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[N.BstSE--a site-specific nickase from Bacillus stearothermophilus SE-589].

作者信息

Abdurashitov M A, Belitchenko O A, Shevchenko A V, Degtiarev S Kh

出版信息

Mol Biol (Mosk). 1996 Nov-Dec;30(6):1261-7.

PMID:9026716
Abstract
摘要

相似文献

1
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Mol Biol (Mosk). 1996 Nov-Dec;30(6):1261-7.
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Characterization of the specific DNA nicking activity of restriction endonuclease N.BstNBI.限制性内切核酸酶N.BstNBI的特异性DNA切口活性的表征
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[A new type of cleavage of the recognition site by the site-specific endonuclease Bst 4.4I from Bacillus stearothermophilus 4.4].[嗜热脂肪芽孢杆菌4.4中位点特异性内切酶Bst 4.4I对识别位点的一种新型切割方式]
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[SegE endonuclease from T4 phage. II. Determination and characteristics of recognition site].[来自T4噬菌体的SegE核酸内切酶。II. 识别位点的确定及特征]
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Bacteriophage lambda DNA maturation and packaging.
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[Purification of recombinant DNA methyltransferase M2.BstSE from nickase-modification system NM.BstSEI and study of the enzyme properties].[从切口酶修饰系统NM.BstSEI中纯化重组DNA甲基转移酶M2.BstSE及其酶学性质研究]
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BstBSI, a restriction endonuclease from Bacillus stearothermophilus BS which recognizes 5'GTATAC3'.BstBSI，一种来自嗜热脂肪芽孢杆菌BS的限制性内切酶，其识别序列为5'GTATAC3'。
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Termination of packaging of the bacteriophage lambda chromosome: cosQ is required for nicking the bottom strand of cosN.噬菌体λ染色体包装的终止：cosQ是切割cosN底部链所必需的。
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Bacteriophage lambda DNA packaging: DNA site requirements for termination and processivity.噬菌体λDNA包装：终止和持续性的DNA位点要求。
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引用本文的文献

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Kinetic Analysis of the Interaction of Nicking Endonuclease BspD6I with DNA.BspD6I 内切酶与 DNA 相互作用的动力学分析。
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Discovery of natural nicking endonucleases Nb.BsrDI and Nb.BtsI and engineering of top-strand nicking variants from BsrDI and BtsI.天然切口核酸内切酶Nb.BsrDI和Nb.BtsI的发现以及BsrDI和BtsI的顶链切口变体的工程改造。
Nucleic Acids Res. 2007;35(14):4608-18. doi: 10.1093/nar/gkm481. Epub 2007 Jun 22.
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Crystallization and preliminary crystallographic analysis of the site-specific DNA nickase Nb.BspD6I.
位点特异性DNA切口酶Nb.BspD6I的结晶及初步晶体学分析
Acta Crystallogr Sect F Struct Biol Cryst Commun. 2005 Mar 1;61(Pt 3):332-4. doi: 10.1107/S174430910500309X.
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Cloning of CviPII nicking and modification system from chlorella virus NYs-1 and application of Nt.CviPII in random DNA amplification.从绿藻病毒 NYs-1 克隆 CviPII 切口和修饰系统及 Nt.CviPII 在随机 DNA 扩增中的应用
Nucleic Acids Res. 2004 Nov 29;32(21):6187-99. doi: 10.1093/nar/gkh958. Print 2004.
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Nucleic Acids Res. 2004 Jul 9;32(12):3661-71. doi: 10.1093/nar/gkh674. Print 2004.
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Restriction endonucleases: classification, properties, and applications.限制性内切核酸酶：分类、特性及应用
Mol Biotechnol. 2003 Mar;23(3):225-43. doi: 10.1385/mb:23:3:225.
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Engineering a nicking endonuclease N.AlwI by domain swapping.通过结构域交换构建切口核酸内切酶N.AlwI
Proc Natl Acad Sci U S A. 2001 Nov 6;98(23):12990-5. doi: 10.1073/pnas.241215698. Epub 2001 Oct 30.
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Converting MlyI endonuclease into a nicking enzyme by changing its oligomerization state.通过改变其寡聚化状态将MlyI核酸内切酶转化为切口酶。
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9
The nicking endonuclease N.BstNBI is closely related to type IIs restriction endonucleases MlyI and PleI.切口核酸内切酶N.BstNBI与IIs型限制性核酸内切酶MlyI和PleI密切相关。
Nucleic Acids Res. 2001 Jun 15;29(12):2492-501. doi: 10.1093/nar/29.12.2492.