Abstract
Plasmid pGV1106, a derivative of the wide-host-range plasmid S-a of the W incompatibility group, was introduced into Rhizobium meliloti 41 by plasmid-mediated mobilization to overcome the restriction of foreign DNA. The mobilized plasmid pKK2 differed from the original pGV1106 by an extra piece of DNA of 1.3 kilobase pairs which supposedly originated from pJB3JI used for mobilization. If pKK2 was isolated from R. meliloti 41, it could be successfully reintroduced by transformation. The transformation frequency was low (10 to 54 colonies per micrograms of plasmid DNA) but reproducible, and several lines of evidence showed that it was the consequence of plasmid DNA uptake. The small size (10.3 kilobases) and elevated copy number (10 to 15 copies per cell) of pKK2 make it a potentially useful cloning vector for the study of symbiotic nitrogen fixation genes of R. meliloti 41.
MeSH Terms
Conjugation, Genetic
DNA Restriction Enzymes
Deoxyribonucleases, Type II Site-Specific
Plasmids
Rhizobium/genetics
Transformation, Bacterial
Chemicals
DNA Restriction Enzymes
CTGCAG-specific type II deoxyribonucleases
Deoxyribonucleases, Type II Site-Specific
GGTACC-specific type II deoxyribonucleases
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Kiss G B
Kálmán Z
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