Neyra C A, Hageman R H
Department of Agronomy, University of Illinois, Urbana, Illinois 61801.
Plant Physiol. 1976 Dec;58(6):726-30. doi: 10.1104/pp.58.6.726.
The observation that exposure of the leaf canopy to increasing concentrations of CO(2) (100-400 mul/l) decreases the influx of nitrate to the leaf blades, but not to the roots or stalks (largely leaf sheaths), was reconfirmed using (15)NO(3) (-). Decreases in leaf nitrate supply were associated with decreases in induction of nitrate reductase, thus supporting the view that the influx of nitrate to a tissue is a major factor in regulation of the level of nitrate reductase. The whole plant (15)N distribution data show that the CO(2) effects were due to decreased influx of nitrate into the leaf blade rather than CO(2)-enhanced nitrate reduction. The decreases in nitrate accumulation by the leaf blade with increases in CO(2) concentration were only partially accounted for by differences in transpiration. Because the initial malate concentration of root tissue (detopped plants) had no subsequent effect on nitrate uptake, it seems unlikely that high levels of malate induced by CO(2) were responsible for the exclusion of nitrate from the leaf blades.Time course changes in nitrate and malate concentrations in root tissue (detopped plants) during nitrate uptake showed that oxidation of extra malate does not stimulate nitrate uptake and that malate is not specifically required as an energy source at the ion carrier level.The observation that nitrate and malate concentrations in corn leaf blades were negatively correlated was reconfirmed with 25 additional corn genotypes. However, using the same tissue, a higher correlation was obtained between malate plus aconitate and nitrate, suggesting that organic acids other than malate could be involved. The proposal that reduction of nitrate in the leaf is stoichiometrically related to malate production is a valid explanation of the relationship only if malate oxidation does not provide NADH for nitrate reduction. However, addition of malate and NAD to crude extracts (in vitro assay) or malate to leaf blade sections (in vivo assay) caused nitrate reduction. Because of these observations and the known intracellular location of NAD-malate dehydrogenase and nitrate reductase, we believe that malate oxidation is one of the major sources of NADH for nitrate reduction in corn leaf blades in situ.
利用¹⁵NO₃⁻再次证实了以下观察结果:将叶冠暴露于浓度不断增加的CO₂(100 - 400 μl/l)环境中会减少硝酸盐向叶片的流入,但不会减少向根或茎(主要是叶鞘)的流入。叶片硝酸盐供应的减少与硝酸还原酶诱导作用的降低相关,从而支持了以下观点:硝酸盐向组织的流入是调节硝酸还原酶水平的主要因素。整株植物的¹⁵N分布数据表明,CO₂的影响是由于硝酸盐向叶片的流入减少,而非CO₂增强了硝酸盐的还原作用。随着CO₂浓度升高,叶片中硝酸盐积累的减少仅部分可由蒸腾作用的差异来解释。由于根组织(去顶植株)的初始苹果酸浓度对硝酸盐吸收没有后续影响,因此由CO₂诱导的高浓度苹果酸导致叶片排斥硝酸盐的可能性似乎不大。在硝酸盐吸收过程中,根组织(去顶植株)中硝酸盐和苹果酸浓度的时间进程变化表明,额外苹果酸的氧化不会刺激硝酸盐吸收,并且在离子载体水平上,苹果酸并非作为能量来源所特别必需的物质。用另外25种玉米基因型再次证实了玉米叶片中硝酸盐和苹果酸浓度呈负相关这一观察结果。然而,在相同组织中,苹果酸与乌头酸之和与硝酸盐之间的相关性更高,这表明除苹果酸外的其他有机酸可能也参与其中。只有当苹果酸氧化不为硝酸盐还原提供NADH时,叶片中硝酸盐还原与苹果酸产生在化学计量上相关这一观点才是对该关系的有效解释。然而,向粗提物中添加苹果酸和NAD(体外测定)或向叶片切片中添加苹果酸(体内测定)会导致硝酸盐还原。基于这些观察结果以及已知的NAD - 苹果酸脱氢酶和硝酸还原酶在细胞内的定位,我们认为苹果酸氧化是玉米叶片原位硝酸盐还原过程中NADH的主要来源之一。