发明授权
US06413758B1 Method for cloning and expression of Bpml restriction endonuclease in E. coli
有权
在大肠杆菌中克隆和表达Bpml限制性内切核酸酶的方法
- 专利标题: Method for cloning and expression of Bpml restriction endonuclease in E. coli
- 专利标题(中): 在大肠杆菌中克隆和表达Bpml限制性内切核酸酶的方法
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申请号: US09693146申请日: 2000-10-20
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公开(公告)号: US06413758B1公开(公告)日: 2002-07-02
- 发明人: Shuang-yong Xu , Jian-ping Xiao , Zhenyu Zhu
- 申请人: Shuang-yong Xu , Jian-ping Xiao , Zhenyu Zhu
- 主分类号: C12N922
- IPC分类号: C12N922
摘要:
The present invention relates to recombinant DNA which encodes the BpmI restriction endonuclease as well as BpmI methyltransferase, expression of BpmI restriction endonuclease from E. coli cells containing the recombinant DNA. BpmI endonuclease is a fusion of two distinct elements with a possible structural domains of restriction-methylation-specificity (R-M-S). This domain organization is analogous to the type I restriction-modification system with three distinct subunits, restriction, methylation, and specificity (R, M, and S). Because BpmI is quite distinct to other type IIs restriction enzymes, it is proposed that BpmI belongs to a subgroup of type II restriction enzymes called type IIf (f stands for fusion of restriction-modification-specificity domains). The Type IIf group of restriction enzyme includes Eco57I, BpmI, GsuI, BseRI and some other restriction enzymes that cut downstream sequences at long distance, 10-20 bp downstream of recognition sequence, such as MmeI (N20/N18)).
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