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转录终止因子ρ与T偶数噬菌体的发育

Transcription termination factor rho and T-even phage development.

作者信息

Zograff Y N, Gintsburg A L

出版信息

Mol Gen Genet. 1980;177(4):699-705. doi: 10.1007/BF00272682.

Abstract

A functional factor rho is necessary for T-even phage development; phages T2 and T4 require different degrees of rho activity. The rho inactivation by ts-mutations in E. coli causes a reduction of some early protein synthesis and an early formation of some proteins normally typical of a later stage. Besides, it weakens the synthesis of some late proteins, impairs the capsid proteins maturation and sharply inhibits phage DNA replication in infected cells. However, in the absence of a functional rho all the proteins required for phage DNA synthesis the formed, indicating that this factor is directly involved in the process of T-even phage DNA replication. A number of rifampicin-resistant mutations supressing the rho 15 mutation and restoring the ability of cells to grow at high temperature were isolated. However these RNA polymerase mutations do not or only partially suppress the effect of rho mutations on T-even phage development and the phage DNA synthesis. The role of rho in DNA transcription and replication during bacteriophage development is discussed.

摘要

功能因子ρ对于T偶数噬菌体的发育是必需的;噬菌体T2和T4需要不同程度的ρ活性。大肠杆菌中ts突变导致的ρ失活会使一些早期蛋白质合成减少,并使一些通常在后期才典型出现的蛋白质提前形成。此外,它会削弱一些晚期蛋白质的合成,损害衣壳蛋白的成熟,并在感染细胞中急剧抑制噬菌体DNA复制。然而,在没有功能性ρ的情况下,噬菌体DNA合成所需的所有蛋白质都能形成,这表明该因子直接参与T偶数噬菌体DNA复制过程。分离出了一些抑制rho 15突变并恢复细胞在高温下生长能力的利福平抗性突变。然而,这些RNA聚合酶突变不会或仅部分抑制rho突变对T偶数噬菌体发育和噬菌体DNA合成的影响。本文讨论了ρ在噬菌体发育过程中DNA转录和复制中的作用。

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