Interaction of AluI, Cfr6I and PvuII restriction-modification enzymes with substrates containing either N4-methylcytosine or 5-methylcytosine
Author:
Publisher
Elsevier BV
Subject
Genetics,Biochemistry,Biophysics,Structural Biology
Reference20 articles.
1. Purification ofMboII methylase (GAAGmA fromMoraxella bovis:site specific cleavage of DNA at nine and ten base pair sequences
2. Recognition sequences of restriction endonucleases and methylases — a review
3. Cytosine modification in DNA by Bcn I methylase yields N 4 -methylcytosine
4. Investigation of restriction-modification enzymes fromM. variansRFL19 with a new type of specificity toward modification of substrate
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2. Overexpression of a lethal methylase, M.TneDI, in E. coli BL21(DE3);Biotechnology Letters;2014-05-28
3. The AplI Restriction-Modification System in an Edible Cyanobacterium, Arthrospira (Spirulina) platensis NIES-39, Recognizes the Nucleotide Sequence 5′-CTGCAG-3′;Bioscience, Biotechnology, and Biochemistry;2013-04-23
4. Translational independence between overlapping genes for a restriction endonuclease and its transcriptional regulator;BMC Molecular Biology;2010
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