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High efficiency introduction of plasmid DNA into glycine treated Enterococcus faecalis by electroporation

โœ Scribed by Cruz-Rodz, ArmandoL. ;Gilmore, MichaelS.


Publisher
Springer
Year
1990
Tongue
English
Weight
354 KB
Volume
224
Category
Article
ISSN
0026-8925

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โœฆ Synopsis


A highly efficient electroporation system for Enterococcus faecalis was developed by systematically optimizing different parameters. One parameter found to be particularly critical for electroporation was cultivation of E. faecalis in medium containing a high glycine concentration, prior to electroporation. Osmotic stabilization of cells with 0.5 M sucrose was also found to be critical during glycine treatment. 10(6) transformants per microgram of plasmid DNA were consistently obtained within 48 h. Electrocompetent preparations of E.-faecalis could be stored at - 70 degrees C without loss of competence.


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Efficient gene delivery into murine ovar
โœ Masahiro Sato; Maya Tanigawa; Natsuko Kikuchi; Shingo Nakamura; Minoru Kimura ๐Ÿ“‚ Article ๐Ÿ“… 2003 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 396 KB

## Abstract Summary: We describe the use of direct injection of circular plasmid DNA and subsequent in vivo electroporation (EP) for efficient gene delivery to the ovarian cells, including follicular cells and oocytes of mice. When Trypan blue (TB) was injected into the central portion of an ovary