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EcoRII甲基化限制系统的基因表达特性。

Peculiarities of gene expression of the EcoRII modification-restriction system.

作者信息

Matvienko N N, Zheleznaya L A, Chernyshova E E, Matvienko N I

机构信息

Branch of Shemyakin-Ovchinnikov, Russian Academy of Sciences, Pushchino, Moscow Region, Russia.

出版信息

Biochemistry (Mosc). 1997 Oct;62(10):1124-7.

PMID:9461634
Abstract

The restriction-modification genes of the EcoRII system have been cloned into plasmids under control of phage-specific promoters T7 and SP6. The transcription was induced by cell infection with the recombinant M13 phages with the corresponding genes of phage RNA-polymerases under control of the Plac-promoter in the presence of IPTG. The induction yields significant amounts of EcoRII DNA-methylase for both phage-specific promoters. In both cases no increase in EcoRII endonuclease expression could be achieved. We hypothesize that the expression of the endonuclease gene is regulated on the translational level.

摘要

EcoRII系统的限制-修饰基因已被克隆到受噬菌体特异性启动子T7和SP6控制的质粒中。转录是通过在IPTG存在的情况下,用携带噬菌体RNA聚合酶相应基因且受Plac启动子控制的重组M13噬菌体感染细胞来诱导的。对于这两种噬菌体特异性启动子,诱导都产生了大量的EcoRII DNA甲基化酶。在这两种情况下,EcoRII内切核酸酶的表达都无法增加。我们推测内切核酸酶基因的表达是在翻译水平上受到调控的。

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