将微型大肠杆菌K12质粒DNA转化为瘤胃农杆菌EHA105细胞用于植物遗传转化的简单安全方法

IF 1 Q3 BIOLOGY Bio-protocol Pub Date : 2025-01-05 DOI:10.21769/BioProtoc.5174
Beenzu Siamalube, Emmanuel Ehinmitan, Maina Ngotho, Justus Onguso, Steven Runo
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引用次数: 0

摘要

农杆菌介导的基因转化方法是开发转基因植物的重要分子生物学技术。植物通过基因工程培育出无病品种,去除作物改良中令人不安的性状,或者加入一种抗原蛋白,使植物成为生产可食用疫苗的绿色工厂。通过成功的转换验证了该方法的鲁棒性,证明了它作为植物生物技术研究人员的标准方法的有效性。它可以将外源DNA引入植物基因组。传统上,植物遗传转化依赖于耗时、昂贵和技术要求高的程序,如电穿孔和嵌合病毒或生物方法,这些方法通常产生可变的转化效率。本研究提出了一种简单且安全的方案,包括一种改进的冻融和热休克混合方法。该方法采用一种简化的质粒微型制备程序,从大肠杆菌K12菌株中分离出高质量的质粒DNA,然后将其靶向转移到大肠杆菌EHA105菌株中。优化后的方法最大限度地减少了DNA降解,最大限度地提高了农杆菌细胞的吸收,使其成为各种基因工程应用的可重复和可访问的方案。转化效率一贯高,提高质粒摄取,同时保持细胞活力,需要最少的专用设备和试剂。拟议的方案具有显著的优势,包括简单、可靠和成本效益,使其成为植物生物技术领域传统技术的一个有价值的替代方案。•使用液氮作为冷冻的代理。•使用用户友好的高拷贝分离试剂盒从合格的细菌细胞中提取质粒DNA。•最多连续五天就足以完成所有手续。
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Simple and Fail-safe Method to Transform Miniprep Escherichia coli Strain K12 Plasmid DNA Into Viable Agrobacterium tumefaciens EHA105 Cells for Plant Genetic Transformation.

Agrobacterium-mediated gene transformation method is a vital molecular biology technique employed to develop transgenic plants. Plants are genetically engineered to develop disease-free varieties, knock out unsettling traits for crop improvement, or incorporate an antigenic protein to make the plant a green factory for edible vaccines. The method's robustness was validated through successful transformations, demonstrating its effectiveness as a standard approach for researchers working in plant biotechnology. It enables the introduction of foreign DNA into plant genomes. Conventionally, plant genetic transformation has relied on time-consuming, costly, and technically demanding procedures, such as electroporation and chimeric viruses or biolistic methods, which usually yield variable transformation efficiencies. This study presents a simple and fail-safe protocol that involves a modified freeze-thaw and heat-shock concoction method. This approach involves a streamlined plasmid miniprep procedure to isolate high-quality plasmid DNA from Escherichia coli K12 strain, followed by a target-specific transfer into A. tumefaciens EHA105 strain. The optimized method minimizes DNA degradation and maximizes uptake by Agrobacterium cells, making it a reproducible and accessible protocol for various genetic engineering applications. The transformation efficiency is consistently high, enhancing plasmid uptake while maintaining cell viability, requiring minimal specialized equipment and reagents. The proposed protocol offers significant advantages, including simplicity, reliability, and cost-effectiveness, positioning it as a valuable alternative to traditional techniques in the field of plant biotechnology. Key features • Uses liquid nitrogen as a proxy for freezing. • Plasmid DNA from competent bacterial cells is extracted using a user-friendly high-copy isolation kit. • A maximum of five consecutive days is sufficient to complete the procedures.

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