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Article: Metabolic Engineering of Pseudomonas putida KT2440 for Complete Mineralization of Methyl Parathion and γ-Hexachlorocyclohexane

TitleMetabolic Engineering of Pseudomonas putida KT2440 for Complete Mineralization of Methyl Parathion and γ-Hexachlorocyclohexane
Authors
Keywordscomplete mineralization
methyl parathion
Pseudomonas putida KT2440
γ-hexachlorocyclohexane
Issue Date2016
Citation
ACS Synthetic Biology, 2016, v. 5, n. 5, p. 434-442 How to Cite?
AbstractAgricultural soils are often cocontaminated with multiple pesticides. Unfortunately, microorganisms isolated from natural environments do not possess the ability to simultaneously degrade different classes of pesticides. Currently, we can use the approaches of synthetic biology to create a strain endowed with various catabolic pathways that do not exist in a natural microorganism. Here, we describe the metabolic engineering of a biosafety Pseudomonas putida strain KT2440 for complete mineralization of methyl parathion (MP) and γ-hexachlorocyclohexane (γ-HCH) by functional assembly of the MP and γ-HCH mineralization pathways. The engineered strain was genetically stable, and no growth inhibition was observed. Such a strain not only would reduce the toxicity of MP and γ-HCH but also would prevent the accumulation of potentially toxic intermediates in the environment. Furthermore, expression of Vitreoscilla hemoglobin improved the ability of the engineered strain to sequester O2. The inoculation of the engineered strain to soils treated with MP and γ-HCH resulted in a higher degradation rate than in noninoculated soils. Moreover, introduced GFP may be used to monitor the activity of the engineered strain during bioremediation. The engineered strain may be a promising candidate for in situ bioremediation of soil cocontaminated with MP and γ-HCH.
Persistent Identifierhttp://hdl.handle.net/10722/352940
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorGong, Ting-
dc.contributor.authorLiu, Ruihua-
dc.contributor.authorZuo, Zhenqiang-
dc.contributor.authorChe, You-
dc.contributor.authorYu, Huilei-
dc.contributor.authorSong, Cunjiang-
dc.contributor.authorYang, Chao-
dc.date.accessioned2025-01-13T03:01:11Z-
dc.date.available2025-01-13T03:01:11Z-
dc.date.issued2016-
dc.identifier.citationACS Synthetic Biology, 2016, v. 5, n. 5, p. 434-442-
dc.identifier.urihttp://hdl.handle.net/10722/352940-
dc.description.abstractAgricultural soils are often cocontaminated with multiple pesticides. Unfortunately, microorganisms isolated from natural environments do not possess the ability to simultaneously degrade different classes of pesticides. Currently, we can use the approaches of synthetic biology to create a strain endowed with various catabolic pathways that do not exist in a natural microorganism. Here, we describe the metabolic engineering of a biosafety Pseudomonas putida strain KT2440 for complete mineralization of methyl parathion (MP) and γ-hexachlorocyclohexane (γ-HCH) by functional assembly of the MP and γ-HCH mineralization pathways. The engineered strain was genetically stable, and no growth inhibition was observed. Such a strain not only would reduce the toxicity of MP and γ-HCH but also would prevent the accumulation of potentially toxic intermediates in the environment. Furthermore, expression of Vitreoscilla hemoglobin improved the ability of the engineered strain to sequester O2. The inoculation of the engineered strain to soils treated with MP and γ-HCH resulted in a higher degradation rate than in noninoculated soils. Moreover, introduced GFP may be used to monitor the activity of the engineered strain during bioremediation. The engineered strain may be a promising candidate for in situ bioremediation of soil cocontaminated with MP and γ-HCH.-
dc.languageeng-
dc.relation.ispartofACS Synthetic Biology-
dc.subjectcomplete mineralization-
dc.subjectmethyl parathion-
dc.subjectPseudomonas putida KT2440-
dc.subjectγ-hexachlorocyclohexane-
dc.titleMetabolic Engineering of Pseudomonas putida KT2440 for Complete Mineralization of Methyl Parathion and γ-Hexachlorocyclohexane-
dc.typeArticle-
dc.description.naturelink_to_subscribed_fulltext-
dc.identifier.doi10.1021/acssynbio.6b00025-
dc.identifier.pmid26854500-
dc.identifier.scopuseid_2-s2.0-84973160909-
dc.identifier.volume5-
dc.identifier.issue5-
dc.identifier.spage434-
dc.identifier.epage442-
dc.identifier.eissn2161-5063-
dc.identifier.isiWOS:000376476900008-

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