Development of chitosan-magnetite aggregates containing Nitrosomonas europaea cells for nitrification enhancement

A cell suspension of the nitrifying bacterium Nitrosomonas europaea obtained after 96-h cultivation was subjected to magnetic separation using chitosan-conjugated magnetite particles (chitosan-magnetite), which have the ability to form aggregates with microbial cells. An equilibrium condition was obtained at room temperature after 30 min and over 90% of the cells were recovered when the chitosan-magnetite concentration was 200 mg/l. The relationship between the cell concentration in the supernatant in equilibrium and the number of cells adsorbed per 1g chitosan-magnetite was expressed by a Freundlich-type adsorption equation. A high nitrifying bacterium activity yield was obtained with a chitosan-magnetite concentration between 100 and 200 mg/l. Repeated batch culture resulted in more N. europaea cells accumulating on the aggregates and as a consequence their nitrification activity improved further. The chitosan-magnetite/cell aggregates were recovered and employed to remove ammonia from artificial wastewater together with PVA-alginate gel beads containing the denitrifying bacterium Paracoccus denitrificans. A higher ammonia removal rate was achieved under aerobic conditions in comparison with that obtained when N. europaea and P. denitrificans were coimmobilized in PVA-alginate gel beads.     

Mechanism of silver nanoparticle toxicity is dependent on dissolved silver and surface coating in Caenorhabditis elegans

The rapidly increasing use of silver nanoparticles (Ag NPs) in consumer products and medical applications has raised ecological and human health concerns. A key question for addressing these concerns is whether Ag NP toxicity is mechanistically unique to nanoparticulate silver, or if it is a result of the release of silver ions. Furthermore, since Ag NPs are produced in a large variety of monomer sizes and coatings, and since their physicochemical behavior depends on the media composition, it is important to understand how these variables modulate toxicity. We found that a lower ionic strength medium resulted in greater toxicity (measured as growth inhibition) of all tested Ag NPs to Caenorhabditis elegans and that both dissolved silver and coating influenced Ag NP toxicity. We found a linear correlation between Ag NP toxicity and dissolved silver, but no correlation between size and toxicity. We used three independent and complementary approaches to investigate the mechanisms of toxicity of differentially coated and sized Ag NPs: pharmacological (rescue with trolox and N-acetylcysteine), genetic (analysis of metal-sensitive and oxidative stress-sensitive mutants), and physicochemical (including analysis of dissolution of Ag NPs). Oxidative dissolution was limited in our experimental conditions (maximally 15% in 24 h) yet was key to the toxicity of most Ag NPs, highlighting a critical role for dissolved silver complexed with thiols in the toxicity of all tested Ag NPs. Some Ag NPs (typically less soluble due to size or coating) also acted via oxidative stress, an effect specific to nanoparticulate silver. However, in no case studied here was the toxicity of a Ag NP greater than would be predicted by complete dissolution of the same mass of silver as silver ions.     

Effect of oxygen concentration on nitrogen removal by Nitrosomonas europaea and Paracoccus denitrificans immobilized within tubular polymeric gel

Tubular gel reactors containing Nitrosomonas europaea and Paracoccus denitrificans, which remove nitrogen from solutions through a process of nitrification and denitrification, require oxygen for ammonia oxidation, the first and rate-limiting step in the process. To accelerate ammonia oxidation, high concentrations of oxygen were applied to the reactors instead of air. Although a 50% O2:N2 gas mixture and pure oxygen were both toxic to free N. europaea cells, they actually accelerated ammonia oxidation by N. europaea immobilized within the tubular gel. Indeed, the rate of ammonia oxidation by a tube exposed to pure oxygen was twice that of one exposed to 20% O2. When the distribution of N. europaea cells within the tubes was investigated using a fluorescently-labeled antibody, colonies were found on the external surface of the tube exposed to 20% O2, but were located at a depth of 120-300 microm from the external surface in the case of the tube exposed to pure oxygen. The region between the external surface of the gel and the colonies apparently acted as a barrier, reducing the diffusion of oxygen and thus protecting the cells from oxygen cytotoxicity.     

Rapid and sensitive Nitrosomonas europaea biosensor assay for quantification of bioavailable ammonium sensu strictu in soil

Knowledge on bioavailable ammonium sensu strictu (i.e., immediately available for cellular uptake) in soil is required to understand nutrient uptake processes in microorganisms and thus of vital importance for plant production. We here present a novel ammonium biosensor approach based on the lithoautotrophic ammonia-oxidizing bacterium Nitrosomonas europaea transformed with a luxAB sensor plasmid. Bioluminescence-based ammonium detection was achieved within 10 min with a quantification limit in liquid samples of ～20 μM and a linear response range up to 400 μM. Biosensor and conventional chemical quantification of ammonium in soil solutions agreed well across a range of sample and assay conditions. The biosensor was subsequently applied for a solid phase-contact assay allowing for direct interaction of biosensor cells with soil particle-associated (i.e., exchangeable plus fixed) ammonium. The assay successfully quantified bioavailable ammonium even in unfertilized soil and demonstrated markedly higher ratios of bioavailable ammonium to water- or 2 M KCl-exchangeable ammonium in anoxic soil than in corresponding oxic soil. Particle-associated ammonium contributed by at least 74% and 93% of the total bioavailable pool in oxic and anoxic soil, respectively. The N. europaea biosensor should have broad relevance for environmental monitoring of bioavailable ammonium and processes depending on ammonium bioavailability.     

Copper toxicity to bioluminescent Nitrosomonas europaea in soil is explained by the free metal ion activity in pore water

The terrestrial biotic ligand model (BLM) for metal toxicity in soil postulates that metal toxicity depends on the free metal ion activity in solution and on ions competing for metal sorption to the biotic ligand. Unequivocal evidence for the BLM assumptions is most difficult to obtain for native soil microorganisms because the abiotic and biotic compartments cannot be experimentally separated. Here, we report copper (Cu) toxicity to a bioluminescent Nitrosomonas europaea reporter strain that was used in a solid phase-contact assay and in corresponding soil extracts and artificial soil solutions. The Cu(2+) ion activities that halve bioluminescence (EC50) in artificial solutions ranged 10(-5) to 10(-7) M and increased with increasing activities of H(+), Ca(2+) and Mg(2+) according to the BLM concept. The solution based Cu(2+) EC50 values of N. europaea in six contaminated soils ranged 2 × 10(-6) to 2 × 10(-9) M and these thresholds for both solid phase or soil extract based assays were well predicted by the ion competition model fitted to artificial solution data. In addition, solution based Cu(2+) EC50 of the solid phase-contact assay were never smaller than corresponding values in soil extracts suggesting no additional solid phase toxic route. By restricting the analysis to the same added species, we show that the Cu(2+) in solution represents the toxic species to this bacterium.     

Structural and functional effects of Cu metalloprotein-driven silver nanoparticle dissolution

Interactions of a model Cu-metalloprotein, azurin, with 10-100 nm silver nanoparticles (NPs) were examined to elucidate the role of oxidative dissolution and protein interaction on the biological reactivity of NPs. Although minimal protein and NP structural changes were observed upon interaction, displacement of Cu(II) and formation of Ag(I) azurin species under aerobic conditions implicates Cu(II) azurin as a catalyst of NP oxidative dissolution. Consistent with NP oxidation potentials, largest concentrations of Ag(I) azurin species were recorded in reaction with 10 nm NPs (>50%). Apo-protein was also observed under anaerobic reaction with NPs of all sizes and upon aerobic reaction with larger NPs (>20 nm), where NP oxidation is slowed. Cu(II) azurin displacement upon reaction with NPs was significantly greater than when reacted with Ag(I)(aq) alone. Regardless of NP size, dialysis experiments show minimal reactivity between azurin and the Ag(I)(aq) species formed as a result of NP oxidative dissolution, indicating Cu displacement from azurin occurs at the NP surface. Mechanisms of azurin-silver NP interaction are proposed. Results demonstrate that NP interactions not only impact protein structure and function, but also NP reactivity, with implications for targeting, uptake, and cytotoxicity.     

无机载银抗菌沸石对涂料流变性能的影响

载银抗菌沸石具有良好的持久性、耐高温性和安全性。通过AR550流变仪研究了采用涂布方式生产载银抗菌纸时,载银抗菌沸石对典型造纸涂料流变性能的影响。研究表明:载银抗菌沸石的加入不会对造纸涂料流变性能产生负面影响,相反它对稠度系数和表观黏度有一定降低作用。对涂料流变曲线拟合研究表明,Herschel-Bulkley模型能较好地拟合涂料的流变曲线,添加载银抗菌沸石后涂料仍具有剪切稀化特性,弹性贮存模量也有一定的降低,而黏性损耗模量与损耗角δ变化不大。     

Controlled evaluation of silver nanoparticle dissolution using atomic force microscopy

Incorporation of silver nanoparticles (AgNPs) into an increasing number of consumer products has led to concern over the potential ecological impacts of their unintended release to the environment. Dissolution is an important environmental transformation that affects the form and concentration of AgNPs in natural waters; however, studies on AgNP dissolution kinetics are complicated by nanoparticle aggregation. Herein, nanosphere lithography (NSL) was used to fabricate uniform arrays of AgNPs immobilized on glass substrates. Nanoparticle immobilization enabled controlled evaluation of AgNP dissolution in an air-saturated phosphate buffer (pH 7.0, 25 °C) under variable NaCl concentrations in the absence of aggregation. Atomic force microscopy (AFM) was used to monitor changes in particle morphology and dissolution. Over the first day of exposure to ≥10 mM NaCl, the in-plane AgNP shape changed from triangular to circular, the sidewalls steepened, the in-plane radius decreased by 5-11 nm, and the height increased by 6-12 nm. Subsequently, particle height and in-plane radius decreased at a constant rate over a 2-week period. Dissolution rates varied linearly from 0.4 to 2.2 nm/d over the 10-550 mM NaCl concentration range tested. NaCl-catalyzed dissolution of AgNPs may play an important role in AgNP fate in saline waters and biological media. This study demonstrates the utility of NSL and AFM for the direct investigation of unaggregated AgNP dissolution.     

Model demonstrating the potential for coupled nitrification denitrification in soil aggregates

A model of reactive, multi-species diffusion has been developed to describe N transformations in spherical soil aggregates, emphasizing the effects of irrigation with reclaimed wastewater. Oxygen demand for respiratory activity has been shown to promote the establishment of anaerobic conditions. Aggregate size and soil respiration rate were identified as the most significant parameters governing the existence and extent of the anaerobic volume in aggregates. The inclusion of kinetic models describing mineralization, nitrification, and denitrification facilitated the investigation of coupled nitrification/denitrification (CND), subject to O2 availability. N-transformations are shown to be affected by effluent-borne NH4+-N content, in addition to elevated BOD and pH levels. Their incremental contribution to O2 availability has been found to be secondary to respiratory activity. At the aggregate level, significant differences between apparent and gross rates of N-transformations were predicted (e.g., NH4+ oxidation and N2 formation), resulting from diffusive constraints due to aggregate size. With increasing anaerobic volume, the effective nitrification rate determined at the aggregates level decreases until its contribution to nitrification is negligible. It was found that the nitrification process was predominantly limited to aggregates <0.25 cm. Assuming that nitrification is the main source for NO3- formation, denitrification efficiency is predicted to peak in medium-sized aggregates, where aerobic and anaerobic conditions coexist, supporting CND. In effluent-irrigated soils, the predicted NO2- formation rate in small aggregates is enhanced when compared to freshwater-irrigated soils. The difference vanishes with increasing aggregate size as anaerobic NO2- consumption exceeds aerobic NO2- formation due to the coupling of nitrification and denitrification.     

Measurement of antioxidants in distilled spirits by a silver nanoparticle assay

Ingestion of antioxidants from the diet is associated with improved health. Total antioxidant capacity as gallic acid equivalents (GAE) of distilled spirits was determined using a modified and validated silver nanoparticle (SNaP) assay utilizing silver nanoparticles pre‐capped with starch and microwave technology. GAE concentrations determined by the SNaP assay for the distilled spirits were validated by high‐performance liquid chromatography (HPLC) measurements of key antioxidant components including gallic acid, ellagic acid, caffeic acid, syringic acid, syringaldehyde and 2‐furaldehyde. SNaP assay and HPLC measurements of GAE were compared via statistical and graphical methods to demonstrate comparability. Application of the assay to 33 different distilled spirits demonstrated good agreement with published literature values, with the highest total antioxidant capacity values observed for bourbon samples followed by whisky, tequila and other types of liqueur. This study is novel for demonstrating the utility of a nanoparticle assay for determination of antioxidant capacity in distilled spirits with validation by HPLC. © 2018 The Institute of Brewing & Distilling     

Application of chitosan-ZnO nanoparticle edible coating to wild-simulated Korean ginseng root

Food Science and Biotechnology - Chitosan-ZnO nanoparticle (ZnONP) edible coating was applied to extend shelf life of wild-simulated Korean ginseng root (WsKG). In antimicrobial testing of various...     

Effect of nano silver coating on thermal protective performance of firefighter protective clothing

The main aim of this experimental work is to find out possible improvement in thermal protective performance of firefighter protective clothing when subjected to different level of radiant heat flux density. Firefighter protective clothing normally consists of three layers: outer shell, moisture barrier and thermal liner. When thermal protective performance of firefighter protective clothing is enhanced, the time of exposure against radiant heat flux is increased, which will provide extra amount of time to firefighter to carry on their work without suffering from severe skin burn injuries. In this study, the exterior side of outer shell was coated with nano-silver metallic particle through magnetron sputtering technology. Coating of outer shell with nano-silver particles was performed at three level of thickness, i.e. 1, 2 and 3?µm, respectively. All the uncoated and silver coated specimens were then characterized on air permeability tester, Permetest and radiant heat transmission machine. It was observed that coating has insignificant difference on the air and water vapor permeability of specimen and a significant decline was recorded for the value of transmitted heat flux density Q_c (kW/m²) and percentage transmission factor (%TF Q_o) as compared to uncoated specimen when subjected to 10 kW/m² and 20?kW/m² indicating improvement of thermal protective performance. These values go on further reduction with increase in thickness of coating layer of nano-silver particles.     

The potential of electrospraying for hydrophobic film coating on foods

There is a continuous need for thinner edible coatings with excellent barrier properties, and this requires new application methods. Electrospraying is known to yield fine droplets of size down to 20 μm, giving the potential of very thin and even coatings. A single electrospraying nozzle was used to characterise droplet formation and investigate the formation of thin films on well-defined surfaces. The experimental droplet size was successfully described as a function of operational parameters and liquid properties using scaling relations. The influence of operating parameters as nozzle height and electrostatic potential were evaluated as well.Thin film deposition was experimentally investigated for sunflower oil electro-sprayed on a highly conductive (aluminium) and insulating target surface (Parafilm). For both aluminium foil and Parafilm the droplet deposition was found to be random. For aluminium foil, being a conductive target, this was expected as repellence between droplets on the surface and new droplets is low, due to charge leakage to the ground. For Parafilm, droplet repellence appeared so large that droplets deposited on larger empty spots or were even pushed away from the surface. To evaluate the film formation performance, Monte Carlo simulations were carried out, and it was found that the method is a useful tool to characterise droplet deposition and film formation characteristics.     

Surface coating of silver nanoparticles on polyethylene for fabrication of antimicrobial milk packaging films

In this study, antimicrobial packaging films were prepared by coating silver (Ag) nanoparticles onto the surface of low density polyethylene (LDPE) films modified by corona air plasma. The possibility of these films for use in the packaging of milk was studied. The influence of input power of the corona discharge treatment on the surface modification and performance of the fabricated Ag/LDPE nanocomposite films was also investigated. The prepared antimicrobial packaging films showed promising antimicrobial efficiency against micro‐organisms that are present in milk and were able to increase the microbial shelf life of the milk. Packages fabricated at corona input powers of 210, 500 and 800 W reached the maximum limit after 5, 8 and 14 days (respectively).     

Some new findings on the potential use of biocompatible silver nanoparticles in winemaking

There is currently an increasing commercial demand for silver nanoparticles (Ag NPs) due to their wide applicability in various markets. Because of their powerful antimicrobial properties, these nanoparticles are frequently used for food-associated consumer products. In this paper, the effect of two Ag NPs coated with biocompatible materials – PEG-Ag NPs 20 (polyethylene glycol) and GSH-Ag NPs (reduced glutathione) – to control microbial growth in wines was assessed. Both Ag NPs were subjected to an in vitro three-step digestion, and changes in their morphology and an assessment of their cytotoxicity against Caco-2 cells were determined. Both Ag NPs were effective against the different microbial population present in tested wines. Regarding their in vitro digestion, the size and shape of the nanoparticles were almost unaltered in the case of GSH-Ag NPs, while in PEG-Ag NPs 20 some particle agglomeration was observed. Overall, these results suggest that Ag NPs may reach the intestine in a nano-scaled form. Finally, Caco-2 cell experiments seemed to exclude toxicity of Ag NPs at the intestinal epithelium.Industrial relevanceTraditionally, sulphur dioxide (SO₂) has been used by oenologists to control the microbial population in wine. As a result of increasing evidence of possible health risks associated with this additive in wine, there has been growing interest in finding new alternatives to replace it. Silver nanoparticles display a broad spectrum of antimicrobial activity, so they could constitute a very promising approach to reducing SO₂ in winemaking.     

空心微珠化学镀银及其织物涂层整理

采用化学镀方法自制金属银包覆空心微珠,并将其应用于织物涂层整理.通过SEM、XRD、导电及电磁屏蔽性能测试得出,化学镀银空心微珠涂层织物具备一定的导电和电磁屏蔽效能,镀银微珠在涂层中起到导电填料的作用,当微珠的填充量达一定密度时,其电阻率值与电磁屏蔽效能值与相同工艺条件下银粉涂层织物接近.