Balachandar D, Kannaiyan S, Ono H, Murooka Y
Department of Agricultural Microbiology, Tamil Nadu Agricultural University, Coimbatore 641 003, India.
Indian J Exp Biol. 2004 Oct;42(10):1028-31.
Among the transposable elements, mini-Tn5 transposon vector has proven to be of greater utility for insertion mutagenesis of variety of Gram negative bacteria. The mini-Tn5 vector containing promoter less egfp gene and gentamycin resistant gene was used for the present study. The transposon vector was introduced to M. huakuii from E. coli S17 by conjugation. The conjugants were screened for stable expression of egfp both in free-living and in nodules of Astragalus sinicus. The result showed that the conjugant #3 showed stable expression of green fluorescent both in free-living and bacteroid stage. The visualization of sym plasmid of wild strain and conjugants showed that conjugant #3 had a fragmentation of large sized plasmid into two but without affecting the nodulating ability. These results clearly indicated that mini-Tn5 vectors (Transposon vectors) the best alternate tools for plasmid vectors for integration of foreign genes in chromosomal DNA or symbiotic plasmid and expression, both in free-living and bacteroid stage of Rhizobium.
在转座元件中,mini-Tn5转座子载体已被证明在多种革兰氏阴性菌的插入诱变中具有更大的实用性。本研究使用了含有无启动子egfp基因和庆大霉素抗性基因的mini-Tn5载体。通过接合作用将转座子载体从大肠杆菌S17引入到华癸中生根瘤菌。对接合子进行筛选,以检测其在自由生活状态和紫云英根瘤中的egfp稳定表达情况。结果表明,接合子#3在自由生活状态和类菌体阶段均显示出绿色荧光的稳定表达。野生菌株和接合子的共生质粒可视化显示,接合子#3的大质粒发生了断裂,分成了两个,但不影响结瘤能力。这些结果清楚地表明,mini-Tn5载体(转座子载体)是用于将外源基因整合到根瘤菌染色体DNA或共生质粒中并在自由生活状态和类菌体阶段进行表达的质粒载体的最佳替代工具。