Botanisches Institut der Universität Bonn, D-5300 Bonn 1, Germany.
Plant Physiol. 1992 Jul;99(3):837-42. doi: 10.1104/pp.99.3.837.
The coordinate appearance of the bispecific NAD(P)H-nitrate reductase (NR; EC 1.6.6.2) and nitrite reductase (NiR; EC 1.7.7.1) was investigated in leaves and roots from European white birch seedlings (Betula pendula Roth). Induction by nitrate and light of both enzymes was analyzed by in vitro assays and by measuring NR- and NiR-encoding mRNA pools with homologous cDNAs as probes. When birch seedlings were grown on a medium containing ammonium as the sole nitrogen source, low constitutive expression of NR and NiR was observed in leaves, whereas only NiR was significantly expressed in roots. Upon transfer of the seedlings to a nitrate-containing medium, mRNA pools and activities of NR and NiR dramatically increased in leaves and roots, with a more rapid induction in leaves. Peak accumulations of mRNA pools preceded the maximum activities of NR and NiR, suggesting that the appearance of both activities can be mainly attributed to an increased expression of NR and NiR genes. Expression of NR was strictly light-dependent in leaves and roots and was repressed by ammonium in roots but not in leaves. In contrast with NR, constitutive expression of NiR was not affected by light, and even a slight induction following the addition of nitrate was found in the dark in roots but not in leaves. No effect of ammonium on NiR expression was detectable in both organs. In leaves as well as in roots, NiR was induced more rapidly than NR, which appears to be a safety measure to prevent nitrite accumulation.
研究了欧洲白桦(Betula pendula Roth)幼苗叶片和根中双特异性 NAD(P)H-硝酸盐还原酶(NR;EC 1.6.6.2)和亚硝酸盐还原酶(NiR;EC 1.7.7.1)的共表达。通过体外测定和使用同源 cDNA 作为探针测定 NR 和 NiR 编码的 mRNA 池,分析了硝酸盐和光照对这两种酶的诱导作用。当白桦幼苗在含有铵盐作为唯一氮源的培养基中生长时,叶片中观察到 NR 和 NiR 的低组成型表达,而根中仅显著表达 NiR。当将幼苗转移到含硝酸盐的培养基中时,叶片和根中 NR 和 NiR 的 mRNA 池和活性急剧增加,叶片中的诱导更为迅速。mRNA 池的最大积累先于 NR 和 NiR 活性的最大活性,表明这两种活性的出现主要归因于 NR 和 NiR 基因的表达增加。NR 的表达在叶片和根中严格依赖于光照,并在根中被铵盐抑制,但在叶片中不受抑制。与 NR 相反,NiR 的组成型表达不受光照影响,甚至在黑暗中添加硝酸盐后在根中发现轻微诱导,但在叶片中没有发现。在两个器官中都没有检测到铵盐对 NiR 表达的影响。在叶片和根中,NiR 的诱导速度快于 NR,这似乎是一种防止亚硝酸盐积累的安全措施。