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1.
Int J Mol Sci ; 24(20)2023 Oct 17.
Article in English | MEDLINE | ID: mdl-37894945

ABSTRACT

Prometryn is a methylthio-s-triazine herbicide used to control the growth of annual broadleaf and grass weeds in many cultivated plants. Significant traces of prometryn are documented in the environment, mainly in waters, soil, and plants used for human and domestic consumption. Previous studies have shown that triazine herbicides have carcinogenic potential in humans. However, there is limited information about the effects of prometryn on the cardiac system in the literature, or the mechanisms and signaling pathways underlying any potential cytotoxic effects are not known. It is important to understand the possible effects of exogenous compounds such as prometryn on the heart. To determine the mechanisms and signaling pathways affected by prometryn (185 mg/kg every 48 h for seven days), we performed proteomic profiling of male mice heart with quantitative liquid chromatography-tandem mass spectrometry (LC-MS/MS) using ten-plex tandem mass tag (TMT) labeling. The data suggest that several major pathways, including energy metabolism, protein degradation, fatty acid metabolism, calcium signaling, and antioxidant defense system were altered in the hearts of prometryn-treated mice. Proteasome and immunoproteasome activity assays and expression levels showed proteasome dysfunction in the hearts of prometryn-treated mice. The results suggest that prometryn induced changes in mitochondrial function and various signaling pathways within the heart, particularly affecting stress-related responses.


Subject(s)
Herbicides , Prometryne , Humans , Animals , Mice , Prometryne/analysis , Prometryne/metabolism , Prometryne/pharmacology , Proteasome Endopeptidase Complex , Chromatography, Liquid , Proteomics , Tandem Mass Spectrometry , Herbicides/toxicity , Plants/metabolism , Mitochondria/metabolism
2.
Sci Total Environ ; 897: 165375, 2023 Nov 01.
Article in English | MEDLINE | ID: mdl-37422222

ABSTRACT

Prometryn (PRO) is frequently detected in shellfish of international trade among triazine herbicides because of its wide application in agriculture and aquaculture worldwide. Nevertheless, the variations of PRO remain unclear in aquatic organisms, which affect the accuracy of their food safety risk assessment. In the present study, the tissue-specific accumulation, biotransformation, and potential metabolic pathway of PRO were reported in oyster species Crassostrea gigas for the first time. The experiments were conducted through semi-static seawater exposure with low and high concentrations of PRO (at nominal concentrations of 10 and 100 µg/L) via daily renewal over 22 days, followed by 16 days of depuration in clean seawater. The characterization of prometryn in oysters was then evaluated through the bioaccumulation behavior, elimination pathway and metabolic transformation, comparing with other organisms. The digestive gland and gonad were found to be the main target organs during uptake. In addition, the highest bioconcentration factor of 67.4 ± 4.1 was observed when exposed to low concentration. The level of PRO in oyster tissues rapidly decreased within 1 day during depuration, with an elimination rate of >90 % for the gill. Moreover, four metabolites of PRO were identified in oyster samples of exposed groups, including HP, DDIHP, DIP, and DIHP, in which HP was the major metabolite. Considering the mass percentage of hydroxylated metabolites higher than 90 % in oyster samples, PRO poses a larger threat to aquatic organisms than rat. Finally, the biotransformation pathway of PRO in C. gigas was proposed, the major metabolic process of which was hydroxylation along with N-dealkylation. Meanwhile, the newly discovered biotransformation of PRO in oyster indicates the importance of monitoring environmental levels of PRO in cultured shellfish, to prevent possible ecotoxicological effects as well as to ensure the safety of aquatic products.


Subject(s)
Crassostrea , Water Pollutants, Chemical , Animals , Rats , Crassostrea/metabolism , Prometryne/metabolism , Commerce , Water Pollutants, Chemical/analysis , Internationality , Seawater
3.
J Hazard Mater ; 446: 130708, 2023 03 15.
Article in English | MEDLINE | ID: mdl-36608577

ABSTRACT

Demethylthio is one of the most important ways for microorganisms to metabolize triazine herbicides. Previous studies have found that the initial reaction of prometryn catabolism in Leucobacter triazinivorans JW-1 was the hydroxylation of its methylthio group, however, the corresponding functional enzyme was not yet clear. In this study, the gene proA was responsible for the initial step of prometryn catabolism from the strain JW-1 was cloned and expressed, and the purified amidohydrolases ProA have the ability to transform prometryn to 2-hydroxypropazine and methanethiol. The optimized reaction temperature and pH of ProA were 45 °C and 7.0, respectively, and the kinetic constants Km and Vmax of ProA for the catalysis of prometryn were 32.6 µM and 0.09 µmol/min/mg, respectively. Molecular docking analyses revealed that different catalysis efficiency of ProA and TrzN (Nocardioides sp. C190) for prometryn and atrazine was due to non-covalent changes in amino acid residues. Our findings provide new insights into the understanding of s-triazine catabolism at the molecular level.


Subject(s)
Herbicides , Prometryne , Prometryne/metabolism , Triazines/metabolism , Molecular Docking Simulation , Herbicides/metabolism , Amidohydrolases , Catalysis , Nocardioides/metabolism
4.
J Hazard Mater ; 443(Pt A): 130202, 2023 02 05.
Article in English | MEDLINE | ID: mdl-36272374

ABSTRACT

Prometryn, 2-methylthio-4,6-bis(isopropylamino)-1,3,5-triazine, is a selective thiomethyl triazine herbicide widely used to control unwanted weeds and harmful insects by inhibiting electron transport in target organisms. Despite having various advantages, herbicides pose as a major threat to the environment and human health due to persistent contamination, bioaccumulation, and damage to non-target organisms. In this study, the developmental toxicity of 5, 10, and 20 mg/L prometryn in zebrafish (Danio rerio) embryos was evaluated and compared to that of the solvent control for 96 h. Several transgenic zebrafish models (fli1a:eGFP, flk1:eGFP, olig2:dsRed and L-fabp:dsRed) were visually assessed to detect fluorescently tagged genes. Results showed that prometryn shortened body length, and induced yolk sac, heart edema, abnormal heart rate, and loss of viability. Fluorescence microscopy revealed that prometryn exposure caused defects in organ development, reactive oxygen species accumulation, and apoptotic cell death. Mitochondrial bioenergetics were also evaluated to determine the effect of prometryn on the electron transport chain activity and metabolic alterations. Prometryn was found to interfere with mitochondrial function, ultimately inhibiting energy metabolism and embryonic development. Collectively, our findings suggest that prometryn is a potential contaminate for non-target sites and organisms, especially aquatic, and emphasize the need to consider the toxic effects of prometryn.


Subject(s)
Herbicides , Water Pollutants, Chemical , Animals , Humans , Prometryne/metabolism , Prometryne/pharmacology , Zebrafish/metabolism , Oxidative Stress , Herbicides/metabolism , Mitochondria , Organogenesis , Embryo, Nonmammalian , Water Pollutants, Chemical/metabolism
5.
Environ Sci Pollut Res Int ; 29(45): 67765-67775, 2022 Sep.
Article in English | MEDLINE | ID: mdl-35522405

ABSTRACT

Cyromazine, a symmetrical triazine insecticide, is used to control dipteran larvae in chicken manure by feeding to the poultry, flies on animals, and leafminers in vegetables. Its extensive use has resulted in the widespread contamination in the environment. In the current study, a cyromazine degrading bacterium (designated strain ZX01) was isolated and characterized from a Chinese ginger cultivated soil by selective enrichment culture method. On the basis of morphological, biochemical characteristics, and 16S rRNA gene sequence, this bacterium showed strong similarity to the Pseudomonadales members and was closely related to the Acinetobacter baumannii group. Spectrophotometric and HPLC analyses revealed that strain ZX01 degraded cyromazine and utilized it as the sole carbon source for its growth. This process hydrolyzes cyromazine to melamine. Strain ZX01 degraded most of the cyromazine in 60 h. Besides, its substrate specificity against four symmetrical triazine herbicides, one triazinone herbicide, as well as 10 insecticides and its antibiotic sensitivity towards eight commercial antibiotics were also tested. At the concentration of 100 µg/mL for 60 h, it could effectively degrade a variety of different pesticides, including atrazine, prometon, simazine, prometryn, enitrothion, diazinon, cypermethrin, and acetamiprid, and the degradation was in the range of 71-87%. In particular, melamine, the main degradation product of cyromazine, was degraded by 47.3%. This microorganism was sensitive to chloramphenicol and tetracycline and intermediate to amoxicillin and trimethoprim. These results highlight that strain ZX01 can be used as a potential biological agent for the remediation of soil, water, or crop contaminated with cyromazine and other symmetrical triazine insecticides.


Subject(s)
Acinetobacter , Atrazine , Herbicides , Insecticides , Pesticides , Zingiber officinale , Acinetobacter/metabolism , Amoxicillin , Animals , Anti-Bacterial Agents/metabolism , Anti-Bacterial Agents/pharmacology , Atrazine/metabolism , Biodegradation, Environmental , Biological Factors/metabolism , Carbon/metabolism , China , Chloramphenicol , Diazinon , Herbicides/metabolism , Insecticides/metabolism , Manure , Pesticides/metabolism , Prometryne/metabolism , RNA, Ribosomal, 16S/genetics , Simazine , Soil , Soil Microbiology , Tetracyclines/metabolism , Triazines/metabolism , Trimethoprim , Water/metabolism
6.
Chemosphere ; 248: 126018, 2020 Jun.
Article in English | MEDLINE | ID: mdl-32035384

ABSTRACT

In recent years, prometryn was utilized as watergrass remover in the aquaculture industry, resulting in the accumulated residual in the aquatic products. The present study focuses on the ozone degradation of prometryn in the Ruditapes philippinarum. The ozone concentration in water increased along with the injection time (60min). The contents of hydroxyl (·OH) and superoxide (O2·-) radicals increased along with the ozone injection time. The effects of temperature, pH, prometryn initial concentration and ozone concentration on the removal efficiency of prometryn were evaluated. The maximum removal efficiency of 86.12% was obtained under the conditions of pH 7, prometryn initial concentration 0.05 mg/kg and the ozone concentration 4.2 mg/L at 28 °C for 30 min. Ion chromatography (IC) and Fourier transform infrared (FT-IR) spectroscopy results show that the S and N atoms in the outer layer of the triazine ring during the prometryn degradation process were oxidized and removed. A total of 30 intermediate compounds were identified using the gas chromatography-mass spectrometry (GC-MS) method. Combined with the IC and FT-IR results, three possible degradation pathways of prometryn were proposed. The prometryn was finally degraded into some small molecules with reduced toxicity by 63.16% for 120 min ozonization treatment. Overall, our work provides a novel approach for prometryn degradation in Ruditapes philippinarum, which can be extended for removing the residues of agricultural and veterinary drugs in other aquatic products.


Subject(s)
Bivalvia/metabolism , Ozone/chemistry , Prometryne/metabolism , Water Pollutants, Chemical/metabolism , Animals , Gas Chromatography-Mass Spectrometry , Hydrogen-Ion Concentration , Hydroxyl Radical/chemistry , Oxidation-Reduction , Spectroscopy, Fourier Transform Infrared , Water , Water Pollutants, Chemical/chemistry
7.
Environ Toxicol Chem ; 39(2): 450-457, 2020 02.
Article in English | MEDLINE | ID: mdl-31569276

ABSTRACT

Plant protection products (PPPs) undergo rigorous regulatory assessment to ensure that they do not pose unacceptable risks to the environment. Elucidation of their fate and behavior in soil is an integral part of this environmental risk assessment. The active substance degradation in soil of PPPs is first assessed in laboratory studies (typically following Organisation for Economic Co-operation and Development [OECD] test guideline 307). Conditions in guideline laboratory studies are far removed from those occurring under agricultural use, and the contribution of crop roots has currently not been assessed. We integrated viable plant root systems, representative of 3 different crop types, into the OECD test guideline 307 design to assess their impact on the dissipation of the herbicide prometryn. Significantly faster decline of parent residue and higher formation of nonextractable residues were observed in all 3 planted systems. This led to a reduction in the time required for 50% of the compound to dissipate (DT50) of approximately one-half in the presence of rye grass and hot pepper and of approximately one-third in the presence of red clover. These findings imply that plants and their associated root networks can have a significant influence on PPP dissipation. Based on these data, greater environmental realism could be added to the standardized laboratory study design by the inclusion of plant root systems into higher tier studies, which, in turn, could serve to improve the environmental risk assessment process. Environ Toxicol Chem 2020;39:450-457. © 2019 SETAC.


Subject(s)
Herbicides/analysis , Prometryne/analysis , Rhizosphere , Soil Pollutants/analysis , Soil/chemistry , Biodegradation, Environmental , Capsicum/growth & development , Capsicum/metabolism , Herbicides/metabolism , Herbicides/toxicity , Lolium/growth & development , Lolium/metabolism , Prometryne/metabolism , Prometryne/toxicity , Risk Assessment , Soil Pollutants/metabolism , Soil Pollutants/toxicity , Trifolium/growth & development , Trifolium/metabolism
8.
Sci Total Environ ; 615: 78-86, 2018 Feb 15.
Article in English | MEDLINE | ID: mdl-28963898

ABSTRACT

The s-triazine herbicides, such as prometryn, have been widely used in agriculture and have raised much public concern over their contamination of water and soil. Leucobacter sp. JW-1 cells were immobilized in polyvinyl alcohol­sodium alginate (PVA-SA) beads and then used to degrade prometryn. Orthogonal array experiments showed that the optimal immobilization conditions of PVA-SA immobilized Leucobacter sp. JW-1 beads (PSLBs) were 3% JW-1 cells (w/v, wet weight), 10-12% (w/v) PVA, 2-3% (w/v) calcium chloride, and an immobilization time of 24-36h. The PSLBs were more tolerance to pH, temperature and salinity changes than free JW-1 cells and were stable and effective for degrading prometryn through six reuse cycles without losing their degradation capacity. The half-life of prometryn degradation by PSLBs at 100mgL-1 in pesticide plant wastewaters were 1.1-6.9h. The rate constants of prometryn degradation by PSLBs in wastewaters ranged from 304 to 576mgL-1day-1, which were approximately 1.25-118 times those of degradation by free JW-1 cells. The PSLBs degraded 99.9% of atrazine, 99.9% of ametryn, 97.8% of propazine, 100.0% of simetryn, 77.9% of simazine, 98.9% of terbuthylazine, 95.2% of prometon, 98.9% of atraton, and 31.6% of terbumeton at an initial concentration of 50mgL-1 of each herbicide in 2days. This study indicates that PSLBs persistently biodegrade s-triazine herbicides better than JW-1 free cells, and can be an efficient, safe and reusable biomaterial for the removal of s-triazine herbicides from contaminated sites.


Subject(s)
Herbicides/metabolism , Leukocidins/metabolism , Prometryne/metabolism , Triazines/metabolism , Wastewater/chemistry , Alginates , Biodegradation, Environmental , Cells, Immobilized , Glucuronic Acid , Hexuronic Acids , Polyvinyl Alcohol
9.
Int J Syst Evol Microbiol ; 68(1): 204-210, 2018 Jan.
Article in English | MEDLINE | ID: mdl-29139349

ABSTRACT

A Gram-stain-positive, rod-shaped, non-motile bacterial strain, designated JW-1T, was isolated from activated sludge collected from the outlet of an aeration tank in a prometryn-manufacturing plant, located in Binzhou City, Shandong province, PR China. Phylogenetic analysis, based on 16S rRNA gene sequences, indicated that strain JW-1T belongs to the genus Leucobacter and its closest neighbours are 'Leucobacter kyeonggiensis' F3-P9 (98.95 % similarity), Leucobacter celer subsp. astrifaciens CBX151T (98.62 %), Leucobacter celer subsp. celer NAL101T (98.53 %), Leucobacter chromiiresistens JG31T (97.86 %) and Leucobacter chironomi DSM 19883T (97.37 %). DNA-DNA hybridization values with the above strains were <55 %. The DNA G+C content of strain JW-1T was 72.6 mol%. The major fatty acids of strain JW-1T were iso-C16 : 0, anteiso-C15 : 0, anteiso-C17 : 0 and iso-C15 : 0. The predominant polar lipids were diphosphatidylglycerol, phosphatidylglycerol and glycolipid. The predominant menaquinone was MK-11. The cell wall amino acids were 2,4-diaminobutyric acid, alanine, glutamic acid, glycine and threonine. Based on the molecular and chemotaxonomic data, as well as the physiological and biochemical characteristics, strain JW-1T is considered to represent a novel species of the genus Leucobacter, for which the name Leucobacter triazinivorans is proposed. The type strain is JW-1T (=DSM 105188T=LMG 30083T).


Subject(s)
Actinomycetales/classification , Herbicides/metabolism , Phylogeny , Prometryne/metabolism , Sewage/microbiology , Actinomycetales/genetics , Actinomycetales/isolation & purification , Aminobutyrates , Bacterial Typing Techniques , Base Composition , Cell Wall/chemistry , China , DNA, Bacterial/genetics , Fatty Acids/chemistry , Glycolipids/chemistry , Nucleic Acid Hybridization , Phospholipids/chemistry , RNA, Ribosomal, 16S/genetics , Sequence Analysis, DNA , Vitamin K 2/chemistry
10.
Biodegradation ; 25(3): 405-15, 2014 Jun.
Article in English | MEDLINE | ID: mdl-24166157

ABSTRACT

A microbial community, selected by its ability to degrade triazinic herbicides was acclimatized by successive transfers in batch cultures. Initially, its ability to degrade prometryn, was evaluated using free cells or cells attached to fragments of a porous support. As carbon, nitrogen and sulfur sources, prometryn, (98.8 % purity), or Gesagard, a herbicide formulation containing 44.5 % prometryn and 65.5 % of adjuvants, were used. In batch cultures, a considerable delay in the degradation of prometryn, presumptively caused by the elevated concentration of inhibitory adjuvants, occurred. When pure prometryn was used, volumetric removal rates remarkably higher than those obtained with the herbicide formulation were estimated by fitting the raw experimental data to sigmoidal decay models, and differentiating them. When the microbial consortium was immobilized in a continuously operated biofilm reactor, the negative effect of adjuvants on the rate and removal efficiency of prometryn could not be detected. Using the herbicide formulation, the consortium showed volumetric removal rates greater than 20 g m(-3) h(-1), with prometryn removal efficiencies of 100 %. The predominant bacterial strains isolated from the microbial consortium were Microbacterium sp., Enterobacter sp., Acinetobacter sp., and Flavobacterium sp. Finally, by comparison of the prometryn removal rates with others reported in the literature, it can be concluded that the use of microbial consortia immobilized in a biofilm reactor operated in continuous regime offer better results than batch cultures of pure microbial strains.


Subject(s)
Biofilms/growth & development , Herbicides/metabolism , Microbial Consortia/physiology , Models, Statistical , Prometryne/metabolism , Water Pollutants, Chemical/metabolism , Actinomycetales/metabolism , Biodegradation, Environmental , Bioreactors , Cells, Immobilized , Enterobacter/metabolism , Flavobacterium/metabolism , Kinetics
11.
Huan Jing Ke Xue ; 34(7): 2894-8, 2013 Jul.
Article in Chinese | MEDLINE | ID: mdl-24028029

ABSTRACT

The purpose of this study was to develop some bacterial strains that could degrade prometryne effectively. Bacteria were screened and purified from sediments of a pesticide plant with the method of domestication with gradient concentrations. Two strains were isolated and named P-1 and P-2, respectively. According to their morphology, physiological, biochemical properties and the analysis of their 16S rRNA gene sequences, the strain P-1 is Gram negative and identified as Ochrobactrum; the strain P-2 is Gram positive and identified as Bacillus. GenBank Accession numbers are HM004554 and HM004555, respectively. Degradation rates of the strains P-1 and P-2 for prometryne concentration with 40 mg x L(-1) were 46.5% and 65.4% after 12 days in the liquid culture experiment, respectively. This study provides an essential material and theoretical foundation for the remediation of prometryne contaminated soils.


Subject(s)
Bacillus/isolation & purification , Herbicides/isolation & purification , Ochrobactrum/isolation & purification , Prometryne/isolation & purification , Bacillus/metabolism , Biodegradation, Environmental , Environmental Pollutants/isolation & purification , Environmental Pollutants/metabolism , Environmental Restoration and Remediation , Herbicides/metabolism , Ochrobactrum/metabolism , Prometryne/metabolism , Sewage/microbiology
12.
Lett Appl Microbiol ; 57(2): 122-8, 2013 Aug.
Article in English | MEDLINE | ID: mdl-23593967

ABSTRACT

UNLABELLED: Prometryn and acetochlor are common herbicides widely used to control weeds in agricultural systems. The impacts of the two herbicides on spore germination, hyphal elongation, the biomass and malondialdehyde content of carrot hairy roots were investigated using a strict in vitro cultivation system associating the Ri T-DNA-transferred carrot hairy roots with Glomus etunicatum. Alternatively, root colonization, daughter spore production and the proportion of hyphae with succinate dehydrogenase (SDH) and alkaline phosphatase (ALP) activities were also investigated. No significant impact on spore germination was noted in the presence of acetochlor at all three concentrations tested, while a significant decrease was observed with prometryn only at the highest concentration. Moreover, an inverse correlation was identified between herbicides concentrations and G. etunicatum root colonization and spore production as well as hyphal SDH and ALP activity, with a positive correlation identified among these four factors. Both herbicides exerted negative effects on the arbuscular mycorrhizal (AM) fungus and symbiosis at increasing concentrations, with prometryn apparently more toxic than acetochlor. Furthermore, the AM symbiotic system was shown to improve biomass, reduce malondialdehyde accumulation and ease lipid peroxidation in carrot hairy roots and decrease damage in host plants, thus enhancing plant tolerance to adverse conditions. SIGNIFICANCE AND IMPACT OF THE STUDY: In this study, the effect of prometryn and acetochlor on the physiology and metabolic activities of the AM fungus Glomus etunicatum were investigated. Our findings demonstrate for the first time, the impact of the two herbicides at three concentrations (0.1, 1 and 10 mg l(-1)) on transformed carrot hairy roots/AM fungus association under strict in vitro culture conditions, which may guide the application of the two herbicides in modern agriculture.


Subject(s)
Daucus carota/microbiology , Glomeromycota/drug effects , Mycorrhizae/drug effects , Prometryne/pharmacology , Symbiosis , Toluidines/pharmacology , Agriculture , Alkaline Phosphatase/metabolism , Biomass , Daucus carota/metabolism , Glomeromycota/physiology , Herbicides/pharmacology , Hyphae/drug effects , Hyphae/enzymology , Lipid Peroxidation , Malondialdehyde/metabolism , Mycorrhizae/physiology , Plant Roots/drug effects , Plant Roots/metabolism , Plant Roots/microbiology , Prometryne/metabolism , Spores, Fungal/drug effects , Spores, Fungal/physiology , Succinate Dehydrogenase/metabolism
13.
Chemosphere ; 87(3): 278-84, 2012 Apr.
Article in English | MEDLINE | ID: mdl-22273183

ABSTRACT

Investigation on organic xenobiotics bioaccumulation/biodegradation in green algae is of great importance from environmental point of view because widespread distribution of these compounds in agricultural areas has become one of the major problems in aquatic ecosystem. Also, new technology needs to be developed for environmental detection and re-usage of the compounds as bioresources. Prometryne as a herbicide is widely used for killing annual grasses in China and other developing countries. However, overuse of the pesticide results in high risks to contamination to aquatic environments. In this study, we focused on analysis of bioaccumulation and degradation of prometryne in Chlamydomonas reinhardtii, a green alga, along with its adaptive response to prometryne toxicity. C. reinhardtii treated with prometryne at 2.5-12.5 µg L(-1) for 4 d or 7.5 µg L(-1) for 1-6 d accumulated a large quantity of prometryne, with more than 2 mg kg(-1) fresh weight in cells exposed to 10 µg L(-1) prometryne. Moreover, it showed a great ability to degrade simultaneously the cell-accumulated prometryne. Such uptake and catabolism of prometryne led to the rapid removal of prometryne from media. Physiological and molecular analysis revealed that toxicology was associated with accumulation of prometryne in the cells. The biological processes of degradation can be interpreted as an internal tolerance mechanism. These results suggest that the green alga is useful in bioremediation of prometryne-contaminated aquatic ecosystems.


Subject(s)
Chlamydomonas reinhardtii/metabolism , Herbicides/metabolism , Prometryne/metabolism , Water Pollutants, Chemical/metabolism , Catalase/metabolism , Chlamydomonas reinhardtii/drug effects , Herbicides/toxicity , Metabolism , Prometryne/toxicity , Reactive Oxygen Species/metabolism , Superoxide Dismutase/metabolism , Water Pollutants, Chemical/toxicity
14.
J Environ Monit ; 13(7): 1935-43, 2011 Jul.
Article in English | MEDLINE | ID: mdl-21655603

ABSTRACT

Prometryne is a selective herbicide of the s-triazine chemical family. Due to its weak absorption onto soil, it readily leaches down through the soil and contaminates underground water. Application of organic manure to soil has become a widespread practice as a disposal strategy to improve soil properties. In this study, we demonstrated the effect of pig manure compost (PMC) and lake-bed sludge (SL) on the sorption/desorption, mobility and bioavailability of prometryne in soil using comprehensive analysis approaches. Downward movement of prometryne was monitored in the packed soil column. Addition of PMC or SL decreased considerably the mobility and total concentration of prometryne in the soil leachate. Bioavailability analyses with wheat plants revealed that addition of the organic matter reduced accumulation of prometryne in tissues and increased plant elongation and biomass. These results indicate that the organic amendments are effective in modifying adsorption and mobility of the pesticide in soil.


Subject(s)
Herbicides/metabolism , Prometryne/metabolism , Soil Pollutants/metabolism , Adsorption , Environmental Monitoring , Geologic Sediments/chemistry , Herbicides/analysis , Kinetics , Manure , Prometryne/analysis , Soil/chemistry , Soil Pollutants/analysis
15.
Environ Toxicol Chem ; 30(3): 622-31, 2011 Mar.
Article in English | MEDLINE | ID: mdl-21298708

ABSTRACT

Rates of pesticide degradation in aquatic ecosystems often differ between those observed within laboratory studies and field trials. Under field conditions, a number of additional processes may well have a significant role, yet are excluded from standard laboratory studies, for example, metabolism by aquatic plants, phytoplankton, and periphyton. These constituents of natural aquatic ecosystems have been shown to be capable of metabolizing a range of crop protection products. Here we report the rate of degradation of six crop protection products assessed in parallel in three systems, under reproducible, defined laboratory conditions, designed to compare aquatic sediment systems which exclude macrophytes and algae against those in which macrophytes and/or algae are included. All three systems remained as close as possible to the Organisation for Economic Co-operation and Development (OECD) 308 guidelines, assessing degradation of parent compound in the total system in mass balanced studies using ((14) C) labeled compounds. We observed, in all cases where estimated, significant increases in the rate of degradation in both the algae and macrophyte systems when compared to the standard systems. By assessing total system degradation within closed, mass balanced studies, we have shown that rates of degradation are enhanced in water/sediment systems that include macrophytes and algae. The contribution of these communities should therefore be considered if the aquatic fate of pesticides is to be fully understood.


Subject(s)
Chlorophyta/metabolism , Pesticides/metabolism , Plants/metabolism , Water Pollutants, Chemical/metabolism , Benzamides/analysis , Benzamides/metabolism , Biodegradation, Environmental , Dioxoles/analysis , Dioxoles/metabolism , Fresh Water/chemistry , Heterocyclic Compounds, 2-Ring/analysis , Heterocyclic Compounds, 2-Ring/metabolism , Hydrogen-Ion Concentration , Kinetics , Models, Chemical , Pesticides/analysis , Phenylurea Compounds/analysis , Phenylurea Compounds/metabolism , Photosynthesis/drug effects , Prometryne/analysis , Prometryne/metabolism , Pyrroles/analysis , Pyrroles/metabolism , Triazoles/analysis , Triazoles/metabolism , Water Pollutants, Chemical/analysis
16.
Pest Manag Sci ; 63(3): 254-60, 2007 Mar.
Article in English | MEDLINE | ID: mdl-17245693

ABSTRACT

A novel bacterial strain FJ1117YT was isolated from an enrichment culture with the herbicide simetryn. The isolate was capable of degrading the herbicide supplied as the sole sulfur source in an aquatic batch culture. The strain FJ1117YT was identified as that belonging to Rhodococcus sp. on the basis of comparative morphology, physiological characteristics and comparison of the 16S rRNA gene sequence. The biodegradation pathway of simetryn was established by isolating the methylsulfinyl analogue as the first metabolite and by identification of the methylsulfonyl intermediate and the hydroxy analogue by liquid chromatography-mass spectrometry (LC-MS) and/or nuclear magnetic resonance (NMR) analysis. The results indicate that the methylthio group was progressively oxidised and hydrolysed by the strain FJ1117YT. The same strain is also able to metabolise other methylthio-s-triazines such as ametryn, desmetryn, dimethametryn and prometryn through similar pathways.


Subject(s)
Herbicides/metabolism , Rhodococcus/metabolism , Triazines/metabolism , Biodegradation, Environmental , Chromatography, Liquid , Herbicides/chemistry , Ions/chemistry , Mass Spectrometry , Nuclear Magnetic Resonance, Biomolecular , Oxidation-Reduction , Prometryne/chemistry , Prometryne/metabolism , RNA, Ribosomal, 16S/classification , RNA, Ribosomal, 16S/genetics , Rhodococcus/classification , Rhodococcus/genetics , Sulfates/chemistry , Triazines/chemistry , Vitamins/chemistry
17.
Environ Sci Technol ; 38(23): 6353-62, 2004 Dec 01.
Article in English | MEDLINE | ID: mdl-15597892

ABSTRACT

The effect of a mixture of 10 compounds, which have previously been identified in an effect-directed analysis as potentially relevant for a specific contaminated riverine sediment (Brack et al. Arch. Environ. Contam. Toxicol. 1999, 37, 164), were investigated for the underlying joint effect. Components identified in an organic sediment extract included several PAHs (benzo[ghi]fluoranthene, benz[a]anthracene, fluoranthene, pyrene, 2-phenylnaphthalene, anthracene, and phenanthrene) plus prometryn, N-phenyl-2-naphthylamine, and parathion-methyl. Experiments were performed using a one-generation algal bioassay with the unicellular green algae Scenedesmus vacuolatus as well as chlorophyll fluorescence quenching analysis to describe the effects of the components and mixtures thereof. Analysis of the mixture effects based on concentration-response modeling of the effect data reveals that indeed effect contributions of several components can be expected although the mixture ratio is not equitoxic and the individual components vary greatly with respect to biological effect. Comparing predicted and observed mixture effects, the combined effect may not be attributed to a joint narcotic effect of the mixture components. Evidently, some of the components act specifically and dissimilar and may therefore be best described in their combined effect by response addition while for others a similar mode of action seems plausible. Chlorophyll fluorescence quenching analysis supports to discriminate between prometryn, N-phenyl-2-naphthylamine, and PAHs. A joint model for calculating the combined effect using concentration addition for the suspected unspecifically acting components in algae (PAHs and parathion-methyl) and subsequently response addition for this group and the other components clearly improves the description of the observed combined effect. Allocation of effect contributions to specific components using toxic units or effect contributions lead to different judgments. The observed combined effect of a 3-compound mixture of prometryn, N-phenyl-2-naphthylamine, and benzo[ghi]fluoranthene is indistinguishable from the effects of the original 10-compound mixture, demonstrating the need in site-specific assessment of complex contamination to account for the mode of action of contaminants. Implications forthe confirmation step in effect-directed analysis of substances causing effects in complex contaminated samples are discussed.


Subject(s)
2-Naphthylamine/analogs & derivatives , Environmental Pollutants/toxicity , Geologic Sediments/analysis , Herbicides/toxicity , Polycyclic Aromatic Hydrocarbons/toxicity , Scenedesmus/drug effects , 2-Naphthylamine/metabolism , 2-Naphthylamine/toxicity , Biological Assay , Complex Mixtures , Drug Interactions , Environmental Pollutants/metabolism , Fluorenes/metabolism , Fluorenes/toxicity , Geologic Sediments/chemistry , Models, Biological , No-Observed-Adverse-Effect Level , Polycyclic Aromatic Hydrocarbons/metabolism , Prometryne/metabolism , Prometryne/toxicity , Regression Analysis , Scenedesmus/physiology , Spectrometry, Fluorescence/methods
18.
J Assoc Off Anal Chem ; 68(4): 750-3, 1985.
Article in English | MEDLINE | ID: mdl-4030649

ABSTRACT

Residue analysis of the herbicide prometryn (2,4-bis(isopropylamino)-6-methylthio-1,3,5-triazine) is widely known, but an analytical method for determining its metabolities or degradation products in addition to the parent chemical has not yet been reported in the literature. The procedure reported here is for the extraction and determination of prometryn and 2 metabolites, 2-amino-4-isopropylamino-6-methyl-thio-1,3,5-triazine and 2,4-diamino-6-methylthio-1,3,5-triazine, in parsley. Crops were extracted with 2-propanol followed by concentration of the extract and partitioning with a minimum amount of hexane in the presence of a large excess of water to remove most of the green pigment. The aqueous phase was divided into 2 equal halves: (A) One-half portion was partitioned with dichloromethane in the presence of saturated sodium chloride solution, the dichloromethane phase was separated, and the aqueous phase was discarded. The organic solvent was evaporated, and the contents were reconstituted in petroleum ether before prometryn analysis. (B) The other half was made slightly alkaline with ammonium hydroxide solution and was partitioned with ethyl acetate in the presence of saturated sodium chloride solution. The ethyl acetate phase was concentrated, centrifuged to remove any turbidity, and analyzed for the 2 metabolities above. Fused silica capillary gas chromatography (GC) with nitrogen-phosphorus (N-P) detection was used for quantitation. The limit of detection was 0.05 mg/kg for all the compounds examined. Recoveries from fortified parsley samples ranged from 59 to 73% at fortification levels of 0.05 to 1.0 mg/kg.


Subject(s)
Herbicides/analysis , Plants/analysis , Prometryne/analysis , Biodegradation, Environmental , Chromatography, Gas , Dealkylation , Indicators and Reagents , Pesticide Residues/analysis , Prometryne/metabolism
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