Rafii F, Franklin W, Cerniglia C E
Division of Microbiology, Food and Drug Administration, Jefferson, Arkansas 72079.
Appl Environ Microbiol. 1990 Jul;56(7):2146-51. doi: 10.1128/aem.56.7.2146-2151.1990.
A plate assay was developed for the detection of anaerobic bacteria that produce azoreductases. With this plate assay, 10 strains of anaerobic bacteria capable of reducing azo dyes were isolated from human feces and identified as Eubacterium hadrum (2 strains), Eubacterium spp. (2 species), Clostridium clostridiiforme, a Butyrivibrio sp., a Bacteroides sp., Clostridium paraputrificum, Clostridium nexile, and a Clostridium sp. The average rate of reduction of Direct Blue 15 dye (a dimethoxybenzidine-based dye) in these strains ranged from 16 to 135 nmol of dye per min per mg of protein. The enzymes were inactivated by oxygen. In seven isolates, a flavin compound (riboflavin, flavin adenine dinucleotide, or flavin mononucleotide) was required for azoreductase activity. In the other three isolates and in Clostridium perfringens, no added flavin was required for activity. Nondenaturing polyacrylamide gel electrophoresis showed that each bacterium expressed only one azoreductase isozyme. At least three types of azoreductase enzyme were produced by the different isolates. All of the azoreductases were produced constitutively and released extracellularly.
开发了一种平板分析法用于检测产生偶氮还原酶的厌氧细菌。通过这种平板分析法,从人类粪便中分离出10株能够还原偶氮染料的厌氧细菌,并鉴定为哈氏真杆菌(2株)、真杆菌属(2个种)、梭状芽孢杆菌、一种丁酸弧菌属细菌、一种拟杆菌属细菌、副腐败梭菌、紧密梭菌和一种梭菌属细菌。这些菌株中直接蓝15染料(一种基于二甲氧基联苯胺的染料)的平均还原速率为每分钟每毫克蛋白质16至135纳摩尔染料。这些酶被氧气灭活。在7株分离菌中,偶氮还原酶活性需要一种黄素化合物(核黄素、黄素腺嘌呤二核苷酸或黄素单核苷酸)。在其他3株分离菌和产气荚膜梭菌中,活性不需要添加黄素。非变性聚丙烯酰胺凝胶电泳显示,每种细菌仅表达一种偶氮还原酶同工酶。不同的分离菌产生至少三种类型的偶氮还原酶。所有的偶氮还原酶都是组成型产生并释放到细胞外的。