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Insights into the microbial degradation pathways of the ioxynil octanoate herbicide

dc.contributor.authorOliveira, Karina O. [UNESP]
dc.contributor.authorSilva, Amanda R.M.
dc.contributor.authorda Silva, Bianca F. [UNESP]
dc.contributor.authorMilagre, Humberto M.S. [UNESP]
dc.contributor.authorMilagre, Cintia D.F. [UNESP]
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.contributor.institutionUniversidade de São Paulo (USP)
dc.date.accessioned2018-12-11T16:51:48Z
dc.date.available2018-12-11T16:51:48Z
dc.date.issued2018-01-01
dc.description.abstractThis paper describes the biodegradation of the ioxynil octanoate herbicide by indigenous microorganisms isolated from herbicide impacted soil-enrichment cultures. Eleven positive hits out of twenty-nine microorganisms screened for nitrile hydratase, nitrilase and amidase activity were further evaluated based on their growth in microtiter plates containing liquid medium with increasing concentrations of herbicide (0.97–250 mM). Two strains were selected from this assay for biodegradation studies and were identified as Lysinibacillus boronitolerans MLH-31 and Bacillus cereus MLH-61. The bacterial degradation of ioxynil octanoate and its biodegradation products were monitored, identified and characterized by liquid chromatography tandem mass spectrometry (HPLC-MS/MS). In addition to 3,5-diiodo-4-hydroxybenzamide and 3,5-diiodo-4-hydroxybenzoic acid, which are commonly detected metabolites, two new metabolites were observed: mono-deiodinated compound 3-iodo-4-hydroxybenzoic acid and the product of Caromatic-CN cleaved 1,3-diiodophenol. The experimentally observed metabolites were correlated with the enzymatic systems involved, revealing the presence of esterases, nitrile hydratases, amidases, nitrilases, dehalogenases and carbon-carbon lyases during biodegradation. Lysinibacillus boronitolerans MLH-31 was found to degrade ioxynil octanoate at a rate of 97% over 7 days through a batch-resting cells experiment, while Bacillus cereus MLH-61 was found to do so at a rate of 75% under the same conditions.en
dc.description.affiliationUNESP – São Paulo State University Institute of Chemistry
dc.description.affiliationUSP – University of São Paulo Institute of Chemistry
dc.description.affiliationUnespUNESP – São Paulo State University Institute of Chemistry
dc.description.sponsorshipConselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)
dc.description.sponsorshipIdCNPq: 384996/2012-4
dc.description.sponsorshipIdCNPq: 560682/2010-7
dc.format.extent258-264
dc.identifierhttp://dx.doi.org/10.1016/j.bcab.2018.01.002
dc.identifier.citationBiocatalysis and Agricultural Biotechnology, v. 13, p. 258-264.
dc.identifier.doi10.1016/j.bcab.2018.01.002
dc.identifier.file2-s2.0-85041634880.pdf
dc.identifier.issn1878-8181
dc.identifier.lattes1425748916849376
dc.identifier.orcid0000-0001-5627-8616
dc.identifier.scopus2-s2.0-85041634880
dc.identifier.urihttp://hdl.handle.net/11449/170638
dc.language.isoeng
dc.relation.ispartofBiocatalysis and Agricultural Biotechnology
dc.relation.ispartofsjr0,479
dc.rights.accessRightsAcesso abertopt
dc.sourceScopus
dc.subjectAmidase
dc.subjectBiodegradation
dc.subjectCarbon-carbon lyase
dc.subjectDehalogenase
dc.subjectIoxynil octanoate
dc.subjectNitrilase
dc.subjectNitrile hydratase
dc.titleInsights into the microbial degradation pathways of the ioxynil octanoate herbicideen
dc.typeArtigopt
dspace.entity.typePublication
relation.isOrgUnitOfPublicationbc74a1ce-4c4c-4dad-8378-83962d76c4fd
relation.isOrgUnitOfPublication.latestForDiscoverybc74a1ce-4c4c-4dad-8378-83962d76c4fd
unesp.author.lattes1425748916849376[5]
unesp.author.orcid0000-0001-5627-8616[5]
unesp.campusUniversidade Estadual Paulista (UNESP), Instituto de Química, Araraquarapt

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