Departamento de Ingeniería Genética de Plantas, CINVESTAV-IPN Unidad Irapuato, Irapuato, Apdo. Postal 629, 36500, Gto., México.
Plant Cell Rep. 1995 May;14(8):482-7. doi: 10.1007/BF00232779.
Escherichia coli cells and tobacco (cv. Xanthi) plants transformed with the hygromycin B phosphotransferase gene were able to grow in culture medium containing glyphosate at 2.0 mM. The growth of tobacco calli in media containing increasing glyphosate concentrations was measured. The ID50 for glyphosate was 1.70±0.03 mM for hygromycin-B resistant plants, and 0.45±0.02 mM for control plants. Regenerated plants and progeny selected for resistance to hygromycin B were tested for glyphosate tolerance by spraying them with Faena herbicide (formulated glyphosate with surfactant) at a dose equal to 0.24 kg/ha. This was two times the dose required to kill 100 percent of the control plants. Phosphotransferase activity was measured in the extracts of the transformed leaves by the incorporation of (32)P from [γ(-32)P]ATP and it was observed that hygromycin B phosphotransferase was able to recognize the molecule of glyphosate as substrate.
用潮霉素 B 磷酸转移酶基因转化的大肠杆菌细胞和烟草(cv. Xanthi)植物能够在含有 2.0mM 草甘膦的培养基中生长。测量了含有不同草甘膦浓度的烟草愈伤组织在培养基中的生长情况。潮霉素 B 抗性植物的草甘膦 ID50 为 1.70±0.03mM,而对照植物的草甘膦 ID50 为 0.45±0.02mM。对再生植物和选择抗潮霉素 B 的后代进行了草甘膦耐受性测试,用 Faena 除草剂(含表面活性剂的草甘膦制剂)喷洒,剂量等于 0.24kg/ha。这是杀死 100%对照植物所需剂量的两倍。通过从 [γ(-32)P]ATP 掺入(32)P 来测量转化叶片提取物中的磷酸转移酶活性,并观察到潮霉素 B 磷酸转移酶能够识别草甘膦分子作为底物。