Koerner J F, Thies S K, Snustad D P
J Virol. 1979 Aug;31(2):506-13. doi: 10.1128/JVI.31.2.506-513.1979.
A protein induced by wild-type T4 phage which is absent in Escherichia coli infected with nuclear disruption-deficient phage (with mutations in gene ndd) was identified by polacrylamide gel electrophoresis. This protein was synthesized at maximum rate at 3 to 6 min after infection. It had a molecular weight of 15,000 determined by sodium dodecyl sulfate-polyacrylamide gel electrophoresis. It was associated with sedimentable fractions of the cell from which it can be dissociated with 1 M guanidine-hydrochloride. The dissociated protein can be partly recovered in a form soluble in dilute buffer after partial purification and dialysis. The occurrence of this protein in a particulate cell fraction is of interest because of the postulated role of the bacterial cell membrane in nuclear disruption.
通过聚丙烯酰胺凝胶电泳鉴定出一种由野生型T4噬菌体诱导产生的蛋白质,该蛋白质在感染了核破坏缺陷型噬菌体(基因ndd发生突变)的大肠杆菌中不存在。这种蛋白质在感染后3至6分钟时以最大速率合成。通过十二烷基硫酸钠-聚丙烯酰胺凝胶电泳测定其分子量为15,000。它与细胞的可沉降部分相关,可通过1M盐酸胍将其从该部分解离。解离后的蛋白质在部分纯化和透析后,可部分以可溶于稀缓冲液的形式回收。这种蛋白质在细胞颗粒部分中的存在令人感兴趣,因为推测细菌细胞膜在核破坏中起作用。