Ghosh S K, Mukhopadhyay N K, Majumder S, Bose S K
Biochem J. 1986 Apr 1;235(1):81-5. doi: 10.1042/bj2350081.
The final purification of the three-fraction enzyme complex mycobacillin synthetase was done by hydroxyapatite column chromatography and sucrose-density-gradient centrifugation; each of the fractions obtained migrates as a single component in SDS/polyacrylamide-gel electrophoresis and gel electrofocusing. The Mr of the enzyme fractions A, B and C by gel filtration is 260 000, 190 000 and 105 000, and that by SDS/polyacrylamide-gel electrophoresis is 252 000, 198 000 and 108 000 respectively. None of the enzyme fractions appears to possess subunit structure.
通过羟基磷灰石柱色谱法和蔗糖密度梯度离心法对三组分酶复合物分枝杆菌素合成酶进行了最终纯化;所获得的每个组分在SDS/聚丙烯酰胺凝胶电泳和凝胶电聚焦中均作为单一成分迁移。通过凝胶过滤法测得的酶组分A、B和C的Mr分别为260 000、190 000和105 000,通过SDS/聚丙烯酰胺凝胶电泳法测得的Mr分别为252 000、198 000和108 000。这些酶组分似乎均不具有亚基结构。