Penicillium griseofulvum F1959, high-production strain of pyripyropene A, specific inhibitor of Acyl-CoA: cholesterol acyltransferase 2

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dc.contributor.authorJung Ho Choi-
dc.contributor.authorMun Chual Rho-
dc.contributor.authorSeung Woong Lee-
dc.contributor.authorJi Na Choi-
dc.contributor.authorHee Jeong Lee-
dc.contributor.authorKyung Sook Bae-
dc.contributor.authorK Kim-
dc.contributor.authorYoung Kook Kim-
dc.date.accessioned2017-04-19T09:11:59Z-
dc.date.available2017-04-19T09:11:59Z-
dc.date.issued2008-
dc.identifier.issn1017-7825-
dc.identifier.urihttps://oak.kribb.re.kr/handle/201005/8649-
dc.description.abstractAcyl-coenzyme A: cholesterol acyltransferase (ACAT) catalyzes cholesterol esterification and plays an important role in the intestinal absorption of cholesterol, hepatic production of lipoproteins, and accumulation of cholesteryl ester within cells. During the course of screening to find ACAT inhibitors from microbial sources, the present authors isolated pyripyropene A from Penicillium griseofulvum F1959. Pyripyropene A, an ACAT2-specific inhibitor, has already been produced from Aspergillus fumigatus. Yet, Aspergillus fumigatus is a pathogen and only produces a limited amount of pyripyropene A, making the isolation of pyripyropene A troublesome. In contrast, Penicillium griseofulvum F1959 was found to produce approximately 28 times more pyripyropene A than Aspergillus fumigatus, plus this report also describes the ideal conditions for the production of pyripyropene A by Penicillium griseofulvum F1959 and its subsequent purification.-
dc.publisherKorea Soc-Assoc-Inst-
dc.titlePenicillium griseofulvum F1959, high-production strain of pyripyropene A, specific inhibitor of Acyl-CoA: cholesterol acyltransferase 2-
dc.title.alternativePenicillium griseofulvum F1959, high-production strain of pyripyropene A, specific inhibitor of Acyl-CoA: cholesterol acyltransferase 2-
dc.typeArticle-
dc.citation.titleJournal of Microbiology and Biotechnology-
dc.citation.number10-
dc.citation.endPage1665-
dc.citation.startPage1663-
dc.citation.volume18-
dc.contributor.affiliatedAuthorJung Ho Choi-
dc.contributor.affiliatedAuthorMun Chual Rho-
dc.contributor.affiliatedAuthorSeung Woong Lee-
dc.contributor.affiliatedAuthorJi Na Choi-
dc.contributor.affiliatedAuthorHee Jeong Lee-
dc.contributor.affiliatedAuthorKyung Sook Bae-
dc.contributor.affiliatedAuthorYoung Kook Kim-
dc.contributor.alternativeName최정호-
dc.contributor.alternativeName노문철-
dc.contributor.alternativeName이승웅-
dc.contributor.alternativeName최지나-
dc.contributor.alternativeName이희정-
dc.contributor.alternativeName배경숙-
dc.contributor.alternativeName김관회-
dc.contributor.alternativeName김영국-
dc.identifier.bibliographicCitationJournal of Microbiology and Biotechnology, vol. 18, no. 10, pp. 1663-1665-
dc.subject.keywordacyl-coenzyme A-
dc.subject.keywordatherosclerosis-
dc.subject.keywordcholesterol acyltransferase (ACAT)-
dc.subject.keywordpenicillium griseofulvum F1959-
dc.subject.keywordpyripyropene A-
dc.subject.localacyl-coenzyme A-
dc.subject.localAcyl-coenzyme A: Cholesterol acyltransferase-
dc.subject.localatherosclerosis-
dc.subject.localAtherosclerosis-
dc.subject.localatheroclerosis-
dc.subject.localcholesterol acyltransferase (ACAT)-
dc.subject.localCholesterol acyltransferase-
dc.subject.localCholesterol acyltransferase (ACAT)-
dc.subject.localcholesterol acyltransferase-
dc.subject.localpenicillium griseofulvum F1959-
dc.subject.localPenicillium griseofulvum F1959-
dc.subject.localpyripyropene A-
dc.subject.localPyripyropene A-
dc.description.journalClassY-
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Jeonbuk Branch Institute > Functional Biomaterial Research Center > 1. Journal Articles
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