Bolton B J, Schmitz G G, Jarsch M, Comer M J, Kessler C
Boehringer Mannheim GmbH, Biochemical Research Center, Penzberg, F.R.G.
Gene. 1988 Jun 15;66(1):31-43. doi: 10.1016/0378-1119(88)90222-3.
A new class-IIS restriction endonuclease, Ksp632I, with novel sequence specificity has been discovered in a non-pathogenic species of Kluyvera. The presence of only a single site-specific activity in this Kluyvera sp. strain 632 enables Ksp632I to be isolated in highly purified form free of contaminating nucleases. Ksp632I recognition sites and cleavage positions were deduced using experimental and computer-assisted mapping and sequencing. The cleavage specificity corresponds to the sequence 5'-CTCTTCN decreases NNN-N-3' 3'-GAGAAGN-NNN increases N-5'. The enzyme recognizes an asymmetric hexanucleotide sequence and cleaves in the presence of Mg2+ ions specific phosphodiester bonds in both DNA strands, 1 and 4 nucleotides distal to the recognition sequence. The staggered cuts generate 5'-protruding ends with single-stranded 5'-phosphorylated trinucleotides. Several slow cleavage sites for Ksp632I were observed on lambda cI857Sam7 DNA. Ksp632I may complement other class-IIS enzymes in the universal restriction approach and may serve as a tool for generating defined unidirectional deletions or insertions.
在克鲁维酵母的一种非致病菌种中发现了一种具有新序列特异性的新型IIS类限制性内切酶Ksp632I。该克鲁维酵母菌株632中仅存在单一的位点特异性活性,这使得Ksp632I能够以高度纯化的形式分离出来,且不含污染性核酸酶。通过实验和计算机辅助的图谱绘制及测序推导得出了Ksp632I的识别位点和切割位置。切割特异性对应于序列5'-CTCTTCN↓NNN-N-3' 3'-GAGAAGN-NNN↑N-5'。该酶识别一个不对称的六核苷酸序列,并在Mg2+离子存在的情况下切割两条DNA链中识别序列下游1和4个核苷酸处的特定磷酸二酯键。交错切割产生带有单链5'-磷酸化三核苷酸的5'-突出末端。在λ cI857Sam7 DNA上观察到了几个Ksp632I的缓慢切割位点。Ksp632I在通用限制方法中可能补充其他IIS类酶,并可作为产生特定单向缺失或插入的工具。