Lee Kwan Hoon, Park Woo Jung, Kim Joo Yun, Kim Han Geun, Lee Jung Min, Kim Jeong Hwan, Park Jeong Woo, Lee Jong Hoon, Chung Sung Kyun, Chung Dae Kyun
Graduate School of Biotechnology and Biomaterial Technology and Business Center, Institute of Life Science and Resources, Kyung Hee University, Suwon 449-701, Korea.
J Microbiol Biotechnol. 2007 Jul;17(7):1213-6.
The vector pCW5 with plasmid pC7, originally isolated in Lactobacillus paraplantarum C7 derived from kimchi, was constructed using a p32 strong promoter, the pC7 replicon, and green fluorescent protein (GFP) as the reporter. The constructed vector was transformed into E. coli and Leuconostoc mesenteroides, and GFP expression detected using a Western blot analysis. GFP fluorescence was recognized in E. coli and Leuconostoc mesenteroides using a confocal microscope. In addition, GFP fluorescence was also clearly detected in several industrially important lactic acid bacteria (LAB), including Lactobacillus bulgaricus, Lactobacillus paraplantarum, and Lactobacillus plantarum. Thus, pCW5 was shown to be effective for Leuconostoc mesenteroides when using GFP as the reporter, and it can also be used as a broad-host-range vector for other lactic acid bacteria.
载体pCW5与质粒pC7最初是从泡菜来源的植物乳杆菌C7中分离得到的,它是利用p32强启动子、pC7复制子以及绿色荧光蛋白(GFP)作为报告基因构建而成的。构建好的载体被转化到大肠杆菌和肠系膜明串珠菌中,并通过蛋白质免疫印迹分析检测GFP的表达。使用共聚焦显微镜在大肠杆菌和肠系膜明串珠菌中识别出了GFP荧光。此外,在几种具有重要工业价值的乳酸菌(LAB)中也清晰地检测到了GFP荧光,包括保加利亚乳杆菌、植物乳杆菌和类植物乳杆菌。因此,当使用GFP作为报告基因时,pCW5对肠系膜明串珠菌显示出有效性,并且它还可以用作其他乳酸菌的广宿主范围载体。