重叠的dam（Gm6ATC）位点处的甲基化并不阻碍同裂酶限制性核酸内切酶AmaI、SalDI和Sbo13I（NruI，TCGCGA）的切割。 - Suppr | 超能文献

Methylation at overlapping dam (Gm6ATC) sites does not block cleavage by the NruI (TCGCGA) isoschizomer restriction endonucleases AmaI, SalDI and Sbo13I.

作者信息

Patel Y, Nelson M, McClelland M

机构信息

Department of Biochemistry and Molecular Biology, University of Chicago, IL 60637.

出版信息

Nucleic Acids Res. 1989 May 11;17(9):3613. doi: 10.1093/nar/17.9.3613.

DOI:10.1093/nar/17.9.3613

原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC317824/

Abstract

摘要

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/951b/317824/628bb1d715ba/nar00126-0283-a.jpg

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引用本文的文献

1

Cloning of NruI and Sbo13I restriction and modification sstems in E. coli and amino acid sequence comparison of M.NruI and M.Sbo13I with other amino-methyltransferases.大肠杆菌中NruI和Sbo13I限制与修饰系统的克隆以及M.NruI和M.Sbo13I与其他氨基甲基转移酶的氨基酸序列比较。

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本文引用的文献

1

Activity of DNA modification and restriction enzymes in KGB, a potassium glutamate buffer.DNA修饰酶和限制酶在谷氨酸钾缓冲液（KGB）中的活性。

Gene Anal Tech. 1988 Sep-Oct;5(5):105-7. doi: 10.1016/0735-0651(88)90005-2.