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Application of a rapid gel method to the sequencing of fragments of 16S ribosomal RNA from Escherichia coli.

机译:快速凝胶方法在大肠杆菌16S核糖体RNA片段测序中的应用。

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摘要

A gel sequencing method has been applied to two 5' end-labelled fragments of the 16S ribosomal RNA from E. coli. The procedure involves partial enzymatic hydrolysis by ribonucleases T1, U2 or A, in order to generate series of end-labelled subfragments terminating in guanine, adenine, or pyrimidine residues, respectively. The two fragments concerned were approximately 75 and 90 nucleotides in length, and both arose from the 3' region of the 16S RNA. The sequences deduced are compared with the published sequence of 16S RNA, and contribute information to the final ordering of the ribonuclease T1 oligonucleotides in the latter, as well as revealing some probable errors.
机译:凝胶测序方法已应用于来自大肠杆菌的两个5S末端标记的16S核糖体RNA片段。该程序包括通过核糖核酸酶T1,U2或A进行部分酶水解,以产生一系列分别终止于鸟嘌呤,腺嘌呤或嘧啶残基的末端标记亚片段。有关的两个片段的长度分别约为75和90个核苷酸,均来自16S RNA的3'区域。将推导的序列与已发布的16S RNA序列进行比较,并为后者中核糖核酸酶T1寡核苷酸的最终排序提供信息,并揭示一些可能的错误。

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