Update on Boron in Higher Plants - Uptake, Primary Translocation and Compartmentation

Abstract: This review focuses on the uptake and primary translocation of boron (B), as well as on the subcellular compartmentation of B and its role in cell walls of higher plants. B uptake occurs via passive diffusion across the lipid bilayer, facilitated transport through major intrinsic proteins (MIPs), and energy-dependent transport through a high affinity uptake system. Whereas the first two represent passive uptake systems, which are constitutively present, the latter is induced by low B supply and is able to establish a concentration gradient for B between the root symplasm and the external medium. At high B supply, a substantial retention of B can be observed at xylem loading, and passive processes are most likely responsible for that. At low B supply, another energy-dependent high affinity transport system for B seems to be induced which establishes an additional concentration gradient between root symplasm and the xylem. The possible significance of all these processes at various B supplies is discussed. The role of soluble B complexes in uptake and primary translocation of B has been evaluated, but the few data available do not allow comprehensive conclusions to be drawn. In any case, there are no indications that soluble B complexes play a major role in either uptake or primary translocation of B. The subcellular compartmentation of B still remains a matter of controversy, but it is unequivocally clear that B is present in all subcellular compartments (apoplasm, cell wall, cytosol and vacuole). The relative distribution of B between these is dependent on plant species and experimental conditions and may vary greatly. Recent results on the well-established role of B in cell walls are summarized and their physiological significance discussed.     

Pathways of Phosphorus Absorption and Early Signaling between the Mycorrhizal Fungi and Plants

This review highlights the key role that mycorrhizal fungi play in making phosphorus (Pi) more available to plants, including pathways of phosphorus absorption, phosphate transporters and plant-mycorrhizal fungus symbiosis, especially in conditions where the level of inorganic phosphorus (Pi) in the soil is low. Mycorrhizal fungi colonization involves a series of signaling where the plant root exudates strigolactones, while the mycorrhizal fungi release a mixture of chito-oligosaccharides and liposaccharides, that activate the symbiosis process through gene signaling pathways, and contact between the hyphae and the root. Once the symbiosis is established, the extraradical mycelium acts as an extension of the roots and increases the absorption of nutrients, particularly phosphorus by the phosphate transporters. Pi then moves along the hyphae to the plant root/fungus interface. The transfer of Pi occurs in the apoplectic space; in the case of arbuscular mycorrhizal fungi, Pi is discharged from the arbuscular to the plant’s root symplasm, in the membrane that surrounds the arbuscule. Pi is then absorbed through the plant periarbuscular membrane by plant phosphate transporters. Furthermore, plants can acquire Pi from soil as a direct absorption pathway. As a result of this review, several genes that codify for high-affinity Pi transporters were identified. In plants, the main family is Pht1 although it is possible to find others such as Pht2, Pht3, Pho1 and Pho2. As in plants, mycorrhizal fungi have genes belonging to the Pht1 subfamily. In arbuscular mycorrhizal fungi we found L1PT1, GiPT, MtPT1, MtPT2, MtPT4, HvPT8, ZmPht1, TaPTH1.2, GmosPT and LYCes. HcPT1, HcPT2 and BePT have been characterized in ectomycorrhizal fungi. Each gene has a different way of expressing itself. In this review, we present diagrams of the symbiotic relationship between mycorrhizal fungi and the plant. This knowledge allows us to design solutions to regional problems such as food production in soils with low levels of Pi.

     

Transport kinetics and metabolism of exogenously applied putrescine in roots of intact maize seedlings

Putrescine metabolism, uptake, and compartmentation were studied in roots of hydroponically grown intact maize (Zea mays L.) seedlings. In vivo analysis of exogenously applied putrescine indicated that the diamine is primarily metabolized by a cell wall-localized diamine oxidase. Time-dependent kinetics for putrescine uptake could be resolved into a rapid phase of uptake and binding within the root apoplasm, followed by transport across the plasma membrane that was linear for 30 to 40 minutes. Concentration-dependent kinetics for putrescine uptake (between 0.05 and 1.0 millimolar putrescine) appeared to be nonsaturating but could be resolved into a saturable (V_max 0.397 micromoles per gram fresh weight per hour; K_m 120 micromolar) and a linear component. The linear component was determined to be cell wall-bound putrescine that was not removed during the desorption period following uptake of [³H]putrescine. These results suggest that a portion of the exogenously applied putrescine can be metabolized in maize root cell walls by diamine oxidase activity, but the bulk of the putrescine is transported across the plasmalemma by a carrier-mediated process, similar to that proposed for animal systems.     

A Relationship between Phosphate Uptake and Membrane Electrical Potential in Excised Roots of Helianthus annuus

Phosphate uptake by excised roots of sunflower (Helianthus annuus)was determined by the disappearance of phosphate from the externalsolution and by the accumulation of phosphate labelled with³²P. Over a 24 h period it was observed that net phosphate uptakedeclined to zero whilst uptake of ³²P continued unabated. Theelectrical PD of the cortical cell membranes declined in parallelwith net phosphate uptake and it was found that both could berestored by creating a pH gradient across the plasmalemma. Itwas concluded that net phosphate uptake was responsible fora component of the membrane PD of the root cortical cells. Key words: Roots, Phosphate, Membranes     

The effect of CCCP on ion fluxes in the stele and cortex of maize roots

Summary The accumulation of ⁸⁶Rb labelled potassium by isolated stelar and cortical tissues from 7-day-old roots of Zea mays has been compared with the levels accumulated by these tissues in the intact root. Cortical tissues have similar uptake eapacities in these two conditions whereas stelar tissues only exhibit an uptake capacity in the intact root system. The uncoupler carbonylcyanide m-chlorophenylhydrazone caused a considerable decrease in the uptake of potassium by these tissues. In the intact root system it prevented ions from the bathing medium reaching the stelar tissues. The efflux pattern from preloaded isolated stelar and cortical tissues was considerably altered by the inhibitor, a promotion of the efflux occurring in both of these tissues.It is concluded that stelar tissues only accumulated ions when these are supplied through the root symplasm and that the stelar plasmalemma has only a limited uptake capacity per se. Stelar uptake is thus a reflection of vacuolar accumulation across the tonoplast. There is no evidence in the present study of a carrier-mediated active secretion of ions across the stelar plasmalemma. The fact that the efflux was promoted rather than depressed by the uncoupler supports the postulate that a passive leakage is the final stage in the transport of ions across the plant root.     

植物对硼元素的吸收转运机制

硼是植物生长发育所必需的微量元素,但是在世界范围内,土壤中硼含量过高或者过低都会对植物生长产生影响,是农业生产上的主要问题.近来人们对硼的吸收转运机制的研究取得了突破性进展,鉴定了一些硼的转运通道和转运蛋白,例如：NIP5;1、NIP6;1、BOR1和BOR4,并对它们的转运机制有了一些了解.植物在硼缺少的情况下首先通过转运通道NIP5;1把硼吸收到共质体,然后通过转运蛋白BOR1运入中柱;在高硼毒害时,通过转运蛋白BOR4把过多的硼转出植物体,同时在植物中增加糖醇的含量,过表达BOR1或BOR4都能改变植物对硼含量变化的耐受性.因此,对植物中硼吸收转运机制的研究将有利于人们通过生物学手段提高作物对土壤中硼过高或过低的抗性.     

On the mechanisms of nectar secretion: revisited

Background and Scope

Models of nectar formation and exudation in multilayered nectaries with modified stomata or permeable cuticle are evaluated. In the current symplasmic model the pre-nectar moves from terminal phloem through the symplasm into the apoplasm (cell walls and intercellular spaces) with nectar formation by either granulocrine or eccrine secretion and its diffusion outwards. It is concluded, however, that no secretory granules are actually produced by the endoplasmic reticulum, and that secretory Golgi vesicles are not involved in the transport of nectar sugar. Therefore, the concept of granulocrine secretion of nectar should be discarded. The specific function of the endomembrane system in nectary cells remains unknown. According to the apoplasmic model, the pre-nectar moves from the terminal phloem in the apoplasm and, on the way, is transformed from phloem sap into nectar. However, viewed ultrastructurally, the unloading (terminal) phloem of nectaries appears to be less active than that of the leaf minor veins, and is therefore not actively involved in the secretion of pre-nectar components into the apoplasm. This invalidates the apoplasmic model. Neither model provides an explanation for the origin of the driving force for nectar discharge.

Proposal

A new model is proposed in which nectar moves by a pressure-driven mass flow in the nectary apoplasm while pre-nectar sugars diffuse from the sieve tubes through the symplasm to the secretory cells, where nectar is formed and sugars cross the plasma membrane by active transport (‘eccrine secretion’). The pressure originates as the result of water influx in the apoplasm from the symplasm along the sugar concentration gradient. It follows from this model that there can be no combinations of apoplasmic and symplasmic pre-nectar movements. The mass-flow mechanism of nectar exudation appears to be universal and applicable to all nectaries irrespective of their type, morphology and anatomy, presence or absence of modified stomata, and their own vascular system.     

Kinetics of Aluminum Uptake in Triticum aestivum L: Identity of the Linear Phase of Aluminum Uptake by Excised Roots of Aluminum-Tolerant and Aluminum-Sensitive Cultivars

The identity of a linear phase of aluminum (Al) uptake in Triticum aestivum was investigated by analysis of the kinetics of Al uptake by excised roots and purified cell wall fractions. Classical interpretation of kinetic data suggests that a linear phase of uptake with time reflects uptake across the plasma membrane; however, in studies with Al the possibility that the linear phase of uptake includes accumulation of Al in both the symplasm and the apoplasm has not been discounted. In our experiments, we observed a linear phase of Al uptake at both ambient and low temperatures, although the rate of uptake at 0°C was 53 to 72% less than at 23°C, depending on cultivars. This nonsaturable phase of uptake at low temperature suggests that a portion of the linear phase of Al uptake is nonmetabolic. Furthermore, analysis of Al in cell wall fractions isolated from excised roots pretreated with Al suggests that the linear phase of uptake includes a cell wall component. When excised roots were pretreated with Al, accumulation of Al in purified cell wall material included a linear phase that could not be desorbed with a 30 minute wash in citrate. The rates of linear-phase accumulation of Al by cell wall material and cell contents were similar. In contrast, the linear phase of in vitro uptake of Al by purified cell wall material was completely desorbed by a 30 minute wash with citrate. These results suggest that the linear phase of Al uptake observed in excised roots of T. aestivum included metabolism-dependent binding of Al in apoplasm.     

Molecular Biology of Sugar Transporters in Plants

Both lower and higher plants have been shown to possess efficient transport systems for the uptake of sugars across the plasmalemma. Genes encoding transport proteins for both mono- and disaccharides have been cloned recently. The main cloning strategies — differential screening, complementation cloning in Saccharomyces cerevisiae, and heterologous screening — are briefly summarized. The relationship of plant sugar transporters to a superfamily of more than 50 uni-, sym-, and antiporters cloned so far is discussed. Various possibilities for heterologous expression (in Schizosaccharomyces pombe, Saccharomyces cerevisiae, Xenopus oocytes) of plant sugar transporters are described and compared. Eight D-glucose transporters (from yeast to Arabidopsis to man) only possess 7% identical amino acids. First site-directed mutations of the Chlorella HUP1 transporter indicate that at least transmembrane helices 5, 7 and 11 line the D-glucose specific path through the membrane. The genomic structures of two plant transporters are outlined; the glycosylation of transport proteins as well as their tissue specificity is discussed.     

Whole Plant Studies using Radioactive 13-Nitrogen: I. TECHNIQUES FOR MEASURING THE UPTAKE AND TRANSPORT OF NITRATE AND AMMONIUM IONS INHYDROPONICALLY GROWN ZEA MAYS

Methods are described for studying the uptake, by hydroponicallygrown Zea mays seedlings, of ammonium and nitrate ions labelledwith radioactive nitrogen-13, which has a half-life often minutes.For nitrate only, some of the activity absorbed by the rootexchanges back out again into the root bathing solution. Theamount of this activity is about five times too large to beattributable to exchange with ions in the root cortical apoplasm.Much of it must be transferred from the root symplasm with ahalf-time of exchange of 2–5 min. After exposing the rootto the labelled solution, equilibrium rates of transport to,and distribution in the shoot were attained within 2 min, fornitrate, or 5 min, for ammonium. The pools within the root,and the transport pathway through which the label passes musttherefore rapidly attain the specific activity of the nutrientsolution. Distribution patterns through the plant are reasonablyconsistent with earlier work on nitrogen assimilation and transport. Key words: Zea mays, Nitrate uptake, Amonium uptake, ¹³N tracer     

超富集植物对重金属耐受和富集机制的研究进展

超富集植物对重金属耐受和富集机制的研究成为近年来植物逆境生理研究的热点,在简要总结细胞壁沉淀、重金属螯合效应、酶活性机制和细胞区室化作用的基础上,概述了超富集植物对重金属的耐受机制,讨论了重金属跨根细胞质膜运输,共质体内运输、木质部运输和跨叶细胞膜运输的富集过程。     

Uptake of Phosphate by White Clover: II. THE EFFECT OF PH ON THE ELECTROGENIC PHOSPHATE PUMP

The effect of pH on the electrogenic phosphate pump in whiteclover roots was investigated. It was found that the pump operatedbetween pH 3.5 and 8.0 with an optimum at 4.3. External pH changesaffected phosphate uptake and PD to the same extent so thata constant relationship between them was maintained. The activityof the pump declined when the carbohydrate supply was cut offby excision of the root or defoliation of the plant but couldbe restored by lowering the pH around the root. It was concludedthat the electrogenic phosphate pump could be driven by a pHgradient across the cell membrane. However, there did not appearto be a direct relationship between the operation of the pumpand extrusion of H⁺ by the root.     

Potassium and Phosphate Uptake in Corn Roots: Further Evidence for an Electrogenic H/K Exchanger and an OH/Pi Antiporter

Evidence is presented that K⁺ uptake in corn root segments is coupled to an electrogenic H⁺/K⁺ -exchanging plasmalemma ATPase while phosphate uptake is coupled to an OH⁻/Pi antiporter. The plasmalemma ATPase inhibitor, diethylstilbestrol, or the stimulator, fusicoccin, altered K⁺ uptake directly and phosphate uptake indirectly. On the other hand, mersalyl, an OH⁻/Pi antiporter inhibitor, inhibited phosphate uptake instantly but only slightly affected K⁺ uptake. Collapse of the proton gradient across the membrane by (p-trifluoromethoxy) carbonyl cyanide phenylhydrazone resulted in immediate inhibition of K⁺ uptake but only later inhibited phosphate uptake. Changing the pH of the absorption solution had opposite effects on K⁺ and phosphate uptake. In addition, a 4-hour washing of corn root tissue induced a 5-fold increase in the rate of K⁺ uptake with little or no lag, but only a 2- to 3-fold increase in phosphate uptake with a 30- to 45-minute lag. Collectively these differences strongly support the coupling of an electrogenic H⁺/K⁺ -exchanging ATPase to an OH⁻/Pi antiporter in corn root tissue.     

Plant Cell Growth in Tissue

Cell walls are part of the apoplasm pathway that transports water, solutes, and nutrients to cells within plant tissue. Pressures within the apoplasm (cell walls and xylem) are often different from atmospheric pressure during expansive growth of plant cells in tissue. The previously established Augmented Growth Equations are modified to evaluate the turgor pressure, water uptake, and expansive growth of plant cells in tissue when pressures within the apoplasm are lower and higher than atmospheric pressure. Analyses indicate that a step-down and step-up in pressure within the apoplasm will cause an exponential decrease and increase in turgor pressure, respectively, and the rates of water uptake and expansive growth each undergo a rapid decrease and increase, respectively, followed by an exponential return to their initial magnitude. Other analyses indicate that pressure within the apoplasm decreases exponentially to a lower value after a step-down in turgor pressure, which simulates its behavior after an increase in expansive growth rate. Also, analyses indicate that the turgor pressure decays exponentially to a constant value that is the sum of the critical turgor pressure and pressure within the apoplasm during stress relaxation experiments in which pressures within the apoplasm are not atmospheric pressure. Additional analyses indicate that when the turgor pressure is constant (clamped), a decrease in pressure within the apoplasm elicits an increase in elastic expansion followed by an increase in irreversible expansion rate. Some analytical results are supported by prior experimental research, and other analytical results can be verified with existing experimental methods.Cell walls perform many functions for plant, algal, and fungal cells. Physical and chemical protection from the environment and physical support for cells and organs are obvious functions. Cell walls also withstand the stresses imposed by turgor pressure and deform irreversibly and reversible (elastically) during expansive growth. Irreversible wall deformations during expansive growth control cell enlargement, size, and shape. Growing and mature (nongrowing) cell walls undergo elastic deformations after changes in turgor pressure caused by changes in water status and environmental conditions. Elastic wall deformations are fundamental to the water relations of plant, algal, and fungal cells. For plant cells in tissues and organs, cell walls are part of the apoplasm pathway that transports water, solutes, and nutrients to cells.Importantly, pressures within the apoplasm (cell walls and xylem) are frequently different from atmospheric pressure during expansive growth of plant cells in tissues and organs. Lower pressures (tensions) are related to transpiration rates from plant organs and to expansive growth of cells in plant organs, e.g. Boyer (1967, 2001), Molz and Boyer (1978), Nonami and Boyer (1987, 1993), Nonami and Hashimoto (1996), Passioura and Boyer (2003), Boyer and Silk (2004), Koch et al. (2004), Wiegers et al. (2009), and the references within. Higher pressures (root pressures) occur during the spring when the soil is well hydrated (e.g. Kramer, 1932). Bleeding sap from cuts and broken stems is evidence of root pressure. Also, higher pressures may occur diurnally, during the night when transpiration rates are low (e.g. Tang and Boyer, 2008). Guttation drops on leaves in the morning are evidence of these higher pressures.Prior research indicates that a significant amount of chemistry and molecular biology occur within cell walls undergoing irreversible deformation during expansive growth (e.g. Cosgrove, 2005; Boyer, 2009). Two questions arise. First, how do pressures within the wall that are different from atmospheric pressure affect the turgor pressure, water uptake, and growth rate of cells in plant organs such as roots, stems, and leaves? Second, how are relevant chemical reactions affected by lower and higher pressures within the wall? The analyses conducted in this article focus on the first question.Previously, equations derived by Lockhart (1965) for wall deformation and water uptake (Growth Equations) were augmented with terms for elastic wall deformation (Ortega, 1985) and transpiration (Ortega et al., 1988). In this article, the previously established Augmented Growth Equations (Ortega, 1985, 1990, 1994, 2004; Ortega et al., 1988; Geitmann and Ortega, 2009) are modified to evaluate the turgor pressure, water uptake, and expansive growth of plant cells in tissue when pressures within the apoplasm are lower and higher than atmospheric pressure. In addition, the pressure within the apoplasm is evaluated after turgor pressure in cells decrease, thus simulating the condition produced by an increase in expansive growth rate of cells in plant tissues and organs. Also, the modified equations are used to determine how the results of stress relaxation experiments conducted on growing plant organs are affected by pressures within the apoplasm that are not atmospheric pressure. Last, the expansive growth of a plant cell is evaluated when pressure within the apoplasm undergoes a semi-instantaneous change while the turgor pressure remains constant, i.e. clamped. Some analytical results are supported by prior experimental research, and some analytical results can be verified with existing experimental methods.     

A phosphate transporter from Medicago truncatula involved in the acquisition of phosphate released by arbuscular mycorrhizal fungi

Many plants have the capacity to obtain phosphate via a symbiotic association with arbuscular mycorrhizal (AM) fungi. In AM associations, the fungi release phosphate from differentiated hyphae called arbuscules, that develop within the cortical cells, and the plant transports the phosphate across a symbiotic membrane, called the periarbuscular membrane, into the cortical cell. In Medicago truncatula, a model legume used widely for studies of root symbioses, it is apparent that the phosphate transporters known to operate at the root-soil interface do not participate in symbiotic phosphate transport. EST database searches with short sequence motifs shared by known phosphate transporters enabled the identification of a novel phosphate transporter from M. truncatula, MtPT4. MtPT4 is significantly different from the plant root phosphate transporters cloned to date. Complementation of yeast phosphate transport mutants indicated that MtPT4 functions as a phosphate transporter, and estimates of the K(m) suggest a relatively low affinity for phosphate. MtPT4 is expressed only in mycorrhizal roots, and the MtPT4 promoter directs expression exclusively in cells containing arbuscules. MtPT4 is located in the membrane fraction of mycorrhizal roots, and immunolocalization revealed that MtPT4 colocalizes with the arbuscules, consistent with a location on the periarbuscular membrane. The transport properties and spatial expression patterns of MtPT4 are consistent with a role in the acquisition of phosphate released by the fungus in the AM symbiosis.     

锰对植物毒害及植物耐锰机理研究进展

含锰矿渣的排放造成了严重的土壤锰污染。揭示锰毒害和植物的耐锰机制对于污染土壤治理具有重要意义。研究表明,高浓度的Mn2＋能够抑制根系Ca2＋、Fe2＋和Mg2＋等元素的吸收及活性,引起氧化性胁迫导致氧化损伤,使叶绿素和Rubisco含量下降、叶绿体超微结构破坏和光合速率降低。而锰超累积植物则具有多种解毒或耐性机制,如区域化、有机酸螯合、外排作用、抗氧化作用和离子交互作用等。根系主要通过有机酸的螯合作用促进植物对Mn^2＋的转运解毒,同时能够将过量的Mn^2＋区域化在根细胞壁中;叶片可通过酚类物质或有机酸螯合Mn^2＋,并将其区域化在叶片表皮细胞和叶肉细胞的液泡中（或通过表皮毛将Mn^2＋排出体外）。其中,金属转运蛋白在植物对Mn^2＋的吸收、转运、累积和解毒过程中发挥着重要作用。     

Focus Issue on Roots: Plant Nutrition: Root Transporters on the Move

Nutrient and water uptake from the soil is essential for plant growth and development. In the root, absorption and radial transport of nutrients and water toward the vascular tissues is achieved by a battery of specialized transporters and channels. Modulating the amount and the localization of these membrane transport proteins appears as a way to drive their activity and is essential to maintain nutrient homeostasis in plants. This control first involves the delivery of newly synthesized proteins to the plasma membrane by establishing check points along the secretory pathway, especially during the export from the endoplasmic reticulum. Plasma membrane-localized transport proteins are internalized through endocytosis followed by recycling to the cell surface or targeting to the vacuole for degradation, hence constituting another layer of control. These intricate mechanisms are often regulated by nutrient availability, stresses, and endogenous cues, allowing plants to rapidly adjust to their environment and adapt their development.Plants take up nutrients and water from the soil and transport them to the leaves to support photosynthesis and plant growth. However, most soils around the world do not provide optimal conditions for plant colonization. Consequently, plants have evolved sophisticated mechanisms to adjust to deficiency or excess of nutrients and water supply. Membrane transport proteins, including channels and transporters, play crucial roles in the uptake of nutrients and water from the soil and in their radial transport to the root vasculature. Newly synthesized membrane transport proteins have to be properly targeted to a defined compartment, usually the plasma membrane, to efficiently ensure their function. The trafficking of membrane transport proteins along the secretory pathway is tightly controlled and involves the recognition of exit signals by gatekeeper protein complexes. After reaching the plasma membrane, membrane transport proteins can be endocytosed and subsequently recycled to the cell surface or targeted to the vacuole for degradation. Because the subcellular localization of proteins directly influences their activity, modulating the localization of membrane transport proteins constitutes a powerful way to control nutrient and water uptake in plants. This review discusses the fundamental mechanisms at stake in membrane protein secretion and endocytosis, with a specific focus on membrane transport proteins, and how endogenous and exogenous cues affect their dynamics to integrate uptake of nutrients and water to plant growth conditions.     

Water transport through plant tissue: the apoplasm and symplasm pathways

A detailed quantitative analysis of water flow through the apoplasm and symplasm of plant tissue is presented. The analysis results in two coupled diffusion equations which describe water transport in the two pathways. Various parameters entering the analysis identify the physical properties of the tissue which control the transport process as the resistance to water flow per cell in the two parallel pathways, the resistance per cell between pathways, and the water capacity per cell in the two pathways. Values for the several resistances and water capacities are estimated from available data, and a model problem is solved wherein a sheet of tissue at an initial water potential of — δ bars is immersed in a container of water. The resulting solutions show that depending on the values assigned to the controlling parameters, local water potential equilibrium between each cell and its cell wall may or may not obtain. In the special case of local equilibrium (water potential in the symplasm and apoplasm pathways essentially equal), the transport process can be described by a single diffusion equation which is derived along with an expression for the tissue diffusivity. It is concluded that the weakest link in the analysis is the estimated value for the permeability of the plasmodesma membrane, and that a logical extension of the theory would be to include the effects of a diffusable solute.     

植物磷营养高效的分子生物学研究进展

挖掘利用植物自身的磷高效营养遗传资源是农业可持续发展的关键。磷高效营养性状涉及根形态、根分泌物、膜与体内磷转运以及菌根等许多方面,表现为数量遗传性状及受多基因控制。近年来,许多高亲和磷转运子基因已被克隆, 磷向地上部转运和磷吸收负反馈调节的控制基因也被发现, 对于根系分泌有机酸和酸性磷酸酶的基因的控制也有了一定的了解, 但目前对于根毛、排根、根构型以及菌根的营养学意义性状的分子生物学研究进展缓慢。