遗传 ›› 2000, Vol. 22 ›› Issue (2): 86-89.

• 论文 • 上一篇    下一篇

抗菌肽D基因导入番茄及转基因植株的鉴定

田长恩1;王正询1;陈韬1;周玉萍1;黄自然2;黄亚东2 TIAN Chang-en1;WANG Zheng-xun1;CHEN Tao1;ZHOU Yu-ping1;HANG Zi-ran2;HANG Ya-dong2   

  1. 1.广州师范学院生物学系,广州 510405 2.华南农业大学蚕桑系, 广州 510642 1.Department of Biology, Guangzhou Teachers College, Guangzhou 510405 2.Department of Sericulture, South China Agricultural University, Guangzhou 510642,China
  • 收稿日期:1900-01-01 出版日期:2000-04-10 发布日期:2000-04-10

Transfer of Antibacterial Peptide D Gene into Tomato and Identification of Transgenic Plants

  • Received:1900-01-01 Online:2000-04-10 Published:2000-04-10

摘要: 用花粉管通道法将柞蚕抗菌肽D基因导入番茄,获得了转基因植株。应用PCR技术、DNA斑点杂交以及Southern印迹分析表明,抗菌肽D基因已整合到番茄基因组;而且,位于目的基因下游的胭脂碱合成酶基因有表达。青枯假单孢菌活体接种结合高发病大田种植试验结果显示,部分转基因植株的子一代具有较强的抗青枯病能力。
Abstract:By using pollen-tube pathway,antibacterial peptide D(AP-D) gene developed from Chinese oak silkwarm was transferred into tomato.PCR,dot and Southern blot analysis confirmed that stable integration of AP-D gene into the tomato genome had occurred.The expression of NOP gene which was localized at downstream of AP-D gene was confirmed with nopaline detection.In comparision with non-transgenicplants,some transgenic plant expressed a stronger resistance value to bacterialwilt disease (Pseudomonas solanacearum).

关键词: 抗菌肽D基因, 花粉通道法, antibacterial peptide-D gene, 青枯病
Key words,
番茄