Investigation on the efficient separation and recovery of Se(IV) and Se(VI) from wastewater using Fe–OOH–bent

Decontamination of the toxic selenium compound, selenite (Se(IV)) and selenate (Se(VI)), from wastewater is imperative for environmental protection. Efficient approaches to remove Se(IV) and Se(VI) are in urgent needs. In this work, an accessible adsorbent Fe–OOH–bent was prepared and applied for the removal of Se(IV) and Se(VI) from wastewater. The batch experimental results demonstrate that Fe–OOH–bent exhibits high adsorption capacities of 5.01 × 10−4 and 2.28 × 10−4 mol/g for Se(IV) and Se(VI) respectively, which are higher than most of the reported bentonite based materials, especially in the case of Se(VI). Moreover, the Fe–OOH–bent displayed superior selectivity towards Se(IV) and Se(VI) even in the presence of excess competitive anions (Cl−, HCO3 −, NO3 −, SO4 2− and PO4 3−) and HA with concentrations of 1000 times higher than Se(IV) and Se(VI). By evaluating the adsorption ratio of Se(IV) and Se(VI), the reusability of Fe–OOH–bent was great through five adsorption-desorption cycles. For practical application, the column experiments were performed with simulated wastewater samples. The breakthrough and eluting curves of Se(IV) and Se(VI) were investigated through the columns packed with Fe–OOH–bent, and the results show that Se(IV) and Se(VI) can be successfully separated and recovered using 0.1 mol/L Na2SO4 (pH = 9.0) and 0.1 mol/L Na3PO4 (pH = 9.0), respectively. Our work provides a new approach for fractional separation as well as the recovery of Se(IV) and Se(VI) from wastewater.

A Novel Assay Method to Determine the β-Elimination of Se-Methylselenocysteine to Monomethylselenol by Kynurenine Aminotransferase 1

Kynurenine aminotransferase 1 (KYAT1 or CCBL1) plays a major role in Se-methylselenocysteine (MSC) metabolism. It is a bi-functional enzyme that catalyzes transamination and beta-elimination activity with a single substrate. KYAT1 produces methylselenol (CH3SeH) via β-elimination activities with MSC as a substrate. This methylated selenium compound is a major cytotoxic selenium metabolite, causing apoptosis in a wide variety of cancer cells. Methylselenol is volatile and possesses extraordinary nucleophilic properties. We herein describe a simple spectrophotometric assay by combining KYAT1 and thioredoxin reductase (TrxR) to detect CH3SeH in a coupled activity assay. The metabolite methylselenol and its oxidized form from MSC metabolism is utilized as a substrate for TrxR1 and this can be monitored spectroscopically at 340 nm. Our results show the feasibility of monitoring the β-elimination of KYAT1 by our assay and the results were compared to the previously described β-elimination assays measuring pyruvate. By using known inhibitors of KYAT1 and TrxR1, we further validated the respective reaction. Our data provide a simple but accurate method to determine the β-elimination activity of KYAT1, which is of importance for mechanistic studies of a highly interesting selenium compound.

[Se(CH2C(O)CH3)3][B12F11NH3]: The first selenium cation with three β-ketone substituents

The reaction of [Se8][B12F11NH3]2 with acetone and subsequent crystallization from acetone/diethyl ether yielded the selenium cation [Se(CH2C(O)CH3)3]+ as a by-product, which is stabilized by the weakly coordinating undecafluorinated anion [B12F11NH3]−. While attempting to crystallize pure [Se8][B12F11NH3]2, the structure of the isolated product, namely, tris(2-oxopropyl)selenium 1-ammonioundecafluorododecaborate, was surprising. The cation [Se(CH2C(O)CH3)3]+ represents the first example for a cationic selenium compound with three ketone functional groups located in the β-position with respect to the selenium atom. The cation possesses almost trigonal–pyramidal C 3 symmetry and forms hydrogen bonds to the ammonio group of the anion.

Synergistic therapeutic efficacy of ebselen and silver ions against multidrug-resistant Acinetobacter baumannii-induced urinary tract infections

Ebselen (EbSe), an organo-selenium compound with well-characterized toxicology and pharmacology, exhibited potent antibacterial activity against glutathione (GSH)-positive bacteria when combined with silver ions (Ag+).

Chiral Chalcogen Bond Donors Based on the 4,4′-Bipyridine Scaffold

Organocatalysis through chalcogen bonding (ChB) is in its infancy, as its proof-of-principle was only reported in 2016. Herein, we report the design and synthesis of new chiral ChB donors, as well as the catalytic activity evaluation of the 5,5′-dibromo-2,2′-dichloro-3-((perfluorophenyl)selanyl)-4,4′-bipyridine as organocatalyst. The latter is based on the use of two electron-withdrawing groups, a pentafluorophenyl ring and a tetrahalo-4,4′-bipyridine skeleton, as substituents at the selenium center. Atropisomery of the tetrahalo-4,4′-bipyridine motif provides a chiral environment to these new ChB donors. Their synthesis was achieved through either selective lithium exchange and trapping or a site-selective copper-mediated reaction. Pure enantiomers of the 3-selanyl-4,4′-bipyridine were obtained by high performance liquid chromatography enantioseparation on specific chiral stationary phase, and their absolute configuration was assigned by comparison of the measured and calculated electronic circular dichroism spectra. The capability of the selenium compound to participate in σ-hole-based interactions in solution was studied by 19F NMR. Even if no asymmetric induction has been observed so far, the new selenium motif proved to be catalytically active in the reduction of 2-phenylquinoline by Hantzsch ester.

Preparation of Organic Seleno cystine Using Locally Isolated Yeast

selenium is a toxic inorganic form at very low concentration to the life, while theorganic-selenium compound sareappre ciableinterest and various of them haveessentialrolesinnutritionalscienceandcellbiochemistry.Selenium-enrichedyeast(Seyeast)isapublicformofseleniumusedtoadditionaldietaryintakeofthisessentialtracemineral.Inthisstudy,weprepareanorganicselenocystinebyusinglocallyisolatedbakeryyeast(Saccharomycescerevisiae).Anovellocallyprepareddateextractmediaenrichedby0.2%potassiumphosphate(KH2PO4),0.6%ammoniumsulfatewasadoptedasalternativeculturemedia.Seleniumsaltwas used in differentconcentrations(30,60,120and240μg/mL),whichwereaddedtotheyeastculturemedia.Whilethebestconcentrationofseleniumaddedwas30μg/mL,itachievedoptimalconditionsforthegrowthof red coloryea stidentical to the standard.Theorganicselenocystine ereanalyzed by High Performance LiquidChromatography (HPLC) and Atomic Absorption Spectrophotometer (AAS) comparing with standard product obtained from Sigma. Results confirmedtheformationofsimilarselenocystineproducts