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1 Department of Microbiology, Oregon State University, Corvallis 97331-3804
2 Marshall Products, Madison, WI 53713
Conditions that allow efficient genetic transformation of dairy Leuconostoc by electroporation were determined. The technique allowed transformation of Leuconostoc mesenteroides ssp. cremoris, Leuconostoc mesenteroides ssp. dextranicum, and Leuconostoc lactis with plasmid pNZ12. Optimized conditions resulted in transformation efficiencies of up to 2 x 106/µg of pNZ12 DNA for L. cremoris 44-4. Further, cloning vectors pNZ18, pGK12, pGK13, pGL3, pBD64, pGB301, pDB101, and pAMß1 from lactococcal, Bacillus, and Escherichia hosts were introduced and maintained by L. cremoris 44-4, extending the range of vectors functional in Leuconostoc.
Key Words: Leuconostoc transformation plasmids
Submitted on August 9, 1990
Accepted on December 28, 1990
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