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利福平诱导携带dnaA突变的大肠杆菌菌株中质粒pBR322的复制。

Rifampicin-induced replication of the plasmid pBR322 in Escherichia coli strains carrying dnaA mutations.

作者信息

Polaczek P, Cieśla Z

出版信息

Mol Gen Genet. 1983;190(2):326-30. doi: 10.1007/BF00330659.

Abstract

The replication pattern of the plasmid pBR322 was examined in the dnaA mutants of Escherichia coli. The rate of pBR322 DNA synthesis is markedly decreased after dnaA cells are shifted to the restrictive temperature of 42 degrees C. However, addition of rifampicin (RIF) to cultures of dnaA strains incubated at 42 degrees C after a lag of 90 min results in a burst of pBR322 synthesis. This RIF-induced pBR322 replication remains dependent on DNA polymerase I activity. Efficient plasmid pBR322 replication is observed at 42 degrees C in the double mutant dnaA46cos bearing an intragenic suppressor of dnaA46. Though replication of pBR322 in dnaA46cos growing at 42 degrees C is initially sensitive to RIF plasmid synthesis is restored after 90 min incubation in the presence of the drug. RIF-induced replication of the plasmid pBR327, lacking the rriB site implicated in RIF-resistant synthesis of the L strand of ColE1-like plasmids (Nomura and Ray 1981; Zipursky and Marians 1981), was observed also in dnaA46 at 42 degrees C.

摘要

在大肠杆菌的dnaA突变体中检测了质粒pBR322的复制模式。将dnaA细胞转移至42℃的限制温度后,pBR322 DNA的合成速率显著降低。然而,在42℃孵育的dnaA菌株培养物中,滞后�90分钟后添加利福平(RIF)会导致pBR322合成爆发。这种RIF诱导的pBR322复制仍然依赖于DNA聚合酶I的活性。在携带dnaA46基因内抑制子的双突变体dnaA46cos中,在42℃观察到了高效的质粒pBR322复制。尽管在42℃生长的dnaA46cos中pBR322的复制最初对RIF敏感,但在药物存在下孵育90分钟后,质粒合成得以恢复。在42℃的dnaA46中也观察到了质粒pBR327的RIF诱导复制,该质粒缺乏与ColE1样质粒L链的RIF抗性合成有关的rriB位点(野村和雷,1981;齐普斯基和马里安斯,1981)。

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