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[受R124因子控制的大肠杆菌菌株中噬菌体λ和P1修饰-限制的特性]

[Characteristics of bacteriophage lambda and P1 modification-restriction in Escherichia coli strains controlled by factor R124].

作者信息

Skavronskaia A G, Aleshkin G I, Demkin V V

出版信息

Genetika. 1979;15(10):1719-23.

PMID:159204
Abstract

The specifities of restriction of bacteriophages P1 and lambda controlled by R plasmids in Escherichia coli have been investigated. The isogenic strains harbouring the plasmids pAS26 coding for restriction endonuclease R.EcoRI, R245 coding for restriction endonuclease R.EcoRII and and R124 have been investigated in the present work. Modification-restriction controlled by R124 has been found to differ in specificity from those controlled by R245 and pAS26. Frequencies of restriction of bacteriophages P1vir and lambdavir specified by R124 pasmid differ from the frequencies in the strains harbouring pAS26 and R245 plasmids as well. The difference is due to the specifity of restriction-modification controlled by R124 plasmid. The data obtained are consistent with the determination of R124 specified restriction-modification activity as a novel one designated R.EcoRIII.

摘要

对大肠杆菌中由R质粒控制的噬菌体P1和λ的限制特异性进行了研究。在本研究中,对携带编码限制性内切酶R.EcoRI的质粒pAS26、编码限制性内切酶R.EcoRII的R245和R124的同基因菌株进行了研究。已发现由R124控制的修饰-限制在特异性上不同于由R245和pAS26控制的修饰-限制。由R124质粒指定的噬菌体P1vir和λvir的限制频率也不同于携带pAS26和R245质粒的菌株中的频率。这种差异是由于R124质粒控制的修饰-限制的特异性所致。所获得的数据与将R124指定的修饰-限制活性确定为一种新的命名为R.EcoRIII的活性一致。

相似文献

1
[Characteristics of bacteriophage lambda and P1 modification-restriction in Escherichia coli strains controlled by factor R124].[受R124因子控制的大肠杆菌菌株中噬菌体λ和P1修饰-限制的特性]
Genetika. 1979;15(10):1719-23.
2
[Effect of recB- and recA-mutations on phage restriction in various modification-restriction plasmid systems of E. coli].[recB和recA突变对大肠杆菌各种修饰-限制质粒系统中噬菌体限制作用的影响]
Mol Gen Mikrobiol Virusol. 1988 May(5):36-41.
3
[Coding R.M.EcoR1-plasmids derived from R-factor].
Genetika. 1978 Aug;14(8):1466-9.
4
[Weakening of bacteriophage lambda EcoK DNA restriction in the presence of plasmid pKM101 ard+. I. General characteristics and genetic localization].[在质粒pKM101 ard+存在下噬菌体λ EcoK DNA限制作用的减弱。I. 一般特性和基因定位]
Mol Biol (Mosk). 1984 Nov-Dec;18(6):1590-6.
5
[Escherichia coli K-12 plasmid R245 controlling EcoRII restriction and DNA modification].
Dokl Akad Nauk SSSR. 1978;238(5):1227-30.
6
[Plasmid recombination stimulated by restriction endonuclease EcoRI in vivo: formation of recombinant plasmids in recA+-cells of E. coli].[体内限制性内切酶EcoRI刺激的质粒重组:大肠杆菌recA⁺细胞中重组质粒的形成]
Mol Gen Mikrobiol Virusol. 1985 Apr(4):15-21.
7
[Conjugative properties of the R factors found in 2 different strains of Escherichia coli].[在两种不同大肠杆菌菌株中发现的R因子的接合性质]
Antibiotiki. 1979 Oct;24(10):761-4.
8
[New DNA modification-restriction plasmid system detected in a clinical strain of Escherichia coli].
Dokl Akad Nauk SSSR. 1980;252(4):993-5.
9
The EcoR124 and EcoR124/3 restriction and modification systems: cloning the genes.EcoR124和EcoR124/3限制与修饰系统:基因克隆
Plasmid. 1985 Nov;14(3):224-34. doi: 10.1016/0147-619x(85)90006-x.
10
[In vivo restriction of Escherichia coli-transforming DNA by endonuclease R.M.EcoRI].[体内内切核酸酶R.M.EcoRI对大肠杆菌转化DNA的限制作用]
Genetika. 1981;17(7):1205-10.

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