Shlomai J, Kornberg A
J Biol Chem. 1980 Jul 25;255(14):6789-93.
Protein n', an enzyme essential for in vitro conversion of single-stranded phiX174 DNA to the duplex replicative form, has been purified about 16,000-fold from Escherichia coli. The enzyme is a single polypeptide chain with a native molecular weight of 76,000; about 70 enzyme molecules are present in an E. coli cell. Nearly homogeneous preparations display an ATPase (dATPase) activity which depends on a unique sequence in the phiX174 DNA. Replicative activity of n' protein and its phiX174 DNA-dependent ATPase activity were present in a constant ratio during the latter stages of purification, upon sedimentation in a glycerol gradient, and during heat inactivation. Further studies of the properties of protein n' are presented in a succeeding paper.
蛋白质n'是一种在体外将单链φX174 DNA转化为双链复制形式所必需的酶,已从大肠杆菌中纯化了约16000倍。该酶是一条天然分子量为76000的单多肽链;大肠杆菌细胞中约有70个酶分子。几乎纯的制剂显示出一种ATP酶(dATP酶)活性,该活性取决于φX174 DNA中的一个独特序列。在纯化的后期、在甘油梯度中沉降以及热失活过程中,n'蛋白的复制活性及其依赖于φX174 DNA的ATP酶活性以恒定比例存在。后续论文将进一步研究蛋白质n'的特性。