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1.
J Hazard Mater ; 430: 128355, 2022 05 15.
Article in English | MEDLINE | ID: mdl-35149497

ABSTRACT

Chloroethenes are common groundwater pollutants, and have been classified as toxic and carcinogenic to humans. The metabolites of chloroethenes, cis-dichloroethene (cis-DCE) and vinyl chloride (VC) commonly accumulate in groundwater due to their recalcitrant reductive dechlorination under anaerobic conditions. Dehalococcoides mccartyi (Dhc) is the key anaerobic bacteria for complete dechlorination of chloroethene, and Clostridium butyricum (C. butyricum) can provide hydrogen for supporting the growth of Dhc. In this study, we co-immobilized Dhc strain BAV1 and C. butyricum in a silica gel to determine the ability of the complete dechlorination of cis-DCE. Our results showed that our immobilized system could protect BAV1 from a high concentration (8 mM) of cis-DCE to carry out complete dechlorination. After the long-term use of our immobilized system, the activity of complete dechlorination was maintained for more than 180 consecutive days. Furthermore, we applied the immobilized system to remediate contaminated groundwater and uncovered the complete dechlorination of cis-DCE into ethene, a non-toxic product, within 28 days. Therefore, this novel co-immobilized system could serve a solution for bioremediation at chloroethene-contaminated sites.


Subject(s)
Chloroflexi , Clostridium butyricum , Trichloroethylene , Biodegradation, Environmental , Chloroflexi/metabolism , Clostridium butyricum/metabolism , Dehalococcoides , Ethylenes , Humans , Silica Gel , Trichloroethylene/metabolism
2.
ACS Appl Mater Interfaces ; 13(39): 46233-46246, 2021 Oct 06.
Article in English | MEDLINE | ID: mdl-34547889

ABSTRACT

While the antibacterial effect of silver nanoparticles (AgNPs) on environmentally beneficial microbes has drawn considerable attention, the stability and microbial toxicity of AgNPs in a system where nitrate reduction is the dominant terminal electron-accepting process remain understudied. Here, we explore the impact of citrate-coated AgNPs (cit-AgNPs) on the growth and metabolism of two metal-sensitive and one nonsensitive bacterial strains under denitrifying conditions. Dose-response analysis revealed that in contrast to the bacteriostatic effect exhibited at 1 ppm, 5 ppm cit-AgNPs were bactericidal to the metal-sensitive strains. It was observed that the growth of the cells initiated Ag(I) formation, and the supplement of chloride (2.7 mM) to the cultures substantially mitigated the bactericidal capacity of cit-AgNPs, indicating that AgNP dissolution to ionic Ag(I) played a key role in AgNP toxicity. Abiotic experiments confirmed that nitrite, not nitrate, had the capacity to oxidize cit-AgNPs. Transcriptomic analysis revealed that (i) the gene encoding for membrane stress was upregulated proportionally to cit-AgNP concentrations; (ii) cit-AgNPs and Ag(I) at higher levels upregulated genes involved in oxidative stress and iron-sulfur clusters, whereas expressions of the genes responsible for electron transport, ATP synthesis, and denitrification were substantially repressed; (iii) the addition of chloride significantly altered the level of transcriptional profiles of all of the genes. These results not only provide evidence of abiotic AgNP oxidation by metabolic intermediate nitrogen species but also suggest that AgNPs and Ag(I) may induce differential toxicity modes to prokaryotes. Our findings reinforce the importance of evaluating the potential ecological toxicity and risks associated with the transformation of nanomaterials.


Subject(s)
Anti-Bacterial Agents/pharmacology , Metal Nanoparticles/chemistry , Silver/pharmacology , Anti-Bacterial Agents/chemistry , Cell Membrane/drug effects , Citrates/chemistry , Cupriavidus/drug effects , Denitrification/drug effects , Drug Stability , Gene Expression Regulation, Bacterial/drug effects , Oxidative Stress/drug effects , Pseudomonas stutzeri/drug effects , Silver/chemistry , Transcriptome/drug effects , Up-Regulation/drug effects
3.
Environ Sci Pollut Res Int ; 27(36): 44757-44770, 2020 Dec.
Article in English | MEDLINE | ID: mdl-32895790

ABSTRACT

Epidemiological studies have proven that children mental health can be affected by environmental pollutants which are believed to be visible in the form of psychological disorder later in their childhood. Moreover, the effects of children mental health are evidently clear in the case of phthalates which have been observed to increase psychological disorder, specifically attention-deficit hyperactivity disorder (ADHD). Hence, the present study aims to conduct a systematic review and provide an overview of the existing literature on the association between urinary phthalate metabolite concentrations and ADHD symptoms among children by emphasizing the confounding factors and limitations. Additionally, this review addressed the possible phthalate mechanism insights in human body including its impact on ADHD symptoms. In this case, 16 epidemiological studies (five cross-sectional, nine cohort and two case control studies) that met all the inclusion criteria were selected out of the total of 427 papers screened to show varying quantitative associations between phthalate exposure and ADHD symptoms among children with confounding factors and limitations in the existing studies in regard to the exposure and outcomes. This review also attempted to present possible explanation on phthalate mechanism in children body and its connection on neurodevelopment and ADHD symptom development which remains unclear in most of the studies. Finally, it is highly recommended for further research to carefully design cohort studies from prenatal to later childhood development with a complete sample size in order to understand phthalate impacts on children health.


Subject(s)
Attention Deficit Disorder with Hyperactivity , Environmental Pollutants , Phthalic Acids , Attention Deficit Disorder with Hyperactivity/chemically induced , Attention Deficit Disorder with Hyperactivity/epidemiology , Child , Cross-Sectional Studies , Female , Humans , Male , Phthalic Acids/adverse effects , Pregnancy
4.
Chemosphere ; 240: 124876, 2020 Feb.
Article in English | MEDLINE | ID: mdl-31542577

ABSTRACT

4-t-octylphenol (4-t-OP), a well-known endocrine disrupting compound, is frequently found in various environmental compartments at levels that may cause adverse effects to the ecosystem and public health. To date, most of the studies that investigate microbial transformations of 4-t-OP have focused on the process mediated by bacteria, ligninolytic fungi, or microbial consortia. There is no report on the complete degradation mechanism of 4-t-OP by non-ligninolytic fungi. In this study, we conducted laboratory experiments to explore and characterize the non-ligninolytic fungal strain Fusarium falciforme RRK20 to degrade 4-t-OP. Using the response surface methodology, the initial biomass concentration and temperature were the factors identified to be more influential on the efficiency of the biodegradation process as compared with pH. Under the optimized conditions (i.e., 28 °C, pH 6.5 with an initial inoculum density of 0.6 g L-1), 25 mg L-1 4-t-OP served as sole carbon source was completely depleted within a 14-d incubation; addition of low dosage of glucose was shown to significantly accelerate 4-t-OP degradation. The yeast estrogenic screening assay further confirmed the loss of estrogenic activity during the biodegradation process, though a longer incubation period was required for complete removal of estrogenicity. Metabolites identified by LC-MS/MS revealed that strain RRK20 might degrade 4-t-OP as sole energy source via alkyl chain oxidation and aromatic ring hydroxylation pathways. Together, these results not only suggest the potential use of non-ligninolytic fungi like strain RRK20 in remediation of 4-t-OP contaminated environments but may also improve our understanding of the environmental fate of 4-t-OP.


Subject(s)
Biodegradation, Environmental , Fusarium/chemistry , Phenols/chemistry , Fungi/metabolism
5.
Environ Sci Pollut Res Int ; 26(17): 17762-17773, 2019 Jun.
Article in English | MEDLINE | ID: mdl-31030402

ABSTRACT

In Taiwan, because of the co-use of some irrigation and drainage canals, a portion of industrial wastewater was directly discharged into irrigation canals or even flowed into rivers or wetlands, causing the heavy metal pollution in waters and sediments. Mercury (Hg) contamination in rivers, irrigation canals, and wetlands has been found in Taiwan, but a thorough investigation on the distribution of Hg and methylmercury (MeHg) in these waters and sediments, which may be present in a greater level with elevating total Hg (THg) concentration and markedly impact human health, is still lacking. In this study, surface waters and surface sediments were sampled from five major rivers, two irrigation canals, two reservoirs, and one wetland in Taiwan, and their THg and MeHg concentrations were quantified. Additionally, statistical analysis was carried out to understand the relationship between sediment properties and MeHg levels. The results showed that irrigation canal sediments were relatively more polluted by Hg and the THg concentrations of some sampling points exceeded the upper limit (i.e., 0.87 mg kg-1) of sediment quality index (SQI) for THg promulgated by Taiwan Environmental Protection Administration, which may be attributed to the co-use of irrigation and drainage canals. Furthermore, the MeHg concentration in irrigation canal sediments was the highest; rivers came in second followed by wetlands. In addition, the Siangshan Wetland was analyzed to have the greatest THg and MeHg concentrations in its surface water. Linear regression analysis also indicated that total organic carbon and clay content substantially affected the MeHg production in sediments.


Subject(s)
Environmental Monitoring , Mercury/analysis , Methylmercury Compounds/analysis , Water Pollutants, Chemical/analysis , Geologic Sediments/analysis , Rivers , Taiwan , Wetlands
6.
Environ Sci Pollut Res Int ; 25(12): 11333-11342, 2018 Apr.
Article in English | MEDLINE | ID: mdl-29546515

ABSTRACT

Phthalates have been blended in various compositions as plasticizers worldwide for a variety of purposes. Consequently, humans are exposed to a wide spectrum of phthalates that needs to be researched and understood correctly. The goal of this review is to focus on phthalate's internal exposure pathways and possible role of human digestion on liver toxicity. In addition, special focus was made on stem cell therapy in reverting liver toxicity. The known entry of higher molecular weight phthalates is through ingestion while inhalation and dermal pathways are for lower molecular weight phthalates. In human body, certain phthalates are digested through phase 1 (hydrolysis, oxidation) and phase 2 (conjugation) metabolic processes. The phthalates that are made bioavailable through digestion enter the blood stream and reach the liver for further detoxification, and these are excreted via urine and/or feces. Bis(2-ethylhexyl) phthalate (DEHP) is a compound well studied involving human metabolism. Liver plays a pivotal role in humans for detoxification of pollutants. Thus, continuous exposure to phthalates in humans may lead to inhibition of liver detoxifying enzymes and may result in liver dysfunction. The potential of stem cell therapy addressed herewith will revert liver dysfunction and lead to restoration of liver function properly.


Subject(s)
Liver/drug effects , Phthalic Acids/toxicity , Diethylhexyl Phthalate , Environmental Exposure/analysis , Humans , Hydrolysis , Liver/metabolism , Plasticizers/metabolism
7.
Mar Pollut Bull ; 125(1-2): 416-425, 2017 Dec 15.
Article in English | MEDLINE | ID: mdl-28964501

ABSTRACT

4-t-Octylphenol (4-t-OP) has become a serious environmental concern due to the endocrine disruption in animals and humans. The biodegradation of 4-t-OP by pure cultures has been extensively investigated only in bacteria and wood-decaying fungi. In this study we isolated and identified 14 filamentous fungal strains from wastewater samples in Taiwan using 4-t-OP as a sole carbon and energy source. The isolates were identified based on sequences from different DNA regions. Of 14 fungal isolates, 10 strains grew effectively on solid medium with a wide variety of endocrine disrupting chemicals as the sole carbon and energy source. As revealed by high-performance liquid chromatography analysis, the most effective 4-t-OP degradation (>70%) in liquid medium was observed in Fusarium falciforme after 15days. To our knowledge, this is the first report on the degradation of 4-t-OP as a sole carbon and energy source by non-ligninolytic fungi.


Subject(s)
Endocrine Disruptors/metabolism , Fungi/metabolism , Phenols/metabolism , Water Pollutants, Chemical/metabolism , Biodegradation, Environmental , Carbon/metabolism , Chromatography, High Pressure Liquid , Fungi/isolation & purification , Taiwan , Wastewater/microbiology
8.
Bioresour Technol ; 226: 55-64, 2017 Feb.
Article in English | MEDLINE | ID: mdl-27987401

ABSTRACT

4-(1,1,3,3-tetramethylbutane)-phenol (4-tert-OP) is one of the most prevalent endocrine disrupting pollutants. Information about bioremediation of 4-tert-OP remains limited, and no study has been reported on the mechanism of 4-tert-OP degradation by yeasts. The yeast Candida rugopelliculosa RRKY5 was proved to be able to utilize 4-methylphenol, bisphenol A, 4-ethylphenol, 4-tert-butylphenol, 4-tert-OP, 4-tert-nonylphenol, isooctane, and phenol under aerobic conditions. The optimum conditions for 4-tert-OP degradation were 30°C, pH 5.0, and an initial 4-tert-OP concentration of 30mgL-1; the maximum biodegradation rate constant was 0.107d-1, equivalent to a minimum half-life of 9.6d. Scanning electron microscopy revealed formation of arthroconidia when cells were grown in the presence of 4-tert-OP, whereas the cells remained in the budding form without 4-tert-OP. Identification of the 4-tert-OP degradation metabolites using liquid chromatography-hybrid mass spectrometry revealed three different mechanisms via both branched alkyl side chain and aromatic ring cleavage pathways.


Subject(s)
Candida/metabolism , Endocrine Disruptors/metabolism , Phenols/metabolism , Biodegradation, Environmental , Chromatography, Liquid , Half-Life , Hydrogen-Ion Concentration , Hydroxylation , Mass Spectrometry , Oxidation-Reduction , Phenols/analysis
9.
J Hazard Mater ; 318: 507-514, 2016 Nov 15.
Article in English | MEDLINE | ID: mdl-27450343

ABSTRACT

While earlier studies have identified the antibacterial activity of carbon nanotubes (CNTs) and proposed that cell membrane damage by direct contact with CNTs is likely the main toxicity mechanism, the relative importance of chemical versus physical properties of CNTs in controlling their bacterial cytotoxicity is understudied. Given that CNT is commonly modified via acid treatment to enhance its dispersivity and surface chemistry, in this study commercially available multi-walled carbon nanotubes (MWCNTs) with high purity were processed carefully by acid reflux, resulting in differences in surface charge of MWCNTs without altering their physical properties. The surface condition of MWCNTs was also modified by adsorption of organic matter to compare bacterial toxicity of functionalized and non-functionalized MWCNTs in suspensions. Results show that although overall electrostatic repulsion and steric obstruction resulted from surface modifications led to elevated dispersivity of MWCNTs and mitigated toxicity on planktonic Escherichia coli cultures, no correlation between the dispersivity and bacterial toxicity of MWCNTs was observed, suggesting that dispersity alone may not be a proper index to estimate the CNT antibacterial effect on planktonic cells in the aqueous phase. In addition, viability recovery of MWCNT-treated cells was observed to be nutrition level-dependent, implying that availability of proper nutrients may be another important factor to be considered when assessing the ecotoxicity of CNTs in the aquatic system.


Subject(s)
Escherichia coli/drug effects , Nanotubes, Carbon , Anti-Bacterial Agents/pharmacology , Cell Membrane/drug effects , Culture Media , Escherichia coli/growth & development , Humic Substances , Phthalic Acids/pharmacology , Static Electricity , Suspensions
10.
Chemosphere ; 154: 375-384, 2016 Jul.
Article in English | MEDLINE | ID: mdl-27070857

ABSTRACT

Recent studies have shown that rice consumption is another critical route of human exposure to methylmercury (MeHg), the most toxic and accumulative form of mercury (Hg) in the food web. Yet, the mechanisms that underlie the production and accumulation of MeHg in the paddy ecosystem are still poorly understood. In 2013 and 2014, we conducted field campaigns and laboratory experiments over a rice growing season to examine Hg and MeHg cycling, as well as associated biogeochemistry in a suite of paddies close to a municipal solid waste incinerator and a coal-fired power plant station in Taiwan. Concentrations of total Hg and MeHg in paddy soil and rice grain at both sites were low and found not to exceed the control standards for farmland soil and edible rice in Taiwan. However, seasonal variations of MeHg concentrations observed in pore water samples indicate that the in situ bioavailability of inorganic Hg and activity of Hg-methylating microbes in the rhizosphere increased from the early-season and peaked at the mid-season, presumably due to the anoxia created under flooded conditions and root exudation of organic compounds. The presence of Hg-methylators was also confirmed by the hgcA gene detected in all root soil samples. Subsequent methylation tests performed by incubating the root soil with inorganic Hg and an inhibitor or stimulant specific for certain microbes further revealed that sulfate-reducers might have been the principal Hg-methylting guild at the study sites. Interestingly, results of hydroponic experiments conducted by cultivating rice in a defined nutrient solution amended with fixed MeHg and varying levels of MeHg-binding ligands suggested that chemical speciation in soil pore water may play a key role in controlling MeHg accumulation in rice, and both passive and active transport pathways seem to take place in the uptake of MeHg in rice roots.


Subject(s)
Environmental Monitoring , Mercury/analysis , Methylmercury Compounds/analysis , Oryza/chemistry , Soil Pollutants/analysis , Soil/chemistry , Biological Availability , Coal , Food Chain , Food Contamination , Humans , Incineration , Methylmercury Compounds/chemistry , Oryza/microbiology , Plant Roots/metabolism , Power Plants , Rhizosphere , Soil Microbiology , Solid Waste , Taiwan , Waste Management , Water/metabolism
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