Paoletti E, Lipinskas B R
J Virol. 1978 Jun;26(3):822-4. doi: 10.1128/JVI.26.3.822-824.1978.
A soluble endoribonuclease activity was extracted from purified vaccinia virus cores by treatment with sodium-deoxycholate and dithiothreitol. The soluble enzyme readily cleaved purified virion-associated high-molecular-weight RNA to limit-sized fragments sedimenting at 8 to 12S. Purified virion-released 8 to 12S polyadenylated mRNA was not degraded by the enzyme extract. The soluble endoribonuclease did not require the presence of ribonucleoside triphosphates for activity.
通过用脱氧胆酸钠和二硫苏糖醇处理,从纯化的痘苗病毒核心中提取出一种可溶性核糖核酸内切酶活性。这种可溶性酶能轻易地将纯化的与病毒粒子相关的高分子量RNA切割成沉降系数为8至12S的有限大小片段。纯化的从病毒粒子释放的8至12S多聚腺苷酸化mRNA不会被该酶提取物降解。该可溶性核糖核酸内切酶的活性不需要核糖核苷三磷酸的存在。