Department of Biochemistry and Applied Molecular Biology, UMIST, M60 1QD, Manchester, UK.
Plant Cell Rep. 1993 May;12(7-8):422-5. doi: 10.1007/BF00234705.
Explants of tomato (Lycopersicon esculentum Mill cv. Ailsa Craig) were co-cultivated with Agrobacterium tumefaciens C58C1Rif(r)::pGSFR1161 in the presence of 20 (μM acetosyringone). Transformed root clones were selected on kanamycin medium and the presence of the nptII gene in the plant DNA confirmed by the polymerase chain reaction. Root clones derived from acetosyringone treatment grew more vigorously in the presence of kanamycin and synthesized a greater amount of NPT-II enzyme. The conclusion is that acetosyringone treatment enhances the transformation process, possibly by stimulating multiple insertions of the T-DNA into the host genome.
番茄(Lycopersicon esculentum Mill cv. Ailsa Craig)外植体与携带 pGSFR1161 的根癌农杆菌 C58C1Rif(r) 在 20μM 乙酰丁香酮的条件下共培养。转化的根克隆在卡那霉素培养基上进行选择,并通过聚合酶链反应确认植物 DNA 中存在 nptII 基因。来自乙酰丁香酮处理的根克隆在卡那霉素存在下生长更旺盛,并合成更多的 NPT-II 酶。结论是乙酰丁香酮处理增强了转化过程,可能通过刺激 T-DNA 插入宿主基因组的多个位置来实现。