To investigate cucumber (Cucumis sativus L.) regeneration from embryogenic calli, shoot tips of aseptically-grown cucumber seedlings were used as explants for establishing tissue cultures. Growth and differentiation of callus were studied by using Murashige and Skoog's (MS) medium containing 0.5-2 mg/L 2,4-D.
Plantlets were induced from the shoot tip culture on the plant growth regulator-free MS medium. Non-embryogenic calli and viscous calli were induced on the medium supplemented with 0.5-2 mg/L 2,4-D, but embryogenic callus was not induced on the same medium.
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