๐”– Bobbio Scriptorium
โœฆ   LIBER   โœฆ

Properties of hybrid plasmids, consisting of parts of the mini-R1 factorRsc11 andColE1

โœ Scribed by Boidol, W. ;Siewert, G. ;Lindenmaier, W. ;Luibrand, G. ;Goebel, W.


Publisher
Springer
Year
1977
Tongue
English
Weight
641 KB
Volume
152
Category
Article
ISSN
0026-8925

No coin nor oath required. For personal study only.


๐Ÿ“œ SIMILAR VOLUMES


Replication of the mini-R1 plasmid Rsc11
โœ Mayer, H. ;Luibrand, G. ;Goebel, W. ๐Ÿ“‚ Article ๐Ÿ“… 1977 ๐Ÿ› Springer ๐ŸŒ English โš– 789 KB

Replication of the multicopy mini-R1 plasmid, Rsc11, is dependent on host replication functions dna A, B, C, E and G but independent of polA1. Chloramphenicol immediately stops its replication. A stable relaxation complex is not formed. Composite plasmids were constructed with Rsc11 and other small

The construction and replication propert
โœ Lane, D. ;Chandler, M. ;Silver, L. ;Bruschi, A. ;Caro, L. ๐Ÿ“‚ Article ๐Ÿ“… 1979 ๐Ÿ› Springer ๐ŸŒ English โš– 545 KB

We have cloned the entire r-determinant of the antibiotic resistance plasmid R100.1 on the plasmic vectors pCR1 and pSC201. We find that the hybrid plasmids segregate from cultures in which replication of the vector is blocked. This suggests that the r-det is not capable of autonomous replication.

The properties of hybrids formed between
โœ Stanisich, Vilma A. ;Bennett, P. M. ๐Ÿ“‚ Article ๐Ÿ“… 1976 ๐Ÿ› Springer ๐ŸŒ English โš– 638 KB

R38, R931-1, and R933 are conjugative plasmids derived from strains of Pseudomonas aeruginosa. They confer resistance to mercuric ions (Hg-r), and do not tranfer from P. aeruginosa to Escherichia coli at detectable frequencies. Hybrids between each of these plasmids and the P-group plasmid, RP1, hav

In vitro system for the replication of t
โœ G. S. Bezanson; W. Goebel ๐Ÿ“‚ Article ๐Ÿ“… 1979 ๐Ÿ› Springer ๐ŸŒ English โš– 794 KB

The in vitro synthesis of the mini R1-factor, Rsc11, was achieved using a soluble Escherichia coli cell-extract system. Triton X-100 lysates of the K12 strain 1101 (Rsc11) fractionated by Sephadex G25 chromatography supported the incorporation of labeled deoxyribonucleotides into covalently-closed c