𝔖 Bobbio Scriptorium
✦   LIBER   ✦

The isolation and characterization of Escherichia coli dnaB::Tn10 insertion mutations

✍ Scribed by Sclafani, Robert A. ;Wechsler, James A. ;Schuster, Heinz


Publisher
Springer
Year
1981
Tongue
English
Weight
737 KB
Volume
182
Category
Article
ISSN
0026-8925

No coin nor oath required. For personal study only.

✦ Synopsis


Exploitation of the ability of the ban protein encoded by phage P1 to compensate for dnaB-defective host mutations, allowed the isolation of dnaB: :Tnl0 insertion mutations. The presence of Plbac prophage was required for survival of dnaB::TnlO mutants, and such lysogens were cryosensitive. The insertions were shown to map in dnaB by transduction and this was confirmed by complementation analysis. The dnaB::TnlO (P1 bac) strains were non-permissive for 2 growth but did support the growth of 2-dnaB + specialized transducing phage. No antigenically active dnaB product could be detected by immunologic assays using either of two methods. In addition, it was shown that the observed cryosensitivity of Plbac suppression was a direct result of reversible inactivation of the ban protein at low temperature.


πŸ“œ SIMILAR VOLUMES


Isolation and properties of Tn10 inserti
✍ Binding, Ron ;Romansky, Gary ;Bitner, Rex ;Kuempel, Peter πŸ“‚ Article πŸ“… 1981 πŸ› Springer 🌐 English βš– 805 KB

Two Tn10 insertions that are in the rac locus of the chromosome of Escherichia coli have been isolated and characterized. The insertions are located at min 29.7 and min 30.0. The insertions are stable when an F123 rac::Tn10 episome is transferred to an F- rac+ recipient, but they are lost at a high

Isolation and characterization of Escher
✍ QuiΓ±ones, Ariel ;Piechocki, Reinhard πŸ“‚ Article πŸ“… 1985 πŸ› Springer 🌐 English βš– 849 KB

To identify the nature and origin of spontaneous mutability we developed a screening procedure suitable to isolate antimutators showing a lower error rate than 10-10 per base per replication. Among about 500,000 mutagenized colonies we found 20 mutants showing a reduced spontaneous mutability. These

Physical mapping of the srl recA region
✍ Willis, David K. ;Uhlin, Bernt Eric ;Amini, Kim S. ;Clark, Alvin J. πŸ“‚ Article πŸ“… 1981 πŸ› Springer 🌐 English βš– 927 KB

A restriction endonuclease map for the enzymes EcoRI, BamHI, SalI, and PstI covering 23.5 kilobase pairs (kb) of the srl recA region of Escherichia coli was constructed. An insertion of the transposon Tn10 in the negative regulatory gene srlR was shown to be located 5.8 kb away from the promoter pro

Transfer of the Ξ” (argF-lac) U169 mutati
✍ Schweizer, Herbert ;Boos, Winfried πŸ“‚ Article πŸ“… 1983 πŸ› Springer 🌐 English βš– 200 KB

To facilitate construction of mutants harboring delta lac for use in gene fusion studies, strains were constructed that carry the transposon Tn10 next to the well defined lac deletion U169. This deletion can now be moved to other Escherichia coli strains in transductional or conjugational crosses by

Insertion mutations in the dam gene of E
✍ Marinus, M. G. ;Carraway, Margaretha ;Frey, Alexis Z. ;Brown, Leif ;Arraj, Judy πŸ“‚ Article πŸ“… 1983 πŸ› Springer 🌐 English βš– 235 KB

The dam gene of E. coli can be inactivated by insertion of Tn9 or Mud phage. Strains bearing these mutations are viable indicating that the dam gene product is dispensable.

Isolation and characterization of the th
✍ Eugenio I. Vivas; Andreina Liendo; Karl Dawidowicz; TomΓ‘s IstΓΊriz πŸ“‚ Article πŸ“… 1994 πŸ› John Wiley and Sons 🌐 English βš– 423 KB

It is known that two gluconokinases are inducibly expressed during the utilization of gluconate by E. coli. One is therrnoresistant (activity stable for 3 h at 30 "C) and the other thermosensitive (losses 75% or more of its activity under the above conditions). The thermoresistant gluconokinase (EC