Meikle A, Killham K, Prosser J I, Glover L A
Department of Molecular and Cell Biology, University of Aberdeen, Marischal College, UK.
FEMS Microbiol Lett. 1992 Dec 1;78(2-3):217-20. doi: 10.1016/0378-1097(92)90029-n.
Genetically modified cells of Pseudomonas fluorescens, chromosomally marked with genes for bioluminescence, were inoculated into sterile soil microcosms. During incubation for 90 days, viable cell concentration did not change significantly but light output, measured by luminometry, decreased, indicating reduced metabolic activity due to lack of substrates. Amendment with nutrients resulted in parallel increases in both luminescence and dehydrogenase activity. Luminometry therefore enables rapid monitoring of the activity of populations of luminescence-marked microbial inocula in the soil, with greater sensitivity and selectivity than traditional techniques.
将经过基因改造、带有生物发光基因且染色体已标记的荧光假单胞菌细胞接种到无菌土壤微观系统中。在90天的培养期间,活细胞浓度没有显著变化,但通过发光测定法测得的光输出量下降,这表明由于缺乏底物,代谢活性降低。添加营养物质后,发光和脱氢酶活性同时增加。因此,发光测定法能够快速监测土壤中发光标记微生物接种体群体的活性,其灵敏度和选择性高于传统技术。