Prest A G, Winson M K, Hammond J R, Stewart G S
Bass Technical Centre, Burton on Trent, UK.
Lett Appl Microbiol. 1997 May;24(5):355-60. doi: 10.1046/j.1472-765x.1997.00064.x.
A plasmid-borne transcriptional fusion between the Escherichia coli nitrate reductase (narG) promoter and the Photorhabdus luminescens lux operon provides E. coli with a highly bioluminescent phenotype in the presence of nitrate. This E. coli biosensor can detect nitrate to a level of 5 x 10(-5) mol l-1 (0.3 ppm), levels relevant to those levels encountered in brewing water. Since induction of the narG promoter requires NarL, the plasmid-based sensor can also be used to interrogate enteric bacteria for the presence of functional homologues of this E. coli regulatory protein. Obesumbacterium proteus, an important bacterial brewery contaminant, failed to provide nitrate-dependent bioluminescence demonstrating divergence in this organism from E. coli in the mechanism of nitrate reductase regulation.
大肠杆菌硝酸盐还原酶(narG)启动子与发光杆菌lux操纵子之间的质粒介导转录融合,使大肠杆菌在有硝酸盐存在时具有高度生物发光表型。这种大肠杆菌生物传感器能够检测低至5×10⁻⁵摩尔/升(0.3 ppm)的硝酸盐,这与酿造用水中遇到的硝酸盐水平相关。由于narG启动子的诱导需要NarL,基于质粒的传感器还可用于检测肠道细菌中是否存在这种大肠杆菌调节蛋白的功能同源物。变形杆菌是啤酒厂一种重要的细菌污染物,它不能产生硝酸盐依赖性生物发光,这表明该生物体在硝酸盐还原酶调节机制上与大肠杆菌存在差异。