scholarly journals Location and nucleotide sequence of the transfer origin of the broad host range plasmid RK2.

1983 ◽  
Vol 80 (12) ◽  
pp. 3595-3598 ◽  
Author(s):  
D. G. Guiney ◽  
E. Yakobson
Keyword(s):  
Nucleotide Sequence ◽  
Host Range ◽  
Broad Host Range ◽  
Broad Host Range Plasmid ◽  
Transfer Origin ◽  
Plasmid Rk2

Nucleotide sequence of korB, a replication control gene of broad host-range plasmid RK2

1987 ◽  
Vol 198 (2) ◽  
pp. 211-222 ◽  
Author(s):  
Jon A. Kornacki ◽  
Paul J. Balderes ◽  
David H. Figurski
Keyword(s):  
Nucleotide Sequence ◽  
Host Range ◽  
Broad Host Range ◽  
Control Gene ◽  
Broad Host Range Plasmid ◽  
Replication Control ◽  
Plasmid Rk2

Nucleotide sequence of the trfA gene of broad host-range plasmid RK2

1984 ◽  
Vol 175 (3) ◽  
pp. 251-262 ◽  
Author(s):  
Christopher A. Smith ◽  
Christopher M. Thomas
Keyword(s):  
Nucleotide Sequence ◽  
Host Range ◽  
Broad Host Range ◽  
Broad Host Range Plasmid ◽  
Plasmid Rk2

Nucleotide sequence of the region of the origin of replication of the broad host range plasmid RK2

1981 ◽  
Vol 181 (1) ◽  
pp. 8-12 ◽  
Author(s):  
David M. Stalker ◽  
Christopher M. Thomas ◽  
Donald R. Helinski
Keyword(s):  
Nucleotide Sequence ◽  
Host Range ◽  
Broad Host Range ◽  
Origin Of Replication ◽  
Broad Host Range Plasmid ◽  
Plasmid Rk2

scholarly journals Promoters of the broad host range plasmid RK2: analysis of transcription (initiation) in five species of gram-negative bacteria.

Genetics ◽  
1992 ◽  
Vol 130 (1) ◽  
pp. 27-36 ◽  
Author(s):  
A Greener ◽  
S M Lehman ◽  
D R Helinski
Keyword(s):  
Host Range ◽  
Transcription Initiation ◽  
Promoter Activity ◽  
Firefly Luciferase ◽  
Broad Host Range ◽  
Gram Negative Bacteria ◽  
Gram Negative ◽  
Broad Host Range Plasmid ◽  
Transcriptional Start Sites ◽  
Plasmid Rk2

Abstract A broad host range cloning vector was constructed, suitable for monitoring promoter activity in diverse Gram-negative bacteria. This vector, derived from plasmid RSF1010, utilized the firefly luciferase gene as the reporter, since the assay for its bioluminescent product is sensitive, and measurements can be made without background from the host. Twelve DNA fragments with promoter activity were obtained from broad host range plasmid RK2 and inserted into the RSF1010 derived vector. The relative luciferase activities were determined for these fragments in five species of Gram-negative bacteria. In addition, four promoters were analyzed by primer extension to locate transcriptional start sites in each host. The results show that several of the promoters vary substantially in relative strengths or utilize different transcriptional start sites in different bacteria. Other promoters exhibited similar activities and identical start sites in the five hosts examined.

Multiple mechanisms for expression of incompatibility by broad-host-range plasmid RK2

1982 ◽  
Vol 152 (3) ◽  
pp. 1078-1090
Author(s):  
R Meyer ◽  
M Hinds
Keyword(s):  
Dna Replication ◽  
Host Range ◽  
Plasmid Dna ◽  
Plasmid Vector ◽  
Broad Host Range ◽  
Plasmid Maintenance ◽  
Broad Host Range Plasmid ◽  
Expression Of Genes ◽  
Plasmid Partitioning ◽  
Plasmid Rk2

By cloning fragments of plasmid DNA, we have shown that RK2 expresses incompatibility by more than one mechanism. One previously identified (R. J. Meyer, Mol. Gen, Genet. 177:155--161, 1979; Thomas et al., Mol. Gen. Genet. 181:1--7, 1981) determinant for incompatibility is linked to the origin of plasmid DNA replication. When cloned into a plasmid vector, this determinant prevents the stable inheritance of a coresident RK2. However, susceptibility to this mechanism of incompatibility requires an active RK2 replicon and is abolished if another replicator is provided. We have also cloned a second incompatibility determinant, encoded within the 54.1- to 56.4-kilobase region of RK2 DNA, which we call IncP-1(II). An RK2 derivative remains sensitive to IncP-1(II), even when it is not replicating by means of the RK2 replicon. The 54.1- to 56.4-kilobase DNA does not confer susceptibility to the IncP-1(II) mechanism, nor does it encode a detectable system for efficient plasmid partitioning. The incompatibility may be related to the expression of genes mapping in the 54.1- to 56.4-kilobase region, which are required for plasmid maintenance and suppression of plasmid-encoded killing functions.

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