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Adventitious shoots were successfully regenerated from hypocotyl explants of in vitro cultures of Euonymus japonicusCu zhi. Hypocotyl slices were cultured on Murashige and Skoog (MS) and B5 basal medium supplemented with variedconcentration of different plant growth-regulators, e.g., α-naphthaleneacetic acid (NAA) and indole-3-butyric acid (IBA)in combination with 6-benzylaminopurine (6-BA) and kinetin. The study showed that shoots could be directly regeneratedfrom hypocotyl explants without the intervening callus phase; MS medium was more suitable for adventitious shootsregeneration. The ability of hypocotyls segments to produce shoots varied depending upon their position on the seedlings.The highest regeneration rate was obtained with hypocotyl segments near to the cotyledon cultured on MS basal mediumsupplemented with 1.5 mg L-1 6-BA and 0.05 mg L-1 NAA (63.64%). The regenerated shoots were readily elongated on thesame medium as used for multiplication and rooted on half-strength MS basal medium supplemented with 1.0 mg L-1 IBAand 100 mg L-1 activated carbon. After being transferred to greenhouse conditions, 96% of the plantlets were successfullyacclimatized. This regeneration system is applied for genetic transformation now.
Adventitious shoots were successfully regenerated from hypocotyl explants of in vitro cultures of Euonymus japonicus Cu zhi. Hypocotyl slices were cultured on Murashige and Skoog (MS) and B5 basal medium supplemented with varied concentration of different plant growth-regulators, eg, alpha-naphthalene acetic acid (NAA ) and indole-3-butyric acid (IBA) in combination with 6-benzylaminopurine (6-BA) and kinetin. The study showed that shoots could be directly regenerated from hypocotyl explants without the intervening callus phase; MS medium was more suitable for adventitious shoots regeneration . The ability of hypocotyls segments to produce shoots varied depending upon their position on the seedlings.The highest regeneration rate was obtained with hypocotyl segments near to the cotyledon cultured on MS basal mediumsupplemented with 1.5 mg L-1 6-BA and 0.05 mg L- 1 NAA (63.64%). The regenerated shoots were often elongated on thesame medium as used for multiplication and rooted on half-strength M After basal medium supplemented with 1.0 mg L-1 IBAand 100 mg L-1 activated carbon. After vegetated to 96% of the plantlets were successfully cloned. This regeneration system is applied for genetic transformation now.