Hubertus V. M. Hamelers, Annemiek Ter Heijne, Tom H. J. A. Sleutels et al.

Applied Microbiology and Biotechnology • 2010

Bioelectrochemical systems (BESs) are emerging technologies which use microorganisms to catalyze the reactions at the anode and/or cathode. BES research is advancing rapidly, and a whole range of applications using different electron donors and acceptors has already been developed. In this mini review, we focus on technological aspects of the expanding application of BESs. We will analyze the anode and cathode half-reactions in terms of their standard and actual potential and report the overpotentials of these half-reactions by comparing the reported potentials with their theoretical potentials. When combining anodes with cathodes in a BES, new bottlenecks and opportunities arise. For application of BESs, it is crucial to lower the internal energy losses and increase productivity at the same time. Membranes are a crucial element to obtain high efficiencies and pure products but increase the internal resistance of BESs. The comparison between production of fuels and chemicals in BESs and in present production processes should gain more attention in future BES research. By making this comparison, it will become clear if the scope of BESs can and should be further developed into the field of biorefineries.

Kerman Kagan

The Japanese Journal of Urology • 2006

Tumor metabolic reprogramming is a core hallmark of cancer, characterized by pathways such as aerobic glycolysis, aberrant lipid metabolism, and glutaminolysis that support rapid proliferation and immunosuppressive microenvironments. Circular RNAs (circRNAs) are highly stable, evolutionarily conserved non-coding RNAs that have emerged as critical modulators of these metabolic shifts. This review aims to systematically elucidate the roles and mechanisms of circRNAs in reprogramming tumor metabolism, and to discuss their clinical potential as biomarkers and therapeutic targets. Through mechanisms including miRNA sponging, protein interactions, regulation of mitochondrial dynamics, and modulation of metabolic enzymes, circRNAs influence key metabolic pathways by targeting glycolytic enzymes, lipid synthesis regulators, and glutaminolysis-related molecules to either facilitate or inhibit their expression. This review systematically summarizes the unique contributions of circRNAs to tumor metabolic reprogramming, highlighting key mechanisms such as regulation of peptide-encoding protein translation, mitochondrial localization function, gene promoter-targeted transcriptional regulation, and cross-pathway metabolic mediation, which underscore their distinct biological advantages and regulatory roles in tumor metabolism. The stability and tissue specificity of circRNAs make them promising diagnostic biomarkers, while their role in drug resistance mediated by metabolic reprogramming highlights their potential as therapeutic targets. Strategies such as circRNA inhibitors, mimics, and nanoparticle-based delivery systems are being explored to modulate tumor metabolism. Despite challenges including complex regulatory networks and limited manipulation tools, advances in high-throughput technologies and clinical trials hold promise for translating circRNA research into novel cancer therapies.

Korneel Rabaey, Simone Bützer, Shelley Brown et al.

Environmental Science & Technology • 2010

Jinyou Shen, Cencen Feng, Yanyan Zhang et al.

Journal of Hazardous Materials • 2012

Bioelectrochemical system (BES) for recalcitrant p-nitrophenol (PNP) removal was investigated in this study. Effective removal of PNP at rates up to 9.14 ± 0.48 mol m(-3)d(-1) was achieved at an energy consumption as low as 0.010 ± 0.002 kWh mol(-1) PNP. PNP removal rate was enhanced with negative cathode potential, increased influent PNP concentration and shortened hydraulic retention time (HRT). Although the coulombic efficiencies at the anode did not exceed 40%, coulombic efficiencies for PNP removal at the cathode were above 70% at various cathode potentials. Compared with conventional anaerobic process, the cosubstrate dosage in BES was significantly reduced due to the high coulombic efficiencies at the cathode. p-Aminophenol (PAP) was identified as the dominant product of PNP reduction at the abiotic graphite cathode of BESs. This study demonstrated that the BES had a potential for efficient removal of nitrophenol pollutants from wastewater.

Kinga Zór, Marc Castellarnau, David Pascual et al.

Biosensors and Bioelectronics • 2011

The analytical method described, based on antibody-antigen bio-recognition and the measuring system for amperometric detection, was designed for accurate, easy to use and cost effective quantification of calpastatin, a meat tenderness biomarker. The novel assay for calpastatin quantification was integrated in a portable electrochemical device known as the Tendercheck system and was used to analyze meat samples collected from animals of different breeds and ages. The data obtained were correlated (R² = 0.62) with Warner Bratzler Shear Force (WBSF) measurements, a routinely used method for meat tenderness determination.

Yang Mu, Jelena Radjenovic, Jinyou Shen et al.

Environmental Science & Technology • 2011

Iodinated X-ray contrast media (ICM) are only to a limited extent removed from conventional wastewater treatment plants, due to their high recalcitrance. This work reports on the cathodic dehalogenation of the ICM iopromide in a bioelectrochemical system (BES), fed with acetate at the anode and iopromide at the cathode. When the granular graphite cathode potential was decreased from -500 to -850 mV vs standard hydrogen electrode (SHE), the iopromide removal and the iodide release rates increased from 0 to 4.62 ± 0.01 mmol m(-3) TCC d(-1) and 0 to 13.4 ± 0.16 mmol m(-3) TCC d(-1) (Total Cathodic Compartment, TCC) respectively. Correspondingly, the power consumption increased from 0.4 ± 1 to 20.5 ± 3.3 W m(-3) TCC. The Coulombic efficiency of the iopromide dehalogenation at the cathode was less than 1%, while the Coulombic efficiency of the acetate oxidation at the anode was lower than 50% at various granular graphite cathode potentials. The results suggest that iopromide could be completely dehalogenated in BESs when the granular graphite cathode potential was controlled at -800 mV vs SHE or lower. This finding was further confirmed using mass spectrometry to identify the dehalogenated intermediates and products of iopromide in BESs. Kinetic analysis indicates that iopromide dehalogenation in batch experiments can be described by a first-order model at various cathode potentials. This work demonstrates that the BESs have a potential for efficient dehalogenation of ICM from wastewater or environmental streams.

Kengo Sasaki, Shin-ichi Hirano, Masahiko Morita et al.

Applied Microbiology and Biotechnology • 2010

Bioelectrochemical reactors (BERs) with a cathodic working potential of -0.6 or -0.8 V more efficiently degraded cellulosic material, i.e., filter paper (57.4-74.1% in 3 days and 95.9-96.3% in 7 days) than did control reactors without giving exogenous potential (15.4% in 3 days and 64.2% in 7 days). At the same time, resultant conversions to methane and carbon dioxide in cathodic working chamber of BERs by application of electrochemical reduction in 3 days of operation were larger than control reactors. However, cumulative methane production in cathodic BERs was similar to those in control reactors after 7 days of operation. Microscopic observation and 16S rRNA gene analysis showed that microbial growth in the entire consortium was higher after 2 days of operation of cathodic BERs as compared with the control reactors. In addition, the number of methanogenic 16S rRNA gene copies in cathodic BERs was higher than in control reactors. Moreover, archaeal community structures constructed in cathodic BERs consisted of hydrogenotrophic methanogen-related organisms and differed from those in control reactors after 2 days of operation. Specifically, the amount of Methanothermobacter species in cathodic BERs was higher within archaeal communities than in those control reactors after 2 days of operation. Electrochemical reduction may be effective for accelerating microbial growth in the start-up period and thereby increasing microbial treatment of cellulosic waste and methane production.

G. Velvizhi, P. Suresh Babu, G. Mohanakrishna et al.

RSC Adv. • 2012

Bioelectrochemistry • 2004

Dieter Sell

Biotechnology • 2001

Sunil A. Patil, Falk Harnisch, Balasaheb Kapadnis et al.

Biosensors and Bioelectronics • 2010

Dongjin Wan, Huijuan Liu, Jiuhui Qu et al.

Bioresource Technology • 2008

A combined bioelectrochemical and sulfur autotrophic denitrification system (CBSAD) was evaluated to treat a groundwater with nitrate contamination (20.9-22.0mgNO(3)(-)-N/L). The reactor was operated continuously for several months with groundwater to maximize treatment efficiency under different hydraulic retention times (HRT) and electric currents. The denitrification rate of sulfur autotrophic part followed a half-order kinetics model. Moreover, the removal efficiency of bioelectrochemical part depended on the electric current. The reactor could be operated efficiently at the HRT ranged from 4.2 to 2.1h (corresponding nitrogen volume-loading rates varied from 0.12 to 0.24 kg N/m(3)d; and optimum current ranged from 30 to 1000 mA), and the NO(3)(-)-N removal rate ranged from 95% to 100% without NO(3)(-)-N accumulation. The pH of effluent was satisfactorily adjusted by bioelectrochemical part, and the sulfate concentration of effluent was lower than 250 mg/L, meeting the drinking water standard of China EPA.

Ka Yu Cheng, Goen Ho, Ralf Cord-Ruwisch

Environmental Science & Technology • 2011

A novel membraneless bioelectrochemical system termed rotatable bioelectrochemical contactor (RBEC) was fabricated and evaluated for its ability to recover useful energy (here methane) from a low organic strength wastewater. We studied the operational characteristics of the RBEC by operating it as a three-electrode electrolysis cell. A stack of conductive disks (each subdivided into two half disks), similar to rotating biological contactors, were rotated with one-half disk immersed in the wastewater and the other into the gas headspace. By carrying out regular half rotations (180° rotation) the anode became the cathode and vice versa. This operation resulted in the build-up of a biofilm that could catalyze both an anodic acetate oxidation and a cathode-driven methanogenesis. Methane production rate was directly proportional to the applied electrical energy. Increase in current density (from 0.16 to 4.1 A m(-2)) resulted in a faster COD removal (from 0.2 to 1.38 kg COD m(-3) day(-1)) and methane production (from 0.04 to 0.53 L L(-1) day(-1)). Of the electrons flowing across the circuit, over 80% were recovered as methane. Such methane production was electrochemically driven by the headspace-exposed cathodic half disks, which released the methane directly to the gas-phase. Energy analysis shows that the new design requires less energy for COD removal than what is typically required for oxygen supply in activated sludge processes. Because the system could operate without wastewater recirculation against gravity; additional pH buffer chemicals; ion-exchange membranes or electrochemical catalysts, it has desirable characteristics for process up-scale. Further, the current report shows the first example of a BES with identical biofilm (due to intermittent polarity inversion) on both electrodes.

Svenja Lohner

Encyclopedia of Applied Electrochemistry • 2014

Small cell lung cancer (SCLC), known for its aggressive nature and resistance to treatment, continues to evade effective targeted therapies. This study investigates the therapeutic potential of Chidamide, a subtype-selective histone deacetylase inhibitor (HDACi), in molecularly distinct SCLC models. In vitro, Chidamide showed dose- and time-dependent cytotoxicity across SCLC-A/N/P subtypes (H69, H526, H446), inhibiting proliferation (IC50: 1.979–4.9 μM) and clonogenicity ( P  < 0.001). It also caused G1/S arrest by increasing p21/p27 levels and decreasing Cyclin E1/CDK2 expression. Mechanistically, Chidamide elevated overall histone H3/H4 acetylation by inhibiting HDAC1/2/3, triggered γ-H2AX-associated DNA damage, and activated mitochondrial apoptosis. Flow cytometry confirmed dose-dependent apoptosis induction (12.45–43.03% across cell lines) and G1-phase accumulation (up to 61.8% in H69). In vivo, oral Chidamide (12.5–25 mg/kg) significantly inhibited xenograft tumor growth, aligning with increased histone acetylation, p21 expression, and Cleaved caspase-3 in treated tumors. Collectively, these results position Chidamide as a promising epigenetic candidate for SCLC therapy, demonstrating preclinical efficacy across molecular subtypes through modulation of chromatin architecture and DNA damage response.

Cristina Tortolini, Marco Frasconi, Gabriele Favero et al.

ECS Meeting Abstracts • 2009

Abstract not Available.

Sandipam Srikanth, Miranda Maesen, Xochitl Dominguez-Benetton et al.

Bioresource Technology • 2014

Bioelectrochemical system (BES) was operated using the enzyme formate dehydrogenase as catalyst at cathode in its free form for the reduction of CO2 into formic acid. Electrosynthesis of formic acid was higher at an operational voltage of -1V vs. Ag/AgCl (9.37mgL(-1) CO2) compared to operation at -0.8V (4.73mgL(-1) CO2) which was strongly supported by the reduction catalytic current. Voltammograms also depicted a reversible redox peak throughout operation at -1V, indicating NAD(+) recycling for proton transfer from the source to CO2. Saturation of the product was observed after 45min of enzyme addition and then reversibility commenced, depicting a lower and stable formic acid concentration throughout the subsequent time of operation. Stability of the enzyme activity after immobilization on the electrode and product yield will be studied further.

Baocheng Huang, Huajun Feng, Meizhen Wang et al.

Bioresource Technology • 2013

The effect of C/N ratios of 2, 2.7, and 3.5 on nitrogen removal in a bioelectrochemical system (BES) was investigated. Starch was used as a carbon source for the electrogenesis phenomenon we observed in a previous study. The results showed that an increased C/N ratio helped the BES to remove nitrate and depress nitrite accumulation but did not increase autotrophic denitrification. Nitrate and total nitrogen removal were increased from 0.69±0.02gm(-3)h(-1) to 1.09±0.16gm(-3)h(-1), and from 0.52±0.08gm(-3)h(-1) to 0.97±0.06gm(-3)h(-1), respectively, when the C/N ratio was increased from 2.0 to 3.5. However, the autotrophic denitrification ratio decreased from 72.74% to 50.23% with the same increase in the C/N ratio. High C/N ratios postponed the excretion of soluble microbial products and increased electrogenesis, but did not improve the anode transformation efficiency.

Zhiwei Wang

Encyclopedia of Membranes • 2014

Yiran Tong, Zhen He

Journal of Hazardous Materials • 2013

This research aims to develop a new approach for in situ nitrate removal from groundwater by using a bioelectrochemical system (BES). The BES employs bioelectricity generated from organic compounds to drive nitrate moving from groundwater into the anode and reduces nitrate to nitrogen gas by heterotrophic denitrification. This laboratory study of a bench-scale BES demonstrated effective nitrate removal from both synthetic and actual groundwater. It was found that applying an electrical potential improved the nitrate removal and the highest nitrate removal rate of 208.2 ± 13.3g NO3(-)-Nm(-3) d(-1) was achieved at 0.8 V. Although the open circuit condition (no electricity generation) still resulted in a nitrate removal rate of 158.5 ± 4.2 gm(-3) d(-1) due to ion exchange, electricity production could inhibit ion exchange and prevent introducing other undesired ions into groundwater. The nitrate removal rate exhibited a linear relationship with the initial nitrate concentration in groundwater. The BES produced a higher current density of 33.4 Am(-3) and a higher total coulomb of 244.7 ± 9.1C from the actual groundwater than the synthetic groundwater, likely because other ions in the actual groundwater promoted ion movement to assist electricity generation. Further development of this BES will need to address several key challenges in anode feeding solution, ion competition, and long-term stability.

Kengo Sasaki, Daisuke Sasaki, Masahiko Morita et al.

Bioresource Technology • 2010

Methanogenic bioreactors, which are packed with supporting material, have attracted attention as an efficient means of degrading garbage. We aimed to increase bioreactor performance by using an electrochemical system to regulate the electrical potential on supporting material. At an organic loading rate of 26.9g dichromate chemical oxygen demand (CODcr)/L/day, reactors with a potential of -0.6 or -0.8V, generated by a cathodic electrochemical reaction, showed greater removal of CODcr and methanogenesis than reactors with a potential of 0.0 or -0.3V, generated by anodic reaction, or control reactors without electrochemical regulation. 16S rRNA gene analysis revealed that the same methanogens were present in all our reactors, but quantitative real-time polymerase chain reaction showed that higher prokaryotic and methanogenic copy numbers were present on cathodic electrodes than on anodic or control electrodes. These results indicate that cathodic electrochemical regulation can support methane fermentation from garbage.

Fangyuan Liang, Yong Xiao, Feng Zhao

Chemical Engineering Journal • 2013

Yoshiyuki Ueno, Yoji Kitajima

Environmental Engineering and Management Journal • 2012

René A. Rozendal, Emilie Leone, Jürg Keller et al.

Electrochemistry Communications • 2009

Fanying Kong, Aijie Wang, Bin Liang et al.

Bioresource Technology • 2013

Bioelectrochemical system (BES) that removes recalcitrant pollutant out of wastewater is of special interest for practice. This study modified the configuration of BES to be a sleeve-type with compact structure. Azo dye (acid orange 7, AO7) in the outer cathode chamber performed a complete decolorization by electrons supplied from acetate oxidized with electricigens in the inner anode chamber. The AO7 decolorization efficiency (DEAO7) was enhanced to be higher than 98% from 0.14 to 2.00 mM. Electrochemical impedance spectroscopy (EIS) analysis showed that the internal resistance of anode, cathode and the whole cell was 26.4, 38.3, and 64.6 Ω, respectively, indicating that the modified configuration with large area and small distance between anode and cathode can result in a lower internal resistance and higher decolorization performance. This is the first study for azo dye decolorization using sleeve-type configuration with highly efficient decolorization by abiotic cathode BES.

Fei Zhang, Jian Li, Zhen He

Bioresource Technology • 2014

Nutrients management is a key task of wastewater treatment and removal of nutrients is usually associated with significant energy/economic cost. A new bioelectrochemical system, named "R(2)-BES", was developed for removing and possibly recovering nutrients from wastewater. This R(2)-BES takes advantage of bioelectricity generation from oxidation of organic compounds to drive ammonium migration out of wastewater, and uses hydroxide ions produced from the cathode reaction as a medium to exchange phosphate ions from wastewater at the same time. Under an applied voltage of 0.8 V, the R(2)-BES removed 83.4 ± 1.3% of ammonium nitrogen and 52.4 ± 9.8% of phosphate, significantly higher than those (3.6 ± 3.7% and 21.1 ± 2.6%) under an open circuit condition. Applying an external voltage can increase current generation, COD removal, and nutrient removal. Those results demonstrate a proof of concept that the R(2)-BES may be potentially applied to remove and recover nutrients through appropriate integration into the existing treatment facilities.

AMY EKECHUKWU

• 2004

Yiran Tong, Zhen He

RSC Advances • 2014

Bo Zhang, Zhen He

RSC Advances • 2012

Min SU, Yong JIANG, Yao ZHANG et al.

Chinese Journal of Appplied Environmental Biology • 2013

James M. Mansell

43rd International Conference on Environmental Systems • 2013

Benjamin Erable, Luc Etcheverry, Alain Bergel

Biofouling • 2011

The paper introduces the concept of the microbial electrochemical snorkel (MES), a simplified design of a "short-circuited" microbial fuel cell (MFC). The MES cannot provide current but it is optimized for wastewater treatment. An electrochemically active biofilm (EAB) was grown on graphite felt under constant polarization in an urban wastewater. Controlling the electrode potential and inoculating the bioreactor with a suspension of an established EAB improved the performance and the reproducibility of the anodes. Anodes, colonized by an EAB were tested for the chemical oxygen demand (COD) removal from urban wastewater using a variety of bio-electrochemical processes (microbial electrolysis, MFC, MES). The MES technology, as well as a short-circuited MFC, led to a COD removal 57% higher than a 1000 Ω-connected MFC, confirming the potential for wastewater treatment.

I-Chung Lo, Chu-Yang Chou

2009 Reno, Nevada, June 21 - June 24, 2009 • 2009

Huanhuan He, Minghua Zhou, Jie Yang et al.

Bioprocess and Biosystems Engineering • 2014

A photosynthetic algal microbial fuel cell (PAMFC) was constructed by the introduction of immobilized microalgae (Chlorella vulgaris) into the cathode chamber of microbial fuel cells to fulfill electricity generation, biomass production and wastewater treatment. The immobilization conditions, including the concentration of immobilized matrix, initial inoculation concentration and cross-linking time, were investigated both for the growth of C. vulgaris and power generation. It performed the best at 5 % sodium alginate and 2 % calcium chloride as immobilization matrix, initial inoculation concentration of 10(6) cell/mL and cross-linking time of 4 h. Our findings indicated that C. vulgaris immobilization was an effective and promising approach to improve the performance of PAMFC, and after optimization the power density and Coulombic efficiency improved by 258 and 88.4 %, respectively. Important parameters such as temperature and light intensity were optimized on the performance. PAMFC could achieve a COD removal efficiency of 92.1 %, and simultaneously the maximum power density reached 2,572.8 mW/m(3) and the Coulombic efficiency was 14.1 %, under the light intensity of 5,000 lux and temperature at 25 °C.

Chansoo Choi, Naixu Hu

Bioresource Technology • 2013

In this study, tetrachloroaurate as an electron acceptor of a microbial fuel cell (MFC) has been studied to discover the parameters that affect the cost-effective recovery of gold. The modeling and equations for calculating the maximum actual efficiency and electrochemical impedance spectroscopic internal resistance of the MFC were also developed. The maximum power density (Pmax) of 6.58 W/m(2) with a fill factor of 0.717 was achieved for 60 mL volumes of 2000 ppm Au(III) catholyte and 12.2 mM acetate anolyte, respectively. The Pmax can also be predicted simply by measuring Rint by EIS. Additionally, the maximum actual MFC efficiency of about 57% was achieved, and the recovery efficiency of Au and the remaining concentration reached 99.89±0.00% and 0.22±0.00 ppm, respectively, for an Au(III) concentration of 200 ppm. The anodic concentration polarization quenching of the MFC strongly supports a mediator mechanism for the electron transfer from the microorganism to the anode.

Yogesh Sharma, Baikun Li

Proceedings of the Water Environment Federation • 2009

Haiming Jiang, Shengjun Luo, Xiaoshuang Shi et al.

Biotechnology Letters • 2012

A system containing a sequential anode-cathode configuration microbial fuel cell and a photobioreactor was developed for continuous treatment of wastewater and electricity generation. Wastewater was treated by the fuel cell to decrease the chemical oxygen demand (COD), phosphorus and nitrogen and to produce electricity. The effluent from the cathode compartment of the cell was continuously fed to an external photobioreactor to remove the remaining P and N using microalgae. Alone, the fuel cell generated a maximum power of 20.3 W/m(3) and achieved removal of 85 % COD, 58 % total phosphorus (TP) and 91 % NH(4) (+)-N. When coupled with the photobioreactor, the system removed 92 % TP and 99 % NH(4) (+)-N. These results demonstrate both the effectiveness and the potential application of the coupled system to continuously treat domestic wastewater and simultaneously generate electricity.

Chun-Hua Feng, Fang-Bai Li, Hong-Jian Mai et al.

Environmental Science & Technology • 2010

In this study, we proposed a new concept of utilizing the biological electrons produced from a microbial fuel cell (MFC) to power an E-Fenton process to treat wastewater at neutral pH as a bioelectro-Fenton (Bio-E-Fenton) process. This process can be achieved in a dual-chamber MFC from which electrons were generated via the catalyzation of Shewanella decolorationis S12 in its anaerobic anode chamber and transferred to its aerated cathode chamber equipped with a carbon nanotube (CNT)/gamma-FeOOH composite cathode. In the cathode chamber, the Fenton's reagents including hydrogen peroxide (H(2)O(2)) and ferrous irons (Fe(2+)) were in situ generated. This Bio-E-Fenton process led to the complete decolorization and mineralization of Orange II at pH 7.0 with the apparent first-order rate constants, k(app) = 0.212 h(-1) and k(TOC) = 0.0827 h(-1), respectively, and simultaneously produced a maximum power output of 230 mW m(-2) (normalized to the cathode surface area). The apparent mineralization current efficiency was calculated to be as high as 89%. The cathode composition was an important factor in governing system performance. When the ratio of CNT to gamma-FeOOH in the composite cathode was 1:1, the system demonstrated the fastest rate of Orange II degradation, corresponding to the highest amount of H(2)O(2) formed.

G. Mohanakrishna, S. Venkata Mohan, P.N. Sarma

Journal of Hazardous Materials • 2010

Microbial fuel cell (MFC; open-air cathode) was evaluated as bio-electrochemical treatment system for distillery wastewater during bioelectricity generation. MFC was operated at three substrate loading conditions in fed-batch mode under acidophilic (pH 6) condition using anaerobic consortia as anodic-biocatalyst. Current visualized marked improvement with increase in substrate load without any process inhibition (2.12-2.48mA). Apart from electricity generation, MFC documented efficient treatment of distillery wastewater and illustrated its function as an integrated wastewater treatment system by simultaneously removing multiple pollutants. Fuel cell operation yielded enhanced substrate degradation (COD, 72.84%) compared to the fermentation process ( approximately 29.5% improvement). Interestingly due to treatment in MFC, considerable reduction in color (31.67%) of distillery wastewater was also observed as against color intensification normally observed due to re-polymerization in corresponding anaerobic process. Good reduction in total dissolved solids (TDS, 23.96%) was also noticed due to fuel cell operation, which is generally not amenable in biological treatment. The simultaneous removal of multiple pollutants observed in distillery wastewater might be attributed to the biologically catalyzed electrochemical reactions occurring in the anodic chamber of MFC mediated by anaerobic substrate metabolism.

Mark Reynolds

UC Merced Undergraduate Research Journal • 2014

Liping Huang, Shaoan Cheng, Daniel J. Hassett et al.

Advances in Water Treatment and Pollution Prevention • 2012

Myelin, essential for rapid nerve conduction and axonal integrity in the central and peripheral nervous systems, is compromised in demyelinating diseases, leading to neurological deficits and progressive neurodegeneration. Although remyelination can occur, regeneration in adults is often limited, resulting in incomplete repair and impaired nerve function. In multiple sclerosis (MS), an immune-mediated demyelinating disease with diverse clinical phenotypes, progression and disability correlate with demyelination and failed remyelination, influenced by genetic and environmental factors. A well-established method to study MS-like demyelination and its cellular and molecular mechanisms utilizes cuprizone (CPZ), extensively studied in adult rodents. Although early-onset demyelination often causes lifelong disability, its pathophysiology remains poorly understood, underscoring the need for models to dissect its biological features. Here, we characterized the effects of early-age CPZ-induced demyelination in juvenile naïve mice, focusing on region-specific vulnerability and neuroinflammatory responses. One-month-old mice were exposed to 0.2% CPZ for five weeks, followed by behavioral, cellular, and transcriptomic analyses. Susceptibility to the early-exposure of CPZ varied between the analysed brain regions. The midline corpus callosum and motor cortex were highly vulnerable, showing marked reductions in myelin together with elevated microglial activation. Other regions, including the hippocampus and amygdala, showed milder susceptibility, often restricted to changes in Mbp or Iba1 transcript levels without corresponding alterations in oligodendrocyte or microglial cell numbers. Behaviorally, early CPZ exposure reduced locomotor activity but did not produce robust anxiety-like or cognitive deficits. Together, these findings reveal distinct regional patterns of early-onset demyelination and neuroinflammation and support CPZ exposure in juvenile mice as a relevant model for multifocal juvenile demyelination, including paediatric-onset MS, and its impact on neurodevelopment.