Abstract
Embryogenic culture was induced from the immature embryos of Quercus serrata using Marashige and Skoog's medium (MS) containing 0.1 μM each of 2,4-d and BAP, and subcultured for seven months before isolation of protoplasts by using 1% Cellulase RS in 0.6 M mannitol solution. Efficient colony formation was obtained when protoplasts were cultured in a liquid MS medium containing 0.6 M mannitol, 3% sucrose and combination of 0.1 μM or 1 μM each of 2,4-d and BAP. Excluding ammonium nitrate from the MS medium resulted in the decrease of the percentage of colony formation. From colonies, both agar culture and liquid culture were sustained in the MS media without mannitol containing no plant growth regulator, or containing 0.1 μM of BAP in combination with 0.1 μM or 1 μM of 2,4-d.
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Abbreviations
- BAP:
-
6-benzylaminopurine
- 2,4-d :
-
2,4-dichlorophenoxyacetic acid
- MS:
-
medium after Murashige & Skoog (1962).
References
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Sasamoto, H., Hosoi, Y. Callus proliferation from the protoplasts of embryogenic cells of Quercus serrata . Plant Cell Tiss Organ Cult 29, 241–245 (1992). https://doi.org/10.1007/BF00034359
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DOI: https://doi.org/10.1007/BF00034359