Olmo-Mira M Francisca, Cabello Purificación, Pino Carmen, Martínez-Luque Manuel, Richardson David J, Castillo Francisco, Roldán M Dolores, Moreno-Vivián Conrado
Departamento de Bioquímica y Biología Molecular, Universidad de Córdoba, Edificio Severo Ochoa, 1a planta, Campus de Rabanales, Córdoba 14071, Spain.
Arch Microbiol. 2006 Oct;186(4):339-44. doi: 10.1007/s00203-006-0149-x. Epub 2006 Aug 3.
A nas gene region from Rhodobacter capsulatus E1F1 containing the putative nasB gene for nitrite reductase was previously cloned. The recombinant His(6)-NasB protein overproduced in E. coli showed nitrite reductase activity in vitro with both reduced methyl viologen and NADH as electron donors. The apparent K ( m ) values for nitrite and NADH were 0.5 mM and 20 microM, respectively, at the pH and temperature optima (pH 9 and 30 degrees C). The optical spectrum showed features that indicate the presence of FAD, iron-sulfur cluster and siroheme as prosthetic groups, and nitrite reductase activity was inhibited by sulfide and iron reagents. These results indicate that the phototrophic bacterium R. capsulatus E1F1 possesses an assimilatory NADH-nitrite reductase similar to that described in non-phototrophic organisms.
先前已克隆了来自荚膜红细菌E1F1的一个nas基因区域,其中包含假定的亚硝酸还原酶nasB基因。在大肠杆菌中过量表达的重组His(6)-NasB蛋白,以还原型甲基紫精和NADH作为电子供体时,在体外表现出亚硝酸还原酶活性。在最适pH和温度(pH 9和30℃)下,亚硝酸和NADH的表观K(m)值分别为0.5 mM和20 μM。光谱显示出的特征表明存在FAD、铁硫簇和西罗血红素作为辅基,并且亚硝酸还原酶活性受到硫化物和铁试剂的抑制。这些结果表明,光合细菌荚膜红细菌E1F1拥有一种类似于非光合生物中所描述的同化型NADH-亚硝酸还原酶。