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M.FokI methylates adenine in both strands of its asymmetric recognition sequence
D Landry1, M C Looney, G R Feehery
1New England Biolabs, Inc., Beverly, MA 01915.
Gene
|April 15, 1989
Abstract:
M.FokI, a type-IIS modification enzyme from Flavobacterium okeanokoites, was purified, and its activity was characterized in vitro. The enzyme was found to be a DNA-adenine methyltransferase and to methylate both strands of the asymmetric FokI recognition sequence: (formula; see text) M.FokI does not methylate single-stranded DNA, nor does it methylate double-stranded DNA at sequences other than FokI sites.