Plant Physiology Division, DSIR, Private Bag, Palmerston North, New Zealand.
Plant Mol Biol. 1985 Jul;5(4):257-63. doi: 10.1007/BF00020643.
The ribulose bisphosphate carboxylase/oxygenase (EC4.1.1.39) (RubisCO) large and small subunit genes from Anacystis nidulans have been cloned as a single fragment into M 13mp10 and pEMBL8 and expressed in Escherichia coli. From M 13mp10 a low yield of enzyme with high specific activity was obtained. The molecular weight of the active enzyme was 260 000 Da and of the inactive enzyme approximately 730 000 Da. The small and large subunits cloned separately did not express activity. The RubisCO gene cloned into pEMBL8 expressed activity up to 22 times that from the M 13 cloned RubisCO DNA. The RubisCO protein produced by the pEMBL cloned gene had a normal MW (550 000). Immunoprecipitation and polyacrylamide gel electrophoresis showed the presence of both large and small subunits.
集胞藻(Anacystis nidulans)的核酮糖-1,5-二磷酸羧化酶/加氧酶(EC4.1.1.39)(RubisCO)大亚基和小亚基基因已被克隆为一个片段,分别插入 M13mp10 和 pEMBL8,并在大肠杆菌中表达。从 M13mp10 获得了低产量但高比活性的酶。活性酶的分子量为 260000Da,失活酶的分子量约为 730000Da。单独克隆的大亚基和小亚基均无活性。克隆到 pEMBL8 的 RubisCO 基因表达的活性是从 M13 克隆的 RubisCO DNA 的 22 倍。由 pEMBL 克隆基因产生的 RubisCO 蛋白具有正常的 MW(550000)。免疫沉淀和聚丙烯酰胺凝胶电泳显示存在大亚基和小亚基。