Purification of Rts1 RepA protein and binding of the protein to mini-Rts1 DNA.

RepA protein, essential for the replication of plasmid Rts1, was purified, and its binding to mini-Rts1 subregions was examined by a DNase I protection assay. RepA protected the incI and incII iterons, a region immediately upstream of the repA promoter, and a 10-base-pair region located between the...

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Pubblicato in:	J Bacteriol
Autori principali:	Kamio, Y, Itoh, Y, Terawaki, Y
Natura:	Artigo
Lingua:	Inglês
Pubblicazione:	American Society for Microbiology (ASM) 1988
Soggetti:	Research Article
Accesso online:	https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC211463/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/3045097/ https://ncbi.nlm.nih.govhttps://doi.org/10.1128/jb.170.9.4411-4414.1988
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