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Photoautotrophic production of macular pigment in a Chlamydomonas reinhardtii strain generated by using DNA-free CRISPR-Cas9 RNP-mediated mutagenesis

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dc.contributor.authorBaek, Kwangryul-
dc.contributor.authorYu, Jihyeon-
dc.contributor.authorJeong, Jooyeon-
dc.contributor.authorSim, Sang Jun-
dc.contributor.authorBae, Sangsu-
dc.contributor.authorJin, EonSeon-
dc.date.accessioned2021-09-02T14:08:31Z-
dc.date.available2021-09-02T14:08:31Z-
dc.date.created2021-06-16-
dc.date.issued2018-03-
dc.identifier.issn0006-3592-
dc.identifier.urihttps://scholar.korea.ac.kr/handle/2021.sw.korea/76889-
dc.description.abstractLutein and zeaxanthin are dietary carotenoids reported to be protective against age-related macular degeneration. Recently, the green alga Chlamydomonas reinhardtii has received attention as a photosynthetic cell factory, but the potential of this alga for carotenoid production has not yet been evaluated. In this study, we selected the C. reinhardtii CC-4349 strain as the best candidate among seven laboratory strains tested for carotenoid production. A knock-out mutant of the zeaxanthin epoxidase gene induced by preassembled DNA-free CRISPR-Cas9 ribonucleoproteins in the CC-4349 strain had a significantly higher zeaxanthin content (56-fold) and productivity (47-fold) than the wild type without the reduction in lutein level. Furthermore, we produced eggs fortified with lutein (2-fold) and zeaxanthin (2.2-fold) by feeding hens a diet containing the mutant. Our results clearly demonstrate the possibility of cost-effective commercial use of microalgal mutants induced by DNA-free CRISPR-Cas9 ribonucleoproteins in algal biotechnology for the production of high-value products.-
dc.languageEnglish-
dc.language.isoen-
dc.publisherWILEY-
dc.subjectLUTEIN-
dc.subjectCAROTENOIDS-
dc.subjectMICROALGAE-
dc.subjectZEAXANTHIN-
dc.subjectXANTHOPHYLLS-
dc.subjectACCUMULATION-
dc.subjectEGG-
dc.titlePhotoautotrophic production of macular pigment in a Chlamydomonas reinhardtii strain generated by using DNA-free CRISPR-Cas9 RNP-mediated mutagenesis-
dc.typeArticle-
dc.contributor.affiliatedAuthorSim, Sang Jun-
dc.identifier.doi10.1002/bit.26499-
dc.identifier.scopusid2-s2.0-85041078024-
dc.identifier.wosid000423672800018-
dc.identifier.bibliographicCitationBIOTECHNOLOGY AND BIOENGINEERING, v.115, no.3, pp.719 - 728-
dc.relation.isPartOfBIOTECHNOLOGY AND BIOENGINEERING-
dc.citation.titleBIOTECHNOLOGY AND BIOENGINEERING-
dc.citation.volume115-
dc.citation.number3-
dc.citation.startPage719-
dc.citation.endPage728-
dc.type.rimsART-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaBiotechnology & Applied Microbiology-
dc.relation.journalWebOfScienceCategoryBiotechnology & Applied Microbiology-
dc.subject.keywordPlusLUTEIN-
dc.subject.keywordPlusCAROTENOIDS-
dc.subject.keywordPlusMICROALGAE-
dc.subject.keywordPlusZEAXANTHIN-
dc.subject.keywordPlusXANTHOPHYLLS-
dc.subject.keywordPlusACCUMULATION-
dc.subject.keywordPlusEGG-
dc.subject.keywordAuthoralgal biotechnology-
dc.subject.keywordAuthorChlamydomonas reinhardtii-
dc.subject.keywordAuthorCRISPR-Cas9-
dc.subject.keywordAuthorlutein-
dc.subject.keywordAuthorzeaxanthin-
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공과대학 (화공생명공학과)
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