Jigami Y, Muraki M, Harada N, Tanaka H
Gene. 1986;43(3):273-9. doi: 10.1016/0378-1119(86)90216-7.
A multicopy plasmid was constructed to direct the synthesis and secretion of human lysozyme (HLY) in Saccharomyces cerevisiae. This plasmid contains a synthetic chicken-lysozyme signal sequence (SIG) and a synthetic HLY structural gene, both inserted between the yeast GAL10 promoter and 2 mu plasmid FLP (flip-flop recombination gene) terminator. The resulting plasmid directed the expression of the hybrid pre-lysozyme, with most of the HLY activity secreted into the culture medium and extracellular periplasmic space. The HLY activity in the culture medium increased with cell growth. The yeast accurately processed the hybrid precursor at the junction between the chicken SIG and the coding sequence downstream, yielding mature HLY. HLY purified from the culture medium was homogeneous and displayed specific activity identical to that of authentic HLY.
构建了一种多拷贝质粒,用于在酿酒酵母中指导人溶菌酶(HLY)的合成与分泌。该质粒包含一个合成的鸡溶菌酶信号序列(SIG)和一个合成的HLY结构基因,二者均插入酵母GAL10启动子和2μm质粒FLP(翻转重组基因)终止子之间。所得质粒指导杂合前溶菌酶的表达,大部分HLY活性分泌到培养基和细胞外周质空间中。培养基中的HLY活性随细胞生长而增加。酵母在鸡SIG与下游编码序列的连接处准确加工杂合前体,产生成熟的HLY。从培养基中纯化的HLY是均一的,其比活性与天然HLY相同。