Study of cellular development and intracellular lipid bodies accumulation in the thraustochytrid Aurantiochytrium sp KRS101

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dc.contributor.authorVelmurugan, Natarajanko
dc.contributor.authorSathishkumar, Yesupathamko
dc.contributor.authorYim, Sung Sunko
dc.contributor.authorLee, Yang Sooko
dc.contributor.authorPark, Min S.ko
dc.contributor.authorYang, Ji Wonko
dc.contributor.authorJeong, Ki Junko
dc.date.accessioned2014-09-01T07:34:42Z-
dc.date.available2014-09-01T07:34:42Z-
dc.date.created2014-06-10-
dc.date.created2014-06-10-
dc.date.created2014-06-10-
dc.date.created2014-06-10-
dc.date.issued2014-06-
dc.identifier.citationBIORESOURCE TECHNOLOGY, v.161, pp.149 - 154-
dc.identifier.issn0960-8524-
dc.identifier.urihttp://hdl.handle.net/10203/189290-
dc.description.abstractTransmission electron, confocal microscopy and FACS in conjunction with two different lipophilic fluorescent dyes, BODIPY 505/515 and Nile Red were used to describe the cellular development and lipid bodies formation in Aurantiochytrium sp. KRS101. TEM results revealed that multi-cellular spores were appeared in sporangium during early-exponential phase, and spores were matured in mid-exponential phase followed by release of spores from sporangium in late-exponential phase. TEM and FACS analyses proved that lipid bodies appeared, developed and degenerated in mid-exponential, early- and late-stationary phases, respectively. The staining results in FACS indicate that BODIPY 505/515 is more effective for the vital staining of intracellular lipid bodies than Nile Red. FACS based single cell sorting also showed healthy growth for BODIPY 505/515 stained cells than Nile Red stained cells. In addition, a quantitative baseline was established either for cell growth and/or lipid accumulation based on cell count, fatty acid contents/composition, and sectional/confocal images of KRS101.-
dc.languageEnglish-
dc.publisherELSEVIER SCI LTD-
dc.titleStudy of cellular development and intracellular lipid bodies accumulation in the thraustochytrid Aurantiochytrium sp KRS101-
dc.typeArticle-
dc.identifier.wosid000335436000019-
dc.identifier.scopusid2-s2.0-84897470315-
dc.type.rimsART-
dc.citation.volume161-
dc.citation.beginningpage149-
dc.citation.endingpage154-
dc.citation.publicationnameBIORESOURCE TECHNOLOGY-
dc.identifier.doi10.1016/j.biortech.2014.03.017-
dc.embargo.liftdate9999-12-31-
dc.embargo.terms9999-12-31-
dc.contributor.localauthorYim, Sung Sun-
dc.contributor.localauthorYang, Ji Won-
dc.contributor.localauthorJeong, Ki Jun-
dc.contributor.nonIdAuthorVelmurugan, Natarajan-
dc.contributor.nonIdAuthorSathishkumar, Yesupatham-
dc.contributor.nonIdAuthorLee, Yang Soo-
dc.contributor.nonIdAuthorPark, Min S.-
dc.description.isOpenAccessN-
dc.type.journalArticleArticle-
dc.subject.keywordAuthorAurantiochytrium sp.-
dc.subject.keywordAuthorTEM analysis-
dc.subject.keywordAuthorBODIPY 505/515-
dc.subject.keywordAuthorNile Red-
dc.subject.keywordAuthorFluorescence-activated cell sorting-
dc.subject.keywordPlusDOCOSAHEXAENOIC ACID PRODUCTION-
dc.subject.keywordPlusFLOW-CYTOMETRY-
dc.subject.keywordPlusCHLAMYDOMONAS-REINHARDTII-
dc.subject.keywordPlusBODY FORMATION-
dc.subject.keywordPlusNILE RED-
dc.subject.keywordPlusMICROALGAE-
dc.subject.keywordPlusEXPRESSION-
dc.subject.keywordPlusSTRAINS-
dc.subject.keywordPlusPUFAS-
dc.subject.keywordPlusGENE-
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