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Cloning of the Escherichia coli recJ chromosomal region and identification of its encoded proteins.

A 9.6-kilobase BamHI-SalI fragment carrying recJ+ was cloned into vector pBR322. Deletion and transposon mutagenesis were used to map the recJ gene on this fragment. The maxicell protein-labeling technique was used to correlate a functional recJ gene with the presence of a polypeptide of 53,000 appa...

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Detalhes bibliográficos
Publicado no:J Bacteriol
Principais autores: Lovett, S T, Clark, A J
Formato: Artigo
Idioma:Inglês
Publicado em: American Society for Microbiology (ASM) 1985
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC218986/
https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/2984175/
https://ncbi.nlm.nih.govhttps://doi.org/10.1128/jb.162.1.280-285.1985
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