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A new procedure for the targeted inactivation of essential bacterial genes.

作者信息

Lukacsovich T, Venetianer P

机构信息

Institute of Biochemistry, Hungarian Academy of Sciences, Szeged.

出版信息

Mol Gen Genet. 1989 Aug;218(2):364-6. doi: 10.1007/BF00331293.

DOI:10.1007/BF00331293
PMID:2674660
Abstract

A new method is described for the exchange of a plasmid encoded mutant gene with its chromosomal counterpart. The method is based on positive selection and is applicable for the exchange of essential genes. The main features of the method are: (1) cloning of an antibiotic resistance marker (without its promoter) downstream of the cloned target gene, thus forming an artificial operon; (2) inactivating the target gene (and consequently also the antibiotic resistance gene) by inserting a strong transcriptional termination signal into it; and (3) selection for double recombinants by means of the antibiotic resistance gene.

摘要

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引用本文的文献

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本文引用的文献

1
Segregation of New Lysogenic Types during Growth of a Doubly Lysogenic Strain Derived from Escherichia Coli K12.源于大肠杆菌K12的双重溶源菌株生长过程中新溶源类型的分离
Genetics. 1954 Jul;39(4):440-52. doi: 10.1093/genetics/39.4.440.
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Gene organization and primary structure of a ribosomal RNA operon from Escherichia coli.大肠杆菌核糖体RNA操纵子的基因组织与一级结构
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Transposon Tn10 provides a promoter for transcription of adjacent sequences.转座子Tn10为相邻序列的转录提供启动子。
Proc Natl Acad Sci U S A. 1982 Aug;79(16):5016-20. doi: 10.1073/pnas.79.16.5016.
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Construction and characterization of new cloning vehicles. VI. Plasmid pBR329, a new derivative of pBR328 lacking the 482-base-pair inverted duplication.新型克隆载体的构建与特性分析。VI. 质粒pBR329,pBR328的一种新衍生物,缺失482个碱基对的反向重复序列。
Gene. 1982 Jan;17(1):79-89. doi: 10.1016/0378-1119(82)90103-2.
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A general method for site-directed mutagenesis in prokaryotes.一种原核生物中定点诱变的通用方法。
Nature. 1981 Jan 1;289(5793):85-8. doi: 10.1038/289085a0.
7
Method for determining whether a gene of Escherichia coli is essential: application to the polA gene.确定大肠杆菌基因是否必需的方法:应用于polA基因。
J Bacteriol. 1984 May;158(2):636-43. doi: 10.1128/jb.158.2.636-643.1984.
8
Deletion of an essential gene in Escherichia coli by site-specific recombination with linear DNA fragments.通过与线性DNA片段进行位点特异性重组在大肠杆菌中缺失必需基因。
J Bacteriol. 1984 Aug;159(2):783-6. doi: 10.1128/jb.159.2.783-786.1984.
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Construction and characterization of a deletion mutant lacking micF, a proposed regulatory gene for OmpF synthesis in Escherichia coli.大肠杆菌中ompF合成的一个假定调控基因micF缺失的缺失突变体的构建与特性分析。
J Bacteriol. 1985 Jun;162(3):1196-202. doi: 10.1128/jb.162.3.1196-1202.1985.
10
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