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Restriction endonucleases of a new type.

作者信息

Petrusyte M, Bitinaite J, Menkevicius S, Klimasauskas S, Butkus V, Janulaitis A

机构信息

ESP Fermentas, Lithuanian S.S.R., U.S.S.R.

出版信息

Gene. 1988 Dec 25;74(1):89-91. doi: 10.1016/0378-1119(88)90259-4.

DOI:10.1016/0378-1119(88)90259-4
PMID:2854813
Abstract
摘要

相似文献

1
Restriction endonucleases of a new type.
Gene. 1988 Dec 25;74(1):89-91. doi: 10.1016/0378-1119(88)90259-4.
2
The sensitivity of DNA cleavage by SpeI and ApaLI to methylation by M.EcoK.SpeI和ApaLI对DNA的切割对M.EcoK甲基化的敏感性。
Nucleic Acids Res. 1988 Jun 10;16(11):5206. doi: 10.1093/nar/16.11.5206.
3
Localization of the type I restriction-modification enzyme EcoKI in the bacterial cell.I型限制修饰酶EcoKI在细菌细胞中的定位。
Biochem Biophys Res Commun. 2000 Apr 2;270(1):46-51. doi: 10.1006/bbrc.2000.2375.
4
Purification and properties of the Eco57I restriction endonuclease and methylase--prototypes of a new class (type IV).Eco57I 限制性内切酶和甲基化酶的纯化及特性——新型(IV 型)的原型
Nucleic Acids Res. 1992 Nov 25;20(22):6043-9. doi: 10.1093/nar/20.22.6043.
5
The purification of restriction endonuclease EcoRI by precipitation involving polyethyleneimine.通过聚乙亚胺沉淀法纯化限制性内切酶EcoRI。
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6
Defining domains in type-I restriction and modification enzymes.
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7
Target recognition by EcoKI: the recognition domain is robust and restriction-deficiency commonly results from the proteolytic control of enzyme activity.EcoKI的靶标识别:识别结构域具有稳健性,限制缺陷通常源于酶活性的蛋白水解调控。
J Mol Biol. 2001 Mar 30;307(3):951-63. doi: 10.1006/jmbi.2001.4543.
8
RsrI restriction-modification enzymes from Rhodobacter sphaeroides.来自球形红杆菌的RsrI限制修饰酶。
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9
Cleavage by the restriction endonuclease Asp718, an isoschizomer of KpnI, is sensitive to Escherichia coli Dcm methylation.限制性内切酶Asp718(KpnI的同裂酶)的切割对大肠杆菌Dcm甲基化敏感。
Nucleic Acids Res. 1987 Nov 11;15(21):9085. doi: 10.1093/nar/15.21.9085.
10
[Substrate specificity of restriction endonuclease Eco781].[限制性内切酶Eco781的底物特异性]
Bioorg Khim. 1985 Nov;11(11):1572-3.

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The role of the methyltransferase domain of bifunctional restriction enzyme RM.BpuSI in cleavage activity.双功能限制酶 RM.BpuSI 的甲基转移酶结构域在切割活性中的作用。
PLoS One. 2013 Nov 4;8(11):e80967. doi: 10.1371/journal.pone.0080967. eCollection 2013.
2
The long march: a sample preparation technique that enhances contig length and coverage by high-throughput short-read sequencing.长征:一种通过高通量短读测序提高重叠群长度和覆盖度的样本制备技术。
PLoS One. 2008;3(10):e3495. doi: 10.1371/journal.pone.0003495. Epub 2008 Oct 22.
3
Binding of MmeI restriction-modification enzyme to its specific recognition sequence is stimulated by S-adenosyl-L-methionine.
S-腺苷-L-甲硫氨酸可刺激MmeI限制修饰酶与其特定识别序列的结合。
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A new Thermus sp. class-IIS enzyme sub-family: isolation of a 'twin' endonuclease TspDTI with a novel specificity 5'-ATGAA(N(11/9))-3', related to TspGWI, TaqII and Tth111II.一种新的嗜热栖热菌属IIS类酶亚家族:具有5'-ATGAA(N(11/9))-3'新特异性的“双”内切酶TspDTI的分离,与TspGWI、TaqII和Tth111II相关。
Nucleic Acids Res. 2003 Jul 15;31(14):e74. doi: 10.1093/nar/gng074.
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Characterization of BseMII, a new type IV restriction-modification system, which recognizes the pentanucleotide sequence 5'-CTCAG(N)(10/8)/.新型IV型限制修饰系统BseMII的特性,该系统识别五核苷酸序列5'-CTCAG(N)(10/8)/。
Nucleic Acids Res. 2001 Feb 15;29(4):895-903. doi: 10.1093/nar/29.4.895.
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A unique restriction endonuclease, BcgI, from Bacillus coagulans.一种来自凝结芽孢杆菌的独特限制性内切酶BcgI。
Nucleic Acids Res. 1993 Feb 25;21(4):987-91. doi: 10.1093/nar/21.4.987.
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In vivo restriction by LlaI is encoded by three genes, arranged in an operon with llaIM, on the conjugative Lactococcus plasmid pTR2030.LlaI的体内限制作用由三个基因编码,这三个基因与llaIM排列在接合型乳酸乳球菌质粒pTR2030上的一个操纵子中。
J Bacteriol. 1995 Jan;177(1):134-43. doi: 10.1128/jb.177.1.134-143.1995.
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Sequence motifs characteristic of DNA[cytosine-N4]methyltransferases: similarity to adenine and cytosine-C5 DNA-methylases.DNA[胞嘧啶-N4]甲基转移酶的特征性序列基序:与腺嘌呤和胞嘧啶-C5 DNA甲基酶的相似性。
Nucleic Acids Res. 1989 Dec 11;17(23):9823-32. doi: 10.1093/nar/17.23.9823.
10
Genetic and sequence organization of the mcrBC locus of Escherichia coli K-12.大肠杆菌K-12的mcrBC基因座的遗传与序列组织
J Bacteriol. 1990 Sep;172(9):4888-900. doi: 10.1128/jb.172.9.4888-4900.1990.