[Molecular cloning and functional analysis of DNA regions of plasmid RP4 determining the incompatibility properties].Genetika. 1986 Aug; 22(8):2025-34.G
Abstract
Sau3A-generated DNA fragments determining incompatibility functions of the plasmid RP4 were cloned on the vectors pTK16 and pBR322. Inc+ recombinant plasmids were divided into two types: 1) expressing incompatibility only towards the homologous RP4 replicon, 2) expressing incompatibility - both towards the homologous RP4 replicon and towards the heterologous replicons of plasmids R906 and R751. For one member of the first type plasmids it was shown that the cloned Inc+-specific insertion derived from the region of location of the EcoRI restriction site. The majority of the Inc+ recombinant plasmids showed asymmetric expression of incompatibility, predominantly eliminating the resident IncP plasmid.
MeSH
Pub Type(s)
Journal Article
Language
rus
PubMed ID
3021575
Citation
Riabchenko, L E., et al. "[Molecular Cloning and Functional Analysis of DNA Regions of Plasmid RP4 Determining the Incompatibility Properties]." Genetika, vol. 22, no. 8, 1986, pp. 2025-34.
Riabchenko LE, Riabchenko NF, Dobrovol'skiĭ P, et al. [Molecular cloning and functional analysis of DNA regions of plasmid RP4 determining the incompatibility properties]. Genetika. 1986;22(8):2025-34.
Riabchenko, L. E., Riabchenko, N. F., Dobrovol'skiĭ, P., Sakanian, V. A., & Alikhanian, S. I. (1986). [Molecular cloning and functional analysis of DNA regions of plasmid RP4 determining the incompatibility properties]. Genetika, 22(8), 2025-34.
Riabchenko LE, et al. [Molecular Cloning and Functional Analysis of DNA Regions of Plasmid RP4 Determining the Incompatibility Properties]. Genetika. 1986;22(8):2025-34. PubMed PMID: 3021575.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR
T1 - [Molecular cloning and functional analysis of DNA regions of plasmid RP4 determining the incompatibility properties].
AU - Riabchenko,L E,
AU - Riabchenko,N F,
AU - Dobrovol'skiĭ,P,
AU - Sakanian,V A,
AU - Alikhanian,S I,
PY - 1986/8/1/pubmed
PY - 1986/8/1/medline
PY - 1986/8/1/entrez
SP - 2025
EP - 34
JF - Genetika
JO - Genetika
VL - 22
IS - 8
N2 - Sau3A-generated DNA fragments determining incompatibility functions of the plasmid RP4 were cloned on the vectors pTK16 and pBR322. Inc+ recombinant plasmids were divided into two types: 1) expressing incompatibility only towards the homologous RP4 replicon, 2) expressing incompatibility - both towards the homologous RP4 replicon and towards the heterologous replicons of plasmids R906 and R751. For one member of the first type plasmids it was shown that the cloned Inc+-specific insertion derived from the region of location of the EcoRI restriction site. The majority of the Inc+ recombinant plasmids showed asymmetric expression of incompatibility, predominantly eliminating the resident IncP plasmid.
SN - 0016-6758
UR - https://www.unboundmedicine.com/medline/citation/3021575/[Molecular_cloning_and_functional_analysis_of_DNA_regions_of_plasmid_RP4_determining_the_incompatibility_properties]_
DB - PRIME
DP - Unbound Medicine
ER -