Interaction of acetamiprid with extracellular polymeric substances (EPS) from activated sludge: A fluorescence study

Extracellular polymeric substances (EPS) are important components of activated sludge and it plays an important role in removing pollutants. The interaction between EPS and organic pollutants is still little known. In the present study, the interaction of soluble/bound EPS with acetamiprid, a neonicotinoid insecticide, was investigated using the three-dimensional excitation–emission matrix (EEM) fluorescence spectroscopy. The fluorescence spectra of EPS revealed that there were two classes of protein-like fluorophores in soluble/bound EPS and one class of fulvic acid-like fluorophore, in addition, in bound EPS. The quenching of protein-like fluorescence by acetamiprid indicated that static quenching (at peak B) and combined quenching (at peak A) occurred simultaneously. The interaction of acetamiprid with EPS was observed to have resulted in the formation of acetamiprid-EPS complexes. The binding constants of the soluble EPS for acetamiprid were greater than those of the bound EPS, indicating the soluble EPS had stronger binding capacity for acetamiprid than the bound EPS. This study confirmed that EPS (soluble/bound) play important roles in biosorption of organic pollutants by activated sludge and also indicated that they may serve as a protective barrier against toxic organic matter, for the microorganisms.Key words: Extracellular polymeric substance (EPS), activated sludge, fluorescence quenching, binding constant, acetamiprid

Rapid flocculation-sedimentation of microalgae with organosilane-functionalized halloysite

Microalgae is a promising feedstock of biofuel for alternating fossil fuels. The major challenge of microalgal biofuels for commercial applications is in designing an efficient harvesting method with high economic feasibility. In this study, a rapid flocculation-sedimentation harvesting method induced by organosilane-functionalized halloysite flocculant was achieved for Scenedesmus dimorphus harvest. The harvesting efficiency was significantly influenced by the pH of microalgal dispersion and the dosage of flocculant. The optimized harvesting condition was pH 3.0 with flocculant dosage of 1.0 g.g(-1) cell dry mass. Under the optimized harvesting condition, microalgae rapidly reached 93% harvesting efficiency within 0.5 min of settling time, and reached 98% harvesting efficiency within 2 min of settling time. The rapid flocculation was attributed to the charge neutralization of the negatively-charged microalgae cells by the positively-charged organosilane-functionalized halloysite flocculant and to the sweep flocculation by organosilane-functionalized halloysite flocculant. The organosilane-functionalized halloysite flocculant did not affect the lipid extraction of microalgae, and not contaminate the extracted residuals. The organosilane-functionalized halloysite flocculant is of high efficient, cost-effective, and eco-friendly, makes it be of promising application for commercial microalgae harvesting.</p

Uranium Bioreduction and Biomineralization

Following the development of nuclear science and technology, uranium contamination has been an ever increasing concern worldwide because of its potential for migration from the waste repositories and long-term contaminated environments. Physical and chemical techniques for uranium pollution are expensive and challenging. An alternative to these technologies is microbially mediated uranium bioremediation in contaminated water and soil environments due to its reduced cost and environmental friendliness. To date, four basic mechanisms of uranium bioremediation-uranium bioreduction, biosorption, biomineralization, and bioaccumulation-have been established, of which uranium bioreduction and biomineralization have been studied extensively. The objective of this review is to provide an understanding of recent developments in these two fields in relation to relevant microorganisms, mechanisms, influential factors, and obstacles

Sorption of cobalt to bone char: Kinetics, competitive sorption and mechanism

Swine bone char is the combustion residues of swine bone. Cobalt adsorption to swine bone char was studied. Batch kinetics studies showed that a rapid uptake occurred during the first 5 min and was followed with a very slow intraparticle diffusion process. The sorption kinetics was ideally conformed to pseudo-second equation, indicating several mechanisms involved in the adsorption process. Equilibrium sorption isotherm studies showed that the Freundlich isotherm model satisfactorily described the sorption data. The presence of co-ions had appreciable inhibiting effects on cobalt uptake by bone char because copper and zinc had higher affinity for the bone char surface than cobalt. Calcium concentration in solution and XRD analysis showed that ion exchange was involved in the removal of Co from solution over a certain initial cobalt concentration range. (C) 2009 Elsevier B.V. All rights reserved

Comparative Analyses of H3K4 and H3K27 Trimethylations Between the Mouse Cerebrum and Testis

AbstractThe global features of H3K4 and H3K27 trimethylations (H3K4me3 and H3K27me3) have been well studied in recent years, but most of these studies were performed in mammalian cell lines. In this work, we generated the genome-wide maps of H3K4me3 and H3K27me3 of mouse cerebrum and testis using ChIP-seq and their high-coverage transcriptomes using ribominus RNA-seq with SOLiD technology. We examined the global patterns of H3K4me3 and H3K27me3 in both tissues and found that modifications are closely-associated with tissue-specific expression, function and development. Moreover, we revealed that H3K4me3 and H3K27me3 rarely occur in silent genes, which contradicts the findings in previous studies. Finally, we observed that bivalent domains, with both H3K4me3 and H3K27me3, existed ubiquitously in both tissues and demonstrated an invariable preference for the regulation of developmentally-related genes. However, the bivalent domains tend towards a “winner-takes-all” approach to regulate the expression of associated genes. We also verified the above results in mouse ES cells. As expected, the results in ES cells are consistent with those in cerebrum and testis. In conclusion, we present two very important findings. One is that H3K4me3 and H3K27me3 rarely occur in silent genes. The other is that bivalent domains may adopt a “winner-takes-all” principle to regulate gene expression

Binding of dicamba to soluble and bound extracellular polymeric substances (EPS) from aerobic activated sludge: A fluorescence quenching study

Binding of dicamba to soluble EPS (SEPS) and bound EPS (BEPS) from aerobic activated sludge was investigated using fluorescence spectroscopy. Two protein-like fluorescence peaks (peak A with Ex/Em = 225 nm/342-344 nm and peak B with Ex/Em = 275/340-344 nm) were identified in SEPS and BEPS. Humic-like fluorescence peak C (Ex/Em = 270-275 nm/450-460 nm) was only found in BEPS. Fluorescence of the peaks A and B for SEPS and peak A for BEPS were markedly quenched by dicamba at all temperatures whereas fluorescence of peaks B and C for BEPS was quenched only at 298 K. A dynamic process dominated the fluorescence quenching of peak A of both SEPS and BEPS. Fluorescence quenching of peak B and C was governed a static process. The effective quenching constants (log K-a) were 4.725-5.293 for protein-like fluorophores of SEPS and 4.23-5.190 for protein-like fluorophores of BEPS, respectively. Log K-a for humic-like substances was 3.85. Generally, SEPS had greater binding capacity for dicamba than BEPS, and protein-like substances bound dicamba more strongly than humic-like substances. Binding of dicamba to SEPS and BEPS was spontaneous and exothermic. Electrostatic force and hydrophobic interaction forces play a crucial role in binding of dicamba to EPS. (C) 2010 Elsevier Inc. All rights reserved.