Kende H, Hahn H, Kays S E
Michigan State University-Atomic Energy Commission Plant Research Laboratory, Michigan State University, East Lansing, Michigan 48823.
Plant Physiol. 1971 Dec;48(6):702-6. doi: 10.1104/pp.48.6.702.
Nitrate reductase activity in excised embryos of Agrostemma githago increases in response to both NO(3) (-) and cytokinins. We asked the question whether cytokinins affected nitrate reductase activity directly or through NO(3) (-), either by amplifying the effect of low endogenous NO(3) (-) levels, or by making NO(3) (-) available for induction from a metabolically inactive compartment. Nitrate reductase activity was enhanced on the average by 50% after 1 hour of benzyladenine treatment. In some experiments, the cytokinin response was detectable as early as 30 minutes after addition of benzyladenine. Nitrate reductase activity increased linearly for 4 hours and began to decay 13 hours after start of the hormone treatment. When embryos were incubated in solutions containing mixtures of NO(3) (-) and benzyladenine, additive responses were obtained. The effects of NO(3) (-) and benzyladenine were counteracted by abscisic acid. The increase in nitrate reductase activity was inhibited at lower abscisic acid concentrations in embryos which were induced with NO(3) (-), as compared to embryos treated with benzyladenine. Casein hydrolysate inhibited the development of nitrate reductase activity. The response to NO(3) (-) was more susceptible to inhibition by casein hydrolysate than the response to the hormone. When NO(3) (-) and benzyladenine were withdrawn from the medium after maximal enhancement of nitrate reductase activity, the level of the enzyme decreased rapidly. Nitrate reductase activity increasd again as a result of a second treatment with benzyladenine but not with NO(3) (-). At the time of the second exposure to benzyladenine, no NO(3) (-) was detectable in extracts of Agrostemma embryos. This is taken as evidence that cytokinins enhance nitrate reductase activity directly and not through induction by NO(3) (-).
麦仙翁离体胚中的硝酸还原酶活性会因硝酸盐(NO₃⁻)和细胞分裂素而增加。我们提出一个问题,即细胞分裂素是直接影响硝酸还原酶活性,还是通过NO₃⁻来影响,是通过放大低内源NO₃⁻水平的效应,还是通过使NO₃⁻可从代谢不活跃区室诱导产生。用苄基腺嘌呤处理1小时后,硝酸还原酶活性平均提高了50%。在一些实验中,早在添加苄基腺嘌呤30分钟后就能检测到细胞分裂素反应。硝酸还原酶活性在4小时内呈线性增加,并在激素处理开始后13小时开始下降。当胚在含有NO₃⁻和苄基腺嘌呤混合物的溶液中孵育时,得到了相加反应。脱落酸抵消了NO₃⁻和苄基腺嘌呤的作用。与用苄基腺嘌呤处理的胚相比,在由NO₃⁻诱导的胚中,较低浓度的脱落酸就能抑制硝酸还原酶活性的增加。酪蛋白水解物抑制硝酸还原酶活性的发展。对NO₃⁻的反应比激素反应更容易受到酪蛋白水解物的抑制。当硝酸还原酶活性最大增强后从培养基中去除NO₃⁻和苄基腺嘌呤时,该酶的水平迅速下降。由于再次用苄基腺嘌呤处理,硝酸还原酶活性再次增加,但用NO₃⁻处理则不然。在第二次接触苄基腺嘌呤时,在麦仙翁胚提取物中未检测到NO₃⁻。这被视为细胞分裂素直接增强硝酸还原酶活性而非通过NO₃⁻诱导的证据。