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噬菌体λ与质粒之间高效的依赖RecABC的同源重组需要噬菌体ninR区域基因。

Efficient RecABC-dependent, homologous recombination between coliphage lambda and plasmids requires a phage ninR region gene.

作者信息

Hollifield W C, Kaplan E N, Huang H V

机构信息

Department of Microbiology and Immunology, Washington University School of Medicine, St. Louis, MO 63110.

出版信息

Mol Gen Genet. 1987 Dec;210(2):248-55. doi: 10.1007/BF00325690.

Abstract

A phage lambda gene that gives a 100-fold increase in recombinant frequencies for RecABC pathway-mediated, phage-plasmid homologous recombination (Shen and Huang 1986) maps to ninG (orf 204) of lambda. We call this gene rap, for recombination adept with plasmid. A similar determinant exists in Charon 4A and maps in phi 80-derived sequences, between nin5 and the Rz homology with lambda. The absence of the Rap+ phenotype from certain lambda vectors explains the inefficiency of screening the resulting phage libraries using phage-plasmid homologous recombination. The mapping of rap permits the construction of lambda vectors more suitable for this screening technique.

摘要

一个噬菌体λ基因,它能使RecABC途径介导的噬菌体 - 质粒同源重组的重组频率提高100倍(Shen和Huang,1986),定位于λ的ninG(orf 204)。我们将这个基因称为rap,即与质粒重组能力强的意思。在Charon 4A中存在一个类似的决定因素,定位于源自φ80的序列中,在nin5和与λ的Rz同源序列之间。某些λ载体缺乏Rap +表型,这解释了使用噬菌体 - 质粒同源重组筛选所得噬菌体文库效率低下的原因。rap的定位使得构建更适合这种筛选技术的λ载体成为可能。

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