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枯草芽孢杆菌RNA聚合酶对phi29 DNA和EcoRI片段的体外转录

Transcription in vitro of phi29 DNA and EcoRI fragments by Bacillus subtilis RNA polymerase.

作者信息

Inciarte M R, Viñuela E, Salas M

出版信息

Eur J Biochem. 1976 Dec;71(1):77-83. doi: 10.1111/j.1432-1033.1976.tb11091.x.

Abstract

EcoRI fragments A, B and C produced from linear phi29 DNA, but not D or E fragments, are transcribed by purified Bacillus subtilis RNA polymerase. The transcription of fragments A and C is initiated preferentially with GTP and to a lesser extent with ATP; the reverse happens in the case of fragment B. The dinucleotides GpU and GpA respectively, compete specifically with the incorporation of [gamma-32P]GTP directed by fragments A and C. The RNA synthesized in vitro by purified B. subtilis RNA polymerase is highly asymmetric. Most of the RNA synthesis directed by fragments A and C is early RNA. However, most of the RNA produced by fragment B is anti-late-RNA. Addition of crude extracts inhibit the transcription of fragment B but not that of fragments A and C.

摘要

由线性phi29 DNA产生的EcoRI片段A、B和C可被纯化的枯草芽孢杆菌RNA聚合酶转录,但D或E片段则不能。片段A和C的转录优先以GTP起始,其次是ATP;片段B的情况则相反。二核苷酸GpU和GpA分别与片段A和C指导的[γ-32P]GTP掺入特异性竞争。纯化的枯草芽孢杆菌RNA聚合酶体外合成的RNA高度不对称。片段A和C指导的大部分RNA合成是早期RNA。然而,片段B产生的大部分RNA是抗晚期RNA。添加粗提物会抑制片段B的转录,但不会抑制片段A和C的转录。

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