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