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BsuRI 限制修饰系统的核苷酸序列。

Nucleotide sequence of the BsuRI restriction-modification system.

作者信息

Kiss A, Posfai G, Keller C C, Venetianer P, Roberts R J

出版信息

Nucleic Acids Res. 1985 Sep 25;13(18):6403-21. doi: 10.1093/nar/13.18.6403.

Abstract

The genes of the 5'-GGCC specific BsuRI restriction-modification system of Bacillus subtilis have been cloned and expressed in E. coli and their nucleotide sequence has been determined. The restriction and modification genes code for polypeptides with calculated molecular weights of 66,314 and 49,642, respectively. Both enzymes are coded by the same DNA strand. The restriction gene is upstream of the methylase gene and the coding regions are separated by 780 bp. Analysis of the RNA transcripts by S1-nuclease mapping indicates that the restriction and modification genes are transcribed from different promoters. Comparison of the amino acid sequences revealed no homology between the BsuRI restriction and modification enzymes. There are, however, regions of homology between the BsuRI methylase and two other GGCC specific modification enzymes, the BspRI and SPR methylases.

摘要

枯草芽孢杆菌5'-GGCC特异性BsuRI限制修饰系统的基因已在大肠杆菌中克隆并表达,其核苷酸序列也已确定。限制酶基因和甲基化酶基因分别编码计算分子量为66,314和49,642的多肽。两种酶由同一条DNA链编码。限制酶基因位于甲基化酶基因的上游,编码区被780 bp隔开。通过S1核酸酶图谱分析RNA转录本表明,限制酶基因和甲基化酶基因从不同的启动子转录。氨基酸序列比较显示,BsuRI限制酶和甲基化酶之间没有同源性。然而,BsuRI甲基化酶与另外两种GGCC特异性甲基化酶BspRI和SPR甲基化酶之间存在同源区域。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/53a2/321967/94e741160346/nar00312-0019-a.jpg

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