| Literature DB >> 5073742 |
J P Brockes, P R Brown, K Murray.
Abstract
The bacteriophage P1 modification enzyme, assayed by the specific methylation of unmodified bacteriophage 82 DNA, has been purified 500-fold from a bacteriophage P1 lysogen of Escherichia coli. The enzyme catalyses the incorporation of approximately 20-24 methyl groups per bacteriophage 82 DNA molecule. The sole product of methylation is 6-methylaminopurine. Methylation of unmodified bacteriophage DNA confers protection against a challenge by purified bacteriophage P1 restriction enzyme. The pH optimum is 6.0-6.25: the apparent K(m) for S-adenosyl-l-methionine is 5x10(-6)m.Entities:
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Year: 1972 PMID: 5073742 PMCID: PMC1178554 DOI: 10.1042/bj1270001
Source DB: PubMed Journal: Biochem J ISSN: 0264-6021 Impact factor: 3.857