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首页> 外文期刊>Journal of Plant Biochemistry and Biotechnology >A comparative study of transgenic canola (Brassica napus L.) harboring either chimeric or native Chit42 genes against phytopathogenic fungi
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A comparative study of transgenic canola (Brassica napus L.) harboring either chimeric or native Chit42 genes against phytopathogenic fungi

机译:带有嵌合或天然Chit42基因抗植物病原真菌的转基因油菜(Brassica napus L.)的比较研究

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摘要

Canola (Brassica napus L.), an agro-economically important crop in the world, is sensitive to many fungal pathogens. One strategy to combat fungal diseases is genetic engineering through transferring genes encoding the pathogenesis-related (PR) proteins such as chitinase which cause the chitin degradation of fungal cell wall. Chitinase Chit42 from Trichoderma atroviride (PTCC5220) plays an important role in biocontrol and has high antifungal activity against a wide range of phytopathogenic fungi. This enzyme lacks a chitin binding domain (ChBD) which is involved in binding activity to insoluble chitin. In the present study, we investigated the effect of chitin binding domain fused to Chit42 when compared with native Chit42. These genes were over-expressed under the CaMV35S promoter in B. napus, R line Hyola 308. Transformation of cotyledonary petioles was achieved by pBISM2 and pBIKE1 constructs containing chimeric and native Chit42 genes respectively, via Agrobacterium method. The insertion of transgenes in T0 generation was verified through polymerase chain reaction (PCR) and Southern blot analysis. Antifungal activity of expressed chitinase in transgenic plants was also investigated by bioassays. The transgenic canola expressing chimeric chitinase showed stronger inhibition against phytopathogenic fungi that indicates the role of chitin binding domain.
机译:双低油菜籽(甘蓝型油菜)在世界上具有重要的经济意义,对许多真菌病原体都很敏感。对抗真菌疾病的一种策略是通过转移编码致病相关(PR)蛋白(例如几丁质酶)的基因进行基因工程,这些蛋白会导致几丁质降解真菌细胞壁。源自木霉阿奇病毒的几丁质酶Chit42(PTCC5220)在生物防治中起着重要作用,并且对多种植物病原真菌具有很高的抗真菌活性。该酶缺乏甲壳质结合结构域(ChBD),其与不溶性甲壳质的结合活性有关。在本研究中,我们调查了与天然Chit42相比,融合到Chit42的几丁质结合域的作用。这些基因在甘蓝型油菜,R系Hyola 308的CaMV35S启动子下过表达。子叶柄的转化是通过农杆菌法通过分别含有嵌合和天然Chit42基因的pBISM2和pBIKE1构建体实现的。通过聚合酶链反应(PCR)和Southern印迹分析验证了T0代中转基因的插入。还通过生物测定研究了表达的几丁质酶在转基因植物中的抗真菌活性。表达嵌合几丁质酶的转基因双低油菜籽对植物病原性真菌表现出更强的抑制作用,表明几丁质结合域的作用。

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