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首页> 外文期刊>Plant Cell, Tissue and Organ Culture: An International Journal on in Vitro Culture of Higher Plants >Improvements in Agrobacterium-mediated transformation of cassava (Manihot esculenta Crantz) for large-scale production of transgenic plants
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Improvements in Agrobacterium-mediated transformation of cassava (Manihot esculenta Crantz) for large-scale production of transgenic plants

机译:农杆菌介导的木薯转化(Manihot esculenta Crantz)的改良,用于大规模生产转基因植物

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摘要

Cassava (Manihot esculenta Crantz) is a major staple food crop of the humid tropics. As a heterozygous, vegetatively propagated crop, robust transformation protocols must be developed for elite cultivars that allow predictable production of large numbers of independent transgenic plant lines. A high throughput Agrobacterium-mediated transformation system was developed for the elite East African farmer-preferred cassava cultivar TME 204 using the GFP visual marker gene. Inclusion of the antibiotic moxalactam in culture medium used to produce embryogenic target tissues prior to inoculation with Agrobacterium increased recovery of independent GFP-expressing transgenic callus lines by up to 113-fold compared to the control. Enhanced transformation was also observed when TME 204 tissues were pretreated with other cephalosporins, namely cefoperazone, cefoxitin, cefmetazole and cefotaxime. Similar but less dramatic increases in transformation efficiencies were seen for the West African cultivars Oko-iyawo and 60444 when pre-treated with moxalactam. Dilution of Agrobacterium suspensions used for co-culture was found to increase transformation efficiencies, resulting in regeneration at an average of 33 GFP-expressing TME 204 plants per cc settled cell volume at OD600 0.05, compared to 15 plants at the more commonly used OD600 0.5. The optimized transformation systems were successfully utilized for the integration of genetic constructs for disease resistance and nutritional enhancement into more than 750 plants of TME 204.
机译:木薯(Manihot esculenta Crantz)是热带潮湿地区的主要主食作物。作为杂合的,无性繁殖的作物,必须为精英品种开发可靠的转化方案,以允许可预测地生产大量独立的转基因植物。利用GFP视觉标记基因,为东非精英农民首选的木薯品种TME 204开发了高通量农杆菌介导的转化系统。与对照相比,在用农杆菌接种之前将抗生素莫拉西坦包含在用于产生胚发生靶组织的培养基中,使表达独立GFP的转基因愈伤组织的回收率提高了多达113倍。当用其他头孢菌素,即头孢哌酮,头孢西丁,头孢甲唑和头孢噻肟预处理TME 204组织时,也观察到了增强的转化。西非品种Oko-iyawo和60444用莫西内酰胺进行预处理后,转化效率的增加相似但不明显。发现用于共培养的农杆菌悬浮液的稀释可提高转化效率,导致每cc沉降细胞体积平均每33个表达GFP的TME 204植物再生,OD600 0.05,而更常用的OD600 0.5为15植物。优化的转化系统已成功用于将抗病和营养增强的遗传构建体整合到TME 204的750多种植物中。

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