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Purification and characterisation of a novel DNA methyltransferase, M.AhdI

We have cloned the M and S genes of the restriction-modification (R-M) system AhdI and have purified the resulting methyltransferase to homogeneity. M.AhdI is found to form a 170 kDa tetrameric enzyme having a subunit stoichiometry M(2)S(2) (where the M and S subunits are responsible for methylation...

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Autores principales: Marks, Phil, McGeehan, John, Wilson, Geoff, Errington, Neil, Kneale, Geoff
Formato: Artigo
Lenguaje:Inglês
Publicado: Oxford University Press 2003
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Acceso en línea:https://ncbi.nlm.nih.gov/pmc/articles/PMC156732/
https://ncbi.nlm.nih.gov/pubmed/12771207
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