Ivanov S X, Yakimov M, Chelibonova-Lorer H
Institute of General and Comparative Pathology, Bulgarian Academy of Sciences, Sofia.
Cancer Biochem Biophys. 1990 Jul;11(3):195-200.
Comparative studies were carried out on the galactosyltransferase activity in ascites lymphoma cells isolated from mouse with ascitic lymphoma Ly/Ya, in these cells grown in vitro (24 hrs culture), in ascitic fluid and culture medium. The effect of varying amounts of UDP-galactose on transfer rate of galactose to ovomucoid by the cell enzyme (ascitic and cultured lymphoma cells) and by the soluble enzyme (ascitic fluid and culture medium) was studied. The activity of the enzyme in the cell culture medium was 2.5-fold higher than that in ascitic fluid. The apparent Km values for UDP-galactose of the enzyme from both kinds of cells and from the two fluids was 7.14 x 10(-7) M. At saturating concentrations of donor substrate, V values for the cells and culture medium was 765 pmoles/10(6) cells/h and 180 pmoles/10(6) cells/h for the ascitic fluid.
对从患有腹水淋巴瘤Ly/Ya的小鼠中分离出的腹水淋巴瘤细胞、这些体外培养(24小时培养)的细胞、腹水和培养基中的半乳糖基转移酶活性进行了比较研究。研究了不同量的UDP-半乳糖对细胞酶(腹水和培养的淋巴瘤细胞)和可溶性酶(腹水和培养基)将半乳糖转移至卵类粘蛋白的转移速率的影响。细胞培养基中该酶的活性比腹水中的高2.5倍。来自两种细胞和两种液体的酶对UDP-半乳糖的表观Km值为7.14×10⁻⁷ M。在供体底物饱和浓度下,细胞和培养基的V值分别为765皮摩尔/10⁶个细胞/小时,腹水的V值为180皮摩尔/10⁶个细胞/小时。