下胚轴
卡那霉素
根癌农杆菌
转化(遗传学)
开枪
外植体培养
生物
农杆菌
植物
李子
转化效率
Murashige和Skoog培养基
园艺
化学
细菌
生物化学
体外
遗传学
基因
作者
César Petri,Ralph Scorza,C. Srinivasan
标识
DOI:10.1007/978-1-61779-558-9_16
摘要
A high-throughput transformation system for plum has been developed using hypocotyl slices excised from zygotic embryos as the source of explants. The hypocotyl slices are infected in an Agrobacterium tumefaciens suspension and then cocultivated for 3 days in shoot regeneration ¾ MS basal medium supplemented with 9 μM 2,4-dichlorophenoxyacetic acid. Transgenic shoots are regenerated in a medium containing 7.5 μM thidiazuron and elongated in a medium containing 3 μM benzyladenine in the presence of 80 mg/L kanamycin in both media. Transformed shoots are rooted in ½ MS basal medium supplemented with 5 μM NAA and 40 mg/L kanamycin. The transgenic plants are acclimatized in a growth chamber and transferred to a temperature-controlled greenhouse. This protocol has allowed transformation efficiencies up to 42% and enabled the production of self-rooted transgenic plum plants within 6 months of transformation.
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