Wei Wenzhong, Xiang Hua, Tan Huarong
Institute of Microbiology, Chinese Academy of Sciences, Beijing 100080, China.
Wei Sheng Wu Xue Bao. 2003 Jun;43(3):347-53.
A food-grade gene expression system in L. lactis using the lacF gene as selection marker was constructed and further used for food-grade expression of human Cu/Zn superoxide dismutase (Cu/Zn SOD). Firstly, an integrative plasmid pUCEmDE containing homologous fragments with 0.5 kb flank sequences of the lacF gene was constructed. The lacF gene was in-frame deleted by double cross-over between the plasmid pUCEmDE and the chromosomal DNA in L. lactis MG5267 and resulted in a food-grade host WZ103 that was confirmed by PCR and Lac phenotype examination. After that, a complementary plasmid pMG36eF in which the lacF gene was controlled by the strong constitutive promoter P32 was electroporated into WZ103 and resulted in the restoration of Lac+ phenotype, indicating that the lacF function in WZ103 could be complemented by the lacF gene in pMG36eF. Finally, a food-grade plasmid pWZ104 used for the expression of Cu/Zn SOD was constructed, in which the lacF gene was used as a selective marker instead of any antibiotic resistance genes. Expressed Cu/Zn SOD in WZ103 (pWZ104) was demonstrated and showed biological activity through non-denatured PAGE and SOD activity gel-staining.
构建了一种以乳酸乳球菌中的lacF基因作为选择标记的食品级基因表达系统,并进一步用于人铜/锌超氧化物歧化酶(Cu/Zn SOD)的食品级表达。首先,构建了一个整合质粒pUCEmDE,其含有与lacF基因0.5 kb侧翼序列同源的片段。通过质粒pUCEmDE与乳酸乳球菌MG5267中的染色体DNA之间的双交换,lacF基因被框内缺失,从而产生了一个食品级宿主WZ103,通过PCR和Lac表型检测得以证实。之后,将一个互补质粒pMG36eF电穿孔导入WZ103,其中lacF基因由强组成型启动子P32控制,结果导致Lac+表型恢复,表明pMG36eF中的lacF基因可以互补WZ103中的lacF功能。最后,构建了一个用于表达Cu/Zn SOD的食品级质粒pWZ104,其中lacF基因用作选择标记,而非任何抗生素抗性基因。通过非变性聚丙烯酰胺凝胶电泳和SOD活性凝胶染色证明了WZ103(pWZ104)中表达的Cu/Zn SOD具有生物活性。