Morlino G B, Tizzani L, Fleer R, Frontali L, Bianchi M M
Department of Cell and Developmental Biology, University of Rome "La Sapienza," Rome 00185, Italy.
Appl Environ Microbiol. 1999 Nov;65(11):4808-13. doi: 10.1128/AEM.65.11.4808-4813.1999.
Heterologous protein production can be doubled by increasing the copy number of the corresponding heterologous gene. We constructed a host-vector system in the yeast Kluyveromyces lactis that was able to induce copy number amplification of pKD1 plasmid-based vectors upon expression of an integrated copy of the plasmid recombinase gene. We increased the production and secretion of two heterologous proteins, glucoamylase from the yeast Arxula adeninivorans and mammalian interleukin-1beta, following gene dosage amplification when the heterologous genes were carried by pKD1-based vectors. The choice of the promoters for expression of the integrated recombinase gene and of the episomal heterologous genes are critical for the mitotic stability of the host-vector system.
通过增加相应异源基因的拷贝数,异源蛋白产量可提高一倍。我们构建了一种酵母乳酸克鲁维酵母中的宿主-载体系统,该系统在质粒重组酶基因的整合拷贝表达时,能够诱导基于pKD1质粒的载体的拷贝数扩增。当异源基因由基于pKD1的载体携带时,在基因剂量扩增后,我们提高了两种异源蛋白的产量和分泌量,这两种异源蛋白分别是来自酵母嗜腺嘌呤阿苏鲁酵母的葡糖淀粉酶和哺乳动物白细胞介素-1β。用于整合重组酶基因和游离异源基因表达的启动子的选择对于宿主-载体系统的有丝分裂稳定性至关重要。