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An efficient transformation method for the bioplastic-producing 'Knallgas' bacterium Ralstonia eutropha H16

机译:生物塑料生产“Knallgas”细菌Ralstonia eutropha H16的有效转化方法

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摘要

Ralstonia eutropha H16 (also known as Cupriavidus necator H16) is a Gram-negative lithoautotrophic β-proteobacterium with increasing biotechnological applications, including carbon capture and utilization, biopolymer synthesis and biofuel production. Engineering of this organism is supported by the availability of its genome sequence and suitable plasmid systems. However, the lack of a simple and robust transformation method remains a challenge as it limits both the pace and ease of engineering this organism. To overcome this limitation, a systematic study was performed to evaluate the effects of different parameters on the transformation efficiency of R. eutropha H16. The optimized electroporation protocol uses R. eutropha H16 cells grown to OD600 0.6. These cells were made competent by a 15-min incubation in 50 mM CaCl2 , followed by two cell washes and final resuspension in 0.2 M sucrose prior to electroporation using 2.3 kV. This protocol achieved a transformation efficiency of (3.86 ± 0.29) x 10(5) cfu/μg DNA, a 10(3) -fold improvement compared to a previously published value for the same plasmid. This transformation method is a valuable tool for R. eutropha H16 research and will further enable the development of other advanced molecular biology methods for this industrially relevant microorganism.
机译:富营养的Ralstonia eutropha H16(也称为铜尿杆菌necator H16)是革兰氏阴性的自养性β-变形杆菌,具有越来越多的生物技术应用,包括碳捕获和利用,生物聚合物合成和生物燃料生产。其基因组序列和合适质粒系统的可用性支持了该生物的工程改造。但是,缺乏简单而强大的转化方法仍然是一个挑战,因为它限制了对该生物进行工程改造的速度和难度。为了克服此限制,进行了系统的研究,以评估不同参数对富氧罗汉果H16转化效率的影响。优化的电穿孔方案使用生长到OD600 0.6的富营养R. eutropha H16细胞。通过在50 mM CaCl2中孵育15分钟使这些细胞具有感受态,然后进行两次细胞洗涤并最终重悬于0.2 M蔗糖中,然后再使用2.3 kV电穿孔。该协议实现了(3.86±0.29)x 10(5)cfu /μgDNA的转化效率,与以前发布的相同质粒的值相比,提高了10(3)倍。这种转化方法是富营养R. eutropha H16研究的一种有价值的工具,并将进一步为该工业相关微生物开发其他先进的分子生物学方法。

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