Uptake of 3-o-Methylglucose by Healthy and Hypomyces-infected Squash Hypocotyls

Rates of uptake of 3-o-methylglucose (MeG) by squash (Cucurbita maxima) hypocotyl sections from above lesions caused by Hypomyces solani f. sp. cucurbitae, race 1, are 2-fold greater than uptake by comparable tissues from healthy plants. Kinetic analyses indicate (i) that a single (constitutive) carrier system, with a Michaelis constant (Km) of 25 to 30 mm, mediates the transport of MeG into healthy hypocotyl cells and (ii) that an additional (inducible) system with a much lower Km (ca. 2 mm) is present in diseased hypocotyls. In both systems MeG uptake is inhibited competitively by glucose. The inducible transport system (s) in diseased tissues has a higher temperature coefficient, greater sensitivity to metabolic inhibitors and larger accumulation capacity than the one in healthy plants. While the nature of the constitutive system is ambiguous, the inducible carrier mechanism is a typical active transport system. These results indicate that increased rates of uptake and accumulation of metabolites by diseased tissues can be caused by new transport systems.     

Effect of Infection by Hypomyces solani f. sp. Cucurbitac on Apparent Free Space, Cell Membrane Permeability, and Respiration of Squash Hypocotyls

Initial symptoms and increases in respiration, apparent free space, and rate of leakage of amino acids occurred concomitantly in squash (Cucurbita maxima Dcne) hypocotyls infected by Hypomyces solani f. sp. cucurbitae Snyd. and Hans. Young, rapidly expanding lesions had greater respiratory rates and apparent free space than comparable tissues from healthy plants.

Hypocotyl tissues above (1-45 mm) lesions possessed greater endogenous respiratory rates (2-3 times) and lower respiratory quotients than similar tissues from healthy plants. But no differences were found in membrane permeability to nonelectrolytes and water and in apparent free space between cells above lesions and healthy hypocotyls.

Host cells contiguous to fungal hyphae at lesion margins were completely permeable to solutes and failed to accumulate neutral red or exhibit cyclosis.

     

Two components of auxin transport

The transport of indoleacetic acid-1-¹⁴C out of sunflower stem sections has been analyzed by a compartmental analysis procedure in which the radioactivity moving out of the tissue (log per cent) is plotted against time. The analysis indicates that indoleacetic acid is transported via a fast transport system (t_½ of about 30 minutes) and a slow transport system (t_½ about 10 hours). While we do not know the sources of these two pools, by analogy with ion transport studies, the fast efflux is characteristic of transport from the cytoplasm across the plasmalemma and the slow efflux is characteristic of transport across the tonoplast and thus out of the vacuole. Both components of transport are inhibited by 2,3,5-triiodobenzoic acid.     

Nicotine Production by Tissue Cultures of Tobacco as Influenced by Various Culture Parameters

Assimilate efflux from vacuum-infiltrated leaf slices (spinach, barley) into a buffered solution was examined in relation to Ca^{+ +} -activity and osmotic conditions. Efflux from isolated mesophyll protoplasts and from a unicellular green alga (Eremosphaera viridis de Bary) was also measured.In the presence of Ca^{+ +}, assimilate efflux from leaf slices was small (1 to 5 % of the total carbon fixation rate, depending on osmotic conditions). Efflux was drastically stimulated by addition of Ca^{+ +} -chelators. If expressed as µmol carbon mg^-1 chlorophyll h^-1, it reached 50 % of the assimilation rate. Efflux from protoplasts or algae was slow and insensitive to Ca^{+ +} chelators at concentrations which caused fast efflux from leaf slices.Assimilate efflux from leaf slices was rather unspecific. Both in the tissue and the surrounding medium, sucrose was the most abundantly labelled compound (70 to 80 % of total soluble labelled material).A 50 % decrease of efflux was observed when turgor pressure was lowered by addition of sorbitol (200 to 300 mosmol kg^-1). At extremely high sorbitol concentrations (> 1500 mosmol kg^-1) efflux increased again and was relatively less stimulated by EDTA.It is suggested that assimilate efflux from leaf slices is mainly diffusion through open veins and/or plasmodesmata. When these symplastic connections are closed by addition of Ca^{+ +}, the remaining transmembrane flux into the apoplast is small. Thus, assimilate movement from the mesophyll to the phloem appears to be symplastic, not apoplastic as suggested in the literature.     

A simple method for the determination of resistance to gas diffusion in plant organs

A simple method was developed for the determination of resistance coefficients for ethylene diffusion in plant tissues based on the kinetic analysis of the efflux of preloaded ethane gas. Efflux curves were analyzed to obtain first-order rate constants and resistance coefficients. Resistance coefficients determined by the ethane efflux and steady-state methods were found to agree well. Employing the ethane efflux method, it was shown that over 97% of gas exchange of tomato (Lycopersicum esculentum Mill., cv. `Ace') fruits occurs through the stem scar. The resistances to diffusion of tomato skin and stem scar were found to be 280,000 and 300 seconds per centimeter, respectively; the combined resistance of intact tomato fruits was approximately 7,800 seconds per centimeter. The ethane efflux method was employed to show that plastic shrink-wrapping of English cucumbers (Cucumis sativus L. var anglicus Bailey) increased the resistance to ethane diffusion from 1.1 × 10³ to 23 × 10³ seconds per centimeter.     

Sequence of key events in shoot gravitropism

It has recently been shown that asymmetric acid efflux is closely correlated with the gravitropic curvature of plant shoots and roots. The research reported here addresses whether auxin (IAA) redistribution in shoots is the cause or result of asymmetric acid efflux.

When abraded sunflower (Helianthus annuus cv Mammoth) hypocotyls are submerged in 20 millimolar neutral buffer, gravicurvature is greatly retarded relative to 0.2 millimolar controls. Nevertheless, in both buffer systems there is a similar redistribution of [³H]IAA toward the lower surface of gravistimulated sunflower hypocotyls. These results suggest that graviperception initiates IAA redistribution, which in turn results in auxin-induced asymmetric H⁺ efflux across the shoot. This interpretation is reinforced by data showing the effects of removal of the epidermal layers (peeling), osmotic shock, and morphactin treatment on gravicurvature and [³H]IAA redistribution. Peeling and osmotic shock inhibit gravicurvature but not redistribution. Morphactin inhibits both processes but does not inhibit hypocotyl straight growth.

     

Cytohistochemical techniques for calcium localization and their application to diseased plants

Lesion delimitation and resistance of old bean (Phaselous vulgaris L., cv. Red Kidney) plants to Rhizoctonia solani Kühn have been suggested to result from increased calcium pectate formation in walls. Ultrastructural histochemistry was used to determine the site of calcium in tissues adjacent to lesions and in older bean hypocotyls. Hypocotyl lesion tissue and uninoculated control tissue were treated with ammonium oxalate or potassium pyroantimonate during fixation. Treatment with potassium pyroantimonate, but not with oxalate, resulted in granular deposits in cell walls of healthy and lesion tissue. Granules also occurred on the plasma membrane of cells adjacent to lesions and in organelles of damaged cells, but wall granule density was not increased. Cell walls from healthy 24-day-old plants had a greater granule density than those for 8-day-old plants. Wall granules were removed from thin sections with ethylene glycol bis(β-aminoethyl ether)-N,N,N′,N′-tetraacetic acid. Energy dispersive analysis of x-rays also suggested that potassium pyroantimonate localized calcium. Chemical analyses showed that some calcium was retained in tissues after fixation. The results suggest that there are different mechanisms for lesion delimitation and age-induced resistance.     

Analysis of Glycerol-3H Transport in the Frog Oocyte by Extractive and Radioautographic Techniques

The efflux of glycerol-³H from mature R. pipiens oocytes was studied by extractive analysis and by quantitative radioautography using techniques suitable for diffusible solutes. Extractive analysis was used to determine the total cellular concentration of tracer, and radioautography, regional intracellular concentrations, at equilibrium and as a function of efflux time, t_E. The efflux was resolvable into four kinetic fractions: cytoplasmic fast and slow fractions, and nuclear fast and slow fractions. The fast fractions represent freely diffusible glycerol in the two compartments; the solvent space accessible to glycerol is unity in the nucleus (germinal vesicle), but only 0.73 in the cytoplasm. The efflux of both fast fractions from the cell is determined by the permeability of the cortical membrane, with neither the nuclear membrane nor diffusion in the cytoplasm detectably slowing the flux. The permeability at 13.6°C is 2.2 x 10^-5 cm/sec. The slow fractions leave the cell at about one-tenth the rate of the fast; the interpretation is that these fractions represent glycerol bound to impermeant cellular constituents. The size of these constituents is below the radioautographic resolution; in the cytoplasm, they appear not to be the yolk platelets. The extent of binding is about fourfold greater, per milliliter of compartment water, in the cytoplasm than in the germinal vesicle.     

Compartmental efflux analysis and removal of extracellular cadmium from roots

Profiles of ¹⁰⁹Cd efflux from roots into three solutions were determined for young intact plants of Agrostis gigantea and maize. The solutions were (a) nutrient culture medium containing 3 micromolar Cd at room temperature, (b) ice-cold 5 millimolar CaCl₂, and (c) ice-cold 5 millimolar PbCl₂. Efflux profiles were clearly resolved into three easily discernible components having fast, medium, and slow exchange rates. These results were unexpected for the situation where some intracellular Cd was present both as extractable Cd-binding peptide and in electron-dense granules within the cytoplasm and the vacuoles. Adding a fourth compartment to the curve-fitting model produced a splitting of the fast exchanging component. Use of these efflux kinetics to estimate Cd fluxes through membranes was inappropriate. However, they were useful in determining optimal washing times for the removal of extracellular Cd. A 10 minute wash in ice-cold 5 millimolar CaCl₂ is recommended for this purpose for Agrostis and maize roots.     

Potassium Fluxes in Excised Barley Roots

The method of the modified compartmental analysis for excisedroots has been adopted for measuring K⁺-fluxes and compartmentationin barley (Hordeum distichon) roots. Efflux of ⁴²K and ⁸⁶Rbindicated that more than two intracellular compartments wereinvolved in the tracer exchange; the ⁴²K data clearly showedthe components. On the basis of the efflux behaviour of theapical and more basal tissues of the roots, the three componentsof efflux were attributed to the cytoplasm of differentiated(fast) and meristematic tissues (intermediate) and to the vacuoles(slow exchange) of the roots. A model is proposed on the basisof which, the fluxes corresponding to the meristematic and differentiatedtissues of the root can be estimated. Additionally, fluxes ofthe differentiated root tissues were determined by using effluxdata obtained with root segments without apical tissues. Thedata obtained in both ways compare reasonably well and agreeto independent chemical measurements. Comparison of the ⁴²K and ⁸⁶Rb efflux data show strong discriminationof K^– in favour of Rb⁺ and indicate that ⁸⁶Rb is not suitableas a tracer for K⁺ in efflux measurements, at least with barleyroots.     

Zinniol,a phytotoxin,is produced by Phoma macdonaldii

Zinniol, a phytotoxin, has been isolated from culture filtrates of Phoma macdonaldii, the causal agent of stem blight of sunflower (Helianthus annuus L.). The production of zinniol appears to be regulated by one or more compounds in the sunflower plant. Zinniol has been isolated from tissues infected with P. macdonaldii implicating it in the disease process. The hypocotyls of sunflower cultivars react differently to zinniol when injected with concentrations from 3.75 × 10⁻³ M to 7.5 × 10⁻³ M. In the most sensitive reaction, zinniol causes the production of a sunken, discolored lesion.     

Oxidation of high density lipoproteins: characterization and effects on cholesterol efflux from J774 macrophages

Oxidative modification of high density lipoproteins (HDL) may alter their capacity to mediate cellular cholesterol efflux. We studied the kinetics of copper-mediated oxidation of HDL and cholesterol efflux mediated by unmodified and oxidized HDL (oxHDL). Oxidation was measured by increases in absorbance at 234 nm (ΔA234), production of thiobarbituric acid reactive substances (TBARS) and loss of trinitrobenzene sulfonic acid reactivity. Oxidation was dependent on copper concentration and showed a lag phase and propagation phase. Efflux of cholesterol from J774 macrophages measured by appearance of cellular [³H]cholesterol in the medium was lower by 16% after 4 h and 36% after 24 h with oxHDL compared to HDL. OxHDL-mediated efflux was also lower by 27% to 36% at lipoprotein concentrations of 10 to 200 μg protein/ml. Cholesterol efflux correlated negatively with TBARS production (r= −0.97, P < 0.003) and ΔA234 (r = −0.77, P < 0.080). There was no difference in efflux mediated by apoproteins prepared from HDL and oxHDL. Efflux measured by change in cholesterol mass in medium was 78% lower with oxHDL. Inhibition of oxidation with butylated hydroxytoluene maintained the capacity of HDL to stimulate efflux. These results suggest that oxidation of HDL may impair its protective role against atherosclerosis.     

Transport of 3-o-Methylglucose Into and Out of Storage Cells of Daucus carota

The movement of labeled 3-o-methylglucose (MeG) into and out of thin carrot discs has been followed in order to gain information on sugar entry and exit mechanisms. Little or no metabolism of this derivative appears to occur in the tissue, since no products were detected either by chromatography or by analysis of respiratory CO₂.

The curve relating entry to external concentration deviated somewhat from a rectangular hyperbola but suggested a carrier mechanism. Glucose and MeG each competitively inhibited the uptake of the other. K_i for MeG was estimated to be 3 times the K_m for its uptake.

When discs incubated in MeG were transferred to H₂O, MeG lost to the solution from the Free Space was re-absorbed against a 7-fold concentration gradient.

The addition of unlabeled MeG or glucose to the medium surrounding discs which had been maintaining a ratio of internal to external MeG of 75:1 brought about release of stored isotope. This was probably not due to exchange diffusion stricto sensu.

Efflux of previously absorbed isotopic MeG into a medium containing unlabeled MeG or glucose was temperature-sensitive. The kinetics of efflux were complex and did not suggest a simple diffusion process related to overall MeG content. However there is evidence (including the falling rate of exit with time) that slow diffusion (or slow release from adsorption) contributed substantially to efflux. The source of this flow appeared to be neither the readily accessible Free Space nor the main storage compartment. Calculation indicated that the volume of this “slow diffusion compartment” might be about 1% of the total volume of the discs.

     

Cation movement in rat articular and non-articular cartilage and in isolated chondrocytes: calcium influx and efflux

1. Calcium ion influx varies between different types of young adult rat cartilage. Sternal cartilage accumulates significantly less Ca2+ than other cartilage types. 2. Influxes of Ca2+ into young adult and ageing tibial cartilage display no significant differences. 3. Efflux of Ca2+ from sternal and tibial cartilage resolves into exponential phases indicative of three compartments. Tracheal cartilage displays two compartment behaviour only. 4. Efflux of Ca2+ from isolated chondrocytes has different characteristics to cartilage efflux with the third slow compartment reduced. 5. Modification of Ca2+ efflux by lanthanum and barium is suggestive of an exchange of strongly bound extracellular calcium during the slow phase of the efflux from young adult tibial cartilage. 6. The metabolic inhibitor 2,4-dinitrophenol is without effect on the efflux of Ca2+ from tibial articular cartilage. 7. The degree of calcium binding exhibited during efflux depends upon cartilage type. Non-articular sternal cartilage binds calcium more strongly than articular tibial, both binding more strongly than non-articular tracheal cartilage. 8. In articular cartilage calcium binding shows an age-related increase.     

Salt tolerance in crop plants monitored by chlorophyll fluorescence in vivo

The potential of measurements of chlorophyll fluorescence in vivo to detect cellular responses to salinity and degrees of salt stress in leaves was investigated for three crop plants. Sugar beet (Beta vulgaris L.) (salt tolerant), sunflower (Helianthus annuus L.) (moderately salt tolerant), and bean (Phaseolus Vulgaris L. cv Canadian Wonder) (salt intolerant) were grown in pots and watered with mineral nutrient solution containing 100 millimolar NaCl. The fast rise in variable chlorophyll fluorescence yield that is correlated with photoreduction of photosystem II acceptors increased in leaves of sugar beet plants treated with salt suggesting stimulation of photosystem II activity relative to photosystem I. In sunflower, this fast rise was depressed by approximately 25% and the subsequent slow rate of quenching of the chlorophyll fluorescence was stimulated. These differences were more marked in the older mature leaves indicating an increasing gradient of salt response down the plant. The salt effect in vivo was reversible since chloroplasts isolated from mature leaves of salt-treated and control sunflower plants gave similar photosystem II activities. Unlike in sugar beet and sunflower, leaves of salt-treated bean progressively lost chlorophyll. The rate of slow quenching of chlorophyll fluorescence decreased indicating development of a partial block after photosystem II and possible initial stimulation of photosystem II activity. With further loss of chlorophyll photosystem II activity declined. It was concluded that measurements of chlorophyll fluorescence in vivo can provide a rapid means of detecting salt stress in leaves, including instances where photosynthesis is reduced in the absence of visible symptoms. The possible application to screening for salt tolerance is discussed.     

Sucrose efflux and export from the maize scutellum*

Abstract During incubation of maize scutellum slices in fructose, there was an efflux of sucrose. Efflux was constant for at least 4 h at fructose concentrations of 70 or 100 mol m^?3. Efflux was increased by EDTA, and decreased by Ca²⁺. Efflux was independent of pH after EDTA treatment, but increased from untreated slices when the pH was lowered from 7 to 4. Uranyl ion and PCMBS (p-chloro-mercuribenzenesulfonic acid) abolished sucrose uptake, but were only weak inhibitors of sucrose efflux. These results are consistent with efflux occurring by simple diffusion through aqueous pores, but they do not rule out facilitated diffusion. Rates of sucrose export from the scutellum to the root shoot axis were estimated from measurements of axis respiration and dry weight gain. Sucrose efflux from scutellum slices was only 14-22% of the export rate. Sucrose efflux from the whole scutellum was only 3-4% of the export rate. It is concluded that the observed efflux is from leaky cells and does not represent sucrose on the way to the phloem along a path that includes the apoplast. These results support the idea that the path for sucrose from parenchyma cell to sieve tube in the maize scutellum is entirely symplastic.     

Fungi associated with strawberry root rot in Illinois

A qualitative and quantitative study of the fungi associated with apparently healthy and root rot-diseased strawberry main roots was made during a 1-year period. Eighty-one genera were isolated from lesions and stele segments of diseased roots, and tips and segments 5–6 cm from the tip of apparently healthy roots. A diverse mycoflora was isolated from each segment of the root. However, each segment had a typical dominant mycoflora, indicating that a changing mycoflora is associated with the root as it passes from a healthy to a diseased condition.Pythium spp. andRhizoctonia Spp. accounted for 25.09 and 5.67 percent, respectively, of the isolates from Surecrop lesions, and 4.96 and 25.92 percent, respectively, of the isolates from Cyclone lesions.     

Correlations between proton-efflux patterns and growth patterns during geotropism and phototropism in maize and sunflower

By placing seedlings of sunflower (Helianthus annuus L.) or maize (Zea mays L.) on agar plates containing a pH indicator dye it is possible to observe surface pH patterns along the growing seedling by observing color changes of the indicator dye. Using this method we find that in geotropically stimulated sunflower hypocotyls or maize coleoptiles there is enhanced proton efflux on the lower surface of the organ prior to the initiation of curvature. As curvature develops the pattern of differential acid efflux becomes more intense. A similar phenomenon is observed when these organs are exposed to unilateral illumination, i.e. enhanced acid efflux occurs on the dark side of the organ prior to the initiation of phototropic curvature and the pattern of differential acid efflux intensifies as phototropic curvature develops. These observations indicate that differential acid efflux occurs in response to tropistic stimuli and that the acid efflux pattern may mediate the development of tropistic curvatures.     

Amino acid accumulation in frog muscle: I. Steady-state glycine accumulation at o °C

Glycine is not significantly metabolized by frog muscle maintained at o °C in vitro. Nevertheless, in this preparation steady-state levels of [¹⁴C]glycine as high as 20 times the external concentration are attained after 3–6 days at o °C. The concentration gradient at the steady state depends on the external concentration, being highest at low external concentrations (approx. 0.1 mM) and reversed at external concentrations above 10 mM.A plot of the steady-state cellular levels of glycine vs the external concentration reveal linear and saturable components. The linear fraction has an average distribution ratio of 0.54 indicating that glycine is partially excluded from the muscle water at this temperature.Efflux of labeled glycine at o °C from previously loaded frog muscle follows first-order kinetics. The rate constant increases with increasing concentrations of glycine in the external medium (efflux facilitation).The steady-state results are shown to be consistent with an adsorption model for amino acid accumulation as well as a model in which amino acid enters the cell via a carrier and exits via a bidirectional leakage pathway. A model in which efflux proceeds through the carrier does not fit the data. This indicates that an alternative to exchange diffusion is needed to explain the observed efflux facilitation.     

Effect of chlorsulfuron on ethylene evolution from sunflower seedlings

The effect of the herbicide chlorsulfuron (2-chloro-N-[(4-methoxy - 6 - methyl -1, 3,5 - triazin - 2 - yl)aminocarbonyl]benzenesulfonamide) on ethylene production in light-grown sunflower (Helianthus annuus L.) seedlings was examined. Application of chlorsulfuron to the apex stimulated ethylene production in all tissues examined: cotyledons, hypocotyls, and roots. The greatest stimulation occurred in the upper portion of the hypocotyl adjacent to, and including, the cotyledonary node. Ethylene evolution from hypocotyls excised from treated seedlings was stimulated over control levels 1 day after herbicide application and reached a maximum (approx. 75 x control or 17 nl/g f wt/h) 2 to 3 days after treatment. Labeling and inhibitor studies indicated that the ethylene produced was derived primarily from methionine. Chlorsulfuron treatment stimulated the rate of accumulation of the ethylene precursor, 1-aminocyclopropane-1-carboxylic acid (ACC), as well as the ability of the tissue to convert exogenous ACC to ethylene. Chlorsulfuron had little effect on ethylene production when administered to the hypocotylsin vitro. Removal of the cotyledons from treated seedlings reduced the rate of ethylene evolution from the hypocotyls. These results suggest that stimulation of ethylene production in sunflower hypocotyls by chlorsulfuron is not a wound response but rather is dependent on factors derived from the cotyledons.