Avola R, Ragusa N, Castro A, Ricceri G
Boll Soc Ital Biol Sper. 1981 Nov 30;57(22):2235-40.
In rat embryo cell cultures infected with X14 or H-1 parvovirus the PRPP pool and the PRPP synthetase activity have been assayed. A radiometric method, prepared by Authors, based on the conversion of [6-14C) orotate to [6-14C) UMP by the mixed enzyme orotate phosphoribosyltransferase and orotidylate decarboxylase and on the separation of UMP by ascending chromatography, has been utilized. The PRPP pool and te PRPP synthetase activity appeared nearly unmodified in the cells infected with X14 or H-1 parvovirus compared to the mock-infected cells. Therefore, the lowered pyrimidine nucleotide synthesis in infected cells, shown in previous studies, may depend, rather than on the diminished PRPP pool, on the lower PRPP utilization; in fact, some inhibition by metabolites, that may be removed by added PRPP, might occur in the infected cells.
在感染了X14或H-1细小病毒的大鼠胚胎细胞培养物中,对磷酸核糖焦磷酸(PRPP)库和PRPP合成酶活性进行了测定。作者采用了一种放射性方法,该方法基于[6-¹⁴C]乳清酸盐通过混合酶乳清酸磷酸核糖基转移酶和乳清酸核苷酸脱羧酶转化为[6-¹⁴C]尿苷一磷酸(UMP),并通过上行色谱法分离UMP。与模拟感染的细胞相比,在感染X14或H-1细小病毒的细胞中,PRPP库和PRPP合成酶活性几乎没有变化。因此,先前研究中显示的感染细胞中嘧啶核苷酸合成降低,可能不是取决于PRPP库的减少,而是取决于PRPP利用率较低;事实上,感染细胞中可能会发生一些被代谢物抑制的情况,而添加PRPP可能会消除这种抑制。