Shen S X, Li Q L, Yan P F, Zhou B, Ye S Y, Lu Y Y, Wang D B
Sci Sin. 1980 Nov;23(11):1435-42.
The restriction endonucleases, Hin P1 I1), Hin S1 I and Hin S2 I are isolated from three strains of Haemophilus influenzae respectively. By polymin P treatment, ammonium sulphate, precipitation and column chromatography on phosphocellulose and on heparin-Sepharose Hin P1 I is partially purified. No contaminating deoxyribonuclease activities have been detected in this purified enzyme preparation. The fact that the digestion patterns of Hin P2 I and Hha I on phage lambda, plasmids ColE1 an pBR 322 DNAs are identical that they are isoschizomers but theri splitting sites are different. The banding patterns of Hin S1 I and Hin S2 I are also the same as that of Hha I.
限制性内切酶Hin P1 I、Hin S1 I和Hin S2 I分别从三株流感嗜血杆菌中分离得到。通过多聚胺P处理、硫酸铵沉淀以及在磷酸纤维素和肝素-琼脂糖上进行柱层析,对Hin P1 I进行了部分纯化。在这种纯化的酶制剂中未检测到污染的脱氧核糖核酸酶活性。Hin P2 I和Hha I对噬菌体λ、质粒ColE1和pBR 322 DNA的消化模式相同,表明它们是同裂酶,但它们的切割位点不同。Hin S1 I和Hin S2 I的条带模式也与Hha I相同。