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酿酒酵母中脱氧核糖核酸酶的研究。对两种偏好双链DNA的内切核酸酶活性的表征。

Studies on deoxyribonucleases from Saccharomyces cerevisiae. Characterization of two endonuclease activities with a preference for double-stranded DNA.

作者信息

Pinon R, Leney E

出版信息

Nucleic Acids Res. 1975 Jul;2(7):1023-42. doi: 10.1093/nar/2.7.1023.

DOI:10.1093/nar/2.7.1023
PMID:239390
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC343491/
Abstract

Two new endonuclease activities, endonuclease B and endonuclease C, obtained from yeast nuclear preparations have been separated and partially characterized. Endonuclease B has a primary requirement for Mn2+ which cannot be replaced by Mg2+ or Ca2+, and makes single-strand scissions in double-stranded DNA. Endonculease C is activated by either Mn2+ or Mg2+, and makes single-strand scissions with Mg2+, while with Mn2+, scissions are made which result in double-strand breaks. Neither enzyme is active on denatured DNA, and both are inhibited by yeast RNA. Both enzymes exhibit pH optima at pH 5.0 and PH 7.2, and leave 5'-phosphoryl termini.

摘要

从酵母核提取物中获得的两种新的核酸内切酶活性,即核酸内切酶B和核酸内切酶C,已被分离并进行了部分特性鉴定。核酸内切酶B主要需要Mn2+,Mg2+或Ca2+不能替代它,它能在双链DNA中产生单链切口。核酸内切酶C可被Mn2+或Mg2+激活,在有Mg2+时产生单链切口,而在有Mn2+时产生导致双链断裂的切口。这两种酶对变性DNA均无活性,且都受到酵母RNA的抑制。两种酶在pH 5.0和pH 7.2时均表现出最适pH值,并留下5'-磷酸末端。

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Studies on deoxyribonucleases from Saccharomyces cerevisiae. Characterization of two endonuclease activities with a preference for double-stranded DNA.酿酒酵母中脱氧核糖核酸酶的研究。对两种偏好双链DNA的内切核酸酶活性的表征。
Nucleic Acids Res. 1975 Jul;2(7):1023-42. doi: 10.1093/nar/2.7.1023.
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Apurinic endonucleases from Saccharomyces cerevisiae.来自酿酒酵母的脱嘌呤内切核酸酶。
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引用本文的文献

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J Ind Microbiol Biotechnol. 2003 Mar;30(3):175-82. doi: 10.1007/s10295-003-0028-2. Epub 2003 Feb 22.
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Saccharomyces cerevisiae plasmid, Scp or 2 mum: intracellular distribution, stability and nucleosomal-like packaging.酿酒酵母质粒,Scp或2μm:细胞内分布、稳定性及核小体样包装
Nucleic Acids Res. 1980 Aug 11;8(15):3371-91. doi: 10.1093/nar/8.15.3371.
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5
An alkaline sucrose gradient analysis of the mechanism of nuclear DNA synthesis in the yeast Saccharomyces cerevisiae.
Mol Gen Genet. 1978 Aug 17;164(2):217-25. doi: 10.1007/BF00267387.
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The use of a novel plate assay in a search for yeast mutants defective in deoxyribonucleases.利用一种新型平板分析法寻找脱氧核糖核酸酶缺陷的酵母突变体。
Mol Gen Genet. 1977 Apr 29;152(3):219-22. doi: 10.1007/BF00268821.

本文引用的文献

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Protein measurement with the Folin phenol reagent.使用福林酚试剂进行蛋白质测定。
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The DNA of bacteriophage PM 2. Ultracentrifugal evidence for a circular structure.噬菌体PM 2的DNA。关于环状结构的超速离心证据。
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Enzymatic breakage and joining of deoxyribonucleic acid. V. End group labeling and analysis of deoxyribonucleic acid containing single straned breaks.脱氧核糖核酸的酶促断裂与连接。V. 末端基团标记及含单链断裂的脱氧核糖核酸分析
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10
Deoxyribonucleic acid nucleases. II. The effects of metals on the mechanism of action of deoxyribonuclease I.脱氧核糖核酸酶。II. 金属对脱氧核糖核酸酶I作用机制的影响。
J Biol Chem. 1968 Sep 10;243(17):4409-16.