Modification of bacterial cell membrane to accelerate decolorization of textile wastewater effluent using microbial fuel cells: role of gamma radiation

The aim of the present work was to increase bacterial adhesion on anode via inducing membrane modifications to enhance textile wastewater treatment in Microbial Fuel Cell (MFC). Real textile wastewater was used in mediator-less MFCs for bacterial enrichment. The enriched bacteria were pre-treated by exposure to 1 KGy gamma radiation and were tested in MFC setup. Bacterial cell membrane permeability and cell membrane charges were measured using noninvasive dielectric spectroscopy measurements. The results show that pre-treatment using gamma radiation resulted in biofilm formation and increased cell permeability and exopolysaccharide production; this was reflected in both MFC performance (average voltage 554.67 mV) and decolorization (96.42%) as compared to 392.77 mV and 60.76% decolorization for non-treated cells. At the end of MFC operation, cytotoxicity test was performed for treated wastewater using a dermal cell line, the results obtained show a decrease in toxicity from 24.8 to 0 (v/v%) when cells were exposed to gamma radiation. Fourier-transform infrared (FTIR) spectroscopy showed an increase in exopolysaccharides in bacterial consortium exposed to increasing doses of gamma radiation suggesting that gamma radiation increased exopolysaccharide production, providing transient media for electron transfer and contributing to accelerating MFC performance. Modification of bacterial membrane prior to MFC operation can be considered highly effective as a pre-treatment tool that accelerates MFC performance

Molecular Events in the Cell Types of the Olfactory Epithelium during Adult Neurogenesis

BACKGROUND: Adult neurogenesis, fundamental for cellular homeostasis in the mammalian olfactory epithelium, requires major shifts in gene expression to produce mature olfactory sensory neurons (OSNs) from multipotent progenitor cells. To understand these dynamic events requires identifying not only the genes involved but also the cell types that express each gene. Only then can the interrelationships of the encoded proteins reveal the sequences of molecular events that control the plasticity of the adult olfactory epithelium. RESULTS: Of 4,057 differentially abundant mRNAs at 5 days after lesion-induced OSN replacement in adult mice, 2,334 were decreased mRNAs expressed by mature OSNs. Of the 1,723 increased mRNAs, many were expressed by cell types other than OSNs and encoded proteins involved in cell proliferation and transcriptional regulation, consistent with increased basal cell proliferation. Others encoded fatty acid metabolism and lysosomal proteins expressed by infiltrating macrophages that help scavenge debris from the apoptosis of mature OSNs. The mRNAs of immature OSNs behaved dichotomously, increasing if they supported early events in OSN differentiation (axon initiation, vesicular trafficking, cytoskeletal organization and focal adhesions) but decreasing if they supported homeostatic processes that carry over into mature OSNs (energy production, axon maintenance and protein catabolism). The complexity of shifts in gene expression responsible for converting basal cells into neurons was evident in the increased abundance of 203 transcriptional regulators expressed by basal cells and immature OSNs. CONCLUSIONS: Many of the molecular changes evoked during adult neurogenesis can now be ascribed to specific cellular events in the OSN cell lineage, thereby defining new stages in the development of these neurons. Most notably, the patterns of gene expression in immature OSNs changed in a characteristic fashion as these neurons differentiated. Initial patterns were consistent with the transition into a neuronal morphology (neuritogenesis) and later patterns with neuronal homeostasis. Overall, gene expression patterns during adult olfactory neurogenesis showed substantial similarity to those of embryonic brain

Group descent algorithms for nonconvex penalized linear and logistic regression models with grouped predictors

Penalized regression is an attractive framework for variable selection problems. Often, variables possess a grouping structure, and the relevant selection problem is that of selecting groups, not individual variables. The group lasso has been proposed as a way of extending the ideas of the lasso to the problem of group selection. Nonconvex penalties such as SCAD and MCP have been proposed and shown to have several advantages over the lasso; these penalties may also be extended to the group selection problem, giving rise to group SCAD and group MCP methods. Here, we describe algorithms for fitting these models stably and efficiently. In addition, we present simulation results and real data examples comparing and contrasting the statistical properties of these methods

Design of a single chamber air cathode microbial fuel cell using a stainless steel spiral anode and 3D printing techniques for continuous flow dye decolourisation

Microbial fuel cells (MFC) offer a novel solution in wastewater treatment systems. Their capacity for COD removal and concomitant electricity generation are highly attractive properties for reducing costs & environmental impacts in industry. MFCs require expensive membranes & catalysts such as Nafion and platinum respectively to achieve increased power output, but the cost of these materials is prohibitive for real world applications. An air breathing, 1 litre-scale spiral anode MFC was designed (Fig. 1) to provide a high electrode surface area to reactor volume ratio using commonly and cheaply available materials such as stainless steel and activated carbon. Non-platinum group metal catalysts (FeAAPyr family) were integrated into a PVDF cathode fabricated using single step phase inversion to improve rate of the oxygen reduction reaction. Anode surface area was maximized by concertina folding and spiral arrangement and its surface was modified using sulphuric acid, heat treatment & carbon black adsorption to provide a more biocompatible surface for biofilms. The performance characteristics of the designed MFC are currently being investigated. Decolourisation of Acid orange-7 azo dye & COD removal were initially investigated in recirculating batch mode followed by continuous flow configuration with a hydraulic retention time of 36 hours. Optimisation of hydraulic retention times, cathode construction & anode surface modification will present a feasible system for the scale up of microbial fuel cells for industrial use, maximizing COD removal & electricity production

Degradation of azo dyes (Acid orange 7) in a microbial fuel cell: comparison between anodic microbial-mediated reduction and cathodic laccase-mediated oxidation

Microbial fuel cells (MFCs) are a promising technology for the simultaneous treatment of wastewater and electricity production. With regard to azo-dye containing wastewater (e.g. from textile manufacturing), the dyes may be fed via the anode chamber containing electrochemically active bacteria or via the cathode chamber containing laccase enzyme as catalyst for oxygen reduction. This study investigated which of the two approaches is the best with regard to rate of decolourisation of the dye (Acid orange 7), COD reduction and electricity production. The power density was higher for the MFCdye at cathode (25 mW/m2, COD reduction 80%) compared with 18 mW/m2 (COD reduction 69%) for MFCdye at anode (Shewanella oneidensis as catalyst). The decolourisation rate of the dye was not statistically significant between the two approaches with ca. 75% decolourisation achieved in 24 h. The anodic dye degradation products were unstable when exposed to air resulting in what seems to be induced diazotization and regaining of colour. In case of degradation by laccase in the cathode chamber, the decolourisation products were stable and simpler in chemical structure (e.g. presence of aliphatic compounds) as determined by GC-MS. This work suggests that feeding azo dyes in cathode chambers of MFCs containing laccase is a better way of treating the dyes than the commonly used approach of feeding the dye in the anode chamber