Phosphorus acquisition, translocation, and redistribution in maize.

Phosphorus (P) is an essential nutrient for crop growth, making it important for maintaining food security as the global population continues to increase. Plants acquire P primarily via the uptake of inorganic phosphate (Pi) in soil through their roots. Pi, which is usually sequestered in soils, is not easily absorbed by plants and represses plant growth. Plants have developed a series of mechanisms to cope with P deficiency. Moreover, P fertilizer applications are critical for maximizing crop yield. Maize is a major cereal crop cultivated worldwide. Increasing its P-use efficiency is important for optimizing maize production. Over the past two decades, considerable progresses have been achieved in research aimed at adapting maize varieties to changes in environmental P supply. Here, we present an overview of the morphological, physiological, and molecular mechanisms involved in P acquisition, translocation, and redistribution in maize, and combine the advances in Arabidopsis and rice, to better elucidate the progress of P nutrition. Additionally, we summarize the correlation between P and abiotic stress responses. Clarifying the mechanisms relevant to improving P absorption and use in maize can guide future research on sustainable agriculture.

Foliar P Application Cannot Fully Restore Photosynthetic Capacity, P Nutrient Status, and Growth of P Deficient Maize (Zea mays L.).

The essential plant nutrient phosphorus (P) is key for numerous structures and processes in crops and its deficiency can severely restrict yield and quality. As soil P availability for plant uptake is often limited, foliar P application can be an alternative means of supplying P to the plants during the growth period. This study was aimed at investigating the effect of foliar P application on photosynthetic parameters, P nutritional status, and growth of P deficient maize over time. Plants of Zea mays L. cv. Keops were grown with deficient and sufficient amounts of P in hydroponics. Foliar P treatments were applied to P deficient plants and several physiological parameters were monitored for 21 days. The variables measured were leaf gas exchange parameters, SPAD values, foliar P absorption, re-translocation rates, and plant biomass production. Foliar P application significantly increased CO2-assimilation and SPAD values and additionally enhanced biomass production in all plant components. Elemental analysis revealed increased tissue P concentrations following foliar P application compared to P deficient plants. While increased growth of P-deficient plants was steadily promoted by foliar P spraying for the entire experimental period, the positive effect on CO2 assimilation and P concentration was transient and vanished some days after the foliar treatment. P deficiency markedly impaired the efficiency of physiological processes of maize plants. As a conclusion, foliar P fertilisation improved physiological and agronomical plant parameters over time, but failed to restore plant functionality of P deficient maize plants during a prolonged experimental period.

Phosphorus remobilization from rice flag leaves during grain filling: an RNA-seq study.

The physiology and molecular regulation of phosphorus (P) remobilization from vegetative tissues to grains during grain filling is poorly understood, despite the pivotal role it plays in the global P cycle. To test the hypothesis that a subset of genes involved in the P starvation response are involved in remobilization of P from flag leaves to developing grains, we conducted an RNA-seq analysis of rice flag leaves during the preremobilization phase (6 DAA) and when the leaves were acting as a P source (15 DAA). Several genes that respond to phosphate starvation, including three purple acid phosphatases (OsPAP3, OsPAP9b and OsPAP10a), were significantly up-regulated at 15 DAA, consistent with a role in remobilization of P from flag leaves during grain filling. A number of genes that have not been implicated in the phosphate starvation response, OsPAP26, SPX-MFS1 (a putative P transporter) and SPX-MFS2, also showed expression profiles consistent with involvement in P remobilization from senescing flag leaves. Metabolic pathway analysis using the KEGG system suggested plastid membrane lipid synthesis is a critical process during the P remobilization phase. In particular, the up-regulation of OsPLDz2 and OsSQD2 at 15 DAA suggested phospholipids were being degraded and replaced by other lipids to enable continued cellular function while liberating P for export to developing grains. Three genes associated with RNA degradation that have not previously been implicated in the P starvation response also showed expression profiles consistent with a role in P mobilization from senescing flag leaves.

Interdependence of phosphorus, nitrogen, potassium and magnesium translocation by the ectomycorrhizal fungus Paxillus involutus.

• Translocation is shown of phosphorus, nitrogen, potassium and magnesium to a P-deficient host from ectomycorrhizal fungal hyphae. • Mycorrhizal (with Paxillus involutus) and nonmycorrhizal P-deficient spruce (P. abies) seedlings were grown in a two-compartment sand-culture system. Hyphal translocation of nutrients from the inner compartment (penetrated only by hyphae) to the host was measured using mass balance (for N, P and K) or stable isotope (15 N and 25 Mg) methods. • Addition of P to the hyphal compartment strongly stimulated hyphal growth, and this also increased both seedling P status and growth. Hyphae translocated nonlimiting elements in addition to P, contributing 52, 17, 5 and 3-4%, respectively, to total P, N, K or Mg plant uptake. The potential role of the ectomycorrhizal mycelium in K acquisition was demonstrated. Translocation to mycorrhizal seedings of N, K and Mg was strongly reduced when hyphal P-fluxes ceased; this translocation of nonlimiting nutrients depended on simultaneous translocation of P. • The ectomycorrhizal mycelium has an active role in P acquisition from sources not available to roots. Nutrient fluxes within fungal hyphae are interdependent and strong coupling of N, K and Mg fluxes with long-distance P translocation in the mycorrhizal mycelium occurs.

Influence of xylem vascular architecture on the translocation of phosphorus from nodal roots in a genotype of Trifolium repens during undisturbed growth.

Our objective was to establish whether the xylem vascular connections (architecture) of a genotype of Trifolium repens L. had implications for the intraplant allocation of recently assimilated phosphorus (P). One nodal root of each plan! was isolated and fed 32 P-labelled nutrient solution for 24 h. The fed root was either on the parent axis (11-12 nodes proximal CO the apex) or on a branch at the third or fourth node along the branch when counting from the junction with the parent stolon. Allocation patterns were obtained by dissecting plants and assaying each dissected component for 32 P. Under conditions of undisturbed growth in a controlled environment xylem architecture was found to have an important influence on the intraplant distribution of 32 P from nodal roots. Allocation patterns of 32 P were consistent with those predicted from knowledge of the xylem vascular architecture of the genotype and a predominantly acropetal direction of the transpiration stream. For instance, very little 32 P (< 1 % of exported 32 P from the fed root) was found in branches on the opposite side of the stolon to the fed root, and the strong acropetal direction of the transpiration stream resulted in little allocation of 32 P to leaves that had traces that arose from axial bundles at positions proximal to that of the fed root (the leaf subtending the fed root and the next distal leaf had low 32 P content), to all plant organs proximal to the fed root (< 6%) and to all other roots (<4%). The high allocation of 32 P to the branch arising at the same node as the fed root (64%) reflects the numerous links that the- fed root has to vascular bundles in the branch (3-6, of which two are axial bundles) against the single connection it has to the adjacent lower axial bundle in the parent stolon. Allocation of 32 P to the leaf and axillary bud at each node along the branch strongly favoured nodes on the adaxial side, a result consistent with the fact that the root connections are to the upper and lower axial bundles on the adaxial side of the branch. Allocation to a particular node along the branch was also influenced by its nodal position relative to the fed root and the sink strength of its tissues for the transpiration stream.