植物学报 ›› 2007, Vol. 24 ›› Issue (04): 459-464.

• 实验简报 • 上一篇    下一篇

反义4CL与UGPase双价基因在烟草中的转化及表达分析

梁海泳 夏秀英 高晓蓉 苏乔   

  1. 大连理工大学环境与生命学院, 大连 116026
  • 收稿日期:2006-07-04 修回日期:2007-01-07 出版日期:2007-07-01 发布日期:2007-07-01
  • 通讯作者: 夏秀英

Vector Construction with UGPase and anti4CL, and Their Expression in Transgenic Tobacco

Haiyong Liang Xiuying Xia Xiaorong Gao Qiao Su   

  1. School of Environmental and Biological Science and Technology, Dalian University of Technology, Dalian 116026, China
  • Received:2006-07-04 Revised:2007-01-07 Online:2007-07-01 Published:2007-07-01
  • Contact: Xiuying Xia

摘要: 构建了携带紫穗槐尿苷二磷酸葡萄糖焦磷酸化酶(UDP-glucose pyrophosphorylase, UGPase)基因和4-香豆酸: 辅酶A连接酶(4-coumarate: coenzyme A ligase, 4CL)反义基因的双价基因植物表达载体, 用热激法转化至根癌农杆菌LBA4404中, 并用制备的农杆菌工程菌进行了烟草转化。PCR及Southern 杂交结果证实, 双价基因已成功整合到烟草基因组中。综纤维素和硫酸木质素含量测定结果显示, 转基因烟草纤维素含量增加, 木质素含量减少,表明双价基因能够有效表达。

Abstract: We describe our construction of a plant expression vector, which contained an UDP-glucose pyrophosphorylase gene and an anti-sense 4-coumarate: CoA ligase gene. The vector was transferred by use of Agrobacterium tumefaciens into tobacco. Results of PCR and Southern blot analysis indicated that both genes were integrated into the tobacco genome successfully. Holocellulose content was increased and Klason lignin content significantly reduced, which illustrated that the two genes were expressed effectively in the tobacco genome.