Gage D J, Bobo T, Long S R
Department of Biological Sciences, Stanford University, California 94305-5020, USA.
J Bacteriol. 1996 Dec;178(24):7159-66. doi: 10.1128/jb.178.24.7159-7166.1996.
A gene encoding a variant of green fluorescent protein (GFP) of Aequorea victoria was put under the control of a promoter which is constitutive in Rhizobium meliloti. The heterologous GFP gene was expressed at high levels during all stages of symbiosis, allowing R. meliloti cells to be visualized as they grew in the rhizosphere, on the root surface, and inside infection threads. In addition, nodules that were infected with bacteria which were synthesizing GFP fluoresced when illuminated with blue light. GFP-tagged bacteria could be seen inside infection threads, providing the opportunity to measure the growth rate and determine the patterns of growth of R. meliloti residing inside its host plant.
将来自维多利亚多管水母的绿色荧光蛋白(GFP)变体的编码基因置于苜蓿根瘤菌组成型启动子的控制之下。异源GFP基因在共生的所有阶段均高水平表达,使得苜蓿根瘤菌细胞在根际、根表面以及侵染线内生长时都能被观察到。此外,被合成GFP的细菌感染的根瘤在蓝光照射下会发出荧光。在侵染线内可以看到带有GFP标记的细菌,这为测量苜蓿根瘤菌在其宿主植物内的生长速率和确定其生长模式提供了机会。