Abstract
Calli were initiated from flower buds, gynoecia and inflorescence segments of Haworthia magnifica v. Poelln. and subcultured on solid medium. Two liquid culture steps were necessary to prepare the calli for the isolation of protoplasts capable of sustained cell divisions. Plants were regenerated from protoplast-derived calli. The influence of both the osmolality of the culture media and exudates on the viability of protoplasts and protoplast-derived cell colonies is briefly discussed.
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Sun, Y., Heil, B.M., Kahl, G. et al. Plant regeneration from protoplasts of the monocotyledonous Haworthia magnifica v. Poelln.. Plant Cell Tiss Organ Cult 8, 91–100 (1987). https://doi.org/10.1007/BF00040736
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DOI: https://doi.org/10.1007/BF00040736