Irr J D, Jacoby L B
Somatic Cell Genet. 1978 Jan;4(1):111-24. doi: 10.1007/BF01546496.
Human lymphoblasts in long-term culture have the enzyme activities necessary to convert citrulline to arginine: argininosuccinate synthetase and argininosuccinate lyase. Upon transfer from arginine-supplemented to citrulline-supplemented medium, lymphoblasts exhibit a lag period before resuming exponential growth. During this lag the specific activity of argininosuccinate synthetase increases an average of 60-fold. Argininosuccinate lyase activity remains unchanged. If normal lymphoblasts are starved in arginine-deficient medium without citrulline or if argininosuccinate lyase--deficient lymphoblasts are transferred to citrulline-containing medium, argininosuccinate synthetase activity increases linearly for several days and reaches even higher levels. Cycloheximide blocks the increase in enzyme activity. Cells grown in citrulline medium and pulse labeled with 35S-methionine incorporate more 35S-methionine into argininosuccinate synthetase protein than cells grown in arginine; the rate of disappearance of radioactively labeled enzyme is the same in citrulline- and arginine-grown cells. Arginine or a closely related metabolite thus appears to repress the synthesis of argininosuccinate synthetase of human lymphoblasts in culture.
精氨琥珀酸合成酶和精氨琥珀酸裂解酶。当从补充精氨酸的培养基转移到补充瓜氨酸的培养基时,淋巴母细胞在恢复指数生长之前会有一个延迟期。在这个延迟期内,精氨琥珀酸合成酶的比活性平均增加60倍。精氨琥珀酸裂解酶活性保持不变。如果正常淋巴母细胞在不含瓜氨酸的精氨酸缺乏培养基中饥饿培养,或者如果精氨琥珀酸裂解酶缺陷的淋巴母细胞转移到含瓜氨酸的培养基中,精氨琥珀酸合成酶活性会连续几天呈线性增加并达到更高水平。放线菌酮会阻断酶活性的增加。在瓜氨酸培养基中生长并用35S-甲硫氨酸脉冲标记的细胞比在精氨酸培养基中生长的细胞将更多的35S-甲硫氨酸掺入精氨琥珀酸合成酶蛋白中;在瓜氨酸和精氨酸培养基中生长的细胞中,放射性标记酶的消失速率相同。因此,精氨酸或一种密切相关的代谢物似乎会抑制培养的人淋巴母细胞中精氨琥珀酸合成酶的合成。