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Article: Engineering Pseudomonas putida KT2440 for simultaneous degradation of carbofuran and chlorpyrifos

TitleEngineering Pseudomonas putida KT2440 for simultaneous degradation of carbofuran and chlorpyrifos
Authors
Issue Date2016
Citation
Microbial Biotechnology, 2016, v. 9, n. 6, p. 792-800 How to Cite?
AbstractCurrently, chlorpyrifos (CP) and carbofuran are often applied together to control major agricultural pests in many developing countries, in most cases, they are simultaneously detected in agricultural soils. Some cost-effective techniques are required for the remediation of combined pollution caused by multiple pesticides. In this work, we aim at constructing a detectable recombinant microorganism with the capacity to simultaneously degrade CP and carbofuran. To achieve this purpose, CP/carbofuran hydrolase genes and gfp were integrated into the chromosome of a biosafety strain Pseudomonas putida KT2440 using a chromosomal scarless modification strategy with upp as a counter-selectable marker. The toxicity of the hydrolysis products was significantly lower compared with the parent compounds. The recombinant strain could utilize CP or carbofuran as the sole source of carbon for growth. The inoculation of the recombinant strain to soils treated with carbofuran and CP resulted in a higher degradation rate than in noninoculated soils. Introduced green fluorescent protein can be employed as a biomarker to track the recombinant strain during bioremediation. Therefore, the recombinant strain has potential to be applied for in situ bioremediation of soil co-contaminated with carbofuran and CP.
Persistent Identifierhttp://hdl.handle.net/10722/352942
ISSN
2016 Impact Factor: 3.513
2023 SCImago Journal Rankings: 1.185
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorGong, Ting-
dc.contributor.authorLiu, Ruihua-
dc.contributor.authorChe, You-
dc.contributor.authorXu, Xiaoqing-
dc.contributor.authorZhao, Fengjie-
dc.contributor.authorYu, Huilei-
dc.contributor.authorSong, Cunjiang-
dc.contributor.authorLiu, Yanping-
dc.contributor.authorYang, Chao-
dc.date.accessioned2025-01-13T03:01:11Z-
dc.date.available2025-01-13T03:01:11Z-
dc.date.issued2016-
dc.identifier.citationMicrobial Biotechnology, 2016, v. 9, n. 6, p. 792-800-
dc.identifier.issn1751-7907-
dc.identifier.urihttp://hdl.handle.net/10722/352942-
dc.description.abstractCurrently, chlorpyrifos (CP) and carbofuran are often applied together to control major agricultural pests in many developing countries, in most cases, they are simultaneously detected in agricultural soils. Some cost-effective techniques are required for the remediation of combined pollution caused by multiple pesticides. In this work, we aim at constructing a detectable recombinant microorganism with the capacity to simultaneously degrade CP and carbofuran. To achieve this purpose, CP/carbofuran hydrolase genes and gfp were integrated into the chromosome of a biosafety strain Pseudomonas putida KT2440 using a chromosomal scarless modification strategy with upp as a counter-selectable marker. The toxicity of the hydrolysis products was significantly lower compared with the parent compounds. The recombinant strain could utilize CP or carbofuran as the sole source of carbon for growth. The inoculation of the recombinant strain to soils treated with carbofuran and CP resulted in a higher degradation rate than in noninoculated soils. Introduced green fluorescent protein can be employed as a biomarker to track the recombinant strain during bioremediation. Therefore, the recombinant strain has potential to be applied for in situ bioremediation of soil co-contaminated with carbofuran and CP.-
dc.languageeng-
dc.relation.ispartofMicrobial Biotechnology-
dc.titleEngineering Pseudomonas putida KT2440 for simultaneous degradation of carbofuran and chlorpyrifos-
dc.typeArticle-
dc.description.naturelink_to_subscribed_fulltext-
dc.identifier.doi10.1111/1751-7915.12381-
dc.identifier.pmid27418102-
dc.identifier.scopuseid_2-s2.0-84978766161-
dc.identifier.volume9-
dc.identifier.issue6-
dc.identifier.spage792-
dc.identifier.epage800-
dc.identifier.eissn1751-7915-
dc.identifier.isiWOS:000387000900009-

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