Elucidation of the growth delimitation of Dunaliella tertiolecta under nitrogen stress by integrating transcriptome and peptidome analysis

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dc.contributor.authorShin, HyeonSeokko
dc.contributor.authorHong, Seong-Jooko
dc.contributor.authorKim, Hyojinko
dc.contributor.authorYoo, Chanko
dc.contributor.authorLee, Hookeunko
dc.contributor.authorChoi, Hyung-Kyoonko
dc.contributor.authorLee, Choul-Gyunko
dc.contributor.authorCho, Byung-Kwanko
dc.date.accessioned2015-11-20T07:16:44Z-
dc.date.available2015-11-20T07:16:44Z-
dc.date.created2015-08-25-
dc.date.created2015-08-25-
dc.date.created2015-08-25-
dc.date.issued2015-10-
dc.identifier.citationBIORESOURCE TECHNOLOGY, v.194, pp.57 - 66-
dc.identifier.issn0960-8524-
dc.identifier.urihttp://hdl.handle.net/10203/200588-
dc.description.abstractDunaliella tertiolecta LB 999 is an oleaginous microalgae species that produces large quantities of lipid and starch during nitrogen starvation; however, nitrogen starvation also limits the cell growth. In order to understand the underlying mechanisms of this phenomenon, the transcriptome and peptidome of D. tertiolecta LB 999 grown under different nitrogen and light conditions were analyzed. Integration of the de novo assembly of transcriptome sequencing reads with peptidome analysis revealed 13,861 protein-coding transcripts, including 33 transcripts whose expression patterns were significantly altered along with the growth phenotypes. Interestingly, 21 of these genes, which were highly enriched in the plastid region, were associated with chlorophyll synthesis and tetrahydrofolate-mediated C1 metabolism. Furthermore, intracellular glutamate levels are predicted to be the main factor that acts as a switch for the regulation of cell growth and carbon accumulation. These data provide the genetic information of D. tertiolecta for its future applications.-
dc.languageEnglish-
dc.publisherELSEVIER SCI LTD-
dc.titleElucidation of the growth delimitation of Dunaliella tertiolecta under nitrogen stress by integrating transcriptome and peptidome analysis-
dc.typeArticle-
dc.identifier.wosid000358796600009-
dc.identifier.scopusid2-s2.0-84942247234-
dc.type.rimsART-
dc.citation.volume194-
dc.citation.beginningpage57-
dc.citation.endingpage66-
dc.citation.publicationnameBIORESOURCE TECHNOLOGY-
dc.identifier.doi10.1016/j.biortech.2015.07.002-
dc.contributor.localauthorCho, Byung-Kwan-
dc.contributor.nonIdAuthorHong, Seong-Joo-
dc.contributor.nonIdAuthorKim, Hyojin-
dc.contributor.nonIdAuthorLee, Hookeun-
dc.contributor.nonIdAuthorChoi, Hyung-Kyoon-
dc.contributor.nonIdAuthorLee, Choul-Gyun-
dc.description.isOpenAccessN-
dc.type.journalArticleArticle-
dc.subject.keywordAuthorDe novo transcriptome assembly-
dc.subject.keywordAuthorPeptidome analysis-
dc.subject.keywordAuthorDunaliella tertiolecta-
dc.subject.keywordAuthorGrowth limitation-
dc.subject.keywordAuthorMicroalgae-
dc.subject.keywordPlusRNA-SEQ DATA-
dc.subject.keywordPlusC-4 PHOTOSYNTHESIS-
dc.subject.keywordPlusREFERENCE GENOME-
dc.subject.keywordPlusMICROALGAE-
dc.subject.keywordPlusACCUMULATION-
dc.subject.keywordPlusANNOTATION-
dc.subject.keywordPlusSUPPLEMENT-
dc.subject.keywordPlusBIOFUELS-
dc.subject.keywordPlusALGAE-
dc.subject.keywordPlusLIGHT-
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