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通过电穿孔法对副干酪魏斯氏菌DX进行质粒转化。

Plasmid transformation of Weissella paramesenteroides DX by electroporation.

作者信息

Papagianni Maria, Papamichael Emmanuel M

机构信息

Department of Hygiene and Technology of Food of Animal Origin, School of Veterinary Medicine, Aristotle University of Thessaloniki, Thessaloniki 54 124, Greece.

Department of Chemistry, University of Ioannina, Ioannina 45 110, Greece.

出版信息

Anaerobe. 2014 Dec;30:60-4. doi: 10.1016/j.anaerobe.2014.08.013. Epub 2014 Sep 6.

Abstract

The present investigation sought to provide a reliable and highly efficient electrotransformation method for the lactic acid bacterium Weissella paramesenteroides DX. Experiments were carried out with the shuttle vectors pVS44 (2910 bps), pTRKH3 (7766 bps) and its derivative pTRKH3-1 (4855 bps). Several parameters, including the concentration of transforming plasmid DNA, plasmid size, electric field strength, age of the culture, cell density, and the pretreatment of cells with dl-threonine, lysozyme, and combined treatment with lithium acetate and dithiothreitol, were investigated and proved to influence the efficiency of transformation. Electrocompetence was found to peak in the early stationary phase (OD600 1.2). Other optimized conditions included: the concentration of 10 μg/ml transforming DNA, the cell density of 10(10) cells/ml, a high-density electric field pulse of 2.5 kV, 25 μF and 200 Ω, pretreatment of cells with 40 mM dl-threonine and 2000 U/ml lysozyme, and yielded 3.5×10(4) transformants/μg DNA for pVS44 while 1.2×10(4) transformants/μg DNA for the large plasmid TRKH3. Compared to previously reported data, the obtained transformation efficiencies provided an 8.75-fold increase for pVS44 and ensured plasmid stability for 120 generations in non-selective medium.

摘要

本研究旨在为副干酪魏斯氏菌DX提供一种可靠且高效的电转化方法。使用穿梭载体pVS44(2910 bp)、pTRKH3(7766 bp)及其衍生物pTRKH3-1(4855 bp)进行实验。研究了几个参数,包括转化质粒DNA的浓度、质粒大小、电场强度、培养物的菌龄、细胞密度以及用dl-苏氨酸、溶菌酶进行细胞预处理,以及乙酸锂和二硫苏糖醇联合处理,结果证明这些参数会影响转化效率。发现电转化能力在稳定期早期(OD600 1.2)达到峰值。其他优化条件包括:转化DNA浓度为10 μg/ml,细胞密度为10(10)个细胞/ml,2.5 kV、25 μF和200 Ω的高密度电场脉冲,用40 mM dl-苏氨酸和2,000 U/ml溶菌酶对细胞进行预处理,对于pVS44,每μg DNA产生3.5×10(4)个转化子,而对于大质粒TRKH3,每μg DNA产生1.2×10(4)个转化子。与先前报道的数据相比,所获得的转化效率使pVS44提高了8.75倍,并确保质粒在非选择性培养基中稳定120代。

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