Fungicide isopyrazam degradative response toward extrinsically added fungal and bacterial strains.
bacteria
biodegradation
fungi
isopyrazam
pyrazole
Journal
Journal of basic microbiology
ISSN: 1521-4028
Titre abrégé: J Basic Microbiol
Pays: Germany
ID NLM: 8503885
Informations de publication
Date de publication:
Jun 2020
Jun 2020
Historique:
received:
27
01
2020
revised:
25
03
2020
accepted:
28
03
2020
pubmed:
22
4
2020
medline:
15
12
2020
entrez:
22
4
2020
Statut:
ppublish
Résumé
The current research is a pioneer in the evaluation of isopyrazam biodegradation, which has been performed utilizing soil-isolated microbes. Biodisintegrative assays of pure fungal strains, namely Aspergillus flavus (AF), Penicillium chrysogenum (PC), Aspergillus niger (AN), Aspergillus terreus (AT), and Aspergillus fumigatus (AFu), and bacterial strains, namely Xanthomonas axonopodis (XA) and Pseudomonas syringae (PS), were utilized. Initial isopyrazam concentration (10 mg/L) was prepared with an individual microbial suspension and monitored for 35 days. Isopyrazam biotransformation was analyzed quantitatively and qualitatively by UV-visible spectrophotometery and gas chromatography-mass spectroscopy. P. syringae (R
Identifiants
pubmed: 32314411
doi: 10.1002/jobm.201900687
doi:
Substances chimiques
3-(difluoromethyl)-1-methyl-N-(1,2,3,4-tetrahydro-9-isopropyl-1,4-methanonaphthalen-5-yl)pyrazole-4-carboxamide
0
Fungicides, Industrial
0
Norbornanes
0
Pyrazoles
0
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
484-493Informations de copyright
© 2020 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.
Références
Stammler G, Wolf A, Glaettli A, Klappach K. Respiration inhibitors: complex II. In: Ishii H, Hollomon DW, editors. Fungicide resistance in plant pathogens. Tokyo: Springer; 2015. p. 105-7.
Ahmad KS. Adsorption evaluation of herbicide iodosulfuron followed by Cedrus deodora sawdust-derived activated carbon removal. Soil Sed Contam Int J. 2018;28:65-80.
Ahmad KS. Arachis hypogaea activated carbon-assisted removal of 1-(4,6-dimethoxypyrimidin-2-yl)-3-(3-ethylsulfonylpyridin-2-yl) sulfonylurea herbicide in agriculturally adsorbed soils. Int J Environ Sci Technol. 2018;16:6247-58.
Ahmad KS. Sorption and Juglans regia-derived activated carbon-mediated removal of aniline-based herbicide alachlor from contaminated soils. Environ Earth Sci. 2018;77:437-45.
Ahmad KS. Evaluating the adsorption potential of alachlor and its subsequent removal from soils via activated carbon. Soil Sed Cont Int J. 2018;27:249-66.
Watanabe N, Horikoshi S, Kawasaki A, Hidaka H, Serpone N. Formation of refractory ring-expanded triazine intermediates during the photocatalyzed mineralization of the endocrine disruptor amitrole and related triazole derivatives at UV-irradiated TiO2/H2O interfaces. Environ Sci Technol. 2005;39:2320-6.
Ahmad KS. Exploring the potential of Juglans regia-derived activated carbon for the removal of adsorbed fungicide ethaboxam from soils. Environ Monit Assess. 2018;190:737-44.
Iftikhar S, Saleem M, Ahmad KS, Jaffri SB. Synergistic mycoflora-natural farming mediated biofertilization and heavy metals decontamination of lithospheric compartment in a sustainable mode via Helianthus annuus. Int J Environ Sci Technol. 2019;16:1-18.
Iftikhar S, Ahmad KS, Gul MM. Low-cost and environmental-friendly Triticum aestivum-derived biochar for improving plant growth and soil fertility. Commun Soil Sci Plant Anal. 2018;49:2814-27.
Gul MM, Ahmad KS. Chlorsulfuron degradation through bio-augmentation of soils by fungal strains and chemical hydrolysis. J Environ Chem Eng. 2018;6:955-63.
Cheng M, Yan X, He J, Qiu J, Chen Q. Comparative genome analysis reveals the evolution of chloroacetanilide herbicide mineralization in Sphingomonas wittichii DC-6. Arch Microbiol. 2019;201(907):18-918.
Pujar N, Laad S, Premakshi HG, Pattar SV, Mirjankar M, Kamanavalli CM. Biodegradation of phenmedipham by novel Ochrobactrum anthropi NC-1. 3Biotech. 2019;9:52.
Gugnani HC. Ecology and taxonomy of pathogenic aspergilli. Front Biosci. 2003;8:346-57.
Wild CP. Aflatoxin exposure in developing countries: the critical interface of agriculture and health. Food Nutr Bull. 2007;28:S372-S80.
Williams JH, Phillips TD, Jolly PE, Stiles JK, Jolly CM, Aggarwal D. Human aflatoxicosis in developing countries: a review of toxicology, exposure, potential health consequences, and interventions. Am J Clin Nutr. 2004;80:1106-22.
Wasylnka JA, Moore MM. Aspergillus fumigatus conidia survive and germinate in acidic organelles of A549 epithelial cells. J Cell Sci. 2003;116:1579-87.
Sugui JA, Pardo J, Chang YC, Müllbacher A, Zarember KA, Galvez EM, et al. Role of laeA in the regulation of alb1, gliP, conidial morphology, and virulence in Aspergillus fumigatus. Eukaryot Cell. 2007;6:1552-61.
Afiyatullov SS, Zhuravleva OI, Chaikina EL, Anisimov MM. A new spirotryprostatin from the marine isolate of the fungus Aspergillus fumigatus. Chem Nat Compd. 2012;48:95-8.
Amin R, Dupuis A, Aaron SD, Ratjen F. The effect of chronic infection with Aspergillus fumigatus on lung function and hospitalization in patients with cystic fibrosis. Chest J. 2010;137:171-6.
Al Hosni AS, Pittman JK, Robson GD. Microbial degradation of four biodegradable polymers in soil and compost demonstrating polycaprolactone as an ideal compostable plastic. Waste Manag. 2019;97:105-14.
Bignell E. Aspergillus: Molecular Biology and Genomics. In: Machida M, Gomi K, editors. Biotechnology Journal. 5 Horizon Scientific Press; 2010. p. 336-7.
Riba A, Bouras N, Mokrane S, Mathieu F, Lebrihi A, Sabaou N. Aspergillus section Flavi and aflatoxins in Algerian wheat and derived products. Food Chem Toxicol. 2010;48:2772-7.
Lewis MH, Carbone I, Luis JM, Payne GA, Bowen KL, Hagan AK, et al. Biocontrol strains differentially shift the genetic structure of indigenous soil populations of Aspergillus flavus. Front Microbiol. 2019;10:1738.
Doster MA, Cotty PJ, Michailides TJ. Evaluation of the atoxigenic Aspergillus flavus strain AF36 in pistachio orchards. Plant Dis. 2014;98:948-56.
Hasanin MS, Darwesh OM, Matter IA, El-Saie H. Isolation and characterization of non-cellulolytic Aspergillus flavus EGYPTA5 exhibiting selective ligninolytic potential. Biocatal Agric Biotechnol. 2019;17:160-7.
Perera M, Wijayarathna D, Wijesundera, Chinthaka M, Seneviratne G, Jayasena S. Biofilm mediated synergistic degradation of hexadecane by a naturally formed community comprising Aspergillus flavus complex and Bacillus cereus group. BMC Microbiol. 2019;19:19-84.
Pitt JI, Hocking AD. Fungi and food spoilage. New York, NY: Springer; 2009.
Tolouee M, Alinezhad S, Saberi R, Eslamifar A, Zad SJ, Jaimand K, et al. Effect of Matricaria chamomilla L. flower essential oil on the growth and ultrastructure of Aspergillus niger van Tieghem. Int J Food Microbiol. 2010;139:127-13.
Samson RA, Hockstra ES, Frisvad JC, Filtenborg O Introduction to food and airborne fungi. The Netherlands: Centaalbureau Voorschimmelculturs-Utrecht Ponson & Looyen; 2000.
Lass-Flörl C. Treatment of infections due to Aspergillus terreus species complex. J Fungi. 2018;4:83.
Ullmann AJ, Aguado JM, Arikan-Akdagli S, Denning DW, Groll AH, Lagrou K, et al. Diagnosis and management of Aspergillus diseases: executive summary of the 2017 ESCMID-ECMM-ERS guideline. Clin Microbiol Infection. 2018;24:e1-e38.
Ahmad KS. Environmental contaminant 2-chloro-N-(2,6-diethylphenyl)-N-(methoxymethyl) acetamide remediation via Xanthomonas axonopodis and Aspergillus niger. Environ Res. 2020;182:109117.
Naeem H, Ahmad KS, Gul MM. Agrochemical 2-chloro-2',6'-diethyl-N-methoxymethylacetanilide tranformative and sorptive demeanor in agriculturally significant pedospheric environs. Int J Environ Anal Chem. 2020. 1-20. https://doi.org/10.1080/03067319.2019.1700965
Hand LH, Moreland HJ. Surface water mineralization of isopyrazam according to OECD 309: observations on implementation of the new data requirement within agrochemical regulation. Environ Toxicol Chem. 2014;33:516-24.
Zheng Z, Chen Y, Zhang S, Wang L, Qian X. Determination of isopyrazam residues and its degradation products in cucumber by gas chromatography. J Food Safety Qual. 2016;7:540-4.
Ortiz-Hernández ML, Sánchez-Salinas E, Dantán-González E, Castrejón-Godínez ML. Pesticide biodegradation: mechanisms, genetics and strategies to enhance the process. In: Chamy R, Rosenkranz F, editors. Biodegradation - Life of Science. 2013. p. 251-87.
Sondhia S, Rajput S, Varma RK, Kumar A. Biodegradation of the herbicide penoxsulam (triazolopyrimidine sulphonamide) by fungal strains of Aspergillus in soil. Appl Soil Ecol. 2016;105:196-206.
Sanyal D, Kulshrestha G. Degradation of metolachlor in crude extract of Aspergillus flavus. J Environ Sci Health B. 2004;39:653-64.
Tortella GR, Rubilar O, Castillo M, Cea M, Mella-Herrera R, Diez MC. Chlorpyrifos degradation in a biomixture of biobed at different maturity stages. Chemosphere. 2012;88:224-8.
El-Ghany A, Masmali IA. Fungal biodegradation of organophosphorus insecticides and their impact on soil microbial population. J Plant Pathol Microbiol. 2016;7:1-7.
Varga J, Rigó K, Teren J. Degradation of ochratoxin A by Aspergillus species. Int J Food Microbiol. 2000;59:1-7.
Abrunhosa L, Santos L, Venâncio A. Degradation of ochratoxin A by proteases and by a crude enzyme of Aspergillus niger. Food Biotechnol. 2006;20:231-42.
Mann R, Rehm HJ. Degradation products from aflatoxin B 1 by Corynebacterium rubrum, Aspergillus niger, Trichoderma viride and Mucor ambiguus. Eur J Appl Microbiol Biotechnol. 1976;2:297-306.
Doyle MP, Marth EH. Aflatoxin is degraded by mycelia from toxigenic and nontoxigenic strains of aspergilli grown on different substrates. Mycopathologia. 1978;63:145-53.
Hamid AB, Smith JE. Degradation of aflatoxin by Aspergillus flavus. Microbiology. 1987;133:2023-9.