Xylem‐to‐phloem transfer of boron in broccoli and lupin during early reproductive growth

The aim of this study was to test the hypothesis that newly‐acquired boron (B) undergoes rapid xylem‐to‐phloem transfer in plants with restricted mobility. Analysis of the element accumulation and water usage by shoots of intact broccoli ( Brassica oleracea var. italica Plenck cv. Commander) and lupin ( Lupinus albus L. cv. Ultra) plants provided with a non‐deficient supply of B, revealed that the concentration of various mineral elements (K, P, Mg, Ca, B, Fe, Zn, Mo, Cu, Mn) in xylem sap of intact plants ranged from 0.3 µ M to 3.5 m M , with B being present at 2.9‐3.5 µ M . For each element assayed, the concentration was higher in phloem exudate (1.6 µ M to 91 m M ) than in xylem sap; B was present at about 0.4 m M . Intact broccoli and lupin plants or detached transpiring broccoli shoots were supplied simultaneously with enriched ¹⁰B, strontium (a xylem marker) and rubidium (a xylem/phloem marker) during early reproductive growth. The contents of these three compounds were determined in foliage and florets or fruits as a function of time (i.e. up to 12 h and 4 days for broccoli and lupin plants, respectively), and the content in florets or fruits was expressed as a percent of the total recovered. In general, the percent recovery of both ¹⁰B and rubidium in florets or fruits was similar and markedly greater than that for strontium, even at the earliest harvest times (within 2 h for broccoli and 1 day for lupin). The data indicate that in plants with restricted B mobility, B is supplied to sink tissues in the phloem, and the extent of B xylem‐to‐phloem transfer is closely determined by current uptake.     

Enhanced inflorescence development in tomato by growth substance treatments in relation to 14C-assimilate distribution

Inflorescence development in tomato plants ( Lycopersicon esculentum Mill., cv. King Plus) grown under a low-light regime is promoted by exogenous applications of a mixture of N⁶-benzyladenine (BA) and gibberellins A₄₊₇ (GA) directly on the inflorescence. The photosynthetic rate of the young mature leaf, which feeds the developing inflorescence, and the proportion of ¹⁴C-assimilates exported from the source leaf are not affected by the growth substance treatment, but the pattern of ¹⁴C-assimilate distribution is altered. Assimilate supply to the treated inflorescence increases concomitantly with a decrease in the ¹⁴C import into the apical shoot, reflecting a competition between these two plant parts. The increased assimilate accumulation in the treated inflorescence is apparent 1 day after the first application of BA+GA, and precedes any morphological changes in the reproductive structure. These results are discussed in relation to nutritional hypotheses that regard assimilate supply as limiting for reproductive development.     

Boron compartmentation in roots of sunflower plants of different boron status: A study using the stable isotopes 10B and 11B adopting two independent approaches

The intracellular compartmentation of boron (B) in roots of sunflower plants precultured with 100 μ M B (high B) or 1 μ M B (low B) was studied using two independent approaches. In the first approach, short-term efflux studies using the stable isotopes ¹¹B and ¹⁰B were carried out. In roots of high B plants, the calculated concentrations of B (nmol g_FW ⁻¹) were 52.6 in the cell wall, 7.5 in the vacuole, 27.1 in the cytosol and 48.0 in the free space. In roots of low B plants, the concentrations of B (nmol g_FW ⁻¹) were 43.4 in the cell wall, 2.8 in the vacuole, 17.9 in the cytosol and almost zero in the free space. Although the B supply differed by a factor 100, the B concentrations in the cytosol and the vacuole of low B plants were 66 and 37% of the respective concentrations in high B plants. This suggests an additional role for B in plant metabolism, besides its function in the cell wall. In the second approach, root B pools (cell sap and water-insoluble residue) were determined for comparison, and found to be in good agreement with the results from the efflux study.     

Effects of nitrate on influx, efflux and translocation of potassium in young sunflower plants

Influx, efflux and translocation of K⁺(⁸⁶Rb) were studied in the roots of sunflower seedlings ( Helianthus annuus L. cv. Uniflorus) treated with 0–4.0 m M NO₃⁻ during a 9 day growth period or a 24 h pretreatment period. Roots treated with high levels of NO₃⁻ absorbed and translocated more K⁺(⁸⁶Rb) than seedlings treated with low levels of NO₃⁻. The content of K⁺ in the shoots was, however, higher in seedlings treated with low levels of NO₃⁻, indicating a low rate of retranslocation of K⁺ in those plants. K⁺(⁸⁶Rb) efflux was highest into the low-NO₃⁻ solutions. All effects on K⁺(⁸⁶Rb)-fluxes were more obvious in high-K plants than in low-K plants. The results are discussed in relation to the Dijkshoorn-Ben Zioni hypothesis for K⁺+ NO₃⁻-uptake and translocation in plants.     

Suppression of ammonium uptake by nitrogen supply and its relief during nitrogen limitation

Barley ( Hordeum vulgare , cv. Triumph), wheat ( Triticum aestivum , cv. Kleiber) and oat ( Avena sativa , cv. Tarok) were grown until day 20 in nitrate-containing solutions or in nitrogen-free solutions for periods up to 8 days immediately prior to day 20. They then were exposed for 4 h to complete, nitrate-free solutions containing 0.5 or 2.0 mM ammonium (98 atom%¹⁵N). In all 3 species in 2 experiments, net ammonium uptake was low in plants grown continuously in nitrate, and increased 3 to 4-fold with increasing nitrogen deprivation. Charge balance during net ammonium uptake was largely maintained by the sum of net potassium and net proton efflux. Variations in root ammonium concentration at the time of exposure to the ammonium solutions revealed no consistent pattern with net ammonium uptake, implying that a product of ammonium assimilation may serve as a negative effector for the uptake process. In nitrogen-replete plants, and in those deprived of nitrogen for 2 days, the amounts of endogenous ¹⁴N-ammonium recovered in the ambient ¹⁵N-ammonium solution during the 4-h uptake period were greater than the initial amounts of ¹⁴N-ammonium present in the root tissue. Significant generation of ¹⁴N-ammonium from endogenous organic nitrogen sources was thus evident in all 3 species.     

Free space uptake and influx of Ni2+ in excised barley roots

The effects of switches between high and low nutrient supplies on growth and mineral nutrition of winter wheat ( Triticum aestivum L. cv. Martonvásári-8) were followed in four main developmental phases: tillering, shooting, heading and grain filling. Growth of the shoots was significantly affected by switches. Under low nutrient supply the life cycle was shortened. Root growth was only slightly affected by switches, but an early high nutrient supply followed by low nutrient supply gave an impetus for root development. In general, the growth data indicate that the nutrient status of the plants is determined by the nutrient level supplied during shooting. A high level of nutrients during shooting leads also to high vegetative growth, whereas the best grain yield was obtained by a high dose of nutrients during tillering followed by low nutrient conditions during the shooting stage and later. K⁺(⁸⁶Rb) influx in the roots decreased with age. The potential for K⁺ (⁸⁶Rb) influx was low in plants of high-salt status, but it became high in response to switching to low supply at shooting, whereas later switches had no influence on this function in high-salt plants. The highest K⁺(⁸⁶Rb) influx was found in plants starting with high nutrient supply followed by low-salt conditions; this plant group was outstanding also with respect to its high grain yield.     

The influence of salinity on phosphate uptake and distribution in lupin roots

Treeby, M. T. and van Steveninck, R. F. M. 1988. The influence of salinity on phosphate uptake and distribution in lupin roots. - Physiol. Plant. 72: 617–622.
The uptake and distribution of phosphate in lupin ( Lupinus luteus L. cv. Weiko III) roots under moderate salt (NaCl) stress was studied. Vacuolar inorganic phosphate (PJ concentrations in high phosphate plants were decreased by salt, although whole root P| was unaffected. In low phosphate plants, vacuolar P_i was unaffected by salt while whole root P_i was increased. Phosphate uptake was not altered by salt in high phosphate plants, but was depressed in low phosphate plants. These observations lead to the conclusion that in high phosphate plants P_i accumulates in cytoplasm and/or stele, ultimately giving rise to phosphate toxicity in shoots. Increasing phosphate supply had no effect on Na⁺ accumulation in root cell vacuoles in the epidermis or cortex, but the concentration of Cl⁻ in endodermal vacuoles was lowered.     

Inhibitory and promotive effects of gibberellic acid on floral initiation and development in Poa pratensis and Bromus inermis

Flowering in Poa pratensis L. cv. Holt and Bromus inermis Leyss. cv. Manchar requires exposure to short days (SD) for primary induction to occur, followed by long days (LD) to allow the inflorescence to develop. Weekly sprays with gibberellic acid (GA₃) during primary induction inhibited flower initiation in both P. pratensis and B. inermis . With 10⁻⁴ M GA₃ flowering of P. pratensis was suppressed even after an induction period of 10 weeks. Since both GA₃ and non-inductive LD conditions greatly stimulate leaf elongation, the degree of primary induction was closely negatively correlated with plant height (leaf sheath and blade length) at the end of the induction period. GA₃ application or the interpolation of LD during SD induction were most inhibitory during the later middle part of the SD period, whereas they were stimulatory near the beginning or immediately before the SD period. We suggest that changes in the portfolio or levels of endogenous gibberellins mediate photoperiodic control of growth and floral initiation in these plants. However, GA₃ sprays could not substitute for LD in causing heading and culm elongation in SD induced plants of the two species. The results are discussed in the light of results with other plants with dual floral induction requirements.     

Anion uptake in maize roots: Interactions between chlorate and nitrate

Effects of nitrate, chloride and chlorate ions upon nitrate and chlorate uptake by roots of maize ( Zea mays L., cv. B73) seedlings were examined. Net nitrate uptake, ³⁶ClO₃⁻ influx and ³⁶Cl⁻ influx (the latter two in a background of 0.5 m M KNO₃) displayed similar pH profiles with optima at pH 5.5 and below. External, non-labeled chloride had little effect on the accumulation of ³⁶ClO₃⁻ (both in 5 h and 20 min uptake assays), while nitrate and chlorate had almost identical, marked inhibitory effects. Nitrate pretreatment caused an apparent induction of both ³⁶ClO₃⁻ and ¹⁵NO₃⁻ uptake activities. After 5 h of treatment in nitrate, the uptake activities of chloride- and chlorate-pretreated plants increased to that of nitrate-pretreated plants. During 6 h exposure to chlorate, ³⁶ClO₃⁻ uptake activity of nitrate-pretreated plants decreased to that of chlorate- and chloride-pretreated plants. The results support the existence of a shared nitrate/chlorate transport system in maize roots which is not inhibited by external chloride, and which is induced by nitrate, but not by chlorate or chloride. The suggestion is made that selection of chlorate-resistant mutants of maize can identify nitrate uptake as well as nitrate reductase mutants.     

Time-course of uptake of dissolved inorganic carbon through willow roots in light and in darkness

Uptake of dissolved inorganic carbon (DIC) from a nutrient solution by willow roots was measured in light and darkness and the distribution in the plant of DIC taken up by the roots was determined. It was also studied whether the transport system could be activated by preincubation with dissolved inorganic carbon.
Willow plants ( Salix cv. Aquatica gigantea) grown in hydroponic culture media were preincubated for 2 days with or without 0.74 mM NaHCO₃. After preincubation, either unlabelled or [¹⁴C]-labelled NaHCO₃ was injected into the media and after 1, 5, 10 and 24 h either in light or in darkness the plants were harvested in pieces into liquid nitrogen, lyophilized and burned in a combustion chamber.
¹⁴C was transported through the roots to the shoots and leaves both in light and in darkness, although incorporation of ¹⁴C in darkness was only half of that in light at the end of the 24-h feeding period. Both in light and in darkness the amount of ¹⁴C increased in all parts of willow plants with time. In light the rate of labelling was highest into cuttings and shoots. In darkness more than half of the total label was detected in cuttings of both the non-activated and the activated treatments.
In the shoots the middle part was most strongly labelled after 5 and 10 h, but after 24 h ¹⁴C moved towards the base of the shoot. In the leaves at all feeding times most radioactivity was incorporated into the young, fully open leaves on the upper part of the shoots. Preincubation of plants with unlabelled NaHCO³ in growth media had no clear effect on the rate of DIC uptake either in light or in darkness.     

Altered resource allocation during seed development in Arabidopsis caused by the abi3 mutation

The regulation of whole-plant resource allocation during seed development in Arabidopsis thaliana was investigated by examining growth rate and partitioning of ¹⁴CO₂ in wild-type plants and those carrying the abi3 mutation. Plants carrying the abi3 mutation partitioned more resources into seed development than the wild type. The extra resources were available as a result of delayed senescence of the cauline leaves in the mutant. After supply of ¹⁴CO₂ at later stages of reproductive development differences in patterns of ¹⁴C distribution between mutant and wild type were consistent with long-term changes in growth and allocation. The role of long-distance signals in the regulation of seed yield in Arabidopsis is discussed.     

Phosphorus translocation in salt-stressed cotton

The effect of salinity on plants has usually been studied at high inorganic P concentration ([Pi]) in the nutrient solution, and salinity × Pi interactions have been examined at much higher [Pi] than found in soil solutions. Short-term ³²Pi experiments were carried out to study the effect of salinity (150 m M NaCl) on phosphorus translocation in cotton plants ( Gossypium hirsutum L. cv. Acala SJ-2) grown in nutrient solutions containing 10 μ M [Pi]. The effect of additional Ca to a concentration of 10 μ M was also tested. Salinity inhibited ³²P translocation from root to shoot. This inhibition was more evident at higher [Pi] in the root medium. Increasing [Pi] 33-fold in the solution resulted in a 4.3-fold increase in [³²P] in the root under saline conditions, but only in a 1,8-fold increase in the shoot. In older shoot tissues total [P] was elevated in the salinized plants. In the young tissues, however, total P concentration was higher in control plants. Inhibition of ³²P translocation by salinity was greater from root to young leaves than to mature shoot tissues. Salinity also decreased ³²P recirculation from the cotyledons to the young leaf. Inhibition by salinity of both ³²P translocation and recirculation to young leaves was fully reversed by increasing Ca supply from 1 to 10     

Growth and accumulation of N, K+, Ca2+ and Mg2+ in barley exposed to various nutrient regimes and root/shoot temperatures

Six cultivars of spring barley ( Hordeum vulgare L. cvs Salve, Nümberg II, Bomi, Risø 1508, Mona and Sv 73 608) were grown in water culture for three weeks with various combinations of mineral supply and differential roots/shoot temperatures during the growth period. Most important for growth and accumulation of N, K⁺, Ca²⁺ and Mg²⁺ was the mineral supply, followed by the root temperature and the choice of cultivar. Treatments with low mineral supply or low root temperature induced a uniform reduction in growth and accumulation of the ions studied. The effects of low mineral supply and low root temperature on growth and N accumulation was additive, which indicates that these factors exert their influence independently of each other.
Roots grown at 10°C were smaller and Rb⁺(⁸⁶Rb) influx was higher than in roots grown at 20°C. It is suggested that the control of Rb⁺(⁸⁶Rb) influx is affected by the root temperature and the age of the plants. The higher ⁸⁶Rb⁺ (⁸⁶Rb) influx into the low temperature roots could not compensate for the smaller root size. However, the lower total mineral accumulation made up for the needs of the smaller plants and cannot explain the reduction in growth.     

Growth, contents of K+ and kinetics of K+(86Rb) uptake in barley cultured at different low supply rates of potassium

Plants of barley ( Hordeum vulgare L. cv. Salve) were grown with 6.5–35% relative increase of K⁺ supply per day (RKR) using a special computer-controlled culture unit. After a few days on the culture solution the plants adapted their relative growth rate (RGR) to the rate of nutrient supply. The roots of the plants remained in a low salt status irrespective of the rate of nutrient supply, whereas the concentration of K⁺ in shoots increased with RKR. Both V_max and K_m for K⁺(⁸⁶Rb) influx increased with RKR. It is concluded that with a continuous and stable K⁺ stress, the K⁺ uptake system is adjusted to provide an effective K⁺ uptake at each given RKR. Allosteric regulation of K⁺ influx does not occur and efflux of K⁺ is very small.     

Selenium uptake by Butyrivibrio fibrisolvens and Bacteroides ruminicola

Abstract The uptake and incorporation of ⁷⁵[Se]selenite by Butyrivibrio fibrisolvens and Bacteroides ruminicola were by constitutive systems. Rates of uptake were higher in chemostat culture than in batch culture and there may be some inducible component. Uptake of [⁷⁵Se]selenite was distinct from sulphate or selenate transport, since sulphate and selenate did not inhibit selenite uptake, nor could sulphate or selenate uptake be demonstrated in these organisms. Selenite uptake in B. fibrisolvens had and apparent K _m of 1.74 mM and a V _max of 109 ng Se · min⁻¹· (mg protein)⁻¹. An apparent K _m of 1.76 mM and V _max of 1.5 μg Se · min⁻¹· (mg protein)⁻¹ was obtained for B. ruminicola . [⁷⁵Se]Selenite uptake by both organisms was partially sensitive to inhibition by 2,4-DNP. Uptake by B. fibrisolvens was also partially inhibited by azide and arsenate and in B. ruminicola it was partially inhibited by fluoride. CCCP, CPZ, DCCD or quinine did not inhibit uptake in either B. fibrisolvens or B. ruminicola . Selenite transport by both organisms was sensitive to IAA and NEM and was strongly inhibited by sulphite and nitrite. [⁷⁵Se]Selenite was converted to selenocystine, selenohomocystine and selenomethionine by B. fibrisolvens. B. ruminicola did not incorporate [⁷⁵Se]selenite into organic compounds, but did reduce it to red elemental selenium.     

Utilization of nitrogen from storage and current-year uptake in walnut spurs during the spring flush of growth

[¹⁵N]-depleted (NH₄)₂SO₄ applied to the soil in 1985 resulted in residual labeling of about 16% of the storage nitrogen (N) pool of mature walnut ( Juglans regia L. cv. Serr) trees in 1987. Application of [¹⁵N]-depleted (NH₄)₂SO₄ fertilizer to a different set of mature walnut trees in 1987 allowed monitoring of the kinetics and utilization of N from current year uptake in 1987 and resulted in >20% labeling of fruit N following completion of leaf expansion. Redistribution of storage N to the new growth predominated during the spring flush of growth although N derived from the soil during current-year uptake contributed increasingly during leaf expansion. Labeled N from current year uptake accumulated preferentially in the leaves as compared with reproductive organs during leaf expansion but subsequent to leaf expansion, fruit were more highly labeled with N derived from current-year uptake than leaves. Pistillate flower abortion was coincident with an apparent competition for N among developing vegetative and reproductive organs and preceded the period of significant N contribution from current-year uptake.     

A 10-kDa acyl-CoA-binding protein (ACBP) from Brassica napus enhances acyl exchange between acyl-CoA and phosphatidylcholine

The gene encoding a 10-kDa acyl-CoA-binding protein (ACBP) from Brassica napus was over-expressed in developing seeds of Arabidopsis thaliana . Biochemical analysis of T₂ and T₃ A. thaliana seeds revealed a significant increase in polyunsaturated fatty acids (FAs) (18:2 ^{cis Δ9,12} and 18:3 ^{cis Δ9,12,15}) at the expense of very long monounsaturated FA (20:1 ^{cis Δ11}) and saturated FAs. In vitro assays demonstrated that recombinant B. napus ACBP (rBnACBP) strongly increases the formation of phosphatidylcholine (PC) in the absence of added lysophosphatidylcholine in microsomes from ΔYOR175c yeast expressing A. thaliana lysophosphatidylcholine acyltransferase ( AthLPCAT ) cDNA or in microsomes from microspore-derived cell suspension cultures of B. napus L. cv. Jet Neuf. rBnACBP or bovine serum albumin (BSA) were also shown to be crucial for AthLPCAT to catalyse the transfer of acyl group from PC into acyl-CoA in vitro . These data suggest that the cytosolic 10-kDa ACBP has an effect on the equilibrium between metabolically active acyl pools (acyl-CoA and phospholipid pools) involved in FA modifications and triacylglycerol bioassembly in plants. Over-expression of ACBP during seed development may represent a useful biotechnological approach for altering the FA composition of seed oil.     

Influence of light and darkness and the experimental design on kinetics of K+ (86Rb) influx in roots of intact spring wheat

Seedlings of spring wheat ( Triticum aestivum L. cv. Svenno) were cultivated at 20°C in continuous light or darkness with the roots in nutrient solutions for six days. The plants were starved for K⁺ during different periods of time to produce plants with various K⁺ status. In one cultivation light-grown plants were pretreated in darkness, and vice versa, before the uptake experiment. In all experiments, roots were put in a complete nutrient medium containing 2.0 m M K⁺ radiolabelled with ⁸⁶Rb. The uptake time was varied (5, 60 or 120 min).
The K⁺ concentration in the roots, [K⁺]_root, increased during the course of the uptake experiments, especially in light and at initially low [K⁺]_root, At the same time K⁺ (⁸⁶Rb) influx in the roots decreased. The simoidal relationship obtained between K⁺ (⁸⁶Rb) influx and [K⁺]_root was affected by these changes, and Hill plots gave various Hill coefficients, n_H, depending on the duration of the uptake experiments. n_H from three apparently straight line segments of the same plot, in different [K⁺]_root - intervals, indicated a falling degree of interaction between the binding sites as [K⁺]_root increased. For the dark-grown plants negative cooperativity could not be demonstrated.     

Nutrition of winter wheat during the life cycle. II. Influx and translocation of potassium and phosphorus

Changes in the K, Na and P content of solution-grown and soil-grown winter wheat ( Triticum aestivum L. cv. Martonvásári 8) were followed during the life cycle. In parallel experiments the influx of K⁺(⁸⁶Rb) and H₂³²PO-₄ and the translocation of these ions to the shoot were also measured. The K content increased during the seedling and tillering stages (autumn and winter period), but then decreased rapidly as the temperature rose. The influx and translocation of K⁺ increased during vegetative growth and declined in the generative phase. Na⁺ replaced K⁺ when K⁺ uptake was limited. The P content changed less than the K content, but influx was maximal during elongation. Both influx and translocation slowed greatly in the grain-filling period. For both minerals the ratio of influx to net uptake was estimated for the life cycle. This ratio was high for the soil-grown plants but low for the solution-grown plants, suggesting that the supply of K and P was limiting the growth of the former but not of the latter plants. It is suggested that the transport of K and P during the life cycle is regulated by metabolism-dependent direct routes (i.e. negative feedback mechanisms) during vegetative growth and by passive, indirect routes in the generative stage. The possibility of hormone-directed transport processes is also discussed.     

Influence of aluminium on phosphate and calcium uptake in beech (Fagus sylvatica) grown in nutrient solution and soil solution

The effects of AICI₃ on uptake of Ca²⁺ and phosphate in roots of intact beech ( Fagus sylvatica L. provenance Maramures) plants were studied in nutrient solution and soil solution. Aluminium reduced the concentrations of Ca, Mg and P in plants and increased that of K. In short term experiments, uptake of Ca²⁺(⁴⁵Ca) was reduced by exposure of the roots to Al. The effect of aluminium on Ca²⁺(⁴⁵Ca) uptake was immediate and primarily of a competitive nature, preventing Ca²⁺ from being adsorbed. Uptake of ³²P-phosphate increased with increasing Al concentration up to 0.1 m M and then decreased at higher Al concentrations. The effect of Al on ³²P-phosphate uptake was most pronounced during the first hours of exposure. Growth of plants for 15 days in soil solution, collected from the upper A horizon of a beech forest soil, had no effect on uptake of Ca²⁺(⁴⁵Ca) and ³²P-phosphate, probably because of a low concentration of labile bound monomeric Al and binding of Al to organic compounds. Soil solution from the deeper B horizon reduced Ca²⁺(⁴⁵Ca) uptake and increased ³²P-phosphate uptake in a manner similar to that with Altreatment in nutrient solution. It is concluded that in soil solution from the deeper regions of the soil, mineral uptake by roots was affected by Al.