Niu Yan, Kong Jian, Xu Yi
State Key Laboratory for Microbial Technology, Shandong University, Shanda Nan Road 27, Jinan, 250100, China.
Curr Microbiol. 2008 Nov;57(5):423-8. doi: 10.1007/s00284-008-9223-8. Epub 2008 Sep 4.
Eukaryotic membrane proteins are often difficult to produce in large quantities, which is a significant obstacle for further structural and biochemical investigation. Lactococcus lactis has several properties that are ideal for enhanced expression of eukaryotic membrane proteins. In this article, a novel lactococcal vector was constructed, by inserting a green fluorescent protein (GFP) sequence into the vector pNZ8148. The resulting vector pKj-gfp was applied to the overexpression of an elongase-GFP fusion in L. lactis. After adding nisin, the expression of the fusion was confirmed via microscopy, the conditions were optimized by fluorescent spectroscopy, and the location of the fusion was monitored through in-gel fluorescence, indicating that the fusion was directed into the cytoplasmic membrane and no degradation was observed. The ELKJ-GFP fusion accounted for approximately 15% of the total membrane proteins using PDQuest software. These results indicate that the lactococcal system can be used for the overproduction and convenient detection of eukaryotic membrane proteins.
真核生物膜蛋白通常难以大量生产,这是进一步进行结构和生化研究的重大障碍。乳酸乳球菌具有若干特性,非常适合增强真核生物膜蛋白的表达。在本文中,通过将绿色荧光蛋白(GFP)序列插入载体pNZ8148构建了一种新型乳球菌载体。所得载体pKj-gfp用于在乳酸乳球菌中过表达延伸酶-GFP融合蛋白。添加乳链菌肽后,通过显微镜确认融合蛋白的表达,通过荧光光谱法优化条件,并通过凝胶内荧光监测融合蛋白的定位,表明融合蛋白被导向细胞质膜且未观察到降解。使用PDQuest软件,ELKJ-GFP融合蛋白约占总膜蛋白的15%。这些结果表明,乳球菌系统可用于真核生物膜蛋白的过量生产和便捷检测。