Abstract
The specificity of three DNA methyltransferases M.Alw26I, M.Eco31I and M.Esp3I, isolated from Acinetobacter Iwoffi RFL26, Escherichia coli RFL31 and Hafnia alvei RFL3+, respectively, was determined. All the enzymes methylate both strands of asymmetric recognition sites yielding m5C in the top-strand and m6A in the bottom-strand, as below: 5'-GTm5CTC 5'-GGTm5CTC 5'-CGTm5CTC 3'-Cm6AGAG 3'-CCm6AGAG 3'-GCm6AGAG (M.Alw26I) (M.Eco31I) (M.Esp3I) They are the first members of type IIs methyltransferases that modify different types of nucleotides in the recognition sequence.
MeSH terms
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Acinetobacter / enzymology*
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Base Sequence
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DNA Modification Methylases / metabolism*
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DNA-Cytosine Methylases / metabolism*
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Enterobacteriaceae / enzymology*
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Escherichia coli / enzymology*
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Kinetics
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Molecular Sequence Data
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Oligodeoxyribonucleotides / metabolism
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Site-Specific DNA-Methyltransferase (Adenine-Specific) / metabolism*
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Substrate Specificity
Substances
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Oligodeoxyribonucleotides
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DNA Modification Methylases
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DNA modification methylase Alw26I
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DNA modification methylase Eco31I
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DNA modification methylase Esp3I
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DNA-Cytosine Methylases
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Site-Specific DNA-Methyltransferase (Adenine-Specific)