Yem D W, Williams L S
J Bacteriol. 1973 Feb;113(2):891-4. doi: 10.1128/jb.113.2.891-894.1973.
Two arginyl-transfer ribonucleic acid (tRNA) synthetase (EC 6.1.1.13, arginine: ribonucleic acid ligase adenosine monophosphate) activities were found in extracts of Escherichia coli strains AB1132 and NP2. The two arginyl-tRNA synthetase activities in extracts of strain AB1132 were found to be separable by diethylaminoethyl-cellulose column chromatography, Sephadex column fractionation, and by sucrose density gradient centrifugation. In addition, in the standard assay using extracts of strain AB1132 there were two pH optima for arginyl-tRNA synthetase activity. Furthermore, when arginyl-tRNA synthetase of strain NP2 was fractionated by hydroxylapatite column chromatography, two activities were observed which were similar to those of strain AB1132.
在大肠杆菌菌株AB1132和NP2的提取物中发现了两种精氨酰转移核糖核酸(tRNA)合成酶(EC 6.1.1.13,精氨酸:核糖核酸连接酶单磷酸腺苷)活性。发现菌株AB1132提取物中的两种精氨酰-tRNA合成酶活性可通过二乙氨基乙基纤维素柱色谱、葡聚糖柱分级分离和蔗糖密度梯度离心分离。此外,在使用菌株AB1132提取物的标准测定中,精氨酰-tRNA合成酶活性有两个最适pH值。此外,当菌株NP2的精氨酰-tRNA合成酶通过羟基磷灰石柱色谱分级分离时,观察到两种活性,它们与菌株AB1132的活性相似。