Zobrazení zdroje stránky Aguirrechoate7191

The results indicate that Pseudomonas sp. DSP-1 and Cupriavidus sp. P2 are useful for remediating both CPF extractable and bound residues.Herein, a Fe3O4 decorated attapulgite adsorbent (FA) is fabricated for the removal of Cd(II) from wastewater, and subsequently a feasible strategy for converting the saturated waste adsorbent to CdS/FA photocatalyst is reported. Owing to the in situ growth of Fe3O4 on the attapulgite (ATP), the FA adsorbents exhibit enlarged surface area and increased adsorption sites. More importantly, the strong interaction between Fe3O4 and ATP leads to changes of coordination environment around the O‒Fe‒O bond with the ATP. Based on the results of density functional theory calculations, the electrons are more readily transferred from Fe to O, and the hanging O atoms with more electronegativity act as the efficient adsorption sites for Cd(II), efficiently improving the adsorption performance of the Fe3O4 phases. Furthermore, the waste FA adsorbent could be conveniently separated from the treated water by magnets and converted to CdS/FA photocatalyst, which exhibits satisfying degradation efficiency for tetracycline with low concentration. This work provides a potential strategy to optimize the ATP-based materials for heavy ions adsorption and reutilize the waste adsorbents.Blood mercury reflects the amount available from tissues, which is an indication of the exposure level. Here we confirm that Hg2+ caused hemolytic effects at high concentrations; while at light concentrations, most of the ions were bound to human serum albumin (HSA). The binding mechanism of Hg2+ to HSA has been investigated, which indicated that the presence of Hg2+ significantly perturbed the structure of HSA and quenched the fluorescence of protein in a hybrid dynamic and static mode. Hg2+ was preferably bound to cysteine and cystine, where the R‒S‒S‒R structure is responsible for maintaining the protein's structure by stabilizing the α-helical bundles. The metal-protein interaction mitigated the cellular toxicity as concealed by A498 cell lines. The fundamental and comprehensive data in this work is beneficial to elucidating and understanding the identification and binding mechanisms of heavy metals with proteins, as well as possible risks on human beings and the environment.Limited studies have been carried out on the historical variations of atmospheric polycyclic aromatic hydrocarbons (PAHs), especially in remote regions of the world. In this study, century-long record of PAHs (1916-2018) were reconstructed from tree rings in the remote southeastern Tibetan Plateau (TP). The total concentrations of 15 PAHs varied from 27.5 to 6.05 × 102 ng/g dry weight (dw), with a mean value of 1.40 × 102 ng/g dw. Higher levels of PAHs were observed during World War Ⅱ and the Peaceful Liberation of Tibet, and increasing trends were observed starting from rapid industrialization in India. Both the isomer ratios and the positive matrix factorization model results indicated biomass and coal combustion were the dominant sources of PAHs. The carcinogenic risk of PAHs to local residents was assessed, which might have been negligible in most past periods and lower than in other regions of the world. Nevertheless, since the beginning of the 21st century, the cancer risk has been increasing year by year, indicating more actions are needed to reduce emissions of PAHs. This study provides an idea for reconstructing the pollution history of PAHs at the global scale.Naturally-occurring phenolic acids (PAs) act as humic precursors that participate in the conversion behaviors and coupling pathways of steroidal estrogens (SEs) during laccase-triggered humification processes (L-THPs). Herein, the influences and mechanisms of PAs on Trametes versicolor laccase-evoked 17β-estradiol (E2) conversion kinetics and humification routes were explored. Fungal laccase was fleet in converting &gt; 99% of E2, and the calculated pseudo-first-order velocity constant and half-time values were respectively 0.039 min-1 and 17.906 min. PAs containing an O-dihydroxy moiety such as gallic acid and caffeic acid evidently hampered E2 humification owning to the yielded highly reactive O-quinones reversed E2 radicals by hydrogen transfer mechanism, implying that the inhibition effect was enormously dependent upon the number and position of the phenolic -OH present in humic precursors. Oligomers and polymers with carbon-carbon/oxygen links were tentatively found as E2 main humified species resulting from laccase-evoked successive oxidative-coupling. Note that PAs participating in the humification also encountered oxydehydrogenation, self-polymerization, and cross-binding to E2. Interestingly, the -COOH and -OCH3 groups of PAs could be deprived in radical-caused self/co-polymerization. The generation of humified products not only circumvented the environmental risks of parent compounds but accelerated global carbon sequestration. To our knowledge, this is the first in-depth revelation of the humification pathways and related mechanisms of SEs with humic precursors in aquatic ecosystems by L-THPs.This study used integrated omics technologies to investigate the potential novel pathways and enzymes for 1,4-dioxane degradation by a consortium enriched from activated sludge of a domestic wastewater treatment plant. An unclassified genus belonging to Xanthobacteraceae increased significantly after magnetic nanoparticle-mediated isolation for 1,4-dioxane degraders. Species with relatively higher abundance (&gt; 0.3%) were identified to present high metabolic activities in the biodegradation process through shotgun sequencing. The functional gene investigations revealed that Xanthobacter sp. 91, Xanthobacter sp. 126, and a Rhizobiales strain carried novel 1,4-dioxane-hydroxylating monooxygenase genes. Xanthobacter sp. 126 contained the genes coding for glycolate oxidase, which was the main enzyme responsible for utilization of 1,4-dioxane intermediates through the TCA cycle, and further proven by the specific glycolate oxidase inhibitor, α-hydroxy-2-pyridinemethanesulfonic acid. [https://www.selleckchem.com/products/ABT-263.html ABT-263 in vitro] An expanded and detailed degradation pathway of 1,4-dioxane was proposed on the basis of the three major intermediates (2-hydroxy-1,4-dioxane, ethylene glycol, and oxalic acid) confirmed by metabolomics.