Villalobo A, Roldán J M, Rivas J
Arch Microbiol. 1977 Mar 1;112(2):127-32. doi: 10.1007/BF00429324.
A soluble nitrate reductase from the bacterium Acinetobacter calcoaceticus grown on nitrate has been characterized. The reduction of nitrate to nitrite is mediated by an enzyme of 96000 molecular weight that can use as electron donors either viologen dyes chemically reduced with dithionite or enzymatically reduced with NAD(P)H, through specific diaphorases which utilize viologens as electron acceptors. Nitrate reductase activity is molybdenumdependent as shown by tungstate antagonistic experiments and is sensitive to--SH reagents and metal chelators such as KCN. The enzyme synthesis is repressed by ammonia. Moreover, nitrate reductase activity undergoes a quick inactivation either by dithionite and temperature or by dithionite in the presence of small amounts of nitrate. Cyanate prevents this inactivating process and can restore the activity once the inactivation had occurred, thus suggesting that an interconversion mechanism may participate in the regulation of Acinetobacter nitrate reductase.
已对在硝酸盐上生长的醋酸钙不动杆菌中的一种可溶性硝酸盐还原酶进行了表征。硝酸盐还原为亚硝酸盐是由一种分子量为96000的酶介导的,该酶可以使用连二亚硫酸盐化学还原或通过利用连二亚硫酸盐作为电子受体的特定黄递酶用NAD(P)H酶促还原的紫精染料作为电子供体。钨酸盐拮抗实验表明,硝酸盐还原酶活性依赖于钼,并且对-SH试剂和金属螯合剂(如KCN)敏感。该酶的合成受到氨的抑制。此外,硝酸盐还原酶活性会因连二亚硫酸盐和温度或在少量硝酸盐存在下的连二亚硫酸盐而迅速失活。氰酸盐可防止这种失活过程,并且一旦发生失活,可恢复活性,因此表明一种相互转化机制可能参与了不动杆菌硝酸盐还原酶的调节。