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1
Biochemical and genetic studies of recombination proficiency in Escherichia coli. I. Enzymatic activity associated with recB+ and recC+ genes.大肠杆菌中重组能力的生化与遗传学研究。I. 与recB+和recC+基因相关的酶活性。
Proc Natl Acad Sci U S A. 1970 Apr;65(4):955-61. doi: 10.1073/pnas.65.4.955.
2
Biochemical and genetic studies of recombination proficiency in Escherichia coli. II. Rec+ revertants caused by indirect suppression of rec- mutations.大肠杆菌中重组能力的生化与遗传学研究。II. 由rec-突变的间接抑制导致的Rec+回复突变体
Proc Natl Acad Sci U S A. 1970 Sep;67(1):128-35. doi: 10.1073/pnas.67.1.128.
3
Characteristics of some multiply recombination-deficient strains of Escherichia coli.一些多重重组缺陷型大肠杆菌菌株的特征
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4
Bacteriophage P22 Abc2 protein binds to RecC increases the 5' strand nicking activity of RecBCD and together with lambda bet, promotes Chi-independent recombination.噬菌体P22 Abc2蛋白与RecC结合,增强RecBCD的5'链切口活性,并与λ bet一起促进不依赖于Chi序列的重组。
J Mol Biol. 2000 Feb 18;296(2):385-401. doi: 10.1006/jmbi.1999.3486.
5
An ATP-dependent deoxyribonuclease from Escherichia coli with a possible role in genetic recombination.一种来自大肠杆菌的依赖ATP的脱氧核糖核酸酶,可能在基因重组中发挥作用。
Proc Natl Acad Sci U S A. 1969 Dec;64(4):1292-9. doi: 10.1073/pnas.64.4.1292.
6
Genetic recombination in Escherichia coli: the role of exonuclease I.大肠杆菌中的基因重组:核酸外切酶I的作用。
Proc Natl Acad Sci U S A. 1971 Apr;68(4):824-7. doi: 10.1073/pnas.68.4.824.
7
Differential thermolability of exonuclease and endonuclease activities of the recBC nuclease isolated from thermosensitive recB and recC mutants.从温度敏感型recB和recC突变体中分离出的recBC核酸酶的核酸外切酶和核酸内切酶活性的差异热稳定性。
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8
Formation of the recB-recC DNase by in vitro complementation and evidence concerning its subunit nature.通过体外互补形成recB-recC DNA酶及其亚基性质的证据。
Nat New Biol. 1973 May 16;243(124):75-7.
9
Analysis of temperature-sensitive recB and recC mutations.温度敏感型recB和recC突变的分析
Basic Life Sci. 1975;5A:301-6. doi: 10.1007/978-1-4684-2895-7_39.
10
Suppressibility of recA, recB, and recC mutations by nonsense suppressors.无义抑制基因对recA、recB和recC突变的抑制作用。
J Bacteriol. 1978 May;134(2):590-6. doi: 10.1128/jb.134.2.590-596.1978.

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RecBCD enzyme: mechanistic insights from mutants of a complex helicase-nuclease.RecBCD 酶:从复杂解旋酶-核酸酶的突变体中获得的机制见解。
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RecBCD is required to complete chromosomal replication: Implications for double-strand break frequencies and repair mechanisms.RecBCD蛋白是完成染色体复制所必需的:对双链断裂频率和修复机制的影响。
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How RecBCD enzyme and Chi promote DNA break repair and recombination: a molecular biologist's view.RecBCD 酶和 Chi 如何促进 DNA 断裂修复和重组:分子生物学家的观点。
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RecBCD enzyme and the repair of double-stranded DNA breaks.RecBCD酶与双链DNA断裂的修复
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7
Ultraviolet light-induced mutation in UV-resistant, thermosensitive derivatives of lexA-strains of Escherichia coli K-12.紫外线诱导的大肠杆菌K-12 lexA菌株抗紫外线、温度敏感衍生物中的突变。
Mol Gen Genet. 1975;136(2):95-106. doi: 10.1007/BF00272033.
8
Partial purification and characterization of four endodeoxyribonuclease activities from Escherichia coli K-12.来自大肠杆菌K-12的四种内切脱氧核糖核酸酶活性的部分纯化及特性分析
Nucleic Acids Res. 1974 Jan;1(1):1-17. doi: 10.1093/nar/1.1.1.
9
Genetic requirements of phage lambda red-mediated gene replacement in Escherichia coli K-12.λ噬菌体red介导的大肠杆菌K-12基因置换的遗传要求
J Bacteriol. 2000 Apr;182(8):2336-40. doi: 10.1128/JB.182.8.2336-2340.2000.
10
Salmonella recD mutations increase recombination in a short sequence transduction assay.鼠伤寒沙门氏菌recD突变在短序列转导试验中增加重组。
J Bacteriol. 1994 Jul;176(13):4092-103. doi: 10.1128/jb.176.13.4092-4103.1994.

本文引用的文献

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The deoxyribonucleases of Escherichia coli. II. Purification and properties of a ribonucleic acid-inhibitable endonuclease.大肠杆菌的脱氧核糖核酸酶。II. 一种核糖核酸抑制性内切核酸酶的纯化及特性
J Biol Chem. 1962 Mar;237:819-28.
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The deoxyribonucleases of Escherichia coli. I. Purification and properties of a phosphodiesterase.大肠杆菌的脱氧核糖核酸酶。I. 一种磷酸二酯酶的纯化及性质
J Biol Chem. 1960 May;235:1479-87.
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The enzymatic repair of DNA. I. Formation of circular lambda-DNA.DNA的酶促修复。I. 环状λ-DNA的形成
Proc Natl Acad Sci U S A. 1967 Jul;58(1):240-7. doi: 10.1073/pnas.58.1.240.
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The general recombination system of bacteriophage lambda.噬菌体λ的一般重组系统。
Cold Spring Harb Symp Quant Biol. 1968;33:711-4. doi: 10.1101/sqb.1968.033.01.080.
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Lysis of Escherichia coli with a neutral detergent.用中性去污剂裂解大肠杆菌。
Biochim Biophys Acta. 1967 Dec 19;149(2):476-88. doi: 10.1016/0005-2787(67)90175-x.
6
Endonuclease-I-deficient and ribonuclease I-deficient Escherichia coli mutants.核酸内切酶I缺陷型和核糖核酸酶I缺陷型大肠杆菌突变体。
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7
Genetic analysis of recombination-deficient mutants of Escherichia coli K-12 carrying rec mutations cotransducible with thyA.携带与thyA共转导的rec突变的大肠杆菌K-12重组缺陷型突变体的遗传分析。
J Bacteriol. 1969 Nov;100(2):923-34. doi: 10.1128/jb.100.2.923-934.1969.
8
Characteristics of some multiply recombination-deficient strains of Escherichia coli.一些多重重组缺陷型大肠杆菌菌株的特征
J Bacteriol. 1969 Oct;100(1):231-9. doi: 10.1128/jb.100.1.231-239.1969.
9
Enzymatic DNA degradation in E. coli: its relationship to synthetic processes at the chromosome level.大肠杆菌中的酶促DNA降解:其与染色体水平合成过程的关系。
Cold Spring Harb Symp Quant Biol. 1968;33:259-69. doi: 10.1101/sqb.1968.033.01.030.
10
Genetic location of certain mutations conferring recombination deficiency in Escherichia coli.大肠杆菌中某些导致重组缺陷的突变的基因定位。
J Bacteriol. 1969 Jan;97(1):244-9. doi: 10.1128/jb.97.1.244-249.1969.

大肠杆菌中重组能力的生化与遗传学研究。I. 与recB+和recC+基因相关的酶活性。

Biochemical and genetic studies of recombination proficiency in Escherichia coli. I. Enzymatic activity associated with recB+ and recC+ genes.

作者信息

Barbour S D, Clark A J

出版信息

Proc Natl Acad Sci U S A. 1970 Apr;65(4):955-61. doi: 10.1073/pnas.65.4.955.

DOI:10.1073/pnas.65.4.955
PMID:4909471
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC283009/
Abstract

An adenosine triphosphate-dependent deoxyribonuclease activity has been detected in lysates of recB(+)recC(+) strains. Mutations in recB or recC lead to loss of this activity, suggesting that these two genes determine the nuclease activity. The over-all reaction in crude lysates digests native DNA to nucleoside monophosphates. Complementation between recB21 and recC22 in vivo leads to normal levels of ATP-dependent nuclease activity. No complementation in vitro has been detected. Mutations in a third recombination gene (recA) do not alter significantly the wild-type levels of this nuclease activity.

摘要

在recB(+)recC(+)菌株的裂解物中检测到一种依赖三磷酸腺苷的脱氧核糖核酸酶活性。recB或recC中的突变会导致这种活性丧失,这表明这两个基因决定了核酸酶活性。粗裂解物中的总体反应将天然DNA消化为单磷酸核苷。recB21和recC22在体内的互补作用导致ATP依赖的核酸酶活性达到正常水平。在体外未检测到互补作用。第三个重组基因(recA)中的突变不会显著改变这种核酸酶活性的野生型水平。