Xi C, Lambrecht M, Vanderleyden J, Michiels J
F.A. Janssens Laboratory of Genetics, K.U.Leuven, Heverlee, Belgium.
J Microbiol Methods. 1999 Feb;35(1):85-92. doi: 10.1016/s0167-7012(98)00103-1.
The gfp gene, encoding the green fluorescent protein, was combined with the gusA gene, coding for the beta-glucuronidase enzyme, in mini-Tn5 transposon derivatives for use in Gram-negative bacteria. These mini-Tn5 elements allow simultaneously monitoring of gene expression and localization of the marked bacteria. Introduction of the resultant mini-Tn5 transposons into Rhizobium etli, Azospirillum brasilense and Pseudomonas stutzeri allowed us to visualise the interaction of these bacteria with their host plant. The dual-marker mini-Tn5 transposons constitute a powerful new tool for studying gene expression and ecology of bacteria in the environment and during the interaction with plants.
编码绿色荧光蛋白的gfp基因与编码β-葡萄糖醛酸酶的gusA基因在mini-Tn5转座子衍生物中结合,用于革兰氏阴性菌。这些mini-Tn5元件可同时监测基因表达和标记细菌的定位。将所得的mini-Tn5转座子导入费氏中华根瘤菌、巴西固氮螺菌和施氏假单胞菌,使我们能够观察这些细菌与其宿主植物的相互作用。双标记mini-Tn5转座子是研究环境中以及与植物相互作用过程中细菌的基因表达和生态学的强大新工具。