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Regeneration of insertionally inactivated streptococcal DNA fragments after excision of transposon Tn916 in Escherichia coli: strategy for targeting and cloning of genes from gram-positive bacteria.

The conjugative transposon Tn916 (15 kilobases), originally identified in Streptococcus faecalis DS16, has been cloned as an intact element on the pBR322-derived vector pGL101 in Escherichia coli. The EcoRI F' (EcoRI F::Tn916) fragment of pAM211 (pAD1::Tn916) was cloned into the single EcoRI site of...

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Detalles Bibliográficos
Publicado en:J Bacteriol
Principais autores: Gawron-Burke, C, Clewell, D B
Formato: Artigo
Idioma:Inglês
Publicado: American Society for Microbiology (ASM) 1984
Assuntos:
Acceso en liña:https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC215615/
https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/6330031/
https://ncbi.nlm.nih.govhttps://doi.org/10.1128/jb.159.1.214-221.1984
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