Shen T C, Ramadoss C S, Vennesland B
Biochim Biophys Acta. 1982 Jun 4;704(2):227-34. doi: 10.1016/0167-4838(82)90150-9.
Demolybdo-nitrate reductase (cytochrome c reductase) (NADH: acceptor oxidoreductase, EC 1.6.99.3) of Chlorella vulgaris can be activated in vitro to nitrate reductase by insertion of Mo from molybdate into the apoprotein. Evidence is here presented that reduction of the enzyme by reduced pyridine nucleotides inhibits the process of molybdenum insertion. This report also describes the effect of molybdate and tungstate concentration on the activation process. The activation is sigmoidally related to molybdate concentration with a calculated Hill coefficient of NH = 3. At suboptimal molybdate concentrations, tungstate stimulates enzyme activation by molybdate; but at saturating molybdate concentrations, tungstate is inhibitory. These facts are regarded as an indication that molybdate and tungstate are both positive effectors of molybdenum incorporation, but that they are competitors for the active Mo center.
普通小球藻的去钼硝酸还原酶(细胞色素c还原酶)(NADH:受体氧化还原酶,EC 1.6.99.3)可在体外通过将钼酸盐中的钼插入脱辅基蛋白而被激活为硝酸还原酶。本文提供的证据表明,还原型吡啶核苷酸对该酶的还原作用会抑制钼的插入过程。本报告还描述了钼酸盐和钨酸盐浓度对激活过程的影响。激活作用与钼酸盐浓度呈S形关系,计算得出的希尔系数NH = 3。在次优钼酸盐浓度下,钨酸盐会刺激钼酸盐对酶的激活;但在钼酸盐饱和浓度下,钨酸盐具有抑制作用。这些事实被视为表明钼酸盐和钨酸盐都是钼掺入的正效应物,但它们是活性钼中心的竞争者。