Purification, cloning and sequence analysis of RsrI DNA methyltransferase: lack of homology between two enzymes, RsrI and EcoRI, that methylate the same nucleotide in identical recognition sequences.

RsrI DNA methyltransferase (M-RsrI) from Rhodobacter sphaeroides has been purified to homogeneity, and its gene cloned and sequenced. This enzyme catalyzes methylation of the same central adenine residue in the duplex recognition sequence d(GAATTC) as does M-EcoRI. The reduced and denatured molecula...

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Pubblicato in:	Nucleic Acids Res
Autori principali:	Kaszubska, W, Aiken, C, O'Connor, C D, Gumport, R I
Natura:	Artigo
Lingua:	Inglês
Pubblicazione:	Oxford University Press 1989
Accesso online:	https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC335309/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/2690017/ https://ncbi.nlm.nih.govhttps://doi.org/10.1093/nar/17.24.10403
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