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作物学报 ›› 2008, Vol. 34 ›› Issue (05): 783-789.doi: 10.3724/SP.J.1006.2008.00783

• 作物遗传育种·种质资源·分子遗传学 • 上一篇    下一篇

转阿特拉津氯水解酶基因烟草的获得及其生物降解能力分析

王绘砖;陈喜文;王永芹;蔡宝立;陈德富*   

  1. 南开大学生命科学学院, 天津300071
  • 收稿日期:2007-07-26 修回日期:1900-01-01 出版日期:2008-05-12 网络出版日期:2008-05-12
  • 通讯作者: 陈德富

Obtainment of atzA-Transgenic Tobacco Plants and Analysis of Their Phytoremediation Capability

WANG Hui-Zhuan,CHEN Xi-Wen,WANG Yong-Qin,CAI Bao-Li,CHEN De-Fu*   

  1. College of Life Sciences, Nankai University, Tianjin 300071, China
  • Received:2007-07-26 Revised:1900-01-01 Published:2008-05-12 Published online:2008-05-12
  • Contact: CHEN De-Fu

摘要: 阿特拉津氯水解酶(AtzA)能有效催化有毒的阿特拉津脱氯生成无毒的羟基阿特拉津。本文将来自假单胞菌ADP的atzA-ADP和来自节杆菌AD1的atzA-NK分别插入Ti载体pBin438, 构建了atzA植物表达载体pBin438-atzA- ADP和pBin438-atzA-NK。并通过农杆菌介导法将其转入烟草, 经基因组PCR筛选及RT-PCR分析, 获得16株转atzA-ADP烟草株系和11株转atzA-NK烟草株系。在含150 mg L-1阿特拉津的1/2MS培养基上生长50 d时, 株系401的降解能力最高, 达79.26%, 远高于野生型烟草的0.47%, 说明转基因烟草可用于建立阿特拉津残留环境的植物修复系统。

关键词: 阿特拉津氯水解酶, 转基因, 农杆菌介导法, 烟草, 阿特拉津降解能力

Abstract: Atrazine (2-chloro-4-ethylamino-6-isopropylamno-1,3,5-triazine) is a wildly used herbicide in the world for controlling broad-leaf weeds in corn and sugarcane. However, atrazine is degraded slowly in the environment with an average half-life ranging from 4 to 57 weeks, and has been detected in soil as well as in ground and surface water in several countries. Atrazine chlorohydrolase (AtzA) catalyses the hydrolytic dechlorination and detoxification of atrazine to hydroxyatrazine, a non-herbicidal and non-toxic substance and is more strongly sorbed to soil than atrazine. In the present paper, atzAs were amplified from pMD4 plasmid (containing atzA-ADP) and pET21b-atzA-NK plasmid (containing atzA-NK), and inserted into plant expression plasmid pBin438. The recombinant plasmid was successfully introduced into tobacco leaf disks by Agrobacterium-mediated transformation and 136 plantlets were regenerated from selected medium contained 20 mg L-1 kanamycin and 150 μg mL-1 atrazine, and then were subjected to analyses of PCR and RT-PCR. The PCR using primers atzA-7/atzA-2, atzA-5/atzA-8, and atzA-7/atzA-8, which are specific for atzA, revealed that 42 of 72 (58.3%) pBin438-atzA-ADP and 38 of 64 (59.4%) of pBin438-atzA-NK regenerated plants were transgenic, respectively. Further RT-PCR indicated that 38.1% (16 of 42) of atzA-ADP and 28.9% (11 of 38) of atzA-NK, expressed AtzA in transgenic tobacco plants, respectively. After 50 days’ growth on 1/2MS medium contained 150 mg L-1 atrazine, the transgenic plants degraded a large amount of atrazine presented in the medium with degrading as high as 79.26% in line 401, whereas 0.47% in the wild type. These results indicated that the transgenic tobacco plants can catalyze atrazine effi-ciently.

Key words: Atrazine chlorohydrolase (AtzA), Transgenic, Agrobacterium-mediate transformation, Tobacco, Phytoremediation capability of atrazine

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