In vitro plant regeneration from embryogenic cell suspension culture of Astragalus chrysochlorus (Leguminoseae)
AFRICAN JOURNAL OF BIOTECHNOLOGY, vol.7, no.9, pp.1250-1255, 2008 (SCI-Expanded, Scopus)
- Publication Type: Article / Article
- Volume: 7 Issue: 9
- Publication Date: 2008
- Journal Name: AFRICAN JOURNAL OF BIOTECHNOLOGY
- Journal Indexes: Science Citation Index Expanded (SCI-EXPANDED), Scopus
- Page Numbers: pp.1250-1255
- Keywords: somatic embryogenesis, propagation, indole-3-acetic acid, flow cytometry, CYCLOARTANE TRITERPENE GLYCOSIDES, SOMATIC EMBRYOGENESIS, HIGH-FREQUENCY, CALLUS, GROWTH, ADSURGENS, ROOTS, INDUCTION, HYPOCOTYL, EXPLANTS
- Istanbul University Affiliated: Yes
Abstract
In vitro plant regeneration was achieved from embryogenic cell suspension culture of Astragalus chrysochlorus. When 30-day-old aseptically grown seedlings were cultured on Murashige and Skoog ( MS) medium containing 0.1 mg/l-naphthaleneacetic acid (NAA) plus 1.0 mg/16- benzyladenine ( BA), friable callus was formed within two weeks from the mesocotyl of the seedling. After three weeks, proliferated actively growing calli were transferred to MS liquid medium containing 2,4-dichlorophenoxyacetic acid ( 2,4-D), indole-3-acetic acid (IAA) or NAA and subcultured at two week intervals. After two weeks, induction of somatic embryos up to the torpedo stage occured at all tested concentrations of 2,4-D, IAA or NAA. Somatic embryos developed only in MS medium containing 0.5 mg/l IAA within two weeks and 2% of globular embryos were developed into the cotyledonary stage embryos. Eighty one percent of somatic embryos cultured in MS medium supplemented with 0.5 mg/l IAA were found to be diploid by flow cytometric analysis. Plantlet propagation was achieved on half strength MS liquid medium supplemented with 3% (w/v) sucrose after four weeks of culture. After a month on half strength MS medium [1.5% (w/v) sucrose and 0.8% (w/v) agar] 29 of 71 shoots developed into rooted plantlets.