Takasaki Y, Hori K
Department of Biochemistry, Saga Medical School, Japan.
Protein Eng. 1990 Mar;3(4):273-7. doi: 10.1093/protein/3.4.273.
Rat aldolase C cDNA was inserted in an Escherichia coli expression vector to construct the rat aldolase C expression plasmid, pRAC42. This plasmid produces active rat aldolase C in the transfected E. coli host cells. The characteristics of the purified enzyme, e.g. mol. wt, electrophoretic mobilities and kinetic parameters, are indistinguishable from those of authentic rat brain aldolase C. Three different tetrameric hybrid forms, C3A, C2A2 and CA3, in addition to C4 and A4, were found to be produced in the host cell when E.coli was co-transfected with expression plasmids for rat aldolase C and for human aldolase A. Similarly, the hybrid forms, C3B, C2B2 and CB3, in addition to C4 and B4, were also produced in the cells when co-transfected with the plasmids for rat aldolase C and for human aldolase B.
将大鼠醛缩酶C的互补DNA(cDNA)插入大肠杆菌表达载体中,构建大鼠醛缩酶C表达质粒pRAC42。该质粒在转染的大肠杆菌宿主细胞中产生有活性的大鼠醛缩酶C。纯化酶的特性,如分子量、电泳迁移率和动力学参数,与天然大鼠脑醛缩酶C的特性无法区分。当大肠杆菌与大鼠醛缩酶C和人醛缩酶A的表达质粒共转染时,发现宿主细胞中除了产生C4和A4外,还产生三种不同的四聚体杂合形式,即C3A、C2A2和CA3。同样,当与大鼠醛缩酶C和人醛缩酶B的质粒共转染时,细胞中除了产生C4和B4外,也产生杂合形式C3B、C2B2和CB。