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Arsenic exposure in humans has been implicated in the development of a myriad of non-cancerous and cancerous diseases. A reductionist approach to understanding this unusual phenomenon would suggest that arsenic-induced perturbation of a small number of fundamental biological processes could manifest as this diverse array of disease endpoints. Endocytosis is a fundamental cellular process involved in the internalization and transport of various extracellular molecules and membranous components. BEAS-2B, a human bronchial epithelial cell line, was used to characterize the effects of chronic arsenite exposure on endocytosis. Fluorophore-labeled bovine albumin, human transferrin, and human low-density lipoprotein (LDL) were the substrates utilized to measure endocytosis in BEAS-2B cells. The uptake of albumin in unexposed BEAS-2B cells is both dose-dependent and temperature sensitive. Chronic arsenite exposure in BEAS-2B cells increased the uptake of albumin by 3.4-fold after 8 hours of uptake relative to unexposed BEAS-2B cells. Pharmacological studies utilizing endocytosis inhibitors suggested that the uptake of albumin in both unexposed and arsenite-exposed BEAS-2B cells occurs through a combination of receptor-mediated endocytosis and macropinocytosis. Chronic arsenite exposure in BEAS-2B cells also increased the endocytic uptake of transferrin by 2.9-fold at 30 minutes and LDL by 1.3-fold at 2 hours relative to unexposed BEAS-2B cells. Together, the data suggests that chronic arsenite exposure can increase the rate of endocytosis. This novel finding could add mechanistic insight to the conundrum of arsenic-associated human diseases.

Arsenic is the most pervasive environmental toxic substance. As a consequence of its ubiquity, nearly every organism has genes for resistance to inorganic arsenic. In one project I examined the role of glutaredoxin 2 (Grx2) in reduction of arsenate to arsenite. I demonstrated that Grx2 has both glutaredoxin thiol transfer activity and glutathione S-transferase (GST) activity. In a second project investigated arsenic resistance in a microbiome organism. I discovered that the human gut microflora B. vulgatus has eight continuous genes in its genome and these genes form an arsenical-inducible transcriptional unit. In two other projects I investigated the properties of two As(III) S-adenosylmethionine (SAM) methyltransferase (ArsM in microbes and AS3MT in animals). In this project we demonstrate that most fungal species have ArsM orthologs with only three conserved cysteine residues, and AfArsM from Aspergillus fumigatus methylates only MAs(III) and not As(III). For human, arsenic methylation process is thought to be protective from acute high-level arsenic exposure. However, with long term low-level exposure, hAS3MT is thought to produce intracellular methylarsenite (MAs(III)) and dimethylarsenite (DMAs(III)), which are considerably more toxic than inorganic As(III) and may contribute to arsenic-related diseases. Several single nucleotide polymorphisms (SNPs) in putative regulatory elements of the hAS3MT gene have been shown to be protective. In contrast, three previously identified exonic SNPs (R173W, M287T and T306I) may be deleterious. I identified five additional intragenic variants in hAS3MT (H51R, C61W, I136T, W203C and R251H). I purified the eight polymorphic hAS3MT proteins and characterized their enzymatic properties. Each enzyme had low methylation activity through decreased affinity for substrate, lower overall rates of catalysis and/or lower stability. I propose that amino acid substitutions in hAS3MT with decreased catalytic activity lead to detrimental responses to environmental arsenic and may increase the risk of arsenic-related diseases.

The apatite crystal structure-A5(TO4)3X-allows for complex substitutions of various minor and trace elements including volatile constituents, rare earth elements, and redox sensitive elements (e.g., As, Mn, Fe, S) (Piccoli and Candela, 1994; Piccoli and Candela, 2002; Pan and Fleet, 2002; Teiber et al., 2015; Harlov, 2015). In this study, apatite grains from 19 intrusions across northeastern Nevada with varied petrogenetic and metallogenic properties were analyzed by electron probe microanalysis (EPMA) to obtain major and trace element abundances. Systematic variations in Sr and REE concentrations in apatite grains from granitic host rocks are the result of competition with pre-existing and coexisting minerals in silicate melts. The presence of zoning in cathodoluminescence colors combined with high Sr concentrations in apatite from many of the Eocene granodiorite rocks suggest magma mixing affected the geochemical evolution in many of the Eocene igneous systems. In addition, high Sr concentrations in apatite grains from Late Cretaceous two-mica granites may reflect significant magmatic input from lower crustal and/or mantle sources despite the felsic nature of these intrusive rocks.A new EPMA analytical routine to measure arsenic down to detection limits of approximately 20 ppm allowed a more extensive characterization of As concentration in igneous apatite than has previously been published. Still, correlations between As and other trace-element concentrations are not evident, which may reflect the simple substitution of As5+ for P5+ in the apatite structure. Petrologic controls on As content include redox state, indicated by the high Asapat/Asbulk-rock in relatively oxidized intrusive rocks. An additional control is competition among other magmatic phases, exsolving aqueous fluids, or sulfide melts, indicated by enrichment of As in apatite cores relative to apatite rims. Past studies on redox-sensitive elements in igneous apatite have focused on Mn and S, but with further investigation, As may also prove to be a key redox-sensitive trace element in apatite for interpreting igneous and hydrothermal processes.

Arsenic (As) exposure is associated with cancer, lung and cardiovascular disease, yet the mechanisms involved are not clearly understood. Elevated matrix metalloproteinase-9 (MMP-9) levels are also associated with these diseases, as well as with exposure to water As. Our objective was to evaluate the effects of dietary components of inorganic As (iAs) intake on serum MMP-9 concentration at differing levels of tap water As. In a cross-sectional study of 214 adults, dietary iAs intake was estimated from 24-h dietary recall interviews using published iAs residue data; drinking and cooking water As intake from water samples and consumption data. Aggregate iAs intake (food plus water) was associated with elevated serum MMP-9 in mixed model regression, with and without adjustment for covariates. In models stratified by tap water As, aggregate intake was a significant positive predictor of serum MMP-9 in subjects exposed to water As≤10 μg/l. Inorganic As from food alone was associated with serum MMP-9 in subjects exposed to tap water As≤3 μg/l. Exposure to iAs from food and water combined, in areas where tap water As concentration is ≤10 μg/l, may contribute to As-induced changes in a biomarker associated with toxicity.

As aquaporinas são proteínas de membrana presentes em quase todos os órgãos e tecidos de animais e plantas, onde desempenham funções que vão além do transporte de água, transportando também moléculas como ureia, ácido bórico, ácido silícico, amônia, dióxido de carbono e arsênio. Em plantas, as aquaporinas podem ser classificadas de acordo com suas sequências de aminoácidos em cinco subfamílias: proteínas intrínsecas da membrana plasmática (PIPs), proteínas intrínsecas de tonoplastos (TIPs), proteínas intrínsecas do tipo nodulina 26 (NIPs), proteínas intrínsecas pequenas (SIPs) e proteínas intrínsecas não caracterizadas (XIPs). Dados genômicos determinam o número de genes de aquaporinas em 33 para arroz, 35 para Arabidopsis, 71 para algodão e 66 para soja. Dentre as principais culturas utilizadas como alimento, o arroz é particularmente eficiente no acúmulo do semimetal altamente tóxico e carcinogênico arsênio (As), representando um risco significativo para a saúde humana Assim, o principal objetivo deste trabalho é elucidar o papel das aquaporinas no transporte de As em arroz. Utilizando cultivares que apresentam susceptibilidade diferencial ao arsênio, foi analisada a expressão dos genes de aquaporinas em resposta ao tratamento com arsenito em diferentes condições. Para a caracterização dos genes de aquaporinas diferencialmente expressos, foram realizados ensaios de complementação funcional em leveduras. Nossos resultados indicam que membros das subfamílias NIP, TIP, PIP e SIP podem estar envolvidos no transporte e metabolismo de As em arroz, dentre estes, quatro podem estar envolvidos no transporte de As para dentro da célula e seis membros podem estar envolvidos no transporte de As para os vacúolos, fazendo com que essas proteínas sejam candidatas a estratégias de melhoramento genético e fitorremediação. / Aquaporins are membrane proteins present in almost all organs and tissues of animals and plants, where they perform functions that go beyond water transport, also transporting molecules such as urea, boric acid, silicic acid, ammonia, carbon dioxide and arsenic. In plants, aquaporins can be classified according to their ami-no acid sequences into five subfamilies: plasma membrane intrinsic proteins (PIPs), tonoplast intrinsic proteins (TIPs), nodulin-26 like intrinsic proteins (NIPs), small intrinsic proteins (SIPs) and uncharacterized intrinsic proteins (XIPs). Genomic data set the number of aquaporin genes in 33 for rice, 35 for Arabidopsis, 71 for cotton and 66 for soybean. Among the main crops used as food, rice is particularly effi-cient in the accumulation of the highly toxic and carcinogenic metalloid arsenic, thus representing a significant risk to human health. Therefore, the main goal of this work is to elucidate the role of aquaporins in the transport of arsenic in rice. Using cultivars with differential susceptibility to arsenic, the expression of aquaporin genes in response to the arsenite treatment under different conditions was ana-lyzed. For the characterization of differentially expressed aquaporin genes, func-tional complementation assays were performed in yeast cells. Our results indicate that members of the subfamilies NIP, TIP, PIP and SIP may be involved in the transport and metabolism of arsenic in rice, of these, four may be involved in the transport of As into the cell and six members may be involved in transporting As to the vacuoles, making these proteins candidates to genetic improvement strategies and phytoremediation.

Silicalite-1 crystals and hollow tube structures were synthesized and functionalized with amine and sulfur containing groups. The adsorption behavior of metal ions (Pb2+, CrO4-) in aqueous solution was investigated on nanocrystalline zeolites functionalized with amines and thiols. Nanocrystalline zeolites with a diameter of 30-50 nm and external surface areas around 100 m2/g were functionalized with 3-aminopropyltriethoxysilane (3-APTES) and 3-mercaptopropyltrimethoxysilane (3-MPTMS). The materials were characterized by 29Si magic angle spinning nuclear magnetic resonance spectroscopy and x-ray diffraction. The adsorption of metal ions from aqueous solutions of Pb (NO3)2 and Na2Cr2O7 was measured by inductively coupled plasma-atomic emission spectroscopy. The effects of various conditions such as pH and concentration were studied to optimize adsorption. Adsorption on functionalized mesoporous silica (MS) was conducted for comparison to the functionalized zeolites. Magnetic zeolite/iron composites were prepared using nanoscale and commercial faujasite zeolites. The composites were functionalized with amine groups to facilitate chromate adsorption under acidic conditions. The materials were characterized using nitrogen adsorption, scanning electron microscopy, thermogravametric analysis, FTIR spectroscopy, and Mossbauer spectroscopy. The adsorption of chromium was evaluated using inductively coupled plasma-optical emission spectroscopy (ICP/OES) to monitor solution chromium quantitatively. The removal of the composites with a magnet was demonstrated. The materials were then evaluated for the adsorption of Cr6+ using ICP-OES to detect chromium. Iron containing zeolite composites were prepared using nanoscale faujasite zeolites. The composites were functionalized with amine groups and Fe ions to facilitate arsenate(As V) adsorption under a variety of pH conditions. The materials were characterized using nitrogen adsorption, X-ray diffraction, thermogravametric analysis and FTIR spectroscopy, and Mossbauer spectroscopy. The adsorption of arsenic was evaluated using inductively coupled plasma-optical emission spectroscopy (ICP/OES) to monitor solution concentration quantitatively. The removal of the composites with a magnet was demonstrated. Kinetics and pH dependence of the adsorption were studied.

Colloid-borne Heavy Metals in the Drainage Gallery of an Abandoned Zn-Pb-Ag Mine (in German). The colloid inventories and the colloid-borne heavy metals in the Rothschönberger Stolln adit, the main drainage gallery of the Freiberg, Germany, mining district, were investigated. This adit runs from Freiberg to the village of Rothschönberg, where it flows into the river Triebisch, a tributary of the river Elbe. The water of the adit is a typical mine water from a flooded ore mine. The main reason for choosing the Rothschönberger Stolln adit for colloid investigations was that ample knowledge concerning the origin of the water and the geology of its catchment area exists. The aim was to characterize the colloids at the mouth of the adit and to elucidate if important contaminants occur in a colloid-borne form. A colloid concentration of about 1 mg/L was found. The particles have a size of 50 to 150 nm. They primarily consist of iron and aluminum oxyhydroxide and carry trace elements such as Pb, As, Cu, Y, La. The contaminants Pb and As are almost entirely colloid-borne. Colloids can have both a retarding and a stimulating influence on the transport of contaminants. The existence of colloids should be taken into account if mine waters flow to the biosphere or if mine waters are to be purified by permeable reactive barriers.

No description available.

Arsenic is a notorious poison due to its high toxicity, worldwide distribution, and lack of any taste and colour once dissolved. The abundance of arsenic in Earth’s crust makes that it can naturally find its way into food and drinking water. Rapid and reliable detection of arsenic, directly in the field, is critical to support evidence-based decision-making in choosing irrigation or drinking water sources. Current cost-effective colourimetric techniques are associated with poor accuracy, health risks, and unacceptable levels of false negatives. Arsenic-specific cellular sensors, or biosensors, may present an inexpensive, safe, and renewable alternative, yet they have long been criticized for unsatisfactory sensing performance, and inconsistency of the outcome. This, in addition to the lack of suitable instruments capable of measuring the signals produced by these biosensors, has led to very few solutions reaching market. The goal of my thesis research was to test hypotheses that improve our fundamental understanding of As species biogeochemistry in simple and complex environmental matrices to then develop a new arsenic monitoring interface, one that would be both simple and accessible to the general public. Using a combination of wild-type and mutant strains, I managed to detail both the internal regulation of arsenic, and the external drivers of arsenic bioavailability. I started by designing a defined exposure protocol that achieved, for the first time, equimolar uptake of over 94% of the added As(III) and As(V) into the cells. By developing this control early into my thesis, I then worked to reintroduce commonly found constituents of environmental waters that are thought to impact arsenic uptake. This direct testing approach uncovered fundamentals of environmental arsenic redox chemistry such as As(III) photooxidation in solution, environmental ligand exchanges, and biological transport pathways. Simplifying a complex exposure protocol for use by the general public required automation of the data analysis steps. This consists of several hundred lines of code, capable of analyzing, normalizing and stabilizing biosensor output to improve the consistency and robustness of this system. These algorithms were then integrated into a new arsenic monitoring interface, one that was built and designed specifically for dehydrated biosensors. This portable, low-cost spectrometer achieved a fluorescent detection range that rivals expensive and sophisticated laboratory equipment at a fraction of the price, and without the need for a computer to compile the measurements. In contrast to highly criticized colorimetric techniques, the biosensor exposure protocol exceeds in operational use, reliability and detection limit. At its core, my thesis research provides a new and complete arsenic testing solution, one capable of measuring both As(III) and As(V) at levels relevant to the World Health Organization and Canadian guidelines for arsenic content in water (10 µg/L). It also provides a new method capable of selectively discriminating between arsenic species, thereby providing an inexpensive and high-throughput arsenic speciation method. I hope this work will help kickstart development of a marketable solution that empowers individuals to test and to monitor the quality of their water sources.