Rolton H A, Keir H M
Biochem J. 1974 Nov;143(2):403-9. doi: 10.1042/bj1430403.
The activities of dCMP deaminase and DNA polymerase I increased twofold and fivefold in BHK-21/C13 cells after infection by the virus of herpes simplex. The increases were greatly diminished, and under certain conditions prevented, by inclusion of actinomycin D or cycloheximide in the cell-virus system during the infective cycle. The dCMP deaminase purified from infected cells harvested 8h after infection differed from the deaminase purified from non-infected cells inasmuch as (a) it was more resistant to heating at 37 degrees C; (b) the substrate (dCMP) concentration at half-maximum velocity was lower; (c) maximum activation was achieved by a lower concentration of dCTP; (d) it was more resistant to inhibition by dTTP; and (e) it behaved differently when assayed in the presence of a herpes-virus-specific antiserum. The DNA polymerase activity in the infected cells was markedly decreased in the presence of the herpes-virus-specific antiserum.
单纯疱疹病毒感染后,BHK - 21/C13细胞中的dCMP脱氨酶和DNA聚合酶I的活性分别增加了两倍和五倍。在感染周期中,若在细胞 - 病毒系统中加入放线菌素D或环己酰亚胺,这些增加会大幅减少,在某些情况下甚至可被阻止。从感染后8小时收获的感染细胞中纯化得到的dCMP脱氨酶,与从未感染细胞中纯化得到的脱氨酶不同,具体表现为:(a) 它在37℃下更耐热;(b) 达到最大反应速度一半时的底物(dCMP)浓度更低;(c) 较低浓度的dCTP即可实现最大激活;(d) 它对dTTP抑制的抗性更强;(e) 在疱疹病毒特异性抗血清存在下进行测定时,其表现不同。在疱疹病毒特异性抗血清存在的情况下,感染细胞中的DNA聚合酶活性显著降低。