Plant regeneration from protoplasts ofIris germanicaL.
โ Scribed by K. Shimizu; T. Yabuya; T. Adachi
- Publisher
- Springer
- Year
- 1996
- Tongue
- English
- Weight
- 411 KB
- Volume
- 89
- Category
- Article
- ISSN
- 0014-2336
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โฆ Synopsis
Protoplasts were isolated enzymatically from suspension cultures derived from embryogenic calli induced by leaf base culture of Iris germanica . In protoplast culture, the effects of glucose concentration, different sugars and combinations of 2,4-D and KIN on protoplast division and colony formation were examined . N6 medium supplemented with 0 .1-1 mg/l 2,4-D, 1 mg/l KIN, 200mg/l casein hydrolysate, 250 mg/l proline, 0 .2 M glucose and 20 g/l agarose was suitable for protoplast division and colony formation . When colonies formed were transferred onto hormone-free MS medium, many plantlets were regenerated through somatic embryogenesis . Thus, we could establish a plant regeneration system from protoplasts of I. germanica .
๐ SIMILAR VOLUMES
Protoplasts were isolated from leaves of axenic shoot cultures of Felicia bergeriana (Kingfisher Daisy) and Brachycome iberidifolia (Swan River Daisy) and from callus cultures of Felicia. Plants were regenerated from all three sources and since both species are of ornamental value (blue flowered) th
Cultured protoplasts of young, unexpanded leaves of the wild lettuce, Lactuca perennis, divided to produce cell colonies in an agarose-solidified, modified MS medium with reduced levels of inorganic salts, together with 2,4-D, NAA and zeatin at 0.2, 0.1 and 0.5 mg 1-1 respectively. Organogenesis fol
Protoplasts were isolated from young leaves or etiolated shoot apices. For initiation of divisions the protoplasts were embedded in sodium alginate and cultivated in MS or MI medium supplemented with 2.2 ixM BA, 2.6 p~M NAA and 2.2 p~M 2,4-dichlorophenoxyacetic acid. The protoplasts of all seven lin