Schiessl S, Schmieger H
Institut für Genetik und Mikrobiologie (Lehrstuhl Genetik), Universität München, BRD.
Intervirology. 1990;31(5):255-64. doi: 10.1159/000150160.
Packaging genes 3 of Salmonella phage P22 wild type and two mutants with altered packaging properties (HT12/4 and NT1/1) have been cloned in an expression vector. By plasmid transduction, it has been shown that the amino terminus of gene 3 is not functional in DNA packaging when fused with the Escherichia coli lacZ gene. The reconstituted genes 3, however, express functional gp3. The transduction experiments also have shown that the pac signal, which is part of gene 3, is intact in all three phages. Expression of gene product gp3 has been demonstrated in the minicell system.
沙门氏菌噬菌体P22野生型的包装基因3以及两个具有改变包装特性的突变体(HT12/4和NT1/1)已被克隆到一个表达载体中。通过质粒转导表明,当基因3的氨基末端与大肠杆菌lacZ基因融合时,其在DNA包装中无功能。然而,重构的基因3表达有功能的gp3。转导实验还表明,作为基因3一部分的pac信号在所有三种噬菌体中都是完整的。基因产物gp3的表达已在小细胞系统中得到证实。