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Effect of liquid pulses with 6-benzyladenine on the induction of somatic embryogenesis from coffee (Coffea arabica L.) callus cultures

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dc.contributor.author Papanastasiou, I en
dc.contributor.author Soukouli, K en
dc.contributor.author Moschopoulou, G en
dc.contributor.author Kahia, J en
dc.contributor.author Kintzios, S en
dc.date.accessioned 2014-06-06T06:48:26Z
dc.date.available 2014-06-06T06:48:26Z
dc.date.issued 2008 en
dc.identifier.issn 01676857 en
dc.identifier.uri http://dx.doi.org/10.1007/s11240-007-9326-0 en
dc.identifier.uri http://62.217.125.90/xmlui/handle/123456789/4147
dc.subject Cell culture en
dc.subject Embryo germination en
dc.subject Indirect somatic embryogenesis en
dc.subject Leaf explant en
dc.subject Redox status en
dc.subject.other Cell growth en
dc.subject.other Free radicals en
dc.subject.other Lipids en
dc.subject.other Plants (botany) en
dc.subject.other Embryo germination en
dc.subject.other Indirect somatic embryogenesis en
dc.subject.other Leaf explant en
dc.subject.other Redox status en
dc.subject.other Cell culture en
dc.subject.other Coffea arabica en
dc.title Effect of liquid pulses with 6-benzyladenine on the induction of somatic embryogenesis from coffee (Coffea arabica L.) callus cultures en
heal.type journalArticle en
heal.identifier.primary 10.1007/s11240-007-9326-0 en
heal.publicationDate 2008 en
heal.abstract We investigated the effect of the physical state of the nutrient medium on the induction of somatic embryogenesis on cell cultures derived from coffee (Coffea arabica L.). Non-embryogenic callus tissues were pulsed initially with 50 μM 6-benzyladenine (BA) for 6, 24 or 48 h in half-strength liquid Murashige and Skoog (MS) medium. After pretreatment, calli were transferred to agar-solidified half-strength MS medium supplemented with 50 μM BA ('standard induction medium'). Control callus tissues were incubated directly on the solid standard induction medium. Callus growth was promoted by longer pretreatment periods. Formation of globular somatic embryos was observed on callus tissues pretreated with BA for 24 or 48 h, which developed fully to cotyledonary-stage within only 2 weeks after transfer to agar-solidified medium supplemented with BA. No embryo formation occurred in control cultures. Pretreatment with BA in liquid medium was associated with changes in the redox status of cultured cells, such as alterations of the ascorbate-glutathione redox systems and the accumulation of free radicals and oxidized lipids, as well as the possible reduction of cytochrome c-mediated apoptotic pathways. In particular, the induction of somatic embryogenesis was highly positively correlated (r 2 = 0.822) with the accumulation of protein carbonyls. The physiological role of BA as an inducer of both embryonic differentiation and cellular death is discussed. © 2007 Springer Science+Business Media B.V. en
heal.journalName Plant Cell, Tissue and Organ Culture en
dc.identifier.issue 2 en
dc.identifier.volume 92 en
dc.identifier.doi 10.1007/s11240-007-9326-0 en
dc.identifier.spage 215 en
dc.identifier.epage 225 en


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