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噬菌体 phi 29 的抗阿非迪霉素突变体:DNA 聚合酶改变的遗传学证据。

Aphidicolin-resistant mutants of bacteriophage phi 29: genetic evidence for altered DNA polymerase.

作者信息

Matsumoto K, Kim C I, Urano S, Ohashi M, Hirokawa H

出版信息

Virology. 1986 Jul 15;152(1):32-8. doi: 10.1016/0042-6822(86)90368-5.

Abstract

Aphidicolin-resistant mutants (Aphr) of Bacillus subtilis bacteriophage phi 29 were isolated after mutagenesis with hydroxylamine. Efficiency of plating (e.o.p.) of the resistant mutants was not reduced at 500 microM aphidicolin, although e.o.p. of wild type phi 29 was less than 10(-5) at the same concentration of aphidicolin. By recombination and complementation analyses, both sites of the mutations, aph-71 and aph-101, of Aphr71 and Aphr101, respectively, were mapped in gene 2 which encodes phi 29 DNA polymerase. The activity of wild type phi 29 DNA polymerase, in a partially purified fraction, was inhibited by aphidicolin. DNA polymerases from Aphr71 and Aphr101, prepared in the same manner as that of wild type, were resistant to the drug. These results indicate that the acquisition of the aphidicolin resistance of Aphr71 and Aphr101 of bacteriophage phi 29 results from a structural alteration of phi 29 DNA polymerase which reduces sensitivity to aphidicolin.

摘要

用羟胺诱变后,分离出了枯草芽孢杆菌噬菌体φ29的抗阿非迪霉素突变体(Aphr)。在500微摩尔阿非迪霉素存在的情况下,抗性突变体的平板接种效率(e.o.p.)并未降低,而野生型φ29在相同浓度的阿非迪霉素下平板接种效率低于10^(-5)。通过重组和互补分析,分别将Aphr71和Aphr101的突变位点aph-71和aph-101定位到编码φ29 DNA聚合酶的基因2中。在部分纯化的组分中,野生型φ29 DNA聚合酶的活性受到阿非迪霉素的抑制。以与野生型相同的方式制备的来自Aphr71和Aphr101的DNA聚合酶对该药物具有抗性。这些结果表明,噬菌体φ29的Aphr71和Aphr101对阿非迪霉素抗性的获得是由于φ29 DNA聚合酶的结构改变,从而降低了对阿非迪霉素的敏感性。

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