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大肠杆菌中λ原噬菌体诱导后RNA聚合酶亚基和终止因子ρ的逃逸合成

Escape synthesis of RNA polymerase subunits and termination factor rho following induction of prophage lambda in Escherichia coli.

作者信息

Nakamura Y, Ikeuchi T, Imai M, Yura T

出版信息

Mol Gen Genet. 1977 Feb 15;150(3):317-24. doi: 10.1007/BF00268131.

Abstract

Synthesis of RNA polymerase subunits and of transcription termination factor p was studied after thermoinduction of prophage lambdac1857 located at several unusual sites on the chromosome of Escherichia coli. When a lysogen carrying the prophage at the bfe gene was induced at 42 degrees C, the rate of synthesis of core polymerase subunits (alpha, beta and beta') rapidly decreased, followed by a marked increase after about 10 min. The latter increase was observed specifically in the "bfe lysogen" and not in any of the other lysogens tested. Similarly, the rate of synthesis of p factor increased appreciably in the induced ilv lysogen carrying the prophage at the ilv gene, and possibly in the bfe lysogen as well, but not in other lysogens examined. Taken together with other evidence, these results suggest that the enhanced syntheses of beta and beta' subunits of RNA polymerase and of p factor observerd represent "escape synthesis", resulting from the close linkage of the prophage genome to the respective structural genes. In contrast, omega factor synthesis was stimulated upon induction of any of the lysogens used without respect to the site of prophage location, suggesting the involvement of an entirely different mechanism.

摘要

在位于大肠杆菌染色体几个不同寻常位点的原噬菌体λc1857热诱导后,研究了RNA聚合酶亚基和转录终止因子ρ的合成。当携带位于bfe基因处原噬菌体的溶原菌在42℃诱导时,核心聚合酶亚基(α、β和β')的合成速率迅速下降,约10分钟后显著增加。后一种增加在“bfe溶原菌”中特异性观察到,而在任何其他测试的溶原菌中未观察到。同样,在携带位于ilv基因处原噬菌体的诱导型ilv溶原菌中,ρ因子的合成速率明显增加,bfe溶原菌中可能也是如此,但在其他检测的溶原菌中没有增加。结合其他证据,这些结果表明,观察到的RNA聚合酶β和β'亚基以及ρ因子的合成增强代表“逃逸合成”,这是由于原噬菌体基因组与各自结构基因的紧密连锁所致。相比之下,在诱导任何所用的溶原菌时,ω因子的合成均受到刺激,而与原噬菌体的位置无关,这表明涉及一种完全不同的机制。

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