Rattray E A, Prosser J I, Killham K, Glover L A
Department of Molecular and Cell Biology, Marischal College, University of Aberdeen, Scotland.
Appl Environ Microbiol. 1990 Nov;56(11):3368-74. doi: 10.1128/aem.56.11.3368-3374.1990.
Measurement of light output by luminometry was used to estimate quantitatively the cell concentrations of luminescent strains of Escherichia coli in liquid culture and inoculated into soil. Strains were constructed in which luciferase production was autoinducible or constitutive. In the former, light output per cell varied considerably during growth but was constant in constitutive strains. In liquid culture, the lower detection limit was in the order of 10(2) cells ml-1. Sensitivity was reduced by approximately 1 order of magnitude for cells inoculated into soil, when 2 x 10(2) to 6 x 10(3) cells g of soil-1 could be detected. Light output measurements were obtained within 5 min of sampling, and luminometry therefore potentially offers a rapid and sensitive detection technique for genetically engineered microorganisms.
通过发光度测量法来测定光输出,以此定量估算液体培养并接种到土壤中的发光大肠杆菌菌株的细胞浓度。构建了荧光素酶产生为自动诱导型或组成型的菌株。在前者中,每个细胞的光输出在生长过程中变化很大,但在组成型菌株中是恒定的。在液体培养中,检测下限约为10(2)个细胞毫升-1。接种到土壤中的细胞的灵敏度降低了约1个数量级,此时可检测到2×10(2)至6×10(3)个细胞克土壤-1。在采样后5分钟内即可获得光输出测量结果,因此发光度测量法有可能为基因工程微生物提供一种快速灵敏的检测技术。