Avola R, Castro A, Ricceri G
Boll Soc Ital Biol Sper. 1981 Nov 30;57(22):2241-7.
In rat embryo cell cultures infected with X14 or H-1 parvovirus and in mock-infected cell cultures the activity of some enzymes involved in purine nucleotide interconversion and in "adenylate cycle" was determined. The enzymatic activities have been assayed on 100,000 x g supernatant by spectrophotometric methods, measuring the absorbance variation in U.V. and by radiometric methods, resolving the radioactive products of reaction by TLC on PEI cellulose. The results indicated a decrease of the enzymatic activities that degrade purine nucleosides and nucleotides in infected cells compared to the controls. Some different behaviour patterns showed the enzymes involved in base salvage pathway; adenine phosphoribosyltransferase did not show a significant modification of activity, whereas hypoxanthine (guanine) phosphoribosyltransferase increased slightly in X14 virus-infected cells. The behaviour of the above mentioned enzymatic activities may be considered as a mechanism of purine nucleotide saving, coupled to an active salvage pathway for the synthesis of nucleotides required for the viral replication.
在感染了X14或H - 1细小病毒的大鼠胚胎细胞培养物以及模拟感染的细胞培养物中,测定了参与嘌呤核苷酸相互转化和“腺苷酸循环”的一些酶的活性。通过分光光度法在100,000×g上清液中测定酶活性,测量紫外吸光度变化,并通过放射性方法,在聚乙二胺纤维素上用薄层层析法分离反应的放射性产物。结果表明,与对照相比,感染细胞中降解嘌呤核苷和核苷酸的酶活性降低。参与碱基补救途径的酶表现出一些不同的行为模式;腺嘌呤磷酸核糖转移酶的活性没有显著改变,而次黄嘌呤(鸟嘌呤)磷酸核糖转移酶在感染X14病毒的细胞中略有增加。上述酶活性的行为可被视为嘌呤核苷酸节约的一种机制,与病毒复制所需核苷酸合成的活跃补救途径相关。