Combining localized PCR mutagenesis and natural transformation in direct genetic analysis of a transcriptional regulator gene, pobR.

We present a procedure for efficient random mutagenesis of selected genes in a bacterial chromosome. The method combines PCR replication errors with the uptake of PCR-amplified DNA via natural transformation. Cloning of PCR fragments is not required, since mutations are transferred directly to the c...

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書目詳細資料

發表在:	J Bacteriol
Principais autores:	Kok, R G, D'Argenio, D A, Ornston, L N
格式:	Artigo
語言:	Inglês
出版:	American Society for Microbiology (ASM) 1997
主題:	Research Article
在線閱讀:	https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC179249/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/9209043/ https://ncbi.nlm.nih.govhttps://doi.org/10.1128/jb.179.13.4270-4276.1997
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