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来自流感嗜血杆菌Rf的一种新型限制性内切酶的纯化及特性

Purification and properties of a new restriction endonuclease from Haemophilus influenzae Rf.

作者信息

Kauc L, Piekarowicz A

出版信息

Eur J Biochem. 1978 Dec;92(2):417-26. doi: 10.1111/j.1432-1033.1978.tb12762.x.

Abstract

Haemophilus influenzae Rf 232, showing the phenomena of restriction and modification, contains an endonuclease that inactivates in vitro the biological activity of DNAs lacking the strain-specific modification. This specific restriction endonuclease has been purified to near homogeneity by a procedure that includes DNA-agarose chromatography. This highly purified enzyme requires ATP and Mg2+ for activity and is stimulated by S-adenosylmethionine. The enzyme seems to cleave DNA at well-defined sites, since it produces a specific pattern of bands upon agarose gel electrophoresis. The enzyme has no ATPase activity. A methylase activity is observed in the course of the endonucleolytic reaction, which probably protects some of the DNA sites from cleavage.

摘要

流感嗜血杆菌Rf 232表现出限制与修饰现象,它含有一种核酸内切酶,该酶在体外可使缺乏该菌株特异性修饰的DNA生物活性失活。这种特异性限制核酸内切酶已通过包括DNA-琼脂糖层析在内的方法纯化至接近均一。这种高度纯化的酶的活性需要ATP和Mg2+,并受S-腺苷甲硫氨酸的刺激。该酶似乎在明确的位点切割DNA,因为它在琼脂糖凝胶电泳时产生特定的条带模式。该酶没有ATP酶活性。在内切核酸反应过程中观察到一种甲基化酶活性,它可能保护一些DNA位点不被切割。

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