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Kinetic Study of the Biodegradation of Acephate by Indigenous Soil Bacterial Isolates in the Presence of Humic Acid and Metal Ions

Many bacteria have the potential to use specific pesticides as a source of carbon, phosphorous, nitrogen and sulphur. Acephate degradation by microbes is considered to be a safe and effective method. The overall aim of the present study was to identify acephate biodegrading microorganisms and to inv...

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Autores principales: Singh, Simranjeet, Kumar, Vijay, Singla, Sourav, Sharma, Minaxi, Singh, Dhananjaya P., Prasad, Ram, Thakur, Vijay Kumar, Singh, Joginder
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7175145/
https://www.ncbi.nlm.nih.gov/pubmed/32168777
http://dx.doi.org/10.3390/biom10030433
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author Singh, Simranjeet
Kumar, Vijay
Singla, Sourav
Sharma, Minaxi
Singh, Dhananjaya P.
Prasad, Ram
Thakur, Vijay Kumar
Singh, Joginder
author_facet Singh, Simranjeet
Kumar, Vijay
Singla, Sourav
Sharma, Minaxi
Singh, Dhananjaya P.
Prasad, Ram
Thakur, Vijay Kumar
Singh, Joginder
author_sort Singh, Simranjeet
collection PubMed
description Many bacteria have the potential to use specific pesticides as a source of carbon, phosphorous, nitrogen and sulphur. Acephate degradation by microbes is considered to be a safe and effective method. The overall aim of the present study was to identify acephate biodegrading microorganisms and to investigate the degradation rates of acephate under the stress of humic acid and most common metal ions Fe(III) and copper Cu(II). Pseudomonas azotoformanss strain ACP1, Pseudomonas aeruginosa strain ACP2, and Pseudomonas putida ACP3 were isolated from acephate contaminated soils. Acephate of concentration 100 ppm was incubated with separate strain inoculums and periodic samples were drawn for UV—visible, FTIR (Fourier-transform infrared spectroscopy) and MS (Mass Spectrometry) analysis. Methamidophos, S-methyl O-hydrogen phosphorothioamidate, phosphenothioic S-acid, and phosphenamide were the major metabolites formed during the degradation of acephate. The rate of degradation was applied using pseudo-first-order kinetics to calculate the half-life (t(1/2)) values, which were 14.33–16.72 d(−1) (strain(s) + acephate), 18.81–21.50 d(−1) (strain(s) + acephate + Cu(II)), 20.06 –23.15 d(−1) (strain(s) + acephate + Fe(II)), and 15.05–17.70 d(−1) (strains + acephate + HA). The biodegradation efficiency of the three bacterial strains can be ordered as P. aeruginosa > P. putida > P. azotoformans. The present study illustrated the decomposition mechanism of acephate under different conditions, and the same may be applied to the removal of other xenobiotic compounds.
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spelling pubmed-71751452020-04-28 Kinetic Study of the Biodegradation of Acephate by Indigenous Soil Bacterial Isolates in the Presence of Humic Acid and Metal Ions Singh, Simranjeet Kumar, Vijay Singla, Sourav Sharma, Minaxi Singh, Dhananjaya P. Prasad, Ram Thakur, Vijay Kumar Singh, Joginder Biomolecules Article Many bacteria have the potential to use specific pesticides as a source of carbon, phosphorous, nitrogen and sulphur. Acephate degradation by microbes is considered to be a safe and effective method. The overall aim of the present study was to identify acephate biodegrading microorganisms and to investigate the degradation rates of acephate under the stress of humic acid and most common metal ions Fe(III) and copper Cu(II). Pseudomonas azotoformanss strain ACP1, Pseudomonas aeruginosa strain ACP2, and Pseudomonas putida ACP3 were isolated from acephate contaminated soils. Acephate of concentration 100 ppm was incubated with separate strain inoculums and periodic samples were drawn for UV—visible, FTIR (Fourier-transform infrared spectroscopy) and MS (Mass Spectrometry) analysis. Methamidophos, S-methyl O-hydrogen phosphorothioamidate, phosphenothioic S-acid, and phosphenamide were the major metabolites formed during the degradation of acephate. The rate of degradation was applied using pseudo-first-order kinetics to calculate the half-life (t(1/2)) values, which were 14.33–16.72 d(−1) (strain(s) + acephate), 18.81–21.50 d(−1) (strain(s) + acephate + Cu(II)), 20.06 –23.15 d(−1) (strain(s) + acephate + Fe(II)), and 15.05–17.70 d(−1) (strains + acephate + HA). The biodegradation efficiency of the three bacterial strains can be ordered as P. aeruginosa > P. putida > P. azotoformans. The present study illustrated the decomposition mechanism of acephate under different conditions, and the same may be applied to the removal of other xenobiotic compounds. MDPI 2020-03-11 /pmc/articles/PMC7175145/ /pubmed/32168777 http://dx.doi.org/10.3390/biom10030433 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Singh, Simranjeet
Kumar, Vijay
Singla, Sourav
Sharma, Minaxi
Singh, Dhananjaya P.
Prasad, Ram
Thakur, Vijay Kumar
Singh, Joginder
Kinetic Study of the Biodegradation of Acephate by Indigenous Soil Bacterial Isolates in the Presence of Humic Acid and Metal Ions
title Kinetic Study of the Biodegradation of Acephate by Indigenous Soil Bacterial Isolates in the Presence of Humic Acid and Metal Ions
title_full Kinetic Study of the Biodegradation of Acephate by Indigenous Soil Bacterial Isolates in the Presence of Humic Acid and Metal Ions
title_fullStr Kinetic Study of the Biodegradation of Acephate by Indigenous Soil Bacterial Isolates in the Presence of Humic Acid and Metal Ions
title_full_unstemmed Kinetic Study of the Biodegradation of Acephate by Indigenous Soil Bacterial Isolates in the Presence of Humic Acid and Metal Ions
title_short Kinetic Study of the Biodegradation of Acephate by Indigenous Soil Bacterial Isolates in the Presence of Humic Acid and Metal Ions
title_sort kinetic study of the biodegradation of acephate by indigenous soil bacterial isolates in the presence of humic acid and metal ions
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7175145/
https://www.ncbi.nlm.nih.gov/pubmed/32168777
http://dx.doi.org/10.3390/biom10030433
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