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Enzymatic Synthesis of Anabolic Steroid Glycosides by Glucosyltransferase from Terribacillus sp. PAMC 23288

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dc.contributor.authorYu, Eun-Ji-
dc.contributor.authorYamaguchi, Tokutaro-
dc.contributor.authorLee, Joo-Ho-
dc.contributor.authorLim, A-Rang-
dc.contributor.authorLee, Jun Hyuck-
dc.contributor.authorPark, Hyun-
dc.contributor.authorOh, Tae-Jin-
dc.date.accessioned2021-08-31T04:46:46Z-
dc.date.available2021-08-31T04:46:46Z-
dc.date.created2021-06-19-
dc.date.issued2020-04-
dc.identifier.issn1017-7825-
dc.identifier.urihttps://scholar.korea.ac.kr/handle/2021.sw.korea/56765-
dc.description.abstractThe application of steroids has steadily increased thanks to their therapeutic effects. However, alternatives are required due their severe side effects; thus, studies on the activities of steroid derivatives are underway. Sugar derivatives of nandrolone, which is used to treat breast cancer, as well as cortisone and prednisone, which reduce inflammation, pain, and edema, are unknown. We linked O-glucose to nandrolone and testosterone using UDP-glucosyltransferase (UGT-1) and, then, tested their bioactivities in vitro. Analysis by NMR showed that the derivatives were 17 beta-nandrolone beta-D-glucose and 17 beta-testosterone beta-D-glucose, respectively. The viability was higher and cytotoxicity was evident in PC12 cells incubated with rotenone and, testosterone derivatives, compared to the controls. SH-SY5Y cells incubated with H2O2 and nandrolone derivatives remained viable and cytotoxicity was attenuated. Both derivatives enhanced neuronal protective effects and increased the amounts of cellular ATP.-
dc.languageEnglish-
dc.language.isoen-
dc.publisherKOREAN SOC MICROBIOLOGY & BIOTECHNOLOGY-
dc.subjectSYNAPTIC PLASTICITY-
dc.subjectSPECIAL-ISSUE-
dc.subjectOLDER MEN-
dc.subjectTESTOSTERONE-
dc.subjectESTROGEN-
dc.subjectESTRADIOL-
dc.subjectBRAIN-
dc.subjectGLYCOSYLATION-
dc.subjectGLUCOSIDES-
dc.subjectACTIVATION-
dc.titleEnzymatic Synthesis of Anabolic Steroid Glycosides by Glucosyltransferase from Terribacillus sp. PAMC 23288-
dc.typeArticle-
dc.contributor.affiliatedAuthorPark, Hyun-
dc.identifier.doi10.4014/jmb.1911.11057-
dc.identifier.scopusid2-s2.0-85084167140-
dc.identifier.wosid000530070400016-
dc.identifier.bibliographicCitationJOURNAL OF MICROBIOLOGY AND BIOTECHNOLOGY, v.30, no.4, pp.604 - 614-
dc.relation.isPartOfJOURNAL OF MICROBIOLOGY AND BIOTECHNOLOGY-
dc.citation.titleJOURNAL OF MICROBIOLOGY AND BIOTECHNOLOGY-
dc.citation.volume30-
dc.citation.number4-
dc.citation.startPage604-
dc.citation.endPage614-
dc.type.rimsART-
dc.type.docTypeArticle-
dc.identifier.kciidART002580575-
dc.description.journalClass1-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.description.journalRegisteredClasskci-
dc.relation.journalResearchAreaBiotechnology & Applied Microbiology-
dc.relation.journalResearchAreaMicrobiology-
dc.relation.journalWebOfScienceCategoryBiotechnology & Applied Microbiology-
dc.relation.journalWebOfScienceCategoryMicrobiology-
dc.subject.keywordPlusSYNAPTIC PLASTICITY-
dc.subject.keywordPlusSPECIAL-ISSUE-
dc.subject.keywordPlusOLDER MEN-
dc.subject.keywordPlusTESTOSTERONE-
dc.subject.keywordPlusESTROGEN-
dc.subject.keywordPlusESTRADIOL-
dc.subject.keywordPlusBRAIN-
dc.subject.keywordPlusGLYCOSYLATION-
dc.subject.keywordPlusGLUCOSIDES-
dc.subject.keywordPlusACTIVATION-
dc.subject.keywordAuthorTestosterone-
dc.subject.keywordAuthornandrolone-
dc.subject.keywordAuthorglucosylation-
dc.subject.keywordAuthorneuroprotective activity-
dc.subject.keywordAuthorrotenone-induced apoptosis-
dc.subject.keywordAuthorsteroid-
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