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dc.contributor.authorZare, K
dc.contributor.authorKhosrowshahli, M
dc.contributor.authorNazemiyeh, H
dc.contributor.authorMovafeghi, A
dc.contributor.authorAzar, AM
dc.contributor.authorOmidi, Y
dc.date.accessioned2018-08-26T08:09:48Z
dc.date.available2018-08-26T08:09:48Z
dc.date.issued2011
dc.identifier.urihttp://dspace.tbzmed.ac.ir:8080/xmlui/handle/123456789/50480
dc.description.abstractCallus induction and proliferation of Echium italicum L. (Boraginaceae) were investigated using cotyledon, hypocotyl and root explants. Calli were initiated and established using B5, LS, 1/2LS and White media supplemented with different auxins, including 2,4-dichlorophenoxyacetic acid (2,4-D), indole-3-acetic acid (IAA) and 1-naphthaleneacetic acid (NAA) in combination with kinetin. The maximum pigmented callus induction (100%) was observed in the White medium. The n-hexane extract of proliferated callus tissues were analysed by TLC and HPLC. The major secondary metabolite was separated by preparative HPLC and its structure was elucidated by UV, H-1 and C-13-NMR spectroscopy. As a result, shikonin acetate was identified by various spectroscopic methods from callus culture of E. italicum. These findings highlight the shikonin production potential of the E. italicum callus, which may be considered as a new source for the production of shikonin and its derivatives for industrial use.
dc.language.isoEnglish
dc.relation.ispartofNATURAL PRODUCT RESEARCH
dc.subjectEchium italicum
dc.subjectpigmented callus
dc.subjectpreparative HPLC
dc.subjectshikonin acetate
dc.subjecttissue culture
dc.titleCallus culture of Echium italicum L. towards production of a shikonin derivative
dc.typeArticle
dc.citation.volume25
dc.citation.issue16
dc.citation.spage1480
dc.citation.epage1487
dc.citation.indexWeb of science
dc.identifier.DOIhttps://doi.org/10.1080/14786410902804857


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