Walker D H, Anderson T F
J Virol. 1970 Jun;5(6):765-82. doi: 10.1128/JVI.5.6.765-782.1970.
Lysates of P1 from all hosts tested contained at least three morphological variants with respect to head size. These were termed "big" (P1B), "small" (P1S), and "minute" (P1M). Since successive clonings of plaques isolated on many different hosts failed to change the proportions of the variants, we concluded that the production of variants was a function of the P1 genome rather than that of the host. In the electron microscope, the heads appeared to be icosadeltahedra, having face-to-face head diameters of 86 +/- 2 nm, 65 +/- 2 nm, and 47 +/- 2 nm. Assuming the head capsids to be composed of the same protein subunits, these diameters were compatible with T = 16, 9, and 4 with a lattice constant (intercapsomere distance) of 12 to 13 nm. The tails of all variants were morphologically indistinguishable. Each consisted of a hollow tail tube surrounded by a contractile sheath attached to the head by means of a "head-neck connector" which could be a specialized vertex capsomere. In CsCl gradients, a number of bands were observed. One band contained the majority of P1B particles and 99% of the plaque-forming units. Two other bands contained P1S particles whose densities suggested a content of about 40 and 60% of the complete P1B genome. The less dense of these two bands also contained defective P1B particles with a calculated content of only 60% of the complete genome. The P1S particles tested injected their deoxyribonucleic acid (DNA) into host cells and killed them. Genetic markers contained in this band could be rescued by infectious P1B particles, confirming the evidence of Ikeda and Tomizawa that this fraction contains P1 DNA.
所有测试宿主的P1裂解物在头部大小方面至少包含三种形态变体。这些变体被称为“大”(P1B)、“小”(P1S)和“微小”(P1M)。由于在许多不同宿主上分离的噬菌斑连续克隆未能改变变体的比例,我们得出结论,变体的产生是P1基因组的功能,而非宿主的功能。在电子显微镜下,头部似乎是二十面体,面对面的头部直径分别为86±2纳米、65±2纳米和47±2纳米。假设头部衣壳由相同的蛋白质亚基组成,这些直径与T = 16、9和4兼容,晶格常数(衣壳粒间距离)为12至13纳米。所有变体的尾部在形态上无法区分。每个尾部都由一个空心尾管组成,周围是一个收缩鞘,通过一个“头颈连接器”连接到头部,该连接器可能是一个特殊的顶点衣壳粒。在氯化铯梯度中,观察到了多个条带。一个条带包含了大部分P1B颗粒和99%的噬菌斑形成单位。另外两个条带包含P1S颗粒,其密度表明含有约40%和60%的完整P1B基因组。这两个条带中密度较小的那个还包含缺陷P1B颗粒,其计算含量仅为完整基因组的60%。测试的P1S颗粒将其脱氧核糖核酸(DNA)注入宿主细胞并杀死它们。该条带中包含的遗传标记可以被感染性P1B颗粒拯救,这证实了池田和富泽的证据,即该部分含有P1 DNA。