- Turkish Journal of Agriculture and Forestry
- Volume:34 Issue:4
- Regeneration and histological analysis of snake melon (Cucumis melo var. flexuosus (L.) Naudin) by d...
Regeneration and histological analysis of snake melon (Cucumis melo var. flexuosus (L.) Naudin) by direct organogenesis
Authors : Yeşim YALÇIN MENDİ, Selay ELDOĞAN, Rafael GUTAKEV
Pages : 309-317
View : 17 | Download : 8
Publication Date : 2010-08-01
Article Type : Research Paper
Abstract :In vitro morphogenesis of Cucumis melo var. flexuosus insert ignore into journalissuearticles values(L.); Naudin was studied by direct organogenesis. Induction of adventitious buds was obtained from distal and proximal parts of the cotyledon incubated on Murashige and Skoog insert ignore into journalissuearticles values(1962); medium containing different concentrations of 6-benzyladenine insert ignore into journalissuearticles values(BA); insert ignore into journalissuearticles values(0.0, 0.5, 1.0, and 2.0 mg L-1); and indole-3-acetic acid insert ignore into journalissuearticles values(IAA); insert ignore into journalissuearticles values(0.0, 0.1, and 0.5 mg L-1);. The best organogenesis was obtained from the proximal part of the cotyledon on medium containing 0.5 mg L-1 BA and 0.5 mg L-1 IAA insert ignore into journalissuearticles values(88%);. This concentration was used for histological analysis. Less regeneration was obtained on media containing 1.0 mg L-1 BA insert ignore into journalissuearticles values(75%); or 1.0 mg L-1 BA and 0.1 mg L-1 IAA insert ignore into journalissuearticles values(60%);. Plant recovery was much greater from proximal rather than distal explants. A callus formed on almost every explant on media supplemented with BA. Histological analyses showed that the formation of early shoot apical meristems was observed in 14-day-old tissues and meristematic structures were seen in 17-day-old tissues. The first shoot was formed after 21 days. By this time, the surface was covered with leaf primordia and leaves, mostly without accompanying buds.Keywords : Key words Cell division, cucurbits, in vitro, regeneration, tissue culture