Articles
USE OF PETIOLE SEGMENTS OF ACTINIDIA CHINENSIS (KLWI) FOR PLANT DIFFERENTIATION AND PRODUCTION OF FRIABLE CALLI FOR PROTOPLAST ISOLATION
Article number
212_117
Pages
687 – 690
Language
Abstract
Petiole segments of Actinidia chinensis produced meristems 4weeks after inoculation on MS medium with sucrose reduced to 20g.1-1 and 1mg.1-1 zeatin/0.025mg.1-1IAA, without adenine.
Plantlets differentiation was accomplished 1 month after transfer to MS medium with macro and micronutrients reduced to ½, sucrose 20g.1-1, 0.5mg.1-1 zeatin/0.025mg.1-1IAA and adenine omitted.
Efficient rooting was obtained by soaking the basal cutting surface of plantlets in 20mg.1-1IBA for 24h followed by immediate potting. 1 month after, vigorous well rooted plants were obtained.
Plantlets differentiation was accomplished 1 month after transfer to MS medium with macro and micronutrients reduced to ½, sucrose 20g.1-1, 0.5mg.1-1 zeatin/0.025mg.1-1IAA and adenine omitted.
Efficient rooting was obtained by soaking the basal cutting surface of plantlets in 20mg.1-1IBA for 24h followed by immediate potting. 1 month after, vigorous well rooted plants were obtained.
Kiwi green calli transferred to MS medium with sucrose reduced to 20 g.1-1 plus mannitol 10g.1-1 and 0.5mg.1-12, 4-D/0.05mg.1-1NAA became friable and suitable for protoplasts isolation.
High yields of viable protoplasts (about 90%) were obtained using 2% cellulase and 1% macerozyme in a developed culture medium.
Authors
M. Salomé, S. Pais, M. Margarida Oliveira, J. Barroso
Keywords
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