Cofactor-Free Light-Driven Whole-Cell Cytochrome P450 Catalysis

Cited 74 time in webofscience Cited 67 time in scopus
  • Hit : 493
  • Download : 0
DC FieldValueLanguage
dc.contributor.authorPark, Jong Hyunko
dc.contributor.authorLee, Sahng-Hako
dc.contributor.authorCha, Gun Suko
dc.contributor.authorChoi, Dasomko
dc.contributor.authorNam, Dong-Heonko
dc.contributor.authorLee, Jaehyungko
dc.contributor.authorLee, Jung-Kulko
dc.contributor.authorYun, Chul-Hoko
dc.contributor.authorJeong, Kijunko
dc.contributor.authorPark, Chan-Beumko
dc.date.accessioned2015-04-08T05:12:53Z-
dc.date.available2015-04-08T05:12:53Z-
dc.date.created2015-03-19-
dc.date.created2015-03-19-
dc.date.created2015-03-19-
dc.date.issued2015-01-
dc.identifier.citationANGEWANDTE CHEMIE-INTERNATIONAL EDITION, v.54, no.3, pp.969 - 973-
dc.identifier.issn1433-7851-
dc.identifier.urihttp://hdl.handle.net/10203/195633-
dc.description.abstractCytochromes P450 can catalyze various regioselective and stereospecific oxidation reactions of non-functionalized hydrocarbons. Here, we have designed a novel light-driven platform for cofactor-free, whole-cell P450 photo-biocatalysis using eosin Y (EY) as a photosensitizer. EY can easily enter into the cytoplasm of Escherichia coli and bind specifically to the heme domain of P450. The catalytic turnover of P450 was mediated through the direct transfer of photoinduced electrons from the photosensitized EY to the P450 heme domain under visible light illumination. The photo-activation of the P450 catalytic cycle in the absence of cofactors and redox partners is successfully conducted using many bacterial P450s (variants of P450 BM3) and human P450s (CYPs 1A1, 1A2, 1B1, 2A6, 2E1, and 3A4) for the bioconversion of different substrates, including marketed drugs (simvastatin, lovastatin, and omeprazole) and a steroid (17 beta-estradiol), to demonstrate the general applicability of the light-driven, cofactor-free system.-
dc.languageEnglish-
dc.publisherWILEY-V C H VERLAG GMBH-
dc.titleCofactor-Free Light-Driven Whole-Cell Cytochrome P450 Catalysis-
dc.typeArticle-
dc.identifier.wosid000348372200044-
dc.identifier.scopusid2-s2.0-84920771048-
dc.type.rimsART-
dc.citation.volume54-
dc.citation.issue3-
dc.citation.beginningpage969-
dc.citation.endingpage973-
dc.citation.publicationnameANGEWANDTE CHEMIE-INTERNATIONAL EDITION-
dc.identifier.doi10.1002/anie.201410059-
dc.contributor.localauthorJeong, Kijun-
dc.contributor.localauthorPark, Chan-Beum-
dc.contributor.nonIdAuthorCha, Gun Su-
dc.contributor.nonIdAuthorLee, Jung-Kul-
dc.contributor.nonIdAuthorYun, Chul-Ho-
dc.type.journalArticleArticle-
dc.subject.keywordAuthorcofactors-
dc.subject.keywordAuthorcytochromes P450-
dc.subject.keywordAuthorenzymatic catalysis-
dc.subject.keywordAuthorphotocatalysis-
dc.subject.keywordAuthorphotoinduced electron transfer-
dc.subject.keywordPlusARTIFICIAL PHOTOSYNTHESIS-
dc.subject.keywordPlusLABORATORY EVOLUTION-
dc.subject.keywordPlusEOSIN-Y-
dc.subject.keywordPlusP450BM3-
dc.subject.keywordPlusREGENERATION-
dc.subject.keywordPlusHYDROXYLATION-
dc.subject.keywordPlusENZYMES-
dc.subject.keywordPlusBIOCATALYST-
dc.subject.keywordPlusCYCLOPROPANATION-
dc.subject.keywordPlusMONOOXYGENASES-
Appears in Collection
CBE-Journal Papers(저널논문)MS-Journal Papers(저널논문)
Files in This Item
There are no files associated with this item.
This item is cited by other documents in WoS
⊙ Detail Information in WoSⓡ Click to see webofscience_button
⊙ Cited 74 items in WoS Click to see citing articles in records_button

qr_code

  • mendeley

    citeulike


rss_1.0 rss_2.0 atom_1.0