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利用DNA聚合酶I的引发合成来研究噬菌体φX-174 DNA的基因间序列。

The use of primed synthesis by DNA polymerase I to study an intercistronic sequence of phiX-174 DNA.

作者信息

Donelson J E, Barrell B G, Weith H L

出版信息

Eur J Biochem. 1975 Oct 15;58(2):383-95. doi: 10.1111/j.1432-1033.1975.tb02385.x.

Abstract

A decadeoxynucleotide complementary to ten nucleotides in the major ribosome-protected fragment of phiX-174 plus-strand DNA has been chemically synthesized and used as a primer for DNA polymerase I on phiX-174 plus-strand DNA as template. The sequence of the first 40 nucleotides incorporated onto the decadeoxynucleotide has been determined. This sequence extends further the sequence of the intercistronic region preceding gene G and shows the presence of another termination codon. The sequence was determined by using manganese as the activating cation for DNA polymerase I which allows ribonucleotides to be incorporated as well as deoxyribonucleotides. The ribo-substituted product was then cleaved specifically at the ribonucleotide residues to generate a series of overlapping ribo-terminated fragments whose sequences were sufficient to determine the complete sequence of the first 40 nucleotides. No evidence for misincorporation by DNA polymerase I in the presence of manganese was detected.

摘要

一种与φX - 174正链DNA主要核糖体保护片段中的十个核苷酸互补的十聚脱氧核苷酸已被化学合成,并用作以φX - 174正链DNA为模板的DNA聚合酶I的引物。已确定掺入到该十聚脱氧核苷酸上的前40个核苷酸的序列。该序列进一步扩展了基因G之前的基因间区域的序列,并显示存在另一个终止密码子。该序列是通过使用锰作为DNA聚合酶I的激活阳离子来确定的,这使得核糖核苷酸以及脱氧核糖核苷酸都能被掺入。然后在核糖核苷酸残基处特异性切割核糖取代产物,以产生一系列重叠的核糖终止片段,其序列足以确定前40个核苷酸的完整序列。未检测到在锰存在下DNA聚合酶I错掺入的证据。

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