Heterologous overexpression of sfCherry fluorescent protein in Nannochloropsis salina

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dc.contributor.authorKang, Nam Kyuko
dc.contributor.authorChoi, Gang-Gukko
dc.contributor.authorKim, Eun Kyungko
dc.contributor.authorShin, Sung Eunko
dc.contributor.authorJeon, seungjibko
dc.contributor.authorPark, Min S.ko
dc.contributor.authorJeong, Ki Junko
dc.contributor.authorJeong, Byeong-ryoolko
dc.contributor.authorChang, Yong Keunko
dc.contributor.authorYang, Ji-Wonko
dc.contributor.authorLee, Bongsooko
dc.date.accessioned2016-04-14T02:54:53Z-
dc.date.available2016-04-14T02:54:53Z-
dc.date.created2015-11-20-
dc.date.created2015-11-20-
dc.date.issued2015-08-
dc.identifier.citationBiotechnology Reports, v.8, pp.10 - 15-
dc.identifier.issn2215-017X-
dc.identifier.urihttp://hdl.handle.net/10203/203700-
dc.description.abstractOleaginous microalgae of the Nannochloropsis genus are considered excellent candidates for biofuels and value-added products owing to their high biomass productivity and lipid content. Here, we report the first overexpression and detection of a heterologous sfCherry fluorescent protein in Nannochloropsis salina in order to develop a transformation toolbox for future genetic improvements. Particle bombardment was employed for transformation, and expression of Shble under the control of TUB and UEP promoters, cloned from N. salina, was used to confer resistance to Zeocin antibiotics, resulting in 5.9 and 4.7 transformants per 10 cells, respectively. Stable integration of the markers into the genome was confirmed using a restriction enzyme site-directed amplification (RESDA) PCR. The expression of sfCherry fluorescent protein was confirmed by Western blot analysis and confocal microscopy. These results suggest new possibilities of efficient genetic engineering of Nannochloropsis for the production of biofuels and other biochemicals.-
dc.languageEnglish-
dc.publisherElsevier BV-
dc.titleHeterologous overexpression of sfCherry fluorescent protein in Nannochloropsis salina-
dc.typeArticle-
dc.identifier.scopusid2-s2.0-84940995623-
dc.type.rimsART-
dc.citation.volume8-
dc.citation.beginningpage10-
dc.citation.endingpage15-
dc.citation.publicationnameBiotechnology Reports-
dc.identifier.doi10.1016/j.btre.2015.08.004-
dc.contributor.localauthorJeong, Ki Jun-
dc.contributor.localauthorJeong, Byeong-ryool-
dc.contributor.localauthorChang, Yong Keun-
dc.contributor.localauthorYang, Ji-Won-
dc.contributor.nonIdAuthorKim, Eun Kyung-
dc.contributor.nonIdAuthorPark, Min S.-
dc.description.isOpenAccessY-
dc.subject.keywordAuthorHeterologous protein expression-
dc.subject.keywordAuthorParticle bombardment-
dc.subject.keywordAuthorRestriction enzyme site-directed amplification (RESDA) PCR-
dc.subject.keywordAuthorsfCherry fluorescent protein-

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