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T4诱导的tRNA细胞内浓度的调节。

Regulation of the intracellular concentration of T4 induced tRNA.

作者信息

Fario M, Cascino A

出版信息

Mol Gen Genet. 1977 Sep 21;155(1):61-5. doi: 10.1007/BF00268561.

Abstract

We have studied the biosynthesis of T4 induced tRNA's upon infection of E. coli BE cells in low phosphate (l.p.) medium (10(-4) M PO---4). Under out experimental conditions the onset of phage DNA synthesis occurs about 15 min after infection, while the first intracellular phage appears one hour later. Amounts of newly synthesized DNA and phage burst size are equivalent to the values obtained in standard (M9) medium (10(-1) M PO---4). We present evidence that the synthesis of mature tRNA's and of at least one dimeric precursor drastically declines 20 min after infection. In addition we show that T4 induced tRNA molecules are stable and that the triphosphate nucleoside precursor pool does not change significantly during infection. Therefore we conclude that T4 induce tRNA molecules behave similarly to other early gene products.

摘要

我们研究了在低磷酸盐(l.p.)培养基(10⁻⁴ M PO₄³⁻)中感染大肠杆菌BE细胞后T4诱导的tRNA的生物合成。在我们的实验条件下,噬菌体DNA合成在感染后约15分钟开始,而第一个细胞内噬菌体在一小时后出现。新合成的DNA量和噬菌体爆发大小与在标准(M9)培养基(10⁻¹ M PO₄³⁻)中获得的值相当。我们提供的证据表明,感染后20分钟,成熟tRNA和至少一种二聚体前体的合成急剧下降。此外,我们表明T4诱导的tRNA分子是稳定的,并且三磷酸核苷前体池在感染期间没有显著变化。因此,我们得出结论,T4诱导的tRNA分子的行为与其他早期基因产物相似。

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