Bioscience, Biotechnology, and Biochemistry
Online ISSN : 1347-6947
Print ISSN : 0916-8451
Transformation of Pseudomonas putida by Electroporation
Kazuhiro IwasakiHiroo UchiyamaOsami YagiTeruyo KurabayashiKozo IshizukaYoshichika Takamura
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JOURNAL FREE ACCESS

1994 Volume 58 Issue 5 Pages 851-854

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Abstract

The optimum electrotransformation conditions were determined for Pseudomonas putida PpY101 with plasmid pSUP104 (9.5kb) and pSR134 (18.6kb). Field strength was a very important parameter for electrotransformation efficiency. Optimum efficiencies (1.1x 105 transformants/μg DNA) with pSUP104 and pSR134 were obtained at a field strength of 12. 5 kV/cm, a time constant of about 4.5 ms (resistance setting of 200 Ω), a supercoiled DNA concentration of 100 ng/ml, and a cell concentration of 109/ml. Because the effciency obtained is high enough, electrotransformation is useful for the direct cloning of P. putida PpY101. No significant relationship between plasmid size and electrotransformation efficiency was observed. These efficiencies were about 4.5 times higher than those using the MgCl2 method. Under these conditions, electrotransformation efficiencies of relaxed plasmid DNA treated with topoisomerase I and that linearized by EcoRI digestion were high.

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