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枯草芽孢杆菌重组过程的遗传学和酶学研究。

Genetic and enzymic studies on the recombination process in Bacillus subtilis.

作者信息

Mazza G, Fortunato A, Ferrari E, Canosi U, Falaschi A, Polsinelli M

机构信息

Istituto di Genetica, Università di Pavia, Italy.

出版信息

Mol Gen Genet. 1975;136(1):9-30. doi: 10.1007/BF00275445.

DOI:10.1007/BF00275445
PMID:16094963
Abstract

We have isolated recombination deficient mutants of Bacillus subtilis on the basis of their sensitivity to methyl-methane-sulfonate or ultraviolet light, or of their inability to be transformed on solid medium. We have analyzed the mutants for several recombination and repair properties; we have grouped them in 5 classes on the basis of their phenotype and tested them for the activity of several enzymes acting on DNA, ie. DNA polymerase, polynucleotide ligase, ATP dependent DNase, and a DNase acting on single-stranded DNA. One mutant was found reduced in the latter DNase. Some of the mutants have been mapped, and they correspond to three different genes denominated rec D, rec F and rec G. All the recombination deficient mutants of B. subtilis described in the literature have been grouped in 7 classes; the mutations belong to 13 (and possibly 15) different genes distributed along the map. A coherent nomenclature and the criteria for a standard study of the rec mutants are proposed.

摘要

我们基于枯草芽孢杆菌对甲磺酸甲酯或紫外线的敏感性,或其在固体培养基上无法被转化的特性,分离出了重组缺陷型突变体。我们分析了这些突变体的几种重组和修复特性;根据它们的表型将其分为5类,并检测了它们对几种作用于DNA的酶的活性,即DNA聚合酶、多核苷酸连接酶、依赖ATP的DNA酶和作用于单链DNA的DNA酶。发现有一个突变体的后一种DNA酶活性降低。其中一些突变体已被定位,它们对应于三个不同的基因,分别命名为rec D、rec F和rec G。文献中描述的枯草芽孢杆菌所有重组缺陷型突变体已被分为7类;这些突变属于沿图谱分布的13个(可能15个)不同基因。本文提出了一个连贯的命名法以及rec突变体标准研究的标准。

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J Bacteriol. 1993 Jul;175(14):4290-7. doi: 10.1128/jb.175.14.4290-4297.1993.
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Anti-SOS effects induced in Bacillus subtilis by a phi 105 mutant prophage.

本文引用的文献

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TRANSFORMATION OF BIOCHEMICALLY DEFICIENT STRAINS OF BACILLUS SUBTILIS BY DEOXYRIBONUCLEATE.脱氧核糖核酸对枯草芽孢杆菌生化缺陷菌株的转化
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9
Repair-defective mutants of Alteromonas espejiana, the host for bacteriophage PM2.埃氏交替单胞菌(噬菌体PM2的宿主)的修复缺陷型突变体。
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ENZYMATIC SYNTHESIS OF DEOXYRIBONUCLEIC ACID. XIV. FURTHER PURIFICATION AND PROPERTIES OF DEOXYRIBONUCLEIC ACID POLYMERASE OF ESCHERICHIA COLI.脱氧核糖核酸的酶促合成。十四。大肠杆菌脱氧核糖核酸聚合酶的进一步纯化及性质
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Properties of a Bacillus subtilis strain lacking DNA polymerase I.一株缺乏DNA聚合酶I的枯草芽孢杆菌菌株的特性
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