Inhibition of diacylglycerol acyltransferase by phenylpyropenes produced by Penicillium griseofulvum F1959

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dc.contributor.authorSeung Woong Lee-
dc.contributor.authorMun Chual Rho-
dc.contributor.authorJung Ho Choi-
dc.contributor.authorK Kim-
dc.contributor.authorY S Choi-
dc.contributor.authorHyun Sun Lee-
dc.contributor.authorYoung Kook Kim-
dc.date.accessioned2017-04-19T09:12:23Z-
dc.date.available2017-04-19T09:12:23Z-
dc.date.issued2008-
dc.identifier.issn1017-7825-
dc.identifier.uri10.4014/jmb.0800.079ko
dc.identifier.urihttps://oak.kribb.re.kr/handle/201005/8728-
dc.description.abstractA bacterium designated strain BD-a59, able to degrade all six benzene, toluene, ethylbenzene, and o-, m-, and p-xylene (BTEX) compounds, was isolated by plating gasoline-contaminated sediment from a gasoline station in Geoje, Republic of Korea, without enrichment, on minimal salts basal (MSB) agar containing 0.01% yeast extract, with BTEX as the sole carbon and energy source. Taxonomic analyses showed that the isolate belonged to Pseudoxanthomonas spadix, and until now, the genus Pseudoxanthomonas has not included any known BTEX degraders. The BTEX biodegradation rate was very low in MSB broth, but adding a small amount of yeast extract greatly enhanced the biodegradation. Interestingly, degradation occurred very quickly in slurry systems amended with sterile soil solids but not with aqueous soil extract. Moreover, if soil was combusted first to remove organic matter, the enhancement effect on BTEX biodegradation was lost, indicating that some components of insoluble organic compounds are nutritionally beneficial for BTEX degradation. Reverse transcriptase PCR-based analysis of field-fixed mRNA revealed expression of the tmoA gene, whose sequence was closely related to that carried by strain BD-a59. This study suggests that strain BD-a59 has the potential to assist in BTEX biodegradation at contaminated sites.-
dc.publisherKorea Soc-Assoc-Inst-
dc.titleInhibition of diacylglycerol acyltransferase by phenylpyropenes produced by Penicillium griseofulvum F1959-
dc.title.alternativeInhibition of diacylglycerol acyltransferase by phenylpyropenes produced by Penicillium griseofulvum F1959-
dc.typeArticle-
dc.citation.titleJournal of Microbiology and Biotechnology-
dc.citation.number11-
dc.citation.endPage1788-
dc.citation.startPage1785-
dc.citation.volume18-
dc.contributor.affiliatedAuthorSeung Woong Lee-
dc.contributor.affiliatedAuthorMun Chual Rho-
dc.contributor.affiliatedAuthorJung Ho Choi-
dc.contributor.affiliatedAuthorHyun Sun Lee-
dc.contributor.affiliatedAuthorYoung Kook Kim-
dc.contributor.alternativeName이승웅-
dc.contributor.alternativeName노문철-
dc.contributor.alternativeName최정호-
dc.contributor.alternativeName김관회-
dc.contributor.alternativeName최용석-
dc.contributor.alternativeName이현선-
dc.contributor.alternativeName김영국-
dc.identifier.bibliographicCitationJournal of Microbiology and Biotechnology, vol. 18, no. 11, pp. 1785-1788-
dc.identifier.doi10.4014/jmb.0800.079-
dc.subject.keywordDiacylglycerol acyltransferase (DGAT)-
dc.subject.keywordHepG2 cell-
dc.subject.keywordPenicillium griseofulvum F1959-
dc.subject.keywordPhenylpyropene-
dc.subject.keywordTriglyceride-
dc.subject.localdiacylglycerol acyltransferase-
dc.subject.localdiacylglycerol acyltansferase (DGAT)-
dc.subject.localDiacylglycerol acyltransferase-
dc.subject.localDiacylglycerol acyltransferase (DGAT)-
dc.subject.localHepG2 cells-
dc.subject.localHepG2 cell-
dc.subject.localpenicillium griseofulvum F1959-
dc.subject.localPenicillium griseofulvum F1959-
dc.subject.localPhenylpyropene-
dc.subject.localtriglyceride-
dc.subject.localTriglycerides-
dc.subject.localTriglyceride-
dc.subject.localtriglyceride (TG)-
dc.description.journalClassY-
Appears in Collections:
Jeonbuk Branch Institute > Functional Biomaterial Research Center > 1. Journal Articles
Ochang Branch Institute > Natural Product Research Center > 1. Journal Articles
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