원문정보
Penicillin-G 첨가 배지에서 배양한 코리네형 세균의 전기장 충격법에 의한 고효율 형질전환
초록
영어
Using the shuttle vector pECCGl between Escherichia coli and Corynebacterium glutamicum and C. glutamicum strain JS231 grown in the medium supplemented with penicillin-G, which inhibits the formation of cross-links in the peptidoglycan of bacterial cell wall, various parameters involved in electroporation system including resistance, electric field strength, capacitance, DNA concentration, and cell density were investigated independently and optimized for the high efficiency transformation of coryneform bacteria. Using cells grown with 0.3U/ml of penicillin-G and harvested at A600 of 0.7-0.8, transformation efficiencies of 107-l08 transformants/ug of DNA with Corynebcctertum glutamicum strain JS231 and wild type ATCC13032 were achieved under conditions of 12.5kV/cm of electric field strength, 400 ohms of resistance, 25uF of capacitance, 3108 cells per transformation(1.21010 cells/ml) and 100ng of plasmid DNA per transformation.
목차
INTRODUCTION
MATERIALS AND METHODS
Bacterial strains and plasmids
Media and bacterial cultivation
Plasmid DNA preparation and DNA manipulations
Electroporation equipment and electroporation procedure
RESULTS
Optimization of conditions for C. glulamicum electroporation
Resistance :
Electric field strength :
Capacitance :
DNA concentration :
Cell density :
DISCUSSION
ABBREVIATIONS
ACKNOWLEDGMENT
요약
REFERENCES
