Department of Biology, McMaster University, Hamilton, Ontario, Canada L8S 4K1.
Plant Physiol. 1976 Apr;57(4):572-6. doi: 10.1104/pp.57.4.572.
A comparison of induction and inactivation of nitrate reductase and two of its component activities, namely FMNH(2)-nitrate reductase and NO(3) (-)-induced NADH-cytochrome c reductase, was made in roots and leaves of corn (Zea mays L. var. W64A x 182E). The three activities were induced in parallel in both tissues when NO(3) (-) was supplied. WO(4) (=) suppressed the induction of NADH- and FMNH(2)-nitrate reductase activities in root tips and leaves. The NO(3) (-)-induced NADH-cytochrome c reductase activity showed a normal increase in roots treated with WO(4) (=). In leaves, on the other hand, there was a marked superinduction of the NO(3) (-)-induced NADH-cytochrome c reductase in the presence of WO(4) (=).The half-life values of NADH-nitrate reductase and FMNH(2)-nitrate reductase measured by removing NO(3) (-) and adding WO(4) (=) to the medium, were 4 hours in root tips and 6 hours in excised leaves. Addition of NO(3) (-) in the induction medium together with WO(4) (=) gave partial protection of NADH-nitrate reductase and FMNH(2)-nitrate reductase activities in both root tips and leaves with a t(0.5) of 6 and 8 hours, respectively. NO(3) (-) also reduced the loss of nitrate reductase activity from mature root sections. In the presence of cycloheximide, both NADH-nitrate reductase and NO(3) (-)-induced NADH-cytochrome c reductase activities were lost at similar rates in root tips. NO(3) (-) protected the loss of NO(3) (-)-induced NADH-cytochrome c reductase to the same extent as that of NADH-nitrate reductase.
对玉米(Zea mays L. var. W64A x 182E)的根和叶进行了硝酸还原酶及其两种组成活性(即 FMNH(2)-硝酸还原酶和 NO(3)(-)诱导的 NADH-细胞色素 c 还原酶)的诱导和失活比较。当供应 NO(3)(-)时,这三种活性在两种组织中平行诱导。WO(4)(=)抑制根尖和叶片中 NADH 和 FMNH(2)-硝酸还原酶活性的诱导。在 WO(4)(=)处理的根中,NO(3)(-)诱导的 NADH-细胞色素 c 还原酶活性正常增加。另一方面,在叶片中,在 WO(4)(=)存在下,NO(3)(-)诱导的 NADH-细胞色素 c 还原酶出现明显的超诱导。通过从培养基中去除 NO(3)(-)和添加 WO(4)(=)来测量 NADH-硝酸还原酶和 FMNH(2)-硝酸还原酶的半衰期值,在根尖中为 4 小时,在离体叶片中为 6 小时。在诱导培养基中添加 NO(3)(-)和 WO(4)(=)一起,分别在根尖和叶片中对 NADH-硝酸还原酶和 FMNH(2)-硝酸还原酶活性提供部分保护,t(0.5)分别为 6 和 8 小时。NO(3)(-)还减少了成熟根段硝酸还原酶活性的丧失。在环己酰亚胺存在下,NADH-硝酸还原酶和 NO(3)(-)诱导的 NADH-细胞色素 c 还原酶活性在根尖中以相似的速率丧失。NO(3)(-)对 NO(3)(-)诱导的 NADH-细胞色素 c 还原酶丧失的保护程度与 NADH-硝酸还原酶相同。