Autor: |
Lourdes Castelblanque, Begoña GarcÃa-Sogo, Benito Pineda, Vicente Moreno |
Zdroj: |
Plant Cell, Tissue & Organ Culture; Jan2010, Vol. 100 Issue 1, p107-112, 6p |
Abstrakt: |
Abstract  A simple and efficient protocol for plant regeneration from protoplasts of the potted plant Kalanchoe blossfeldiana Poelln. is reported. Mesophyll protoplasts were isolated from axenic leaves after a preculture. The enzymatic digestion of the tissue with a solution containing 0.4% Cellulase Onozuka R-10 and 0.2% Driselase yielded 6.0 Ã 105 protoplasts per gram fresh weight after density gradient purification. Protoplasts were cultured in the dark at an initial density of 1 Ã 105 protoplasts per milliliter in a liquid medium with 320 mM mannitol, 130 mM sucrose, 2.3 μM 2,4-dichlorophenoxy acetic acid (2,4-D), 5.4 μM 1-naphthaleneacetic acid (NAA) and 2.2 μM 6-benzyladenine (BA). Cell wall regeneration was observed within 4 days of culture and cell division began after 5â7 days. When cultured in a liquid medium with 5.4 μM NAA and 8.9 μM BA, protoplast-derived colonies proliferated until small visible calli, and adventitious buds appeared after transfer to photoperiod conditions. Developed shoots were rooted on a solid medium supplemented with 0.6 μM indole-3-acetic acid (IAA) and successfully established under greenhouse conditions. The process required 4 months from isolation to rooted plants and the best conditions found gave a plant regeneration efficiency of 6.4 plants per 1 Ã 105 protoplasts. This is the first protocol reported for plant regeneration from protoplasts for a Crassulaceae family species. [ABSTRACT FROM AUTHOR] |
Databáze: |
Complementary Index |
Externí odkaz: |
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