Abstract
The effects of culture media, culture modes, and carbon sources on plating efficiencies of protoplasts of two genotypes of Asparagus officinalis L. were investigated. Protoplasts grew best in a semisolid culture system containing half-strength MS medium with 1 mg NAA/liter, 0.5 mg zeatin/liter, 0.6 M glucose, and 0.1% Gelrite. The plating efficiencies were 12.5% and 8.1% for genotypes G 203 and G 171, respectively. Embryogenic calli were produced from protoplast-derived microcalli after culturing on MS medium with 1 mg 2,4-D, 3% sucrose, and 0.2% Gelrite. The somatic embryos were initiated, matured, and then germinated to plantlets in MS medium containing 0.1 mg NAA/liter, 0.3 mg 2-iP/liter (EMM), and different levels of carbohydrates. Transfer of somatic embryos from EMM with 10% glucose to EMM containing 2% sucrose produced the highest number of bipolar embryos and plantlets. The plantlets regenerated shoots and roots in MS medium with 3% sucrose, 0.1 mg NAA/liter, 0.1 mg kinetin/liter, and 1.28 mg ancymidol/liter. Cytological analysis of these plants revealed 2n = 20 chromosomes.
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