Agrobacterium- Mediated Transformation of Tobacco Plants using Walnut Polyphenol Oxidase Gene

F. Khodadadi, M. Tohidfar, K. Vahdati, C. Leslie
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Abstract

Polyphenol oxidase (PPO) is a well-recognized copper-containing enzyme which can catalyze oxidation of a great variety of phenolic compounds. PPO is found in diverse microorganisms, plants, and animals. To examine the anti-pathogenic role of PPO in walnut (Juglans regia L.), Agrobacterium tumefaciens strain LBA4404 was used to transform tobacco (Nicotiana tobacum L.) explants. Recombinant binary vector pBI121, containing the walnut JrPPO gene and the nptII gene as a selectable marker, was incorporated into A. tumefaciens. MS medium supplemented with 50 mg/l of kanamycin and 200 mg/l of cefotaxime was used as a selection medium. Plantlets were regenerated from putatively transgenic calli and polymerase chain reaction and Southern blot analysis were performed to confirm the integration of JrPPO into the genome. To evaluate the function of PPO in pathogen resistance, transgenic tobacco plants were exposed to Pseudomonas syringae pv. tabaci. According to symptom progress and quantitative analyses, although there was no significant difference in transgenic tobacco, but mean comparison showed that disease severity of transgenic tobacco was less than wild plants. Finally, it may be concluded that PPO has a notable function in the resistance process in walnut, but tobacco transgenic plants might not be a suitable test plant to examine the resistance role of PPO in walnut.
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农杆菌介导的核桃多酚氧化酶基因转化烟草植株的研究
多酚氧化酶(PPO)是一种公认的含铜酶,可以催化多种酚类化合物的氧化。PPO存在于多种微生物、植物和动物中。为研究多酚氧化酶(PPO)对核桃(Juglans regia L.)的抗病原菌作用,采用根癌农杆菌LBA4404对烟草(Nicotiana tobacum L.)外植体进行转化。将核桃JrPPO基因和nptII基因作为选择标记的重组二元载体pBI121导入到瘤胃拟南杆菌中。选用MS培养基,添加50 mg/l卡那霉素和200 mg/l头孢噻肟作为选择培养基。通过聚合酶链反应和Southern blot分析证实JrPPO已整合到基因组中。为了研究PPO在烟草抗性中的作用,将转基因烟草暴露于丁香假单胞菌中。烟。根据症状进展和定量分析,虽然转基因烟草之间无显著性差异,但平均比较表明转基因烟草的疾病严重程度低于野生植物。由此可见,PPO在核桃抗病过程中具有显著的作用,但烟草转基因植株可能不是检验PPO在核桃抗病作用的合适试验植物。
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