nZVI particles production for the remediation of soil and water polluted by inorganic Lead

The present study deals with experiments of Pb removal by nano-Zero Valent Iron (nZVI) in aqueous solution and in soil. Synthetic Pb aqueous solutions were treated by nZVI, at a fixed Pb concentration of 100 mg L-1 , varying nanoparticles initial concentration in the range between 27 and 270 mg nZVI L-1 . A kinetic study was carried out: Pb adsorption followed a first order kinetic, and half life times between 11 and 26.66 min were determined. Soil samples were first characterized, and Pb speciation and concentration by sequential extractions was determined. Adsorption tests were then carried out at three selected amounts of nZVI, to allow Pb stabilization in the soil matrix. To evaluate the treatment efficiency, sequential extractions were also performed on the treated samples

Hexavalent chromium reduction in manganese-rich soils by ZVI nanoparticles: the influence of natural organic matter and manganese oxides

Hexavalent chromium reduction by nano Zero-Valent Iron (nZVI) has been proved fast and efficient, mainly due to nanoparticles large specific surface area and high chemical reactivity. In this work the influence of natural organic matter and manganese oxide was investigated, through a set of experimental tests carried out on a real polluted soils naturally rich in manganese. Soil samples were characterized in terms of initial concentration of Cr, Cr(VI), Mn, pH, and TOC and three different nZVI solutions were used (120, 360 and 600 mg nZVI L-1 ) for the treatment. At selected interval times (0, 5, 10, 15, 30, 60, 120 min) a slurry sample was filtered and Cr(VI) residual concentration and pH were measured. The same procedure was carried out on an artificial spiked soil, characterized by a similar TOC and poor of Mn. Furthermore the two soils were mixed with different amounts of leonardite, to evaluate the influence of NOM on treatment efficiency

Continuous production of KNO3 nanosalts for the fertilization of soil by means of a Spinning Disk Reactor

In this study the production of high soluble material nanoparticles was successfully performed by means of a spinning disk reactor (SDR). This result was possible due to the use of a potassium nitrate saturated solution, which was continuously recycled back to the reactor after removal of the produced solid nanoparticles. Several process configurations were checked. It appears to be mandatory that the recycled saturated solution must be free of residual nanoparticles since their presence would lead to heterogeneous nucleation. In this respect, a small amount of nitric acid was added to the stream to permit the residual nanoparticle dissolution. Moreover, a spiral wounded piping system was developed in order to increase both the contact time and the mixing condition of the saturated solution with the added acid before entering the SD

Performance analysis of multi-hop framed ALOHA systems with virtual antenna arrays

We consider a multi-hop virtual multiple-input-multiple-output system, which uses the framed ALOHA technique to select the radio resource at each hop. In this scenario, the source, destination and relaying nodes cooperate with neighboring devices to exploit spatial diversity by means of the concept of virtual antenna array. We investigate both the optimum number of slots per frame in the slotted structure and once the source-destination distance is fixed, the impact of the number of hops on the system performance. A comparison with deterministic, centralized re-use strategies is also presented. Outage probability, average throughput, and energy efficiency are the metrics used to evaluate the performance. Two approximated mathematical expressions are given for the outage probability, which represent lower bounds for the exact metric derived in the paper

The Role of Histone H4 Biotinylation in the Structure of Nucleosomes

Background: Post-translational modifications of histones play important roles in regulating nucleosome structure and gene transcription. It has been shown that biotinylation of histone H4 at lysine-12 in histone H4 (K12Bio-H4) is associated with repression of a number of genes. We hypothesized that biotinylation modifies the physical structure of nucleosomes, and that biotin-induced conformational changes contribute to gene silencing associated with histone biotinylation. Methodology/Principal Findings: To test this hypothesis we used atomic force microscopy to directly analyze structures of nucleosomes formed with biotin-modified and non-modified H4. The analysis of the AFM images revealed a 13% increase in the length of DNA wrapped around the histone core in nucleosomes with biotinylated H4. This statistically significant (p,0.001) difference between native and biotinylated nucleosomes corresponds to adding approximately 20 bp to the classical 147 bp length of nucleosomal DNA. Conclusions/Significance: The increase in nucleosomal DNA length is predicted to stabilize the association of DNA with histones and therefore to prevent nucleosomes from unwrapping. This provides a mechanistic explanation for the gene silencing associated with K12Bio-H4. The proposed single-molecule AFM approach will be instrumental for studying the effects of various epigenetic modifications of nucleosomes, in addition to biotinylation

On the spontaneous stochastic dynamics of a single gene: complexity of the molecular interplay at the promoter

International audienceBACKGROUND: Gene promoters can be in various epigenetic states and undergo interactions with many molecules in a highly transient, probabilistic and combinatorial way, resulting in a complex global dynamics as observed experimentally. However, models of stochastic gene expression commonly consider promoter activity as a two-state on/off system. We consider here a model of single-gene stochastic expression that can represent arbitrary prokaryotic or eukaryotic promoters, based on the combinatorial interplay between molecules and epigenetic factors, including energy-dependent remodeling and enzymatic activities. RESULTS: We show that, considering the mere molecular interplay at the promoter, a single-gene can demonstrate an elaborate spontaneous stochastic activity (eg. multi-periodic multi-relaxation dynamics), similar to what is known to occur at the gene-network level. Characterizing this generic model with indicators of dynamic and steady-state properties (including power spectra and distributions), we reveal the potential activity of any promoter and its influence on gene expression. In particular, we can reproduce, based on biologically relevant mechanisms, the strongly periodic patterns of promoter occupancy by transcription factors (TF) and chromatin remodeling as observed experimentally on eukaryotic promoters. Moreover, we link several of its characteristics to properties of the underlying biochemical system. The model can also be used to identify behaviors of interest (eg. stochasticity induced by high TF concentration) on minimal systems and to test their relevance in larger and more realistic systems. We finally show that TF concentrations can regulate many aspects of the stochastic activity with a considerable flexibility and complexity. CONCLUSIONS: This tight promoter-mediated control of stochasticity may constitute a powerful asset for the cell. Remarkably, a strongly periodic activity that demonstrates a complex TF concentration-dependent control is obtained when molecular interactions have typical characteristics observed on eukaryotic promoters (high mobility, functional redundancy, many alternate states/pathways). We also show that this regime results in a direct and indirect energetic cost. Finally, this model can constitute a framework for unifying various experimental approaches. Collectively, our results show that a gene - the basic building block of complex regulatory networks - can itself demonstrate a significantly complex behavior

Activation of transcription factors by extracellular nucleotides in immune and related cell types

Extracellular nucleotides, acting through P2 receptors, can regulate gene expression via intracellular signaling pathways that control the activity of transcription factors. Relatively little is known about the activation of transcription factors by nucleotides in immune cells. The NF-κB family of transcription factors is critical for many immune and inflammatory responses. Nucleotides released from damaged or stressed cells can act alone through certain P2 receptors to alter NF-κB activity or they can enhance responses induced by pathogen-associated molecules such as LPS. Nucleotides have also been shown to regulate the activity of other transcription factors (AP-1, NFAT, CREB and STAT) in immune and related cell types. Here, we provide an overview of transcription factors shown to be activated by nucleotides in immune cells, and describe what is known about their mechanisms of activation and potential functions. Furthermore, we propose areas for future work in this new and expanding field