Gromkova R, Goodgal S H
J Bacteriol. 1976 Aug;127(2):848-54. doi: 10.1128/jb.127.2.848-854.1976.
A type I restriction enzyme from Haemophilus influenzae, Hind I, which requires adenosine 5' -triphosphate and 5-adenosyl methionine, was studied for its activity on transfecting and transforming deoxyribonculeic acid (DNA). The enzyme reduced the size of unmodified bacteriophage S2 DNA from 37 X 10(6) daltons to approximately 10 X 10(6) daltons, but did not affect modified S2 DNA. Unmodified transforming DNA was attacked in vitro by Hind I; however, relatively low levels of inactivation were obtained for single markers, and linked transformants were inactivated as a function of the distance between markers. In contrast, unmodified bacterial DNA was not inactivated in vivo for either single or linked markers by the Hind I restriction system, probably because the segments generated by Hind I were still capable of being integrated in vivo. The lack of preferential inactivation of markers by the enzyme suggests that it makes random breaks in the DNA.
对来自流感嗜血杆菌的I型限制酶Hind I进行了研究,该酶需要5'-三磷酸腺苷和5-腺苷甲硫氨酸,研究其对转染和转化脱氧核糖核酸(DNA)的活性。该酶将未修饰的噬菌体S2 DNA的大小从37×10⁶道尔顿降至约10×10⁶道尔顿,但不影响修饰的S2 DNA。未修饰的转化DNA在体外受到Hind I的攻击;然而,单个标记的失活水平相对较低,并且连锁转化体的失活是标记之间距离的函数。相比之下,未修饰的细菌DNA在体内对于单个或连锁标记都不会被Hind I限制系统失活,这可能是因为Hind I产生的片段仍能够在体内整合。该酶对标记缺乏优先失活表明它在DNA中产生随机断裂。