Strokovskaya L I, Skuratovskaya I N, Gudz-Gorban A P, Zherebtsova E N, Prima V I, Kok I P
Arch Virol. 1979;59(4):331-43. doi: 10.1007/BF01317473.
DNA preparations from nuclear polyhedrosis virus (NPV) of Galleria mellonella L. (GmL) were fractionated in high ionic strength neutral sucrose gradient. This procedure allowed a separation of supercoiled infectious DNA molecules with contour length of 48--52 microns from infectious open ring DNA molecule, and noninfectious linear DNA molecules of the same size. In addition a heterogeneity of supercoiled DNA molecules was detected. Covalently closed DNA molecules did not contain protein or ribonucleotide ligands which could be digested by pronase or pancreatic RNase treatment. It is concluded from data on the infectivity of different molecular forms of DNA and reassociation kinetics studies, that the genome of GmL NPV is a unique ring nucleotide sequence with a molecular weight of about 90--100 X 10(6).
从大蜡螟核型多角体病毒(GmL NPV)中提取的DNA制剂在高离子强度中性蔗糖梯度中进行分级分离。该程序能够将轮廓长度为48 - 52微米的超螺旋感染性DNA分子与感染性开环DNA分子以及相同大小的非感染性线性DNA分子分离开来。此外,还检测到超螺旋DNA分子的异质性。共价闭合的DNA分子不含有可被链霉蛋白酶或胰核糖核酸酶处理消化的蛋白质或核糖核苷酸配体。根据不同分子形式DNA的感染性数据和复性动力学研究得出结论,GmL NPV的基因组是一个分子量约为90 - 100×10⁶的独特环状核苷酸序列。