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Mineralization of the herbicide swep by a two-strain consortium and characterization of a new amidase for hydrolyzing swep
BACKGROUND: Swep is an excellent carbamate herbicide that kills weeds by interfering with metabolic processes and inhibiting cell division at the growth point. Due to the large amount of use, swep residues in soil and water not only cause environmental pollution but also accumulate through the food...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6945715/ https://www.ncbi.nlm.nih.gov/pubmed/31910844 http://dx.doi.org/10.1186/s12934-020-1276-9 |
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author | Zhang, Long Hang, Ping Zhou, Xiyi Dai, Chen He, Ziyi Jiang, Jiandong |
author_facet | Zhang, Long Hang, Ping Zhou, Xiyi Dai, Chen He, Ziyi Jiang, Jiandong |
author_sort | Zhang, Long |
collection | PubMed |
description | BACKGROUND: Swep is an excellent carbamate herbicide that kills weeds by interfering with metabolic processes and inhibiting cell division at the growth point. Due to the large amount of use, swep residues in soil and water not only cause environmental pollution but also accumulate through the food chain, ultimately pose a threat to human health. This herbicide is degraded in soil mainly by microbial activity, but no studies on the biotransformation of swep have been reported. RESULTS: In this study, a consortium consisting of two bacterial strains, Comamonas sp. SWP-3 and Alicycliphilus sp. PH-34, was enriched from a contaminated soil sample and shown to be capable of mineralizing swep. Swep was first transformed by Comamonas sp. SWP-3 to the intermediate 3,4-dichloroaniline (3,4-DCA), after which 3,4-DCA was mineralized by Alicycliphilus sp. PH-34. An amidase gene, designated as ppa, responsible for the transformation of swep into 3,4-DCA was cloned from strain SWP-3. The expressed Ppa protein efficiently hydrolyzed swep and a number of other structural analogues, such as propanil, chlorpropham and propham. Ppa shared less than 50% identity with previously reported arylamidases and displayed maximal activity at 30 °C and pH 8.6. Gly449 and Val266 were confirmed by sequential error prone PCR to be the key catalytic sites for Ppa in the conversion of swep. CONCLUSIONS: These results provide additional microbial resources for the potential remediation of swep-contaminated sites and add new insights into the catalytic mechanism of amidase in the hydrolysis of swep. |
format | Online Article Text |
id | pubmed-6945715 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-69457152020-01-09 Mineralization of the herbicide swep by a two-strain consortium and characterization of a new amidase for hydrolyzing swep Zhang, Long Hang, Ping Zhou, Xiyi Dai, Chen He, Ziyi Jiang, Jiandong Microb Cell Fact Research BACKGROUND: Swep is an excellent carbamate herbicide that kills weeds by interfering with metabolic processes and inhibiting cell division at the growth point. Due to the large amount of use, swep residues in soil and water not only cause environmental pollution but also accumulate through the food chain, ultimately pose a threat to human health. This herbicide is degraded in soil mainly by microbial activity, but no studies on the biotransformation of swep have been reported. RESULTS: In this study, a consortium consisting of two bacterial strains, Comamonas sp. SWP-3 and Alicycliphilus sp. PH-34, was enriched from a contaminated soil sample and shown to be capable of mineralizing swep. Swep was first transformed by Comamonas sp. SWP-3 to the intermediate 3,4-dichloroaniline (3,4-DCA), after which 3,4-DCA was mineralized by Alicycliphilus sp. PH-34. An amidase gene, designated as ppa, responsible for the transformation of swep into 3,4-DCA was cloned from strain SWP-3. The expressed Ppa protein efficiently hydrolyzed swep and a number of other structural analogues, such as propanil, chlorpropham and propham. Ppa shared less than 50% identity with previously reported arylamidases and displayed maximal activity at 30 °C and pH 8.6. Gly449 and Val266 were confirmed by sequential error prone PCR to be the key catalytic sites for Ppa in the conversion of swep. CONCLUSIONS: These results provide additional microbial resources for the potential remediation of swep-contaminated sites and add new insights into the catalytic mechanism of amidase in the hydrolysis of swep. BioMed Central 2020-01-07 /pmc/articles/PMC6945715/ /pubmed/31910844 http://dx.doi.org/10.1186/s12934-020-1276-9 Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Zhang, Long Hang, Ping Zhou, Xiyi Dai, Chen He, Ziyi Jiang, Jiandong Mineralization of the herbicide swep by a two-strain consortium and characterization of a new amidase for hydrolyzing swep |
title | Mineralization of the herbicide swep by a two-strain consortium and characterization of a new amidase for hydrolyzing swep |
title_full | Mineralization of the herbicide swep by a two-strain consortium and characterization of a new amidase for hydrolyzing swep |
title_fullStr | Mineralization of the herbicide swep by a two-strain consortium and characterization of a new amidase for hydrolyzing swep |
title_full_unstemmed | Mineralization of the herbicide swep by a two-strain consortium and characterization of a new amidase for hydrolyzing swep |
title_short | Mineralization of the herbicide swep by a two-strain consortium and characterization of a new amidase for hydrolyzing swep |
title_sort | mineralization of the herbicide swep by a two-strain consortium and characterization of a new amidase for hydrolyzing swep |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6945715/ https://www.ncbi.nlm.nih.gov/pubmed/31910844 http://dx.doi.org/10.1186/s12934-020-1276-9 |
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