The effect of recA mutation on the expression of EcoKI and EcoR124I hsd genes cloned in a multicopy plasmid
Jazyk angličtina Země Spojené státy americké Médium print
Typ dokumentu časopisecké články
PubMed
9821288
DOI
10.1007/bf02818573
Knihovny.cz E-zdroje
- MeSH
- bakteriální geny MeSH
- bakteriální proteiny genetika metabolismus MeSH
- DNA restrikčně-modifikační enzymy genetika metabolismus MeSH
- Escherichia coli enzymologie genetika růst a vývoj MeSH
- klonování DNA MeSH
- mutace MeSH
- plazmidy genetika MeSH
- proteiny z Escherichia coli * MeSH
- RecA-rekombinasy genetika MeSH
- regulace genové exprese u bakterií * MeSH
- restrikční endonukleasy typu I genetika metabolismus MeSH
- restrikční enzymy genetika metabolismus MeSH
- síran hořečnatý farmakologie MeSH
- teplota MeSH
- Publikační typ
- časopisecké články MeSH
- Názvy látek
- bakteriální proteiny MeSH
- DNA restrikčně-modifikační enzymy MeSH
- endodeoxyribonuclease EcoKI MeSH Prohlížeč
- endodeoxyribonuclease EcoR124I MeSH Prohlížeč
- HsdR protein, E coli MeSH Prohlížeč
- HSDS protein, Bacteria MeSH Prohlížeč
- proteiny z Escherichia coli * MeSH
- RecA-rekombinasy MeSH
- restrikční endonukleasy typu I MeSH
- restrikční enzymy MeSH
- síran hořečnatý MeSH
Type I restriction-modification (R-M) endonucleases are composed of three subunits--HsdR, required for restriction, and HsdM and HsdS which can produce a separate DNA methyltransferase. The HsdS subunit is required for DNA recognition. In this paper we describe the effect of cloned EcoKI and EcoR124I hsd genes on the resulting R-M phenotype. The variability in the expression of the wild type (wt) restriction phenotype after cloning of the wt hsd genes in a multicopy plasmid in Escherichia coli recA+ background suggests that the increased production of the restriction endonuclease from pBR322 is detrimental to the cell and this leads to the deletion of the cloned hsd genes from the hybrid plasmid and/or inactivation of the enzyme. The effect of a mutation in E. coli recA gene on the expression of R-M phenotype is described and discussed in relation to the role of the cell surface and the localization of the restriction endonuclease in the cell.
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Annu Rev Biochem. 1969;38:467-500 PubMed
Folia Microbiol (Praha). 1994;39(6):452-8 PubMed
J Mol Biol. 1970 May 28;50(1):111-27 PubMed
Mol Gen Genet. 1983;190(1):92-100 PubMed
Gene. 1992 Mar 1;112(1):21-7 PubMed
Nucleic Acids Res. 1993 Feb 11;21(3):373-9 PubMed
Genetics. 1954 Jul;39(4):440-52 PubMed
Folia Microbiol (Praha). 1985;30(1):17-24 PubMed
Mol Gen Genet. 1980;180(1):35-46 PubMed
Ann Inst Pasteur (Paris). 1954 Dec;87(6):653-73 PubMed
J Mol Biol. 1969 May 14;41(3):459-72 PubMed
J Bacteriol. 1953 Feb;65(2):113-21 PubMed
Genetics. 1965 Nov;52(5):1043-50 PubMed
J Biol Chem. 1981 Jul 25;256(14):7573-82 PubMed
Annu Rev Genet. 1991;25:585-627 PubMed
Mol Gen Genet. 1974;135(1):51-60 PubMed
J Bacteriol. 1971 May;106(2):539-42 PubMed
Nucleic Acids Res. 1979 Nov 24;7(6):1513-23 PubMed
Gene. 1977;2(2):95-113 PubMed
J Mol Biol. 1992 Oct 5;227(3):597-601 PubMed
J Bacteriol. 1978 Jun;134(3):1141-56 PubMed
Gene. 1990 May 31;90(1):125-8 PubMed
J Mol Biol. 1983 May 5;166(1):1-19 PubMed
Genet Res. 1969 Apr;13(2):227-40 PubMed
Virology. 1972 Jun;48(3):679-89 PubMed
Ann N Y Acad Sci. 1983;411:383-8 PubMed
Plasmid. 1985 Nov;14(3):224-34 PubMed
J Gen Microbiol. 1980 Jul;119(1):231-8 PubMed
Proc Natl Acad Sci U S A. 1989 Apr;86(7):2281-5 PubMed
Microbiol Rev. 1993 Jun;57(2):434-50 PubMed
Folia Microbiol (Praha). 1994;39(2):162-5 PubMed
J Gen Microbiol. 1972 Jul;71(2):403-5 PubMed
J Gen Microbiol. 1973 Dec;79(2):257-64 PubMed
Functional coupling of duplex translocation to DNA cleavage in a type I restriction enzyme