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Effect-directed identification of novel aryl hydrocarbon receptor-active aromatic compounds in coastal sediments collected from a highly industrialized area

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dc.contributor.authorGwak, Jiyun-
dc.contributor.authorCha, Jihyun-
dc.contributor.authorLee, Junghyun-
dc.contributor.authorKim, Youngnam-
dc.contributor.authorAn, Seong-Ah-
dc.contributor.authorLee, Sunggyu-
dc.contributor.authorMoon, Hyo-Bang-
dc.contributor.authorHur, Jin-
dc.contributor.authorGiesy, John P.-
dc.contributor.authorHong, Seongjin-
dc.contributor.authorKhim, Jong Seong-
dc.date.accessioned2022-07-18T01:22:44Z-
dc.date.available2022-07-18T01:22:44Z-
dc.date.issued2022-01-
dc.identifier.issn0048-9697-
dc.identifier.issn1879-1026-
dc.identifier.urihttps://scholarworks.bwise.kr/erica/handle/2021.sw.erica/108040-
dc.description.abstractIn this study, we identified major aryl hydrocarbon receptor (AhR) agonists in the sediments from Yeongil Bay (n = 6) using effect-directed analysis. Using the H4IIE-luc bioassays, great AhR-mediated potencies were found in aro-matic fractions (F2) of sediment organic extracts from silica gel column chromatography and sub-fractions (F2.6- F2.8) from reverse phase-HPLC. Full-scan mass spectrometric analysis using GC-QTOFMS was conducted to identify novel AhR agonists in highly potent fractions, such as F2.6-F2.8 of S1 (Gumu Creek). Selection criteria for AhR-active compounds consisted of three steps, including matching factor of NIST library (>_70), aromatic structures, and the number of aromatic rings (>_4). Fifty-nine compounds were selected as tentative AhR agonist candidates, with the AhR-mediated activity being assessed for six compounds for which standard materials were available commercially. Of these compounds, 20-methylcholanthrene, 7-methylbenz[a]anthracene, 10-methylbenz[a]pyrene, and 7,12-dimethylbenz[a]anthracene exhibited significant AhR-mediated potency. Relative potency values of these com-pounds were determined relative to benzo[a]pyrene to be 3.2, 1.4, 1.2, and 0.2, respectively. EPA positive matrix fac-torization modeling indicated that the sedimentary AhR-active aromatic compounds primarily originated from coal combustion and vehicle emissions. Potency balance analysis indicated that four novel AhR agonists explained 0.007% to 1.7% of bioassay-derived AhR-mediated potencies in samples. (c) 2021 Elsevier B.V. All rights reserved.-
dc.format.extent9-
dc.language영어-
dc.language.isoENG-
dc.publisherELSEVIER-
dc.titleEffect-directed identification of novel aryl hydrocarbon receptor-active aromatic compounds in coastal sediments collected from a highly industrialized area-
dc.typeArticle-
dc.publisher.location네델란드-
dc.identifier.doi10.1016/j.scitotenv.2021.149969-
dc.identifier.scopusid2-s2.0-85113943362-
dc.identifier.wosid000709082400004-
dc.identifier.bibliographicCitationSCIENCE OF THE TOTAL ENVIRONMENT, v.803, pp 1 - 9-
dc.citation.titleSCIENCE OF THE TOTAL ENVIRONMENT-
dc.citation.volume803-
dc.citation.startPage1-
dc.citation.endPage9-
dc.type.docTypeArticle-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaEnvironmental Sciences & Ecology-
dc.relation.journalWebOfScienceCategoryEnvironmental Sciences-
dc.subject.keywordPlusRESOLUTION MASS-SPECTROMETRY-
dc.subject.keywordPlusIN-SILICO MODELS-
dc.subject.keywordPlusDIOXIN-LIKE-
dc.subject.keywordPlusRELATIVE POTENCIES-
dc.subject.keywordPlusSOURCE APPORTIONMENT-
dc.subject.keywordPlusHOUSEHOLD DUST-
dc.subject.keywordPlusPAHS-
dc.subject.keywordPlusWATER-
dc.subject.keywordPlusOIL-
dc.subject.keywordPlusMARINE-
dc.subject.keywordAuthorAryl hydrocarbon receptor-
dc.subject.keywordAuthorH4IIE-luc bioassay-
dc.subject.keywordAuthorGC-QTOFMS-
dc.subject.keywordAuthorFull-scan screening analysis-
dc.subject.keywordAuthorIndustrial area-
dc.identifier.urlhttps://www.sciencedirect.com/science/article/pii/S0048969721050440?via%3Dihub-
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ERICA 공학대학 (ERICA 해양융합공학과)
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