Cytogenetics and Biotechnology Laboratory, Department of Botany Osmania University, Hyderabad 500 007.
* Tissue Culture Laboratory, Agricultural Research Institute, Rajendranagar, Hyderabad
Somatic embryogenesis was obtained from long term callus cultures of leaf bud in half strength MS medium supplemented with both 0.5 mg/1 2,4–0 +1.0 mg/1 NAA and 0.5 mg/1 2,4–0. However, further development of the somatic embryos into plants was obtained only from the 0.5 mg/1 2,4–0 supplemented cultures. Half strength MS medium supplemented with 0.5 mg/1 2,4–0 + 1.0 mg/1 NAA + 0.5 mg/1 BAP yielded only non-embryogenic callus. Isozyme patterns were studied to distinguish between non-embryogenic and embryogenic calli and also between non-viable and viable somatic embryos in embryogenic calli. Specific isoperoxidases and isoesterases were found to be associated with the development of viable somatic embryos.
Somatic embryogenesis, isozyme analysis, rose, micropropagation