Microbial Cells Research Articles

Microbial Biofilm Inhibition Using Magnetic Cross-Linked Polyphenol Oxidase Aggregates.

Microbial biofilm accumulation poses a serious threat to the environment, presents significant challenges to different industries, and exhibits a large impact on public health. Since there has not been a conclusive answer found despite various efforts, the potential green and economical methods are being focused on, particularly the innovative approaches that employ biochemical agents. In the present study, we propose a bio-nanotechnological method using magnetic cross-linked polyphenol oxidase aggregates (PPO m-CLEA) for inhibition of microbial biofilm including multidrug resistant bacteria. Free PPO solution showed only 55-60% biofilm inhibition, whereas m-CLEA showed 70-75% inhibition, as confirmed through microscopic techniques. The carbohydrate and protein contents in biofilm extracellular polymeric substances (EPSs) were reduced significantly. The m-CLEA demonstrated reusability up to 5 cycles with consistent efficiency in biofilm inhibition. Computational work was also done where molecular docking of PPO with microbial proteins associated with biofilm formation was conducted, resulting in favorable binding scores and inter-residual interactions. Overall, both in vitro and in silico results suggest that PPO interferes with microbial cell attachment and EPS formation, thereby preventing biofilm colonization.

Influence of Fiber Diameter of Polycaprolactone Nanofibrous Materials on Biofilm Formation and Retention of Bacterial Cells.

To develop microbiologically safe nanofibrous materials, it is crucial to understand their interactions with microbial cells. Current research indicates that the morphology of nanofibers, particularly the diameter of the fibers, may play a significant role in biofilm formation and retention. However, it has not yet been determined how the fiber diameter of poly-ε-caprolactone (PCL), one of the most widely used biopolymers, affects these microbial interactions. In this study, two nanofibrous materials electrospun from PCL (PCL45 and PCL80) with different fiber diameter and characteristic distance δ between fibers were compared in terms of their ability to support or inhibit bacterial biofilm formation and retain bacterial cells. Strains of Escherichia coli (ATCC 25922 and ATCC 8739) and Staphylococcus aureus (ATCC 25923 and ATCC 6538) were used as model bacteria. Biofilm formation rate and retention varied significantly between the E.coli and S.aureus strains (p < 0.05) for the tested nanomaterials. In general, PCL showed a lower tendency to be colonized by the tested bacteria compared to the control material (polystyrene). Fiber diameter did not influence the biofilm formation rate of S.aureus strains and E.coli 25922 (p > 0.05), but it did significantly impact the biofilm formation rate of E.coli 8739 and biofilm morphology formed by all of the tested bacterial strains. In PCL45, thick uniform biofilm layers were formed preferably on the surface, while in PCL80 smaller clusters formed preferably inside the structure. Further, fiber diameter significantly influenced the retention of bacterial cells of all the tested strains (p < 0.001). PCL45, with thin fibers (average fiber diameter of 376 nm), retained up to 7 log (CFU mL-1) of staphylococcal cells (100% retention). The overall results indicate PCL45's potential for further research and highlight the nanofibers' morphology influence on bacterial interactions and differences in bacterial strains' behavior in the presence of nanomaterials.

Taurolidine and Heparin as Catheter Lock Solution for Central Venous Catheters in Hemodialysis.

Chronic kidney disease can lead to end-stage renal disease, and the prevalence is increasing. Many patients starting hemodialysis require central venous catheters (CVCs). Catheter-related bloodstream infections (CRBSIs) are a common complication and lead to significant morbidity and mortality. Interventions to prevent CRBSI include antimicrobial lock therapy but concern for the development of antimicrobial resistance and adverse effects. Nonantimicrobial antiseptics as catheter lock solutions have also been used. Taurolidine and heparin catheter lock solution is first approved by the Food and Drug Administration for the prevention of CRBSI in patients on hemodialysis. Taurolidine has a unique mechanism of action and favorable safety profile. Taurolidine and heparin catheter lock solution have both antimicrobial and anticoagulant properties. Taurolidine is derivative of the amino acid taurine, and heparin is derived from porcine intestinal mucosa. Taurolidine not only damages microbial cell walls but also prevents the adherence of microorganisms to biological surfaces, preventing biofilm formation. Taurolidine and heparin catheter lock solution is intended to be used intraluminally within the catheter and should be aspirated. Because it is used locally, limited pharmacokinetic and pharmacodynamic data are available. The LOCK-IT-100 trial is a randomized, double-blind, phase 3 study, which included 795 end-stage renal disease patients on hemodialysis with CVC. Taurolidine and heparin was compared with the control heparin alone. The results of the study showed a 71% risk reduction in CRBSI for taurolidine and heparin arm (95% confident interval, 38%-86%, P = 0.0006). Other studies have also shown that taurolidine lock solution leads to decreased CRBSI episodes. Several systematic reviews and meta-analysis consisted of taurolidine in adult, and pediatric populations also showed reduction in the incidence of CRBSIs. Taurolidine and heparin lock solution represents a novel preventive strategy for those undergoing hemodialysis through a CVC by reducing the risk of CRBSI. This is significant progress because there are no other similar options available for patients for whom catheters are the only options for their life-saving treatment.

New regulatory role of Znf1 in transcriptional control of pentose phosphate pathway and ATP synthesis for enhanced isobutanol and acid tolerance.

To develop a cost-effective microbial cell factory for the production of biofuels and biochemicals, an understanding of tolerant mechanisms is vital for the construction of robust host strains. Here, we characterized a new function of a key metabolic transcription factor named Znf1 and its involvement in stress response in Saccharomyces cerevisiae to enhance tolerance to advanced biofuel, isobutanol. RNA-sequencing analysis of the wild-type versus the znf1Δ deletion strains in glucose revealed a new role for transcription factor Znf1 in the pentose phosphate pathway (PPP) and energy generation. The gene expression analysis confirmed that isobutanol induces an adaptive cell response, resulting in activation of ATP1-3 and COX6 expression. These genes were Znf1 targets that belong to the electron transport chain, important to produce ATPs. Znf1 also activated PPP genes, required for the generation of key amino acids, cellular metabolites, and maintenance of NADP/NADPH redox balance. In glucose, Znf1 also mediated the upregulation of valine biosynthetic genes of the Ehrlich pathway, namely ILV3, ILV5, and ARO10, associated with the generation of key intermediates for isobutanol production.Using S. cerevisiae knockout collection strains, cells with deleted transcriptional regulatory gene ZNF1 or its targets displayed hypersensitivity to isobutanol and acid inhibitors; in contrast, overexpression of ZNF1 enhanced cell survival. Thus, the transcription factor Znf1 functions in the maintenance of energy homeostasis and redox balance at various checkpoints of yeast metabolic pathways. It ensures the rapid unwiring of gene transcription in response to toxic products/by-products generated during biofuel production. Importantly, we provide a new approach to enhance strain tolerance during the conversion of glucose to biofuels.

Microbe-cellulose hydrogels as a model system for particulate carbon degradation in soil aggregates

Abstract Particulate carbon (C) degradation in soils is a critical process in the global C cycle governing greenhouse gas fluxes and C storage. Millimeter-scale soil aggregates impose strong controls on particulate C degradation by inducing chemical gradients of e.g., oxygen, as well as limiting microbial mobility in pore structures. To date, experimental models of soil aggregates have incorporated porosity and chemical gradients but not particulate C. Here, we demonstrate a proof-of-concept encapsulating microbial cells and particulate C substrates in hydrogel matrices as a novel experimental model for soil aggregates. Ruminiclostridium cellulolyticum was co-encapsulated with cellulose in millimeter-scale polyethyleneglycol-dimethacrylate (PEGDMA) hydrogel beads. Microbial activity was delayed in hydrogel-encapsulated conditions, with cellulose degradation and fermentation activity being observed after 13 days of incubation. Unexpectedly, hydrogel encapsulation shifted product formation of R. cellulolyticum from an ethanol-lactate-acetate mixture to an acetate-dominated product profile. Fluorescence microscopy enabled simultaneous visualization of the PEGDMA matrix, cellulose particles, and individual cells in the matrix, demonstrating growth on cellulose particles during incubation. Together, these microbe-cellulose-PEGDMA hydrogels present a novel, reproducible experimental soil surrogate to connect single cells to process outcomes at the scale of soil aggregates and ecosystems.

A streamlined workflow for a fast and cost-effective count of tyndallized probiotics using flow cytometry

The use of dead probiotics and their cellular metabolites seems to exhibit immunomodulatory and anti-inflammatory properties, providing protection against pathogens. These inanimate microorganisms, often referred to as tyndallized or heat-killed bacteria, are a new class of probiotics employed in clinical practice. Safety concerns regarding the extensive use of live microbial cells have increased interest in inactivated bacteria, as they could eliminate shelf-life problems and reduce the risks of microbial translocation and infection. Culture-dependent methods are not suitable for the quality assessment of these products, and alternative methods are needed for their quantification. To date, bacterial counting chambers and microscopy have been used for tyndallized bacteria enumeration, but no alternative validated methods are now available for commercial release. The aim of the present study is to design a new method for the qualitative and quantitative determination of tyndallized bacterial cells using flow cytometric technology. Using a live/dead viability assay based on two nucleic acid stains, thiazole orange (TO) and propidium iodide (PI), we optimized a workflow to evaluate bacterial viability beyond the reproduction capacity that provides information about the structural properties and metabolic activities of probiotics on FACSVerse without using beads as a reference. The data obtained in this study represent the first analytical application that works effectively both on viable and non-viable cells. The results provided consistent evidence, and different samples were analyzed using the same staining protocol and acquisition settings. No significant discrepancies were highlighted between the declared specification of commercial strain and the analytical data obtained. For the first time, flow cytometry was used for counting tyndallized bacterial cells as a quality control assessment in probiotic production. This aspect becomes important if applied to medical devices where we cannot boast metabolic but only mechanical activities.

Biological Performance of Hexadeca-Substituted Metal Phthalocyanine/Reduced Graphene Oxide Nanobioagents.

This study presents a tetra-substituted phthalonitrile derivative, namely, diethyl 2-(3,4-dicyano-2,5-bis(hexyloxy)-6-(4-(trifluoromethoxy)phenoxy)phenyl)malonate (a), cyclotetramerizing in the presence of some metal salts. The resultant hexadeca-substituted metal phthalocyanines [M= Co, Zn, InCl)] (b-d) were used for the modification of reduced graphene oxide for the first time. The effect of the phthalonitrile/metal phthalocyanines on biological features of reduced graphene oxide (rGO) was extensively examined by the investigation of antioxidant, antimicrobial, DNA cleavage, cell viability, and antibiofilm activities of nanobioagents (1-4). The results were compared with those of unmodified rGO (nanobioagent 5), as well. Modification of reduced graphene oxide with the synthesized compounds improved its antioxidant activity. The antioxidant activities of all the tested nanobioagents also enhanced as the concentration increased. The antibacterial activities of all the nanobioagents improved by applying the photodynamic therapeutic (PDT) method. All the phthalonitrile/phthalocyanine-based nanobioagents (especially phthalocyanine-based nanocomposites) exhibited DNA cleavage activities, and complete DNA fragmentation was observed for nanobioagents (1-4) at 200 mg/L. They can be used as potent antimicrobial and antimicrobial photodynamic therapy agents as well as Escherichia coli microbial cell inhibitors. As a result, the prepared nanocomposites can be considered promising candidates for biomedicine.

Development of microbial desalination cells for the treatment of reverse osmosis reject water: A new benchtop approach

To address the growing global demand for usable water, there is an immediate necessity to enhance wastewater treatment systems. A continuous mode adaption of the conventional three-chamber microbial desalination cell (MDC) configuration was used, with gravity facilitating the flow of residential reject water for desalination. Initially, operating in batch mode with a 100mL treatment volume, the single microbial desalination machine was expanded to 300mL in continuous mode, capable of treating 5L of home refuse water over 36 days. The batch mode MDC had a maximum current and power density of 3.81µA/cm2 and 0.337µW/cm2, resulting in 76% desalination and 83.9% COD eradication rates. Scaling up increased the MDC's performance, reaching a maximum of 0.45µW/cm2 and 5.31µA/cm2, which was 1.3 times greater than batch mode operation. The current work demonstrates the feasibility of microbial desalination cells and their novel approach for treating much higher quantities of reverse osmosis (R.O.) saline water in a comparable period of roughly 36 days. It emphasizes the actual limits when dealing with real-world wastewater samples, presenting a unique path for biotechnology by simultaneously generating bio-electricity and tackling future contaminants. Furthermore, incorporating desalination chambers with microbial fuel cells increases efficiency and opens up new options for enhanced wastewater treatment, resource recovery, and bioenergy generation. This pioneering strategy uses innovative membrane technologies and microbial optimization approaches to push the limits of desalination.

A Comparative Analysis of Capping and Reducing Agents of Microbial Cell Aspergillus niger and Bacillus subtilis for Biosynthesis of Ag Doped ZnO Nanoparticles

In this study, green synthesis of of Ag doped ZnO (AZNPR) has been carried out using the sol-gel method at pH 8.0, using two types of microbial cells, namely Aspergillus niger and Bacillus subtilis as capping and reducing agents. This work centred on the phytomediated biosynthesis and characterisation of AZNPR and its biological utility. Based on infrared analysis, phytochemicals present in microbial cells are extracellular enzymes namely proteolytic, amylolytic, lipolytic, cellulolytic, and pectinase, which can be extracted from A. niger and B. subtilis and are responsible for controlling the growth of AZNPR. The formation of AZNPR was characterised using different analyses. The FTIR shows absorption band located at ∼864 cm-1 that shows the interaction between Ag and ZnO. The XRD results showed the presence of crystalline AZNPR in the forms of hexagonal wurtzite ZnO and Ag. Microstructural and size examination showed that AZNPR was in the form of nanorods with homogeneous distribution with a size of rods in A. niger media 137.0 nm, while in B. subtilis media 197.4 nm. The Ag-ZnO nanorods revealed the ability to inhibit Candida albicans species, a fungus causing infectious disease, with an inhibition zone measuring 2.1-3.2 mm at 24 hours.

Evaluation of electromethanogenesis in a microbial electrolysis cell using nylon cloth as a separator: Reactor performance and metagenomic analysis

This study aimed to propose a novel approach for simultaneous CO2 abatement and energy storage in microbial electrolysis cells (MECs). The methane (CH4) production from CO2 was achieved in a graphite granule–filled cathodic compartment of an MEC separated by a modified nylon cloth. Using the modified nylon cloth in MEC significantly reduced membrane internal resistance compared with the control where a commercial proton exchange membrane (PEM) was used (PEM: 1746 ± 80 TΩ/cm; nylon cloth: 251 ± 8 TΩ/cm). Consequently, CH4 production realized 72.9 ± 24.4 mL/(L ∙ d) with an average energy efficiency of 121 ± 39% compared with halted electromethanogenesis in PEM-equipped MEC. Metagenomics affirmed the predominance of hydrogenotrophic methanogens Methanocorpusculum and Methanobacterium. Moreover, H2-mediated methanogenesis contributed significantly to electromethanogenesis in nylon-MEC. This study demonstrated that the bioelectrochemical conversion of CO2 into CH4 in a nylon-MEC could be viable for CO2 sequestration combined with energy storage (power to gas).

Advancing autotrophic nitrogen removal in low C/N ratio wastewater: Innovative application of supercapacitor to enhance microbial electrolysis cells

This study presents a novel approach, the Supercapacitor Microbial Electrolysis Cell (SC-MEC), which utilizes a supercapacitor as an external power source to enhance the efficiency of autotrophic nitrogen removal in low C/N ratio wastewater. The results demonstrated that the SC-MEC system, operating under anaerobic conditions and devoid of any organic carbon source, exhibited exceptional performance in ammonia oxidation and total nitrogen (TN) removal when solely relying on ammonia nitrogen as the electron donor. Operating at a voltage of 1.8 V with a capacitance capacity of 30 F, ammonium oxidation rated up to 56.51 mg/L/day and TN removal rated up to 54.64 mg/L/day, in which 97% of ammonium nitrogen was converted to gaseous nitrogen. Furthermore, the charging and discharging process of supercapacitors autonomously regulated the bipolar potentials. Cyclic voltammetry (CV) analysis showed the significantly enhanced electrochemical activity of the SC-MEC system during the reaction process. Based on in-situ CV test results, it was inferred that this enhancement was associated with extracellular electron transfer mediators. The microbial community analysis revealed a process of synchronous nitrification and denitrification (SND) coupled with anammox, involving multiple genera, such as Candidatus Kuenenia, Nitrosomonas, Truepera, and Bosea. In conclusion, this study highlights the tremendous potential of SC-MEC in achieving efficient autotrophic nitrogen removal, offering more feasible and economical solutions for addressing low C/N water pollution issues.

Exploring the effects of diverse extraction methods on nanoemulsion formulation using betel leaf essential oil: Assessing antibacterial efficacy against pathogenic microorganisms

The present study focused on observing the impact of different pretreatments applied on betel leaves powder (BLP) before extraction of essential oil (EO) on the formulation and characterization of BLP-EO-nanoemulsion (NE). BLP-EO nanoemulsion was produced from different BLP-EO (C, CP, MW, CPAMW treated BLP-EO), surfactant (tween 80), and distilled water by ultrasonic probe method and their particle size, polydispersity index (PDI), zeta potential, turbidity, viscosity, refractive index, whiteness index and antibacterial properties were investigated. Significant differences were observed among the nanoemulsions prepared from EO obtained using different pretreatment. The CPAMW-BLP-EO- nanoemulsion prepared with 1% oil concentration and 1:3 oil to surfactant concentration showed the smallest particle size (98.00 ± 0.92 nm), lowest PDI value (0.21 ± 0.01) and zeta potential value (−24.73 ± 1.37) followed by MW, CP and C-BLP-EO-NE due to high concentration of chemical composition that effectively bind with a surfactant. Similarly, better physical properties were obtained for CPAMW-BLP-EO-NE. This CPAMW treated BLP-EO nanoemulsion was the most effective against Gram-positive bacteria like Staphylococcus aureus with an inhibition zone of 12.5 mm than Gram-negative bacteria like Salmonella spp and Escherichia coli with an inhibition zone of 9.4 mm, and 8.5 mm respectively followed by MW, CP, and C treated BLP-EO-NE. In conclusion, the potent antibacterial activity of the nanoemulsion is due to its higher concentration of oxygenated terpenoids and smaller particle size, facilitating effective transport of active compounds and enhancing interactions with microbial cell membranes. Therefore, the CPAMW pre-treated BLP-EO nanoemulsions showed great potential to be incorporated into water-based food products and beverages as flavoring and antimicrobial agents.

Development of an H2 fuel cell electrochemical system powered by Escherichia coli cells

Because of the growing high importance of the development of biocatalytic fuel cell (FC) technologies for renewable energy-producing and testing systems for medical or environmental purposes, in this study, we constructed and demonstrated an H2 FC voltammeter working with graphite sample testing micro-strips and based on Escherichia coli microbial cells. Presented H2 FC voltammeter that provides fast and precise testing of bio-electrochemical possible reactions in biosamples for H2 and other gases, is automated with software which works in NI LabVIEW programming environment, has amplifier cascade system with high internal resistance, temperature controlling and resistance cascade. Microbial Hydrogenase (Hyd) enzymes reversibly catalyze the formation and oxidation of H2. Isolation and characterization of O2-tolerant [NiFe]-hydrogenases (Hyds) have given rise to new concepts in H2 FC. Escherichia coli and [NiFe]-Hyds can be applied as a biocatalyst anode in biofuel cells (BFCs). We evaluated the efficiency of applying the 3 µl (1.5 mg cell dry weight) E. coli intact cells or crude extracts on 0.5 cm2 as anode catalyzers in the bio-electrochemical system. The highest electrical potential (up to 0.7 V) was achieved with bacterial whole cells, which were grown on glucose and glycerol.

Integration of genome-scale metabolic model with biorefinery process model reveals market-competitive carbon-negative sustainable aviation fuel utilizing microbial cell mass lipids and biogenic CO2

Integration of genome-scale metabolic model with biorefinery process model reveals market-competitive carbon-negative sustainable aviation fuel utilizing microbial cell mass lipids and biogenic CO2

Chain elongation in continuous microbial electrosynthesis cells: The effect of pH and precursors supply

Microbial electrosynthesis (MES) enables the production of carbon-neutral chemicals using CO2 as a carbon source. Acetic acid is the main MES product, but recent studies show the direct production of elongated carboxylic acids, e.g., butyric and caproic acid. However, the production of elongated acids in MES systems is still inefficient due to the low growth rates of acetogenic bacteria and to limited solventogenic rates. Subsequently, researchers have produced elongated carboxylic acids directly from acetic acid or have operated MES systems at low pH to favor solventogenesis. However, the effect the addition of different chain elongation precursors and the operation pH exerts in the bioelectrochemical production of elongated acids remains unclear. To investigate this, three pH-controlled MES systems were operated in this study with continuous liquid and gas supply. MES systems elongating acetic acid at pH 6 achieved higher butyric (0.71 vs. 0.42 g L−1) and caproic acid (0.71 vs. 0.42 g L−1) titers in the absence of CO2 sparging. Additionally, lowering the pH to 5 in the MES systems fed with CO2 and acetic acid improved the elongated acids titers, reaching 0.72 g L−1 butyric and 0.33 g L−1 caproic acid. The 16 S rRNA analysis showed the community was dominated by Oscillibacter at pH 6, and by Clostridium at pH 5. Furthermore, the first scanning electron microscopy pictures revealing biofilm stratification in MES cathodes were taken in this study, where homogeneous rod-shaped bacteria biofilm layers, in contact with the graphite cathode, were covered by heterogeneous biofilm layers.

An In Vitro Study on the Application of Silver-Doped Platelet-Rich Plasma in the Prevention of Post-Implant-Associated Infections.

Implant therapy is a common treatment option in dentistry and orthopedics, but its application is often associated with an increased risk of microbial contamination of the implant surfaces that cause bone tissue impairment. This study aims to develop two silver-enriched platelet-rich plasma (PRP) multifunctional scaffolds active at the same time in preventing implant-associated infections and stimulating bone regeneration. Commercial silver lactate (L) and newly synthesized silver deoxycholate:β-Cyclodextrin (B), were studied in vitro. Initially, the antimicrobial activity of the two silver soluble forms and the PRP enriched with the two silver forms has been studied on microbial planktonic cells. At the same time, the biocompatibility of silver-enriched PRPs has been assessed by an MTT test on human primary osteoblasts (hOBs). Afterwards, an investigation was conducted to evaluate the activity of selected concentrations and forms of silver-enriched PRPs in inhibiting microbial biofilm formation and stimulating hOB differentiation. PRP-L (0.3 µg/mm2) and PRP-B (0.2 µg/mm2) counteract Staphylococcus aureus, Staphylococcus epidermidis and Candida albicans planktonic cell growth and biofilm formation, preserving hOB viability without interfering with their differentiation capability. Overall, the results obtained suggest that L- and B-enriched PRPs represent a promising preventive strategy against biofilm-related implant infections and demonstrate a new silver formulation that, together with increasing fibrin binding protecting silver in truncated cone-shaped cyclic oligosaccharides, achieved comparable inhibitory results on prokaryotic cells at a lower concentration.

Porewater microbiomes in buried wetland soils: Synergic effects of water chemistry and redox gradients associated with hydrological processes

Abstract Interstitial water or pore water occupies the space between soil particles and provides “hotspots” and “fluvial networks” for microbial activities in floodplain soil. However, to date, we know very little about the microorganisms living in pore water and how they respond to environmental changes. This study aimed to understand microbial distribution and assemblage in riparian pore waters, and how they respond to water chemistry and redox gradients associated with hydrological processes. We analysed the annual changes of porewater microbial communities from the east and west banks of the White Clay Creek, a site at the Christina River Basin – Critical Zone Observatory, Pennsylvania, USA. Microbial abundances were quantified by epifluorescence microscopy and detailed community structures were characterised by high‐throughput sequencing. Water chemistry and redox gradients were also monitored and recorded, and their interactions with porewater microbiomes were analysed using correlations and multivariate analyses. Abundance of microbial cells increased during summer and late autumn. Wetland porewater microbiomes mainly contained Acidobacteria, Bacteroidetes, Nitrospirae and Proteobacteria, and microbiome structures were easily distinguishable from those in the underlying hyporheic gravel layer. Seasonal dynamics of bacterial community structure in the east and west wetlands were distinct, responding to floodplain topography and associated hydrological/geochemical processes. Iron (Fe)‐cycling bacteria (mainly Gallionellaceae and Rhodoferax spp.) dominated the porewater microbiome, and their relative abundance was significantly higher in the east than the west wetland. Furthermore, Fe‐oxidising bacteria (Gallionellaceae) were negatively correlated with Fe‐reducing bacteria (Rhodoferax spp.) at the east wetland. Microbial abundances (cell density) in pore waters showed similar seasonal patterns across stream banks, but microbial community structure did not. Microbiome assembly in pore water is correlated with water chemistry and redox gradients primarily associated with local hydrological processes. As a consequence of their significance for carbon (C) mineralisation and Fe reduction at terrestrial–aquatic interfaces, microbiomes in riparian pore waters and associated microbial activity play an essential role in C and mineral dynamics. These findings will inform future studies of the response of freshwater ecosystems to hydrological dynamics influenced by global climate change.

Exploring the role of domesticated resistors in batch-mode microbial desalination cell

Microbial Desalination Cells (MDCs) are an electrochemical process that harnesses microbial reactions to simultaneously treat wastewater, generate power, and desalinate water. By utilizing microbial decomposition of organic pollutants in wastewater, MDCs offer a sustainable and energy-efficient alternative to conventional desalination technologies. The technical framework of MDCs emphasizes the integration of water-electricity principles, making them promising for future applications in seawater desalination, wastewater treatment, resource recovery, and water softening. This study investigates the impact of acclimation resistance, represented by four different domesticated resistors values of 1 kΩ, 100Ω, 51Ω, and 10Ω, on the performance of MDCs. Larger acclimation resistors exhibit higher power performance, with the case of 100Ω achieving a power density of 0.33 mA/m2 and the case of 1 kΩ achieving the highest current density of 1.90 mA/m2. Furthermore, the case with an acclimation resistance of 1 kΩ exhibits superior performance in terms of chemical oxygen demand (COD) removal, achieving a removal rate of 76.3% on day 1. Conversely, the case with an acclimation resistance of 10Ω demonstrates the best desalination performance, achieving a desalination rate of 9.0%. It should be noted that the optimal performance in terms of COD removal and desalination capacity varies due to the various operational mechanisms involved. . The findings of this study provide valuable insights for enhancing the performance of MDCs in future applications, enabling further improvements in their efficiency and effectiveness.

Effects of microbial electrolysis cell on anaerobic digestion of food waste: Acidification and recovery

The effects of a microbial electrolysis cell (MEC) applying 1.2 V on the acidification and recovery in the anaerobic digestion (AD) of food waste were studied by semi-continuous experiments. The experimental results showed that the MEC reduced the accumulation of volatile fatty acids (VFAs), enhanced acidification, accelerated the conversion of VFAs during recovery, and accelerated recovery by decreasing the relative abundance of Aminobacterium and norank_f__W27 and increasing that of Methanobacterium. The MEC reduced the production of propionic and butyric acids by decreasing the abundance of functional enzymes (such as fumarate reductase, propionate CoA-transferase, phosphate butyryltransferase, and butyrate kinase) and bacteria (such as Aminobacterium and norank_f__W27). The MEC increased the rates of four AD steps with a maximal rate of 11.47–32.32 %. The MEC promoted electron transfer by enriching the electroactive bacterium Trichococcus (10.91–28.80 %) and Methanosaeta (8.17–24.43 %). The MEC increased the abundance of the most critical functional enzymes in the bacterial community during the entire test and those in the archaeal community during recovery.

A Self-Assembled MOF-Escherichia Coli Hybrid System for Light-Driven Fuels and Valuable Chemicals Synthesis.

The development of semi-artificial photosynthetic systems, which integrate metal-organic frameworks (MOFs) with industrial microbial cell factories for light-driven synthesis of fuels and valuable chemicals, represents a highly promising avenue for both research advancements and practical applications. In this study, an MOF (PCN-222) utilizing racemic-(4-carboxyphenyl) porphyrin and zirconium chloride (ZrCl4) as primary constituents is synthesized. Employing a self-assembly process, a hybrid system is constructed, integrating engineered Escherichia coli (E. coli) to investigate light-driven hydrogen and lysine production. These results demonstrate that the light-irradiated biohybrid system efficiently produce H2 with a quantum efficiency of 0.75% under full spectrum illumination, the elevated intracellular reducing power NADPH is also observed. By optimizing the conditions, the biohybrid system achieves a maximum lysine production of 18.25mg L-1, surpassing that of pure bacteria by 332%. Further investigations into interfacial electron transfer mechanisms reveals that PCN-222 efficiently captures light and facilitates the transfer of photo-generated electrons into E. coli cells. It is proposed that the interfacial energy transfer process is mediated by riboflavin, with facilitation by secreted small organic acids acting as hole scavengers for PCN-222. This study establishes a crucial foundation for future research into the light-driven biomanufacturing using E. coli-based hybrid systems.