Perry L J, Heyneker H L, Wetzel R
Gene. 1985;38(1-3):259-64. doi: 10.1016/0378-1119(85)90226-4.
The phage T4 gene coding for lysozyme has been cloned into a plasmid under control of the (trp/lac) hybrid tac promoter and expressed in Escherichia coli with no significant toxic effect to actively growing cells. E. coli D1210 (lacIq) transformed with this plasmid produced active T4 lysozyme at levels up to 2% of the cellular protein after induction with isopropyl-beta-D-thiogalactoside. A strain producing active lysozyme was shown to be under a selective disadvantage when co-cultured with a similar strain producing inactive lysozyme. Purified strains, however, are reasonably stable in culture and under normal storage conditions.
编码溶菌酶的噬菌体T4基因已被克隆到一个受(色氨酸/乳糖)杂交tac启动子控制的质粒中,并在大肠杆菌中表达,对活跃生长的细胞没有明显的毒性作用。用该质粒转化的大肠杆菌D1210(lacIq)在用异丙基-β-D-硫代半乳糖苷诱导后,产生的活性T4溶菌酶水平高达细胞蛋白的2%。当与产生无活性溶菌酶的类似菌株共培养时,产生活性溶菌酶的菌株显示出选择性劣势。然而,纯化的菌株在培养和正常储存条件下相当稳定。