Strontium Transport,Distribution, and Toxic Effects on Maize Seedling Growth

Two-day-old seedlings of maize (Zea mays L.) were incubated on 3 mM and 35 M solutions of Sr(NO₃)₂, and the toxic effects of strontium were assessed by measuring, in the course of four days of incubation, the daily increments of the primary root length and also the root and shoot length by day 7 of incubation, and the length of the fully elongated cells. Sodium rhodizonate, a reagent developing the colored complex with Sr, was used to follow Sr distribution in maize tissues and organs following 2, 24, 48, and 168 h of incubation. Sr was found in all root tissues as soon as after 24 h of incubation; it accumulated mostly in the cell apoplast, whereas its content in the protoplasts was considerably lower. Strontium readily crossed the endodermal barrier via the symplast and was immobilized predominantly in the pericycle cell walls; therefore, it did not hamper root branching. Strontium did not affect the final cell length and hindered root growth (at the concentration of 3 mM) by inhibiting cell division. In the shoots, Sr was found in the xylem cell walls in the vascular bundles of coleoptile, mesocotyl, and leaves on the second day of incubation, an evidence for high Sr mobility. We conclude that the transport of Sr differs from the transport of such heavy metals, as Cd, Pb, and Ni, and is similar in many aspects to the distribution of calcium, another alkaline earth metal, probably due to similar physical and chemical properties of their ions.     

Effects of heavy metals and strontium on division of root cap cells and meristem structural organization

In order to define relations between the behavior of quiescent center cells and the condition of root cap cells, effects of various metal salts on the root meristem structure, root growth, and division of root cap cells were investigated. Two-day-old maize (Zea mays L., cv. Diamant) seedlings were incubated on solutions containing 35 μM Ni(NO₃)₂), 10 μM Pb(NO₃)₂, or 3 mM Sr(NO₃)₂ in the absence or in the presence of 3 mM Ca(NO₃)₂. Toxic effects of metals were assessed from inhibition of the primary root length increment following 24-h and 48-h incubations as compared to the roots grown on water or on 3 mM Ca(NO₃)₂ solution. Metal localization in the root apex tissues following 24-h and 48-h incubations was determined using histochemical techniques. Cell lengths in three upper layers of root cap columella were determined, and the mitotic index in these cells was calculated. In the absence of Ca(NO₃)₂, the metals were found both in the meristem and in the root cap. Pb and Sr were revealed primarily in the cell walls, and Ni, in the cell protoplasts. In the presence of Ca(NO₃)₂, metal content in all root tissues was decreased, and their toxic effect on root growth was ameliorated. Pb and Ni inhibited cell division in the root cap. Pb caused an increase in the root cap cell length as early as following 24-h incubation, and Ni, only following 48-h incubation. Pb activated division of quiescent center cells in the direction of root cap. These effects, as well as possible involvement of dermatogen and cortex cells, resulted in a regrowth of a new root cap already after a 24-h incubation period. In this case, the meristem was transformed from a closed structure into the open one. Following 48-h incubation, Ni brought about only few divisions of quiescent center cells in the direction of root cap. It was suggested that inhibition of divisions of the root cap upper layer cells and a decrease in the sloughing off its cells can stimulate the quiescent center cell divisions. A similarity of the quiescent center and animal stem cells is discussed.     

Distribution and Toxic Effects of Cadmium and Lead on Maize Roots

Two-day-old seedlings of maize (Zea mays L.) were incubated on Cd and Pb nitrate solutions at the concentrations that inhibited root growth approximately by 50% after two-day-long incubation (LC₅₀; 10^–4 and 10^–3 M, respectively) or completely terminated growth of the primary root after one-day-long incubation (LC; 5 × 10^–4 and 10^–2 M, respectively). Cd and Pb contents were measured using an anodic inversion voltammetric technique in a flow injection system and a histochemical method. At LC₅₀, Cd and Pb were discerned, by histochemical techniques, in all root apical tissues, whereas in the root hair zone, the heavy metals were primarily accumulated in the apoplast of the rhizodermis and cortex and to a lesser extent, in the vascular tissues and parenchyma cells surrounding the metaxylem vessels. Insignificant accumulation of Cd and Pb in the pericycle probably explains why root branching was tolerant to these agents. At LC, Cd and Pb were found in the apoplast of all root tissues, in accordance with the practically complete inhibition of root growth and branching. Irrespectively of Cd and Pb concentrations in the external solution, the metal contents in the root apex exceeded those in the basal region. Procion dyes were used to assess cell death inflicted by Cd and Pb. At LC, the root cap and meristematic cells perished, together with the rhizodermal cells and the outer cortical cells of the root apex, whereas only the rhizodermal cells in the root apical region died at LC₅₀. The evidence that Cd and Pb cross the endodermal barrier at LC presumes that, at lower metal concentrations, the Casparian strip and plasmalemma of the endodermis regulate the transport of these metals into the central cylinder. The authors conclude that the identical barriers control Cd and Pb transport in root tissues.     

Enhancement of nickel and lead accumulation and their toxic growth-inhibitory effects on amaranth seedlings in the presence of calcium

The effects of Ni(NO₃)₂ and Pb(NO₃)₂ on Amaranthus sp. L. root growth and the effect of calcium on heavy metal (HM) accumulation in the growing root zone and root growth inhibition were studied. The seeds were germinated in the Pb(NO₃)₂ solutions at concentrations of 50, 100, 200, 500 and 700 μM or Ni(NO₃)₂ solutions at concentrations of 10, 50, 70, 100, and 500 μM in the presence of 100 μM Ca(NO₃)₂ or without it. HM toxicity was assesses in 7 days after seed sowing by the root length. Distribution of HM over the tissues of the growing root part was examined histochemically. Ni was more toxic to root growth than Pb. In the presence of Ca, Ni and Pb accumulation in the amaranth root growing part increased markedly, and this enhanced their growth-inhibitory of action. A comparison of results obtained in this work and available from the literature permitted a conclusion that the routes of HM penetration into the root differ in different plant species, and this determines ambiguity of protective Ca action.     

The effects of lead,nickel, and strontium nitrates on cell division and elongation in maize roots

The effects of Pb, Sr, and Ni nitrates on the root growth, its cell division and elongation were studied. Two-day-old maize seedlings were incubated on the 35 μM Ni(NO₃)₂, 10 μM Pb(NO₃)₂, or 3 mM Sr(NO₃)₂ in the presence or absence of 3 mM Ca(NO₃)₂. Metal toxicity was evaluated after the inhibition of root growth for the first and second days of incubation in comparison with the roots kept on water or Ca(NO₃)₂ solution. The contents of metals were determined in the apical (the first centimeter from the tip) and basal (the third centimeter from the kernel) root parts by voltamperometry and atomic-absorption spectrophotometry. We measured the length of the meristem, the length of the fully elongated cells, counted the mitotic index (MI) in the meristem and the number of meristematic cells in the cortex row; we also calculated duration the cell cycle. In the absence of Ca(NO₃)₂, the metal content in the apical root region was higher than in basal one. In the presence of Ca(NO₃)₂, we observed reverse ratio most pronounced in the case of Pb and Sr. All metals tested markedly reduced MI in the cortex, which was determined by the increase in the cell cycle duration and accompanied by the meristem shortening. These metals affected differently cell division and elongation: Ni inhibited mainly cell division and to a lesser degree their elongation, whereas Sr and Pb affected both cell division and elongation; only Sr treatment resulted in the increased length of the fully elongated cells. In the presence of Ca, all studied growth indices changed less than in the absence of Ca, which was manifested in the less severe suppression of the root growth and was in agreement with the lower accumulation of the metals in the root tips. Possible causes for the heavy metal action on growth are discussed in connection with the specificity of their transport and accumulation.     

Cotton root and shoot response to localized supply of nitrate,phosphate and potassium: Split-pot studies with nutrient solution and vermiculitic soil

Vertical stratification of plant-available K in vermiculitic soil profiles contributes to a late-season K deficiency that limits cotton (Gossypium hirsutum L.) yields on affected soils. Split-root solution culture and split-pot soil experiments were conducted to determine whether root distribution and cultivar differences in root extension in these stratified profiles result from a compensatory response to localized enrichment with NO₃-N, PO₄-P, and/or K in the root zone. Compensatory root growth was greatest in response to localized NO₃-N enrichment. For two cultivars examined in solution culture, 74% of new root development occurred in the half-pot providing 90% of the total NO₃-N supply. Only 60% of cultivar root development occurred in the half-pot providing 90% of the PO₄-P. No compensatory root growth was observed in response to localized K enrichment. In the split-pot system, the proportion of total root surface area developing in a half-pot was highly correlated with localized soil NO₃-N levels (r²=0.81), while increased K availability in one half of the root zone did not affect root distribution. Mean soil NO₃-N supply to the whole root system determined shoot N accumulation (r²=0.97). Shoot K accumulation was not related to soil K availability but was strongly correlated with mean root surface area density (r²=0.86). Cultivar Acala GC510, known to be less sensitive to K deficiency than Acala SJ-2, had significantly larger root diameter in all nutrient-supply environments. Under conditions of K stress, Acala GC510 had increased root branching and allocated greater dry matter to roots relative to shoots than Acala SJ-2. The results demonstrate that K acquisition by cotton is strongly influenced by the quantity and distribution of NO₃-N in the root zone through its effects on root proliferation, and that distinct cultivar differences associated with crop performance on low K soils can be detected in short-term, solution culture growth systems.     

A comparative study between two citrus rootstocks: Effect of nitrate on the root morpho-topology and net nitrate uptake

Root morpho-topology and net nitrate uptake of two citrus seedlings, Volkamer Lemon and Carrizo Citrange, grown at two nitrogen supplies (NO₃-N 5 M and 1000 M, respectively) were studied. Root morphological and topological parameters were gauged by an image-specific analysis system (WinRHIZO). Net nitrate uptake was estimated using the nitrate depletion method. The main findings showed that Carrizo seedlings had a dichotomous branching root system characterized by high root tip numbers and long 2^nd order lateral roots. Conversely, Volkamer root systems had a herringbone structure with a long tap root and 1^st order lateral root. Nitrate treatment did not seem to affect the pattern of the two genotypes, except for the 2^nd order lateral roots (Carrizo more than Volkamer) and root/shoot ratio and root mass ratio (Volkamer more than Carrizo) that were significantly different at low nitrate supply. Nitrate treatments induced a diverse net nitrate uptake regulation between citrus rootstocks. Indeed, at low nitrate supply, Carrizo showed a more efficient nitrate acquisition process in terms of: 1) higher net nitrate uptake maximum of the inducible high affinity transport system or full induction (A), (2) higher cumulative nitrate uptake (A_t) and (3) lower t₁ parameter defined as the half time of the net nitrate uptake rate of the inducible transport system during the induction phase, compared to Volkamer. Conversely, at the high nitrate level, only the genotypical difference of the t₁ parameter was maintained. The results suggested that, at the low nitrate level, the morphological root traits such as higher 2^nd order lateral roots and greater root tip numbers of the Carrizo compared with Volkamer seedlings, enhance the capacity to absorb nitrate from nutrient solution.     

Resistance of Surface Phosphohydrolases of Barley Root Cells to Nickel Salts Is One of Factors of Plant Adaptation to Excessive Nickel in the Environment

We studied the effect of nickel ions on the activity of ecto-phosphohydrolases (acid phosphatase and Ca-stimulated nucleotidase) from root surface of etiolated barley seedlings as well as from root microsomal fraction. The presence of nickel nitrate (25 M) proved to stop root growth and insignificantly (on average by 20%) decreased specific hydrolytic activity of both enzymes determined on root surface as well as in the root microsomal fraction. At the same time, direct addition of nickel to the incubation mixture when measuring the substrate hydrolysis demonstrated high resistance of the microsomal fraction enzymes to the salts. A significant decrease in Ca-stimulated nucleotidase activity was observed only for nickel nitrate concentrations above 100 M, reaching 50–60% for 3 mM Ni(NO₃)₂. The presence of an activator ion as well as extended duration of the microsomal fraction pretreatment with nickel nitrate (2.5 h) did not increase its effect on the enzyme activity. The pattern of nickel effect on acid phosphatase activity depended on the presence of magnesium ions in the mixture but did not change after extended duration of the microsomal fraction pretreatment (3 h). Inhibition of acid phosphatase activity in the presence of magnesium was observed only for nickel nitrate concentrations above 500 M being no more than 20% for 3 mM Ni(NO₃)₂. Hence, the hydrolytic enzymes of the apoplast of plant root cells have different tolerance to nickel salts. We propose that an insignificant decrease in specific activity of surface hydrolases of plant roots grown on a medium containing nickel salts in concentrations inhibiting growth processes (25 M) is not related to direct effect of Ni on the apoplastic enzymes. The significance of hydrolytic enzyme resistance in plant adaptation to high nickel content in the soil is discussed.     

Comparative Impacts of Heavy Metals on Root Growth as Related to Their Specificity and Selectivity

Two-day-old maize (Zea mays L.) seedlings were incubated on the solutions of Ag, Cd, Pb, Zn, Cu, Tl, Co, and Hg salts (0.001 to 3 g/l). Toxicity of heavy metals was assessed as the inhibition of root growth on the first, second, and third days, the change in the length of the lateral root zone, and the duration of lateral root development from the first division in pericycle to emergence. For all salts under study, the ratio of the lethal concentration to the lowest concentration slowing down root growth was about ten, and growth inhibition was not almost enhanced in the course of three days. With concentrations calculated as g/l, metal toxicity declined in the following order: Cu Tl > Ag > Cd > Hg > Co > Zn > Pb; for molar concentrations, the order was the following: Tl³⁺ > Cu²⁺ > > Ag⁺ > Hg²⁺ Cd²⁺ > Zn²⁺ Pb²⁺ Co²⁺. Duration of lateral root development was least affected by heavy metals. Metal affinity of biological compounds for SH-groups was closely correlated (r = 0.9) with the molar concentration that inhibited primary root growth by 50%. Because of the narrow range of effective concentrations, only slightly increasing inhibition over the exposure time, tolerant root branching, and close relationship between the toxicity and the constant of binding to SH-groups, we conclude that the salts under study exert nonselective inhibition and root growth is slowed down due to the general toxicity of heavy metals rather than selective inhibition of any particular process or processes.     

Effects of anaerobic conditions on water and solute relations,and on active transport in roots of maize (Zea mays L.)

The effects of anoxia on water and solute transport across excised roots of young maize plants (Zea mays L. cv. Tanker) grown hydroponically have been studied. With the aid of the root pressure probe, root pressure (P_r), root hydraulic conductivity (Lp_r), and root permeability (P_sr), and reflection ( _sr) coefficients were measured using potassium nitrate (a typical nutrient salt) and sodium nitrate (an atypical nutrient salt) as solutes. During a period of 10–15 h, anaerobic treatment (0.0–0.2 g O₂·m^-3 in root medium) caused a decrease of root pressure by 0.01–0.28 MPa (by 10–80% of original root pressure) after a short transient increase. For a time period of 5 h, the decrease in the stationary root pressure was not reversible. Under anaerobic conditions, roots still behaved like osmometers and were not leaky. The root hydraulic conductivity measured in osmotic experiments (osmotic solute: NaNO₃) was smaller by one to two orders of magnitude than that measured in the presence of hydrostatic gradients. Both the osmotic and hydrostatic hydraulic conductivity decreased during anaerobic treatment by 28 and 44%, respectively, at a constant reflection coefficient of the solutes ( _sr=0.3–1.0). As with root pressure, changes in root permeability to water and solutes were not reversible within 5 h. Under aerobic conditions and at low external concentrations (31–59 mOsmol·kg^-1), osmotic response curves were monophasic for KNO₃, i.e. there was no passive uptake of solutes. Response curves became biphasic at higher concentrations (100–150 mOsmol·kg^-1)- For NaNO₃, response curves were biphasic at all concentrations. Presumably, this pattern was a consequence of the fact that potassium had already accumulated in the xylem. During anoxia, accumulation of potassium in the xylem was reduced, and biphasic responses were also obtained at lower potassium concentrations applied to the medium. The results are discussed in terms of a pump/leak model of the root in which anoxia affects both the active ion pumping and the permeability of the root to nutrient salts (leakage). The effects of anaerobiosis on the passive transport properties of the root (Lp_r, P_sr, _sr) are in line with the recently proposed composite transport model of the root.Abbreviations and Symbols A_r root surface area - Lp_r root hydraulic conductivity - Lp_rh hydrostatic hydraulic conductivity of root - Lp_ro osmotic hydraulic conductivity of root - P_r root pressure - P_sr permeability coefficient of root - _sr reflection coefficient of root The authors thank Mr. Walter Melchior for the curve-fitting program used to work out Lp_rh values from root pressure relaxations and Mr. Mohammad Hajirezai (Lehrstuhl für Pflanzenphysiologie, Universität Bayreuth) for making the ATP measurements. The assistance of Mrs. Libuse Badewitz in making the drawings and the technical help of Mr. Burkhard Stumpf are also gratefully acknowledged.     

Ethylene–auxin interactions regulate lateral root initiation and emergence in Arabidopsis thaliana

Plant root systems display considerable plasticity in response to endogenous and environmental signals. Auxin stimulates pericycle cells within elongating primary roots to enter de novo organogenesis, leading to the establishment of new lateral root meristems. Crosstalk between auxin and ethylene in root elongation has been demonstrated, but interactions between these hormones in root branching are not well characterized. We find that enhanced ethylene synthesis, resulting from the application of low concentrations of the ethylene precursor 1-aminocyclopropane-1-carboxylic acid (ACC), promotes the initiation of lateral root primordia. Treatment with higher doses of ACC strongly inhibits the ability of pericycle cells to initiate new lateral root primordia, but promotes the emergence of existing lateral root primordia: behaviour that is also seen in the eto1 mutation. These effects are correlated with decreased pericycle cell length and increased lateral root primordia cell width. When auxin is applied simultaneously with ACC, ACC is unable to prevent the auxin stimulation of lateral root formation in the root tissues formed prior to ACC exposure. However, in root tissues formed after transfer to ACC, in which elongation is reduced, auxin does not rescue the ethylene inhibition of primordia initiation, but instead increases it by several fold. Mutations that block auxin responses, slr1 and arf7 arf19, render initiation of lateral root primordia insensitive to the promoting effect of low ethylene levels, and mutations that inhibit ethylene-stimulated auxin biosynthesis, wei2 and wei7 , reduce the inhibitory effect of higher ethylene levels, consistent with ethylene regulating root branching through interactions with auxin.     

Lateral Root Initiation or the Birth of a New Meristem

Root branching happens through the formation of new meristems out of a limited number of pericycle cells inside the parent root. As opposed to shoot branching, the study of lateral root formation has been complicated due to its internal nature, and a lot of questions remain unanswered. However, due to the availability of new molecular tools and more complete genomic data in the model species Arabidopsis, the probability to find new and crucial elements in the lateral root formation pathway has increased. Increasingly more data are supporting the idea that lateral root founder cells become specified in young root parts before differentiation is accomplished. Next, pericycle founder cells undergo anticlinal asymmetric, divisions followed by an organized cell division pattern resulting in the formation of a new organ. The whole process of cell cycle progression and stimulation of the molecular pathway towards lateral root initiation is triggered by the plant hormone auxin. In this review, we aim to give an overview on the developmental events taking place from the very early specification of founder cells in the pericycle until the first anticlinal divisions by combining the knowledge originating from classical physiology studies with new insights from genetic-molecular analyses. Based on the current knowledge derived from recent genetic and developmental studies, we propose here a hypothetical model for LRI.     

Hydraulic conductivities of competing root systems of Grevillea robustaand maize in agroforestry

Models of water uptake in mixed stands of vegetation commonly assume that water is partitioned among competing root systems in proportion to relative root length densities. Such an approach assumes implicitly that roots of different species have equivalent hydraulic properties. This was tested for root systems of Grevillea robustaA. Cunn. and maize (Zea maysL.) at a semi-arid site in Kenya. The hydraulic conductances for roots of both species were measured in situat the scale of the whole root or root system using a high pressure flow meter (HPFM). Hydraulic conductivities (_r) were expressed per unit root length. Root lengths were estimated for maize plants by soil coring and for G. robustausing a fractal branching model calibrated against soil coring. Mean _r was 1.88×10^–7 ±0.28×10^–7kg s^–1 MPa^–1 m^–1 for G. robustaand 1.25×10^–7 ±0.13×10^–7kg s^–1 MPa^–1 m^–1 for maize. Values of _r were not significantly different (P<0.05), suggesting that the assumption of hydraulic equivalence for root systems of the two species may be valid, at least when hydrostatic gradients are the major driving force for water uptake. Differences in conductivities between these species could arise, however, because of variation in the hydraulic properties of roots not accounted for here, for example because of root age, phenology or responses to the soil environment.     

Resumption of DNA Synthesis and Cell Division in Wheat Roots as Related to Lateral Root Initiation

The arrest of DNA synthesis and termination of cell division in basal meristematic cells as well as the resumption of these processes as related to the initiation of lateral root primordia (LRP) were studied in tissues of Triticum aestivumroots incubated with ³H-thymidine. All cells of the stelar parenchyma and cortex as well as most endodermal and pericycle cells left the mitotic cycle and ceased proliferative activity at the basal end of the meristem and at the beginning of the elongation zone. Some endodermal and pericycle cells started DNA synthesis in the basal part of the meristem and completed it later on during their elongation, but they did not divide. In the cells of these tissues, DNA synthesis resumed above the elongation zone, the cells being located much closer to the root tip than the first newly dividing cells. Thus, the initiation of LRP started much closer to the root tip than it was previously believed judging from the distance of the first dividing pericycle cells from the root tip. DNA synthesizing and dividing cells first appeared in the stelar parenchyma, then, in the pericycle, and later, in the endodermis and cortex. It seems likely that a release from the inhibition of DNA synthesis allows the cells that completed mitotic cycle in the basal part of meristem in the G₁phase to cease the proliferative arrest above the elongation zone and to continue their cycling. The location of the first DNA synthesizing and dividing cells in the stelar parenchyma and pericycle did not strictly correspond to the LRP initiation sites and proximity to the xylem or phloem poles. This indicates that LRP initiation results from the resumption of DNA synthesis in all pericycle and stelar parenchyma cells that retained the ability to synthesize DNA and occurs only in the pericycle sector situated between the two tracheal protoxylem strands, all cells of which terminated their mitotic cycles in the G₁phase.     

Histological analysis of adventitious rooting in Arabidopsis thaliana (L.) Heynh seedlings

ABSTRACT

Adventititous rooting is essential for the post-embryonic growth of the root apparatus in various species. In Arabidopsis thaliana, adventitious rooting has been reported in some mutants, and auxin seems to be the inducer of the process. The objective of the study was to identify the tissues involved in adventitious rooting in the most commonly used ecotypes for molecular and genetic studies (i.e. Columbia, Wassilewskija and Landsberg erecta) both in the presence and absence of exogenous auxin. Seedlings of the three ecotypes were grown under various conditions. When grown under 16 hours light/day for 11 days, all seedlings showed adventitious roots, both with and without auxin, however, both adventitious and lateral rooting were enhanced by exogenous auxin (2 µM naphthaleneacetic acid). Independently of the presence of auxin and of the ecotype, the hypocotyl pericycle produced adventitious roots directly (i.e., according to the same pattern of lateral root formation by the pericycle cells in the primary root). However, in the presence of auxin, roots of indirect origin also, and mainly, formed and their formation was preceded by the exfoliation of the tissues external to the stele. Exfoliation was caused by cell hypertrophy, separation, and disintegration, which mainly involved the endodermis. At the exfoliation site, the pericycle, with a minor contribution of a few endodermal cells, produced the callus from which indirect roots arose. The finding that adventitious rooting occurs in the absence of auxin (all ecotypes) indicates that this process is part of the normal root apparatus in Arabidopsis, with the hypocotyl pericycle as the target tissue of the process. Exogenous auxin alters adventitious rhizogenesis mainly affecting the endodermis response.     

The ultrastructural development of mechanically impeded barley roots. Effects on the endodermis and pericycle

Summary When barley roots,Hordeum vulgare cv Proctor, are grown under a small degree of applied mechanical constraint-2 × 10⁴ Pa-changes in both the endodermis and the underlying pericycle cells are apparent amongst other divergences from the normal patterns of root growth.The appearance of secondary features in both of these tissues has been found to occur much earlier in the overall development of the root. The proportion of the total number of endodermal cells which are suberized is much higher in impeded roots. This corresponds with a smaller proportion of State I loading area presented to the stele for transfer of solutes from the cortex.The orientation of certain divisions in the endodermal cells of impeded roots is not always found to be transverse. Such divisions give rise to units other than the characteristically cuboid-shaped cells of the layer. Tangential divisions in the protoxylem pole mother cells are demonstrated to result in the deposition of xylem parenchyma between endodermis and protoxylem pole cells thus giving rise to an occasionally biseriate pericycle.     

Proteins reacting with cadherin and catenin antibodies are present in maize showing tissue-, domain-, and development-specific associations with endoplasmic-reticulum membranes and actin microfilaments in root cells

Summary With heterologous antibodies raised against animal N-cadherin, -catenin, and -catenin, we have visualized their reactive proteins within cells of maize root apices. Embedding using Steedman's wax allowed us to accomplish tissue-specific analysis which revealed that cells of epidermis, endodermis/pericycle, and outer stele tissues, all of which are tightly associated to each other, are especially enriched with presumed plant homologues of N-cadherin and both catenins. In the root epidermis, trichoblasts initiating root hairs showed prominent accumulations of cadherin-like antigens at outgrowing domains where they co-localize with actin. Close associations of cadherin-like proteins with F-actin were detected in parenchymatic cells of the stele, also at the immunogold electron microscopy level. A possible role of these interesting proteins in membrane-membrane interactions is indicated by their prominent accumulations at endoplasmic-reticulum-enriched pit-field-based plant cell adhesion domains in plasmolyzing cells of maize root apices exposed to mannitol. Intriguingly, these unique adhesion domains of plasmolyzing cells are enriched with endoplasmic-reticulum-resident calreticulin. Cadherin-like, but not catenin-like, proteins were abundant also within the nucleoplasm.Abbreviations AGPs arabinogalactan proteins - EM electron microscopy - ER endoplasmic reticulum - MFs microfilaments - SB stabilizing buffer     

Radial transport of water across cortical sleeves of excised roots ofZea mays L.

The stationary radial volume flows across maize (Zea mays L.) root segments without steles (sleeves) were measured under isobaric conditions. The driving force of the volume flow is an osmotic difference between the internal and external compartment of the root preparations. It is generated by differences in the concentrations of sucrose, raffinose or polyethylene glycol. The flows are linear functions of the corresponding osmotic differences ( ) up to osmotic values which cause plasmolysis. The straight lines obtained pass through the origin. No asymmetry of the osmotic barrier could be detected within the range of driving forces applied ( =±0.5 MPa), corresponding to volume-flow densities of j_{v, s}=±7·10^–8 m·s^–1. Using the literature values for the reflection coefficients of sucrose and polyethylene glycol in intact roots (E. Steudle et al. (1987) Plant Physiol.84, 1220–1234), values for the sleeve hydraulic conductivity of about 1·10^–7 m·s^–1 MPa^–1 were calculated. They are of the same order of magnitude as those reported in the literature for the hydraulic conductivity of intact root segments when hydrostatic pressure is applied.Abbreviations and symbols a _s outer surface of sleeve segment - c concentration of osmotically active solute - j _{v, s} radial volume flow density across sleeve segment - Lp_s hydraulic conductivity of sleeves - Lp_r hydraulic conductivity of intact roots - _N thickness of Nernst diffusion layer - reflection coefficient of root for solute - osmotic value of bulk phase - osmotic coefficient