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通过随机诱变确定NaeI假定结合位点和催化位点的位置。

Location of putative binding and catalytic sites of NaeI by random mutagenesis.

作者信息

Holtz J K, Topal M D

机构信息

Lineberger Comprehensive Cancer Center, University of North Carolina Medical School, Chapel Hill 27599-7295.

出版信息

J Biol Chem. 1994 Nov 4;269(44):27286-90.

PMID:7961638
Abstract

Endonuclease NaeI is a prototype for an unusual group of type II restriction endonucleases that must bind two DNA recognition sequences to cleave DNA. The naeIR gene, expressed from a Ptac promotor construct, was toxic to Escherichia coli in the absence of NaeI-sequence specific methylases. The naeIR gene was mutagenized with N-methyl-N'-nitrosoguanidine; four classes of NaeI variants were isolated in the absence of protecting methylase activity. Class I variants (T60I, E70K) lacked detectable cleavage activity, but displayed good sequence-specific DNA binding. Class II variants (D95N, G141D) displayed 1-5% of the wild-type cleavage activity and normal DNA binding. Class III variants (G131E, G131R, G155D, G245E) displayed significantly attenuated cleavage and binding activities. Class IV variants (G197D, G214R/A219T, G236S, L241P, G245E, G245R, G250E, G270E) lacked both cleavage and binding activities. These results imply two amino acids (Thr-60, Glu-70) essential for catalysis. In addition, two domains are indicated in NaeI: one (Thr-60 to Gly-155) mediates substrate binding and catalysis, the other (Gly-197 to Gly-270) may mediate binding of the activating DNA sequence. Our results are compared with the active site residues of EcoRI, EcoRV, and BamHI.

摘要

核酸内切酶NaeI是一类不同寻常的II型限制性核酸内切酶的原型,这类酶必须结合两个DNA识别序列才能切割DNA。从Ptac启动子构建体表达的naeIR基因,在没有NaeI序列特异性甲基化酶的情况下对大肠杆菌有毒。用N-甲基-N'-亚硝基胍对naeIR基因进行诱变;在没有保护性甲基化酶活性的情况下分离出四类NaeI变体。I类变体(T60I、E70K)缺乏可检测的切割活性,但表现出良好的序列特异性DNA结合能力。II类变体(D95N、G141D)表现出野生型切割活性的1-5%,且具有正常的DNA结合能力。III类变体(G131E、G131R、G155D、G245E)表现出明显减弱的切割和结合活性。IV类变体(G197D、G214R/A219T、G236S、L241P、G245E、G245R、G250E、G270E)既缺乏切割活性也缺乏结合活性。这些结果表明有两个氨基酸(苏氨酸-60、谷氨酸-70)对催化作用至关重要。此外,NaeI中显示出两个结构域:一个(苏氨酸-60至甘氨酸-155)介导底物结合和催化作用,另一个(甘氨酸-197至甘氨酸-270)可能介导激活DNA序列的结合。我们的结果与EcoRI、EcoRV和BamHI的活性位点残基进行了比较。

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