pH Modulation Research Articles

Virus-Based Separation of Rare Earth Elements.

The utilization of biomaterials for the separation of rare earth elements (REEs) has attracted considerable interest due to their inherent advantages, including diverse molecular structures for selective binding and the use of eco-friendly materials for sustainable systems. We present a pioneering methodology for developing a safe virus to selectively bind REEs and facilitate their release through pH modulation. We engineered the major coat protein of M13 bacteriophage (phage) to incorporate a lanthanide-binding peptide. The engineered lanthanide-binding phage (LBPh), presenting ∼3300 copies of the peptide, serves as an effective biological template for REE separation. Our findings demonstrate the LBPh's preferential binding for heavy REEs over light REEs. Moreover, the LBPh exhibits remarkable robustness with excellent recyclability and stability across multiple cycles of separations. This study underscores the potential of genetically integrating virus templates with selective binding motifs for REE separation, offering a promising avenue for environmentally friendly and energy-efficient separation processes.

PH modulation for high capacity and long cycle life of aqueous zinc-ion batteries with β-MnO2/3D graphene-carbon nanotube hybrids as cathode

pH modulation for high capacity and long cycle life of aqueous zinc-ion batteries with β-MnO2/3D graphene-carbon nanotube hybrids as cathode

Translational insights into the hormetic potential of carbon dioxide: from physiological mechanisms to innovative adjunct therapeutic potential for cancer.

Carbon dioxide (CO2), traditionally viewed as a mere byproduct of cellular respiration, plays a multifaceted role in human physiology beyond simple elimination through respiration. CO2 may regulate the tumor microenvironment by significantly affecting the release of oxygen (O2) to tissues through the Bohr effect and by modulating blood pH and vasodilation. Previous studies suggest hypercapnia (elevated CO2 levels) might trigger optimized cellular mechanisms with potential therapeutic benefits. The role of CO2 in cellular stress conditions within tumor environments and its impact on O2 utilization offers a new investigative area in oncology. This study aims to explore CO2's role in the tumor environment, particularly how its physiological properties and adaptive responses can influence therapeutic strategies. By applying a structured translational approach using the Work Breakdown Structure method, the study divided the analysis into six interconnected work packages to comprehensively analyze the interactions between carbon dioxide and the tumor microenvironment. Methods included systematic literature reviews, data analyses, data integration for identifying critical success factors and exploring extracellular environment modulation. The research used SMART criteria for assessing innovation and the applicability of results. The research revealed that the human body's adaptability to hypercapnic conditions could potentially inform innovative strategies for manipulating the tumor microenvironment. This could enhance O2 utilization efficiency and manage adaptive responses to cellular stress. The study proposed that carbon dioxide's hormetic potential could induce beneficial responses in the tumor microenvironment, prompting clinical protocols for experimental validation. The research underscored the importance of pH regulation, emphasizing CO2 and carbonic acid's role in modulating metabolic and signaling pathways related to cancer. The study underscores CO2 as vital to our physiology and suggests potential therapeutic uses within the tumor microenvironment. pH modulation and cellular oxygenation optimization via CO2 manipulation could offer innovative strategies to enhance existing cancer therapies. These findings encourage further exploration of CO2's therapeutic potential. Future research should focus on experimental validation and exploration of clinical applications, emphasizing the need for interdisciplinary and collaborative approaches to tackle current challenges in cancer treatment.

Reversible electrochemical pH modulation in thin-layer compartments using poly(aniline-co-o-aminophenol)

The analysis of many environmental and clinical samples requires the modification of the original pH, which is conventionally carried out by manual/automatic addition of acid, base, or buffering reagents. In the case of decentralized measurements, often, this approach is not plausible. Instead, reagentless alternatives, such as electrochemically activated in-situ pH adjustments, are suitable. Herein, we present a method for electrochemical, reversible pH modulation of thin-layer samples (<100 µm thickness) using the co-polymer poly(aniline-co-o-aminophenol) (PANOA). The PANOA’s electropolymerization strategy was optimized considering the proton exchange properties in the final material. Thus, limiting the maximum anodic potential to 0.85 V and with the number of cyclic scans being ≤150), the optimal pH modulation capabilities were observed. The reversible proton exchange properties of PANOA were quantified by monitoring the pH inside the thin-layer sample (volume of 0.6 µL), which was defined by a 3D-printed microfluidic cell and a pH-sensor placed in a face planar configuration to the PANOA film. A pH value in the range of 2–4 can repeatably be reached in the samples in 3 min, purely by an electrochemical means and without the addition of external reagents. The concept has been demonstrated to acidify samples at environmental pH (artificial samples and Seawater). The outcomes suggest that the family of polyaniline-co-polymers are interesting to be explored and utilized for electrochemically based pH modulation strategies, if careful considerations are taken regarding their electropolymerization process. Overall, such materials could contribute to the development of continuous, decentralized measuring devices requiring acidification for the formal detection of environmental markers, such as nutrients, carbon species speciation and alkalinity, among others.

Enhanced MC1R-signalling and pH modulation facilitate melanogenesis within late endosomes of BLOC-1-deficient melanocytes.

Photoprotective melanins in the skin are synthesised by epidermal melanocytes within specialised lysosome-related organelles called melanosomes. Melanosomes coexist with lysosomes; thus, melanocytes employ specific trafficking machineries to ensure correct cargo delivery to either the endolysosomal system or maturing melanosomes. Mutations in some of the protein complexes required for melanogenic cargo delivery, such as biogenesis of lysosome-related organelles complex 1 (BLOC-1), result in hypopigmentation due to mistrafficking of cargo to endolysosomes. We show that hypopigmented BLOC-1-deficient melanocytes retain melanogenic capacity that can be enhanced by treatment with cAMP elevating agents despite the mislocalisation of melanogenic proteins. The melanin formed in BLOC-1-deficient melanocytes is not generated in melanosomes but rather within late endosomes/lysosomes to which some cargoes mislocalise. Although these organelles generally are acidic, a cohort of late endosomes/lysosomes have a sufficiently neutral pH to facilitate melanogenesis, perhaps due to mislocalised melanosomal transporters and melanogenic enzymes. Modulation of the pH of late endosomes/lysosomes by genetic manipulation or via treatment with lysosomotropic agents significantly enhances the melanin content of BLOC-1-deficient melanocytes. Our data suggest that upregulation of mistargeted cargoes can facilitate reprogramming of a subset of endolysosomes to generate some functions of lysosome-related organelles.

In situ encapsulation of anthocyanin within soybean protein isolate chains driven by pH for detecting the freshness of food

Intelligent indicator labels have been widely demonstrated as functional material to real-time monitor the freshness of food, whereas the migration problem of natural pH-sensitive dyes from the matrix into surface of packaging film restricted the practical application. Herein, a facile in situ encapsulation strategy was proposed to design and fabricate soybean protein isolate (SPI)/carboxymethyl cellulose sodium (CMC)/anthocyanin (Anth) (SCA) composite film as smart labels to monitor the freshness of protein-based foods. Inspired by the stimulation-response behaviors of Mimosa, Anth was in situ wrapped by the spatial structural mutation of SPI chains driven by different pH conditions, in which tannic acid (TA) served as pH modulator. Compared to CMC/Anth composite film free of pH modulation, the cumulative release of Anth from SCA-7.0 composite film was decreased from 90.97%, 82.45% and 70.52% to 64.14%, 53.88% and 39.45% in distilled water, 10% ethanol and 90% ethanol, respectively. Furthermore, the prepared SCA-7.0 composite film possessed reinforced UV-shielding, gas barrier and water resistance performances. When employed as intelligent label, this composite film can be an intelligent indicator label for real-time meat freshness monitoring. A facile strategy was carried out to in situ encapsulate the Anth within matrix, boosting the reliability and lifespan of intelligent packaging in practical application.

Surface Engineering of Tin Oxide Nanoparticles by pH Modulation Facilitates Homogeneous Film Formation for Efficient Perovskite Solar Modules (Adv. Energy Mater. 25/2024)

Surface Engineering of Tin Oxide Nanoparticles by pH Modulation Facilitates Homogeneous Film Formation for Efficient Perovskite Solar Modules (Adv. Energy Mater. 25/2024)

Enhanced immobilization of cadmium and lead in contaminated soil using calcium alginate-modified HAP biochar: Improvements in soil health and microbial diversity

A novel adsorbent, calcium alginate-modified HAP (Hydroxyapatite)-wood ear mushroom sticks biochar (CA-HAPMB), was synthesized to enhance the immobilization of Cd and Pb in soil. Over 150 days, applying CA-HAPMB at concentrations of 0%–3% in contaminated soils from Chenzhou City in Hunan Province (CZ) and Shenyang City in Liaoning Province (SY) resulted in decreased effective concentrations of Cd and Pb. Specifically, in CZ soil, Cd and Pb decreased by 30.9%–69.3% and 31.9%–78.6%, respectively, while in SY soil, they decreased by 27.5%–53.7% and 26.4%–62.3%, respectively. Characterization results, obtained after separating CA-HAPMB from the soil, indicate that complexation, co-precipitation, and ion exchange play crucial roles in the efficient immobilization of Cd and Pb by CA-HAPMB. Additionally, adjusting the amount of CA-HAPMB added allows modulation of soil pH, leading to increased soil organic matter and nutrient content. Following treatment with CA-HAPMB for immobilizing Cd and Pb, soil bacteria abundance and diversity increased, further promoting heavy-metal immobilization.

Amorphous calcium carbonate as a novel potential treatment for osteoarthritis in dogs: a pilot clinical study.

Amorphous calcium carbonate (ACC) is a potential new treatment for canine osteoarthritis (OA) with novel mechanisms based on local pH modulation and targeting bone remodeling, inflammation, and pain. The aim of this pilot exploratory clinical study was to obtain initial data on the potential efficacy and safety of ACC in OA dogs and to determine if further investigation was appropriate using similar assessment methods. In this prospective, randomized, double-blind, controlled pilot study, 41 client-owned dogs were allocated in a 2:1 ratio to ACC: placebo given orally for 56 days. Efficacy assessments included improvements in pain and mobility using owner questionnaires [Canine Brief Pain Inventory (CBPI), Client Specific Outcome Measure (CSOM), and Veterinary Orthopedic Scores (VOS)]. Safety in the study population was monitored by veterinary examinations, clinical pathology, and adverse events. Fifty-three dogs were screened, of which 41 enrolled and served for the safety assessment. Thirty-six dogs were found evaluable for initial efficacy assessment. Three dogs given placebo (21.4%) and one given ACC (4.5%) were removed before day 56 due to owner-perceived pain and were considered treatment failures. There were no serious adverse events or clinically significant treatment-related effects in the study. Overall, ACC was found safe in the small study population. On day 56, proportionally more ACC than placebo dogs were treatment successes based on CBPI (45.5% vs. 21.4%) and CSOM (63.6% vs. 30.8%, respectively); however, these differences were not statistically significant (p = 0.15 and 0.06, respectively). On day 56, within the ACC group but not the placebo group, the CBPI, CSOM, and VOS assessments were lower compared to day 0 and day 14 (p < 0.05). The relatively small number of dogs limited the statistical power of the pilot study in evaluating the efficacy and safety of ACC. Study results support the conduct of larger, appropriately powered studies using similar assessments to confirm whether ACC may be a safe and effective treatment for OA in dogs.

Aptamer molecular gate functionalized mesoporous SiO2@MB controlled-release system for pollutant detection using Ti(Ⅲ) self-doped TiO2 NTs as active photoanode coupled with electrostatic modulation

Atrazine (ATZ) is a widely used herbicide that can cause serious harm to organisms and ecosystems. An immobilization-free photoelectrochemical (PEC) aptasensor has been herein developed for ATZ based on aptamer molecular gate functionalized mesoporous SiO2@MB controlled release system. Compared with traditional immobilization-based sensors, immobilization-free sensors (IFSs) avoid the modification of the recognition element on the electrode surface. Mesoporous SiO2 with large surface area and good biocompatibility can be used as nanocontainers to stably encapsulate the signal shuttle molecule methylene blue (MB). The bifunctional aptamer (APT) is used not only as the recognition element for ATZ but also as the signal switch to block or release MB. In the presence of ATZ, the specific recognition between ATZ and APT will cause the detachment of APT from the surface of SiO2, thus the molecular gate will open and release MB. Due to pH modulation, the positively charged MB can reach the surface of the negatively charged Ti(III) self-doped TiO2 NTs (Ti(III)–TiO2 NTs) electrode to act as an electron donor, which increases the photocurrent. The immobilization-free aptasensor has shown ultrasensitive detection of ATZ with a wide linear range from 1.0 pM to 100.0 nM and a low detection limit of 0.1 pM. In addition, the sensor has excellent selectivity, stability and anti-interference ability, and has been used in real water sample analysis successfully. This strategy has provided a new idea for the design of advanced immobilization-free PEC sensors for environmental pollutant detection.

Advancing BiVO4 Photoanode Activity for Ethylene Glycol Oxidation via Strategic pH Control.

The photoelectrochemical (PEC) conversion of organic small molecules offers a dual benefit of synthesizing value-added chemicals and concurrently producing hydrogen (H2). Ethylene glycol, with its dual hydroxyl groups, stands out as a versatile organic substrate capable of yielding various C1 and C2 chemicals. In this study, we demonstrate that pH modulation markedly enhances the photocurrent of BiVO4 photoanodes, thus facilitating the efficient oxidation of ethylene glycol while simultaneously generating H2. Our findings reveal that in a pH = 1 ethylene glycol solution, the photocurrent density at 1.23 V vs. RHE can attain an impressive 7.1 mA cm-2, significantly surpassing the outputs in neutral and highly alkaline environments. The increase in photocurrent is attributed to the augmented adsorption of ethylene glycol on BiVO4 under acidic conditions, which in turn elevates the activity of the oxidation reaction, culminating in the maximal production of formic acid. This investigation sheds light on the pivotal role of electrolyte pH in the PEC oxidation process and underscores the potential of the PEC strategy for biomass valorization into value-added products alongside H2 fuel generation.

In Situ pH Modulation for Enhanced Chemical Sensing: Strategies and Applications

AbstractpH is one of the key parameters in chemistry and impacts almost all chemical and biological processes. Also, within analytical chemistry and sensing, pH plays a critical role. This review underscores the critical role of pH manipulation in overcoming analytical challenges posed by complex sample matrices and dynamic environmental conditions. It explores the available tools to control pH at a local scale and how those are or can be applied to improve sensor performance. We focus on four key areas where pH modulation has been or could be leveraged to advance chemical sensing capabilities: i) sensing alkalinity and buffer capacity, ii) sample pretreatment, iii) sensing pH dependent analytes and iv) reducing biofouling. We analyze existing strategies, but also try to identify unexplored possibilities which may have potential and can be exploited for sensing.

Magnesium microspheres to enhance lipiodol-mediated transarterial chemo-embolization (TACE) of hepatocellular carcinoma: From bench to a pilot clinical study.

e16204 Background: Transarterial chemoembolization (TACE) has been extensively used in clinic to treat unresectable hepatocellular carcinoma (HCC). However, arterial embolization would worsen the hostile physicochemical features in the tumor microenvironment (TME) by further reducing its pH and increasing hypoxia, leading to immunosuppressive TME and drug resistance. Methods: Magnesium microspheres (Mg MSs), acting as H2 donors and pH modulators, were prepared via gas atomization pulverization. Characterization included inverted optical microscopy, SEM, and XRD analysis. Their H2 generation and acid neutralization capabilities were confirmed. The Lip-Mg dispersion (Mg MSs dispersed in lipiodol) was tested for therapeutic efficacy in H22 murine liver tumor-bearing mice, 4T1, and CT26 subcutaneous tumor models, as well as in vivo interventional TAE therapy for rabbit orthotopic liver tumors. The modulated capacities of Lip-Mg in H2 gas generation, acid neutralization, and promotion of antitumor immune response were investigated in vivo. Finally, a single-center, single-arm, open-label trial (ChiCTR2200064999) evaluated the safety and efficacy of TACE treatment with Lip-Mg (M-TACE) in Chinese HCC patients. Results: Inverted optical microscopy and SEM images confirmed uniform, smooth Mg microspheres (~60 μm) with a grayish-white color. In acidic buffer (pH 6.4), Mg microspheres rapidly increased pH, as measured by pH meter or fluorescent probe. Lip-Mg treatment significantly inhibited tumor growth compared to controls, prolonging mouse survival by ~2-fold, validated in 4T1 and CT26 models. Ultrasonic and multispectral fluorescence imaging demonstrated Lip-Mg's ability to release H2 and neutralize pH in vivo, reversing the immunosuppressive tumor microenvironment. Clinical study showed manageable treatment-related adverse events, with no unexpected toxicities and negligible impact on serum magnesium levels, confirming the safety of Mg microspheres for M-TACE. According to mRECIST, M-TACE exhibited high CR (61.5%), PR (38.5%), and ORR (100%) rates, with an overall response rate and CR rate of 90% and 60%, respectively. Conclusions: Metallic Mg microspheres (~60 μm) were developed to enhance lipiodol-mediated TAE/TACE for HCC. When combined with lipiodol and injected, they neutralized the acidic TME, triggered hydrogen therapy, and reversed immunosuppression, effectively inhibiting tumor growth. Lip-Mg showed superior outcomes to lipiodol alone for TAE therapy, with M-TACE treatment exhibiting higher ORR and CR rates than cTACE. Post-M-TACE, adverse events were managed well without treatment discontinuations. Our study introduces Mg microspheres as a promising embolic device for M-TACE therapy, potentially improving TACE benefits. Clinical trial information: ChiCTR2100050327.

Zeolite-Loaded Hydrogels as Wound pH-Modulating Dressings for Diabetic Wound Healing.

Wound pH has emerged as a promising therapeutic target in diabetic foot ulcers (DFU). Here, we aimed to develop a microparticle-loaded hydrogel for pH modulation in wound fluid. In a screen of polymeric and inorganic microparticles, zeolites were identified as pH-modulating microparticles. Zeolites were encapsulated in a calcium cross-linked alginate hydrogel, a biocompatible matrix clinically used as a wound dressing. This hydrogel potently neutralized hydroxide ions in serum-containing simulated wound fluid. These findings encourage a further development of this pH-modulating device as a molecular therapeutic system for DFUs.

PH Modulation of Super-Assembled Heteromembranes for Sustainable Chiral Sensing.

Enantioselective sensing and separation represent formidable challenges across a diverse range of scientific domains. The advent of hybrid chiral membranes offers a promising avenue to address these challenges, capitalizing on their unique characteristics, including their heterogeneous structure, porosity, and abundance of chiral surfaces. However, the prevailing fabrication methods typically involve the initial preparation of achiral porous membranes followed by subsequent modification with chiral molecules, limiting their synthesis flexibility and controllability. Moreover, existing chiral membranes struggle to achieve coupled-accelerated enantioseparation (CAE). Here, we report a replacement strategy to controllably produce mesoscale and chiral silica-carbon (MCSC) hybrid membranes that comprise chiral pores by interfacial superassembly on a macroporous alumina (AAO) membrane, in which both ion- and enantiomers can be effectively and selectively transported across the membrane. As a result, the heterostructured hybrid membrane (MCSC/AAO) exhibits enhanced selectivity for cations and enantiomers of amino acids, achieving CAE for amino acids with an isoelectric point (pI) exceeding 7. Interestingly, the MCSC/AAO system demonstrates enhanced pH-sensitive enantioseparation compared to chiral mesoporous silica/AAO (CMS/AAO) with significant improvements of 78.14, 65.37, and 14.29% in the separation efficiency, separation factor, and permeate flux, respectively. This work promises to advance the synthesis of two or more component-integrated chiral nanochannels with multifunctional properties and allows a better understanding of the origins of the homochiral hybrid membranes.

Empirical modeling of naphthenic acids precipitation in an idealized system using response surface methodology: impact of factor interactions

Several factors are recognized to affect the precipitation of naphthenic acids from oil; however, their interactions have not been thoroughly assessed. This study uniquely investigated the interactions among six factors affecting naphthenate precipitation from a model oil using Box-Behnken design. The findings indicate an independent quadratic effect of calcium concentration. A notable positive interaction was observed between pH and water cut, while naphthenic acid concentration exhibited substantial negative interactions with pH and water cut, respectively. Optimization revealed low naphthenate precipitation at high naphthenic acid concentrations, suggesting a role for low molecular weight acids in pH regulation. Thus, pH modulation using low molecular weight acids remains a key strategy for preventing naphthenate deposition.

Surface Engineering of Tin Oxide Nanoparticles by pH Modulation Facilitates Homogeneous Film Formation for Efficient Perovskite Solar Modules

AbstractUniform film deposition over an entire substrate is indispensable to achieve efficient perovskite solar modules (PSMs) by minimizing the gap with high‐performance perovskite solar cells (PSCs). Only a few microscopic pinholes on the film in PSMs directly give rise to debase the performance and stimulate the degradation of the devices. Herein, a strategy of the homogeneous and defect‐reduced electron‐transport layer for high‐performance PSMs is reported. pH modulation of tin oxide (SnO2) nanoparticles colloidal dispersion by a small amount of nitric acid (HNO3) addition leads to the removal of hydroxy groups on the SnO2 surface acting as electronic defects as well as superb regularity of the thin films by forming a network of the SnO2 nanoparticles. The surface engineering of SnO2 nanoparticles brings out the high performance of 23.7% efficiency for a unit cell, 20.3% efficiency for a 24.5 cm2 minimodule, and 19.0% efficiency for a 214.7 cm2 submodule, respectively, where all efficiencies are averaged from results obtained by the reverse/forward scan. In outdoor tests with the submodules, a target PSM generates 16.5% higher cumulative electricity for a month as compared to a control PSM. Furthermore, under damp heat environments, the target PSM maintains 80% efficiency compared to an initial efficiency of 1080 h.

Integrative Salt Selection and Formulation Optimization: Perspectives of Disproportionation and Microenvironmental pH Modulation.

We report a novel utilization of a pH modifier as a disproportionation retardant in a tablet formulation. The drug molecule of interest has significant bioavailability challenges that require solubility enhancement. In addition to limited salt/cocrystal options, disproportionation of the potential salt(s) was identified as a substantial risk. Using a combination of Raman spectroscopy with chemometrics and quantitative X-ray diffraction in specially designed stress testing, we investigated the disproportionation phenomena. The learnings and insight drawn from crystallography drove the selection of the maleate form as the target API. Inspired by the fumarate form's unique stability and solubility characteristics, we used fumaric acid as the microenvironmental pH modulator. Proof-of-concept experiments with high-risk (HCl) and moderate-risk (maleate) scenarios confirmed the synergistic advantage of fumaric acid, which interacts with the freebase released by disproportionation to form a more soluble species. The resultant hemifumarate helps maintain the solubility at an elevated level. This work demonstrates an innovative technique to mediate the solubility drop during the "parachute" phase of drug absorption using compendial excipients, and this approach can potentially serve as an effective risk-mitigating strategy for salt disproportionation.

Advancing Agricultural Sustainability: Vermicomposting as a Biochemical Pathway for Improved Soil Health and Climate Resilience

This comprehensive review explores the multifaceted role of vermicomposting in sustainable agriculture, emphasizing its biochemical processes and impact on soil systems. Beginning with the concept, the document delves into the intricacies of the vermicomposting process, including the selection of suitable earthworm species for vermiculture. It further examines the biochemical transformations that occur during vermicomposting, such as the optimization of the carbon to nitrogen ratio, alterations in organic carbon content, and the modulation of soil pH and electrical conductivity. The accumulation of heavy metals and the transformation of nitrogen and phosphorus are also discussed, alongside the process of humification. Subsequently, the profound effects of vermicompost on soil properties, highlighting its influence on physical characteristics, organic matter content, mineralization, and nutrient dynamics, as well as the enhancement of humus content was deeply reviewed. The document also investigates the implications of vermicomposting on plant growth and yield, providing insights into its potential to increase agricultural productivity. Additionally, the review addresses the impact of vermicomposting on greenhouse gas emissions, underscoring its significance in the context of climate-smart farming practices. Arising from detailed synthesis of the findings, vermicomposting is a pivotal component of climate-resilient agriculture, offering a pathway to healthier soil ecosystems and a sustainable future.

Electrochemical-coupled sulfur-driven autotrophic denitrification for nitrogen removal from raw landfill leachate: Evaluation of performance and mechanisms

The cost-effective and environment-friendly sulfur-driven autotrophic denitrification (SdAD) process has drawn significant attention for advanced nitrogen removal from low carbon-to-nitrogen (C/N) ratio wastewater in recent years. However, achieving efficient nitrogen removal and maintaining system stability of SdAD process in treating low C/N landfill leachate treatment have been a major challenge. In this study, a novel electrochemical-coupled sulfur-driven autotrophic denitrification (ESdAD) system was developed and compared with SdAD system through a long-term continuous study. Superior nitrogen removal performance (removal efficiency of 89.1 ± 2.5 %) was achieved in ESdAD system compared to SdAD process when treating raw landfill leachate (influent total nitrogen (TN) concentration of 241.7 ± 36.3 mg-N/L), and the effluent TN concentration of ESdAD bioreactor was as low as 24.8 ± 5.1 mg-N/L, which meets the discharge standard of China (< 40 mg N/L). Moreover, less sulfate production rate (1.3 ± 0.2 mg SO42−−S/mgNOx−−N vs 1.7 ± 0.2 mg SO42−−S/mgNOx−−N) and excellent pH modulation (pH of 6.9 ± 0.2 vs 5.8 ± 0.4) were also achieved in the ESdAD system compared to SdAD system. The improvement of ESdAD system performance was contributed to coexistence and interaction of heterotrophic bacteria (e.g., Rhodanobacter, Thermomonas, etc.), sulfur autotrophic bacteria (e.g., Thiobacillus, Sulfurimonas, Ignavibacterium etc.) and hydrogen autotrophic bacteria (e.g., Thauera, Comamonas, etc.) under current stimulation. In addition, microbial nitrogen metabolic activity, including functional enzyme (e.g., Nar and Nir) activities and electron transfer capacity of extracellular polymeric substances (EPS) and cytochrome c (Cyt-C), were also enhanced during current stimulation, which facilitated the nitrogen removal and maintained system stability. These findings suggested that ESdAD is an effective and eco-friendly process for advanced nitrogen removal for low C/N wastewater.