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机构地区:[1]中国科学院上海植物生理研究所植物分子遗传国家重点实验室,上海200032
出 处:《Acta Botanica Sinica》1994年第9期657-663,共7页Acta Botanica Sinica(植物学报:英文版)
基 金:"863"计划资助课题
摘 要:用根癌农杆菌(Agrobacterium tum efaciens)共培养法把外源基因导入甘蓝型油菜(Brassi-ca napusL.)主要栽培品种“云北2 号”,获得转基因植株。所用外植体为带有1—2 m m 子叶柄的完整子叶,根癌农杆菌为A208SE(pTiT37-SE, pROA93)。Ti质粒pROA93 带有NPTⅡ及GUS嵌合基因。共培养2 天后转到附加25 m g/L卡那霉素的分化培养基(MS+ 4.5 m g/LBAP)上。AgNO3 和羧苄青霉素促进芽的分化,头孢霉素则有抑制作用。最高转化频率为27% 。把分化出的茎芽切下,插入含有25 m g/L卡那霉素的生根培养基中。羧苄青霉素不利于根的形成。把完整抗性植株移入盛土壤的盆中,生长状况良好。测定β-葡糖苷酸酶活性,84% 明显高于对照。以NPTⅡ基因作探针进行Southern blot分析。Seeds of Brassica napus L.cv.“Yunbei 2” were surface sterilized and germinated on hormone free MS medium.After 4—5 days the cotyledons were excised in such a way that each has a 1—2 mm petiole was remained at its base.These cotyledons were used as the explants for tissue culture and genetic transformation.This paper first deals with the improvement of the medium for shoot regeneration.Of the elements tested, AgNO 3 and carbenicillin enhanced shoot regeneration.The highest frequency (52%) was obtained on MS medium containing 4 5 mg/L BAP, 20 μmol/L AgNO 3 and 500 mg/L carbenicillin.An efficient gene transfer system based on the regeneration procedure was established.After 2 days of cocultivation with Agrobacterium tumefaciens strain A208SE (pTi T37 SE, pROA93), the explants were transferred onto selection medium containing 25 mg/L kanamycin.After 1 5 months shoots emerged from 27% of the explants inoculated.They were excised and transferred onto rooting medium containing 25 mg/L kanamycin and 200 mg/L cefotaxime which is better than carbenicillin for root induction.Whole plants were transplanted into pots, and grew well in the phytotron.Transformation was confirmed by β glucuronidase assay and Southern blotting analysis.
分 类 号:S565.403.2[农业科学—作物学]
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