Auxin-Stimulated NADH Oxidase Purified from Plasma Membrane of Soybean

NADH oxidation by plasma membrane vesicles purified from hypocotyls of etiolated soybean seedlings by two-phase partition was stimulated 2- to 3-fold by auxins, indole-3-acetic acid, 2,4-dichlorophenoxy acetic acid (2,4-D), and α-naphthaleneacetic acid. The stimulation was concentration dependent in the presence or absence of detergent with a maximum for 2,4-D at 1 micromolar. The NADH oxidation activity was solubilized with the zwitterionic detergent CHAPS and purified by ion exchange chromatography and gel filtration approximately 2000-fold over the total homogenate. Both the partially purified fraction and an active band from nondenaturing gel electrophoresis revealed the same three bands when analyzed by denaturing gel electrophoresis. When obtained from plasma membrane vesicles from the region of rapid cell elongation, the NADH oxidase complex retained auxin responsiveness throughout purification (3- to 5-fold stimulation by 1 micromolar 2,4-D).     

Glycosphingolipid Domains on Cell Plasma Membrane

In this study we analyzed by immunofluorescence, laser confocal microscopy, immunoelectron microscopy and label fracture technique the ganglioside distribution on the plasma membrane of several different cell types: human peripheral blood lymphocytes (PBL), Molt-4 lymphoid cells, and NIH 3T3 fibroblasts, which mainly express monosialoganglioside GM3, and murine NS20Y neuroblastoma cells, which have been shown to express a high amount of monosialoganglioside GM2. Our observations showed an uneven distribution of both GM3 and GM2 on the plasma membrane of all cells, confirming the existence of ganglioside-enriched microdomains on the cell surface. Interestingly, in lymphoid cells the clustered immunolabeling appeared localized over both the microvillous and the nonvillous portions of the membrane. Similarly, in cells growing in monolayer, the clusters were distributed on both central and peripheral regions of the cell surface. Therefore, glycosphingolipid clusters do not appear confined to specific areas of the plasma membrane, implying general functions of these domains, which, as structural components of a cell membrane multimolecular signaling complex, may be involved in cell activation and adhesion, signal transduction and, when associated to caveolae, in endocytosis of specific molecules.     

Effect of Ground Cover on Splash Dispersal of Phytophthora cactorum from Strawberry Fruits

Abstract A rain simulator was used to investigate the influence of various ground covers (soil, straw, sand, and plastic) on splash dispersal of Phytophthora cactorum , the cause of leather rot of strawberry. Potted strawberry plants were held in a concentric circle by a wood frame, 30 cm from an inoculum source of 10 infected fruits with sporulating lesions. The canopy was exposed to 15 and 30 min of generated rain at intensities of 15 and 30 mm/h. Plastic mulch had the highest resulting fruit disease, incidence (e.g., ca. 80% of fruit infected at 30 min duration and 15 mm/h rain), followed by soil and sand (36–47%), then straw (ca. 15%). Except for straw, there was lower incidence at 30 than at 15 mm/h. There was a general increase in disease incidence over time.     

Studies on Antagonistic Effects of Trichoderma Isolates Against Phytophthora cactorum

Bioassays were used to demonstrate the antibiotic effect of Trichoderma isolates on P. cactorum. When both fungi were grown on benomyl-containing PDA medium, the mycelial growth of Trichoderma was suppressed. However, the production of antibiotics by this fungus remained active, leading to inhibition of the mycelial growth of P. cactorum. The antibiotic effect of Trichoderma on zoospores and cysts was tested on a PDA substrate precultured with Trichoderma on cellophane sheets. On the substrate of some Trichoderma isolates, lysis of zoospores, formation of extracellular vesicles, and hypertrophy of the water expulsion vesicle did occur, both resulting in the death of the zoospores. Conidial suspensions of Trichoderma isolates also induced zoospore lysis. It is presumed that membrane-active peptide antibiotics (peptaibols) are involved in zoospore lysis. The peptaibol paracelsin caused lysins of zoospores at a concentration of 2.5 × 10^?4 M. The effect on cysts depended on the Trichoderma isolate tested and the age of Trichoderma preculture. Old cultures (after beginning of sporulation) affected cysts more severely than young cultures (before sporulation) which usually were not lethal to the cysts but induced preferably microsporangium formation, inhibition of cyst germination, and retardation of germ tube growth.     

Relative Resistance of Four Peach Rootstocks to Phytophthora cactorum and Phytophthora megasperma

Shoot samples of four peach rootstocks that are important to the peach industry in Greece: KID I, GF305, GF677, and PR204, were inoculated with Phytophthora cactorum and Phytophthora megasperma in the field and in the glasshouse and were then evaluated with regard to susceptibility. The pathogenicity of P. cactorum and P. megasperma to peach rootstocks was confirmed with an excised twig assay. The peach rootstocks showed differential susceptibility to P. cactorum . GF305 was the least susceptible and KID I was the most susceptible, which suggests that the latter rootstock is unsuitable for orchards in which the conditions are favourable for Phytophthora diseases. GF677 and PR204 were moderately susceptible. The plants that were inoculated with P. megasperma in the field and in the glasshouse showed no sign of infection whereas twigs inoculated in vitro with P. megasperma developed necrosis. GF305 was the most resistant, KID I was the most susceptible and PR204 and GF677 were moderately resistant. The present results demonstrate that none of the four peach rootstocks used in this study was completely resistant to P. cactorum , particularly when rootstocks were flooded periodically to enhance disease development. Therefore an integrated approach including host and resistance cultural practices is recommended to manage diseases caused by P. cactorum in peach orchards in Greece.     

Properties of Partially Purified Malate Synthase from Euglena gracilis

SYNOPSIS. Properties of partially purified malate synthase from Euglena gracilis were characterized. The pH optimum is 7.0 and the temperature optimum about 30 C; the activation energy is 12,000 calories. A Km of 4 × 10⁻⁵ M was found for both reactants, glyoxylate and acetyl-CoA. The reaction is partially inhibited by a number of normal metabolites, suggesting allosteric control; glycolate is severely inhibitory. The enzyme is not active in cells grown with phototrophic nutrition, but is found in all heterotrophic cells grown on a wide range of carbon sources; the specific activity is greatly dependent on carbon source. High rates of oxygen consumption are usually, but not always, correlated with high enzyme levels.     

Agarose Medium for Germination of Oospores of Phytophthora cactorum

When oospores of Phytophthora caetorum from 30-day-old culture were treated with 0.25% KMnO₄ for 20 min and incubated at 24°C under light for 10 days, 65–75% germinated on water agar and water agarose but only 1–21% germinated on V-8 agar and S+L agar. Water agarose was selected because germinated oospores formed restrieted colonies on this medium that could be isolated easily. KMnO₄ treatment killed sporangia, chlamydospores and mycelial fragments present in oospore suspensions. Under the above conditions, approximately 44% of oospores from 10-day-old culture germinated and the optimum germination rate of about 75% was obtained when oospores reached about 20 days old.     

Effect of Bacterial Antagonist on Phytopthora cactorum and Apple Crown Rot

Bacterial antagonist B8 produced an inhibition zone with each of four Phytophthora cactorum isolates on corn meal agar (CMA) plates. Infections with three P. cactorum isolates were significantly reduced when the soil was simultaneously inoculated with B8. Growth of P. cactorum was completely inhibited on CMA amended with 40–100 per cent 10 fold concentrated B8 extract. Percent oospore germination of P. cactorum was significantly reduced when B8 was present in suspension for 9, 12 and 15 days from inoculation. Survival of oospores was significantly reduced at 60 and 90 mm depths in soil. Bacterial antagonist B8 significantly reduced the population of viable P. cactorum oospores in the top 30 mm of soil where oospores generally survive.     

Selective Interaction Model and Photoreceptor Cell Membrane

A mathematical model is proposed in order to describe, from the thermodynamic point of view, the changes in the photoreceptorcell membrane induced by light stimuli. The phenomenologicalbackground is the increase of the fly microvillar membrane ionicconductivity as a consequence of Ca^++-Na⁺ affinity modification under light action. On the basis of the analogywith the model of protein interaction in mixed solvents, themodel is focused on the selective interaction between ionchannels gates and two ionic ligands. Three possible theoretical cases are examined.     

Interaction between Cell Wall and Plasma Membrane via RGD Motif is Implicated in Plant Defense Responses

Integrin- and vitronectin-like proteins were found to existin the pea plasma membrane and cell wall, respectively. Thehexapeptide GRGDSP but not GRGESP inhibited either the bindingof cell wall protein(s) to plasma membrane protein(s) or thedefense response. A possible role of linkage via RGD motif inplant defenses is discussed. (Received April 20, 1998; Accepted September 1, 1998)     

Main compounds responsible for off-odour of strawberries infected by Phytophthora cactorum

AIMS: Volatile compounds present in strawberries infected with Phytophthora cactorum, especially those responsible for the characteristic off-odour of such fruits were the subject of this study. METHODS AND RESULTS: Six strawberry varieties (Redgauntlet, Selva, Korona, Tenira, Real, Pegasus) inoculated with P. cactorum strain (PC-5), isolated from naturally infected fruit and one variety inoculated with 15 strains of P. cactorum in the laboratory were analysed. All the samples had a distinct, to a various degree, off-odour reminiscent of watercolour paint with phenolic notes. Volatile compounds were isolated by solid phase microextraction and simultaneous distillation extraction methods. To detect compounds responsible for the characteristic off-odour, gas chromatography-olfactometry was used. Two compounds were found to be responsible for the characteristic off-odour of strawberries infected by P. cactorum: 4-ethyl phenol and 4-ethyl-2-metoxy phenol (4-ethyl guaiacol). The content of these compounds in infected varieties ranged from 1.12 to 22.56 mg kg(-1) and 0.14-1.05 mg kg(-1) respectively. Other volatile compounds, not detected in noninoculated sound strawberries, were also identified: camphene, 1-octene-3-ol, 3-octanone, o-cymene, phenyl methanol, cis-linaloloxide, nonanal, phenyl ethyl alcohol, 2-undecanone and alpha-muurolene. SIGNIFICANCE AND IMPACT OF THE STUDY: Volatile compounds responsible for the characteristic off-odour of strawberries infected with P. cactorum were identified. Also compounds produced as a result of P. cactorum growth on strawberry fruit were characterized.     

Characteristics and Regulatory Properties of the H+-ATPase in a Plasma Membrane Fraction Purified from Arabidopsis thaliana

The aqueous two-phase partitioning technique was utilized to isolate a plasma membrane (PM) fraction from etiolated seedlings of Arabidopsis thaliana. The purification procedure adopted yielded a fraction highly enriched in PM as compared to inner membranes, with a recovery of about 30%, as judged from the activities of PM markers such as vanadate-sensitive ATPase, FC binding and UDP-glucose sterol glucosyltransferase. The purified PM fraction displayed vanadate-sensitive H⁺ pumping activity. Its purity was confirmed by the biochemical characteristics of its ATPase activity assayed in the absence of Ca²⁺: sensitivity to vanadate (IC₅₀ ca. 1 μM), Mg²⁺-dependence, insensitivity to molybdate, oligomycin and nitrate, pH optimum at 6.6. The PM H⁺-ATPase activity was stimulated by fusicoccin and by a controlled treatment of the PM with trypsin. In both cases stimulation was much stronger on the activity assayed at pH 7.5 than on the activity at pH 6.6. Moreover, neither fusicoccin nor the treatment with trypsin stimulated the portion of activity (30 to 40% at pH 7.5) which decayed upon preincubation of the PM in assay medium without ATP.     

Effects of Metalaxyl, Fosetyl-Al, Dimethomorph and Cymoxanil on Phytophthora cactorum of Peach Tree

The activity of metalaxyl, fosetyl-Al, dimethomorph, and cymoxanil against Phytophthora crown rot of peach trees was examined. Application of fosetyl-Al or metalaxyl by painting the trunk (150 g/l) of 3-year-old PR204 trees was inhibitory to growth of the fungus but neither dimethomorph nor cymoxanil were effective. Application of metalaxyl as a soil drench suppressed canker development when the treated trees were subsequently inoculated with Phytophthora cactorum . Fosetyl-Al significantly reduced the growth of fungus compared with cymoxanil, dimethomorph and control but it was not as effective as metalaxyl. Again, dimethomorph and cymoxanil did not influence canker development. Both metalaxyl and fosetyl-Al were active for at least 21 days after applications. Strips of trunk bark were removed from trees, that had been drenched with the tested chemicals 20 days before, and inoculated on the cambium side with P. cactorum . Metalaxyl was the most effective fungicide and fosetyl-Al significantly reduced the development of fungus compared with dimethomorph, cymoxanil and the untreated strips. Colonization of strips treated with dimethomorph was significantly less than untreated strips. In contrast, cymoxanil did not inhibit the growth of fungus. Application of metalaxyl or fosetyl-Al as trunk paint or a soil drench appear to be effective procedures for preventing Phytophthora rot of peach trees.     

Effect of Neutral Salts on Spectral Characteristics of Undegraded Phytochrome Partially Purified from Etiolated Pea Shoots

Spectral characteristics of partially purified undegraded peaphytochrome were investigated in different ionic conditions.At the red-light-induced photostationary state in low ionicstrength buffer phytochrome had reduced absorbance in its far-redpeak as reported previously. Elevation of the ionic strengthof the buffer reversibly increased the absorbance in the far-redregion at the photostationary state. It was found that the effectof increase of ionic strength was strengthened secondarily bychaotropicity of salts. It was confirmed that phytochrome preparations of low ionicstrength contained a photosensitive component(s) other thanthe red-light-absorbing form (P_R) and farred- light-absorbingform (P_FR) during photochemical transformation, as well as duringthe first several min in the dark after phototransformation.At high ionic strength, phytochrome became a two-component systemcomposed of only P_R and P_FR at the redlight-induced photostationarystate though a significant accumulation of another component(s)occurred during phototransformations. Increasing ionic strengthalso enhanced A723 of phytochrome at the red-light-induced photostationarystate. The effect could result from either an increased molefraction of P_FR at the photostationary state induced by redlight, or a change in the extinction coefficients of P_FR. ¹ Present address: Division of Biological Regulation, NationalInstitute for Basic Biology, Myodaijicho, Okazaki 444, Japan (Received March 18, 1981; Accepted August 3, 1981)     

壳梭孢素对质膜H~ -ATPase活力影响机制的研究进展

壳梭孢素 (FC)作为一种重要的研究工具广泛用于研究酸介导的生长反应和依赖于质子推动力的膜运输系统 ,FC刺激质膜H _ATPase的活性是通过FC结合蛋白 (FCBP)与H _ATPase发生作用。FCBP是 1 4_3_3蛋白家族成员之一     

Some Properties of Partially Purified Pyruvate Kinase from Euglena gracilis Klebs var. bacillaris

A method of purification of pyruvate kinase (EC 2.7.1.40) from light-grown Euglena gracilis var. bacillaris was developed which yielded an enzyme preparation purified 115-fold over crude extracts. During organelle formation, levels of pyruvate kinase in extracts prepared from cells engaged in light-induced chloroplast development do not change significantly. The enzyme has a molecular weight of approximately 240,000 and a requirement for both K⁺ and Mg²⁺. Fructose 1,6-diphosphate activates the enzyme when the concentration of phosphoenol-pyruvate is limiting; it does not activate when the concentration of ADP is limiting. ATP, citrate, and Ca²⁺ are inhibitors of the enzyme and inhibit the fructose 1,6-diphosphate stimulation of the enzyme activity. ATP inhibition is only partially reversed by high concentrations of fructose 1,6-diphosphate. Further reversal of inhibition can be achieved by dialysis. Ca²⁺-dependent inhibition can be reversed by a chelating agent but not by increased concentrations of Mg²⁺.