Department of Botany and Plant Sciences, University of California, Riverside, California 92521.
Plant Physiol. 1986 Jul;81(3):774-9. doi: 10.1104/pp.81.3.774.
The accumulation of arginine in leaves of four citrus rootstock cultivars during P deficiency has been demonstrated to be due to increased de novo synthesis rather than decreased catabolism or increased protein degradation (E Rabe, CJ Lovatt, 1984, Plant Physiol 76: 747-752). In this report, we provide evidence (a) that the increased activity of the arginine biosynthetic pathway observed for citrus rootstocks grown under P-deficient conditions for 7 months is due to an increase in the concentration of ammonia in leaves of P-deficient plants and (b) that ammonia accumulation and removal through arginine systhesis are early responses to phosphorus deficiency for both a woody perennial, rough lemon (Citrus limon), and an herbaceous annual, summer squash (Cucurbita pepo). Transferring 5-day-old squash plants to a phosphorus-deficient nutrient solution for only 10 days resulted in a 2-fold increase in the concentration of nitrate in the youngest fully expanded leaves (YFE). Concomitantly, the specific activity of nitrate reductase doubled and the ammonia content of P-deficient YFE leaves increased to a concentration significantly greater that of leaves from healthy control plants (P < 0.05). Consistent with increased availability of ammonia, the incorporation of NaH(14)CO(3) into arginine plus urea doubled during phosphorus deficiency and arginine accumulated. Despite the accumulation of nitrate and ammonia in YFE leaves during phosphorus deficiency, the total nitrogen content of these leaves was less than that of the healthy control plants. Similar results were obtained for rough lemon. Nitrate content of the YFE leaves increased 1.5- and 3.0-fold in plants deprived of phosphorus for 6 and 12 weeks, respectively. Ammonia content of the leaves increased as P deficiency progressed to 1.4 +/- 0.08 mg (+/- se, n = 4) per gram dry weight, a level 1.8-fold greater than that of the P-sufficient control plants. During P deficiency de novo arginine biosynthesis in rough lemon increased 10-fold. Immersing the petiole of YFE leaves from P-sufficient squash and rough lemon plants in 50 millimolar NH(4) (+) for 3 hours resulted in the accumulation of ammonia in the leaves, and a 4-fold increase in the incorporation of NaH(14)CO(3) into arginine plus urea. Taken together, these results provide strong evidence that the accumulation of nitrate and ammonia in leaves is an early response of both woody and herbaceous plants to P deprivation. The data are consistent with the hypothesis that increased de novo arginine biosynthesis in leaves during P deficiency is in response to ammonia content of the leaves.
在缺磷条件下,四种柑橘砧木品种叶片中精氨酸的积累被证明是由于新合成的增加,而不是由于降解或蛋白质降解减少(E Rabe,CJ Lovatt,1984,植物生理学 76:747-752)。在本报告中,我们提供了证据(a)在缺磷条件下生长 7 个月的柑橘砧木中观察到的精氨酸生物合成途径活性增加是由于缺磷植物叶片中氨浓度增加所致,以及(b)氨的积累和通过精氨酸合成去除是木本多年生植物柠檬和草本一年生植物南瓜对磷缺乏的早期反应。将 5 天大的南瓜植物转移到缺磷的营养液中仅 10 天,导致最年轻的完全展开叶片(YFE)中硝酸盐浓度增加了 2 倍。同时,硝酸还原酶的比活性增加了一倍,缺磷 YFE 叶片中的氨含量增加到显著高于健康对照植物叶片的浓度(P <0.05)。与氨的可用性增加一致,在磷缺乏期间,NaH(14)CO(3)掺入精氨酸加尿素增加了一倍,并且精氨酸积累。尽管 YFE 叶片在缺磷期间积累了硝酸盐和氨,但这些叶片的总氮含量低于健康对照植物。柠檬的结果类似。分别剥夺磷 6 和 12 周后,YFE 叶片中的硝酸盐含量增加了 1.5-和 3.0 倍。随着磷缺乏的进展,叶片中的氨含量增加到 1.4 +/- 0.08 mg(+/ - se,n = 4)/克干重,比磷充足的对照植物高 1.8 倍。在柠檬中,缺磷时新合成的精氨酸生物合成增加了 10 倍。将来自磷充足的南瓜和柠檬植物的 YFE 叶片的叶柄在 50 毫摩尔 NH(4)(+)中浸泡 3 小时会导致叶片中氨的积累,并使 NaH(14)CO(3)掺入精氨酸加尿素的量增加 4 倍。综上所述,这些结果为硝酸盐和氨在叶片中的积累是木本和草本植物对磷缺乏的早期反应提供了有力的证据。这些数据与假设一致,即在缺磷时,叶片中新合成的精氨酸增加是对叶片中氨含量的反应。