) and Fn(355) (R2 = 0.705, p < 0.01). This neural network model facilitates the creation of a novel fast assessment tool by highlighting the connection between DOM features and the trophic state index. By enabling swift experimental measurements, this model offers a high-resolution monitoring solution for tracking the eutrophication of plateau lakes and rivers.

Deciphering the role of extracellular polymeric substances in the adsorption and biotransformation of organic micropollutants during anaerobic wastewater treatment

Extracellular polymeric substances (EPS) participate in the removal of organic micropollutants (OMPs), but the primary pathways of removal and detailed mechanisms remain elusive. We evaluated the effect of EPS on removal for 16 distinct chemical classes of OMPs during anaerobic digestion (AD). The results showed that hydrophobic OMPs (HBOMPs) could not be removed by EPS, while hydrophilic OMPs (HLOMPs) were amenable to removal via adsorption and biotransformation of EPS. The adsorption and biotransformation of HLOMPs by EPS accounted up to 19.4 ± 0.9 % and 6.0 ± 0.8 % of total removal, respectively. Further investigations into the adsorption and biotransformation mechanisms of HLOMPs by EPS were conducted utilizing spectral, molecular dynamics simulation, and electrochemical analysis. The results suggested that EPS provided abundant binding sites for the adsorption of HLOMPs. The binding of HLOMPs to tryptophan-like proteins in EPS formed nonfluorescent complexes. Hydrogen bonds, hydrophobic interactions and water bridges were key to the binding processes and helped stabilize the complexes. The biotransformation of HLOMPs by EPS may be attributed to the presence of extracellular redox active components (c-type cytochromes (c-Cyts), c-Cyts-bound flavins). This study enhanced the comprehension for the role of EPS on the OMPs removal in anaerobic wastewater treatment.

The Impact of Bisphenol A on the Anaerobic Sulfur Transformation: Promoting Sulfur Flow and Toxic H2S Production.

Bisphenol A (BPA), as a typical leachable additive from microplastics and one of the most productive bulk chemicals, is widely distributed in sediments, sewers, and wastewater treatment plants, where active sulfur cycling takes place. However, the effect of BPA on sulfur transformation, particularly toxic H2S production, has been previously overlooked. This work found that BPA at environmentally relevant levels (i.e., 50-200 mg/kg total suspended solids, TSS) promoted the release of soluble sulfur compounds and increased H2S gas production by 14.3-31.9%. The tryptophan-like proteins of microbe extracellular polymeric substances (EPSs) can spontaneously adsorb BPA, which is an enthalpy-driven reaction (ΔH = -513.5 kJ mol-1, ΔS = -1.60 kJ mol-1K -1, and ΔG = -19.52 kJ mol-1 at 35 °C). This binding changed the composition and structure of EPSs, which improved the direct electron transfer capacity of EPSs, thereby promoting the bioprocesses of organic sulfur hydrolysis and sulfate reduction. In addition, BPA presence enriched the functional microbes (e.g., Desulfovibrio and Desulfuromonas) responsible for organic sulfur mineralization and inorganic sulfate reduction and increased the abundance of related genes involved in ATP-binding cassette transporters and sulfur metabolism (e.g., Sat and AspB), which promoted anaerobic sulfur transformation. This work deepens our understanding of the interaction between BPA and sulfur transformation occurring in anaerobic environments.

Synergetic conditioning via oxalic acid enhanced Fe2+/CaO2 and skeleton construct to achieve deep dewatering of sewage sludge

Extracellular polymeric substance (EPS) with highly hydrophilic groups and sludge with high compressibility are determined sludge dewaterability. Herein, Fe2+ catalyzed calcium peroxide (CaO2) assisted by oxalic acid (OA) Fenton-like process combined with coal slime was applied to improve sludge dewaterability. Results demonstrated that the sludge treated by 0.45/1/1.1-OA/Fe2+/CaO2 mM/g DS, the water content (WC), specific resistance to filtration and capillary suction time dropped to 53.01%, 24.3 s and 1.2 × 1012 m/kg, respectively. Under coal slime ratio as 0.6, WC and compressibility were further reduced to 42.72% and 0.66, respectively. The hydroxyl radicals generated by OA/Fe2+/CaO2 under near-neutral pH layer by layer collapsed EPS, resulting in the degradation and migration of inner releasing components and the exposure of inner sludge flocs skeleton. The hydrophilic tryptophan-like protein of TB-EPS were degraded into aromatic protein of S-EPS and exposed inner hydrophobic sites. The protein secondary structures were transformed by destroying hydrophilic functional groups, which were attributed to the reducing α-helix ratio and reconstructing β-sheet. Moreover, coal slime as the skeleton builder lowered compressibility and formed more macropores to increase the filterability of pre-oxidized sludge for the higher intensity of rigid substances. This study deepened the understanding of OA enhanced Fenton-like system effects on sludge dewaterability and proposed a cost-effective and synergistic waste treatment strategy in sludge dewatering.

Redox mediator chlorophyll accelerates low-temperature biological denitrification with responses of extracellular polymers and changes in microbial community composition

Low temperatures limit the denitrification wastewater in activated sludge systems, but this can be mitigated by addition of redox mediators (RMs). Here, the effects of chlorophyll (Chl), 1,2-naphthoquinone-4-sulfonic acid (NQS), humic acid (HA), and riboflavin (RF), each tested at three concentrations, were compared for denitrification performance at low temperature, by monitoring the produced extracellular polymeric substances (EPS), and characterizing microbial communities and their metabolic potential. Chl increased the denitrification rate most, namely 4.12-fold compared to the control, followed by NQS (2.62-fold increase) and HA (1.35-fold increase), but RF had an inhibitory effect. Chl promoted the secretion of tryptophan-like and tyrosine-like proteins in the EPS and aided the conversion of protein from tightly bound EPS into loosely bound EPS, which improved the material transfer efficiency. NQS, HA, and RF also altered the EPS components. The four RMs affected the microbial community structure, whereby both conditionally abundant taxa (CAT) and conditionally rare or abundant taxa (CRAT) were key taxa. Among them, CRAT members interacted most with the other taxa. Chl promoted Flavobacterium enrichment in low-temperature activated sludge systems. In addition, Chl promoted the abundance of nitrate reduction genes narGHI and napAB and of nitrite reduction genes nirKS, norBC, and nosZ. Moreover, Chl increased abundance of genes involved in acetate metabolism and in the TCA cycle, thereby improving carbon source utilization. This study increases our understanding of the enhancement of low-temperature activated sludge by RMs, and demonstrates positive effects, in particular by Chl.

Advanced oxidation process/coagulation coupled with membrane distillation (AOP/Coag-MD) for efficient ammonia recovery: Elucidating biofouling control performance and mechanism

The inadequate understanding of the biofouling formation mechanism and the absence of effective control have inhibited the commercial application of membrane distillation (MD). In this study, an advanced oxidation process (AOP)/coagulation-coupled (Coag) membrane distillation system was proposed and exhibited the potential for MD ammonia recovery (recovery rate: 94.1%). Extracellular polymeric substances (EPS) and soluble microbial products (SMP) components such as humic acid and tryptophan-like proteins were disrupted and degraded in the digestate. The curtailment and sterilizing efficiency of AOP on biofilm growth was also verified by optical coherence tomography (OCT) in situ real-time monitoring and confocal laser scanning microscopy (CLSM). Peroxymonosulfate (PMS) was activated to generate sulfate (SO4•-) and hydroxyl radicals (HO•), which altered the microbial community. After oxidative treatment, 16 S rRNA sequencing indicated that the dominant phylum of the microbial community evolved into Firmicutes. Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway analysis demonstrated that free radicals produced by PMS could disrupt cells' signaling molecules and interactions. In conjunction with these analyses, the mechanisms of response to free radical attack by Gram-negative bacteria, Gram-positive bacteria, and fungi were revealed. This research provided new insights into the field of membrane fouling control for membrane technology resource recovery processes, broadening the impact of AOP applications on microbiological response and fate in the environment.

Mechanistic insight into the aggregation ability of anammox microorganisms: Roles of polarity, composition and molecular structure of extracellular polymeric substances

The chemical characteristics of extracellular polymeric substances (EPS) of anammox bacteria (AnAOB) play a crucial role in the rapid enrichment of AnAOB and the stable operation of wastewater anammox processes. To clarify the influential mechanisms of sludge EPS on AnAOB aggregation, multiple parameters, including the polarity distribution, composition, and molecular structure of EPS, were selected, and their quantitative relationship with AnAOB aggregation was analyzed. Compared to typical anaerobic sludge (anaerobic floc and granular sludge), the anammox sludge EPS exhibited higher levels of tryptophan-like substances (44.82–56.52 % vs. 2.57–39.81 %), polysaccharides (40.02–53.49 mg/g VSS vs. 30.22–41.69 mg/g VSS), and protein structural units including α-helices (20.70–23.98 % vs. 16.48–19.32 %), β-sheets (37.43–42.98 % vs. 25.78–36.72 %), and protonated nitrogen (Npr) (0.065–0.122 vs. 0.017–0.061). In contrast, it had lower contents of β-turns (20.95–27.39 % vs. 28.17–39.04 %). These biopolymers were found to originate from different genera of AnAOB. Specifically, the α-helix-rich proteins were mainly derived from Candidatus Kuenenia, whereas the extracellular proteins related to tryptophan and Npr were closely associated with Candidatus Brocadia. Critically, these EPS components could drive anammox aggregation through interactions. Substantial amounts of tryptophan-like substances facilitated the formation of β-sheet structures and the exposure of internal hydrophobic clusters, which benefited the anammox aggregation. Meanwhile, extracellular proteins with high Npr content played a pivotal role in the formation of mixed protein-polysaccharide gel networks with the electronegative regions of polysaccharides, which could be regarded as the key component in the maintenance of anammox sludge stability. These findings provide a comprehensive understanding of the multifaceted roles of EPS in driving anammox aggregation and offer valuable insights into the development of EPS regulation strategies aimed at optimizing the anammox process.

Bacteria Affect the Distribution of Soil-Dissolved Organic Matter on the Slope: A Long-Term Experiment in Black Soil Erosion

Soil erosion results in dissolved organic matter (DOM) loss and is one of the main paths of soil carbon loss. Bacteria affect the generation and transformation of DOM. However, the effect of bacteria on the composition and slope distribution of DOM has rarely been investigated under field conditions. Based on a long-term experiment of three gradients (3°, 5°, 8°) in a black soil erosion area of Northeast China, the content, composition, and source of DOM were studied. The results showed that the DOM of the 3° and 5° slope was enriched midslope, and the DOM of the 8° slope was enriched downslope. Parallel factor (PARAFAC) analysis indicated that the main substances in DOM were fulvic-like acid, humic-like acid, tryptophan-like protein, and soluble microbial metabolites. The upslope and downslope soils of 3° and 5° slopes showed high DOM bioavailability, while the downslope soil of the 8° slope showed high DOM bioavailability. The content of new DOM in downslope soil increased with the gradient. Bacteria played an important role in the synthesis and transformation of DOM and affected its composition and slope distribution. Verrucomicrobiota, Firmicutes, Planctomycetota, and Gemmatimonadota were the main factors affecting soil DOM. The results could be helpful in understanding the loss mechanism of DOM in eroded black soil and provide support for soil carbon sequestration.

Impact of polyamide microplastics on riparian sediment structures and Cd(II) adsorption: A comparison of natural exposure, dry-wet cycles, and freeze-thaw cycles

Microplastics (MPs) accumulation in sediments has posed a huge threat to freshwater ecosystems. However, it is still unclear the effect of MPs on riparian sediment structures and contaminant adsorption under different hydrological processes. In this study, three concentrations of polyamide (PA) MPs-treated sediments (0.1%, 1%, and 10%, w/w) were subjected to natural (NA) exposure, dry-wet (DW) cycles, and freeze-thaw (FT) cycles. The results indicated that PA MPs-added sediment increased the micro-aggregates by 10.1%−18.6% after FT cycles, leading to a decrease in aggregate stability. The pH, OM, and DOC of sediments were significantly increased in DW and FT treatments. In addition, the increasing concentration of PA MPs showed an obvious decrease in aromaticity, humification, and molecular weight of sediment DOM in FT treatments. Also, high level of MPs was more likely to inhibit the formation of humic-like substances and tryptophan-like proteins. For DW and FT cycles, 0.1% and 1% PA MPs-treated sediments slightly increased the adsorption capacity of Cd(II), which may be ascribed to the aging of MPs. Further correlation analysis found that DW and FT altered the link between DOM indicators, and aggregate stability was directly related to the changes in sediment organic carbon. Our findings revealed the ecological risk of MPs accumulating in riparian sediments under typical hydrological processes.

Triclocarban transformation and removal in sludge conditioning using chalcopyrite–triggered percarbonate treatment

Herein, a facile combination approach of chalcopyrite and sodium percarbonate (CuFeS2+ SPC) was established to augment both TCC removal efficiency and sludge dewatering. Results showed that utilizing the CuFeS2 dosage of 600 mg/g total solids (TS) under the optimal condition, along with the SPC dosage of 12.5 mg/g TS, an initial pH of 4.0, and a reaction duration of 40 min, led to a substantial reduction of 53.9% in the TCC content within the sludge, accompanied by a notable decrease of 36.9% in the water content. Compared to well-studied iron-based advanced oxidation processes, CuFeS2 + SPC treatment proved to be more cost-effective and environmentally friendly. Mechanistic findings demonstrated that •OH oxidation played a significant role in TCC removal, with O2•− and 1O2 acting as secondary factors. During the CuFeS2 + SPC process, the received •OH, O2•−, and 1O2 destroyed the main binding sites of extracellular polymeric substances to TCC, including tryptophan-like protein, amide, CO stretch, and −COO− functional groups. As a result, approximately 50% of TCC was partially degraded within the solid sludge phase after the attack of radicals. Meanwhile, the decreased macromolecular organic compounds in solid sludge attenuated the binding efficacy of TCC, giving rise to the transfer of partial TCC to the liquid phase. Ultimately, the TCC in sludge was successfully removed, and five transformation products were identified. This study significantly contributes to our understanding regarding TCC transformation and removal in the sludge conditioning process.

In-situ sewer sediment self-cleaning by plant ash-driven hydrolysis: Impairing adhesion and hydraulic erosion resistance from gelatinous biopolymer molecule deconstruction

The gelatinous structure and adhesion of sediments induced strong hydraulic erosion resistance and bottom siltation, which brought about serious challenges in sewer management. The in-situ sediment self-cleaning technology with low energy and labor consumption has become urgent demand. This study proposed an innovative plant ash-triggered molecule hydrolysis strategy for driving sewer sediment self-cleaning. Plant ash treatment at the optimal dosage of 0.10 g/g SS promoted molecular deconstruction and dissolution of aromatic proteins (tryptophan-like and tyrosine-like proteins), humic acids (fulvic acid-like and humic acid-like substances) and carbohydrates with secondary structure deflocculation (α-helix to β-turn), meanwhile numerous microbial cells were lysed, contributing to linkage breakage in extracellular polymeric substance (EPS). The gelatinous EPS disruption and outward migration with cohesion reduction were achievable. Sediment adhesion was vulnerable to EPS structural damage, which was degenerated by 91.14 %. Correspondingly, the sediment matrix structure was observably disintegrated into dispersive and small fragments, with increased surface electronegativity and eliminated adhesive bio-agglomeration. Thereby, the sensitivity of sediments to hydraulic erosion was greatly improved. In this case, substantial organic and inorganic sediment particles were solubilized and downstream transported by gravity sewage flow. Such plant ash-triggered hydrolysis provided a sustainable strategy for sediment self-cleaning in “waste control by waste” pattern, which improved sediment floating by 7.25–9.57 times. Considerable economic benefits of 35.56–123.46 CNY/(sewer meter length) were obtained compared with traditional mechanical flushing approaches. The findings might provide theoretical and engineering inspirations for solving sewer sediment issues.

Cadmium immobilization during nitrate-reducing Fe(II) oxidation by Acidovorax sp. BoFeN1: Contribution of bacterial cells and secondary minerals

Microbially nitrate-reducing Fe(II) oxidation (NRFO) is widespread in anoxic environments at circumneutral pH, in which Fe(II) oxidation is considered to be mainly catalyzed by nitrite via chemodenitrification after microbial nitrate reduction. Cadmium (Cd) is toxic to organisms, and its availability is strongly affected by iron (oxyhydr)oxides and/or bacteria. However, it remains unclear how NRFO affects the fate of Cd with environmentally relevant concentrations, and the relative contributions of microbes and secondary minerals to Cd immobilization during NRFO. Here, Acidovorax sp. BoFeN1, a typical NRFO bacterium, was used to investigate the Cd immobilization during NRFO at pH 7.0 with 0.1, 0.5, and 1.0 mg/L Cd, respectively. Higher initial Cd concentration resulted in a higher amount of Cd immobilized in precipitates, but showed stronger inhibition on nitrate reduction, acetate metabolism, and cell growth. The presence of Cd barely influenced the Fe(II) oxidation during NRFO or chemodenitrification, but retarded the mineral transformation to secondary crystalline minerals, i.e., lepidocrocite and goethite. The extracellular polymeric substances deposited in the bacteria-mineral precipitates were rich in tyrosine-like and tryptophan-like proteins with negatively charged amino and carboxyl groups. The STEM-HAADF images with EDX mapping demonstrated that Cd was strongly co-localized with Fe on the cell surface and in the periplasm. Cadmium immobilization experiments with bacterial cells or during chemodenitrification indicated that the bacterial cells and secondary minerals formed during chemodenitrification are comparably important for Cd immobilization in the Cd0.1 treatment, while the secondary minerals played a predominant role in Cd immobilization in the Cd0.5 and Cd1.0 treatments. These results suggested that Cd was likely associated with the secondary iron minerals, which precipitated with the proteins on the cell surface and in the periplasm. Our findings provide a comprehensive understanding of the roles of Cd, bacterial cells, and secondary minerals formed via chemodenitrification, as well as their interactions during the complicated NRFO process at circumneutral pH.

Halophyte Elymus dahuricus colonization regulates microbial community succession by mediating saline-alkaline and biogenic organic matter in bauxite residue

Alkalinity regulation and nutrient accumulation are critical factors in the construction of plant and microbial communities and soil formation in bauxite residue, and are extremely important for sustainable vegetation restoration in bauxite residue disposal areas. However, the establishment and succession of microbial communities driven by plant colonization-mediated improvements in the physicochemical properties of bauxite residues remain poorly understood. Thus, in this study, we determined the saline-alkali properties and dissolved organic matter (DOM) components under plant growth conditions and explored the microbial community diversity and structure using Illumina high-throughput sequencing. The planting of Elymus dahuricus (E. dahuricus) in the bauxite residue resulted in a significant decrease in total alkalinity (TA), exchangeable Na, and electrical conductivity (EC) as well as the release of more tryptophan-like protein compounds and low-molecular-weight humic substances associated with biological activities into the bauxite residue substrate. Taxonomical analysis revealed an initial-stage bacterial and fungal community dominated by alkaline-tolerant Actinobacteriota, Firmicutes, and Ascomycota, and an increase in the relative abundances of the phyla Bacteroidota, Cyanobacteria, Chloroflexi, and Gemmatimonadota. The biological activities of phylum Actinobacteriota, Bacteroidota, and Gemmatimonadota were significantly associated with protein-like and UVA-like humic substances. As eutrophic bacteria, Proteobacteria participate in the transformation of humic substances and can not only utilize small molecules of organic matter and convert them into humic substances but also promote the gradual conversion of humic acids into simple molecular compounds. Our results suggest that plant roots secrete organic matter and microbial metabolites as the main biogenic organic matter that participates in the establishment and succession of the microbial community in bauxite residues. Root length affects bacterial and fungal diversity by mediating the production of protein-like substances.