Clanton D J, Riggsby W S, Miller R V
J Bacteriol. 1979 Mar;137(3):1299-1307. doi: 10.1128/jb.137.3.1299-1307.1979.
EndoR . NgoII, a class II restriction endonuclease isolated from Neisseria gonorrhoeae, was purified to electrophoretic homogeneity. We were able to separate it from another restriction endonuclease of N. gonorrhoeae, NgoI, by phosphocellulose chromatography. NgoII is an isoschizomer of HaeIII, a restriction endonuclease of Haemophilus aegyptius, and was found to recognize the deoxyribonucleic acid nucleotide base sequence GGCC. NgoII was able to digest phage lambda deoxyribonucleic acid over a wide pH range, with optimal activity at pH 8.5. The enzyme has an absolute requirement for Mg2+; maximal enzyme activity was observed at 1 mM Mg2+. The active enzyme has a molecular weight of 65,000 and appears to be composed of six subunits of identical molecular weight (11,000). No methylase activity could be detected in the purified enzyme preparation.
从淋病奈瑟菌中分离出的II类限制性内切酶EndoR. NgoII被纯化至电泳纯。我们能够通过磷酸纤维素层析将其与淋病奈瑟菌的另一种限制性内切酶NgoI分离。NgoII是埃及嗜血杆菌的限制性内切酶HaeIII的同裂酶,被发现可识别脱氧核糖核酸核苷酸碱基序列GGCC。NgoII能够在较宽的pH范围内消化噬菌体λ脱氧核糖核酸,在pH 8.5时活性最佳。该酶对Mg2+有绝对需求;在1 mM Mg2+时观察到最大酶活性。活性酶的分子量为65,000,似乎由六个分子量相同(11,000)的亚基组成。在纯化的酶制剂中未检测到甲基化酶活性。